Catalogo de Genomica ROCHE 2014

Genomics and Cell Research
Instruments and Reagents

2014 Product Index
Dear Valued Customer,
We are pleased to provide you with the 2014 Roche Product Index. In keeping with
our commitment to reduce paper, we have introduced a leaner, easier-to-use product
overview.
Used together with our Roche website, this Product Index helps you to navigate the
following product categories:
Discovery Reagents
Sample Preparation
Laboratory Development Testing
PCR/RT-PCR
Sequencing Solutions
Cell Biology
Browse this listing of proven instruments and reagent systems for pinpointing when to
perform functional assays that analyze gene and protein expression. Find the cutting-
edge products to identify the cellular and molecular mechanisms used by normal and
diseased cells, with the goal of better understanding how we function. We hope the
solutions provided in this index create breakthroughs and improve laboratory efciency.
Thank you for using our high quality and outstanding Roche service.
Best wishes,
Roche
4
www.roche-applied-science.com
Roche Innovates Life Science Research
1. Discovery Reagents
2. Sample Preparation
3. Laboratory Developed Testing
Roche provides a wide variety of essentials for research
laboratories, that are complimentary with the analysis
technologies referred in subsequent chapters. Trust the
high standard of quality and reliability. Thoroughly tested
reagents with superb quality are the driving factors for
success delivering performance you essentially need for
your tricky experiments.
Choose from a broad portfolio for hybridization experiments,
cloning, labeling, enzymatic analysis or simply laboratory
buffers and gels. Basic research made easy.
High quality nucleic acid purication is the gateway to
all genomic analysis. Use proven Roche High Pure Spin
Column products and stabilization/extraction reagents
for state-of-the-art nucleic acid purity and yield. To
streamline your laboratorys automated workow, use the
MagNA Pure Compact and MagNA Pure LC 2.0 Sample
Preparation Systems.
Proven technology and performance reach the next level
with MagNA Pure 96 Automated Sample Preparation
Systems. DNA and/or RNA from up to 96 samples can
be isolated in less than one hour from a broad variety
of sample materials using barcoded, prelled reagents.
Now available for IVD applications.
Improve your cell analysis results. Purify proteins using
cOmplete His-Tag Purication Resin, now applicable
with any buffer with EDTA or DTT for the highest protein
stability without loss of capacity. Proven cOmplete ULTRA
and PhosSTOP Protease Inhibitor Tablets are the easy way
to stabilize the protein you spent days isolating.
The future of rapid laboratory-developed testing powered
by Roche.
The FLOW System offers workow standardization and
data automation while keeping full exibility, from primary
sample to qPCR result.
Acquire optimal results and peace of mind with our multi-
plex-optimized one-step master mix and newly developed
internal control you can rely on from extraction through
qPCR.
Maximize your labs testing potential: Flexibly handle
high sample throughputs and a variety of targets while
minimizing turnaround time. Eliminate sources of error
and embrace a new level of result safety with the FLOW
Systems automated qPCR detection.
5
Roche Innovates Life Science Research
5. Sequencing Solutions
6. Cell Biology
The Roche portfolio of proven DNA sequencing and target
enrichment solutions is advancing research in human health,
agriculture, evolutionary biology and more. The GS FLX+
System and benchtop GS Junior System offer the unique
combination of powerful next-generation sequencing
throughput and the familiarity of long Sanger-like read
lengths (up to 1,000 bp).
SeqCap EZ Libraries and reagents enrich target DNA
regions for a variety of next-generation sequencing plat-
forms, allo wing researchers to selectively sequence the
human exome, human disease-associated genes, or
genomic regions of interest in a wide range of non-human
species. The broad portfolio of products with complete
custo mization enables researchers to achieve best-in-class
target enrichment efciency and uniform coverage in
variant discovery studies.
Easily transfect a large variety of cell types using the
low cytotoxic X-tremeGENE HP or choose between nine
additional Transfection Reagents. Use Liberase Enzyme
Blends to isolate increased numbers of viable primary
cells with high efciency.
The Cedex HiRes Analyzer leads the next generation of
cell culture analysis, featuring high-resolution scanner-
based imaging that enables deeper insights into even
subtle changes in your cell culture. Based on the Trypan
Blue Exclusion Method, this optimized successor to the
world-class Cedex Analyzer offers additional functionality,
precise measurements, and state-of-the-art automation.
4. PCR/RT-PCR
The Roche LightCycler
96 Real-Time PCR Instrument

combines accuracy and speed with convenient handling
using touchscreens and powerful software for data analysis.
The proven LightCycler
480 Real-Time PCR System is the

preferred high-end solution for high-throughput gene
expression and genetic variation analysis.
Roche has mastered the science of enzyme blending to
bring premium performance to PCR and RT-PCR products.
Choose Roches dNTPacks, convenient products that
combine PCR-Grade Nucleotides, thermostable enzymes
and enzyme blends, and all associated products such as
buffers and PCR-enhancing additives in one convenient
pack.
6
Your Link to Product Details
We are proud to present further product details on the following links:
Detailed information about products, local contact, terms and conditions:
Online Catalog on www.roche-applied-science.com
General Information about Legal Statement and Trademarks:
https://www.roche-applied-science.com/new/legal
Regulatory and Patent License Disclaimers for individual products:
www.technical-support.roche.com All 454 Life Sciences products mentioned in this catalog are labeled For life
science research only. Not for use in diagnostic procedures. For License Disclaimer information of 454 Sequencing
products please refer to the Instructions for Use.
7
Table of Contents
1 Discovery Reagents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Nucleic Acid Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Protein Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Antibodies and Detection Substrates . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Nucleotides and Analogs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Catabolic Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Metabolite Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Laboratory Reagents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
2 Sample Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Automated Sample Preparation of Nucleic Acids . . . . . . . . . . . . . . . 43
Manual Sample Preparation of Nucleic Acids . . . . . . . . . . . . . . . . . . . 50
Isolation of Cells - Tissue Dissociation . . . . . . . . . . . . . . . . . . . . . . . . . 53
Degradation of Cellular Components . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Isolation of Proteins . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
3 Laboratory Developed Testing . . . . . . . . . . . . . 60
FLOW System Instruments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
FLOW System -Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
FLOW System -Asseccories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
FLOW System -Disposables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
4 PCR/RT-PCR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
PCR/RT-PCR Enzymes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
qPCR Systems and Associated Products . . . . . . . . . . . . . . . . . . . . . . . 67
qPCR/qRT-PCR Reagents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
RealTime ready . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Universal ProbeLibrary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
5 Sequencing Solutions . . . . . . . . . . . . . . . . . . . . . . . . . 84
GS Junior System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
GS FLX+ System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
GS FLX System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86
Assays . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87
Sequence Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
6 Cell Biology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
Cell Counter and Analyzer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
Cell Imaging Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Transfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Cell Culture Reagents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 94
Mycoplasma Detection and Elimination . . . . . . . . . . . . . . . . . . . . . . . . 96
Growth Factors and Cytokines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96
Reporter Gene Detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
Apoptosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Cytotoxicity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 101
Cell Proliferation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 101
Oncology Research . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102
Virus Research . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 103
7 Alphabetical Product Index . . . . . . . . . . . . . . . . 104
8 Products by Catalog Number . . . . . . . . . . . . . 184

1
Dis
8

www.r

Nu
Lab
Kits
Prod
High

Conv
solut
tripho
kit fo
Nick

Labe
of the
the n
DNA
Rand

Unifo
modi
many
South
SP6/

For in
SP6 o
nonra
hybri
Enz
Prod
DNA

This
conta
trans
Klen

Use t
techn
in rec
oligo
Klen

This s
Sang
be us
the e
Polyn

Use t
DNA
phos
witho
SP6

Trans
prom
Use l
prote
T3 R

Trans
prom
Use l
synth
T4 D

Labe
hybri
must
Gene

scovery
roche-applied-sc
ucleic Acid
beling of Nu
s for Labeling
duct Name
h Prime DNA Lab
venient, rapid rand
ions offer a choice
osphates (
32
P,
35
S,
or many different h
k Translation Kit
l DNA with radioa
e helix, incorporati
nicked site. Use lab
/RNA transfer hyb
dom Primed DNA
ormly label plasmid
fied dNTP. High sp
y hybridization tech
hern and northern
/T7 Transcription
n vitro transcriptio
or T7 promoter. Sy
adioactively labele
dizations, genomic
ymes for Lab
duct Name
A Polymerase I
recombinant DNA
ain DNase I). It can
slation (with added
ow Enzyme
this labeling-grade
niques, such as 3-
cessed DNA ends
nucleotides during
ow Enzyme
sequencing grade
ger DNA sequencin
sed in 3-end label
elongation of oligon
nucleotide Kinas
to phosphorylate 5
or RNA using [
phate exchange, a
out altering their 5
RNA Polymerase
scribe RNA from c
moter. Perform synt
abeled RNA in DN
ection, and synthes
RNA Polymerase
scribe RNA from c
moter. Perform synt
abeled RNA in RN
hesis of capped RN
DNA Polymerase
l 3'-termini of DNA
dization probe. DN
t have 5-protrudin
e 32 Protein in site-
Reagent
cience.com
d Analysis
cleic Acids
g of Nucleic A
eling Kit
om-primed DNA l
e in the selection o
,
3
H, digoxigenin, f
ybridization techn
ctive or modified d
ing labeled nucleo
beled probes in co
bridization, and ISH
A Labeling Kit
d or phage DNA w
pecific activity labe
hniques, including
blots, and in situ
n Kit
on of DNA sequenc
ynthesize labeled R
ed ribonucleotides.
c sequencing, and
beling of Nucl
A Polymerase I is en
n therefore be use
d DNase I) and sec
e enzyme from E. c
-end labeling, rand
to create blunt-en
g site-directed mut
enzyme is specific
ng (dideoxy-chain
ing, random DNA
nucleotides.
se
5' ends of DNA or
-
32
P]-ATP either b
and to remove 3'-p
' ends (at low pH o
e
cloned DNA templa
thesis with labeled
NA/RNA blots, in s
sis of capped RNA
cloned DNA templa
thesis with labeled
NA/DNA blots, ISH
NA in vitro with m7
A, producing highl
NA labeled with re
ng ends. Blunt-end
-directed mutagen
ts
s
Acids
abeling kit. Suppli
of modified deoxyr
fluorescein, biotin,
iques.
dNTPs. Enzymes n
otides as polymeras
lony/plaque hybrid
H.
with any [-
32
P]-d
eled DNA probes a
g gene library scree
hybridizations.
ces cloned downst
RNA using radioact
. Use in DNA/RNA
S1 nuclease stud
leic Acids
ndonuclease-free
d for labeling of D
cond-strand synthe
coli in many molec
dom primed DNA l
nded DNA, and elo
tagenesis.
cally prepared and
termination metho
labeling, fill-in rea
RNA, label 5'-hydr
by direct phosphor
phosphates from R
only).
ates downstream f
d NTPs to generate
situ hybridization, R
A in vitro .
ate downstream fr
d NTPs, generating
, RNase protection
7GpppG or m7Gpp
ly labeled DNA for
ecombinant T4 DNA
d DNA will not wor
nesis.
ed nucleotide
ibonucleoside
, etc). Use this
ick one strand
se proofreads
dization,
dNTP or
are used in
ening,
tream of the
tive or
A
ies.
(does not
DNA by nick
esis of cDNA.
cular biology
labeling, filling
ongation of
d tested for
od). It can also
actions, and
roxyl ends of
rylation or by
RNA or DNA
from an SP6
e labeled RNA.
RNase
rom a T3
g labeled RNA.
n, and
ppA.
r use as
A Polymerase
rk. Use with T4

Cat. No.
11 585 584 001
10 976 776 001
11 004 760 001
10 999 644 001
Cat. No.
10 642 711 001
10 642 720 001
11 008 404 001
11 008 412 001
10 104 531 001
10 174 645 001
10 633 542 001
10 810 274 001
11 487 671 001
11 031 163 001
11 031 171 001
11 004 786 001
11 004 794 001

1 kit for up
labeled nucleo
1 kit for up to
1 kit for
1 kit for up t
2
Pack Size
to 50 labeling reac
otide of choice, 0.0
per assay

o 50 standard labe

up to 50 labeling r

to 2 x 20 transcript

Pack Size
250 U
1,000 U

100 U
500 U

250 U (5 x 10
3
U/m

200 U
1,000 U

1,000 U
5,000 U

1,000 U
5,000 U

100 U
500 U

ctions with a
01 to 2 g DNA
eling reactions
reactions
tion reactions
ml)

Price in
505,10
408,50
452,70
587,00
Price in
146,20
486,00
109,20
438,70
275,00
217,20
864,20
111,90
433,40
111,90
433,40
204,10
771,90

Di

T4 P

Phos
RNA
CMP
label
T7 R

Trans
prom
Use R
synth
Term

Add
fragm
and 3
ddNT
PCR
Prod
PCR

Add
hybri
when
ELISA
PCR

Conv
produ
conve
Micro
PCR

Conv
100 t
ELISA
sequ
PCR

Conv
produ
No. 1
paral
PCR

Gene
low-c
Probe
remo
PCR

For d
PCR.
in PC
produ
PCR

Direc
PCR.
diges
Urac
Hybr

Use i
ELISA

scovery
olynucleotide Kin
phorylate 5'-hydro
and DNA, 3' ends
, forming 5'[
32
P]pC
ing of RNA with T4
RNA Polymerase
scribe RNA from c
moter. Perform synt
RNA in RNA/DNA
hesis, and synthesi
minal Transferase
nucleotides to the
ments, such as for
3-end labeling wit
TPs (e.g ., DIG-ddU
R Product L
duct Name
Fluorescein Lab
mix directly to PCR
dization probes. P
n limited amounts
A, membrane hybr
ELISA, DIG-Labe
venient nonradioac
ucts for detection
entional ethidium
oplate format is ide
ELISA, DIG-Dete
venient, nonradioac
times more sensitiv
A format makes de
ence in large sam
ELISA, DIG-Dete
venient, nonradioac
ucts; 5-pack is the
1636111910), prov
lel testing of a larg
DIG Probe Synth
erate highly sensiti
copy gene detectio
es labeled with alk
oval of digoxigenin
DIG Labeling Mi
direct labeling of am
The PCR DIG labe
CR. The nucleotide
uct combined with
DIG Labeling Mi
ct labeling of ampl
Prevent PCR carry
st contaminating P
il-DNA Glycosylas
ridization Buffer
n combination wit
As for application
Reagent
nase, 3'-phospha
oxyl ends of oligon
s of RNA, and add
Cp. This substrate
4 RNA ligase.
cloned DNA templa
thesis with labeled
blots, ISH, RNase
s of capped RNA
e
3-OH ends of do
homopolymeric ta
th either radioactiv
UTP).
Labeling and
beling Mix
Rs to produce fluo
articularly useful f
of target DNA is a
ridization, or ISH.
eling
ctive method adds
using PCR ELISA;
bromide staining o
eal for automation
ection
ctive method for la
ve than ethidium b
etermining presenc
ple numbers easy.
ection, 5-pack
ctive method for la
e high capacity ver
viding more reage
ge number of sam
hesis Kit
ve hybridization pr
on of rare mRNA in
kaline-labile digoxi
label after detecti
ix
mplification produ
eling mix can repla
concentration ens
h DIG detection.
ix
PLUS

ification products
yover by incorpora
PCR products from
e.
th the PCR ELISA a
in nucleic-acid hyb
ts
atase free
ucleotides and link
a 5'[
32
P]-terminal
is commonly used
ate downstream fr
d NTPs, generating
protection, microa
in vitro .
uble- or single-str
ailing or end-labeli
ve or chemically m
d Detection
rescein-labeled DN
for synthesizing DN
available. Use label
a DIG label to you
100 times more se
of products using
n.
abeling and detect
bromide staining o
ce or absence of s

abeling and detect
rsion of the standa
nts, but lacking co
ples.
robes using PCR. S
n Southern and no
igenin (DIG)-dUTP
ion are stable for o
cts using digoxige
ace the unlabeled
sures maximum yie
using digoxigenin
ating dUTP instead
previous amplifica
and the series of D
bridization reactio
kers, 5' ends of
label to 3'-
d for 3'-end
rom a T7
g labeled RNA.
array target
randed DNA
ng with dNTPs,
modified
NA
NA probes
led probes in
ur PCR
ensitive than
agarose gels.
t PCR products;
n agarose gels.
specific target
ting PCR
ard kit (see Cat.
ontrols. For
Suitable for
orthern blots.
P for easy
over one year.
enin-dUTP in
nucleotide mix
eld of PCR
(DIG)-dUTP in
of dTTP and
ations using
DIG-detection
ns.

10 709 557 001
10 838 292 001
10 881 767 001
10 881 775 001
03 333 566 001
03 333 574 001
Cat. No.
11 636 154 910
11 636 120 910
11 636 111 910
11 965 409 910
11 636 090 910
11 585 550 910
11 835 289 910
11 717 472 001

8,000 U (fo
reacti
24,000 U (fo
reacti
100 l for up
1 kit
1 kit for 1
microplates
detec
1 kit for 4
microplates), th
number of
standar
1 kit for up to 2
volume (one
labeled pro
500 l (2 x 250
reactions of 1
co
2 x 250 l for u
50
200 U
1,000 U

1,000 U
5,000 U

or 20 tailing or 3'-e
ons, 400 U per rea
ons, 400 U per rea

Pack Size
p to 10 PCR reactio
of 100 l

t for up to 50 react

192 detection react
s), allows the semi-
ction of 50 PCR pro

480 detection reac
he number of tests
required sample d
rd and/or control r

25 reactions of 50
e reaction can prod
obe to analyze 650
membrane)

0 l) for up to 2 x 2
00 l final reaction
oncentration 200

up to 2 x 50 reactio
l final reaction vol

100 ml

www.roche
end labeling
action)
end labeling
action)
ons, reactions
tions
tions (two
-quantitative
oducts
tions (five
depends on the
dilutions and
eactions
l final reaction
duce enough
0 cm
2
of blot
25 PCR assays,
n volume, final
M
ons, reactions of
lume
e-applied-science

306,80
947,10
111,90
433,40
100,10
225,20
Price in
338,80
576,00
527,20
911,30
457,50
414,40
414,40
80,70

1
9

e.com

1
Dis
10

www.r

Pro
Kits
Prod
DIG

Nonr
dUTP
subst
dot b
DIG-

Comp
dUTP
probe
and c
DIG-

Comp
chem
labele
South
DIG

Produ
chem
Desig
reage
Kits
Prod
DIG

Nonr
dUTP
detec
chrom
DIG

Comp
(SP6/
effici
and R
DIG

3'-en
using
oligo
mem
DIG

For fa
11-dU
with
blots
Mix
Prod
Bioti

Comp
probe
after
situ ,
Bioti

Labe
polym
north
and i
DIG

Easy-
11-dU
or in
0.65

scovery
roche-applied-sc
oducts for M
s for Labeling
duct Name
DNA Labeling an
radioactive random
P, followed by colo
trates NBT and BC
blots, and colony a
-High Prime DNA
plete, convenient k
P and color detecti
es in 1 hour to ove
colony/plaque hyb
-High Prime DNA
plete, convenient k
milumiluminescent
ed probe in 1 hour
hern/northern blot
Northern Starter
uce DIG-labeled R
miluminescent dete
gned for the novice
ents proven to pro
s for Labeling
duct Name
DNA Labeling Ki
radioactive random
P. Used for in situ
ction. Detect labele
mogenic or chemil
RNA Labeling Ki
plete kit for RNA la
/T7). DIG-labeled r
ency. Used in nort
RNase protection e
Oligonucleotide
nd labeling of oligo
g DIG-11-ddUTP a
nucleotides are us
brane-blot applica
Oligonucleotide
ast and sensitive ta
UTP and recombin
DIG-dUTP are use
or in situ hybridiz
xes and Reag
duct Name
in-High Prime
plete reaction mix
es. Biotin-labeled
overnight incubat
and colony and pl
in RNA Labeling
l RNA with Biotin-
merases (SP6, T3, a
hern, and dot blots
in situ and microa
DNA Labeling M
-to-use nonradioac
UTP. For Southern
situ hybridization;
mM dTTP, 0.35 mM
Reagent
cience.com
Membrane H
g and Detectio
nd Detection Kit
m primed labeling o
r detection using a
CIP. Use labeled pr
nd plaque screeni
A Labeling and De
kit for random prim
on of labeled hybr
ernight incubation.
bridizations.
A Labeling and De
kit for random-prim
detection of labele
r to overnight incu
ts, colony/plaque h
r Kit
RNA probes to use
ection reagents for
e DIG system user
vide successful, re
g
it
m primed labeling o
and filter hybridiza
ed hybrids using a
luminescence AP s
t (SP6/T7)
abeling using DIG-
run-off transcripts
thern/Southern blo
experiments.
3'-End Labeling
onucleotides from
nd recombinant Te
sed as hybridizatio
ations and in situ h
Tailing Kit, 2nd g
ailing of oligonucle
nant Terminal Tran
ed for DNA or RNA
zation.
ents for Labe
for efficient rando
probes are genera
ion. Use in Southe
laque lifts.
Mix
-16-UTP by in vitro
and T7). Labeled R
s, plaque and colon
rray hybridizations
Mix
ctive rapid random
, northern, and do
; 10x solution with
M DIG-11-dUTP.
ts
Hybridization
on
of DNA probes usi
anti-DIG-AP conju
robes in Southern,
ng.
etection Starter
med DNA labeling
rids. Obtain high y
. Use in Southern/
etection Starter
med DNA labeling
ed hybrids. Obtain
ubation. Use in
hybridization.
with the supplied
r northern blotting
r. This Starter Kit c
eproducible results
of DNA probes wit
ations and single-c
anti-DIG-AP conjug
substrates.
-11-UTP by in vitro
are synthesized w
ots, ISH, plaque or
Kit, 2nd generati
14 to 100 nucleotid
erminal Transferas
n probes in all typ
hybridization.
generation
eotides at the 3'-e
nsferase. Oligonucl
A hybridization in m
eling
om primed labeling
ated at high yield w
ern, dot, and northe
o transcription usin
RNA can be used i
ny lifts, RNase prot
s.
m primed labeling m
t blots, colony and
1 mM dATP, dCTP
n
ing DIG-11-
ugate and the
northern, and
Kit I
using DIG-11-
ields of labeled
northern blots,
Kit II
with DIG and
n high yield of
techniques.
ontains the
s.
th DIG-11-
copy gene
gate and
o transcription
with high
colony lifts,
ion
des in length
se. DIG-labeled
pes of
nd using DIG-
leotides tailed
membrane
g of DNA
within 1 hour or
ern blotting, in
ng RNA
n Southern,
tection assays,
mix with Dig-
d plaque lifts,
P, dGTP (each),

Cat. No.
11 093 657 910
11 745 832 910
11 585 614 910
12 039 672 910
Cat. No.
11 175 033 910
11 175 025 910
03 353 575 910
03 353 583 910
Cat. No.
11 585 649 910
11 685 597 910
11 277 065 910

1 kit for up to 2
of 50 blots,
1 kit for up to 1
of 24 blots, 10
1 kit for up to 1
of 24 blots, 1
1 kit for up to 1
of 10 blots, blot
DNA, yielding
1 kit for up to 4
1 kit for up
1 kit for up to 2
oligonucleotide
of a
1 kit for up to
oligonucleotide
of a
100 l for up t
tem
40 l for up
50 l for
Pack Size
5 labeling reaction
10 ng to 3 g per
of 100 cm
2

2 labeling reaction
ng to 3 g DNA p
of 100 cm
2

2 labeling reaction
0 ng to 3 g per a
100 cm
2

0 labeling reaction
ts of 10 x 10 cm
2
r
approx. 20 g labe

Pack Size
0 labeling reaction
DNA per assay

p to 2 x 10 labeling

25 labeling reactio
s per assay corres
30-mer oligonucle

o 25 tailing reactio
e per assay corresp
30-mer oligonucle

Pack Size
o 25 labeling assay
mplate DNA per as

p to 20 transcriptio

up to 25 standard

ns and detection
assay, blots
ns and detection
per assay, blots
ns and detection
assay, blots of
ns and detection
reactions of 1g
eled RNA, each
ns, 10 ng to 3 g
g reactions
ons, 100 pmol of
sponding to 1 g
eotide
ons, 100 pmol
ponding to 1 g
eotide
ys, 0.01 to 3 g
ssay
on reactions
reactions

Price in
801,40
484,80
493,20
508,20
Price in
626,60
590,90
571,60
531,40
Price in
351,60
184,80
164,50

Di

DIG

Mixtu
(SP6/
and R
(each
DIG-

Prem
Obta
incub
dot b
Digo
hydr

For D
via am
with
group
Fluor

RNA
T7, o
enzym
(Sout
Fluor

Conv
prime
at hig
lifts,
Hexa

This
prime
in ma
and n
High

Labe
prime
librar
50 to
Kits
Prod
DIG

Conta
acid
labele
and t
DIG

High
South
chem
meth
Hyb
Prod
DIG

Read
using
Hyb b
nonto
DIG

Block
labele
100 m
made
DIG W

The D
hybri
block

scovery
RNA Labeling M
ure for RNA labelin
/T7/T3). Used in no
RNase protection e
h), 6.5 mM UTP, 3.5
-High Prime
mixed solution for ra
in high yields of la
bation. Use labeled
blots, and colony/p
oxigenin-3-O-me
oxysuccinimide e
DIG labeling of pro
mino groups (unde
NH
2
-groups of pro
p, digoxigenin, is b
rescein RNA Lab
labeling with Fluo
r T3 RNA polymera
me-conjugated an
therns, northerns,
rescein-High Pri
venient enzyme an
ed labeling of DNA
gh yield for use in
ISH, and library sc
anucleotide Mix
10x Hexanucleotid
ed DNA labeling. H
any hybridization t
northern blots, and
h Prime
l DNA with radioa
ers. Labeled probe
ry screening, and i
remove unincorpo
s for Detectio
duct Name
Nucleic Acid Det
ains all reagents to
hybrids. Used in S
ed nucleic acids a
the color substrate
Luminescent Det
ly sensitive, specif
hern/northern blot
miluminescent subs
hods, with shorter e
bridization Re
duct Name
Easy Hyb
dy-to-use blocking
g nonradioactive, d
buffer cannot be u
oxic solution and d
Easy Hyb Granul
king buffer for mem
ed nucleic acid pro
ml of a 1x working
e solutions and lon
Wash and Block
DIG Wash and Blo
dization and DIG d
king solution and m
Reagent
ix
ng using DIG-11-U
orthern/Southern b
experiments; 10x s
5 mM DIG-11-UTP
andom primed DN
abeled probes with
d probes in library
plaque hybridizatio
ethylcarbonyl--
ester
teins and 5'-amino
er gentle condition
oteins or oligonuc
bound by Anti-Dig
beling Mix
orescein-12-UTP by
ases. Detect labele
ti-fluorescein, and
plaque lifts, ISH).
me
d nucleotide mix f
A with fluorescein-
Southern, norther
reening.
de Mix has all poss
High specific activ
echniques for scre
d in situ hybridizat
ctive dCTP using r
es are used in Sout
in situ hybridizatio
orated nucleotides
on
tection Kit
o detect membran
Southern, northern,
re detected using
es NBT and BCIP.
tection Kit
ic detection of DIG
ts and plaque/colo
strate CSPD. Signa
exposure times.
eagents
buffer for all mem
digoxigenin-labeled
used for in situ hyb
does not contain fo
es
mbrane hybridizat
obes (not for ISH).
solution; 6 x 100 m
ng-term storage.
Buffer Set
ck Buffer Set is us
detection. The set
maleic acid, washin
ts
UTP by in vitro tran
blots, ISH, plaque
solution of 10 mM
P.
NA labeling using D
hin one hour or ove
screening, Southe
ns.
-aminocaproic ac
o-substituted oligo
ns). One reactive g
leotides. The other
oxigenin and dete
y in vitro transcrip
ed RNA directly or
d use in hybridizati
or highly efficient
-dUTP. Generate la
n, and dot blots, co
sible sequences fo
ity labeled DNA pr
eening gene librari
tion.
random oligonucle
thern northern, an
ons. Use Quick Spi
s.
e-blotted, DIG-lab
, and dot blots, and
anti-DIG-AP antib
G-labeled nucleic a
ony lifts with anti-D
al is as sensitive as
mbrane hybridizatio
d nucleic acid pro
bridization. The bu
ormamide.
ion using nonradio
. Dissolve granules
ml portions allow f
sed at various step
contains 10x prep
ng, and detection
nscription
or colony lifts,
ATP, CTP, GTP
DIG-11-dUTP.
ernight
ern, northern,
cid-N-
onucleotides
group interacts
r functional
cted.
ption using SP6,
r with an
on techniques
random
abeled probes
olony/plaque
r random
robes are used
ies, Southern
eotides as
d dot blots,
n Columns, G-
beled nucleic
d ISH. DIG-
body conjugate
acids in
DIG-AP and the
s radioactive
on applications
bes. DIG Easy
ffer is a
oactive DIG-
s in water for
for freshly
s of DIG
arations of
buffers.

11 277 073 910
11 585 606 910
11 333 054 001
11 685 619 910
11 585 622 910
11 277 081 001
11 585 592 001
Cat. No.
11 175 041 910
11 363 514 910
Cat. No.
11 603 558 001
11 796 895 001
11 585 762 001

40
160 l for up t
tem
40
100 l for up t
tem
100
200 l fo
1 kit for up
1 kit for u
gr
1
l for up to 20 reac

o 40 labeling assay
mplate DNA per as

5 mg

l for up to 20 reac

o 25 labeling assay
mplate DNA per as

l for up to 50 reac

or up to 50 labelin

Pack Size
p to 40 blots of 10

up to 50 blots of 1

Pack Size
500 ml

ranules for 6 x 100

set for up to 30 blo

www.roche
ctions
ys, 0.01 to 3 g
ssay
ctions
ys, 0.01 to 3 g
ssay
ctions
g assays
cm x 10 cm
0 x 10 cm
ml
ots
e-applied-science

168,70
560,20
190,90
168,70
430,70
60,40
382,80
Price in
413,20
541,40
Price in
279,30
321,10
264,40

1
11

e.com

1
Dis
12

www.r

Bloc

Block
filter
Block
Mem
Prod
Nylo

Matr
(DIG)
RNA,
Stron
hybri
Nylo

Unch
phag
chem
biotin
Hybr

Use t
stand
proce
sequ
Pro
Mix
Prod
DIG

Mixtu
(SP6/
and R
(each
Fluor

RNA
T7, o
enzym
(Sout
Nick

Optim
hybri
to de
chrom
DIG-

Conv
labele
for fil
the D
Bioti

Enzym
Biotin
for fil
High
Ma
Res
Prod
Aat I

Aat I
with
recog
5230
Acc

Acc I
fragm
meth
Acc I

scovery
roche-applied-sc
cking Reagent
king Reagent is us
hybridization and
king reagent does
mbranes
duct Name
on Membranes, p
ix for hybridization
) and biotin, or rad
, or oligonucleotide
ngest signals and l
ds.
on Membranes fo
harged microporou
ge/cosmid libraries
miluminescent/ chr
nylated or radioact
ridization Bags
these bags in nonr
dard radioactive pr
edures. All hybridiz
entially to the sam
oducts for in
xes for Label
duct Name
RNA Labeling M
ure for RNA labelin
/T7/T3). Used in no
RNase protection e
h), 6.5 mM UTP, 3.5
rescein RNA Lab
labeling with Fluo
r T3 RNA polymera
me-conjugated an
therns, northerns,
k Translation Mix
mized enzyme mix
dization. Designed
etect multicopy or v
msomes or interph
-Nick Translation
venient enzyme nu
ed using DIG-11-d
lter hybridization. F
DIG-High Prime kit
in-Nick Translati
me nucleotide mix
n-16-dUTP for use
Prime.
apping and C
striction Enzy
duct Name
II
I recognizes the se
3-cohesive termin
gnition sequence a
I and Zra I.
I
I recognizes the se
ments with 5-cohe
hyladenine and 5-m
I is an isoschizome
Reagent
cience.com
sed to decrease the
the detection of n
not contain BSA.
positively charged
n with nonradioact
dioactive labeling u
e probes, for Sout
owest background
or Colony and Pla
us nylon membran
s with DIG probes a
romogenic substra
tive probes. Pore s
radioactive hybridi
robe hybridizations
zation solutions an
me bag.
n situ Hybrid
ing
ix
ng using DIG-11-U
orthern/Southern b
experiments; 10x s
5 mM DIG-11-UTP
beling Mix
orescein-12-UTP by
ases. Detect labele
ti-fluorescein, and
plaque lifts, ISH).
x
generates sensitiv
d for direct fluorop
very large hybridiz
hase nuclei.
n Mix
cleotide mix to ge
dUTP for in situ hy
For highly sensitive
ts.
on Mix
xture for generating
e in in situ hybridiz
Cloning of N
mes
equence GA*CGT
ni. It is inhibited by
as indicated (*). Aa
equence GT(A,C)
esive termini. It is i
methylcytosine as i
er to Fbl I and Xmi
ts
e background in n
ucleic acid hybrids
d
tive labeling using
using
32
P,
35
S,
3
H
thern, northern an
d obtained with DI
aque Hybridizatio
e for nonradioactiv
and detection with
ates. Use in hybridi
size: 1.2 m.
zation and detecti
s, and western blo
nd blocking buffer
dization
blots, ISH, plaque
solution of 10 mM
P.
ed RNA directly or
ve probes for fluor
phore-labeling of in
zation targets on m
nerate highly sens
ybridization. The m
e filter hybridizatio
g sensitive probes
zation. The mix can
NA
*C and generates
y 5-methylcytosine
at II is a neoschizo
(T,G)*A*C and gen
nhibited by the pre
indicated (*) on the
I.
onradioactive
s. This Roche
digoxigenin
with DNA,
d dot blotting.
G-labeled
on
ve screening of
h
izations with
on procedures,
tting
can be added
nscription
or colony lifts,
ATP, CTP, GTP
ption using SP6,
r with an
on techniques
escence in situ
n situ probes,
metaphase
sitive probes
mix can be used
on probes, use
labeled with
n also be used
on, use Biotin-
fragments
e in the
omer of Ssp
nerates
esence of N6-
e sequence.

11 096 176 001
Cat. No.
11 209 272 001
11 209 299 001
11 417 240 001
11 699 075 001
11 699 083 001
11 666 649 001
Cat. No.
11 277 073 910
11 685 619 910
11 745 808 910
11 745 816 910
11 745 824 910
Cat. No.
10 775 207 001
10 728 438 001

10
20
50 disc
50 discs
40
40
200 l for
160 l for
160 l for
50 g

Pack Size
0 sheets (20 x 30 c
0 sheets (10 x 15 c
1 roll (0.3 x 3 m)
cs (each 82 mm dia
s (each 132 mm d

50 bags

Pack Size
l for up to 20 reac

l for up to 20 reac

r up to 50 labeling

r up to 40 labeling

r up to 40 labeling

Pack Size
250 U (1 - 5 U/l)

500 U (5 U/l)

cm)
cm)
ameter)
iameter)
ctions
ctions
reactions
reactions
reactions
)

88,60
Price in
423,20
235,20
552,10
282,20
525,30
107,50
Price in
168,70
168,70
350,60
508,80
508,80
Price in
53,30
421,60

Di

Afl II

Afl III
fragm
5-me
Afl III
Alu I

Alu I
blunt
5-hyd
Isosc
Apa

Apa
with
indic
Bsp 1
Asp7

Reco
with
meth
inhib
Asp7

Reco
fragm
5-me
not in
Bam

Reco
5'-co
meth
resid
BbrP

Reco
blunt
recog
I, Pm
Bcl I

Reco
cohe
posit
meth
Bfr I

Reco
cohe
meth
I, Ms
Bgl I

Reco
cohe
but is
Bgl II
Bln I

Bln I
5-co
meth
Bsm

Reco
3'-co
sequ
Isosc
BssH

Reco
overh
gene
indic

scovery
II
I recognizes the se
ments with 5-cohe
ethylcytosine at the
I has no known iso
I
recognizes the se
t termini. It is inhib
droxymethylcytosin
chizomer: AluB I.
I
I recognizes the se
3-cohesive termin
ated (*) in the reco
120 I and Psp OMI
700 I (Xmn I)
ognizes the sequen
blunt termini. Inhib
hyladenine at the o
it. Isoschizomers:
718 I
ognizes GGTAC*C
ments with 5 cohe
ethylcytosine as ind
nfluence activity()
mH I
ognizes the sequen
ohesive termini. Ba
hylation, but is inhi
ue as indicated (*)
P I (PmaC I)
ognizes the sequen
t ends. The enzyme
gnition site as indic
aC I, Pml I, and Ps

ognizes the sequen
sive termini. Inhibi
ion of adenine. Inh
hylcytosine. Isoschi
(Afl II)
ognizes the sequen
sive ends. The enz
hylcytosine at the s
pC I, and Vha464
II
ognizes the sequen
sive termini. It is n
s sensitive to 5-me
I has no known iso
I (Avr II)
recognizes the seq
ohesive termini. Th
hylation. Bln I is an
I
ognizes the sequen
ohesive termini.Inh
ence as indicated
chizomers: BsaM I,
H II
ognizes the sequen
hanging ends. Belo
rate large fragmen
ated (*). Isoschizo
Reagent
equence A*C(A,G
esive ends. Afl III is
e site indicated (*)
oschizomers.
quence *AG*CT a
bited by 6-methylad
ne,or 4-methylcyto
equence GGG*CC
ognition sequence
.
nce G*AANNNN
bited by 6-methyla
other A() or presen
MroX I, Pdm I, Xm
C; same sequence
sive ends, not 3 e
dicated (*). Methyl
). Neoschizomer: K
nce GGAT*CC a
m H I is not inhibit
bited by 5- or 4-m
). Isoschizomer: Bs
nce CA*CGTG and
e is inhibited by 5-
cated (*). BbrP I is
spC I.
nce TG*AT*CA, ge
ited by the dam ge
hibited by 5-hydrox
zomers: Fba I, Ksp
nce *CTTAAG and
zyme is inhibited b
site indicated (*). Is
I.
nce AGAT*CT an
not inhibited by ove
ethyl and 5-hydrox
oschizomers.
quence CCTAGG
e enzyme is not kn
isoschizomer of A
nce G*AATGCNN
ibited by 6-methyl
(*). 5-methylcytos
Mva1269 I, Pct I.
nce G*CG*CGC an
ongs to a class of
nts of DNA. Inhibit
mers: BseP I, Pau
ts
G)(T,C)GT and gene
s inhibited by the p
on the recognition
and generates frag
denine, 5-methylcy
osine at the (*) in th
*C and generates
y 5'-methylcytosine
e. Apa I is a neosch
TTC and generate
adenine at the (*).
nce of 5-methylcyt
mn I.
e as Kpn I but gene
nds as from Kpn I
lation of A and cen
Kpn I.
and generates frag
ted by overlapping
methylcytosine at th
stI.
d generates fragm
-methylcytosine wi
s an isoschizomer o
enerating fragmen
ene and methylate
xymethyl-cytosine
p22 I.
d generates fragm
by the presence of
soschizomers: Afl I
nd generates fragm
erlapping dam met
xy-methylcytosine,
G and generates fra
nown to be affecte
Avr II, AspA2 I, and
N and generates fr
adenine within the
ine does not inhib
nd generates fragm
rare-cutter enzyme
ted by 5'-methylcyt
I.
erates
presence of
n sequence.
gments with
ytosine,
he sequence.
s fragments
e at the sites
hizomer to
es fragments
6-
tosine does not
erates
. Inhibited by
ntral C does
ments with
g dam
he internal C
ments with
ithin the
of Acv I, Eco72
nts with 5-
s the 6N-
, but not by 5-
ents with 5-
5-
II, BspT I, Bst98
ments with 5-
thylation (),
as shown (*).
agments with
ed by
d Xma I.
ragments with
e recognition
it ().
ments with 5-
es, which
tosine as

11 209 183 001
10 239 275 001
10 656 267 001
10 703 753 001
10 899 208 001
10 835 277 001
10 814 245 001
10 814 253 001
11 175 050 001
10 220 612 001
10 567 604 001
10 656 275 001
10 798 975 001
11 274 031 001
11 168 860 001
10 693 952 001
11 097 059 001
11 198 939 001
10 348 767 001
10 567 639 001
10 899 224 001
11 175 068 001
11 558 161 001
11 558 170 001
11 292 307 001
11 168 851 001

100 U (5 U/l)

500 U (10 U/l)
2,000 U (10 U/l)

20,000 U (40 U/l)
5,000 U (10 U/l)

500 U (10 U/l)

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)
1,000 U (10 U/l)
2,500 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
50,000 U (40 U/l)
500 U (10 U/l)

500 U (10 U/l)
2,500 U (40 U/l)

500 U (10 U/l)

500 U (10 U/l)
2,000 U (10 U/l)
2,000 U (40 U/l)
10,000 U (40 U/l)
200 U (10 U/l)
1,000 U (10 U/l)

200 U (10 U/l)

200 U (10 U/l)

www.roche

)

)
)
)

)

e-applied-science

261,50
78,80
228,50
317,90
97,90
73,90
68,20
284,20
284,20
29,50
57,90
199,10
199,10
807,70
91,40
68,20
175,10
64,80
68,20
181,90
181,90
534,30
131,80
528,70
114,90
114,90

1
13

e.com

1
Dis
14

www.r

BstX

Reco
with
5-me
enzym
Cfo I

Reco
cohe
simu
Isosc
Cla I

Reco
5'-co
5-me
BshV
Dde

Dde
5-co
5-hy
HpyF
Dpn

Reco
ends
at the
Mal I
Dra I

Dra I
blunt
the s
isosc
Dra I

Dra I
fragm
(*). Is
EclX

Reco
5-co
show
BseX
Eco4

Eco 4
with
as ind
Aor5
EcoR

Eco R
with
or bo
isosc
EcoR

Reco
blunt
(*). It
5-Hyd
Fok I

Reco
5'-co
dista
Neos
Hae

Reco
ends
C*. In
Isosc

scovery
roche-applied-sc
X I
ognizes the sequen
3-overhanging en
ethylcytosine within
me has no known
I (Hha I)
ognizes the sequen
ltaneous presence
chizomers: AspLE I
I
ognizes the sequen
ohesive termini. It is
ethylcytosine as sh
V I, BspD I, BspX I,
I
I recognizes the se
ohesive termini. It i
ydroxymethylcytosi
F3 I.
I
ognizes the sequen
. The enzyme is on
e indicated site (*)
I.
I
recognizes the se
t ends. Dra I is not
ite indicated () on
chizomer of Aha III
III
II recognizes the s
ments with 3-cohe
soschizomer: Ade I
I (Xma III)
ognizes the sequen
ohesive termini. Inh
wn (*). 5-methylcyto
X3 I, BstZ I, Eag I, E
47 III
47 III recognizes th
blunt ends. Eco47
dicated (*). 6-mety
1H I.
R I
RI recognizes the s
5-cohesive termin
oth A residues, and
chizomer to Rsr I.
R V
ognizes the sequen
t ends. Inhibited by
is not inhibited by
droxymethylcytosi
I
ognizes the sequen
ohesive termini. A C
nces from the seq
schizomers: BseG I
III
ognizes the sequen
. Inhibited by 5-me
nhibited by 5-hydro
chizomers: BshF I,
Reagent
cience.com
nce *CC*A(N)5NT
nds. BstX I is inhib
n the recognition s
isoschizomers.
nce G*CG*C and g
ited by 5-methylcy
e of 5-hydroxymeth
, BstHH I, Hha I.
nce *AT*CG*AT a
s inhibited by over
own (*). Isoschizo
Bsu15 I, BsuTU I.
equence *CTNAG
s inhibited by the
ine at the site indic
nce GmAT*C and
nly inhibited by the
if no 6-methylade
equence TTTAAA
inhibited by the p
n the recognition s
.
sequence C*A*CNN
esive termini. It is m
I.
nce *CGG*C*CG a
hibited by 5-methy
osine in position 4
Eco52 I.
he sequence AG*C
III is inhibited by t
yladenine is not inh
sequence G*A*AT
ni. EcoR I is inhibite
d by 5-methylcytos
nce G*ATATC an
y the presence of 6
y the presence of 5
ne. Isoschizomer:
nce GG*ATG(N)9/1
Class II S enzyme w
uence. Inhibited b
I, BstF5 I, BtsC I.
nce GG*CC, gene
ethyl and 5-hydrox
oxymethylcytosine
Bsn I ,BspAN I, Bs
ts
TGG and generates
ited by 6-methylad
sequence as indica
generates fragmen
ytosine, as shown (
hylcytosine at both
nd generates fragm
rlapping dam-meth
mers: Ban III, Bsa2
G and generates fr
presence of 5-me
cated (*). Isoschizo
generates fragme
e occurrence of 5-
enine is present. Is
A and generates fr
presence of 6-meth
sequence. Dra I is
NNGTG and gene
methlation sensitiv
and generates frag
ylcytosine in positio
4 also inhibits. Isosc
CGCT and genera
the presence of 5-
hibiting.Isoschizom
TT*C and generate
ed by 6-methylade
sine as indicated (*
nd generates fragm
6-methyladenine, a
5-methylcytosine (
Eco 32I.
13 and generates f
which cleaves dsD
y 6-methyladenine
erating fragments
xymethylcytosine a
at the external C
uR I, Pho I.
s fragments
denine and
ated (*). The
nts with 3-
(*). Inhibited by
h C residues.
ments with
hylation and
29 I, BseC I,
agments with
ethyl- or
omers: BstDE I,
ents with blunt
methylcytosine
oschizomer:
ragments with
hyladenine at
an
erates
ve as indicated
gments with
on 1 and 5 as
chizomers:
ates fragments
-methylcytosine
mers: Afe I,
es fragments
enine at either
*). Eco RI is an
ments with
as indicated
() or
fragments with
DNA at precise
e as shown (*).
with blunt
at the internal
.

11 117 777 001
11 117 785 001
10 688 541 001
10 404 217 001
10 656 291 001
11 092 758 001
10 835 307 001
10 742 970 001
10 742 988 001
10 827 754 001
10 843 547 001
11 131 397 001
11 167 103 001
10 200 310 001
10 606 189 001
10 703 737 001
11 175 084 001
10 667 145 001
10 667 153 001
11 040 197 001
11 004 816 001
10 693 944 001

250 U (10 U/l)
1,250 U (10 U/l)

1,000 U (10 U/l)

500 U (10 U/l)
2,500 U (10 U/l)
2,500 U (40 U/l)
1,000 U (10 U/l)

200 U (10 U/l)
1,000 U (10 U/l)

5,000 U (10 U/l)

500 U (1 - 5 U/l)

1,000 U (10 U/l)

100 U (5 U/l)

10,000 U (40 U/l)
50,000 U (40 U/l)
5,000 U (10 U/l)
10,000 U (10 U/l)
2,000 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
100 U (1 - 5 U/l)

5,000 U (10 U/l)

)

)
)

)

)
)
)

64,80
261,50
51,50
75,00
299,10
299,10
171,70
85,30
338,80
143,30
274,00
490,00
189,80
52,30
210,30
42,00
52,30
75,00
282,00
282,00
128,50
136,20

Di

Hind

Reco
blunt
inhib
recog
Hind

Reco
5-co
5-hyd
inhib
Hinf

Reco
5-co
5-me
5-hyd
Hpa

Reco
blunt
as ind
Isosc
Kpn

Reco
cohe
both
Ksp

Belon
fragm
gene
of 5'-
Mae

Reco
cohe
inform
FspB
Mae

Reco
cohe
by th
HpyC
Mae

Reco
cohe
not k
Mlu

Reco
cohe
sequ
meth
MluN

Reco
blunt
indic
Mro

Reco
cohe
inhib
Aor13
Mun

Mun
5-co
recog
Mva

Reco
cohe
resid
meth

scovery
d II
ognizes the sequen
ited by 5-hydroxym
gnition sequence.
d III
ognizes the sequen
ohesive termini. Inh
droxymethylcytosin
it (). Isoschizome
I
ognizes the sequen
ohesive termini. Se
ethylcytosine at 3p
droxymethylcytosin
I
ognizes the sequen
dicated (*). 5-meth
chizomers: KspA I.
I
ognizes the sequen
sive termini. Kpn I
C-residues or by 6
I (Sac II)
ngs to a class of ra
ments of genomic
rates fragments w
-methylcytosine. Is
e I
ognizes the sequen
sive termini. Supp
mation is available
I, Bfa I, Xsp I.
e II
ognizes the sequen
sive termini. Supp
e presence of 5-m
CH4 IV.
e III
ognizes the sequen
sive termini. Supp
known to be inhibit
I
ognizes the sequen
ence as indicated
hyladenine (). Isos
N I (Bal I)
ognizes the sequen
t ends. MluN I is in
ated (*). Isoschizo
I (Acc III)
ognizes the sequen
sive ends. Inhibite
ition by overlappin
3H I, BseA I, Bsp13
n I (Mfe I)
I recognizes the s
ohesive termini. Mu
gnition sequence a
I (BstN I)
ognizes sequence *
sive termini. Sensi
ues, and 4-methyl
hyladenine. Isoschi
Reagent
nce GTPyPu*AC a
y 6-methyladenine
methylcytosine at t
Isoschizomer: Hinc
nce *AAG*CTT a
hibited by 6-methy
ne also inhibits. 6-
rs: none known.
nce G*ANTC and
nsitive to 6-methy
position () does no
ne does. Isoschizo
nce GTT*AAC an
y 6-methyladenine
hylcytosine does n
nce GGTACC and
is not inhibited by
6-methyladenine. I
are-cutter enzymes
DNA. Recognizes
with 3'-cohesive en
soschizomers: Sac
nce CTAG and ge
lied with the speci
e concerning meth
nce A*CGT and g
lied with the speci
methylcytosine as in
nce GTNAC and g
lied with the speci
ted by methylation
nce A*CGCGT an
ited by 5-methylcy
(*). It is not influen
schizomers: none k
nce TGGC*CA and
nhibited by overlap
mers: Mls I, Bal I, M
nce T*CCGGA, g
d by 5-methylcyto
ng dam-methylatio
3 I, BspE I, Kpn2 I.
sequence CA*ATT
un I is inhibited by
as indicated. Isosc
*C*C(A,T) GG, ge
tive to simultaneo
cytosine at extena
zomers: BstN I, Bs
ts
and generates frag
e as indicated (*). H
the 3-C residue of
c II.
nd generates fragm
yladenine or 5-met
methyladenine at
d generates fragme
ladenine (*). Prese
ot prevent cleavag
mers: none known
nd generates fragm
e and 5-hydroxyme
ot influence the cl
d generates fragme
y 5-methylcytosine
Isoschizomers:Asp
s which generate l
the sequence CCG
ds. Not sensitive to
II, Sst II.
enerates fragments
ial 2x incubation b
ylation sensitivity.
enerates fragment
ial 2x incubation b
ndicated (*). Isosch
generates fragmen
ial 2x incubation b
n. Isoschizomers: n
nd generates fragm
ytosine within the r
nced by the presen
known.
d generates fragm
pping dcm-methyla
Msc I, Msp20 I.
enerating fragmen
sine(*). In contrast
on(). Isoschizomer
TG and generates
y 6-methyladenine
hizomers: Mfe I.
enerating fragment
us 5-methylation a
al C. Inhibited by 6-
seBI, BstOI, Bst2UI.
gments with
Hind II is
f the
ments with
thylcytosine (*).
A does not
ents with
ence of
e, but
n.
ments with
ethylcytosine
leavage ().
ents with 3-
e at either or
p718 II, Acc65 I.
large
GCGG and
o the presence
s with 5-
uffer. No
Isoschizomers:
ts with 5-
uffer. Inhibited
hizomers:
nts with 5-
uffer. Mae III is
none known.
ments with 5-
recognition
nce of 6-
ments with
ation as
nts with 5'-
t to BseA I, no
rs: Acc III,
fragments with
in the
ts with 5-
at both C
-
.

10 656 305 001
10 656 313 001
10 656 321 001
10 798 983 001
11 274 040 001
10 779 652 001
10 779 679 001
11 274 082 001
10 380 385 001
10 567 647 001
10 742 953 001
10 899 186 001
11 117 807 001
10 822 221 001
10 862 495 001
10 822 230 001
10 822 248 001
10 909 700 001
10 909 718 001
11 526 430 001
11 102 982 001
11 441 337 001
11 288 075 001

22,500 U (3 - 10 U/

5,000 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
50,000 U (40 U/l)
1,000 U (10 U/l)
5,000 U (10 U/l)
20,000 U (40 U/l)
100 U (3 - 10 U/l
500 U (3 - 10 U/l

10,000 U (40 U/l)
5,000 U (10 U/l)

1,000 U (10 U/l)

250 U (1 - 5 U/l)

50 U (1 - 5 U/l)

50 U (1 - 5 U/l)
250 U (1 - 5 U/l)

500 U (10 U/l)
2,500 U (10 U/l)

200 U (10 U/l)

100 U (1 - 5 U/l)

200 U (10 U/l)

5,000 U (10 U/l)

www.roche
l)

)
)
)

)
)
)
)

)
)

e-applied-science

475,30
55,80
98,80
98,80
359,00
69,40
275,10
814,10
75,00
300,10
195,60
121,70
94,40
369,50
347,90
90,90
369,50
69,40
239,90
106,80
353,50
172,80
203,60

1
15

e.com

1
Dis
16

www.r

Mvn

Mvn
blunt
sequ
BstFN
Nar I

Reco
cohe
meth
posit
Nco

Reco
cohe
of 6-
Bsp1
Nde

Nde
with
recog
Isosc
Nde

Reco
cohe
No in
I, Bst
Nhe

Nhe
5-co
recog
Not I

Not I
GCG
by 5-
not in
Nru I

Reco
ends
meth
posit
Nsi I

Nsi I
3-co
5-me
Zsp2
Pst I

Pst I
3-co
and 6
Pvu

Reco
cohe
Inhib
Isosc
Pvu

Pvu I
blunt
recog
Rsa

Reco
ends
howe
inhib

scovery
roche-applied-sc
I (FnuD II)
I recognizes the se
t ends. Mvn I is inh
ence, as indicated
N I, BstU I.
I
ognizes the sequen
sive ends. Inhibite
hylcytosine at the 3
ions. Isoschizomer
I
ognizes the sequen
methyladenine doe
9 I.
I
I recognizes the se
5-cohesive termin
gnition sequence a
chizomers: FauND
II (Mbo I)
ognizes the sequen
nhibition by 5-meth
tMB I, Dpn II, Kzo9
I
I recognizes the se
ohesive termini. Nh
gnition sequence a
I
is a rare-cutter en
GG*C*CGC, gener
-methylcytosine as
nhibiting (). Isosch
I
ognizes the sequen
. Inhibited by over
hylcytosine is inhib
ion of the C. Isosc

recognizes the seq
ohesive termini. Ns
ethylcytosine is not
I.
recognizes the seq
ohesive termini. Pst
6-methyladenine, a
I
ognizes the sequen
sive termini. Not in
bited by 5-methylcy
chizomers: BpvU I,
II
I recognizes the se
t ends. Pvu II is inh
gnition sequence a
I
ognizes the sequen
. Rsa I is not inhib
ever, the presence
iting as indicated
Reagent
cience.com
equence *CGCG
hibited by 5-methy
(*).Isoschizomers
nce GG*CGCC an
d by 5-methylcyto
3'-position and by 5
rs: Mly113 I.
nce *CCATGG an
ited by 5-methylcy
es not influence th
equence CAT*AT
ni. Nde I is inhibite
as indicated (*), bu
I.
nce G*ATC, gener
ited by overlapping
hylcytosine. Isosch
9 I, Mbo I, Sau3A I.
equence GCTAG*
he I is inhibited by
as indicated (*). Iso
nzyme and recogn
rating fragments w
s shown (*). 5-meth
hizomers: CciN I.
nce T*CGCG*A, g
lapping dam-meth
iting(*) or not inhi
hizomers: BtuM I,
quence ATGC*AT
si I is inhibited by 6
t inhibiting. Isosch
quence *CTGCA
t I is inhibited by th
nce CGAT*CG, g
nhibited by overlap
ytosine as shown (
Mvr I, Ple19 I.
equence CAG*CT
hibited by 5'- and 4
nce GT*AC and g
ited by the presen
of 6-methyladenin
(*). Isoschizomers:
ts
and generates fra
ylcytosine within th
: Acc II, Bsh1236 I,
nd generates fragm
sine as shown (*).
5'-hydroxymethylc
nd generates fragm
ytosine as indicated
he cleavage (). Iso
TG and generates
ed by 6-methyladen
ut not by 5-methylc
rating fragments w
g dam-methylation
hizomers: BfuC I, B
*C and generates f
5'-methylcytosine
oschizomers: AsuN
izes the sequence
with 5-cohesive te
hylcytosine in the 5
generating fragme
hylation as shown(
biting(), dependin
Bsp68 I.
T and generates fr
6-methyladenine, a
izomers: EcoT22 I,
G and generates f
he presence of 5-m
oschizomers: BspM
enerating fragmen
pping dam-methyl
(*) and 4-methylcy
TG and generates f
4'-methylcytosine w
oschizomers: none
generates fragmen
ce of 5-methylcyto
ne or 4-methylcyto
: Afa I.
gments with
he recognition
, BspFN I,
ments with 5-
Inhibited by 4-
cytosine in all
ments with 5-
d (*). Presence
oschizomers:
fragments
nine within the
cytosine ().
with 5-
n as shown (*).
Bsp143 I, BssM
fragments with
within the
NH I.

rmini. Inhibited
5'-C position is
ents with blunt
(*). 5-
ng on the
ragments with
as indicated (*).
Mph1103 I,
fragments with
methylcytosine
MA I.
nts with 3-
ation ().
ytosine.
fragments with
within the
e known.
nts with blunt
osine (),
osine is

11 062 573 001
11 103 024 001
10 835 315 001
10 835 323 001
11 047 698 001
11 040 219 001
11 040 227 001
11 040 243 001
10 885 843 001
10 885 851 001
10 885 860 001
11 014 706 001
11 014 714 001
11 037 668 001
10 776 777 001
10 909 831 001
10 909 840 001
10 621 625 001
10 621 633 001
10 798 991 001
10 650 129 001
10 650 137 001
10 642 690 001
10 642 703 001
10 729 124 001
10 729 132 001
11 047 671 001

200 U (10 U/l)

1,000 U (10 U/l)

200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (40 U/l)
200 U (10 U/l)
1,000 U (10 U/l)

1,000 U (5 U/l)

200 U (10 U/l)
1,000 U (10 U/l)
1,500 U (40 U/l)
200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (40 U/l)
1,000 U (10 U/l)

200 U (10 U/l)
1,000 U (10 U/l)

3,000 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
500 U (5 U/l)
100 U (5 U/l)

1,000 U (10 U/l)
5,000 U (10 U/l)

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)

)
)

109,10
251,10
104,60
393,40
393,40
86,40
344,50
314,90
72,80
291,00
345,60
90,90
351,40
351,40
364,40
97,80
269,40
90,90
225,20
225,20
331,90
84,20
51,10
213,80
72,80
291,00
291,00

Di

Sac

Reco
cohe
meth
(). Is
Sal I

Sal I
5-co
meth
Isosc
Sau3

Reco
termi
5- an
Isosc
Sca

Sca I
blunt
indic
SexA

SexA
with
(*). Is
Sfi I

Analy
GGC
Inhib
Cs is
Sfu I

Reco
cohe
insen
BspT
Sma

Reco
Not i
other
Neos
Spe

Reco
cohe
and 5
I, Ahl
Sph

Reco
cohe
meth
hydro
Ssp

Ssp I
blunt
as ind
Stu I

Stu I
blunt
indic
Swa

Swa
with
geno
Isosc
Taq I

Taq l
cohe
indic

scovery
I (Sst I)
ognizes the sequen
hylcytosine at the o
soschizomers: Psp1
recognizes the seq
ohesive termini. Sa
hyladenine within t
chizomers: none kn
3A I
ognizes sequence
ini. No inhibition b
nd 4-methylcytosin
chizomers: Mbo I, N
I
recognizes the se
t ends. Sca I is not
ated (). Isoschizo
A I
AI recognizes the se
5'-cohesive termin
soschizomers: Mab
yze and clone larg
C*CNNNNNGGC
bited by 5-methylcy
not inhibiting ().
I (Asu II)
ognizes the sequen
nsitive to 5-methylc
T104 I, BstB I, Csp4
I
ognizes sequence*C
nhibited by 5-meth
r positions or 4-me
schizomers: Cfr9 I,
I
ognizes the sequen
sive termini. Spe I
5-methylcytosine
l I.
I
ognizes the sequen
hylcytosine at 3'-C(
oxymethylcytosine
I
recognizes the se
t ends. The enzyme
dicated (*). Isosch
I
recognizes the seq
t ends. Stu I is inhi
ated (*). Isoschizo
I
I recognizes the se
blunt ends. The en
omes. No informati
chizomers: Smi I.
I
recognizes the se
sive termini. Taq I
ated (*). Isoschizo
Reagent
nce GAG*CTC an
ited by 5-methylcy
other C does not in
124B I, Sst I.
quence GT*CG*A
l I is inhibited by 5
he recognition seq
nown.
GAT*C. Generate
by dam gene which
ne, 5-hydroxymethy
Nde II, Dpn II and
equence AGTAC
inhibited by the p
mers: Ass I, BmcA
equence AC*C(T
ni. SexA I is dcm m
b I.
e DNA fragments.
CC. Generates frag
ytosine at central C
Isoschizomers: no
nce TTCG*AA an
ited by 6-methylad
cytosine (). Isosch
45 I, Nsp V.
CC*CGGG. Gene
hylcytosine at mid
ethylcytosine in eit
TspM I, Xma I, Xm
nce *A*CTAGT an
is inhibited by the
( mA?m CTAGT) a
nce GC*ATG?C. G
ited by 6-methylad
() or simultaneous
at both Cs. Isosch
equence AAT*ATT
e is inhibited by th
izomers: none kno
quence AGG*C*C
bited by the prese
mers: Aat I, Eco14
equence ATTTAA
nzyme is very usefu
on is available con
equence TCG*A a
is inhibited by ove
mers: Tth HB8 I.
ts
nd generates fragm
ytosine at the centr
nhibit, nor does 6-m
AC and generates f
5-methylcytosine a
quence as indicate
es fragments with
h methylates N6 of
ylcytosine inhibit a
others.
CT and generates fr
presence of 5-meth
A I, Zrm I.
T,A)GGT and gener
methylation sensitiv
. Recognizes the se
gments with 3-co
C (*). 5-methylcyto
one.
nd generates fragm
denine as indicated
hizomers: Bpu14 I,
erates fragments w
dle C(). 5-methylc
ther position inhibi
maC I.
nd generates fragm
e presence of N6-m
as shown (*) . Isosc
enerates fragment
denine(*). No inhib
s presence of 5-
hizomers: Bbu I, Pa
T and generates fr
he presence of 6-m
own.
CT and generates f
ence of 5-methylcy
7 I, Pce I, SseB I.
AAT and generates
ul for digesting GC
ncerning methylati
and generates frag
erlapping dam-met
ments with 3-
ral C (*). 5-
methyladenine
fragments with
and N6-
ed (*).
5-cohesive
f adenine ().
at C(*).
ragments with
hylcytosine, as
rates fragments
ve as indicated
equence
hesive termini.
osine at other
ments with 5-
d (*), but is
Bsp119 I,
with blunt ends.
cytosine at
its(*).
ments with 5'-
methyladenine
chizomers: Bcu
ts with 3-
bition by 5-
ae I
ragments with
methyladenine
fragments with
ytosine as
s fragments
C-rich bacterial
on sensitivity.
gments with 5'-
thylation, as

10 669 792 001
10 669 806 001
11 047 655 001
10 348 783 001
10 567 663 001
11 047 612 001
10 709 751 001
10 775 266 001
11 497 995 001
11 288 024 001
11 288 059 001
11 243 497 001
10 220 566 001
10 656 348 001
11 047 639 001
11 008 943 001
11 008 951 001
11 207 644 001
10 606 120 001
11 026 534 001
11 026 542 001
11 026 950 001
10 972 975 001
10 753 351 001
11 047 680 001
11 371 517 001
10 567 671 001
11 175 114 001

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)
500 U (10 U/l)
2,500 U (10 U/l)
2,500 U (40 U/l)
500 U (1 - 5 U/l)

2,500 U (10 U/l)

200 U (10 U/l)

1,250 U (10 U/l)
5,000 U (40 U/l)

2,000 U (10 U/l)

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)
200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (40 U/l)
500 U (10 U/l)
2,500 U (10 U/l)
2,500 U (40 U/l)
200 U (10 U/l)
1,000 U (10 U/l)

500 U (10 U/l)
2,500 U (40 U/l)

200 U (10 U/l)

2,500 U (10 U/l)
10,000 U (10 U/l)

www.roche

)

)
e-applied-science

90,90
340,00
340,00
53,40
203,60
203,60
185,40
261,90
152,30
240,90
792,40
103,40
104,60
365,00
365,00
90,90
351,40
351,40
268,20
931,20
931,20
121,70
269,40
78,50
314,90
103,40
104,60
309,10

1
17

e.com

1
Dis
18

www.r

Tru9

Tru9
cohe
availa
Xba

Reco
termi
gene
hydro
Xho

Xho I
with
meth
PaeR
SuR
Prod
SuRE

10x o
selec
Tris-a
mM d
SuRE

10x o
deter
diges
merc
SuRE

10x o
deter
diges
dithio
SuRE

10x o
deter
diges
(at +
SuRE

10x o
deter
diges
dithio
SuRE

One s
and H
been
activi
Clo
Prod
rAPid

Rapid
inact
requi
deph
Alka

Calf I
phos
cloni
Highe
Alka

Use t
phos
enzym
conc

scovery
roche-applied-sc
I
I recognizes the se
sive termini. No in
able. Isoschizomer
I
ognizes sequence T
ini. Requires at lea
which methylates
oxymethylcytosine
I
I recognizes the se
5-cohesive termin
hyladenine and 5-m
R7 I, Sfr274 I, Sla I,
RE/Cut Buffer
duct Name
E/Cut Buffer A
optimized incubatio
ct 100% activity or
acetate, 660 mM p
dithiothreitol, pH 7
E/Cut Buffer B
optimized incubatio
rmined to select 10
sts. 100 mM Tris-H
captoethanol, pH 8
E/Cut Buffer H
optimized incubatio
rmined to select 10
sts. 500 mM Tris-H
oerythritol, pH 7.5
E/Cut Buffer L
optimized incubatio
rmined to select 10
sts. 100 mM Tris-H
37C).
E/Cut Buffer M
optimized incubatio
rmined to select 10
sts. 100 mM Tris-H
oerythritol, pH 7.5
E/Cut Buffer Set
set containing 1 m
H for DNA restricti
determined in eac
ity in double-diges
ning of DNA
duct Name
d Alkaline Phosp
d, efficient dephos
ivated at +75C fo
ired after restrictio
osphorylated DNA
aline Phosphatase
Intestinal Alkaline
phates from DNA
ng efficiency by pr
er conc. 20 U/l en
aline Phosphatase
this calf intestinal a
phates from DNA
me (20 U/l), conv
entration (1 U/l)
Reagent
cience.com
equence TTAA a
formation concern
rs: Mse I, Tru1 I.
T*CTAGA. Genera
ast two nucleotide
s 6N of adenine inh
inhibit at (*). Isosc
equence *CT*CG*
ni. Xho I is inhibited
methylcytosine as i
Str I, Tli I.
rs
on buffer for RE di
to calculate activit
potassium-acetate,
7.9 (at +37C).
on buffer for restri
00% activity or to c
HCl, 1 M NaCl, 50 m
.0 (at +37C).
HCl, 1 M NaCl, 100
(at +37C).
HCl, 100 mM MgCl
HCl, 500 mM NaCl,
(at +37C).
for Restriction E
ml 10x solutions ea
ion digests. Activit
ch buffer to select
sts.
Fragments
phatase
sphorylation of 5 e
or 2 minutes. No ad
on and dephospho
A directly in ligatio
e
Phosphatase (1 U
or RNA in small-s
reventing self ligat
nzyme is also avai
e
alkaline phosphata
or RNA. This prep
venient for large-sc
is also available.
ts
nd generates frag
ning methylation se
ates fragments wit
es around target se
hibits; 5-methylcyt
chizomers: none.
*AG and generates
d by the presence
indicated (*). Isosc
igests. Activity dete
ty in double-digest
, 100 mM magnesi
cition digests. Act
calculate activity in
mM MgCl
2
, 10 mM
cition digests. Act
mM MgCl
2
, 10 m
cition digests. Act
2
, 10 mM dithioery
cition digests. Act
100 mM MgCl
2
, 1
nzymes
ch of SuRE/Cut Bu
ty of all restriction
t 100% activity or to
ends of DNA and R
dditional purificatio
rylation. Use the
n reactions.
/l) removes 5'-te
scale experiments,
tion of linearized v
lable.
ase to remove 5'-te
p has a high conce
cale experiments. A
ments with 5-
ensitivity is
th 5-cohesive
equence; dam
tosine and 5-
s fragments
of 6-
chizomers:
ermined to
ts. 330 mM
ium acetate, 5
tivity
n double-
M 2-
tivity
n double-
mM
tivity
n double-
ythritol, pH 7.5
tivity
n double-
10 mM
uffer A, B, L, M,
enzymes has
o calculate
RNA. Rapidly
on steps
rminal
enhancing
vector DNA.
erminal
entration of
A lower

11 464 825 001
10 674 257 001
10 674 265 001
10 674 273 001
11 047 663 001
10 703 770 001
10 703 788 001
10 899 194 001
Cat. No.
11 417 959 001
11 417 967 001
11 417 991 001
11 417 975 001
11 417 983 001
11 082 035 001
Cat. No.
04 898 133 001
04 898 141 001
10 713 023 001
11 097 075 001

1,000 U (10 U/l)

1,000 U (10 U/l)
5,000 U (10 U/l)
20,000 U (10 U/l)
20,000 U (40 U/l)
2,500 U (40 U/l)
12,500 U (40 U/l)
5,000 U (10 U/l)
Pack Size
5 x 1 ml

5 x 1 ml

5 x 1 ml

5 x 1 ml

5 x 1 ml

1 set

Pack Size
1,000 U (1 U/l)
5,000 U (1 U/l)

1,000 U (1 U/l)

1,000 U (20 U/l)

)
)

)

251,10
45,50
105,80
400,20
400,20
53,40
216,00
102,30
Price in
25,80
25,80
25,80
25,80
25,80
23,40
Price in
90,70
363,80
88,70
103,40

Di

Isopr

Isopr
lac o
analo
Meg

Very
large
episo
chrom
Rapi

Fast,
or blu
fragm
linea
Rapi

Cova
plasm
recirc
just 5
T4 D

Use T
Catal
hydro
nicks
pBR3

Selec
cleav
sites
inact
pUC

Plasm
orien
many
coli b
Stora

Box w
stora
Mo
Prod
DNA

For s
mole
gene
23.1
DNA

DNA
in So
label
DNA

For s
deter
restri
DNA

DNA
in So
label
DNA

For s
deter
restri
DNA

For s
deter
restri

scovery
ropyl--D-thioga
ropyl--D-thiogal
operon. It binds an
og of galactose tha
ganuclease I-Sce
rare-cutter endon
e DNA fragments, a
omal DNA, cloned
mosomal DNA isol
d DNA Dephos &
efficient dephosph
unt-end DNA frag
ments into plasmid
r DNA, and library
d DNA Ligation K
lently joins sticky-
mid or phage vecto
cularizing linear D
5 minutes at room
DNA Ligase
T4 DNA ligase to jo
lyzes formation of
oxyl- and 5'-phosp
s in dsDNA are als
322 DNA
ctable plasmid for
vage sites in the am
in the tetracycline
ivating these drug
18 DNA
mid for loning doub
ntation with respec
y unique sites for c
by transformation.
age Box
with removable sty
ge of 50 microcen
lecular Weigh
duct Name
A Molecular Weig
ize distribution an
cular weight deter
rated by restriction
kbp.
A Molecular Weig
Molecular Weight
outhern blot analys
ing and detection.
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
outhern blot analys
ing and detection.
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
Reagent
alactoside
actoside (IPTG) is
d inactivates the la
at cannot be cleave
e I
uclease. Use in ad
and for mapping b
mammalian DNA
lated from pulsed-
& Ligation Kit
horylation (10 min
ments. Minimizes
d and phage vector
y generation.
Kit
- or blunt-end DNA
ors, adding linkers
NA. Contains all re
temperature.
oin sticky- or blun
phosphodiester bo
phate ends in doub
o closed by T4 DN
cloning of recomb
mpicillin gene, or C
e gene, allow foreig
resistance genes.
ble-digested restri
ct to the lac promo
cloning of foreign

yrofoam insert (0.5
ntrifuge tubes. Tem
ht Markers
ght Marker II
alysis using agaro
rmination of doubl
n digests, PCR, an
ght Marker II, DIG
t Marker II, DIG-la
sis when using the
Size range: 0.12 to
ght Marker III
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker III, DI
t Marker III, DIG-la
sis when using the
Size range: 0.12 to
ght Marker IV
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker V
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ts
a very effective in
ac repressor. It is
ed by -galactosi
dapter cloning and
bacterial or yeast c
fragments, or mam
-field gels.
) and ligation (5 m
application times w
rs, linker ligation, r
A fragments for clo
to plasmids or oth
eagents needed fo
t-ended DNA frag
onds between neig
ble-stranded DNA.
NA Ligase.
binant DNA. Pst I a
Cla I, Hind III, Bam
gn DNA to be inse
.
iction fragments in
oter. Polylinker (MC
DNA. Easily introd
to 2.0 ml capacity
mperature-resistant
se gels. Simplifies
e-stranded DNA f
d RT-PCR. Size ran
G-labeled
beled, is used as a
DIG System for nu
o 23.1 kbp.
plifies accurate mo
fragments generate
e range: 0.12 to 21
IG-labeled
abeled, is used as
DIG System for nu
o 21.2 kbp.
plifies accurate mo
fragments generate
e range: 0.07 to 19
plifies accurate mo
fragments generate
e range: 8 to 587 b
ducer of the
a chemical
idase.
subcloning of
chromosomes,
mmalian
min) of sticky-
when cloning
recircularizing
oning into
her DNAs, and
or ligation in
gments.
ghboring 3'-
. Single-strand
and Pvu I
HI, and Sal I
erted for
n either
CS) provides
duced into E.
y) for the
t to -70C.
accurate
fragments
nge: 0.12 to
a size standard
ucleic acid
olecular weight
ed by
1.2 kbp.
a size standard
ucleic acid
olecular weight
ed by
9.3 kbp.
olecular weight
ed by
bp.

10 724 815 001
11 411 446 001
11 362 399 001
04 898 117 001
04 898 125 001
11 635 379 001
10 481 220 001
10 716 359 001
10 799 009 001
10 481 238 001
10 885 819 001
10 800 058 001
Cat. No.
10 236 250 001
11 218 590 910
10 528 552 001
11 218 603 910
11 418 009 001
10 821 705 001

1 kit
1 kit
1 kit for up
50 g in 200 l
50
50 g in 200 l
50
50 g in 200 l
50 g in 200 l
1 g
5 g

1,000 U

for up to 160 reac

p to 40 DNA ligatio

100 U (1 U/l)
500 U (1 U/l)
500 U (5 U/l)
200 l 1 A
260
unit

50 g (200 l)

1 box

Pack Size
(1 A
260
unit) for up

00 l (5 g, 10 g/m

(1 A
260
unit) for up

00 l (5 g, 10 g/m

(1 A
260
unit) for up

(1 A
260
unit) for up

www.roche
tions
ctions
on reactions
t
p to 50 gel lanes
ml)
p to 50 gel lanes
ml)
p to 50 gel lanes
p to 50 gel lanes
e-applied-science

82,20
308,00
414,90
174,60
499,50
286,10
87,20
275,50
275,50
212,30
468,30
7,40
Price in
100,10
205,30
111,00
205,30
161,70
152,00

1
19

e.com

1
Dis
20

www.r

DNA

For s
deter
restri
DNA

DNA
stand
acid
DNA

For s
deter
restri
DNA

DNA
stand
acid
DNA

For s
deter
restri
DNA

DNA
stand
acid
DNA

For s
deter
restri
DNA

For s
deter
restri
DNA

For s
deter
restri
DNA

For s
deter
restri
addit
DNA
Mark

Allow
Temp
cleav
agaro
DNA

For s
deter
restri
DNA

For s
deter
restri
RNA

RNA
size s
nucle
RNA

RNA
size s
nucle
RNA

RNA
size s
nucle

scovery
roche-applied-sc
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
dard in Southern b
labeling and detec
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
dard in Southern b
labeling and detec
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
dard in Southern b
labeling and detec
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
tional band of 2642
A Molecular Weig
ker)
ws accurate sizing
plate PCR System o
ved with rare-cuttin
ose gels. Size rang
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
standard in northe
eic acid labeling an
A Molecular Weig
Molecular Weight
standard in northe
A Molecular Weig
Molecular Weight
standard in northe
Reagent
cience.com
ght Marker VI
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker VI, DI
t Marker VI, DIG-la
blot analysis when
ction. Size range: 0
ght Marker VII
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker VII, D
t Marker VII, DIG-l
blot analysis when
ght Marker VIII
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker VIII, D
t Marker VII, DIG-l
blot analysis when
ght Marker IX
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker X
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker XIII (5
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker XIV (1
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
2 bp.
ght Marker XV (E
of DNA fragments
or restriction diges
ng restriction endo
ge: 2.3 to 48.5 kbp.
ght Marker XVI (2
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker XVII (
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker I, DIG
t Marker I, digoxig
ern blot analysis wh
nd detection. Size
ght Marker II, DIG
t Marker II, digoxig
nd detection. Size
ght Marker III, DI
t Marker III, digoxi
nd detection. Size
ts
plifies accurate mo
fragments generate
e range: 0.15 to 2.
IG-labeled
abeled, is used as
using the DIG Sys
0.15 to 2.1 kbp.
plifies accurate mo
fragments generate
e range: 0.081 to 8
DIG-labeled
labeled, is used as
using the DIG Sys
0.081 to 8.57 kbp.
plifies accurate mo
fragments generate
e range: 19 to 111
DIG-labeled
labeled, is used as
using the DIG Sys
19 - 1114 bp.
plifies accurate mo
fragments generate
e range: 72 to 135
plifies accurate mo
fragments generate
e range: 100 bp to
50 bp ladder)
plifies accurate mo
fragments generate
e range: 50 to 750
100 bp ladder)
plifies accurate mo
fragments generate
e range: 100 to 15
Expand DNA Mole
s generated by the
st of high molecula
onucleases and se
250 bp ladder)
plifies accurate mo
fragments generate
e range: 0.25 to 3.0
(500 bp ladder)
plifies accurate mo
fragments generate
e range: 0.5 to 5.0
G-labeled
enin (DIG)-labeled
hen the DIG System
range: 0.3 to 6.9 k
G-labeled
genin (DIG)-labele
hen the DIG System
range: 1.5 to 6.9 k
G-labeled
genin (DIG)-labele
hen the DIG System
range: 0.3 to 1.5 k
olecular weight
ed by
1 kbp.
a size
stem for nucleic
olecular weight
ed by
8.57 kbp.
s a size
stem for nucleic
olecular weight
ed by
4 bp.
s a size
stem for nucleic
olecular weight
ed by
3 bp.
olecular weight
ed by
o 12.2 kbp.
olecular weight
ed by
bp.
olecular weight
ed by
00 bp and an
ecular Weight
e Expand Long
ar weight DNA
eparated on
olecular weight
ed by
0 kbp.
olecular weight
ed by
kbp.
d is used as a
m is used for
kb.
d is used as a
m is used for
kb.
ed is used as a
m is used for
kb.

11 062 590 001
11 218 611 910
11 209 264 001
11 669 940 910
11 336 045 001
11 449 451 910
11 449 460 001
11 498 037 001
11 721 925 001
11 721 933 001
11 721 615 001
11 855 638 001
11 855 646 001
11 526 529 910
11 526 537 910
11 373 099 910

50 g in 200 l
50
50 g in 200 l
50
50 g in 200 l
500
50 g in 200 l
100 g in 400
50 g (1 A
2
50 g in 200 l
50 g in 200 l
50 g in 200 l
(1 A
260
unit) for up

00 l (5 g, 10 g/m

(1 A
260
unit) for up

00 l (5 g, 10 g/m

(1 A
260
unit) for up

0 l (10 g/ml) (5

(1 A
260
unit) for up

l (2 A
260
units) fo
lanes

260
unit) for up to 5

(1 A
260
unit) for up

50 g (1 A
260
unit)

(1 A
260
unit) for up

(1 A
260
unit) for up

4 g (200 l)

2 g (200 l)

2 g (200 l)

p to 50 gel lanes
ml)
p to 50 gel lanes
ml)
p to 50 gel lanes
g)
p to 50 gel lanes
or up to 50 gel
50 gel lanes
p to 50 gel lanes
)
p to 50 gel lanes
p to 50 gel lanes

152,00
203,90
152,00
231,40
173,70
256,00
190,70
125,60
132,80
139,80
121,90
115,70
115,70
355,50
392,50
322,50

Di

Nuc
Nuc
Prod
Actin

Actin
quan
hybri
huma
DIG-

Estim
hybri
temp
DIG-

Estim
probe
of DI
temp
Car
Prod
COT

Use C
repet
(CISS
hybri
COT

Supp
DNA
hybri
captu
DNA

The r
preve
DNA
dena
DNA

This
diges
Glyc

Mole
preci
repla
picog
Hum

Prepa
(buffy
const
Expa
RNA

For s
synth
hybri
RNA

16S-
gel e
struc
RNA

For s
prote
polyp
proce

scovery
cleic Acids,
cleic Acids an
duct Name
n RNA Probe, DIG
n RNA Probe, DIG-
tity of various RNA
dization and north
an cell lines and tis
-labeled Control
mate the yield of DI
dization probe in S
plate DNA and app
-labeled Control
e in Southern and
G-labeled neo-RN
plate DNA (fragme
rrier and Com
duct Name
Human DNA
COT Human DNA
titive DNA in in situ
S) hybridizations, h
dizations.
Human DNA, Flu
presses cross-hybr
probes are hybrid
dizations, such as
ure, and nucleic ac
A, MB-grade
ready-to-use solut
ents nonspecific hy
hybridizations. Ad
turing are not requ
A, lambda
high quality prepa
sts, amplification o
ogen
ecular biology grad
pitation of nucleic
ace tRNAs or sonic
gram amounts of D
man Genomic DNA
aration of high mo
y coat). Suitable fo
truction, and the re
nd System.
A
tudies which use n
hesizing system. Th
dization.
A, 16S- and 23S-r
and 23S-ribosoma
lectrophoresis and
cture and function
A, MS2
tructural/functiona
ein-synthesizing sy
peptide synthesis. A
edures.
Reagent
Probes and
nd Probes, DI
G-labeled
-labeled is ideal fo
A species. Applicat
hern blot analysis t
ssue samples.
DNA
IG-labeled nucleic
Southern blots. Th
prox. 250 ng synthe
RNA
IG-labeled RNA or
northern blots. Th
NA (760 bp length)
nts of 798 and 328
mpetitor Nucle
to suppress cross-
u hybridizations, c
hybridization to mic
uorometric Grade
ridization to human
dized in situ . Use in
comparative geno
cid labeling and de
ion is directly adde
ybridization in all t
ddition of NaCl, so
uired.
ration of Lambda
of large DNA targe
de Glycogen is use
c acids (DNA or RN
cated DNAs; 20 g
DNA or RNA from
A
olecular weight DN
or Southern hybrid
eliable amplificatio
natural RNA in a in
he product is also
ribosomal
al RNA is used as
d ultracentrifugatio
of ribosomes.
al studies using na
ystems, initiation, e
Also used as a car
ts
d Carrier
IG-labeled
r evaluating the qu
tions include in sit
to evaluate RNA fr
c acids or use as a
e solution contain
esized DIG-labeled
r use as a control h
he solution contain
and 0.5 g pSPT1
81 bp).
eic Acids
-hybridization to h
chromosome in situ
croarrays, and filte
e
n repetitive DNA w
n FISH and DNA m
ome hybridization,
etection.
ed to the hybridiza
types of membrane
nication or shearin
DNA is used for re
ets, and as a PCR c
ed as a carrier for t
NA). As an inert m
g (1 l solution) pre
a volume of 1 ml.
NA isolated from hu
dization analysis, ge
on of large DNA ta
n vivo and in vitro
used as a carrier R
a molecular weigh
on; also used to stu
atural RNA in in viv
elongation, and ter
rrier in sensitive RN
uality and
tu
rom various
control
s 1 g
d DNA.
hybridization
ns approx. 5 g
8-neo
human
u suppression
er
when human
microarray
sequence
ation mix. It
e or in situ
ng, and
estriction
control.
the
aterial it may
ecipitates
uman blood
enomic library
argets by the
protein-
RNA in in situ
ht standard in
udy the
vo and in vitro
rmination of
NA purification

Cat. No.
11 498 045 910
11 585 738 910
11 585 746 910
Cat. No.
11 581 074 001
05 480 647 001
11 467 140 001
10 745 782 001
10 901 393 001
11 691 112 001
10 109 223 001
10 206 938 001
10 165 948 001

50 l (5 g/
50 l (10
1
5
Pack Size
2 g

/ml DIG-labeled pl

00 g/ml DIG-labe

Pack Size
500 g (500 l)

1 ml (1 mg/ml)

500 mg (50 ml)

1 ml (5 A
260
units)

20 mg (1 ml)

100 g

100 g

ml (100 A
260
units

500 l (10 A
260
unit

www.roche
asmid DNA)
led RNA)
)
s)
ts)
e-applied-science

Price in
399,40
118,30
118,30
Price in
161,10
425,60
197,80
119,10
99,50
181,50
66,60
129,20
123,10

1
21

e.com

1
Dis
22

www.r

Tran
Prod
tRNA

tRNA
preve
nega
tRNA

tRNA
preve
to im
a lyop
tRNA

tRNA
preve
to im
lyoph
Hist
Prod
Histo

Natu
Histo
pack
the p
Histo

Lysin
kinas
exit s
forma
Histo

Histo
in the
globu
nucle
Pro
Gen
Prod
DIG

Nonr
prepa
comp
detec
Lab
Kits
Prod
Bioti

The k
such
Pero

Comp
acces
antib
immu

scovery
roche-applied-sc
nsfer Ribonuc
duct Name
A
A is used as a com
ent nonspecific bin
tive); supplied as a
A
A is used as a com
ent nonspecific bin
prove recovery of
philizate.
A
A is used as a com
ent nonspecific bin
prove recovery of
hilizate.
tones
duct Name
one
ral mixture of histo
ones are highly alk
age and order the
primary component
one H1
ne-rich preparation
ses. The linker hist
sites of the DNA, lo
ation of higher ord
one H3
one H3 from calf th
e structure of chro
ular domain and a
eosome "beads on
otein Anal
ne Expressio
duct Name
Gel Shift Kit, 2nd
radioactive detectio
aring 3'-end-labele
plexes in gel mobil
cts as little as 20 fm
beling of Pro
s for Labeling
duct Name
in Protein Labelin
kit is suitable for th
as immunohistoch
oxidase Labeling
plete kit for labelin
ssible primary ami
bodies with POD, a
unoblotting. All req
Reagent
cience.com
cleic Acids
petitor in pre- and
nding of the probe
a lyophilizate.
petitor in pre- and
nding of the probe
diluted samples. F
petitor in pre- and
nding of the probe
diluted samples. F
ones H1, H2A, H2B
aline proteins foun
DNA into structur
t of chromatin.
n from calf thymus
tone H1 binds the
ocking the DNA in
der structure.
hymus is one of the
omatin in eukaryoti
long N-terminal ta
a string" structure
lysis
on Analysis
d generation
on of sequence-sp
ed oligonucleotide
lity shift assays. Co
mol of the control
oteins
g of Proteins
ng Kit
he labeling of prote
hemistry, immunob
Kit
ng water-soluble b
no groups with PO
nd downstream us
quired reagents ar
ts
d hybridization solu
e. From E. coli MRE
e. It can also be use
From brewer's yeas
From baker's yeast
B, H3, and H4 from
nd in eukaryotic ce
ral units (nucleoso
s used as a substra
nucleosome and t
nto place and allow
e five histone prote
ic cells. Featuring
ail, H3 is involved
e.
pecific DNA bindin
e probes that detec
onvenient and sens
oligo.
eins with biotin fo
blotting, and ELISA
biomolecules with r
OD. Ideal for coupl
se in ELISA, IHC, a
e supplied.
utions to
E 600 (RNase
utions to
ed as a carrier
st, supplied as
utions to
ed as a carrier
t, supplied as a
m calf thymus.
ell nuclei that
omes). They are
ate for protein
he entry and
wing the
eins involved
a main
in the
ng proteins. For
ct DNA-protein
sitive kit
r applications,
A.
reactive and
ing of
and

Cat. No.
10 109 541 001
10 109 550 001
10 109 517 001
10 109 525 001
10 109 495 001
10 109 509 001
Cat. No.
10 223 565 001
10 223 549 001
11 004 875 001
11 034 758 001
Cat. No.
03 353 591 910
Cat. No.
11 418 165 001
11 829 696 001

1 kit for up to 2
reactions wi
reactions, chem
for up to 20
oligonucleotid
1 kit for
1 kit for
Pack Size
100 mg
500 mg

100 mg
500 mg

100 mg
500 mg

Pack Size
10 mg

1 mg
5 mg

1 mg

Pack Size
20 Oligonucleotide
ith DIG-11-ddUTP,
miluminescent det
blots, DNA binding
de for up to 20 con
Pack Size
r up to 5 labeling r


e 3'-end labeling
, 200 binding
tection reaction
g protein and
ntrol reactions
reactions
reactions

Price in
249,20
992,50
127,50
447,80
155,10
609,30
Price in
193,80
200,10
707,10
200,10
Price in
715,20
Price in
282,90
494,10

Di

Mar
Prod
Alka

Calf I
its am
for co
Alka

Alkal
amin
direc
ELISA
-G

Use f
be co
direc
chrom
Pero

For o
Perox
moie
dialys
Pero

Perox
as we
used
a salt
Mar
Prod
Alka

Activ
prima
witho
rabbi
Pero

Use P
solub
For c
shee
Det
Det
Prod
Anti-

Detec
tagge
immu
10-fo
Anti-

Detec
conta
immu
Since
label
Anti-

Detec
tagge
strep
fold l
Anti-

Detec
weste
mono
mono

scovery
rker Enzymes
duct Name
aline Phosphatase
Intestine Alkaline P
mino groups. This
onjugation without
aline Phosphatase
ine Phosphatase r
o and carbohydrat
ctly for conjugation
As, microarrays, an
Galactosidase
for labeling enzym
oupled to other pro
matography. Supp
oxidase (POD)
oxidation of electro
xidase (POD) to pr
ty. Use reconstitut
sis. Grade I salt-fre
oxidase (POD)
xidase (POD) can
ell as its carbohyd
directly for conjug
t-free lyophilizate.
rker Enzymes
duct Name
aline Phosphatase
vated Alkaline Phos
ary amino groups
out pre-activation t
it, mouse, sheep, a
oxidase (POD), ac
Peroxidase (POD),
ble substances wit
coupling of Ig, Ig Fa
p, and goat with P
tection of Pr
tection of Epit
duct Name
-HA (12CA5)
ct native influenza
ed protein contain
unoprecipitation, a
old lower conc., us
-HA High Affinity
ct native influenza
ain the HA epitope
unoprecipitation, a
e it is a rat monocl
ing.
-HA-Biotin
ct native influenza
ed protein in weste
ptavidin fluorescent
ower conc. using A
-HA-Biotin, High
ct HA-tagged reco
ern and dot blottin
oclonal, it is possib
oclonals for double
Reagent
s without Pre
e
Phosphatase can b
ready-to-use enzy
t prior dialysis; EIA
e recombinant, h
recombinant can b
te groups. The en
n without prior dial
nd western blot an
e immunoassay te
oteins via its SH-g
lied as lyophilizate
on donors by epoxi
roteins via its amin
ted solution directl
ee lyophilizate.
be coupled to othe
rate moiety. The re
gation without prio
s with Pre-ac
e (AP), activated
sphatase labels wa
(peptides/proteins
to label Ig, Ig Fab,
and goat.
ctivated
activated,without
h reactive and acc
ab, and Ig F(ab')
2

POD. Use in ELISA,
roteins
tope-Tagged
a hemagglutinin pr
ing the HA epitope
and western and do
e Anti-HA High Af
y
a hemagglutinin an
e in ELISA, immuno
and western and do
onal, use with mur
a hemagglutinin pr
ern blots and imm
t or POD systems.
Anti-HA-Biotin, Hi
Affinity (3F10)
ombinant proteins
ng, and ELISA. Sinc
ble to use it in conj
e labeling.
ts
e-activation
be coupled to othe
yme solution can b
A Grade, 10 mg/ml
highly active
be coupled to prote
zyme solution can
ysis. Applications
nalysis.
echniques. -Galac
roups. Use recons
ysis or gel permea
e.
idation of double b
no groups and its c
ly in conjugation w
er proteins via its a
econstituted solutio
or dialysis. EIA grad
ctivation
d
ater-soluble substa
s) with alkaline pho
and Ig F(ab')
2
frag
pre-activation to l
cessible primary am
fragments from ra
IHC, and immuno
Proteins
rotein and recombi
e in immunocytoch
ot blots. For highe
ffinity.
nd recombinant pro
ocytochemistry,
ot blots.
rine monoclonals f
rotein and recombi
unofluorescence w
Obtain higher sen
igh Affinity.
with high sensitivi
ce Anti-HA-High A
junction with muri
er proteins via
e used directly
solution.
eins via its
be used
include
ctosidase can
tituted solution
ation
bonds. Couple
carbohydrate
without prior
amino groups,
on can be
de, supplied as
ances carrying
osphatase. Use
gments from
abel water-
mino groups.
abbit, mouse,
oblotting.
inant epitope-
hemistry,
r sensitivity at
oteins that
for double
inant HA-
with
nsitivityat 10-
ity using
Affinity is a rat
ine

Cat. No.
10 567 752 001
03 359 123 001
10 745 731 001
10 108 090 001
10 814 407 001
Cat. No.
11 464 752 001
11 428 861 001
Cat. No.
11 583 816 001
11 666 606 001
11 867 423 001
11 867 431 001
11 666 851 001
12 158 167 001

10 m
app
100
Pack Size
15 mg (1.5 ml)

10 mg (500 l)

25 mg

25,000 U

100 mg

Pack Size
mg (approx. 40 mg

prox. 40 mg lyophil

Pack Size
200 g (lyo.)
5 mg (5 mg/ml)

50 g
500 g

g (0.2 mg/ml; 50

50 g

www.roche
lyo.)
izate
00l)
e-applied-science

Price in
647,10
440,80
657,00
277,60
301,80
Price in
542,40
362,90
Price in
466,50
1.322,90
347,10
2.945,40
350,80
524,30

1
23

e.com

1
Dis
24

www.r

Anti-

Loca
sharp
using
Anti-
Anti-

Use A
recom
immu
used
Anti-

Singl
blotti
HA-P
need
Anti-

For s
blot a
Since
conju
Anti-

Spec
of ex
immu
Anti-

Spec
vecto
immu
tagge
Anti-

Singl
blotti
indep
epito
Anti-

For s
weste
effici
to C-
Anti-

Anti-
native
that c
immu
Anti-

Use f
recom
dot b
need
HA P

The s
gentl
contr
anti-H
c-my

The s
C-ter
can b
chrom

scovery
roche-applied-sc
-HA-Fluorescein
lize recombinant H
per images with cle
g unlabeled Anti-H
-HA-Fluorescein, H
-HA-Fluorescein
Anti-HA-Fluoresce
mbinant HA-tagge
unofluorescence. S
with murine mono
-HA-Peroxidase
e-step detection o
ng. For higher sen
Peroxidase High Af
for a secondary d
-HA-Peroxidase,
ingle-step detectio
analysis and ELISA
e Anti-HA High Aff
unction with murin
-His
6

ific and sensitive d
pression vector us
unocytochemistry,
-His
6
(2)
ific, sensitive detec
or. For immunoblot
unofluorescence, E
ed proteins than C
-His
6
-Peroxidase
e-step detection o
ng and ELISA. Rea
pendent of epitope
pe with high sens
-His
6
-Peroxidase
ingle-step detectio
ern and dot blot an
ently recognizes N
-terminal tagged p
-c-myc
-c-myc (clone 9E10
e human c-myc pr
contain the c-myc
unocytochemistry,
-c-myc-Peroxida
for single-step det
mbinant epitope-ta
blots and western b
for a secondary d
Peptide
synthetic HA Pepti
y elute tagged fus
rol to verify immun
HA and HA-tagged
yc peptide
synthetic peptide E
rminus of human c
be used in compet
matography of pro
Reagent
cience.com
HA-tagged protein
eaner background
HA. For higher sens
High Affinity.
, High Affinity
ein, High Affinity fo
ed proteins using f
Since the antibody
oclonals for double
of HA-tagged reco
nsitivity at 10-fold l
ffinity. Use of Anti-
detection step.
High Affinity
on of HA-tagged r
A.
finity is a rat mono
ne monoclonals for
detection for histid
sed. For immunoblo
immunofluorescen
ction of histidine-t
tting, immunoprec
ELISA. More efficie
C-tagged proteins.
e
of His
6
-tagged rec
acts with native an
e-sequence locatio
itivity.
e (2)
on of His
6
-tagged
nalysis and ELISA.
N-terminal histidine
roteins.
0) is used for the im
rotein and recomb
epitope in western
and immunopreci
ase
tection of native hu
agged proteins tha
blots. Use of Anti-c
detection step.
de YPYDVPDYA is
sion proteins from
nospecificity, and in
d fusion proteins.
EQKLISEEDL, comp
c-myc protein, is re
tition experiments,
oteins that contain
ts
s by immunofluore
d compared to indi
sitivity at 10-fold lo
or direct detection
low cytometry and
y is a rat monoclon
e labeling.
mbinant proteins b
lower concentratio
-HA-Peroxidase el
recombinant protei
r double labeling.
dine-tagged protein
otting, immunopre
nce, and ELISA.
tagged proteins re
ipitation, immunoc
ently recognizes N
ombinant proteins
nd denatured tagge
on. Recognizes the
recombinant prote
Anti-His
6
-Peroxid
e-tagged proteins
mmunochemical d
binant epitope tag
n and dot blots,
pitation.
uman c-myc prote
at contain the c-my
c-myc-Peroxidase
s recognized by An
immunocomplexe
n competition expe
prising 10-amino a
ecognized by Anti-
including affinity
this epitope.
escence. Yields
rect methods
ower conc., use
of
d
al, it can be
by western
on, use Anti-
iminates the
ins by western
ble to use it in
ns regardless
ecipitation,
gardless of
cytochemistry,
-terminal-
s by western
ed proteins
e C-terminal
6

eins by
dase (2) more
in comparison
detection of
ged proteins
in and
yc epitope in
eliminates the
nti-HA. Use to
s, as positive
eriments using
acids from the
-c-myc and

11 666 878 001
11 988 506 001
11 667 475 001
12 013 819 001
11 922 416 001
04 905 318 001
11 965 085 001
04 905 270 001
11 667 149 001
11 667 203 001
11 814 150 001
11 666 975 001
11 667 246 001

50
2
100 g (500 l)

25 g

g (0.1 mg/ml; 500

25 U (25 g)

100 g

200 l

50 U

80 U

200 g (lyophilizate
5 mg (1 ml)

500 g (500 l)

5 mg

5 mg

0 l)
e)

352,10
326,80
408,60
408,60
334,90
355,30
388,40
414,60
417,90
1.322,90
407,40
549,80
495,00

Di

Wes
Prod
Lum

Chem
PVDF
high
hours
BM C

Ideal
sensi
than
sensi
Lum

Chem
PVDF
sensi
allow
Lum

Chem
PVDF
espec
for m
BM C

Ideal
<10 p
than
mem
West

10x s
expe
mem
PVD

Ideal
low b
color
Light
Lum

Lumi
is ide
chem
techn
Lum

Lumi
is ide
chem
techn
ELIS
Prod
BM C

Chem
conve
ELISA
sourc
BM C

Subs
syste
ELISA
forma
Bloc

This
bindi

scovery
stern Blotting
duct Name
i-Light
PLUS
Weste
miluminescent POD
F or nitrocellulose
sensitivity western
s, allowing for mul
Chemiluminesce
chemiluminescen
itivity is required. O
colorimetric metho
itive as radioactivit
i-Light
PLUS
Weste
miluminescent POD
F or nitrocellulose
itivity western blott
wing multiple expos
i-Light Western B
miluminescent POD
F or nitrocellulose
cially when quanti
multiple exposures.
Chemiluminesce
substrate (POD) f
pg antigen in west
other nonradioact
branes.
tern Blocking Re
solution used as a
riments. The reage
brane, membrane
F Western Blottin
membrane for we
background bindin
rimetric and chemi
t Western-Blotting
i-Film Chemilum
-Film Chemilumin
eal for detecting th
miluminescent subs
niques.
i-Film Chemilum
-Film Chemilumin
eal for the detectio
miluminescent subs
niques.
SAs
duct Name
Chemiluminesce
miluminescent sub
enient and highly
A and SEAP report
ces, such as intest
Chemiluminesce
trate solution for p
ems for highly sens
A and use with a m
at) or tube-format
cking Reagent
Blocking Reagent
ng sites in ELISA p
Reagent
g Reagents
ern Blotting Kit (M
D substrate detect
membranes using
n blotting requiring
ltiple exposures.
ence Western Blo
nce system for wes
Obtain 1 to 3 order
ods. Chemilumine
ty with shorter exp
ern Blotting Subs
D substrate detect
membranes using
ting, requiring qua
sures.
Blotting Substrat
D substrate detect
membranes. For h
fication is required
ence Western Blo
for protein and nuc
tern blots. Shows a
tive or radioactive
eagent, Solution
general blocking a
ent is used in steps
washing steps, an
ng Membranes
estern and dot blot
ng generate excelle
iluminescent detec
Substrates.
minescent Detecti
escent Detection F
he signals from alk
strates (e.g ., CSPD
minescent Detecti
escent Detection F
on of signals from a
strates (e.g., CSPD
ence ELISA Subst
strate system base
sensitive method t
ter gene assays. M
ine, placenta, milk
ence ELISA Subst
peroxidase-based
sitive, enhanced ch
microplate chemilu
luminometers.
preparation is use
procedures. Suppl
ts
Mouse/Rabbit)
s 1-5 pg antigen b
mouse/rabbit ant
g quantification. Si
otting Kit (Mouse
stern and dot blots
rs of magnitude hi
scence image is at
posure.
strate
s 1-5 pg antigen b
secondary antibo
antification. Signal
te
s 10-50 pg antigen
high-sensitivity wes
d. Signal lasts >3 h
otting Substrate (
cleic acid detectio
at least 10-fold hig
detection systems
agent during weste
s such as blocking
nd diluting detectio
ts. Strong sample r
ent signal-to-noise
ction. Ideal for use
ion Film
Film 7.1 x 9.4 inche
kaline phosphatase
D) in membrane hy
ion Film
Film 8 x 10 inches,
alkaline phosphata
D) in membrane hy
trate (AP)
ed on CSPD provid
to detect alkaline p
Measures AP from v
k, and bacteria.
trate (POD)
(POD, HRP) secon
hemiluminescence
uminescence reade
ed for the blocking
ied as a yellowish
blotted onto
tibodies. For
gnal lasts >9
e/Rabbit)
s where high
gher sensitivity
t least as
blotted onto
dies. For high
lasts >9 hrs,
n blotted onto
stern blotting,
hours, allowing
(POD)
n. Sensitivity:
gher sensitivity
on PVDF
ern blotting
g the
on antibodies.
retention and
e ratios in
e with Lumi-
es, 18 x 24 cm
e
ybridization
20.3 x 25.4 cm
ase
ybridization
des a
phosphatase in
various
ndary detection
e. Optimized for
er (96-well
g of nonspecific
powder.

Cat. No.
12 015 218 001
11 520 709 001
12 015 196 001
12 015 200 001
11 500 694 001
11 500 708 001
11 921 673 001
11 921 681 001
03 010 040 001
11 666 916 001
11 666 657 001
Cat. No.
11 759 779 001
11 582 950 001
11 112 589 001

1 kit
1 kit
100 m
400 m
1 set
1 set
100
6 x 10
1
100 films (
100 films (
250 ml for u
27 g for
Pack Size
(1,000 cm
2
memb

(2,000 cm
2
memb

ml (1,000 cm
2
mem

ml (4,000 cm
2
mem

(4,000 cm
2
memb
(1,000 cm
2
memb

ml (10 blots, 100 c
00 ml (60 blots, 100

roll (30 cm x 3.00

(7.1 x 9.4 inches, 1

(8 x 10 inches, 20.3

Pack Size
150 ml

up to 2.500 wells or

one liter blocking

www.roche
brane)
brane)
mbrane)
mbrane)
brane)
brane)
cm
2
)
0 cm
2
)
m)
8 x 24 cm)
3 x 25.4 cm)
r 1.000 tubes
solution
e-applied-science

Price in
812,50
417,20
497,50
230,80
344,40
165,60
91,40
321,90
300,50
305,40
298,10
Price in
387,30
201,80
49,60

1
25

e.com

1
Dis
26

www.r

Gly
End
Prod
-A

Use
polys
enzym
Endo

Use r
glyco
glyco
N-Gly
O-Gl

Relea
threo
acid)
glyco
N-Gl

N-Gly
recom
glyco
fucos
N-Gl

N-Gly
recom
glyco
fucos
N-Gl

N-Gly
glyca
core
solut
Lyso

Use L
of pro
heali
to iso
Exo
Prod
Amy

Amyl
activi
termi
polys
Amy

Amyl
activi
termi
polys
-G

Use
Provi
crysta
-G

For h
analy
prepa
immu
Neur

From
(2,
glyco
hydro

scovery
roche-applied-sc
ycoprotein A
doglycosidase
duct Name
Amylase
-Amylase for the
saccharides contai
me produces -d
oglycosidase H
recombinant Endo
oproteins. Endoglyc
opeptides and prot
ycosidase A to cle
lycosidase
ases Gal-(1,3)-Ga
onine are hydrolyze
prevent hydrolysis
oproteins before pr
lycosidase F
ycosidase F PNGa
mbinant from E.col
opeptides and glyc
se residues presen
lycosidase F
ycosidase F PNGa
mbinant from E.col
opeptides and glyc
se residues presen
lycosidase A
ycosidase A from s
an chains from glyc
fucose residues p
ion.
ozyme
Lysozyme from hen
otoplasts, bacterio
ng), food and drin
olation of nucleic a
glycosidases
duct Name
yloglucosidase
oglucosidase is us
ity: approx. 6 U/mg
inal glucoses that
saccharide of mult
yloglucosidase
oglucosidase is us
ity: approx. 6 U/mg
inal glucoses that
saccharide of mult
Galactosidase
-Galactosidase t
ded as a suspensi
alline.
Glucuronidase
hydrolysis of steroid
ysis, and to detect
aration to cleave g
unoassays, or othe
raminidase (Siali
m Vibrio cholerae ; h
3-, 2,6-, 2,8-li
oproteins, and glyc
olytic cleavage of s
Reagent
cience.com
Analysis
es
e hydrolyzation of
ning 3 or more
extrins.
glycosidase H for
cosidase H hydroly
teins. It cleaves on
eave glycopeptides
aINAc from O-glyc
ed. Substituents at
s and must be rem
rotein sequencing.
se F of Flavobacter
li ; hydrolyzes all ty
coproteins unless t
nt in insect and pla
se F of Flavobacter
coproteins unless t
sweet almond mea
copeptides, even t
resent in insect an
n egg white for ce
olysis, pharmacolog
ks (flavor enhance
acids.
s
sed for the determ
g lyo. at +25C wit
are 1,4- or 1,6
iple glucose units;
sed for the determ
g lyo. at +25C wit
are 1,4- or 1,6
iple glucose units;
to produce a calib
on in 3.2 M ammo
d conjugates (gluc
benzodiazepine in
glucuronides prior
er analytical metho
idase)
hydrolyzes termina
nked to oligo-, po
colipids). For glyco
sialic acid from bio
ts
1,4-glycosidic b
1,4-linked D-Gluco
the deglycosylatio
yzes N-linked oligo
ly high mannose s
s.
cans. Bindings to s
t the disaccharide
moved. For deglyco
.
rium meningosepti
ypes of N-glycan c
they carry -1-3
ant glycoproteins. I
rium meningosepti
ypes of N-glycan c
they carry -1-3
ant glycoproteins L
al; hydrolyzes all ty
those carrying
nd plant glycoprote
ell wall degradation
gy (anti-inflammat
er), and sample pre
ination of starch. S
th glycogen as sub
6-linked to an olig
supplied as lyoph
th glycogen as sub
6-linked to an olig
supplied as suspe
ration curve in enz
onium sulfate, pH a
curonides) in urine
n small doses. Use
to GC-MS, HPLC,
ods.
al N- or 0-acylneur
ly-, mucopolysacc
conjugate structur
ological material.
bonds in
ose units. The
n of
osaccarides of
structures. Use
serine and
(e.g., sialic
osylation of
icum ,
chains from
3 linked core
In solution.
icum ,
chains from
3 linked core
Lyophilizate.
ypes of N-
1,3-bound
eins. In
n, preparation
tory, tissue
eparation prior
Specific
bstrate. Cleaves
o- or
hilizate.
Specific
bstrate. Cleaves
o- or
ension.
zymatic assays.
approx. 6,
e, in doping
during sample
raminic acids
harides,
ral studies and

Cat. No.
10 102 814 001
11 088 726 001
11 643 053 001
11 347 101 001
11 365 169 001
11 365 177 001
11 365 185 001
11 365 193 001
11 642 995 001
10 837 059 001
Cat. No.
11 202 332 001
11 202 367 001
10 102 857 001
10 105 031 001
03 707 580 001
03 707 598 001
03 707 601 001
11 080 725 001

Pack Size
50 mg (5 ml)

1 U (200 l)
2.5 U (500 l)

25 mU

100 U (0.1 ml)
250 U (0.25 ml)

100 U
250 U

5 mU (0.1 ml)

10 g

Pack Size
500 U
3,500 U

100 mg (10 ml)

1,500 U

1 ml
5 ml
15 ml
1 U

Price in
127,20
406,10
749,00
328,90
243,20
456,00
243,20
456,00
431,00
245,90
Price in
98,30
364,10
131,40
185,00
49,90
181,80
491,90
104,00

Di

Neur

From
acyln
muco
sialic
Neur

From
acids
etc).
2,8
Kits
Prod
DIG

Analy
of se
nitroc
tissue
Pro
Prot
Prod
Carb

Use C
succe
prote
argin
Endo

Use E
and f
Endo

Use E
sequ
Papa

For c
immu
prote
Requ
Peps

Use P
medi
yield
from
Plasm

Use P
used
resea
Plasm

Use P
used
resea
Plasm

Plasm
plasm
Pron

Mix o
single
tissue
of gly
Thro

Use T
prote
Throm

scovery
raminidase (Siali
m Arthrobacter urea
neuraminic acids,
opolysaccharides,
c acids from glycoc
raminidase (Siali
m Clostridium perfrin
s (2,3-, 2,6-,
In contrast to othe
8 sialic acids are cl
s for Glycan A
duct Name
Glycan Different
yze and characteri
lected lectins. In a
cellulose membran
e sections.
oteases
teases
duct Name
boxypeptidase B
Carboxypeptidase
essive cleavage of
eins. Specific Activ
nine as the substra
oproteinase Glu-C
Endoproteinase Gl
for sequence analy
oproteinase Lys-C
Endoproteinase Ly
ence analysis.
ain
complete proteolyti
unoglobulins, and
eins and produces
uires 0.5% cysteine
sin
Pepsin for nonspec
a. Pepsin provides
biologically active
pig gastric mucos
min, bovine
Plasma, bovine in c
for protein structu
arch. The enzyme c
min, human
Plasmin, human in
for protein structu
arch. The enzyme c
minogen
minogen from hum
minogen activators
nase
of nonspecific end
e amino acids. Deg
e dissociation alon
ycopeptides from g
ombin
Thrombin in coagu
ein-structure analy
mbin contains EDT
Reagent
idase)
afaciens ; hydrolyze
2,3-, 2,6-, or
glycoproteins, and
conjugates of a wid
idase)
ingens ; hydroyzes
2,8-linked to oligo
er neuraminidases
leaved with similar
Analysis
iation Kit
ze carbohydrate st
addition to differen
nes, lectins can ide
B for the sequenc
f basic amino acids
ity - approx. 150 U
ate.
C (V8 Protease)
u-C (V8 Protease)
ysis.
C
ys-C for protein str
ic cleavage of prot
tissue dissociation
glycopeptides from
e for activity.
cific hydrolysis of p
s a limited hydrolys
e fragments. Pepsin
sa.
coagulation resear
ure analysis, seque
converts fibrin into
coagulation resea
ure analysis, seque
man serum is used
s; substrate of t-PA
o- and exoproteas
grade protein duri
ng with collagenas
glycoproteins.
ulation, biochemica
ysis. The enzyme co
TA and additional s
ts
es terminal N- or 0
2,8-linked to olig
d glycolipids. Comp
de variety of biolog
terminal N- or 0-a
o-, poly-, mucopol
, cleaves 2,3 fas
r velocity as 2,6.
tructures by the sp
tiating glycoprotei
entify carbohydrate
ce analysis of prote
s from the C-termi
U/mg at +25C with
for protein structu
ructure analysis an
teins, limited hydro
n. Solubilizes integ
m purified proteog
proteins and pepti
sis of native immun
n is an aspartic en
rch and in medica
ence analysis, and
o soluble products
arch and medical r
ence analysis, and
o soluble products
to determine the a
A.
ses that digest prot
ng DNA and RNA
se and trypsin. Use
al and medical res
onverts fibrinogen
stabilizing agents.
0-
go-, poly-, and
pletely remove
gical materials.
acylneuraminic
lysaccharides,
ter than 2,6;
pecific binding
ins bound to
e structures on
eins by
nus of
h hippuryl-L-
ure analysis
nd for
olysis of native
ral membrane
glycans.
des in acidic
noglobulins to
doproteinase
l research. It is
biochemical
.
research. It is
biochemical
.
activity of
tein down to
A isolation. For
e in production
search, and
to fibrin.

10 269 611 001
11 585 886 001
Cat. No.
11 210 238 001
Cat. No.
10 103 233 001
10 791 156 001
10 476 986 001
10 108 014 001
10 108 057 001
10 602 370 001
10 602 361 001
10 874 477 001
10 165 921 001
11 459 643 001
10 602 400 001

1 kit for the de
1 U (100 l)

5 U

Pack Size
etection on 25 blot
cm

Pack Size
5 mg (1 ml)

2 mg

3 U

100 mg (10 ml)

1 g

5 U (1 ml)

5 U (0.5 ml)

20 U

1 g
5 g

20 U

www.roche
ts, each 10 x 10
e-applied-science

262,60
190,90
Price in
620,40
Price in
182,70
147,60
325,60
130,70
84,30
216,90
201,00
234,20
108,30
396,10
125,70

1
27

e.com

1
Dis
28

www.r

Prot
Prod
Chym

Use C
chym
for pe
Endo

Endo
purifi
mapp
solut
Endo

Endo
speci
analy
Endo

Endo
is a h
analy
Endo

Endo
is a h
sequ
polya
Tryps

Diges
prote
analy
prote
Tryps

Use t
struc
and t
to cro
Tryps

Spec
chrom
spect
chym
Sub
Prod
Chro

Use C
prote
Chro

Use C
prote
Chro

Use C
prote
Chro

Use C
in pu
used
Univ

Use a
activi
Prote
fluori

scovery
roche-applied-sc
teases, Sequ
duct Name
motrypsin Seque
Chymotrypsin Sequ
motrypsin alone or
eptide mapping, fi
oproteinase Arg-
oproteinase Arg-C
ied, specific cystei
ping, fingerprinting
ion, gels, or on me
oproteinase Asp-
oproteinase Asp-N
ific metalloproteas
ysis.
oproteinase Glu-C
oproteinase Glu-C
highly purified and
ysis and for sequen
oproteinase Lys-C
oproteinase Lys-C S
highly purified, spe
ence analysis. Suit
acrylamide gels, or
sin Sequencing G
st proteins in solut
ein-structure elucid
ysis, and translocat
eins in polyacrylam
sin Sequencing G
to generate glycop
cture elucidation, tr
translocation studi
oss-linking.
sin recombinant,
ifically digests pro
matographic meth
trometry. Tested fo
motrypsin, and othe
bstrates for th
duct Name
omozym PK
Chromozym PK as
eases, specifically p
omozym PL
Chromozym PL as
omozym TH
Chromozym TH as
eases, specifically t
omozym t-PA
Chromozym t-PA a
urified preparations
to evaluate the co
versal Protease S
as a general subst
ities, such as conta
ease Substrate can
imetrically in a hom
Reagent
cience.com
encing Grade
encing Grade
uencing Grade for
in combination wit
ngerprinting, and
C Sequencing G
Sequencing Grade
ne protease to cle
g, and sequence a
embrane blots.
-N Sequencing G
Sequencing Grad
se used for protein
C Sequencing Gr
Sequencing Grade
specific serine pr
nce analysis.
C Sequencing Gr
Sequencing Grade
ecific serine protea
table to digest pro
r on blotting memb
Grade
tion, in gels, or on
dation, tryptic map
tion studies. It is s
mide gels.
Grade, modified
peptides from purif
ryptic mapping, fin
es. Enzyme resista
, Proteomics Gra
oteins separated by
ods during sample
or the absence of p
er contaminating p
he Determina
a substrate for the
plasma kallikrein i
a substrate for the
plasmin in aqueou
a substrate for the
thrombin in aques
as a substrate for t
s and in cell cultur
ontent of one-chai
Substrate
rate for proteases
amination in enzym
n be measured spe
mogeneous assay.
ts
e
r the hydrolysis of
th other proteases
sequence analysis
rade
e from C. histolytic
ave proteins/pepti
nalysis, and to dig
Grade
e is a highly purifi
n structure and seq
rade
e from Staphylococ
otease used for pr
rade
e from Lysobacter
ase for protein stru
oteins in solution, in
branes.
blotting membran
pping, fingerprintin
uitable for the dige
fied glycoproteins
ngerprinting, seque
ance to autolysis is
ade
y 2D gel electroph
e preparation for m
porcine trypsin (se
proteases.
ation of Prote
e determination of
n citrated plasma.
e determination of
us solutions.
e determination of
ous solutions.
the determination
re supernatants. It
n and two-chain t-
and to detect trac
me preparations. T
ectrophotometrical
proteins by
s. It is suitable
s.
cum is a highly
ides for
est protein in
ed and
quence
ccus aureus V8
rotein structure
enzymogenes
ucture and
n
nes. Use for
ng, sequence
estion of
in protein-
ence analysis,
s increased due
oresis or liquid
mass
erine protease),
ases
f serine
f serine
f serine
of t-PA, both
can also be
-PA.
ce protease
The Universal
ly and

Cat. No.
11 418 467 001
11 370 529 001
11 054 589 001
11 420 488 001
11 047 817 001
11 420 399 001
11 047 825 001
11 420 429 001
11 047 841 001
11 418 475 001
11 418 025 001
11 418 033 001
03 708 969 001
03 708 985 001
Cat. No.
10 378 445 001
10 378 461 001
10 206 849 001
11 585 398 001
11 093 037 001
11 734 334 001

Pack Size
4 x 25 g

3 x 5 g

3 x 2 g
2 g

3 x 50 g
50 g

3 x 5 g
5 g

4 x 100 g
4 x 25 g

4 x 25 g
4 x 100 g

4 x 100 g
4 x 25 g

Pack Size
20 mg

20 mg

20 mg
100 mg

20 mg

40 mg

Price in
101,60
305,00
403,90
161,80
397,10
157,90
326,30
128,30
278,10
76,20
112,30
379,80
287,20
94,30
Price in
369,90
362,60
290,60
1.199,50
333,70
565,00

Di

An
Det
Prod
Strep

Use S
immu
and w
phos
Strep

Use S
immu
and w
phos
Strep

Use S
immu
coval
Strep

Use S
immu
Strep
Strep

Ideal
vitro
High
the m
Strep

Use S
solid
hapte
detec
Det
Prod
Anti-

Use A
digox
in situ
Anti-

Use A
digox
in situ
Anti-

Anti-
using
weste
light-
Anti-

Detec
colon
immu
nonra
north
Anti-

Detec
in gly
immu
cann
Anti-

Detec
dot b
fragm
sensi
Anti-

Detec
Immu
Perox

scovery
ntibodies a
tection of Bi
duct Name
ptavidin-AP
Streptavidin-AP to
unohistocytochem
western blotting. S
phatase. Supplied
ptavidin-AP
Streptavidin-AP to
unohistocytochem
western blotting. S
phatase. Supplied
ptavidin--Gal
Streptavidin--Ga
unohistocytochem
lently coupled to
ptavidin-POD
Streptavidin-POD t
unohistocytochem
ptavidin is covalent
ptavidin Mutein M
for gentle purifica
expressed biotiny
binding capacity a
matrix.
ptavidin, recomb
Streptavidin, recom
phases (e.g., micr
ens and antibodies
ction systems.
tection of D
duct Name
-Digoxigenin
Anti-Digoxigenin a
xigenin-labeled co
u hybridization, an
-Digoxigenin
Anti-Digoxigenin a
xigenin-labeled co
u hybridization, an
-Digoxigenin, Fab
-Digoxigenin, FAB
g ELISA, immunoh
ern blotting. Prefer
-chain specific ant
-Digoxigenin-AP
ct digoxigenin-lab
ny/plaque hybridiza
unohistocytochem
adioactive DNA se
hern blotting.
-Digoxigenin-Flu
ct digoxigenin-lab
ycoconjugate resea
unohistocytochem
ot be used for me
-Digoxigenin-PO
ct digoxigenin-lab
blots. Obtain highe
ments conjugated t
itivity. Not evaluate
-Digoxigenin-PO
ct digoxigenin-lab
unohistocytochem
xidase substrates i
Reagent
and Detec
iotinylated M
detect biotinylate
istry,
Streptavidin is cova
as clear, colorless
detect biotinylate
istry, ISH,
as a clear, colorle
al to detect biotiny
istry, and western
-galactosidase fr
to detect biotinylat
istry, in situ hybrid
tly coupled to hors
Matrix
ation of biotinylate
ylated proteins usin
and multiple reuse
binant
mbinant from Strep
roplates, beads etc
s in universal imm
IG-labeled M
antibody (clone 1.7
mpounds using EL
nd western blotting
antibody from shee
mpounds using EL
nd western blotting
b fragments
Fragments detect
istocytochemistry,
rentially used for s
ti-sheep conjugate
P, Fab fragments
eled compounds u
ation, ELISA, gel s
equncing blots, and
uorescein, Fab fra
eled compounds u
arch, fluorescent in
istry, and in situ h
mbrane applicatio
OD (poly), Fab fra
eled compounds i
r signal-to-noise v
to unpolymerized
ed in immunohisto
OD, Fab fragment
eled compounds u
include DAB and B
ts
ction Subs
Molecules
d compounds usin
alently coupled to a
s solution.
d nucleic acids in
ess solution.
ylated compounds
blotting. Streptavid
rom E. coli .
ted compounds in
dization, and weste
seradish peroxidas
d proteins. Tested
ng RTS AviTag Bio
e permits cost-effe
ptomyces avidinii f
c.), as well with bio
unological streptav
Molecules
71.256) for the dete
LISA, immunohisto
g.
ep for the detectio
LISA, immunohisto
g.
digoxigenin-labele
in situ hybridizati
secondary detectio
e.
using cDNA arrays
hift assays,
dization, RNase pro
d Southern, weste
agments
using digoxigenin-
ybridization. The a
ns.
agments
n ELISA, Southern
values compared to
HRP (ELISA). Use
ochemistry.
s
using dot blots, EL
dization, and weste
BM Blue.
trates
ng ELISA,
alkaline
ELISA,
alkaline
in ELISA,
din is
ELISA,
ern blotting.
se.
for use with in
otinylation Kits.
ective use of
for coating of
otin-labeled
vidin/biotin
ection of
ocytochemistry,
n of
ocytochemistry,
ed compounds
on, and
on using a
s,
otection,
rn, and
-labeled sugars
n (FISH),
antibody
n, western, and
o Anti-Dig-Fab
for high
ISA,
ern blotting.

Cat. No.
11 089 161 001
11 093 266 910
11 112 481 001
11 089 153 001
03 708 152 001
11 721 666 001
11 721 674 001
Cat. No.
11 333 062 910
11 333 089 001
11 214 667 001
11 093 274 910
11 207 741 910
11 633 716 001
11 207 733 910

5 m
Pack Size
1,000 U (1 ml)

150 U (200 l)

500 U

500 U

ml settled resin volu

1 mg
5 mg

Pack Size
100 g

200 g

1 mg

150 U (200 l)

200 g

50 U

150 U

www.roche
ume
e-applied-science

Price in
336,20
139,90
279,20
239,40
445,60
155,40
569,20
Price in
255,50
152,50
159,40
191,90
210,20
320,30
210,20

1
29

e.com

1
Dis
30

www.r

Anti-

Use A
comp
resea
immu
Det
Prod
Anti-

Detec
immu
The a
antib
Anti-

Detec
immu
weste
immu
Anti-

Detec
immu
weste
immu
Sub
Che
Prod
CDP

Chem
ultra-
acids
and d
CDP

Read
Enab
labele
For S
CSPD

Chem
extre
labele
shift
CSPD

Read
enab
nonra
For b
Chr
Prod
BCIP

For a
South
is ins
disso
BCIP

Use B
immu
react
can b
BM P

Color
north
situ
bottle

scovery
roche-applied-sc
-Digoxigenin-Rh
Anti-Digoxigenin-R
pounds using digo
unohistocytochem
tection of Fl
duct Name
-Fluorescein
ct fluorescein-labe
unohistocytochem
antibody is not sta
body in sandwich-E
-Fluorescein-AP,
ct fluorescein-labe
unohistocytochem
ern blots. Use the
unohistochemistry
-Fluorescein-POD
ct fluorescein-labe
unohistocytochem
ern blots. Conjuga
unohistochemistry
bstrates for
emiluminesce
duct Name
-Star
miluminescent sub
-sensitive visible li
s on film or lumine
dot blots, and gel s
-Star , ready-to-
dy-to-use chemilum
bles fast, ultra-sens
ed nucleic acids o
Southern, dot, and
D
miluminescent sub
mely fast and sens
ed nucleic acids o
assays, and seque
D ready-to-use
dy-to-use chemilum
ling extremely fast
adioactively labele
blotting, gel shift as
romogenic Su
duct Name
P
alkaline phosphata
hern and western
soluble in water. Th
olved (50 mg/ml) in
P
BCIP for alkaline p
unohistocytochem
tion product has a
be visually detecte
Purple
rimetric AP substra
hern, and Southern
hybridization. Use
e with no mixing o
Reagent
cience.com
odamine, Fab fra
Rhodamine to dete
oxigenin-labeled su
n situ hybridization
luorescein-l
eled compounds u
bilized with protein
ELISAs and labelin
, Fab fragments
eled compounds in
conjugate in ELISA
with an anti-mous
D, Fab fragments
eled compounds in
te only usable in E
using anti-mouse
Detection
ent Substrate
strate for alkaline
ght detection of no
scence imager sys
shift assays.
use
minescent substrat
sitive visible light d
n film/luminescen
northern blots, ge
strate for alkaline
n film or luminesc
encing.
minescent substrat
t and sensitive visi
ed nucleic acids on
ssays, and sequen
ubstrates for
se detection using
blotting. The react
he blue color can b
n dimethylformami
phosphatase detec
istry and Southern
blue color and is
d. Supplied as a p
ate for immunohist
n blotting, colony a
stabilized substrat
or reconstitution.
ts
agments
ect digoxigenin-lab
ugars in glycoconju
n (FISH),
ybridization.
labeled Mol
sing ELISA,
dization, and weste
n and is suitable a
ng procedures.
n ELISA,
dization, Southern,
A, immunoblotting
se Ig fluorescein, F
s
n ELISA,
dization, Southern,
ELISA, immunoblot
e Ig fluorescein, Fa
es for AP
phosphatase, ena
onradioactively lab
stems. For Souther
te for alkaline pho
detection of nonrad
ce imagers.
l shift assays.
phosphatase, ena
detection of nonra
cence imagers. For
te for alkaline pho
ble light detection
n film or luminesce
cing.
AP
g immunohistocyto
tion product has a
be visually detecte
ide.
tion using
n and western blott
insoluble in water.
owder.
tocytochemistry, w
and plaque hybridi
te solution directly
beled
ugate
lecules
ern blotting.
as a coating
dot, and
g, and
Fab2 fragment.
dot, and
tting, and
b2 fragment.
bling fast,
beled nucleic
rn, northern,
sphatase.
dioactively
bling
dioactively
r blotting, gel
sphatase,
n of
ence imagers.
ochemistry and
blue color and
ed. BCIP is
ting. The
. The blue color
western,
zation, and in
y from the

11 207 750 910
Cat. No.
11 426 320 001
11 426 338 910
11 426 346 910
Cat. No.
11 685 627 001
11 759 051 001
12 041 677 001
11 655 884 001
11 755 633 001
Cat. No.
11 383 221 001
10 760 994 001
11 585 002 001
11 442 074 001

200 g

Pack Size
100 g

150 U (200 l)

150 U

Pack Size
1 ml
2 x 1 ml

2 x 50 ml

1 ml

2 x 50 ml

Pack Size
3 ml (150 mg)

250 mg
1 g

100 ml

210,20
Price in
320,90
223,90
189,60
Price in
286,10
514,80
410,90
237,90
227,20
Price in
86,20
123,50
434,20
86,70

Di

Fast

Used
with
organ
using
INT/

Color
phos
blot,
NBT

For u
Solub
hybri
weste
NBT

For u
colon
north
Supp
NBT/

Read
colon
and w
nitroc
NBT/

Stock
color
and w
nitroc
Fluo
Prod
AttoP

AttoP
phos
sensi
subst
HNP

Comb
nonra
used
and c
Chr
Prod
ABTS

ABTS
(abso
ABTS

For p
perox
as a
phos
ABTS

Ideal
mark
displa
perbo
ABTS

ABTS
immu
solut
diluti
ABTS

Ideal
mark
subst
sodiu

scovery
Red Tablets
d as a substrate in
alkaline phosphata
nic solvent, which
g organic solvent-c
BCIP Stock Solu
rimetric substrate s
phatase (AP) in bl
and for application
use in the sensitive
ble in water, aqueo
dization, immunoh
ern blots, and to d
ny/plaque hybridiza
hern, and western
plied as 100 mg/ml
/BCIP Ready-to-
dy-to-use tablets fo
ny/plaque lifts, imm
western blots, and
cellulose and nylon
/BCIP Stock Solu
k solution for sens
rimetric AP substra
western blots, and
cellulose and nylon
orescent Sub
duct Name
Phos
Phos is a highly se
phatase-conjugate
itive by a factor of
trate 4-methylumb
PP Fluorescent De
bined with Fast Re
adioactively labele
for nonradioactive
colony and plaque
romogenic Su
duct Name
S
S substrate is a per
orbance), chromat
S Buffer
preparing the enzym
xidase as the mark
powder: sodium p
phate.
S Buffer
enzyme immunoa
ker enzyme. The re
ay "over" after sev
orate, citric acid, d
S Solution
S Solution is an ide
unoassays with ho
ion is supplied as
on.
S Tablets
substrate for enzy
ker enzyme. Each t
trate solution. The
um perborate, citric
Reagent
immunohistocytoc
ase. The Fast Red
may cause proble
containing mounti
tion
solution for the se
otting protocols, in
ns in immunohisto
e detection of alkal
ous buffer, and DM
histocytochemistry
etect proteins/glyc
ation, immunohisto
blots, and to detec
l solution in 70% D
-Use Tablets
or sensitive detecti
munohistocytochem
to detect proteins
n membranes.
ution
itive detection of a
ate is used in immu
to detect proteins
n membranes.
bstrates for AP
nsitive substrate fo
ed secondary dete
100 than the most
belliferyl-phosphat
etection Set
ed, HNPP is used fo
ed probe in in situ
e blots: Southern,
hybridizations.
ubstrates for
roxidase substrate
ographically homo
me immunoassay
ker enzyme for hig
erborate, citric aci
assay substrate usi
action's high sens
veral minutes. Supp
disodium hydrogen
eal chromogenic s
rseradish peroxida
one component re
yme immunoassay
ablet contains 50 m
buffer solution for
c acid, and disodiu
ts
chemistry and wes
reaction product i
ms for in situ hybr
ng media.
ensitive detection o
ncluding Southern
ocytochemistry.
line phosphatase u
MF. For colony/plaq
y, ISH, Southern, no
coconjugates. Crys
line phosphatase u
ocytochemistry, IS
ct proteins and gly
DMF.
ion of alkaline pho
mistry, ISH, Southe
s/glycoconjugates.
alkaline phosphata
unohistocytochem
s and glycoconjuga
P
or ELISA using alk
ection systems. It is
t commonly used f
e (MUP).
or fluorescent dete
hybridization. HNP
northern, DNA seq
POD
e for ELISA. Purity:>
ogeneous.
buffer when using
h reaction sensitiv
d, disodium hydro
ing horseradish pe
sitivity can cause a
plied in solution: s
n phosphate.
ubstrate for enzym
ase as a marker en
eagent, ready-to-u
ys with horseradish
mg ABTS substrate
r ABTS substrate c
um hydrogen phos
stern blotting
s soluble in
ridization when
of alkaline
blot, western
using BCIP.
que
orthern,
stalline form.
using BCIP. For
SH, Southern,
ycoconjugates.
osphatase. For
ern, northern,
Use with
ase. The
mistry, Southern
ates. Use with
kaline
s more
fluorescence
ection of a
PP alone is
quencing blots,
>98%
g horseradish
vity. Supplied
ogen
eroxidase as a
utoreaders to
odium
me
nzyme. ABTS
se at working
h peroxidase as
e, for a 50 ml
consists of
sphate.

11 496 549 001
11 681 460 001
11 585 029 001
11 383 213 001
11 697 471 001
11 681 451 001
Cat. No.
11 681 982 001
11 758 888 001
Cat. No.
10 102 946 001
11 112 597 001
11 204 530 001
11 684 302 001
11 112 422 001

1 set for u
3 x 100 ml (f
20 tablets (ea
20 tablets

3 ml

5 g

3 ml (300 mg)

20 tablets

8 ml

Pack Size
up to 1,800 wells 1

1 set

Pack Size
2 g

16.7 g (for 1 l)

125 ml

for 1,500 to 3,000 E

ach tablet is for 50
solution)

www.roche
00 l each
ELISA assays)
0 ml substrate
e-applied-science

85,40
130,20
551,90
108,40
146,40
110,00
Price in
542,40
441,40
Price in
57,90
48,30
29,40
177,20
65,90

1
31

e.com

1
Dis
32

www.r

ABTS

Ideal
mark
subst
sodiu
BM B

Read
appli
sensi
react
BM B

BM B
ELISA
phen
nonto
DAB

DAB
of ap
and w
Sub
Prod
CPRG

Color
The r
be ev
X-Ga

Use X
produ
meth
detec
Sub
Prod
D(-)

Use f
extra
toget
biolu
Mic
Prod
Strep

Strep
and f
steril
for ce
Strep

Strep
for co
steril
suita
Strep

Strep
bindi
immu
Not s
Strep

Strep
are u
Plate
coati

scovery
roche-applied-sc
S Tablets
substrate for enzy
ker enzyme. Each t
trate solution. The
Blue POD Substr
dy-to-use colorime
cations, such as w
itive than DAB and
tions using alkaline
Blue POD Substr
Blue POD Substrat
A applications. The
ylendiamine (oPD)
oxic.
B Substrate
Substrate is a colo
pplications, such as
western and dot b
bstrates for
duct Name
G
rimetric determina
reaction product h
valuated photomet
al
X-Gal for immunoh
uct has a blue colo
hanol. It is not solu
cted.
bstrates for Lu
duct Name
-Luciferin
for the luminometr
cts. It is a natural s
ther with firefly luc
minescence.
croplates fo
duct Name
ptaWell (transpa
ptaWell, streptavidi
fluorescent protein
ization procedure
ell culture purpose
ptaWell (transpa
olorimetric and flu
e as sterilization p
ble for cell culture
ptaWell, High Bin
ng capacity are us
unoassays. Not ste
suitable in cell cult
ptaWell, High Bin
used in colorimetric
s are not sterile as
ng. Not suitable fo
Reagent
cience.com
yme immunoassay
ablet contains 5 m
buffer solution for
c acid, and disodiu
rate, precipitating
tric peroxidase sub
western , northern,
d produces less ba
e phosphatase det
rate, soluble
te, soluble, is an id
e reagent shows h
) or ABTS substrat
or substrate for pe
s immunohistocyto
lotting.
-Galactosida
tion of -Gal activ
as a dark red colo
trically at 574 or 57
histocytochemistry
or and is soluble in
ble in water. The b
uciferase
ric determination o
substrate of lucife
ciferase for the det
or Immunoas
arent 96-well)
in-coated micropla
n immunoassays. T
would impair the s
es.
arent, 12 x 8-well
in-coated micropla
orescent protein im
rocedures impair t
e.
nd (transparent,
in-coated micropla
sed in colorimetric
erile as sterilization
ture.
nd (transparent,
in-coated micropla
c and fluorescent n
s sterilization proce
or cell culture.
ts
ys with horseradish
mg ABTS substrate
r ABTS substrate c
um hydrogen phos
g
bstrate solution fo
and Southern blot
ackground staining
tection.
eal ready-to-use s
igher sensitivity th
tes and can be cla
eroxidase and is us
ochemistry, in situ
ase
vity in cell extracts
78 nm.
y applications. The
n dimethylformami
blue color can be v
of Luc gene activity
rase from firefly an
termination of ATP
ssays
ates can be used f
The plates are not
streptavidin coatin
l strips)
ates (12 x 8-well st
mmunoassays. The
the streptavidin co
12 x 8-well strips
c and fluorescent n
n impairs streptavid
96-well)
ates with high bind
nucleic acid immu
edures impair stre
h peroxidase as
, for a 5 ml
consists of
sphate.
r a variety of
tting. It is more
g than
solution for
han o-
assified as
sed in a variety
hybridization,
and ELISA.
water. It can
reaction
ide and
visually
y in cell
nd is used
P using
or colorimetric
sterile as any
ng. Not suitable
trips) are used
e plates are not
oating. Not
s)
trips) with high
nucleic acid
din coating.
ding capacity
unoassays.
ptavidin

11 204 521 001
11 442 066 001
11 484 281 001
11 718 096 001
Cat. No.
10 884 308 001
10 651 745 001
10 703 729 001
10 745 740 001
11 680 293 001
Cat. No.
11 626 353 001
Cat. No.
11 734 776 001
11 664 778 001
11 645 692 001
11 989 685 001

20 tablets (e
1
5 plates (
5 plates (
1
each tablet is for 5
solution)

100 ml

100 ml

1 pack

Pack Size
250 mg

250 mg
2.5 g
1 g
100 mg
Pack Size
50 mg

Pack Size
15 plates (96 wells

12 x 8 well strips a


15 plates (96 wells

ml substrate
s)
and frame)
and frame)
s)

53,70
107,10
66,50
184,50
Price in
87,30
148,00
1.122,10
492,50
91,90
Price in
716,80
Price in
745,00
317,00
229,20
657,00

Di

Nu
Deo
Prod
Deox

PCR-
RT-P
sodiu
color
Deox

Use f
prime
vials:
solut
dATP

Use d
ampl
clear
dATP

Use d
reage
react
of the
dCTP

Use d
ampl
mM c
dCTP

Suita
as rev
sequ
solut
dGTP

Use d
ampl
100 m
dGTP

Suita
as rev
sequ
solut
dTTP

Use d
ampl
mM c
dTTP

Suita
as rev
sequ
solut
dUTP

For s
react
DNA
conta
dUTP

Use d
requi
conta
Supp

scovery
ucleotides
oxynucleotid
duct Name
xynucleoside Trip
-Grade set for app
CR, DNA labeling,
um salts of dATP, d
rless solutions in w
xynucleoside Trip
for sequencing/cyc
er extension, and a
dATP, dCTP, dGTP
ion of the lithium s
P
dATP, lithium salt,
ification reactions
, colorless solution
P
dATP, PCR Grade s
ents are required:
tions, and sequenc
e sodium salt (pH
P
dCTP, lithium salt,
ification reactions
clear, colorless sol
P
able for application
verse transcription
encing/cycle sequ
ion of the sodium
P
dGTP, lithium salt,
ification reactions
mM clear, colorless
P
verse transcription
encing/cycle sequ
ion of the sodium
P
dTTP, lithium salt, f
ification reactions
P
verse transcription
encing/cycle sequ
ion of the sodium
P
equencing, labelin
tions. DNA contain
glycosylase. This
amination; 100 mM
P
dUTP, PCR Grade f
ired: RT, PCR, RT-P
amination between
plied as 100 mM so
Reagent
and Anal
des
phosphate Set
lications requiring
sequencing. Cont
dCTP, dGTP, dTTP
water (pH 8.3).
phosphate Set
cle sequencing, la
all types of amplific
P, dTTP; each cont
salt (pH 7).
for DNA sequenci
or primer-extensio
n of the lithium sal
sodium salt for ap
reverse transcripti
cing. Supplied as 1
8.3).
for DNA sequenci
or primer-extensio
lution of the lithium
ns where high-qua
n, PCR, RT-PCR, D
uencing analysis. It
salt (pH 8.3).
for DNA sequenci
or primer-extensio
s solution of the lit
ns where high-qua
n, PCR, RT-PCR, D
salt (pH 8.3).
for DNA sequenci
or primer-extensio
lution of lithium sa
ns where high-qua
n, PCR, RT-PCR, D
uencing analysis. T
salt (pH 8.3).
ng, primer extensio
ning dUTP is susce
allows dUTP to be
M lithium salt solut
for applications wh
PCR, labeling, sequ
n PCRs to eliminat
olution of the sodiu
ts
ogs
high-quality reage
tains individual via
at 100 mM concen
beling, reverse tra
cation reactions. S
tains 100 mM clea
ing, labeling, and a
on reactions. dATP
t (pH 7).
plications where h
on, PCR, RT-PCR,
00 mM clear colo
on reactions. Supp
m salt (pH 7).
ality reagents are re
NA labeling reacti
t is a 100 mM clea
on reactions. It is s
thium salt (pH 7).
NA labeling reacti
t is a 100 mM clea
ng, labeling, and a
on reactions. Supp
alt (pH 7).
NA labeling reacti
This is a 100 mM cl
on,and all types of
eptible to hydrolysi
e used to prevent c
tion.
here high-quality r
uencing. Avoid car
e a source of false
um salt.
ents: RT, PCR,
als of the
ntration. Clear,
nscription,
Set contains 4
ar, colorless
all types of
P is a 100 mM
high-quality
DNA labeling
rless solution
all types of
plied as a 100
equired, such
ons, and
r colorless
all types of
supplied as a
equired, such
ons, and
r colorless
all types of
plied as a 100
equired, such
ons, and
lear colorless
amplification
is using uracil-
carryover
reagents are
rryover
e positives.

Cat. No.
03 622 614 001
11 969 064 001
11 277 049 001
11 922 505 001
11 051 440 001
03 732 681 001
11 934 511 001
11 969 013 001
11 051 458 001
03 732 690 001
11 934 520 001
11 969 021 001
11 051 466 001
03 732 703 001
11 934 538 001
11 969 030 001
11 051 482 001
03 732 711 001
11 934 546 001
11 969 048 001
11 420 470 001
03 732 720 001
11 934 554 001
11 969 056 001

4 x 1,250 l (4 x
37,500 rea
4 x 250 l (4 x
6,250 rea
4 x
40 x 100 l
250 l (25
standard
4 x 1,250
250 l (25
standard
1,250 l (125
31,250 stand
250 l (25 m
a
4 x 1,250
250 l (25 m
6,250 stand
1,250 l (125
standard
250 l (25
standard
4 x 1,250
250 l (25
standard
1,250 l (125
standard
250 l (25 m
a
4 x 1,250
250 l (25
standard
1,250 l (125
standard
250 l (25
standard
4 x 1,250
250 l (25
standard
1,250 l (125
standard
Pack Size
x 125 mol, 4 x 100
actions at 20 l fin
x 25 mol, 4 x 100
actions at 20 l fina

x 10 mol (4 x 100
l (40 x 10 mol, 40

mol, 100 mM) for
d PCR assays of 20

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) 100
dard PCR assays o
mol) for up to 6,250
assays of 20 l eac

l (4 x 125 mol, 4
mol, 100 mM) 100
dard PCR assays o
mol, 100 mM) fo
d PCR assays of 20
mol, 100 mM) for
d PCR assays of 20

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
assays of 20 l eac

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
mol, 100 mM) for
d PCR assays of 20

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20

www.roche
0 mM) for up to
nal volume
mM) for up to
al volume
l)
x 100 mM)
r up to 6,250
0 l each
x 100 mM)
r up to 6,250
0 l each
0 mM, for up to
of 20 l each
standard PCR
ch
x 100 mM)
mM, for up to
f 20 l each
or up to 31,250
0 l each
r up to 6,250
0 l each
x 100 mM)
r up to 6,250
0 l each
or up to 31,250
0 l each
standard PCR
ch
x 100 mM)
r up to 6,250
0 l each
or up to 31,250
0 l each
r up to 6,250
0 l each
x 100 mM)
r up to 6,250
0 l each
or up to 31,250
0 l each
e-applied-science

Price in
1.061,20
235,50
126,10
885,00
68,80
1.029,80
89,10
328,70
68,80
1.029,80
89,10
328,70
68,80
1.029,80
89,10
328,70
68,80
1.029,80
89,10
328,70
94,30
1.029,80
89,10
328,70

1
33

e.com

1
Dis
34

www.r

PCR

Conv
dCTP
Wate
cDNA
PCR

Read
each
react
dUTP
Did
Prod
Dide

2',3'-
prime
Kleno
ddAT
the s
Rib
Prod
Ribo

Suita
DNA
ATP,
solut
ATP

Suita
prepa
salt s
ATP

Aden
form.
deter
ATP

ATP i
lumin
speci
tripho
CTP

CTP,
such
is tes
GTP

GTP,
a cel
GTP

Suita
prepa
salt s
UTP

This s
trans
100 m

scovery
roche-applied-sc
Nucleotide Mix
venient, easy-to-us
P, dGTP, and dTTP,
er. Optimized for di
A synthesis, and p
Nucleotide Mix
P
dy-to-use premixed
at 10 mM, and dU
tions. Prevent carry
P instead of dTTP b
deoxynucleo
duct Name
eoxynucleoside T
Dideoxynucleoside
er catalyzed by
ow enzyme and ar
TP, ddCTP, ddGTP,
odium salt (pH 8.3
bonucleotide
duct Name
onucleoside Triph
able for in vitro tra
sequencing. This
CTP, GTP, and TTP
aration is tested fo
solution, 100 mM, p
nosine-5'-triphosph
. It can be used for
rmination of Lucife
is supplied as the
nometric determina
ial quality preparat
osphate in crystal
a 100 mM solution
as in vitro RNA tr
sted for the absenc
disodium salt, is r
l-free system.
solution, 100 mM, p
special quality pre
scription since it is
mM solution of the
Reagent
cience.com
se, clear colorless s
each at 10 mM co
irect use in all type
rimer-extension.
PLUS

d solution of sodiu
UTP at 30 mM. Opt
yover contaminatio
by pretreatment wi
otides
Triphosphate Set
e triphosphates inh
e used in Sanger s
ddTTP; each a 10
3).
es
hosphate Set
nscription reaction
special quality set
P, each containing
salt (pH 7).
ns such as in vitro
or the absence of R
pH 7.
hate is supplied as
r applications, suc
erase activity in ce
disodium salt. Use
ation of Luciferase
tion contains high
form.
n of the lithium sa
ranscription. This s
ce of RNases.
equired as a coenz
ns such as in vitro
or the absence of R
pH 7.
eparation of UTP is
tested for the abs
e lithium salt (pH 7
ts
solution of sodium
oncentration in PC
es of amplification
m salts of dATP, d
timized for most am
on using PCR prod
ith Uracil-DNA Gly
hibit chain elongat
sequencing. Conta
mM clear colorles
ns and RNA polym
t consists of 4 sepa
g a 100 mM clear, c
RNA transcription
RNases. Supplied a
s the disodium salt
h as the luminome
ll extracts.
e in applications, s
e activity in cell ext
ly purified adenos
lt, is suitable for ap
special quality prep
zyme for protein b
RNA transcription
RNases. Supplied a
s suitable for in vitr
sence of RNases. U
7).
m salts of dATP,
CR Grade
reactions,
dGTP, dCTP,
mplification
ducts with
ycosylase.
tion of a
ains 4 vials:
ss solution of
merase-directed
arate vials of
colorless
n. The
as a lithium
t in crystal
etric
uch as the
tracts. This
ine-5'-
pplications
paration of CTP
biosynthesis in
n. The
as a lithium
ro RNA
UTP is a

11 581 295 001
11 814 362 001
11 888 412 001
Cat. No.
03 732 738 001
Cat. No.
11 277 057 001
11 140 965 001
10 127 523 001
10 127 531 001
10 519 979 001
10 519 987 001
11 140 922 001
10 106 399 001
11 140 957 001
11 140 949 001

200 l 10 mM, e
l
2,000 l (10 x
5,000 reaction
2 x 100 l f
reactions o
4 x 100
4 x 200 l
400
400
400
400
each, for up to 500
final reaction volu
x 200 l) 10 mM, e
ns of 20 l final rea

for up to 10 mM, e
of 20 l final react

Pack Size
l (4 x 1 mol; 10 m

Pack Size
(4 x 20 mol, 100

l (40 mol, 100 m

5 g
10 g

1 g
5 g

l (40 mol, 100 m

250 mg

l (40 mol, 100 m

l (40 mol, 100 m

0 reactions of 20
me
each, for up to
action volume
ach, for 500
ion volume
mM each)
mM, each)
mM)
mM)
mM)
mM)

60,00
445,60
120,80
Price in
228,40
Price in
222,30
108,40
56,60
92,60
50,50
199,40
108,40
198,00
108,40
108,40

Di

Pol
Prod
Poly

Poly(
work
tail to
(mRN
Poly

Use a
activi
single
this l
Poly

Poly(
chain
Poly

Use a
bioph
It is a
the d
Nuc
Prod
Bioti

Subs
trans
with
conju
Bioti

Nonr
can r
Detec
using
Bioti

For n
trans
(Tran
color
Bioti

Subs
rever
using
colon
Digo

Subs
vitro
of 35
the D
Digo

Subs
Repla
Use t
South
Digo

Subs
trans
labele
and r
Digo

Subs
rever
recom
DNA
Fluor

Subs
vitro
hybri
Fluor

scovery
ynucleotide
duct Name
(A)
(A) has a chain len
king solution is 0.5
o an RNA molecule
NA) for translation
(A) x (dT)
15

as a primer for rev
ity of reverse trans
e strand of poly(A)
ong strand of poly
(dA)
(dA) was prepared
n length is 250-500
[d(I-C)]
as a template for R
hysical investigatio
also used as a prim
determination of sm
cleotides fo
duct Name
in-11-CTP
trate for RNA poly
scription in RNA la
Biotin-16-UTP. De
ugate or ELISA wit
in-16-UTP
radioactively label
replace UTP as a s
ct labeled RNA wit
g a Streptavidin-AP
in-16-dUTP
nonradioactive DNA
slation. Substrate fo
nscriptor). Detect u
r or chemiluminesc
in-16-ddUTP
trate for DNA poly
rse transcriptase (T
g TdT. Biotin-labele
ny/plaque screens,
oxigenin-11-UTP
trate for SP6, T3, a
transcription RNA
to 65. Detect labe
DIG Nucleic Acid D
oxigenin-11-dUTP
trate for Taq, E. co
aces dTTP in nick t
this alkaline-labile
hern blots planned
oxigenin-11-dUTP
salation, random pr
ed DNA needs to
reprobing, use DIG
oxigenin-11-ddUT
trate for E. coli DN
rse transcriptase. Id
mbinant TdT. DIG-
/RNA transfers, IS
rescein-12-UTP
transcription for R
dization and direc
rescein-AP, or Anti
Reagent
es
ngth of 2,100 to 10,
mg/ml. Polyadeny
e. This process pro
.
verse transcriptase
sriptases. Consists
). Short (15 bp) se
y(A).
from dATP using
0 bases and varies
RNA polymerases a
ons.
mer template with
mall amounts of dIT
r Labeling
ymerase (SP6/T3/T
beling. For higher
etect labeled RNA w
th Strepavidin-AP.
RNA during in vitr
ubstrate for SP6, T
th a fluorescent st
P conjugate.
A labeling by rand
or TdT, DNA polym
using streptavidin-
cent substrate (CS
ymerase I, TdT, Taq
Transcriptor). Labe
ed oligo is used fo
, and in situ hybrid
and T7 RNA Polym
A labeling reaction
eled RNA using An
Detection (color or
P, alkali-labile
oli DNA polymeras
transalation, rando
formulation when
d.
P, alkali-stable
oli polymerase, RT
rimed labeling, and
survive alkaline tre
G-11-dUTP, alkali-l
TP
NA polymerase, T4
deal for 3'-end lab
labeled oligos can
H, and colony/plaq
and T7 RNA Polym
RNA labeling. Dete
ct fluorescence or d
i-Fluorescein-POD
ts
,000 nucleotides. T
ylation is the additi
oduces mature me
s and can be appl
of 1 long (at least
quences of dT are
terminal transfera
s by lot.
and as a DNA mod
Kornberg DNA po
TP, dGTP, and dCT
T7). Replaces CTP i
more uniform labe
with fluorescent st
ro transcription. Bi
T3, and T7 RNA po
treptavidin conjuga
dom priming, PCR,
merase I, Taq, and
alkaline phosphat
PD, CDP-Star ).
q, T4 DNA polymer
el the 3'-end of olig
or DNA/RNA transf
dization..
merases. Replaces U
using a percent D
nti-DIG-AP and ch
chemiluminescen
se, RT, and termina
om primed labeling
n stripping and rep
T, and TdT. Replace
d PCR. Use when t
eatment. For memb
labile.
4 /T7 DNA polyme
beling of oligonucle
n be used as a prob
que screening.
merase. Can replace
ect labeled RNA by
detection by ELISA
D.
The suggested
on of a poly(A)
essenger RNA
ied to test the
t 1,000 bp),
e hybridized to
se. Mean
del for
lymerase for
TP.
in in vitro
el density, use
treptavidin
iotin-16-UTP
olymerase.
ate or by ELISA
or nick
RT
ase and a
rase, and
gonucleotides
fers,
UTP in the in
Dig-UTP ratio
oose one of
t) Kits.
al transferase.
g, and PCR.
probing of
es dTTP in nick
the DIG-
brane stripping
rase, Taq, and
eotides with
be for
e UTP in in
y in situ
A using Anti-

Cat. No.
10 108 626 001
10 108 677 001
10 223 581 001
10 108 812 001
11 219 847 001
Cat. No.
04 739 205 001
11 388 908 910
11 093 070 910
11 427 598 910
03 359 247 910
11 209 256 910
11 573 152 910
11 573 179 910
11 093 088 910
11 558 706 910
11 570 013 910
11 363 905 910
11 427 857 910

25
25
50
25
57
25
25
125
25
125
5 x 125
25
25
Pack Size
100 mg

5 A
260
units

5 A
260
units

10 A
260
units
50 A
260
units

Pack Size
l (250 nmol) (10 m

l (250 nmol) (10 m

0 l (50 nmol) (1 m

5 l (25 nmol) (1 m

l (200 nmol, 3.5 m
l (250 nmol, 10 m

5 l (25 nmol) (1 m
5 l (125 nmol) (1 m

5 l (25 nmol) (1 m
5 l (125 nmol) (1 m
l (5 x 125 nmol) (5
5 l (25 nmol; 1 mM

l (250 nmol) (10 m

www.roche
mM)
mM)
mM)
mM)
mM)
mM)
mM)
mM)
mM)
mM)
5 x 1 mM)
M)
mM)
e-applied-science

Price in
130,10
141,20
193,20
139,80
523,30
Price in
253,90
253,90
286,00
263,40
196,10
260,60
225,80
826,40
225,80
826,40
3.325,20
274,20
354,70

1
35

e.com

1
Dis
36

www.r

Fluor

Subs
trans
and P
or EL
Tetra

Used
trans
Labe
hybri
Mo
Prod
7-De

7-De
termi
comp
stretc
m7G

Use t
Polym
Nuc
Prod
AMP

Comp
hydro
cleav
veno
ATP-

ATP-
Hydro
thiop
Supp
ATP-

ATP-
Hydro
thiop
Supp
GTP-

GTP-
hydro
the s
powd
5-Br

5-Bro
that c
studi
sister
Ca
Enz
Prod
Acid

Acid
phos
lyoph
+25
Aden

Aden
used
inosin
phos

scovery
roche-applied-sc
rescein-12-dUTP
trate for terminal t
scriptase. Replaces
PCR. Use labeled p
LISA with Anti-Fluo
amethyl-Rhodam
d in nonradioactive
slation, random-pri
led probes show r
dization for direct
odified Nucle
duct Name
eaza-2'-deoxy-gu
aza-2'-deoxy-guan
ination sequencing
pression problems
ches of DNA.
G(5')ppp(5')G
the nucleotide, m7
merase promoter s
cleotide Ana
duct Name
P-PNP
petitive inhibitor of
olyzing between th
vage between the
m phosphodiester
--S
-S is a substrate
olyzed very slowly
phosphorylated, pro
plied as a lithium sa
--S
-S is a substrate
olyzed very slowly
phosphorylated, pro
plied as a tetralithiu
--S
--S activates gua
olyzed enzymatical
timulation of aden
der.
romo-2'-deoxyuri
omo-2'-deoxyuridi
can be incorporate
es of DNA synthes
r chromatid exchan
atabolic An
zymes
duct Name
Phosphatase
Phosphatase grad
phohydrolase [aci
hilizate. Specific ac
C with 4-nitrophen
nosine Deaminas
nosine Deaminase
for the determina
ne analogs. Solutio
phate, pH approxi
Reagent
cience.com
P
transferase, DNA p
s dTTP in random p
probes for ISH with
orescein-AP.
mine-5-dUTP
e labeling of DNA.
imed labeling, PCR
red fluorescence a
fluorescence dete
eotides
uanosine-5'-triph
nosine-5'-triphosp
g methods, in plac
in gel electrophor
7G(5')ppp(5')G, tog
systems to initiate i
alogs
f ATP-dependent s
he a- and -phos
- and -phosph
rase and adenylate
e and inhibitor of A
by phosphatases
oteins are resistan
alt, 100 mM solutio
by phosphatases
oteins are resistan
um salt powder.
anine-nucleotide-b
lly. It inhibits GTPa
nylate cyclase. Sup
idine
ne is an immunoc
ed into DNA instea
sis, and to detect m
nge (SCE).
nalysis
de II (orthophospho
d optimum]) from
ctivity is approxima
nyl phosphate as t
se (ADA)
(adenosine amino
tion of adenosine
on in 50% glycerol
mately 6.
ts
polymerase I, Taq,
primed labeling, ni
h direct fluorescen
Replaces dTTP in
R, 3-tailing, and cD
nd are suitable for
ection.
hosphate
phate is used in did
ce of dGTP to overc
resis when sequen
gether with the SP
in vitro RNA synth
systems. Substrate
phorus atom, yet r
horus atom. Subst
e cyclase.
ATP-dependent en
and most ATPases
nt to protein phosp
on, pH 7.
ATP-dependent en
and most ATPases
nt to protein phosp
binding proteins, a
ases more potently
plied as a tetralith
hemically detectab
ad of thymidine. Us
mutagenic substan
oric-monoester
potato is supplied
ately 2 U/mg lyoph
the substrate.
ohydrolase) from c
analogs to the cor
l (v/v), 10 mM pota
and reverse
ick translation,
nce detection
nick
DNA synthesis.
r in situ
deoxy-chain
come
ncing GC-rich
P6 and T7 RNA
hesis.
e for enzymes
resistant to
trate of snake
nzyme systems.
s. Once
phatases.
nzyme systems.
s. Once
phatases.
and is slowly
y than GTP in
ium salt
ble nucleotide
sed for in vivo
nces using
d as a
hilizate at
calf intestine is
rresponding
assium

11 373 242 910
11 534 378 910
Cat. No.
10 988 537 001
10 904 988 001
Cat. No.
10 102 547 001
11 162 306 001
10 102 342 001
10 220 647 001
10 280 879 001
Cat. No.
10 108 227 001
10 102 105 001

25
25
20
5 l (25 nmol) (1 m

5 l (25 nmol) (1 m

Pack Size
0 l (2 mol, 10 m

5 U (at 260 nm)

Pack Size
25 mg

20 mol (200 l)

25 mg

10 mg

1 g

Pack Size
500 mg

10 mg (2 ml)

mM)
mM)
mM)

257,90
241,80
Price in
95,70
170,90
Price in
203,70
469,10
410,50
319,50
70,00
Price in
276,90
192,40

Di

Aden

Aden
used
inosin
appro
Alco

Alcoh
syste
Spec
ethan
Alde

Aldeh
NAD
prote
Alka

Alkal
phos
selec
Poly(
Asco

Remo
(asco
mate
oxalic
Carn

Key e
endo
from
acylC
Citra

Catal
enzym
mole
Crea

Enzym
of cre
dipho
Spec
lyoph
Form

Most
dehy
cyste
-G

-G
as a s
appro
32,00
-G

Susp
gene
fluore
galac
Gluc

Gluco
cofac
3.2 M
Gluc

Gluco
cofac
phos
solut
Gluc

Gluco
mese
Addit
amm

scovery
nosine Deaminas
nosine Deaminase
for the deaminatio
ne analogs. Suspe
oximately 6.
ohol Dehydrogena
hol Dehydrogenas
ems. Substrate spe
ific activity is appr
nol as the substrat
ehyde Dehydroge
hyde Dehydrogena
PH recycling syste
ein at +25C with a
aline Phosphatase
ine Phosphatase g
phohydrolase [alk
ctive cleavage of te
(U) is not cleaved.
orbate Oxidase S
ove ascorbic acid f
orbate, vitamin C)
erial, such as detec
c acid in urine dur
nitine Acetyltrans
enzyme in the met
oplasmic reticulum
an acyl-CoA thioe
CoA/CoA in subcel
ate Lyase (CL)
lyzes the cleavage
me complex that c
cular weights abo
atine Kinase (CK)
me expressed by v
eatine and consum
osphate.
ific Activity - appro
hilizate at +37C).
mate Dehydrogen
t widely used in co
drogenase is a dim
eine residue which
Galactose Dehydr
alactose Dehydrog
suspension in 3.2
oximately 6. It is a
00 D).
Galactose Dehydr
ension in 3.2 M am
for -galactose D
escens strain BMT
ctosidase promote
cose-6-Phosphat
ose-6-Phosphate D
ctor recycling syste
M ammonium sulfa
cose-6-Phosphat
ose-6-Phosphate D
phate. Grade I from
ion, pH approx. 6.
cose-6-Phosphat
ose-6-Phosphate D
enteroides is a com
tional reagent gluc
onium sulfate solu
Reagent
se (ADA)
(adenosine amino
on of adenosine an
ension in 3.2 M am
ase (ADH)
e from yeast is a c
cificity is limited to
rox. 300 U/mg enzy
te.
enase
ase from yeast is a
ems. Specific activi
acetaldehyde as th
e (AP)
grade I (orthophos
aline optimum]) fr
erminal phosphate
Spatula
from aqueous solu
interferes with the
ction of erythrocyte
ring research studi
sferase
abolic pathway in
. Catalyzes the rev
ester to carnitine a
llular compartmen
of citrate to aceta
consists of three di
ut 54,000, 32,000, a
)
various tissues and
mes ATP to create
ox. 350 U/mg lyop
nase
ofactor recycling sy
mer of two identica
is essential for ac
rogenase
genase from Pseud
M ammonium sulf
dimer with subuni
rogenase S
mmonium sulfate,
Dehydrogenase S
TU 102, placed und
r in the plasmid pU
te Dehydrogenas
Dehydrogenase (G
ems for NADPH. G
ate solution, pH ap
te Dehydrogenas
Dehydrogenase (G
ems for NADPH. A
m yeast. Suspensi
te Dehydrogenas
Dehydrogenase (G
mponent of cofacto
cose-6-phosphate
ution, pH approx. 6
ts
ohydrolase) from c
nalogs to the corre
mmonium sulfate so
component of NAD
o low molecular we
yme protein at +25
a component of NA
ity is approx. 20 U/
he substrate.
sphoric-monoester
rom calf intestine i
groups from oligo
utions where ascor
e investigation of s
es in urine or deter
ies.
mitochondria, per
versible transfer of
nd regulates the r
ts.
ate and oxaloaceta
fferent polypeptide
and 10,000, respec
d cells. Catalyzes th
phosphocreatine a
hilizate at +25C (
ystems for NADH.
al subunits. The en
ctivity or structural
domonas fluoresce
fate, 1 mM EDTA,
its of equal size (s
1 mM EDTA, pH a
is from the Pseudo
der the control of a
UR 51.
se (G6P-DH)
G6P-DH) is a comp
Grade II from yeast
prox. 6.
se (G6P-DH)
G6P-DH) is a comp
Additional reagent
ion in 3.2 M ammo
se (G6P-DH)
G6P-DH) from Leuc
or recycling system
. Suspension in 3.2
6.
calf intestine is
esponding
olution, pH
DH recycling
eight alcohols.
5C with
ADH and
/mg enzyme
r
s used for
onucleotides.
rbic acid
sample
rmination of
roxisomes, and
acyl groups
atio of
te, and is an
e chains with
ctively.
he conversion
and adenosine
(800 U/mg
Formate
nzyme has a
integrity.
ens is provided
pH
ubunit =
approx. 6. The
omonas
an E. coli -
ponent of
. Suspension in
ponent of
glucose-6-
onium sulfate
conostoc
ms for NADPH.
2 M

10 102 121 001
10 127 558 001
10 171 832 001
10 108 138 001
10 108 146 001
10 736 619 001
10 103 241 001
10 354 074 001
10 127 566 001
10 736 988 001
10 244 678 001
10 837 016 001
10 104 973 001
10 104 981 001
10 662 046 001
10 127 671 001
10 737 232 001
10 127 655 001
10 165 875 001

10 mg (1 ml)

1 g (34 ml)

250 U

1,500 U
7,500 U

25 spatulas

5 mg (1 ml)

120 U

100 mg
500 mg

80 U
250 U

1 mg (1 ml)
5 mg (1 ml)

50 U

10 mg (2 ml)
25 mg (5 ml)

5 mg (1 ml)

1,000 U (1 ml)

www.rochee-applied-science

164,80
492,30
211,00
63,80
256,00
72,40
172,00
163,30
99,70
398,80
125,70
294,90
59,20
209,70
264,60
192,40
364,10
310,90
105,40

1
37

e.com

1
Dis
38

www.r

-G

Used
urine
prepa
drugs
Gluta

Gluta
for N
BSA
Gluta

Gluta
nonn
ketog
and L
Gluta

Gluta
synth
Gluta

A cru
gluta
perox
to GS
Glyc

Glyce
provi
appro
subst
Hexo

For th
biolo
sacch
assay
Hexo

Hexo
yeast
sulfat
G6P-
3-Hy

3-Hyd
hydro
L-La

L-Lac
-ke
in su
L-La

L-Lac
-ke
in su
L-Ma

L-Ma
enzym
using
glyce
L-Ma

L-Ma
enzym
using
amm
Lucif

Dete
activi
relea
suffic

scovery
roche-applied-sc
Glucuronidase/Ar
d for simultaneous
e and other biologi
are protoplasts, in
s in urine.
amate Dehydrog
amate Dehydrogen
NAD(P) and NAD(P
as a stabilizer, and
amate-Oxaloace
amate-Oxaloacetat
natural L-amino ac
glutarate, catalyzes
L-glutamate.
amate-Pyruvate
amate-Pyruvate Tra
hesis of nonnatura
athione Reductas
ucial flavoenzyme i
athione is used by g
xide and is then co
SH by glutathione
erol-3-Phosphat
erol-3-Phosphate D
ded as a suspensi
ox. 6. Specific activ
trate (optimized co
okinase (HK)
he determination o
gical research sam
harides which con
y of many glycosid
okinase/Glucose
okinase/Glucose-6-
t/Leuconostoc ove
te suspension, pH
-DH. Ratio of HK:G
ydroxybutyrate D
droxybutyrate Deh
oxymonocarboxylic
actate Dehydroge
ctate Dehydrogena
etoacids to -hyd
spension in 3.2 M
actate Dehydroge
ctate Dehydrogena
etoacids to -hyd
spension in 3.2 M
alate Dehydroge
alate Dehydrogena
me that reversibly
g the reduction of
erol (v/v), pH appro
alate Dehydroge
alate Dehydrogena
me that reversibly
g the reduction of
onium sulfate solu
ferase
rmine ATP in ATP
ity of enzymes suc
sed per molecule A
cient for 5,000 ATP
Reagent
cience.com
rylsulfatase
hydrolysis of -glu
cal fluids. Use to r
enzyme immobiliz
enase (GlDH)
nase is a compone
P)H. The formulatio
d ADP as an activa
tate Transamina
te Transaminase (G
cids from -keto a
s the conversion o
Transaminase (G
ansaminase (GPT)
l L-amino acids fro
se (GR)
in the antioxidant d
glutathione peroxi
onverted to oxidize
reductase.
te Dehydrogenas
Dehydrogenase (G
on in 3.2 M ammo
vity: approx. 170 U
onditions).
of D-glucose, D-fru
mples. It may also b
vert to glucose or
des.
e-6-Phosphate De
-Phosphate Dehyd
erproducer. It is pr
approx. 6. Prepare
G6P-DH is approx. 2
Dehydrogenase (3
hydrogenase (3-HB
c acids, or the reve
enase (L-LDH)
ase from hog mus
droxycarboxylic aci
ammonium sulfat
enase (L-LDH)
ase from rabbit mu
droxycarboxylic aci
ammonium sulfat
nase (L-MDH)
ase (L-MDH) from
catalyzes the oxid
NAD
+
to NADH. S
oximately 7.
nase (L-MDH)
ase (L-MDH) from
catalyzes the oxid
NAD
+
to NADH. S
ution, pH approx. 6
generating or ATP
ch as creatine kina
ATP in biolumines
P determinations in
ts
ucuronides and su
remove cell walls f
zation studies, and
ent of cofactor recy
on contains buffer
ator.
se (GOT)
GOT) is used for th
acids. In the presen
f L-aspartate to ox
GPT)
from pig heart is
om -keto acids.
defense system. R
dase to detoxify hy
ed glutathione whi
se (GDH)
GDH) from rabbit m
onium sulfate solut
U/mg at +25C with
uctose, and D-sorb
be used to assay o
fructose, making i
ehydrogenase (H
drogenase is from
rovided as a 3.2 M
ed by mixing hexo
2:1 (protein conten
3-HBDH)
BDH) selectively ox
erse reaction.
cle is used for the
ds, or reverse reac
e solution, pH app
uscle is used for th
ds, or reverse reac
e solution, pH app
pig heart (mitocho
ation of malate to
Supplied in solutio
pig heart (mitocho
ation of malate to
Supplied in suspen
6
P consuming react
se/ATPases. One p
scence assays. One
n concentration 0.1
ulfate esters in
rom yeast to
to determine
ycling systems
substances,
he synthesis of
nce of a-
xaloacetate
used for the
Reduced
ydrogen
ch is recycled
muscle is
tion, pH
h DAP as the
bitol in food or
other
it useful in the
HK/G6P-DH)
ammonium
kinase and
nt).
xidizes (R)-3-
reduction of
ction. Provided
prox. 6.5.
he reduction of
ction. Provided
prox. 7.
ondrial) is an
oxaloacetate
n in 50%
ondrial) is an
oxaloacetate
nsion in 3.2 M
tions, and
photon is
e milligram is
1 nM to 1 M.

10 127 060 001
10 127 698 001
10 197 734 001
10 105 554 001
10 737 046 001
10 105 589 001
10 737 127 001
10 105 678 001
10 127 752 001
10 127 779 001
11 426 362 001
10 127 825 001
10 737 275 001
10 127 833 001
10 127 841 001
10 107 085 001
10 127 230 001
10 127 876 001
10 127 884 001
10 127 248 001
10 127 256 001
10 127 914 001
10 411 523 001

2 ml
10 ml

3,000 U

10 mg (1 ml)
25 mg (2.5 ml)

10 mg (1 ml)
25 mg (2.5 ml)

5 mg (1 ml)

10 mg (1 ml)
100 mg (10 ml)

1,500 U (1 ml)

15 mg (5 ml)
30 mg (10 ml)

10 mg (2 ml)
25 mg (5 ml)

100 mg (10 ml)

10 mg (2 ml)
25 mg (5 ml)
100 mg (10 ml)
5 mg (1 ml)

5 mg (1 ml)
25 mg (5 ml)

1 mg protein

66,70
245,90
47,80
143,10
270,20
122,80
225,30
134,40
105,40
650,50
85,40
156,20
275,80
134,40
294,90
251,10
43,40
86,80
293,50
56,60
56,60
159,10
148,90

Di

Lucif

Bacte
the d
forme
NAD

Use w
and f
activi
subst
Nitra

Nitra
nitrat
prepa
Nucl

Nucle
rever
produ
Phos

Phos
of ke
sulfat
Pyro

Inorg
pyrop
prote
amm
Pyru

Pyruv
Catal
mole
amm
Pyru

Pyruv
Catal
mole
(v/v),
Sorb

Redu
relate
Xant

Catal
oxida
purin
EDTA
Coe
Prod
Acet

Acety
using
group
Purity
NAD

Nicot
It act
provi
NAD

Nicot
It act
provi
NAD

NAD
This
NAD

NAD
This

scovery
ferase
erial luciferase use
determination of NA
ed or consumed. F
D(P)H:FMN Oxido
with luciferase from
for reactions in wh
ity: approx. 7 U/mg
trate, and NADH a
ate Reductase
te Reductase is us
te in culture media
aration is a crucial
leoside Monopho
eoside Monophos
rsible transfer of a
ucing adenosine d
sphoglucose Isom
phoglucose Isome
etoses to aldoses. S
te, pH approximate
ophosphatase, ino
ganic pyrophospha
phosphate to form
ein, RNA, and DNA
onium sulfate, pH
vate Kinase (PK)
vate Kinase from ra
lyzes the transfer o
cule of pyruvate a
onium sulfate solu
vate Kinase (PK)
vate Kinase from ra
cule of pyruvate a
, pH approx. 6.
bitol Dehydrogen
uces L-iditol to L-s
ed sugar alcohols.
thine Oxidase (XO
lyzes oxidation of h
ation of xanthine to
nes in some specie
A, pH approx. 8.
enzymes
duct Name
tyl-Coenzyme A
yl-Coenzyme A is u
g radioisotopes. CA
ps from acetylcoen
y: 85% acetyl-CoA
D
tinamide adenine d
ts as a coenzyme i
ded as a lyophiliza
D
tinamide adenine d
ts as a coenzyme i
ded as a lyophiliza
DH
H is the reduced f
NADH Grade I, dis
DH
H is the reduced f
NADH Grade II, di
Reagent
ed together with N
AD(P)H, and for re
From Photobacteriu
oreductase
m Photobacterium
hich NAD(P)H is fo
g lyophilizate at +2
as the coenzyme.
sed for nitrate dete
a, and determinatio
l step. Deproteinat
osphate Kinase
phate Kinase is a l
phosphate group
diphosphate and a
merase (PGI)
erase (PGI) from ye
Supplied as a susp
ely 6.
organic (PPase)
atase (PPase) catal
orthophosphate. I
A synthesis. Suppli
6.
)
abbit muscle is an
of a phosphate gro
nd 1 molecule of A
ution, pH approx. 6
)
abbit muscle is an
of a phosphate gro
nd 1 molecule of A
ase (SDH)
orbose. Also acts o
Allows the reduct
OD)
hypoxanthine to xa
o uric acid. Plays a
es. Suspension in 3
used to assay CAT
AT enzyme activity
nzyme A to chloram
A (enzymatic/absor
dinucleotide is a c
n redox reactions.
ate.
dinucleotide is a c
n redox reactions.
ate.
form of nicotinamid
sodium salt is prov
form of nicotinamid
sodium salt is sup
ts
AD(P)H:FMN oxid
eactions in which N
um fischeri .
fischeri to determ
ormed or consume
25C and pH 7.0 w
ermination: Assay o
on of NO
3
in serum
tion is required for
liver enzyme that c
from adenosine tr
nucleoside diphos
east is used for the
pension in 3.2 M am
lyzes the hydrolysi
It plays an importa
ed in suspension i
n enzyme involved
oup from PEP to A
ATP. Suspension in
6.
n enzyme involved
oup from PEP to A
ATP. Solution in 50
on D-glucitol and
tion of ketones to p
anthine and can fu
an important role in
3.2 M ammonium s
T enzyme activity in
y catalyzes the tran
mphenicol.
rbance), 2% Li.
coenzyme found in
This NAD Grade I
coenzyme found in
This NAD Grade I
de adenine dinucle
vided as an amorph
de adenine dinucle
pplied as an amorp
doreductase for
NAD(P)H is
mine NAD(P)H,
d. Specific
with FMN as the
of nitrite and
m. Sample
r good results.
catalyzes the
riphosphate,
sphate.
e isomerization
mmonium
s of inorganic
ant role in
in 3.2 M
in glycolysis.
DP, yielding 1
n 3.2 M
in glycolysis.
DP, yielding 1
0% glycerol
other closely
polyols.
urther catalyze
n catabolism of
sulfate, 10 mM
n cell extracts
nsfer of acetyl
all living cells.
, free acid is
all living cells.
I, free acid is
eotide (NAD).
hous powder.
eotide (NAD).
phous powder.

10 476 498 001
10 476 480 001
10 981 249 001
10 107 948 001
10 127 396 001
10 128 139 001
10 108 987 001
10 128 155 001
10 128 163 001
10 109 045 001
10 109 339 001
10 110 434 001
Cat. No.
10 101 893 001
10 101 907 001
11 585 371 001
10 127 965 001
10 127 973 001
10 127 981 001
10 127 990 001
10 621 650 001
10 107 735 001
10 128 023 001

10 m
10 m
2 mg protein

20 U

20 U

mg (60 mg lyophiliz

2 mg (1 ml)
10 mg (1 ml)

1 mg (1 ml)

10 mg (1 ml)
100 mg (10 ml)

10 mg (1 ml)

mg (60 mg lyophiliz

20 U (1 ml)

Pack Size
10 mg
50 mg
200 mg
1 g
5 g

1 g
5 g
10 g
500 mg

1 g

www.roche
zate)
zate)
e-applied-science

152,90
232,70
186,40
197,90
40,40
137,20
109,70
84,10
333,70
79,40
312,10
99,70
Price in
102,40
436,40
1.466,90
84,10
284,60
59,20
241,50
433,50
159,10
147,30

1
39

e.com

1
Dis
40

www.r

NAD

Nicot
anab
requi
amor
NAD

NAD
provi
Sub
Prod
Crea

Subs
mole
phos
Gluc

Gluco
comp
enter
subst
Phos

Use P
pyruv
Enz
Prod
N-Ac

Use N
(appr
gluco
N-Ac

Stand
resea
gluco
Hitac
N-Ac

Addit
life sc
Acety
2,3-D

2,3-D
dipho
scien
Free

Enzym
samp
resea
role o
L-Ca

Dete
enzym
the te
Gluc

Fast,
deter
scien
is com

scovery
roche-applied-sc
DP
tinamide adenine d
olic reactions, suc
ire NADPH as a re
rphous powder.
DPH
PH is the reduced
ded as an amorph
bstrates for
duct Name
atine phosphate
trate for creatine k
cule that serves as
phates in skeletal
cose-6-phosphat
ose-6-Phosphate i
pound is very com
ring a cell will beco
trate for glucose-6
sphoenol-pyruva
Phosphoenol-pyru
vate kinase.
zymatic Test
duct Name
cetyl--D-Glucos
N-Acetyl--D-Glu
rox. 50 tests) for th
osaminidase in urin
cetyl--D-Glucos
dard for the determ
arch samples with
osaminidase. It can
chi 705, 704, and E
cetyl--D-Glucos
tional control solut
cience research sa
yl--D-glucosam
Diphosphoglycer
Diphosphoglycerate
osphoglycerate in
nce research applic
Fatty Acids, Half
matic colorimetric
ples from serum an
arch tool to increas
of free fatty acids i
arnitine
rmine L-carnitine
matic UV test. Line
est solution. For us
cosidase Assay
sensitive, specific
rmination of neutra
nce research applic
mpatible with micr
Reagent
cience.com
dinucleotide phosp
ch as lipid and nuc
educing agent. NAD
form of NADP
+
. N
hous powder bottle
Enzymatic A
kinase. The enzym
s a rapidly mobiliza
muscle and brain.
e
s glucose sugar p
mon in cells, as th
ome phosphorylate
6-phosphatase.
ate
vate PEP, monopo
ts
saminidase (NAG
ucosaminidase (NA
he determination o
ne in life science r
saminidase Stan
mination of NAG a
the aid of the Test
n be used in autom
pos 5060.
saminidase Cont
tion for the determ
amples with the aid
inidase on automa
rate (2,3-DPG)
e (2,3-DPG) is use
blood in the range
cations.
f Micro Test
assay to determin
nd plasma. The tes
se scientific knowl
in blood.
levels in seminal p
earity in the range
se in life science re
colorimetric assay
al -glucosidase
cations. Cannot be
roplate and cuvette
ts
phate is a coenzym
cleic acid synthesis
DP disodium is su
NADPH tetrasodiu
ed under nitrogen.
Analysis
e is a phosphoryla
able reserve of hig
.
hosphorylated on
e vast majority of g
ed in this way. It is
otassium salt as a s
G)
AG) in a colorimet
of N-Acetyl--D-
research applicatio
ndard (NAG Stand
ctivity in urine life
t-Combination N-A
mated analyzers, su
trol (NAG Contro
mination of NAG ac
d of the Test-Com
ated analyzers.
ed for the determin
e of 0.02 - 0.15 m
ne free fatty acids i
st combination is in
ledge about the ph
plasma, serum, or u
of 5.6 - 112 M L-
esearch applicatio
y for the quantitati
in human semen s
e used in other spe
e formats.
me used in
s, which
pplied as an
m salt is
ated creatine
gh-energy
carbon 6. This
glucose
s used as a
substrate for
tric assay
ons.
dard)
science
Acetyl--D-
uch as the
ol)
ctivity in urine
bination N-
nation of 2,3-
ol in life
n research
ntended as a
hysiological
urine using this
-carnitine in
ns.
ve
samples in life
ecimens. Assay

10 128 031 001
10 128 040 001
10 128 058 001
10 240 354 001
10 107 824 001
10 621 692 001
10 621 706 001
Cat. No.
10 621 714 001
10 621 722 001
10 127 647 001
10 108 294 001
Cat. No.
10 875 406 001
10 982 962 001
11 164 368 001
10 148 334 001
11 383 175 001
11 242 008 001
11 742 027 001

ap
1 kit fo
app
approximately
approxim
1 kit fo
100 mg
500 mg
1 g
5 g
100 mg
500 mg
1 g
Pack Size
5 g
10 g

5 g

1 g

Pack Size
pproximately 50 tes

5 x 3 ml

3 x 1 ml

or approximately 3

proximately 5 x 10 t

3 x 10 tests (test c
mately 3 x 10 determ

or 30 tests and 10

sts
30 tests
tests
combination for
minations)
blanks

66,40
262,70
396,10
1.549,00
199,40
791,80
1.462,40
Price in
98,30
179,20
116,90
294,90
Price in
605,60
189,30
98,20
352,10
604,20
462,60
363,50

Di

Me
Prod
Nitrit

Semi
wate
and b
the p
Nitric

Dete
Nitra
nicot
of the
Lab
Alb
Prod
Bovi

Spec
chec
prote
Bovi

Stabi
when
prote
elect
Bovi

Highe
meta
ligan
in low
Buf
Prod
Buffe

Stabl
resist
for th
temp
Buffe

Stabl
resist
for th
temp
Buffe

Stabl
resist
for th
temp
Buffe

Stabl
resist
for th
temp
DTT

For lu
extra
prote
mono
Form

Color
hybri
elect
to sta

scovery
etabolite A
duct Name
te/Nitrate, Color
-micro method for
r, plant material, fo
biological samples
presence of nitrate
c Oxide, Colorim
rmination of nitric
te present in the s
tinamide adenine d
e enzyme nitrate re
boratory R
bumins
duct Name
ne Serum Album
ial BSA quality for
ked for the absenc
eases, and is used
ne Serum Album
lize enzymes to pr
n proteins are in lo
ein blocker, media
rophoresis and pro
ne Serum Album
est quality BSA. Us
bolism in biologica
d binding, and inv
w concentration.
ffers and Bu
duct Name
ers in a Box, Prem
e 10x solution of P
tant to enzymatic a
he absence of nucl
perature.
ers in a Box, Prem
e 20x solution of S
tant to enzymatic a
he absence of nucl
perature.
ers in a Box, Prem
e 10x solution of T
tant to enzymatic a
he absence of nucl
perature.
ers in a Box, Prem
e 10x solution of T
tant to enzymatic a
he absence of nucl
perature.
uminometric deter
cts. Superb protec
eins/enzymes (com
othiols in the reduc
mamide
rless liquid suitable
dization. Formamid
rophoresis by deio
abilize single stran
Reagent
Analysis
imetric Test
r determining nitrit
oodstuffs, drugs, c
s. Nitrate reduced t
reductase.
metric Assay
oxide via nitrite in
sample is reduced
dinucleotide phosp
eductase.
Reagents
min
r molecular biology
ce of DNases, nick
to stabilize enzym
min Fraction V
revent proteolysis a
ow concentration. S
supplement, and a
otein determinatio
min Fraction V, fat
sed for fatty acid a
al systems, identify
vestigate ionic bind
uffer Compo
mixed PBS Buffe
PBS, filtered throug
and nonenzymatic
lease or protease a
mixed SSC Buffe
SSC, filtered throug
and nonenzymatic
lease or protease a
mixed TAE Buffer
TAE, filtered throug
and nonenzymatic
lease or protease a
mixed TBE Buffer
TBE, filtered throug
and nonenzymatic
lease or protease a
mination of Lucife
ctive reagent for su
mpared to -merc
ced state and qua
e for denaturing g
de is used as an R
onizing RNA. In ca
ds of denatured D
ts
te and/or nitrate to
cosmetics, and env
to nitrite by reduce
n biological fluids i
to nitrite by reduc
phate (NADPH) in
y. This albumin pre
king activity, RNase
es.
and denaturation,
Suitable as a buffe
as a protein standa
ns.
tty acid free
and lipid research.
y transport mecha
ding. Ideal if protei
onents
er, 10x
gh 0.2 m pore siz
degradation. Each
activity, and stores
er, 20x
gh 0.2 m pore siz
degradation. Each
r, 10x
gh 0.2 m pore siz
degradation. Each
r, 10x
gh 0.2 m pore siz
degradation. Each
erase gene activity
ulfhydryl groups of
captoethanol). Mai
ntitatively reduces
els and nucleic ac
RNA stabilizer in ge
pillary electrophor
DNA.
o investigate
vironmental
ed NADPH in
n a microplate.
ced
the presence
eparation is
es, and
especially
er component,
ard in
Study lipid
nisms, study
ns are present
ze membrane,
h lot is tested
s easily at room
ze membrane,
h lot is tested
s easily at room
ze membrane,
h lot is tested
s easily at room
e membrane,
h lot is tested
s easily at room
in cell
f
ntains
s disulfides.
cid
el
resis, it is used

Cat. No.
11 746 081 001
11 756 281 001
Cat. No.
10 711 454 001
10 735 078 001
10 735 086 001
10 735 094 001
10 735 108 001
10 775 835 001
Cat. No.
11 666 789 001
11 666 681 001
11 666 690 001
11 666 703 001
10 197 777 001
10 708 984 001
11 583 786 001
11 814 320 001

1 test combina
1 test
Pack Size
ation for approxim

combination for 9

Pack Size
20 mg (1 ml)

50 g
100 g
500 g
1 kg
50 g

Pack Size
4 l

4 l

4 l

4 l

2 g
10 g
25 g
500 ml

www.roche
ately 64 assays
6 wells
e-applied-science

Price in
262,10
458,30
Price in
120,40
123,30
220,80
887,30
1.296,70
409,60
Price in
114,30
127,20
127,20
116,60
inquire
183,80
417,60
91,10

1
41

e.com

1
Dis
42

www.r

Guan

Suita
stron
Tris b

Tris B
comp
prepa
Tris h

Tris H
biolo
comb
Elec
Prod
Agar

Agar
prepa
analy
phag
Agar

Agar
analy
of hig
Agar

Agar
bp). I
sizing
fragm
scovery
roche-applied-sc
nidine thiocyanat
able as denaturing
nger denaturant tha
base
Base is extensively
ponent of buffer so
aration is free of p
hydrochloride
Hydrochloride is ex
gy as a buffering a
bination with Tris B
ctrophoresi
duct Name
rose LE
ose LE (low electro
arative gel electrop
ysis of PCR, examin
ge DNA, and separ
rose MP
ose MP is a high s
ytical and preparat
gh molecular weig
rose MS
ose MS is ideal fo
It can be used in s
g, and STR analysi
ments that differ by
Reagent
cience.com
te
agent for proteins
an guanidine hydr
y used in biochemi
olutions, especially
roteases, DNases
xtensively used in
agent in incubation
Base for preparatio
s Reagents
oendosmosis) is id
phoresis of nucleic
nation of RE digest
ration of RNA.
strength, multipurp
tive electrophoresi
ht DNA via pulse f
r separation of sm
separation of PCR p
s. Agarose MS dis
y only 4 base pairs

ts
s. Guanidine thiocy
rochloride.
stry and molecular
y for nucleic acid s
and RNases.
biochemistry and
n mixtures. It is us
on of Tris-HCl buff
deal for routine ana
c acids. Applicatio
tsfrom plasmid, co
pose agarose deve
s of nucleic acids
field gel electroph
all DNA fragments
products, genotyp
scriminates betwee
s.
yanate is a
r biology as a
solutions. This
molecular
ed in
fers.
alytical and
ns include
osmid, and -
eloped for
and separation
oresis (PFGE).
s (50 to 1500
ing, allele
en DNA

11 685 929 001
10 708 976 001
11 814 273 001
10 812 846 001
Cat. No.
11 685 660 001
11 685 678 001
03 573 788 001
11 388 983 001
11 388 991 001
11 816 586 001

500 g

1 kg
5 kg

500 g

Pack Size
100 g
500 g

500 g bulk
100 g
500 g
100 g

307,60
171,40
588,20
170,50
Price in
244,70
828,80
inquire
219,10
768,50
595,00

Sa

Au
Ma
Mag
Mag
Prod
Mag

Auto
using
ready
stand
Mag
Prod
Mag

Read
acids
Instru
Mag

Read
acids
Instru
Mag

Read
RNA
blood
Mag

For ri
purifi
confi
Mag

For ri
purifi
confi
conta
Mag

Use t
purifi
for in
lysate
Mag

Use t
purifi
for in
lysate
Mag

Use t
purifi
for in
lysate
Mag
Prod
Mag

Dispo
by M
Quali
eleva
Mag

Plate
for co
to mi
Mag

Deep
Pure
proce

ample Pr
utomated S
agNA Pure S
gNA Pure 96
gNA Pure 96 Sy
duct Name
gNA Pure 96 Instr
mated high-throug
g flexible software-
y-to-use reagents.
dard volume samp
gNA Pure 96 Sy
duct Name
gNA Pure 96 DNA
dy-to-use reagents
s from up to 200 l
ument. External lys
gNA Pure 96 DNA
dy-to-use reagents
s from up to 1,000
ument. External lys
gNA Pure 96 Cellu
dy-to-use reagents
using the MagNA
d, up to 1x10
6
cult
gNA Pure 96 Syst
insing the MagNA
ication run. Using
guration, the instr
gNA Pure 96 Syst
insing the MagNA
ication run. Using
guration, the instr
ainers.
gNA Pure 96 Exte
this reagent with t
ication of total nuc
n vitro diagnostic p
es.
gNA Pure 96 Bact
this reagent with t
es.
gNA Pure 96 DNA
this reagent with t
es.
gNA Pure 96 Sy
duct Name
gNA Pure 96 Filte
osable pipetting tip
MagNA Pure 96 Inst
ity Control procedu
ated temperatures.
gNA Pure 96 Outp
for collecting elua
ooling by maximizi
nimize the risk of
gNA Pure 96 Proc
p well plates with 9
96 Instruments; nu
edures; inert to ch
eparatio
Sample Pr
Systems
System
ystem - Instrum
rument
ghput instrument f
-driven protocols a
Typical run takes
les.
ystem - Kits
A and Viral NA Sm
s in two prefilled se
l sample volumes u
sis is optional.
A and Viral NA La
l sample volume
sis is optional.
ular RNA Large V
A Pure 96 Instrume
tured cells, up to 2
tem Fluid (Interna
A Pure 96 Instrume
the internal system
ument can be run
tem Fluid (Extern
A Pure 96 Instrume
the external system
ument is on a tabl
ernal Lysis Buffer
he MagNA Pure 9
cleic acids (DNA/R
purposes, and for s
terial Lysis Buffe
he MagNA Pure 9
cleic acids (DNA/R
purposes, and for s
A Tissue Lysis Bu
he MagNA Pure 9
cleic acids (DNA/R
purposes, and for s
ystem - Dispos
er Tips (1,000 l)
ps for 1,000 l volu
truments; nuclease
ures; inert to chem

put Plate
ates containing pu
ing contact with co
dead volume that
cessing Cartridge
96 wells for sample
uclease free accor
emical leaching at
on
reparation
ment
for nucleic acid pu
and barcoded, pref
less than one hou
mall Volume Kit
ealed trays for pur
using the MagNA
arge Volume Kit
ealed trays for pur
using the MagNA
Volume Kit
ealed trays for pur
ent from 400/800
0 mg tissue, or eq
al)
nt reagent head d
m fluid and liquid w
as a tabletop instr
nal)
nt reagent head d
m fluid and liquid
e that also holds t
r
6 System for the is
RNA) from biologic
stabilization of nuc
er
6 System for the is
RNA) from biologic
uffer
6 System for the is
RNA) from biologic
stabilization of DN
sables
ume with aerosol f
e free according to
mical leaching at lo
urified nucleic acid
ooling block; wells
cannot be pipetted
e
e processing steps
rding to current Qu
t low and elevated
n of Nucle
urification
filled trays with
ur for 96
ifying nucleic
Pure 96
ifying nucleic
A Pure 96
ifying total
l lysed whole
uivalent.
uring a
waste
rument.
uring a
waste
the external
solation and
cal specimens
cleic acids with
solation and
cal specimens
cleic acids with
solation and
cal specimens
NA in tissue
filters for use
o current
ow and
s; optimized
s are v-shaped
d.
s using MagNA
uality Control
temperatures.

ic Acids
Cat. No.
06 541 089 001
Cat. No.
06 543 588 001
06 374 891 001
05 467 535 001
06 430 112 001
06 640 729 001
06 374 913 001
06 374 921 001
06 640 702 001
Cat. No.
06 241 620 001
06 241 611 001
06 241 603 001

1 instrumen
3 sets
3 set
3 set
3,8
Pack Size
nt, control unit and

Pack Size
s for 192 isolations

ts for 96 isolations


2 containers

1 container

1 bottle (100 ml)

1 bottle (20 ml)

1 bottle (100ml)

Pack Size
840 filter tips (40x9

60 plates

36 cartridges

www.roche
d accessories
s each
each
each
96)
e-applied-science

Price in
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire

2
43

e.com

2

2
Sa
44

www.r

Mag

Use t
use. T
pierc
Mag

Barco
Instru
intern
Mag
Prod
Mag

Holde
Mag

This a
in the
of the
Mag

This a
matri
plate
Mag

Drop
and c
Mag

MagN
Mag

MagN
Mag

MagN
Mag

MagN
Mag

Use a
tande
Mag

MagN
Mag

MagN
Mag

MagN
Mag

Reag
of Ma
Mag

Need
Instru
Mag
Mag
Prod
Mag

Table
samp
Light
tubes

ample Pr
roche-applied-sc
gNA Pure 96 Seal
to reseal MagNA P
There is no need t
ced when removing
gNA Pure 96 Inter
oded tubes for pre
uments. These tub
nal controls during
gNA Pure 96 Sy
duct Name
gNA Pure 96 Plate
er for custom plate
gNA Pure 96 Ligh
adapter is used to
e MagNA Pure 96
e LightCycler
480
gNA Pure 96 Arch
adapter is used to
ix storage tubes, in
is placed on top o
gNA Pure 96 Drop
catcher and attac
cleaning MagNA P
gNA Pure 96 Barc
NA Pure 96 Barcod
gNA Pure 96 Tip R
NA Pure 96 Tip Ra
gNA Pure 96 Bott
NA Pure 96 Bottle
gNA Pure 96 Purif
NA Pure 96 Purific
gNA Pure 96 Reag
as replacement rac
em after the first k
gNA Pure 96 Was
NA Pure 96 Waste
gNA Pure 96 Inter
NA Pure 96 Interna
gNA Pure 96 Was
NA Pure 96 Waste
gNA Pure 96 Reag
gent loop unit for u
agNA Pure 96 Inst
gNA Pure 96 Nee
dle set for user rep
ument reagent pip
gNA Pure LC
gNA Pure LC Sy
duct Name
gNA Pure LC 2.0 I
etop instrument bo
ple material and fo
tCycler
Capillarie
s. Process up to 32
eparatio
cience.com
ling Foil
Pure 96 reagent tra
o remove the seal
g reagent to minim
rnal Control Tube
eparing internal co
es are ideal for the
g a run.
ystem - Additio
e Holder
es in the MagNA P
htCycler 480 Ada
fix the 96-well Lig
Instrument. This p
0 Multiwell Plate 9
hive Plate Adapte
fix 96-well plates
n MagNA Pure 96
of the 96-well plate
p Catcher
ched Drop Catcher
Pure 96 Instrument
code Scanner
de Scanner for rep
Rack
ack for replacemen
tle Rack
Rack for replacem
fication Rack
cation Rack for rep
gent Rack
ck or for storing a
kit.
ste Rack
e Rack for replacem
rnal Waste Conta
al Waste Containe
ste Cover
e Cover for replace
gent Loop Unit
user replacement o
truments.
dle Set of 4
placement of the ne
petting heads.
C System
ystem - Instrum
Instrument
oth for automated
or pipetting into PC
es, 96-well plate, PC
2 samples in one ru
on
ays and output pla
ing foil prior to nex
mize risk of cross-c
e
ontrols using MagN
e automated proce
onal Products
Pure 96 Instrument
pter
ghtCycler
480 Mu
perforated plate is
96 for access to ea
er 4S
with no snap-lock
Instruments. The p
es with non-snap-
r Fleece for runnin
ts.
placement.
nt.
ment.
placement.
second purificatio
ment.
ainer
er for replacement.
ement.
onto the reagent p
eedles on MagNA
ment
nucleic acid isolat
CR reaction vessel
CR tubes, and 1.5
un in 16-180 min.
ates for later
xt use. Foil is
contamination.
NA Pure 96
essing of
t.
ultiwell Plate 96
placed on top
ch well.
k for tubes, e.g.,
perforated
-lock tubes
g, maintaining
on kit used in

ipetting head
A Pure 96
tion from crude
s, such as
ml reaction

06 241 638 001
06 374 905 001
Cat. No.
06 541 283 001
06 638 996 001
06 639 003 001
06 541 119 001
06 541 143 001
06 541 151 001
06 541 178 001
06 541 208 001
06 541 224 001
06 541 259 001
06 541 267 001
06 541 275 001
06 541 127 001
06 541 194 001
Cat. No.
05 197 686 001

1 in
1 instrument w
mo
100 foils

150 tubes (15x10)

Pack Size
1 plate holder
1 adapter

1 adapter

1 drop catcher

1 barcode scanne
1 tip rack
1 bottle rack
1 purification rack
1 reagent rack

1 waste rack
ternal waste conta
1 waste cover
1 reagent loop uni

1 set of 4 needles

Pack Size
with integrated PC
nitor, and accesso

)
r
k
ainer
it
s
C, touchscreen
ories

inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire

Sa

Mag
Prod
Mag

Isolat
1x10
3
Instru
Syste
Mag

Addit
Isolat
lysis
stabi
Mag

Isolat
Instru
lysate
with
instru
Mag

Isolat
types
purifi
Exter
Mag

Isolat
blood
Resu
block
Mag

Isolat
tissue
for RT
syste
Mag

For a
blood
purifi
north
Mag

Addit
III (Ti
inhib
RNA.
Mag

Isolat
serum
Purifi
qPCR
Mag

Isolat
whol
high
high
Mag

Isolat
plasm
elute
Light
blood
Mag
Buffe

Addit
plasm
MagN
Nucle
Instru

ample Pr
gNA Pure LC Sy
duct Name
gNA Pure LC DNA
te high quality DN
3
to 1x10
6
blood o
uments. Resulting
ems, standard bloc
gNA Pure LC DNA
tional Lysis/Bindin
tion Kit I and Mag
of mammalian blo
lization of nucleic
gNA Pure LC DNA
te high-purity DNA
uments. External ly
es and difficult to h
LightCycler
Syste
uments.
gNA Pure LC DNA
te high-purity bact
s, up to 100 l volu
ied DNA for PCR w
rnal lysis protocols
gNA Pure LC DNA
te high-purity geno
d, blood cells, or cu
lting DNA is ideal
k cyclers and other
gNA Pure LC RNA
te total RNA from
es using MagNA P
T-PCR using Light
ems.
gNA Pure LC RNA
automated isolation
d cells or cultured
ied RNA in RT-PCR
hern blots, and for
gNA Pure LC RNA
tional lysis buffer f
ssue) and MagNA
its RNases during
. Use to homogeni
gNA Pure LC Tota
te high-purity tota
m, plasma, or whol
ied nucleic acids a
R and qRT-PCR us
gNA Pure LC Tota
te high-purity tota
e blood using Mag
sensitivity in down
performance PCR
gNA Pure LC Tota
te total nucleic aci
ma using MagNA P
d in 50-100 l. Nu
tCycler
Systems a
d.
gNA Pure LC Tota
er Refill
ma, and to stabilize
NA Pure LC Total
eic Acid Isolation K
uments.
eparatio
ystem - Kits
A Isolation Kit I
A from 20 to 200
r cultured cells us
DNA is eluted in 1
ck cyclers and othe
A Isolation Kit I
ng Buffer for use w
NA Pure LC DNA
od, blood cells, or
acids.
A Isolation Kit II (
A from 1 to 10 mg
ysis protocols allow
homogenize samp
ems, block cyclers
A Isolation Kit III
terial and fungal D
ume, using MagNA
with LightCycler
S
for BAL, sputum,
A Isolation Kit - L
omic DNA from 20
ultured cells using
for qPCR using Li
r real-time PCR ins
A Isolation Kit III
fresh-frozen or for
Pure LC Instrumen
tCycler
Instrumen
A Isolation Kit - H
n of total RNA from
cells using MagNA
R with LightCycler
gene expression a
A Isolation Tissue
for use with the M
A Pure LC Instrume
cell lysis, releasin
ze tissue with Mag
al Nucleic Acid Is
l nucleic acids (vir
le blood using Ma
are eluted in 50-10
ing LightCycler
S
al Nucleic Acid K
l viral nucleic acid
gNA Pure LC Instr
nstream applicatio
with LightCycler

al Nucleic Acid Is
ds (viral DNA/RNA
Pure LC Instrumen
cleic acids are ide
and block cyclers.
al Nucleic Acid Is
for the lysis of mam
e nucleic acids. Us
Nucleic Acid Isolat
Kit - Large Volume
on
l mammalian who
ing MagNA Pure L
100 l. Ideal for Lig
er real-time PCR in
Lysis/Binding B
with the MagNA Pu
Isolation Kit Larg
cultured cells, and
(Tissue)
tissue with MagN
w DNA purification
ples. Use purified D
s and other real-tim
(Bacteria, Fungi
DNA from many dif
A Pure LC Instrume
Systems and block
CSF, and urine.
Large Volume
0 l to 1 ml of mam
g MagNA Pure LC
ghtCycler
System
struments.
(Tissue)
rmalin-fixed paraff
nts. Resulting RNA
nts and other real-
High Performance
m up to 200 l who
A Pure LC Instrum
r
Systems, block
analysis.
e Lysis Buffer - R
agNA Pure LC RN
ents. This reagent
g and stabilizing m
gNA Lyser Instrum
solation Kit
ral DNA/RNA) from
gNA Pure LC Instr
00 l. Nucleic acids
Systems and block
Kit - High Perform
s from 1 ml serum
uments. This kit ac
ns. Use purified nu
Systems and bloc
solation Kit - Larg
A) from up to 1 ml
nts. Purified nucleic
eal for qPCR and q
Do not use this ki
solation Kit - Lys
mmalian blood, ser
se in combination w
tion Kit, MagNA P
e on MagNA Pure
ole blood or
LC
ghtCycler

nstruments.
Buffer - Refill
ure LC DNA
ge Volume. For
d the
A Pure LC
n from FFPE
DNA for PCR
me PCR
)
fferent sample
ents. Use
k cyclers.
mmalian whole
Instruments.
ms, standard
fin-embedded
from is ideal
-time PCR
e
ole blood or 10
6

ments. Use
cyclers,
Refill
NA Isolation Kit
efficiently
mRNA and total
ment.
m up to 200 l
ruments.
s are ideal for
k cyclers.
mance
m, plasma, or
chieves very
ucleic acids for
ck cyclers.
ge Volume
l serum and
c acids are
RT-PCR using
t for whole
is/Binding
rum, or
with the
Pure LC Total
LC

Cat. No.
03 003 990 001
03 246 752 001
03 186 229 001
03 264 785 001
03 310 515 001
03 330 591 001
03 542 394 001
03 604 721 001
03 038 505 001
05 323 738 001
03 264 793 001
03 246 779 001

1 kit
1 kit
1 kit
1 kit for up to 9
1 kit
1 kit
1 kit
1 kit
1 kit
Pack Size
for up to 192 isola

100 ml

for up to 192 isola

for up to 192 isola

96 to 288 isolations
sample volume

for up to 192 isola

for up to 192 reac

70 ml

for up to 192 isola

for up to 288 isola

for up to 192 isola

100 ml

www.roche
ations
ations
ations
s, depending on
ations
ctions
ations
ations
ations
e-applied-science

Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

2
45

e.com

2

2
Sa
46

www.r

Mag

Isolat
oligo
LC In
Syste
Mag

Use t
cultu
be im
LC In
mRN
Mag
Prod
Mag

These
purifi
Remo
using
Mag

Reag
on th
MagN
Mag

Reag
on th
buffe
Tub L
Mag

Reac
MagN
nucle
with
Mag

Large
Instru
head
Mag

Smal
With
when
Mag

Reag
of Ma
and V
Pure
Mag

Reag
on th
MagN
Mag

Samp
acids
Instru
Comp
Mag

The T
purifi
reduc
posit
Mag

Tub L
medi
term
also c

ample Pr
roche-applied-sc
gNA Pure LC mRN
te high-quality mR
(dT) and streptavid
nstruments. Use pu
ems and block cyc
gNA Pure LC mRN
this optimized buff
red cells, and to st
mmediately process
nstruments. Use bu
A HS Kit.
gNA Pure LC Sy
duct Name
gNA Pure LC Cart
e adhesive films se
ied nucleic acids. T
ove a sample by pe
g a new Cartridge
gNA Pure LC Med
gent containers for
he stage of MagNA
NA Pure LC Tub L
gNA Pure LC Med
gent containers for
he stage of MagNA
er volume and V-sh
Lids (small, mediu
gNA Pure LC Proc
ction vessels for sa
NA Pure LC Instru
eic acids. Each pro
8 wells each.
gNA Pure LC Rea
e (50 - 1000 l volu
uments. With integ
nozzles when dis
gNA Pure LC Rea
l (5 - 50 l volume
integrated filters t
n eluting nucleic ac
gNA Pure LC Rea
gent containers for
agNA Pure LC Inst
V-shaped bottom m
LC Tub Lids (large
gNA Pure LC Rea
gent containers for
he stage of MagNA
NA Pure LC Tub L
gNA Pure LC Sam
ple reaction plates
s from magnetic be
uments. Each cartr
patible with standa
gNA Pure LC Tip S
Tip Stand is for tem
ication runs using
ces the number of
ions, so that the n
gNA Pure LC Tub
Lid Seals are for us
um, large). They p
storage after purif
catch liquid drops
eparatio
cience.com
NA HS Kit
RNA from 1 x 10
7
m
din-coated magne
urified mRNA for q
lers for gene expre
NA Isolation Kit I
fer to lyse mamma
tabilize mRNA. Lys
sed or after long-t
uffer in combinatio
ystem - Dispos
tridge Seal
eal the MagNA Pu
They prevent evap
erforating the seal
Seal.
dium Reagent Tu
r storing up to 20 m
A Pure LC Instrume
ids (small, medium
dium Reagent Tu
A Pure LC Instrum
haped bottom min
m).
cessing Cartridge
mples and purifica
ment when purifyi
ocessing cartridge
ction Tip (large)
ume) reaction tips
grated filters to pre
pensing reagents
ction Tip (small)
e) reaction tips for
to prevent contam
cids and during po
gent Tub (large)
r 100 ml of MagNA
truments. Tub mar
minimizes dead vo
e).
gent Tub (small)
r storing up to 3.5 m
A Pure LC Instrume
ids (small, medium
mple Cartridge
for aliquoting prim
eads, and sample s
ridge has 32 (4 x 8
ard 8-well multich
Stand
mporary storage of
MagNA Pure LC I
f tips required for a
ozzle head can bri
Lid Seal
se with all MagNA
prevent evaporative
fication using Mag
during robotic arm
on
mammalian blood
etic particles with M
qRT-PCR with Ligh
ession analysis.
Lysis Buffer R
alian whole blood,
sed and stabilized
term storage using
on with the MagNA
sables
ure Cartridge when
poration and conta
l of the well, and th
ub 20
ml of MagNA Pure
ents. Tubs are sea
m).
ub 30
ml of MagNA Pure
ments. Tub marking
imizes dead volum
e
ation reagents pipe
ing DNA, RNA, mR
has 64 wells, arran
s for MagNA Pure
event contaminatio
and separating ma

r MagNA Pure LC
ination of pipetting
ost-elution pipettin
A Pure LC reagents
rkings estimate bu
olume. Seal tubs us
)
ml of MagNA Pure
ents. Tubs are sea
m).
mary samples, elut
storage using Mag
8) wells, each with
annel pipettes.
f tips for multiple u
Instruments. The T
a purification run.
iefly store small or
A Pure LC Tub Lids
e reagent loss and
gNA Pure LC Instru
m movements.
cells using
MagNA Pure
htCycler

Refill
blood and
samples can
g MagNA Pure
A Pure LC
n storing
mination.
hen reseal
e LC reagents
led using
e LC reagents
gs estimate
me. Use with
etted by the
RNA, and total
nged in 8 rows
LC
on of pipetting
agnetic bead.
Instruments.
g head nozzles
ng.
s on the stage
ffer volume
sing MagNA
e LC reagents
led using
ting nucleic
gNA Pure LC
1.5 ml volume.
use during
Tip Stand
It has 8
r large tips.
s (small,
permit long-
uments. They

03 267 393 001
03 246 744 001
Cat. No.
03 118 827 001
03 004 058 001
03 045 501 001
03 004 147 001
03 004 171 001
03 004 180 001
03 004 040 001
03 004 066 001
03 004 112 001
03 004 155 001
03 004 104 001

1 kit
960 tips (30 pre
960 tips (30 pre
for up to 192 isola

2 x 35 ml

Pack Size
200 seals

150 tubs

50 tubs

160 cartridges

e-packed trays ea

e-packed trays ea

120 tubs

150 tubs

120 cartridges

200 tip stands

400 seals

ations
ch with 32 tips)
ch with 32 tips)

inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Sa

Mag

Reag
lids r
receiv
remo
Mag

Reag
These
perfo
surfa
Mag

These
Box o
tips f
Instru
Mag

Auto
waste
react
MagN
Mag

The W
LC pu
conta
salts
Mag
Prod
Mag

One a
Plate
adap
Light
Mag

Barco
2844
area
Mag

One
Printe
Labe
Mag

One
docu
prints
MagN
Mag

Cooli
(0.2 m
vials.
post-
Mag

Cooli
Elutio
A-Rin
trans
Mag

Cooli
conta
using
posit
Mag

Cooli
Light
the p
sixtee
reage

ample Pr
gNA Pure LC Tub
gent Tub Lids for th
reduce evaporative
ving up to 8 reacti
oved as tips are ext
gNA Pure LC Tub
e lids reduce evap
orations for receivin
aces are removed a
gNA Pure LC 2.0 W
e Waste Bags are
of MagNA Pure LC
from 5 to 7 runs. Th
ument.
gNA Pure LC Was
clavable MagNA P
e slide of the Mag
tion tips discarded
NA Pure LC 2.0 Ins
gNA Pure LC Was
Waste Bottle collec
urification runs. Th
act with potentially
in the lysis buffers
gNA Pure LC Sy
duct Name
gNA Pure LC 2.0 L
adapter for approp
96 in the MagNA
ter is placed onto
tCycler
480 Multi
gNA Pure LC Barc
ode labels for use
. These barcode la
of the MagNA Pur
gNA Pure LC Barc
Barcode Printer Ri
er TLP 2844 to pro
ls.
gNA Pure LC Barc
Barcode Printer TL
mentation during
s barcodes created
NA Pure LC Samp
gNA Pure LC Coo
ing Block for holdi
ml, 96-well plate),
It fits directly onto
-elution pipetting o
gNA Pure LC Coo
ing Block for holdi
on Module of the M
ngs with purified n
sferred to an instru
gNA Pure LC Coo
ing Block for holdi
aining LightCycler
g MagNA Pure LC
ions for 1.5 ml rea
gNA Pure LC Coo
ing Block for holdi
tCycler
Capillarie
post-elution progra
en 1.5 ml reaction
ents.
eparatio
Lid (large)
he MagNA Pure LC
e reagent loss. Eac
ion tips, ensuring t
tracted.
Lid (small, medi
he MagNA Pure LC
porative reagent los
ng up to 8 reaction
as tips are extracte
Waste Bags
only for use with t
C 2.0 Instruments. T
hey cannot be use
ste Bags
Pure LC Waste Bag
NA Pure LC 1.0 In
by the robot. They
strument.
ste Bottles
cts up to 330 ml liq
hese autoclavable
y infectious materi
s.
ystem - Additio
LightCycler
480
priate orientation o
Pure LC Cooling B
the 96-well PCR P
iwell Plate 96 is the
code Labels
with the MagNA P
abels are suitable f
re LC Sample Cart
code Printer Ribb
ibbon for use with
oduce barcodes on
code Printer TLP
LP 2844 for sample
MagNA Pure LC p
d by MagNA Pure
le Cartridges and/
ling Block, 96-w
ng either one Ligh
or 0.2 ml 8-strip vi
o block cyclers, an
of master mixes by
ling Block, A-Rin
ng 1 or 2 A-Rings
MagNA Pure LC S
nucleic acids and P
ument platform for
ling Block, LC Ce
ng 32 LightCycler
Capillaries for au
Instruments. This
ction tubes for ma
ling Block, LC Sa
ng the LightCycler
es for robotic pipet
am of MagNA Pure
tube positions for
on
C Reagent Tubs (la
h Tub Lid has 8 pe
that liquid on tip s
um)
C Reagent Tubs (s
ss. Each Tub Lid h
n tips, ensuring tha
ed.
the MagNA Pure L
They can receive u
ed with the MagNA
gs are only for use
strument. They co
y cannot be used w
quid waste during
Waste Bottles prev
al and the irritating
onal Products
0 Plate Adapter
of the LightCycler
Block, 96-well PCR

Plate Cooling Block
en positioned corr
Pure LC Barcode P
for the new barcod
tridge.
bon
the MagNA Pure
n the MagNA Pure
2844
e identification, tra
purification runs. T
LC Software Versi
/or non-barcode-la
well PCR Plate
htCycler
480 Mul
ials, or 0.2 ml singl
d can be used for
y MagNA Pure LC
ng
with barcodes. Us
oftware for autom
PCR reagents. A-R
testing.
entrifuge Adapte
Centrifuge Adap
utomated post-elu
Cooling Block also
aster mixes and oth
ample Carousel
r
Sample Carous
tting of up to 32 ca
e LC Instruments. I
master mixes and
arge). These
erforations for
urfaces are
small, medium).
as 8
at liquid on tip
LC 2.0 Waste
used reaction
A Pure LC 1.0
e with the tip
llect used
with the
MagNA Pure
vent user
g chaotropic
480 Multiwell
R Plate. The
k. The
rectly.
Printer TLP
de labeling
LC Barcode
LC Barcode
acking, and
This device
ion 3.0 for the
abeled tubes.
tiwell Plate
le reaction
automated
Instruments.
se the Post
ated filling of
Rings are then
ers
pters
ution pipetting
o has fifteen
her reagents.
sel with
apillaries using
It also has
d other

03 004 074 001
03 004 082 001
05 324 157 001
03 004 201 001
03 004 198 001
Cat. No.
05 323 983 001
03 531 520 001
03 531 538 001
03 576 094 001
12 189 674 001
03 201 287 001
12 190 664 001
12 189 704 001

25 b
1,000
1 cooling bloc
120 lids

300 lids

bags (for 5 runs ea

200 bags

40 bottles

Pack Size
1 adapter

labels (10 mm x 6

1 ribbon

1 barcode printer

1 cooling block

1 cooling block

ck (with 32 LightCy
adapters)

1 cooling block

www.roche
ach)
0 mm)
r
ycler centrifuge
e-applied-science

inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

2
47

e.com

2

2
Sa
48

www.r

Mag

Cooli
elutio
Block
Caro
Mag

Greas
servic
greas
Softw
Mag

The M
MagN
liquid
MagN
Mag

Kit w
nozzl
pipet
MagN
Mag

The M
holdi
MagN
Mag

Addit
conta
5 to 5
distin
Mag

Addit
conta
50 to
distin
Mag

This
MagN
Wast
Mag

Repla
Bottle
the re
tray.
Mag

One a
Bags
tips a
bag i
Mag

One a
a Ma
2.0 W
Instru
Mag
Mag
Prod
Mag

Benc
samp
purifi
stand

ample Pr
roche-applied-sc
gNA Pure LC Coo
ing Block for holdi
on pipetting by Ma
k as required with
usel, LC Centrifuge
gNA Pure LC Grea
sing station, pads,
cing of MagNA Pu
sing, the greasing
ware greasing prog
gNA Pure LC Liqu
MagNA Pure LC L
NA Pure LC Instru
ds from the reagen
NA Pure LC Waste
gNA Pure LC O-R
with a vial of grease
le head O-rings an
tting accuracy of th
NA Pure Compact
gNA Pure LC Rea
MagNA Pure LC R
ng two large reage
NA Pure LC Instru
gNA Pure LC Tip R
tional Tip Rack for
aining MagNA Pur
50 l. These Tip Ra
nguish them from t
gNA Pure LC Tip R
tional Tip Rack for
aining MagNA Pur
1000 l. These Tip
nguish them from t
gNA Pure LC 2.0 T
is a replacement w
NA Pure LC 2.0 Ins
te Slide into the M
gNA Pure LC Was
acement accessory
e of all MagNA Pu
eagent/sample sta
gNA Pure LC 2.0 W
additional Waste B
s are fixed to the M
are discarded by th
n the waste box.
gNA Pure LC 2.0 W
additional Waste B
agNA Pure LC 2.0 W
Waste Box Lid. Use
ument into the was
gNA Pure Co
gNA Pure Com
duct Name
gNA Pure Compa
chtop instrument fo
ples, such as blood
ied nucleic acid in
dard cyclers, and d
eparatio
cience.com
ling Block, Reac
ng thirty-two 1.5 m
agNA Pure LC Inst
the MagNA Pure
e Adapters, or 96-
asing Set
O-rings and grea
ure LC nozzlehead
station is placed o
gram performs the
uid Waste Funnel
iquid Waste Funne
ments. The robotic
nt/sample stage th
e Bottle.
Ring Maintenance
e and 12 sets of 8 O
nd for periodic rep
he nozzle head of
Instruments.
gent Reservoir R
Reagent Reservoir R
ent tubs and six m
ments.
Rack
r small reaction tip
re LC Reaction Tip
acks for small tips
the Tip Racks for l
Rack
r large reaction tips
re LC Reaction Tip
p Racks for large t
the Tip Racks for s
Tip Waste Slide
waste slide. Used r
strument through t
agNA Pure LC 2.0
ste Bottle Tray
y tray holding the
ure LC Instruments
age into the MagN
Waste Box
Box for holding Ma
MagNA Pure LC 2.0
he MagNA Pure LC
Waste Box Lid
Box Lid. The MagN
Waste Bag which i
d tips are discarde
ste bag in the was
ompact System
pact System -
ct Instrument
or automated nucl
d, serum, plasma, o
PCR, RT-PCR on
downstream applic
on
ction Tubes
ml reaction tubes f
truments. Combine
Cooling Blocks for
well PCR Plate.
ase for automated
O-Rings. For auto
on the Instrument s
e process.
l
el is a replacement
c nozzle head pipe
rough this funnel
e Kit
O-rings to prolong
lacement of O-ring
both MagNA Pure
Rack
Rack is an addition
medium/small reag
ps for holding 3 tip
ps (small), each wit
are colored yellow
arge tips which ar
s for holding 3 tip
ps (large), each wit
tips are colored blu
small tips which ar
reaction tips are di
the MagNA Pure L
Waste Box.
MagNA Pure LC L
s. The robot pipets
A Pure LC Waste
agNA Pure LC 2.0
0 Waste Box Lid. U
C 2.0 Instrument in
NA Pure LC 2.0 Wa
is fixed to the Mag
ed by the MagNA
ste box.
m
Instrument
eic acid purificatio
or cells in 1540 m
LightCycler
Instr
cations.
for use in post-
e this Cooling
r either the LC
or manual
omated
stage, and the
t accessory for
ets unused
into the
g the life of
gs, ensuring
e LC and
nal rack for
ent tubs in
trays
th a capacity of
w to easily
re blue.
trays
th a capacity of
ue to easily
re yellow.
scarded by the
LC 2.0 Tip
Liquid Waste
liquids from
Bottle on this
Waste Bags.
Used reaction
nto the waste
aste Box holds
gNA Pure LC
Pure LC 2.0
on from 1-8
minutes. Use
uments,

12 189 666 001
03 561 402 001
03 253 805 001
03 561 429 001
03 253 767 001
03 253 783 001
03 253 775 001
05 324 122 001
03 253 813 001
05 323 991 001
05 324 114 001
Cat. No.
03 731 146 001

1
1 vial of
1 instrument w
moni
1 cooling block

1 set

liquid waste funn

grease and 12 x 8

1 reagent rack

1 tip rack

1 tip rack

1 slide

1 waste bottle tray

1 box

1 lid

Pack Size
with integrated PC
itor and barcode re

el
8 O-rings
y
C, touchscreen
eader

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire

Sa

Mag
Prod
Mag

Read
from
using
PCR
PCR
Mag

Use w
Kit I t
cultu
MagN
Mag

Read
from
using
PCR
PCR
Mag

Read
from
MagN
Light
Mag

This a
MagN
for lo
one n
Mag

Use t
Isolat
from
stand
Mag
Prod
Mag

One a
Instru
Mag

One a
Instru
Mag

One a
Instru
Mag

One a
Instru
Mag

One a
Instru
Mag

One a
Instru
Ma
Mag
Prod
Mag

Quick
appli
lysis
kits. E

ample Pr
gNA Pure Com
duct Name
gNA Pure Compa
dy-to-use reagents
mammalian cells
g MagNA Pure Com
with LightCycler

instruments.
gNA Pure Bacteri
with the MagNA P
to isolate bacterial
res. For automatio
NA Lyser Instrume
gNA Pure Compa
dy-to-use reagents
mammalian cells
g MagNA Pure Com
with LightCycler

instruments.
gNA Pure Compa
dy-to-use reagents
tissue, blood cells
NA Pure Compact
tCycler
Systems,
gNA Pure Compa
accessory is requir
NA Pure Compact
ost or contaminated
nucleic acid extrac
gNA Pure DNA Tis
the MagNA Pure C
tion Kit I - Large V
mammalian tissue
dard cyclers, and in
gNA Pure Com
duct Name
gNA Pure Compa
additional Cartridg
ument.
gNA Pure Compa
additional Drip Tra
ument.
gNA Pure Compa
additional Drop Ca
ument.
gNA Pure Compa
additional Elution
ument.
gNA Pure Compa
additional Tube Ra
ument.
gNA Pure Compa
additional Waste T
ument.
agNA Lyser S
gNA Lyser In
duct Name
gNA Lyser Instrum
kly and completely
cations. Use in com
buffers from the M
Easily integrates in
eparatio
pact System -
ct Nucleic Acid I
s in prefilled, sealed
and viral nucleic a
mpact Instruments
Systems, standard
a Lysis Buffer
Pure Compact and
DNA from urine,
on and convenienc
ent and Green Bea
ct Nucleic Acid I
and viral nucleic a
mpact Instruments
Systems, standard
ct RNA Isolation
s, and whole blood
Instruments. Use
microarrays, and g
ct Tip Tray Kit
red when perform
Instrument. The T
d tip trays. One tip
ction.
ssue Lysis Buffer
Compact Instrumen
Volume, and its rea
e. Use purified DN
n downstream app
pact System -
ct Cartridge Rac
ge Rack for use wi
ct Drip Tray
ay for use with the
ct Drop Catcher
atcher for use with
ct Elution Tube R
Tube Rack for use
ct Tube Rack
ack for use with th
ct Waste Tank
Tank for use with t
System
strument
ment
y homogenize tissu
mbination with Ma
MagNA Pure LC or
nto your laboratory
on
Kits and Reag
Isolation Kit I
d cartridges for pu
acids in a volume u
s. Use purified DN
d cyclers and othe
MagNA Pure Com
BAL, sputum, CSF
ce, combine lysis b
ads.
Isolation Kit I - La
d cartridges for pu
acids in a volume u
s. Use purified DN
d cyclers and othe
Kit
d cartridges for pu
d in a volume up to
RNA for RT-PCR w
gene expression sy
ing the Leakage T
Tip Tray Kit is also a
p tray contains all d
r
nt, MagNA Pure C
ady-to-use buffer t
A with LightCycler
plications.
Additional Pro
ck
th the MagNA Pur
e MagNA Pure Com
h the MagNA Pure
Rack
e with the MagNA
he MagNA Pure Co
the MagNA Pure C
ue for many extrac
agNA Lyser Green
r MagNA Pure Com
y workflow.
ents
urifying DNA
up to 400 l
A for PCR/RT-
er real-time
mpact Isolation
F, swabs, and
uffer with the
arge Volume
urifying DNA
up to 1 ml
A for PCR/RT-
er real-time
urifying RNA
o 200 l using
with
ystems.
Test using the
a replacement
disposables for
Compact
to isolate DNA
r
Systems,
oducts
re Compact
mpact
e Compact
Pure Compact
ompact
Compact
ction
Beads and
mpact isolation

Cat. No.
03 730 964 001
04 659 180 001
03 730 972 001
04 802 993 001
03 753 166 001
04 805 160 001
Cat. No.
03 788 237 001
04 347 005 001
03 788 270 001
03 788 288 001
03 788 296 001
03 788 300 001
Cat. No.
03 358 968 001
03 358 976 001

1 kit
1 kit
1 kit
1 instrume
1 instrume
Pack Size
t for up to 32 isolat

20 ml lysis buffer



10 tip trays

100 ml lysis buffer

Pack Size
1 cartridge rack

1 drip tray

1 drop catcher

1 tube rack

1 tube rack

1 waste tank

Pack Size
ent (110 V, plus ac
ent (220 V, plus ac

www.roche
tions
tions
tions
r
ccessories)
ccessories)
e-applied-science

Price in
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire

2
49

e.com

2

2
Sa
50

www.r

Mag
Prod
Mag

Addit
samp
one s
MagN
Mag

One a
temp
Lyser
Lyser
Mag

2.0 m
Use i
biolo
and M
Ma
Kits
Prod
Agar

The A
fragm
fragm
prime
DNA

Easily
South
Elimi
reage
DNA

Rapid
or bu
diges
purifi
Geno

Prepa
using
can b
sequ
Geno

Prepa
using
can b
sequ
Geno

Conv
with
durin
numb
High

For fa
- 10
Isolat
array
High

Use t
bp. Is
cDNA
mole
High

Purify
Use p
sequ
fragm

ample Pr
roche-applied-sc
gNa Lyser Di
duct Name
gNA Lyser Rotor
tional MagNA Lyse
ple tubes for tissue
shipped with the M
NA Lyser Rotor Co
gNA Lyser Rotor C
additional MagNA
perature of up to 16
r Rotor at +2 to +8
r Instrument. Use w
gNA Lyser Green
ml sample tubes wi
n the MagNA Lyse
gical materials usi
MagNA Pure Com
anual Sam
s for DNA P
duct Name
rose Gel DNA Ext
Agarose DNA Extra
ments from standa
ments are suitable
ed labeling, and se
A Isolation Kit for
y and quickly isola
hern blots, restrict
nates organic extr
ents.
A Isolation Kit for
dly isolate DNA fro
uffy coat samples.
sts, and Southern b
ication steps, and
opure Plasmid M
are highly purified
g a modified alkalin
be used in transfec
encing, and clonin
opure Plasmid M
are highly purified
be used in transfec
encing, and clonin
opure Buffer Set
venient, ready-to-u
the Genopure Plas
ng the isolation, pro
ber plasmids.
h Pure FFPET DNA
ast and convenien
m thick sections
ted DNA is suitabl
ys), and sequencin
h Pure PCR Clean
this kit to selective
solate PCR produc
A, and concentrate
cular biology tech
h Pure PCR Produ
y and concentrate
purified DNA direc
encing, cloning, lig
ments that are >10
eparatio
cience.com
sposables an
er Rotors. Each Ma
e homogenization.
MagNA Lyser Instr
ooling Blocks to inc
Cooling Block
A Lyser Rotor Cooli
6 sample tubes be
8C. Identical to th
with additional roto
Beads
th ceramic beads
er Instrument to d
ng lysis buffers su
pact isolation kits.
mple Prepa
urification
traction Kit
action Kit efficient
rd or low melting p
for ligation, transf
equencing.
Cells and Tissue
ates DNA from mos
ion digests, PCR/lo
actions, anion exc
Mammalian Blo
om 1 -10 ml mamm
Use in PCR or long
blots. Eliminate org
chaotropic reagen
Midi Kit
plasmid DNA in m
ne lysis method. P
ction, PCR, restrict
ng.
Maxi Kit
plasmid DNA in la
ne lysis method. P
ng.
for Low-Copy Nu
use, nuclease-free
smid Kits. Doubling
ovides better yield
A Isolation Kit
t isolation and pur
of formalin-fixed,
e for qPCR, microa
g.
nup Micro Kit
ely isolate small DN
cts from amplificati
e dilute solutions.
niques.
uct Purification K
amplified DNA (o
ctly in downstream
gation, and PCR. E
00 bp in length.
on
nd Additional
agNA Lyser Rotor
These rotors are id
ument. Use with a
crease throughput
ing Block for main
eing loaded onto th
e one shipped wit
ors to increase thr
to purify RNA, mR
isrupt cells, tissues
upplied with the M

aration of
tly isolates small an
point agarose. Re
formation, RE diges
es
st cells and tissues
ong PCR, and sequ
hange columns, a
ood
malian whole blood
g PCR, sequencing
ganic extractions,
nts.
medium quantities
urified plasmid DN
tion digestion, Sou
arge quantities (up
urified plasmid DN
tion digestion, Sou
umber Plasmids
buffers for use in
g the volume of th
s of plasmid DNA
rification of genom
paraffin-embedde
array analysis (CG
NA fragment sizes
ion and other reac
Use purified DNA
Kit
or DNA from other
m applications, suc
Efficiently recovers
s
holds up to 16
dentical to the
additional
t.
taining the
he MagNA
h the MagNA
roughput.
RNA, and DNA.
s, and other
agNA Pure LC
Nucleic A
nd large DNA
covered DNA
sts, random
s. Use for
uencing.
nd chaotropic
d, lymphocyte,
g, restriction
column
(up to 100 g)
NA from E. coli
thern blotting,
p to 500 g)
NA from E. coli
thern blotting,
combination
he buffers
from low-copy
mic DNA from 5
d tissue.
H, methylation
25 bp to 100
ctions, purify
in most
reactions).
h as labeling,
DNA

Cat. No.
03 359 093 001
03 359 085 001
03 358 941 001
Acids
Cat. No.
11 696 505 001
11 814 770 001
11 667 327 001
03 143 414 001
03 143 422 001
04 634 772 001
06 650 767 001
04 983 912 001
11 732 668 001
11 732 676 001

100 tubes (
1 kit
1 kit (10 isola
or 5
1 kit for up to
1 kit f
1 kit f
1 set buffer fo
1
1 kit fo
1 kit f
1 kit fo
Pack Size
2 rotors

1 cooling block

(prefilled with cera

Pack Size
t for max. 100 reac

ations of 400 mg e
5 x 10
7
cultured ce

25 purifications of

for up to 20 prepar

for up to 10 prepar

or up to 20 maxi pr
preps

kit for 50 isolation

or up to 200 purific

for up to 50 purific

amic beads)
ctions
each for tissue
ells)
f 10 ml samples
rations
rations
reps or 60 midi
ns
cations
cations
cations

Price in
inquire
inquire
inquire
Price in
182,80
234,80
242,60
149,40
172,30
137,80
258,00
280,10
109,00
458,50

Sa

High

Purify
cultu
treatm
SNP
High

Quick
cultu
trans
High

Quick
whol
inclu
PCR,
High

Purify
same
colum
direc
High

Use t
Nucle
Viral
be pr
Kits
Prod
High

For fa
m th
Macr
isolat
High

Isolat
direc
of mR
Light
High

Purifi
inclu
RNA
quan
High

Rapid
cells.
purifi
RNas
High

Isolat
fresh
sectio
Light
High

Quick
liver,
north
const
High

Quick
fluids
analy
mRN

Isolat
homo
Use i
and c

ample Pr
h Pure PCR Temp
y nucleic acids fro
red cells, and tissu
ment with lysozym
detection, blotting
h Pure Plasmid Is
kly prepare up to 1
res. Use directly fo
sfection, and to gen
h Pure Viral Nucle
kly purify viral nuc
e blood. When usi
ding viral nucleic a
directly after eluti
h Pure Viral Nucle
y viral nucleic acid
e principle as the H
mn assembly purif
ct use in PCR and R
h Pure Viral Nucle
this Buffer Set in c
eic Acid Kit, the H
Nucleic Acid Larg
rocessed.
s for RNA Pu
duct Name
h Pure FFPET RNA
ast convenient isol
hick sections of fo
rodissected sample
ted RNA for qRT-P
h Pure FFPE RNA
te total RNA from
ct use in RT-PCR. Is
RNA in RT-PCR us
tCycler
Carousel-
h Pure miRNA Iso
ies and enriches s
ding formalin-fixed
in northern blots,
tification with RT-
h Pure RNA Isolat
dly isolate small am
Blood, yeast, and
ied and intact RNA
se protection, and
h Pure RNA Paraf
te total RNA from
-frozen tissue for
ons is ideal for rela
tCycler
Carousel-
h Pure RNA Tissu
kly purify total inta
spleen, lung, and
hern blotting, RNas
truction, and in vit
h Pure Viral RNA
kly purify viral RNA
s, or cell culture su
ysis directly after e
NA Capture Kit
te highly purified p
ogenization, and im
mmobilized mRNA
cDNA-AFLP.
eparatio
plate Preparation
m different sample
ue. Bacteria and ye
me or lyticase. Use
g, etc.
solation Kit
15 g highly purifie
or PCR, sequencin
nerate labeled hyb
eic Acid Kit
cleic acids (DNA, R
ng whole blood, to
acids. Use purified
on in water.
eic Acid Large Vo
ds from serum, plas
High Pure Viral Nu
ies larger sample v
RT-PCR.
eic Acid Buffer S
combination with th
igh Pure Viral Nuc
ge Volume Kit whe
urification
A Isolation Kit
lation and purifica
rmalin-fixed, paraf
es or biopsy mater
PCR and microarra
Micro Kit
formalin-fixed, par
solated RNA is sui
sing real-time PCR
-Based and the 48
olation Kit
mall (micro) RNAs
d/FFPE sections, a
miRNA array hybr
PCR on the LightC
tion Kit
mounts of high qu
bacteria require a
A in RT-PCR, north
much more.
ffin Kit
formalin-fixed par
use in RT-PCR. Th
ative quantification
-Based System.
e Kit
act RNA from mam
heart. Use isolated
se protection, prim
tro translation.
Kit
A from mammalian
upernatants. Isolate
elution in PCR grad
poly (A)
+
RNA from
mmobilize in strept
A directly for qualit
on
Kit
e materials, such a
east require a spec
purified nucleic ac
ed plasmid DNA fr
g, cloning, in vitro
bridization probes.
RNA) from serum,
otal nucleic acids a
d nucleic acids in P
olume Kit
sma, or whole bloo
cleic Acid Kit. An
volumes up to 2.5
Set
he High Pure 16 Sy
cleic Acid Kit, or th
n larger sample vo
tion of total RNA f
ffin-embedded tiss
rial can also be use
ay analysis.
raffin-embedded t
itable for relative q
R systems such as t
80 Systems.
s from animal cells
nd plant material.
ridization, and rela
Cycler
480 System
ality total RNA from
a pre-lysis treatme
hern blotting, prime
raffin-embedded ti
he quality of RNA f
n of mRNA with RT
mmalian tissues, su
d RNA directly in R
mer extension, cDN
n serum, plasma, o
ed viral RNA is use
de water.
m cells and tissue
tavidin-coated 0.2
tative and quantita
as whole blood,
cific prelysis
cids in PCR,
rom bacterial
transcription,
plasma, or
are isolated
PCR and RT-
od, using the
innovative spin
ml. Ideal for
ystem Viral
e High Pure
olumes must
from 5 to 10
sue.
ed. Use
tissues for
quantification
the
s and tissues,
Use purified
tive
m.
m cultured
nt. Use the
er extension,
ssue and
from paraffin
T-PCR on the
uch as mouse
RT-PCR,
NA library
other body
ed for RT-PCR
after lysis and
ml PCR tubes.
ative RT-PCR

11 796 828 001
11 754 777 001
11 754 785 001
11 858 874 001
05 114 403 001
12 011 875 001
Cat. No.
06 650 775 001
04 823 125 001
05 080 576 001
11 828 665 001
03 270 289 001
12 033 674 001
11 858 882 001
11 787 896 001

1 kit fo
1 kit f
1 kit fo
1 kit fo
1 kit
1 set
1
1 kit
1 kit for
1 kit
1 kit
1 kit
1 kit fo
1 kit




for up to 100 isola

Pack Size


up to 50 miRNA is


for up to 100 isola



for up to 192 reac

www.roche
cations
cations
cations
cations
tions
ations
ns
tions
solations
tions
ations
tions
cations
ctions
e-applied-science

279,90
102,60
448,30
335,70
259,70
146,30
Price in
inquire
308,00
324,80
238,70
477,20
238,70
363,50
459,70

2
51

e.com

2

2
Sa
52

www.r

mRN

Isolat
cells,
north
Isolat
mRN

Isolat
with
yield
blotti
Rea
Prod
Red

Used
lyses
cells
use w
RNA

Easy-
For s
bone
long-
Strep

Polyd
biotin
partic
succe
TriPu

Prepa
DNA
synth
dena
Col
Prod
mini

Read
quick
of ex
sequ
mini

Read
quick
from
mini

Read
quick
from
limit:
Quic

Read
uninc
react
dsDN
Quic

Read
uninc
react
dsDN
Quic

Read
unlab
react
RNA:

ample Pr
roche-applied-sc
NA Isolation Kit
te highly purified m
or tissue (without
hern blotting, cDNA
te at least 70 g of
NA Isolation Kit fo
te high-quality mR
RNA/DNA Stabiliz
of 50 to 200 ng m
ng, cDNA library p
agents for Is
duct Name
Blood Cell Lysis
d for isolate DNA a
red blood cells in
free of red blood c
with other species.
A/DNA Stabilizati
-to-use reagent fo
imultaneous cell ly
e marrow samples.
-term storage.
ptavidin Magneti
disperse paramagn
n-labeled molecule
cles/ml. Magnetic
essfully used in ma
ure Isolation Rea
are total RNA, gen
-free RNA in north
hesis, RT-PCR. Use
tured protein in SD
lumns for Pu
duct Name
Quick Spin DNA
dy-to-use, microce
k, efficient purifica
cess dye-labeled d
encing. Exclusion
Quick Spin Oligo
dy-to-use, microce
k and efficient rem
end-labeled oligo
Quick Spin RNA
dy-to-use, microce
k and efficient rem
RNA labeled by p
= 20 bases
ck Spin Columns
dy-to-use disposab
corporated nucleot
tions. Use in low-s
NA: <10 base pairs
ck Spin Columns
dy-to-use disposab
corporated nucleot
tions. Use in low-s
NA: <72 base pairs
ck Spin Columns
dy-to-use disposab
beled or radioactiv
tions. Use in low-s
: <12 bases. Samp
eparatio
cience.com
mature mRNA from
t isolation of total R
A synthesis, RT-PC
f poly (A)
+
RNA.
or Blood/Bone M
RNA from blood or
zation Reagent for
RNA/ml blood can
preparation, and m
solation
Buffer
and RNA, this read
human whole blo
cells, for use in do

on Reagent for B
r collection of sam
ysis and stabilizatio
Also ideal for nuc
ic Particles
netic particles for f
es. Supplied in sus
separation of biot
any applications.
agent
nomic DNA, and pr
herns, in vitro tran
e RNA-free DNA in
DS-PAGE and wes
urification
A Columns
ntrifuge-compatib
tion of DNA from
dideoxynucleotide
limit: = 20 bp
o Columns
ntrifuge-compatib
moval of unincorpo
nucleotides. Exclu
A Columns
ntrifuge-compatib
moval of unincorpo
olymerase or end-
for radiolabeled
ble columns quickl
tides from DNA la
peed, swinging-bu
s. Sample size: up
for radiolabeled
ble columns quickl
tides from DNA la
peed, swinging-bu
s. Sample size: up
for radiolabeled
ble columns quickl
vely labeled RNA fr
peed swinging-bu
ple size: up to 50
on
m RNA preparation
RNA). Use isolated
CR, in vitro translat
Marrow
r bone marrow lysa
Blood/Bone Marro
n be used in RT-PC
more.
y-to-use buffer pr
od, yielding intact
wnstream applicat
Blood/Bone Marr
mples for nucleic ac
on of nucleic acids
cleic acid stabilizat
fast separation of a
spension, containin
in-labeled molecu
rotein from a singl
slation, RNase pro
n PCR and cloning
stern blots.
le chromatography
labeling reactions,
terminators prior t
le chromatography
rated radiolabeled
sion limit: = 8 bp
le chromatography
rated radiolabeled
-labeling technique
DNA purification
y and efficiently re
beling and polyme
ucket centrifuges.
to 50 l.
DNA purification
beling and polyme
ucket centrifuges.
to 100 l.
RNA purification
y, efficiently separ
rom nucleotides an
ucket centrifuges. E
l.
ns, cultured
d mRNA in
tion, etc.
ates preserved
ow. Resulting
CR, northern
referentially
white blood
tions. Not for
row
cid isolation.
s in blood and
tion during
a variety of
ng 10 mg
les is
e sample. Use
otection, cDNA
g. Use
y columns for
, and removal
to fluorescent
y columns for
nucleotides
y columns for
nucleotides
es. Exclusion
n
emove
erization
Exclusion limit
n
emove
erization
Exclusion limit
n
rate small
nd labeling
Exclusion limit

11 741 985 001
11 934 333 001
Cat. No.
11 814 389 001
11 934 317 001
11 641 778 001
11 641 786 001
11 667 157 001
11 667 165 001
Cat. No.
11 814 419 001
11 814 397 001
11 814 427 001
11 273 922 001
11 273 949 001
11 273 965 001
11 273 973 001
11 273 990 001

1 kit (for
1 kit (for up
(1.5
100 ml (for 50
sam
500 ml (for
isolation of at leas
poly (A)
+
RNA)

to 30 (100) isolatio
5 ml) sample volum

Pack Size
0 to 500 reactions,
mple size 1 to 500

r up to 50 ml samp

2 ml
10 ml

50 ml
200 ml

Pack Size
50 columns

50 columns

50 columns

20 columns
50 columns

20 columns
50 columns

20 columns

st 70 g of
ons from 5 ml
mes)
depending on
l)
ple material)

348,90
587,60
Price in
51,00
96,10
189,80
719,10
160,20
530,90
Price in
206,40
206,40
222,90
188,00
420,50
188,00
420,50
280,60

Sa

Quic

Read
unlab
react
RNA:
Iso
Lib
Prod
Liber

Maxi
conta
non-c
provi
Liber

Maxi
conta
non-c
prote
Liber

Maxi
conta
a non
more
Liber

Maxi
conta
a non
ensu
Liber

Maxi
conta
a non
disso
Liber

Dete
these
Blend
appli
Cru
Prod
Colla

Disso
mam
suspe
viabil
Colla

Disso
mam
suspe
and v
Colla

Disso
blood
estab
integ
Colla

Use t
hepa
such
adipo

ample Pr
ck Spin Columns
dy-to-use disposab
beled or radioactiv
tions. Use in low-s
:<72 bases. Sampl
olation of C
erase Purifi
duct Name
rase DH Researc
mize yield of isolat
ains highly purified
clostridial neutral
des high experime
rase DL Researc
clostridial neutral
ein) for delicate ap
rase TH Researc
n-clostridial neutra
e difficult targets.
rase TL Research
res experimental r
rase TM Researc
ociation application
rase Research G
rmine the optimal
e five 5 mg vials of
ds, each with diffe
cability.
ude Collagen
duct Name
agenase A
ociate tissue (lung,
mary gland, blood
ensions to establis
lity, and functional
agenase B
mary gland, blood
ensions to establis
viability are import
agenase D
d vessels, brain, et
blish primary cell c
rity of cell-surface
agenase H
to dissociate tissue
tocytes from rat liv
as for large vesse
ocytes from epidid
eparatio
for radiolabeled
ble columns quickl
vely labeled RNA fr
peed swinging-bu
le size: up to 100
Cells - Tis
ed Enzyme
ch Grade
ted cells using this
d collagenase isofo
protease. Exceptio
ental reproducibilit
h Grade
d collagenase isofo
protease. Gentle a
plications.
h Grade
d collagenase isofo
al protease. More a
h Grade
d collagenase isofo
al protease. Except
reproducibility.
ch Grade
d collagenase isofo
al protease. Excelle
ns.
rade Selection K
collagenase produ
f highly pure Libera
rent levels of aggr
nase Enzym
, heart, muscle, bo
d vessels, brain, etc
sh primary cell cult
lity are important.
, heart, muscle, bo
tant.
, heart, muscle, bo
c.), and prepare si
culture systems. Us
e proteins are impo
es to establish prim
ver and for the pre
el endothelial cells,
ymal fat pads of ra
on
RNA purification
rom nucleotides an
l.
ssue Disso
Blends
s new enzyme blen
orms blended with
onal lot-to-lot cons
ty.
s new enzyme blen
orms blended with
activity (low activity
s new enzyme blen
orms blended with
aggressive proteas
s new enzyme blen
orms blended with
tional lot-to-lot con
s new enzyme blen
orms blended with
ent overall applicab
Kit
uct for your applica
ase Research Grad
ressiveness, specif
mes
one, liver, kidney, c
c.), and prepare sin
ture systems. Use
ture systems. Use
one, liver, mammar
ngle-cell suspensi
se when functiona
ortant.
mary cell cultures.
eparation of other t
, and for the isolati
ats.
n
rate small
nd labeling
Exclusion limit
ociation
nd that
h Dispase
, a
sistency
nd that
h Dispase
, a
y per mg
nd that
h Thermolysin,
se activity for
nd that
h Thermolysin,
nsistency
nd that
h Thermolysin,
bility in
ation using
de Enzyme
icity, and
cartilage,
ngle-cell
when yield,
cartilage,
ngle-cell
when yield
ry, kidney,
ions to
lity and
Isolate
types of cells,
ion of

11 274 015 001
Cat. No.
05 401 054 001
05 401 089 001
05 401 160 001
05 466 202 001
05 401 135 001
05 401 151 001
05 401 020 001
05 401 119 001
05 401 127 001
05 401 046 001
Cat. No.
10 103 578 001
10 103 586 001
11 088 793 001
11 088 807 001
11 088 815 001
11 088 831 001
11 088 858 001
11 088 866 001
11 088 882 001
11 074 032 001
11 074 059 001
11 087 789 001

1
1
1
1
20 columns

Pack Size
10 mg (2 x 5 mg)
100 mg (2 x 50 mg

10 mg (2 x 5 mg)
100 mg (2 x 50 mg

10 mg (2 x 5 mg)
100 mg (2 x 50 mg

10 mg (2 x 5 mg)

10 mg (2 x 5 mg)
100 mg (2 x 50 mg

1 kit (5 x 5 mg)

Pack Size
100 mg
500 mg
2.5 g
100 mg
500 mg
2.5 g
100 mg
500 mg
2.5 g
100 mg
500 mg
2.5 g

www.roche

g)

g)

g)

g)
e-applied-science

280,60
Price in
333,00
1.367,50
62,50
402,70
82,10
611,50
36,50
108,50
642,40
213,30
Price in
59,00
251,90
1.009,90
59,00
251,90
1.009,90
59,00
251,90
1.009,90
59,00
250,90
1.009,90

2
53

e.com

2

2
Sa
54

www.r

Colla

Use t
high
and r
epidi
Colla

Colla
variet
Colla
deter
Oth
Prod
Disp

Rapid
Relea
cultu
suspe
Disp

Rapid
Relea
cultu
suspe
De
Prod
DNa

DNas
endo
for is
as a
DNa

DNas
degra
DNA
this e
DNa

DNas
isolat
DNA
DNa

Degr
to rem
after
sensi
Nucl

Endo
dsDN
yield
vitro
Prote

Activ
grade
from
lyoph
Prote

Activ
grade
from
mg/m
RNas

RNas
RNA.

ample Pr
roche-applied-sc
agenase P
collagenase activi
rat. The preparatio
dymal fat pads of
agenase/Dispase
agenase/Dispase

ty of different tissu
agenase/Dispase

rmined empirically
her Dissocia
duct Name
pase
I (neutral p
d, gentle disruption
ases single cells fo
re to transfer to a
ension.
pase
II (neutral
re to transfer to a
ension.
egradation
duct Name
se I
se I, Grade II from
onuclease that requ
solation procedures
lyophilizate.
se I
se I (double-strand
ades DNA. During
which causes cell
extracellular DNA.
se I recombinant
se I, recombinant,
tion procedures, a
during sample pre
se I recombinant
rades DNA in appl
move genomic DN
in vitro transcripti
itive regions in euk
lease S7
onuclease preferen
NA and RNA. Cleav
3'-mono- and olig
translation system
einase K, recomb
ve endopeptidase i
e enzyme isolates
tissues/cell lines,
hilizate. Also availa
einase K, recomb
ve endopeptidase i
e enzyme isolates
tissues/cell lines,
ml in 10 mM Tris. A
se
se from bovine pan
. This is a crude m
eparatio
cience.com
ty, you can isolate
n is also used to is
rats.
e

is used for the pre
ues and organs. Th
for preparation of
y.
ating Enzyme
protease, grade I
n of cellular matrix
or primary cell cult
secondary culture
protease, grade
secondary culture
n of Cellula
bovine pancreas i
uires bivalent catio
s for proteins (e.g
d specific endonuc
tissue dissociatio
l clumping. Adding
Lyophilized.
t
grade I is used for
nalysis of chromat
eparation.
t, RNase-free
ications sensitive t
NA from RNA prep
ion, perform nick t
karyotic DNA.
ntially cleaves sing
ves 5'-phosphodie
gonucleotides. Rem
ms and in RNA seq
binant, PCR Grad
nactivates endoge
nucleic acids for P
and promotes bac
able in solution.
binant, PCR Grad
nactivates endoge
nucleic acid for PC
and promotes bac
Available lyophilize
ncreas is used for
ixture of RNases.
on
mary cell cultures.
pancreatic islets f
solate adipocytes f
eparation of cells f
he suitability of
f a particular cell ty
es
)
x in many tissues a
ure or harvesting c
e. Prevents cell clum
II)
x in many tissues a
ure or harvesting c
ar Compo
s a double-strand-
ons for maximal ac
., membrane prote
clease) from bovin
n, some cells are ly
g DNase I to the b
r eliminating DNA
tin structure, and e
to the presence of
arations, isolate D
translations, and to
le-strand substrate
ester bonds of RNA
move endogenous
quencing.
de
enous RNases and
PCR and native RN
cterial cell lysis. Su
de
enous RNases/DNa
CR and native RNA
cterial cell lysis. So
ed.
the removal and d
Because of its
from mouse
from
from a wide
ype must be
and organs.
cells already in
mping in
and organs.
cells already in
mping in
onents
-specific
ctivity. It is used
eins). Supplied
e pancreas
ysed, releasing
uffer degrades
during protein
eliminating
RNase. Used
NA-free RNA
o map DNase-
es, as well as
A and DNA to
RNA from in
DNases. PCR-
NA and DNA
pplied as a
ases. PCR-
A and DNA
olution: 14 to 22
degradation of

11 213 857 001
11 213 865 001
11 213 873 001
10 269 638 001
11 097 113 001
Cat. No.
04 942 086 001
04 942 078 001
Cat. No.
10 104 159 001
11 284 932 001
04 536 282 001
04 716 728 001
10 107 921 001
03 115 801 001
03 115 836 001
03 115 852 001
03 115 879 001
03 115 828 001
03 115 844 001
03 115 887 001
10 109 134 001

10 x approx. 2
5
10,000 U (pr
100 mg
500 mg
2.5 g
100 mg
500 mg

Pack Size
mg (filtered throu
size membrane)

5 x 1 g (non-sterile

Pack Size
100 mg

100 mg

2 x 10,000 U

rovided with incub

15,000 U

2 x 250 mg
25 mg
4 x 250 mg
100 mg
5 ml
25 ml
1.25 ml
500 mg

gh 0.2 m pore
e)
bation buffer)

80,80
326,40
1.296,50
130,80
454,20
Price in
753,70
435,30
Price in
58,20
157,20
119,20
213,30
169,50
364,80
37,70
590,50
82,30
113,40
453,90
51,40
128,50

Sa

RNas

RNas
that a
isolat
RNas

Cleav
of DN
site-s
and r
RNas

Use R
RNA
solut
RNas

Effici
prepa
deoxy
a boi
Iso
Cel
Prod
cOm

Rapid
inhib
extra
IMAC
cOm

Rapid
inhib
extra
prepa
cOm

Rapid
inhib
in ce
EDTA
Pro
Prod
cOm

Excel
prote
cOmp
cOm

Supe
of se
bacte
cOm

High
prote
cOmp
cOm

Supe
serin
yeast

ample Pr
se A
se A from bovine p
acts on single-stra
tion of DNA. For D
se H
ves RNA in RNA:D
NA synthesis, elim
specific cleavage o
removal of poly (A)
se T1
RNase T1 from Asp
fingerprinting; sup
ion, pH 6.
se, DNase-free
ently removes con
arations. Heteroge
yribonuclease. Use
ling step. Solution
olation of P
ll Lysis Kits
duct Name
mplete Lysis-M
d, gentle mammali
ition of protease a
cts. Produces high
C, use with cOmple
mplete Lysis-M ED
d, gentle mammali
ition of protease a
cts. Obtain higher
aration allows use
mplete Lysis-B (2x
d, gentle bacterial
ition of protease a
ll extracts. Obtain
A-free preparation
otease Inhib
duct Name
mplete ULTRA Tab
llent inhibition of s
ein protection in ba
plete His-Tag Purif
mplete ULTRA Tab
erb protein protect
rine, cysteine, and
erial, yeast, and ma
mplete ULTRA Tab
inhibition of serin
plete His-Tag Purif
mplete ULTRA Tab
erb protein protect
e, cysteine, and as
t, and mammalian
eparatio
pancreas is a pyrim
anded RNA. For an
DNA isolation, RNa
DNA hybrids. Use in
ination of mRNA in
of RNA, detection o
) sequences of mR
pergillus oryzae fo
pplied as a supens
ntaminating RNA fr
eneous mixture of r
e directly in any D
: 500 g/ml.
Proteins
withcOmple
ian cell lysis in 5 m
activity (serine, cys
her yields of protei
ete His-Tag Purific
DTA-free
yields of protein t
in IMAC.
x) EDTA-free
cell lysis in 10 min
higher yields of pr
allows use in IMA
itors - Cock
blets, glass vials
serine, cysteine, me
acterial, yeast, and
fication Resin for I
blets, EDTA-free,
ion combined with
aspartic protease
ammalian cell type
blets, Mini, EASY
e, cysteine, metallo
blets, Mini, EDTA
ion combined with
spartic proteases fo
cell types.
on
midine-specific end
nalytical purposes a
ase A needs to be b
n in vivo RNA-prim
n 2nd-strand cDN
of RNA:DNA regio
RNA.
or RNA sequence a
sion in 3.2 M amm
rom plasmid or ge
ribonucleases, pre
NA isolation techn
ete Tablets
minutes and simult
teine, metalloprote
n than using sonic
cation Resin.
minutes and simult
teine, metalloprote
than using sonicat
nutes and simultan
teine, but not meta
rotein than using s
AC.
ktail Tablets
etallo- and asparti
d mammalian cell t
IMAC.
glass vials
h ease of use: High
es for protein prote
es.
Ypack
o- and aspartic pro
d mammalian cell t
IMAC.
A-free, EASYpack
h ease of use: High
or protein protecti
doribonuclease
and for
boiled.
med initiation
A synthesis,
ons in dsDNA,
analysis and
onium sulfate
enomic DNA
epared free of
nique, without
aneous
eases) in cell
cation. For
aneous
eases) in cell
ion. EDTA-free
neous
alloproteases)
sonication.
s
ic proteases for
types. Use new
hest inhibition
ection in
oteases for
types. Use new
k
h inhibition of
on in bacterial,

10 109 142 001
10 109 169 001
10 786 357 001
10 109 193 001
11 119 915 001
Cat. No.
04 719 956 001
04 719 964 001
04 719 948 001
Cat. No.
05 892 988 001
06 538 304 001
05 892 953 001
06 538 282 001
05 892 970 001
05 892 791 001

1 kit for the ly
1 kit for the ly
1 kit
2 glass via
6 glass via
2 glass vials ea
6 glass vials ea
30 tablets (in
packs, each ta
10 m
30 tablets (in
packs, each ta
10 m
25 mg
100 mg

100 U

100,000 U

500 g (1 ml)

Pack Size
ysis of up to 100 g
cells

ysis of up to 100 g
cells

for up to 20 extrac

Pack Size
als each containing
(with EDTA)
als each containing
(with EDTA)

ach containing 10
free
ach containing 10
free

ndividually packed
ablet is sufficient f
ml extraction solut

ndividually packed
ml extraction solut

www.roche
of mammalian
of mammalian
ctions
g 10 tablets
g 10 tablets
tablets, EDTA-
tablets, EDTA-
d in foil blister
for a volume of
tion)
d in foil blister
for a volume of
tion)
e-applied-science

37,70
101,40
388,00
60,70
154,00
Price in
314,90
314,90
234,20
Price in
262,40
707,30
262,40
630,40
158,40
158,40

2
55

e.com

2

2
Sa
56

www.r

cOm

Rely
and m
New
Supp
cOm

Rely
and m
New
Supp
cOm

Rely
EDTA
types
cOm

Rely
EDTA
types
cOm

Rely
and m
New
Supp
cOm

Rely
and m
New
Supp
cOm

Rely
EDTA
types
cOm

Rely
EDTA
types
Pro
Prod
Antip

Antip
to a s
than
fold h
Apro

Prote
cultu
chym
quan
Best

Besta
leuci
locat
carbo
Calp

Stron
and I
prote
weig
Chym

Chym
inhib

ample Pr
roche-applied-sc
mplete
on proven perform
metalloproteases i
for EDTA inhibitio
plied in glass vials.
mplete
on proven perform
metalloproteases i
for EDTA inhibitio
plied in EASYpacks
mplete, EDTA-free
on proven perform
A-free Tablets inhi
s as cOmplete ULT
mplete, EDTA-free
on proven perform
A-free Tablets inhi
s as cOmplete ULT
mplete, Mini
on proven perform
metalloproteases i
for EDTA inhibitio
plied in a glass vial
mplete, Mini
on proven perform
metalloproteases i
for EDTA inhibitio
plied in EASYpacks
mplete, Mini, EDTA
on proven perform
A-free Tablets inhi
s as cOmplete ULT
mplete, Mini, EDTA
on proven perform
A-free Tablets inhi
s as cOmplete ULT
otease Inhib
duct Name
pain dihydrochlo
pain dihydrochlorid
small extent. Note:
leupeptin. The inh
higher than that of
otinin
ect proteins during
re studies. Used fo
motrypsin on immo
tification of kallikr
tatin
atin is an inhibitor
ne aminopeptidase
ed on the surface
oxypeptidases.
pain Inhibitor I
ng inhibitor of Ca
2+
I. Inhibits calpain,
ein kinase C. Most
ht and lack of cha
mostatin
mostatin is a mixtu
itor of -, -,
eparatio
cience.com
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
s .
e
mance combined w
bit serine and cyst
TRA Tablets. Suppl
e
mance combined w
bit serine and cyst
TRA Tablets. Suppl
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
.
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
s .
A-free
mance combined w
bit serine and cyst
TRA Tablets. Suppl
A-free
mance combined w
bit serine and cyst
TRA Tablets. Suppl
itors - Indiv
oride
de inhibits papain
: Antipain is more
hibitory potency of
f elastatinal.
g isolation/purificat
or purification of u
bilized aprotinin, p
rein activity.
of aminopeptidase
e, tripeptide amino
of mammalian cel
+
-dependent neutr
which activates m
likely membrane p
rged residues.
re of chymostatins
-, and -chymotr
on
Tablets inhibit serin
pes as cOmplete U
mplete His-Tag Pur
pes as cOmplete U
mplete His-Tag Pur
with high convenie
teine proteases in
ied in glass vials.
with high convenie
teine proteases in
ied in EASYpacks
pes as cOmplete U
mplete His-Tag Pur
pes as cOmplete U
mplete His-Tag Pur
with high convenie
teine proteases in
ied in a glass vial.
with high convenie
teine proteases in
ied in EASYpacks
vidual Inhibit
and trypsin. Plasm
specific for papain
antipain is approx
tion, increasing ce
urokinase, trypsin, a
protein-folding stu
es, such as aminop
opeptidase, and am
ls. Does not inhibi
ral cysteine protea
myosin light chain k
permeable due to
s a, b and c and is
rypsin.
ne, cysteine,
ULTRA Tablets.
rification Resin.
ne, cysteine,
ULTRA Tablets.
rification Resin.
nce. cOmplete
the same cell
nce. cOmplete
the same cell
.
ne, cysteine,
ULTRA Tablets.
rification Resin.
ne, cysteine,
ULTRA Tablets.
rification Resin.
nce. cOmplete
the same cell
nce. cOmplete
the same cell
.
tors
min is inhibited
n and trypsin
ximately 100-
ell lifetime in
and
dies, and
peptidase B,
minopeptidases
it
ases calpain I
kinase and
low molecular
a specific

11 697 498 001
11 836 145 001
04 693 116 001
05 056 489 001
11 873 580 001
04 693 132 001
11 836 153 001
04 693 124 001
11 836 170 001
04 693 159 001
Cat. No.
11 004 646 001
10 236 624 001
10 981 532 001
11 583 794 001
10 874 515 001
11 086 090 001
11 004 638 001

20 tablets in a
for a volum
3 x 20 tablet
sufficient fo
20 tablets (in
packs, each ta
50 m
3 x 20 table
sufficient f
20 tablets in a
for a volum
20 tablets (in
packs; each ta
50 m
25 tablets in a
for a volum
30 tablets (in
packs, each ta
10 m
25 tablets in a
for a volum
30 tablets (in
packs, each ta
10 m
glass vial, each tab
me of 50 ml extract
ts in a glass vial, e
or a volume of 50 m
solution

ndividually packed
ml extraction solut

ets in glass vials, ea
for a volume of 50
me of 50 ml extract

ndividually packed
ml extraction solut

me of 10 ml extract

ndividually packed
ml extraction solut

me of 10 ml extract

ndividually packed
ml extraction solut

Pack Size
10 mg

10 mg
50 mg
100 mg
10 mg

25 mg

10 mg

blet is sufficient
ion solution
each tablet is
ml extraction
d in foil blister
for a volume of
tion)
ach tablet is
ml solution
blet is sufficient
ion solution
d in foil blister
for a volume of
tion)
blet is sufficient
ion solution
d in foil blister
for a volume of
tion)
blet is sufficient
ion solution
d in foil blister
for a volume of
tion)

257,20
692,90
257,20
617,70
257,20
257,20
136,00
163,10
136,00
163,10
Price in
185,70
69,70
275,40
488,00
183,30
224,80
185,70

Sa

E-64

Stron
cathe
of pro
betw
Leup

Prote
prote
alpha
the re
2
-

2
-M
endo
speci
uroki
Pefa

Spec
comp
value
block
Pefa

Spec
comp
attac
conc
Peps

Prote
inves
class
pharm
PMS

Inhib
prote
most
solub
Prote

Each
a wid
and s
resor
Tryps

Use t
Inhib
cultu
tissue
Tryps

Use t
Inhib
medi
kallik
Pho
Prod
Phos

Use n
Inhib
almo
deph
Kin
Prod
Stau

Most
depe
effec
, diac

ample Pr
4
ng, irreversible inhi
epsin B and L, bro
oteins and enzyme
een the SH compo
peptin
ect proteins during
ease inhibitor. Leup
a-amino group. It i
eaction by dialysis
Macroglobulin
Macroglobulin is a
oproteinases. Not a
ific for one or a lim
inase, factor XIIa, a
bloc
SC
ific, potent, irrever
pared to PMSF or D
es. Completely inac
ker of thrombin in
bloc
SC PLUS
ific, potent irrevers
pared to PMSF or D
hment of Pefabloc
entration for longe
statin
ect proteins and en
stigation of enzyme
sifications. For affin
macological, HIV, a
SF
bits serine protease
ease papain [revers
t cysteine or aspart
ble, water-stable a
ease Inhibitors S
inhibitor in the se
de variety of protea
sensitively verified
rufin-labeled).
sin Inhibitor
to terminate tissue
bits trypsin, factor X
re media. Does no
e kallikrein. From s
sin Inhibitor
to terminate tissue
bits trypsin, plasmin
a. Does not inhibit
krein. From chicken
osphatase In
duct Name
sSTOP
non-toxic tablets to
bition of acid/alkali
st any tissue or ce
osphorylation in F
nase Inhibito
duct Name
urosporine
t potent PKC inhib
ndent protein kina
tively than with er
cylglycerol, or phos
eparatio
ibitor of papain an
melain, and ficin d
es. Inhibition of thi
onents.
g isolation from tiss
peptin is a tripepti
s highly soluble in
s.
a protease inhibito
affected are endop
mited number of se
and endoproteinas
rsible inhibitor of s
DFP with higher st
ctivates proteinase
serum and plasma
sible inhibitor of se
DFP. Pefabloc
SC
c
SC to proteins.
er incubation times
nzymes during isol
e mechanisms, bio
nity chromatograph
and cancer researc
es (chymotrypsin, t
sible by DTT treatm
tic proteases. Pefa
lternative.
Set
et can be used sep
ases. Effectiveness
using the Univers
e disaggregation an
Xa, plasmin, and p
ot inhibit metallo-,
soybean.
e disaggregation an
n, and plasma kall
t metallo-, cysteine
n egg white.
nhibitors
o protect your prot
ne, serine/threonin
ell type. PhosSTOP
FFPE tissue section
ors
itor known. Also in
ases. Protein tyrosi
bstatin and genist
spholipids.
on
nd cysteine proteas
during isolation and
ol proteases is non
sues or membrane
de derivative with
n water and can be
r that blocks most
proteinases that are
equences (tissue k
se Lys-C).
serine proteases. N
tability at physiolog
e K. Unlike PMSF, e
a.
erine proteases. N
C and the PLUS ad
They can be used
s at alkaline pH.
ation and purificat
ological function, a
hy, and structural,
ch.
trypsin, thrombin, c
ment]). Does not in
abloc
SC is a non
parately or as cockt
s of protease inhib
sal Protease Substr
nd for subcultivati
lasma kallikrein in
cysteine, aspartic
nd for subcultivati
ikrein activity in se
e, aspartic proteas
tein from dephosp
ne and tyrosine ph
Tablets prevent
ns.
nhibits cAMP- and
ine kinases are blo
ein. Does not com
ses, such as
d purification
n-competitive
es using this
an acetylated
e removed from
t
e highly
kallikrein,
Nontoxic
gical pH
excellent
ontoxic
dditive prevent
at higher
tion. Facilitates
and protease
cysteine
nhibit metallo-,
ntoxic, water-
tails to inhibit
ition is quickly
rate (casein,
on procedures.
n serum-free
proteases, or
on procedures.
erum-free
es, or tissue
phorylation.
hosphatases in
d cGMP-
ocked more
mpete with Ca
2+

10 874 523 001
11 585 681 001
11 017 101 001
11 017 128 001
11 034 626 001
11 529 048 001
10 602 442 001
11 429 868 001
11 429 876 001
11 585 916 001
11 873 601 001
11 873 628 001
10 253 286 001
11 359 053 001
11 524 488 001
10 837 091 001
11 359 061 001
11 206 893 001
10 109 886 001
10 109 878 001
Cat. No.
04 906 837 001
04 906 845 001
Cat. No.
11 055 682 001

set I (100 mg P
set II (1 g Pefab
1 set (10 in
20 tablet
(each tablet
10 tablet
(each tablet
10 mg
25 mg

5 mg
25 mg
50 mg
100 mg
25 inhibitor units

100 mg
1 g
500 mg
Pefabloc
SC; 5 m
solution)
bloc
SC; 2 x 25 m
solution)

2 mg
10 mg
50 mg
10 g
25 g

ndividual protease

50 mg

1 g

Pack Size
ts in EASYpacks (fo
for 10 ml cell extra
ts in EASYpacks (fo
for 10 ml cell extra

Pack Size
500 g

www.roche
l PSC-Protector
ml PSC-Protector
e inhibitors)
oil blister)
act or buffer)
oil blister)
act or buffer)
e-applied-science

270,20
542,80
82,90
292,80
418,40
630,90
108,30
101,60
505,30
271,40
153,60
724,60
42,60
163,10
457,00
97,70
184,40
346,30
50,90
128,20
Price in
190,00
101,10
Price in
426,00

2
57

e.com

2

2
Sa
58

www.r

Me
Prod
CHA

For s
of bo
n-Oc

n-Oc
solub
dialys
Noni

Solub
comp
stabi
0.25
Noni

Solub
comp
stabi
nitrog
Sodi

Pure
appli
Trito

Comm
durin
elect
inject
Trito

Comm
isolat
elect
CMC
Twee

Use T
mem
for a
and i
Chr
Prod
Anti-

Easy
mam
of HA
weste
Anti-

Easy
mam
prote
prote
cOm

High-
tagge
enab
cOm

Prepa
above

ample Pr
roche-applied-sc
embrane Pro
duct Name
APS
olubilization of me
oth the sulfobetaine
ctylglucoside
ctylglucoside is a m
bilization and recon
sis. CMC: 14.5 mM
idet P40 Substitu
bilize membrane p
plexes. Also includ
lize enzymes such
mM.
idet P40 Substitu
bilize membrane p
plexes. Also includ
lize enzymes such
gen in injection via
um Dodecyl Sulf
quality preparatio
cations as a denat
on X-100
monly used non-io
ng isolation of mem
rophoresis. Aqueo
tion vials. CMC: ap
on X-100
monly used non-io
tion of membrane-
rophoresis. Suppli
C: approx. 0.2 mM a
en 20
Tween 20 to solub
brane-protein com
subsequent prote
mmunoblotting. C
romatograp
duct Name
-HA Affinity Matr
method for immun
malian, bacterial, a
A-tagged proteins
ern blotting or silv
-Protein C Affinit
method for immun
ein C-tagged prote
eins by western blo
mplete His-Tag Pu
-capacity IMAC m
ed proteins from ly
les compatibility w
mplete His-Tag Pu
acked columns wit
e). Fully compatibl
eparatio
cience.com
otein Solubil
embrane proteins.
e-type and bile-ac
mild, nonionic, non
nstitution of memb
M at +25C.
ute
roteins during isol
ed in buffers for m
as Taq. Supplied
ute
roteins during isol
ed in buffers for m
as Taq. Aqueous
als. CMC: 0.25 mM
fate (SDS)
n, suitable in most
turing agent for pr
onic detergent solu
mbrane-protein co
ous solution, 10% (
pprox. 0.2 mM at +
onic detergent for
-protein complexes
ed as a viscous liq
at +25C
ilize membrane pr
mplexes. Due to its
in detection by UV
CMC: approx. 0.06 m
hy Products
rix
noprecipitation of
and yeast extracts
from crude extrac
er staining.
ty Matrix
noprecipitation of
and yeast extracts
eins from crude ext
otting or silver stai
urification Resin
atrix for convenien
ysates. Proprietary
with EDTA and DTT
urification Colum
th cOmplete His-T
le with standard pu
on
lization
CHAPS combines
cid detergents. CM
-denaturing deterg
brane proteins. Eas
lation of membran
microplate assays a
as a Gel under nitr
lation of membran
microplate assays a
solution, 10% (w/v
M.
t routine electroph
roteins.
ubilizes membrane
mplexes. Used for
(w/v), filled under n
+25C.
solubilizing memb
s. It is also used fo
quid.
roteins during isola
s low UV absorban
V light absorption.
mM.
s
HA-tagged protein
and column affini
cts. Analyze tagged
protein C-tagged
and affinity purific
tracts. For analyzin
ning.
nt single-step purif
nickel-chelate che
T with minimal nic
mn
Tag Purification Re
urification systems
the properties
MC: 4 mM.
gent for the
sily removed by
e-protein
and used to
rogen. CMC:
e-protein
and used to
v), filled under
horetic
e proteins
r native gel
nitrogen in
branes during
or native gel
ation of
ce, it is ideal
Used in ELISA
ns from
ity purification
d proteins by
proteins from
cation of
ng tagged
fication of His-
emistry
kel leakage.
sin (see
s.

Cat. No.
10 810 118 001
10 810 126 001
10 634 425 001
11 754 599 001
11 332 473 001
11 667 289 001
11 332 481 001
10 789 704 001
11 332 465 001
Cat. No.
11 815 016 001
11 815 024 001
05 893 682 001
05 893 801 001
06 781 543 001
06 781 535 001

1 ml
1 ml
25 m
200 m
Pack Size
10 g
50 g

10 g

100 ml

5 x 10 ml

1 kg

5 x 10 ml

100 ml

5 x 10 ml

Pack Size
l (settled resin volu


ml (settled resin vol
ml (settled resin vo

5 x 1 ml
1 x 5 ml

ume)
ume)
lume)
olume)

Price in
277,50
1.239,90
741,50
122,30
102,40
359,50
83,50
53,40
116,70
Price in
852,30
473,20
290,40
1.583,60
179,00
130,00

Sa

Imm
Prod
Prote

Affin
for th
for th
mitog
Prote

Affin
from
enter
cultu
Imm

For th
Prote
solub
Imm

For th
Prote
solub
Fus
Prod
Ente

Enter
used
activa
Rest

High
acid
sequ
of rec
ample Pr
munoprecip
duct Name
ein G Agarose
ity chromatograph
he purification of Ig
he absence of stap
genic.
ein A Agarose
ity chromatograph
many species. Tes
rotoxins. Use to pu
re supernatant.
unoprecipitation
he immunoprecipit
ein A Agarose. The
bilization, stabilizat
unoprecipitation
he immunoprecipit
ein-G-Agarose. The
sion Protein
duct Name
rokinase
rokinase is a highly
for the cleavage o
ates trypsinogen to
triction Protease
ly purified, special
sequence IleGlu
ence may also be
combinant fusion
eparatio
pitation Reag
hy using Protein G
gG from many spe
phylococcal entero
hy using Protein A
sted for the absenc
urify mouse monoc
n Kit (Protein A)
tation of proteins f
e kit contains all re
tion, and the immu
n Kit (Protein G)
tion, and the immu
Cleavage
y purified preparat
of fusion proteins a
o trypsin.
Factor Xa
quality serine pro
GlyArg with a
used as a restricti
proteins.

on
gents
agarose is the me
ecies. Recombinant
toxins that are kno
agarose is ideal fo
ce of staphylococc
clonal antibodies fr
from cellular extra
eagents necessary
unopurification of p
from cellular extra
eagents necessary
tion from calf intes
at definite cleavag
otease, recognizing
a high degree of s
on cleavage site fo
ethod of choice
t form is tested
own to be
or purifying IgG
cal
rom ascites or
cts using
for cell lysis,
proteins.
cts using
y for cell lysis,
proteins.
stine and is
e site;
g the amino
pecificity. This
or processing

Cat. No.
05 015 952 001
11 243 233 001
11 719 416 001
05 015 979 001
11 134 515 001
11 719 408 001
11 719 394 001
11 719 386 001
Cat. No.
11 334 115 001
11 351 311 001
11 179 896 001
11 585 924 001

15 m
5 ml
2 ml
15 m
5 ml
2 ml
1 kit
1 kit
Pack Size


Pack Size
3 x 30 g
3 x 250 g

3 x 250 g
3 x 100 g

www.roche
lume)
ume)
ume)
lume)
ume)
ume)
tions
tions
e-applied-science

Price in
2.043,70
877,20
438,00
1.238,00
531,50
265,80
279,40
332,30
Price in
287,80
1.115,30
1.064,70
765,50

2
59

e.com

3

3
La
60

www.r

FLO
Prod
FLOW

The F
of pri
Cartr
FLOW

The F
Light
FLO
Prod
FLOW

The F
data
Mana
FLOW

The F
(one
Hand
FLO
Prod
Rack

The R
holdi
Rack

The R
which
FLOW

FLOW
Rack

The R
FLOW

The F
96 Pr
Instru
Prim

The P
MagN
Rack

The R
Flow
FLOW

The F
Light
FLOW

The F
used
FLOW

The F
used
FLOW

The F
Pure
FLOW

The F
Outp

aboratory
roche-applied-sc
OW System
duct Name
W Primary Samp
FLOW Primary Sam
imary and/or seco
ridges.
W PCR Setup Ins
FLOW PCR Setup I
tCycler
480 Instru
OW System
duct Name
W Software 1.0
FLOW Software 1.0
exchange between
agement Systems.
W Control Unit in
FLOW Control Unit
Control Unit is nee
dling Instrument, P
OW System
duct Name
k Sample Carrier
Rack Sample Carri
ng up to 32 prima
k Sample Carrier
Rack Sample Carri
h is used for holdi
W 32 Vial Carrier
W 32 Vial Carrier w
k Tip Carrier, TIP-
Rack Tip Carrier, is
W Processing Ca
FLOW Processing C
rocessing Cartridg
ument.
mary Sample Hand
Primary Sample Ha
NA Pure lysis buffe
k Tube Carrier Fil
Rack Tube carrier
32 Vial Carriers fo
W PCR Setup LC4
FLOW PCR Setup L
tCycler
480 Multi
W PCR Setup LC4
FLOW PCR Setup L
for cooling the Lig
W PCR Setup LC4
FLOW PCR Setup L
for cooling the Lig
W Output Plate C
FLOW Output Plate
96 Output Plates.
W PCR Setup Out
FLOW PCR Setup O
ut Plate.
y Develo
cience.com
m - Instru
le Handling Instr
mple Handling Inst
ndary samples into
strument
Instrument is for a
ument.
m - Softw
0 controls the FLOW
n FLOW compone
nclusive Monitor
t is used in conjun
eded for each of th
PCR Setup Unit, an
m - Assec
r, SMP-CAR-32-A
er, comes in a set
ry sample tubes.
r, SMP-CAR-24-A
er, SMP-CAR-24-A
ng up to 24 prima
r
with Adaptors for th
-CAR-480-A00, f
s used for holding
artridge Carrier
Cartridge Carrier i
e on the FLOW Pri
dling Reagent Ca
andling Reagent C
ers.
lling
Filling is used to s
or tube loading
480 Multiwell Pla
LC480 Multiwell Pl
iwell Plates.
480 Multiwell Pla
LC480 Multiwell Pl
ghtCycler
480 M
480 Multiwell Pla
LC480 Multiwell Pl
ghtCycler
480 M
Carrier
e Carrier enables t
tput Plate Coolin
Output Plate Cooli
ped Test
uments
rument
trument is for auto
o MagNA Pure 96
utomated PCR set
ware
W process and ma
nts and Laboratory
nction with the FLO
he following: Prima
d System Control)
ccories
A00, Set of 3
of 3 each of which
A00, Set of 4
A00, comes in a se
ry sample tubes.
he FLOW Instrume
for 480 tips
up to 5 tip trays (9
s used to place a M
imary Sample Han
arrier
Carrier is used for h
ecure Rack Sampl
ate Carrier
late Carrier is used
ate Cooling Bloc
late Cooling Block
ultiwell Plates 96.
ate Cooling Bloc
late Cooling Block
ultiwell Plates 384
the placement of u
ng Block
ng Block is used f
ting
mated transfer
Processing
tup on the
anages the
y Information
OW System
ary Sample
).
h is used for
et of 4 each of
ent.
96 tips each).
MagNA Pure
dling
holding
le Carriers and
d to hold the
ck (96 well)
k (96 well) is
ck (384 well)
k (384 well) is
.
up to 5 MagNA
or cooling the

Cat. No.
07 101 937 001
07 101 996 001
Cat. No.
07 102 097 001
07 101 929 001
Cat. No.
04 639 529 001
04 639 502 001
07 127 014 001
04 639 545 001
07 101 970 001
07 101 988 001
04 639 618 001
07 102 020 001
07 102 046 001
07 102 054 001
07 102 062 001
07 162 367 001

1
1 co
1 c
1 proc
1 rack
1 m
1 c
1 co
Pack Size
1 instrument

1 instrument

Pack Size
1 software packag

ontrol unit with mo

Pack Size
set of 3

set of 4

carrier with adapto
1 rack tip carrier

cessing cartrigde c

1 reagent carrier

k-tube carrier fillin

multiwell plate car

cooling block (96 w

ooling block (384 w

1 plate carrier

1 cooling block

e
onitor
ors
carrier
g rack
rier
well)
well)

Price in
inquire
inquire
Price in
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

La

FLO
Prod
Tip H

The T
with
Instru
Solid

The S
Samp
Plast

The P
on a
Kit V

For in
FLOW

The F
FLOW
Light

High-
Instru
used
Light
Light

High-
Instru
for re
Light
Light

Preve
assay
clear)
evapo
FLOW

The 2
FLOW
Setup
aboratory
OW System
duct Name
High Vol, 1 ml wit
Tip High Vol tips co
the FLOW Primary
ument.
d Waste Bag
Solid Waste Bag ho
ple Handling Instru
tic Chute
Plastic Chutes can
Hamilton Trolley.
VFV Consumables
nstallation purpose
W PCR Setup Ins
FLOW PCR Setup I
W PCR Setup Instru
tCycler
480 Mu
-performance reac
uments, 96-well ve
for real-time PCR
tCycler
480 Instru
tCycler
480 Mu
-performance reac
uments, 384-well v
eal-time PCR and m
tCycler
480 Instru
tCycler
480 Sea
ent evaporation an
ys in LightCycler

) using the LightC
oration during cyc
W Tubes (2 ml)
2 ml Screw Cap Tu
W Primary Sample
p Instrument (PSU
y Develo
m - Dispo
th Filter
ome in a set of 3.8
y Sample Handling
olds the waste pro
ument.
be used in combi
s ML STAR
es only.
strument 50 l Fil
Instrument 50 l F
ument.
ultiwell Plate 96,
ction device tailor-
ersion.LightCycler
and melting curve

ument, 96-well ver
ultiwell Plate 384
version.Use LightC
melting curve anal
ument, 384-well ve
aling Foil
nd contamination w
480 Multiwell Plat
Cycler
480 Instrum
cling or storage.
ubes, can be used
Handling Instrume
).
ped Test
osables
840 1 ml filter tips a
and the FLOW PC
oducts of the FLOW
nation with the So
lter Tips
ilter Tips are used
white, 4 barcode
-made for the Ligh
480 Multiwell Pla

e analysis applicat
rsion.
4 white, 4 barcod
-made for the Ligh
Cycler
480 Multiw
lysis applications w
ersion.
when running real-
tes (96 or 384 well
ment. Strong adhes
as secondary tube
ent (PSH) and for t
ting
and are used
CR Setup
W Primary
olid Waste Bag
with the
es
htCycler
480
ates 96 are
tions with the
des
htCycler
480
well Plates 384
with the
-time PCR
ls, white or
sion prevents
es for the
the FLOW PCR

Cat. No.
04 639 642 001
05 530 873 001
04 639 669 001
04 639 626 001
07 102 127 001
05 220 319 001
05 217 555 001
04 729 757 001
07 128 894 001

1
5 x 10 p
5 x 10 p
Pack Size
1 set of 3.840

25 per roll

1 set of 10 chutes

1 kit
2 sets of 5 x 96 tip

plates without seal

plates without seal

50 foils

280 tubes per box

www.roche
s
ps
ling foils
ling foils
x
e-applied-science

Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

3
61

e.com

4

4
PC
62

www.r

PC
Pro
Prod
Tran

Reco
fragm
and L
end l
Tran

Reve
trans
intere
quan
Tran

Reve
reage
time
Light
First

Synth
sequ
gene
quan
cDNA

Synth
librar
gene
for hy
Expa

A RN
ampl
RACE
Expa
huma
Reve

For tr
prepa
M-M
Full-l
Reve

For u
DNA
end l
hybri
5'/3'

Analy
Ends
3 en
react
Add
Prod
Prote

Inhib
trans
degra
PCR,
prepa

CR/RT-PC
roche-applied-sc
CR/RT-PCR
oducts for Tw
duct Name
scriptor Reverse
ombinant reverse tr
ments up to 14 kb.
LightCycler
and o
abeling, first stran
scriptor High Fid
rse transcribe RNA
scriptases. Optimiz
est and sequence
titative RT-PCR wi
scriptor First Str
rse transcribe all t
ents for first-strand
instruments, inclu
tCycler
480 Syste
Strand cDNA Sy
hesize 1st strand c
ence-specific prim
rate cDNA librarie
tify mRNA to mon
A Synthesis Syst
hesize ready-to-us
ries, for substractiv
s, and to in vitro t
ybridization on mic
and Reverse Tran
Nase H
-
reverse tr
ification of long RN
E. A two-step RT-P
nd Long Template
an dystrophin RNA
erse Transcriptas
ranscription of RN
aration and synthe
MuLV lacks endonu
ength copies of la
erse Transcriptas
up to 12 kb first- an
sequencing. Also
abeling of DNA fra
dization, and geno
RACE Kit, 2nd G
yze mRNA structu
(RACE). Generate
ds from low-copy
tion products witho
ditional Prod
duct Name
ector RNase Inhi
bits a wide spectru
scription reactions
adation. Use in ma
RNase protection
aration of RNase-f
CR
cience.com
R Enzyme
wo-Step RT-
e Transcriptase
ranscriptase for ro
Used in two-step
other real-time PC
d cDNA synthesis
delity cDNA Synth
A with increased fi
ed for two-step RT
transcriptomes. St
ith LightCycler
Sy
and cDNA Synth
types of RNA from
d cDNA synthesis
ding LightCycler

ems.
ynthesis Kit for R
cDNA as the startin
mers, poly(dT)
15
pri
es, first step in diffe
nitor expression.
tem
se ds cDNA to con
ve hybridization to
ranscribe whole cD
croarrays.
nscriptase
ranscriptase for tw
NA targets, genera
PCR using Expand
e was used to amp
A.
se M-MuLV
A fragments up to
esis of 1st-strand c
uclease activity and
arge mRNA are obt
se AMV
nd second-strand
used for primer ex
agments, generati
omic footprint expe
Generation
re and expression
e full-length cDNA
RNA, amplify and
out cloning.
ducts for Tw
ibitor
m of RNases also
(up to +60C) to p
any techniques: cD
, in vitro virus repl
free antibodies.
es
-PCR
obust transcription
RT-PCR using the
CR systems. Ideal fo
s, RACE, and more.
hesis Kit
idelity compared to
T-PCR. Use to clon
tudy gene express
ystems.
hesis Kit
a variety of source
reactions up to 14
Carousel-Based
RT-PCR (AMV)
ng reaction for RT
imers, or random p
erential display of
struct non-directio
enrich differential
DNA to generate l
wo-step RT-PCR, es
ation of cDNA libra
Reverse Transcrip
lify up to 13.5 kb c
o 10 kb. Use in cDN
cDNA for RT-PCR.
d has lower RNase
tained.
cDNA synthesis a
xtension, RNA seq
on of single-strand
eriments.
by Rapid Amplific
As, isolate and char
clone rare mRNA
wo-Step RT-
in in challenging
protect RNA samp
DNA synthesis, RT-
lication, transcripti
of RNA
ermal cyclers
or sequencing,
.
o other reverse
ne genes of
ion using
es. Includes all
4 kb on all real-
and
PCR. Use with
primers to
mRNA, or
onal cDNA
lly expressed
abeled cRNA
specially
aries, and 5'/3'
ptase and
cDNA from
NA library
Unlike AMV,
e H activity.
nd dideoxy
quencing, 3'-
ded probes for
cation of cDNA
racterize 5or
, and sequence
-PCR
reverse
les from
-PCR, qRT-
ion/translation,

Cat. No.
03 531 287 001
03 531 295 001
03 531 317 001
05 081 955 001
05 081 963 001
05 091 284 001
04 379 012 001
04 896 866 001
04 897 030 001
11 483 188 001
11 117 831 001
11 785 826 001
11 785 834 001
11 062 603 001
10 109 118 001
03 353 621 001
Cat. No.
03 335 399 001
03 335 402 001

2,000 U (4 x
of 50 l fina
Transcri
500 U for up to
each contain
250 U for up to
each contain
1 kit for up
1 kit
1 kit
1 kit for up to 5
1 kit
1 kit
1 kit for up to
1 kit
1 kit
10
Pack Size
x 500 U) for up to 2
l volume each con
ptor Reverse Trans
50 reactions of 50
ning 10 U Transcri
Transcriptase
25 reactions of 50
ning 10 U Transcri
Transcriptase
to 50 reactions an
reaction
for up to 200 reac
for up to 100 reac
50 reactions, inclu
reactions
for up to 100 reac
for up to 200 reac
30 reactions, inclu
reactions


1,000 U (20 l)
5,000 U (100 l)

500 U

1,000 U


Pack Size
2,000 U
0,000 U (5 x 2,000

200 reactions
ntaining 10 U
scriptase
0 l final volume
iptor Reverse
0 l final volume
iptor Reverse
nd 10 control
ctions
ctions
ding 10 control
ctions
ctions
uding 5 control
tions
tions
U)

Price in
946,00
266,10
162,70
413,20
1.087,40
598,10
332,40
484,00
869,90
244,00
651,70
99,80
377,70
231,50
490,40
478,50
Price in
134,00
496,80

PC

Pro
Prod
Tran

Sens
gene
impro
ampl
Tth D

Perfo
temp
cloni
ampl
Titan

Sens
tube
ampl
enzym
Titan

Analy
up to
inhib
reliab
Enz
Prod
Apta

Reco
& imm
One-
range
FastS

Therm
PCR
and o
setup
FastS

Therm
supe
Ideal
prior
FastS

Enzym
fourfo
multi
Conta

CR/RT-PC
oducts for O
duct Name
scriptor One-Ste
itive and specific o
-specific primers.
oved performance
ification, including
DNA Polymerase
orm reverse transc
peratures, allowing
ng, and analysis o
ification of RNA at
n One Tube RT-P
itive, quick and rep
system reverse tra
ifies cDNA with a
me blend from the
n One Tube RT-P
yze RNA from man
o 6 kb. Includes rea
itor, and PCR-grad
ble analysis of RNA
zymes for PC
duct Name
aTaq Fast DNA Po
ombinant Taq polym
mediate activation
-for-all < 30 min p
e, including GC-RI
Start Taq DNA Po
mostable modified
nucleotide mix. De
optimized buffer. Id
p and prior to initia
Start Taq DNA Po
mostable, chemica
rb results due to it
tool for hot start P
to initial denatura
Start High Fidelit
me blend with ben
old higher accurac
plex PCR, RT-PCR
ains ready-to-use
CR
ne-Step RT-
ep RT-PCR Kit
one-step endpoint
Combines high-yie
of a hot start syst
g GC-rich RNA.

ription and DNA a
its use in RT-PCR
f gene expression
t least 1 kb length
CR System
producible analysi
anscribes RNA into
thermal cycling re
e Expand High Fide
CR Kit
ny sources (animal
agents, control prim
de water to perform
A with high fidelity
CR
olymerase
merase with aptam
. Comes with optim
rotocol for superb
CH templates.
olymerase, dNTP
recombinant Taq
elivers superb resu
deal for hot start; e
al denaturation.
olymerase, 5 U/
ally modified recom
ts unique enzyme
PCR, since it stays
ation step.
ty PCR System, d
nefits of FastStart T
cy and ability to am
R, GC-RICH templa
PCR Nucleotide M
-PCR
RT-PCR analysis o
eld reverse transcr
em for high-fidelit
amplification at ele
R for detection, qua
at the RNA level.
.
s of RNA with high
o cDNA (AMV) up
eaction using an op
elity PCR System.
l, plant, human, vir
mers, nucleotides,
m RT-PCR. For qui
y.
mer mediated, reve
mized buffer syste
results in a broad
Pack
polymerase with r
ults with unique en
enzyme stays inact
l
mbinant Taq polym
design and optimi
inactive during PC
dNTPack
Taq DNA Polymera
mplify fragments u
te amplification, d
Mix.
of RNA using
ription and
ty, high-yield
evated
antification,
For RT-PCR
h fidelity. One-
to 6 kb and
ptimized
ral, bacterial)
RNase
ick, sensitive,
ersible hot start
m for fast PCR.
template
ready-to-use
nzyme design
tive during
merase. Delivers
zed buffer.
CR setup and
ase with
p to 5 kb. For
ifficult PCRs.

Cat. No.
04 655 877 001
04 655 885 001
11 480 022 001
11 855 476 001
11 939 823 001
Cat. No.
06 879 110 001
06 879 128 001
04 738 314 001
04 738 357 001
04 738 381 001
04 738 403 001
04 738 420 001
12 032 902 001
12 032 929 001
12 032 937 001
12 032 945 001
12 032 953 001
04 738 284 001
04 738 292 001

1 kit for up to 5
1 kit for
500 U (2 x 250
final volume
50 reactions
100 U for up to
each conta
500 U (2 x 250
final volume e
1,000 U (4 x 25
l final volume
2,500 U (10 x 2
50 l final volu
Ta
5,000 U (20 x 2
50 l final volu
Ta
100 U for up to
each conta
500 U (2 x 250
final volume e
2,500 U (10 x 2
50 l final volu
Ta
5,000 U (20 x 2
50 l final volu
Ta
125 U for up to
each conta
500 U (2 x 250
final volume ea
Pack Size
50 reactions of 50
control reactions
up to 150 reaction

U) for up to 200 re
each containing 2
Polymerase

100 reactions

, including 10 cont

Pack Size
100 units
1,000 units

50 reactions of 50
aining 2 U FastStar
Polymerase
U) for up to 250 re
ach containing 2 U
DNA Polymerase
50 U) for up to 500
each containing 2
DNA Polymerase
250 U) for up to 1,2
me each containin
aq DNA Polymeras
me each containin
aq DNA Polymeras
50 reactions of 50
aining 2 U FastStar
Polymerase
U) for up to 250 re
ach containing 2 U
DNA Polymerase
1,000 U (4 x 250 U
250 U) for up to 12
me each containin
aq DNA Polymeras
me each containin
aq DNA Polymeras
50 reactions of 50
ining 2.5 U FastSta
Polymerase
U) for up to 200 re
ach containing 2.5
DNA Polymerase

www.roche
l including 10
s of 50 l
eactions of 50 l
2.5 U Tth DNA
trol reactions
0 l final volume
rt Taq DNA
eactions of 50 l
U FastStart Taq
reactions of 50
U FastStart Taq
250 reactions of
ng 2 U FastStart
se
500 reactions of
ng 2 U FastStart
se
0 l final volume
rt Taq DNA
eactions of 50 l
U FastStart Taq
U)
250 reactions of
ng 2 U FastStart
se
500 reactions of
ng 2 U FastStart
se
0 l final volume
art Taq DNA
eactions of 50 l
U FastStart Taq
e-applied-science

Price in
326,30
717,70
322,00
576,50
530,90
Price in
43,00
286,00
119,40
486,10
837,20
1.991,10
3.349,20
119,40
486,10
837,20
1.991,10
3.349,20
152,20
497,50

4
63

e.com
4

4

4
PC
64

www.r

FastS

Enzym
Polym
fragm
RICH
GC-R

Blend
temp
Solut
Conta
GC-R

Blend
diffic
RICH
high
Pwo

High
Use f
yield
temp
Pwo

For h
gene
RICH
Perfo
Expa

Enzym
outst
PCR.
Conta
Expa

Enzym
outst
PCR,
ampl
Expa

For c
Use t
mix, a
PCR,
Expa

Amp
enzym
produ
ampl
Expa

Amp
buffe
and D
large
Taq D

Manu
docu
in ph
prime
.

CR/RT-PC
roche-applied-sc
Start High Fidelit
me blend that com
merase with fourfo
ments up to 5 kb. U
H template amplific
RICH PCR System
d of Taq Polymeras
plates up to 5 kb. E
tion deliver superb
ains ready-to-use
RICH PCR System
d of Taq DNA Poly
ult templates up to
H Resolution Solutio
yield and accuracy
SuperYield DNA
fidelity PCR up to
for site-directed m
and 18-fold highe
plates (GC RICH So
SuperYield DNA
high fidelity PCR up
expression. Highe
H Solution ensures
orm digests directly
and High Fidelity
P
me blend for robus
tanding yield, spec
Develop a new am
ains ready-to-use
and High Fidelity
P
me blend for robus
tanding yield, spec
primer extension,
ification assay or o
and Long Range d
consistent, accurate
the specially desig
and optimized blen
and large-fragme
and 20 kb
PLUS
PCR
lify genomic DNA
me blend amplify p
uce fragments 23
ification. Contains
and 20 kb
PLUS
PCR
lify genomic DNA
er and enzyme blen
DNA produce frag
e-fragment amplific
DNA Polymerase
ufactured under G
mentation require
harmaceutical and
er-extension react
CR
cience.com
ty PCR System
mbines the benefits
old higher accuracy
Use for multiplex P
cation, and difficult
m, dNTPack
se and a proofread
Enhanced processiv
b performance in P
nucleotide mix.
m
ymerase and a pro
o 5 kb. Enhanced p
on deliver superb
y.
A Polymerase, dN
3 kb. Contains rea
mutagenesis, clonin
er fidelity than Taq
olution).
A Polymerase
p to 3 kb, site-dire
er yield and 18-fold
high performance
y in PCR mix.
PLUS
PCR System,
st amplification of
cificity, sensitivity, a
mplification assay o
PCR Nucleotide M
PLUS
PCR System
st amplification of
carryover prevent
optimize an existin
dNTPack
e amplification of
ned buffer set, ult
nd of thermostable
ent amplification.
R System, dNTPa
fragments up to 3
products >20 kb. C
kb long. Use in PC
ready-to-use PCR
R System
fragments up to 3
nd to amplify prod
ments of 23 kb in
cation.
e, GMP Grade
GMP regulations. M
ments of research
biotechnology ind
ions (sequencing,
s of FastStart Taq D
y with the abilty to
PCR, sequencing, R
t PCRs.
ding polymerase a
vity and GC-RICH
PCR (high yield and
ofreading polymer
processivity and th
performance in PC
NTPack
ady-to-use PCR Nu
ng, and gene expre
. High performanc
cted mutagenesis,
d higher fidelity th
e using difficult tem
dNTPack
fragments up to 5
and accuracy. Use
or optimize an exis
Mix.
fragments up to 5
and accuracy. Use
tion, to develop a n
ng one.
long, 5 to 20 kb PC
rapure PCR-grade
e DNA polymerase
ack
35 kb. Optimized bu
Control primers an
CR, RT-PCR, large-
R Nucleotide Mix.
35 kb. Includes an o
ucts over 20 kb. C
length. Use in PCR
Meets high quality
h and development
dustry. Use in PCR,
labeling).
DNA
o amplify
RT-PCR, GC-
mplify difficult
Resolution
d accuracy).
rase amplify
he unique GC-
CR, providing
ucleotide Mix.
ession. Higher
ce with difficult
, cloning, and
an Taq. GC-
mplates.
5 kb with
in PCR/RT-
sting one.
5 kb with
in PCR/RT-
new
CR products.
e nucleotide
es for PCR, RT-
uffer and
nd DNA
-fragment
optimized
Control primers
R, RT-PCR, and
and
t laboratories
RT-PCR, and

03 553 361 001
03 553 400 001
04 743 784 001
12 140 306 001
04 743 750 001
04 340 850 001
04 340 868 001
04 743 725 001
04 743 733 001
03 300 226 001
03 300 234 001
04 829 034 001
04 829 042 001
04 829 069 001
04 743 814 001
11 811 002 001
03 734 927 001

2,500 U (10 x 2
50 l final v
FastSt
500 U (2 x 250
final volume ea
100 U for up to
each co
100 U for up to
each co
100 U for up to
each contain
500 U (2 x 250
final volum
Supe
100 U for up to
each contain
125 U for up
volume each
500 U (2 x 250
final volume ea
500 U (2 x 250
final volume ea
2,500 U (10 x 2
20 l final volu
175 U for up
volume each
700 U for up
volume each
3,500 U (5 x 70
20 l final volum
200 U for up to
each co
200 U for up to
each co
1,000 U for up
volume eac
volume each conta
tart Taq DNA Polym
U) for up to 200 re
ach containing 2.5
DNA Polymerase

50 reactions of 50
ntaining 2 U enzym

50 reactions of 50
ntaining 2 U enzym

40 reactions of 50
ning 2.5 U Pwo Sup
Polymerase

U) for up to 200 re
me each containing
erYield DNA Polym
40 reactions of 50
ning 2.5 U Pwo Sup
Polymerase

p to 125 reactions
h containing 1 U e
U) for up to 500 re
ach containing 1 U

U) for up to 500 re
ach containing 1 U
ume each containi
blend

p to 125 reactions
containing 1.4 U e
p to 500 reactions
containing 1.4 U e
00 U) for up to 2,5
me each containin
blend
40 reactions of 50
ntaining 5 U enzym

40 reactions of 50
ntaining 5 U enzym

p to 2,000 reaction
ch containing 0.5 U
Polymerase

000 reactions of
aining 2.5 U
merase
eactions of 50 l
U FastStart Taq
0 l final volume
me blend
0 l final volume
me blend
0 l final volume
perYield DNA
eactions of 50 l
g 2.5 U Pwo
merase
0 l final volume
perYield DNA
of 20 l final
enzyme blend
eactions of 20 l
U enzyme blend
eactions of 20 l
U enzyme blend
500 reactions of
ng 1 U enzyme
of 20 l final
enzyme blend
of 20 l final
enzyme blend
00 reactions of
ng 1.4 U enzyme
0 l final volume
me blend
0 l final volume
me blend
s of 20 l final
U Taq DNA

2.107,90
497,50
206,60
206,60
118,40
467,30
118,40
131,30
517,30
517,30
2.072,30
172,30
591,20
2.239,00
199,40
204,30
690,90

PC

Taq D

Taq D
prepa
PCR
react
Taq D

Taq D
produ
PCR,
label
Taq D

Taq D
rigoro
ready
prime
Taq D

Lowe
conve
conc
exten
Expa

Enzym
three
resul
ready
Expa

Expa
resul
to Ta
targe
Pwo

High
fold l
extre
chara

CR/RT-PC
DNA Polymerase
DNA Polymerase, d
aration (5 U/l) of
Nucleotide Mix. U
tions, such as sequ
DNA Polymerase
DNA Polymerase (
uced using rigorou
and other primer-
ing.
DNA Polymerase
DNA Polymerase, d
ously tested prepa
y-to-use PCR Nucl
er-extension react
DNA Polymerase
er concentration of
enient pipetting of
entration (5 U/l)
nsion reactions (se
and High Fidelity
me blend that deliv
efold greater fidelit
ts for genomic targ
y-to-use PCR nucl
and High Fidelity
nd High Fidelity Sy
ts with twofold hig
q. Choose this sys
ets up to 5 kb, in PC
DNA Polymeras
thermal stability p
ower than Taq DN
mely accurate DN
acterization of rare
CR
e, dNTPack
dNTPack combine
recombinant Taq
se for PCR, RT-PC
uencing and labeli
e, 5 U/l
(5 U/l) is ideal for
us purity and quali
-extension reaction
e (1 U/l), dNTPa
dNTPack combine
aration (1U/l) of r
leotide Mix. Use fo
ions (sequencing,
e, 1 U/l
f recombinant Taq
f small amounts of
Taq. Use in PCR, R
equencing, labeling
PCR System, dN
vers superior resu
ty compared to Taq
gets up to 5 kb, in
eotide mix.
PCR System
ystem is an enzym
gher yield and thre
stem for the most s
CR/RT-PCR.
e
polymerase with an
NA Polymerase). Id
A synthesis, such
e mutations.
es our standard, rig
with convenient, r
CR, and other prime
ng.
r routine PCR. The
ity standards for us
ns, such as sequen
ack
es our low concent
ecombinant Taq w
or PCR, RT-PCR, an
labeling).
allows more accu
f enzyme. Identical
RT-PCR, and other
g).
NTPack
lts with twofold hig
q. Use for the mos
PCR and RT-PCR
e blend delivering
eefold greater fidel
sensitive PCR resu
n extremely low er
deal for application
as high fidelity PC
gorously tested
ready-to-use
er-extension
enzyme is
se in PCR, RT-
ncing and
tration,
with convenient,
nd other
urate and
l to our higher
r primer-
gher yield and
st sensitive PCR
. Contains
superior
lity compared
lts for genomic
ror rate (18-
ns that require
CR and

04 728 858 001
04 728 866 001
04 728 874 001
04 728 882 001
04 728 904 001
11 146 165 001
11 146 173 001
11 418 432 001
11 435 094 001
11 596 594 001
04 738 225 001
04 738 241 001
11 647 679 001
11 647 687 001
04 738 250 001
04 738 268 001
04 738 276 001
11 732 641 001
11 732 650 001
11 759 078 001
11 644 947 001
11 644 955 001

5,000 U (20 x 25
20 l final vo
100 U for up
volume eac
500 U (2 x 250
l final volume
1,000 U (4 x 25
20 l final vo
2,500 U (10 x 2
20 l final vo
100 U for up
volume eac
500 U for up
volume eac
1,000 U (4 x 25
20 l final vo
5,000 U (20 x 25
20 l final vo
2,500 U (10 x 2
50 l final vo
250 U for up
volume eac
1,000 U (4 x 25
20 l final vo
250 U for up
volume eac
1,000 U (4 x 25
20 l final vo
100 U for up to
each con
500 U (2 x 250
final volume ea
2,500 U (10 x 2
50 l final volum
100 U for up to
each con
500 U (2 x 250
final volume ea
2,500 U (10 x 2
50 l final volum
100 U for up
volume eac
500 U (2 x 250
l final volume
50 U) for up to 10,
lume each contain
DNA Polymerase
p to 200 reactions
ch containing 0.5 U
Polymerase
U) for up to 1,000
e each containing
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase
lume each contain
DNA Polymerase
p to 200 reactions
ch containing 0.5 U
Polymerase
to 1,000 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase
50 U) for up to 10,
lume each contain
DNA Polymerase
lume each contain
DNA Polymerase
p to 500 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase

p to 500 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase

40 reactions of 50
ntaining 2.6 U enzy
U) for up to 200 re
ch containing 2.6
me each containin
blend
40 reactions of 50
ntaining 2.6 U enzy
U) for up to 200 re
ch containing 2.6
me each containin
blend
p to 40 reactions o
ch containing 2.5 U
Polymerase
U) for up to 200 r
e each containing 2
Polymerase

www.roche
000 reactions of
ning 0.5 U Taq
of 20 l final
U Taq DNA
reactions of 20
0.5 U Taq DNA
00 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
of 20 l final
U Taq DNA
s of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq
of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq
0 l final volume
yme blend
eactions of 50 l
U enzyme blend
000 reactions of
ng 2.6 U enzyme
0 l final volume
yme blend
eactions of 50 l
U enzyme blend
000 reactions of
ng 2.6 U enzyme
of 100 l final
U Pwo DNA
reactions of 100
2.5 U Pwo DNA
e-applied-science

2.703,80
89,00
356,00
640,50
1.480,10
89,00
356,00
640,50
2.703,80
1.480,10
202,60
640,50
202,60
640,50
123,10
492,10
1.969,60
123,10
492,10
1.969,60
136,60
547,10

4
65

e.com
4

4

4
PC
66

www.r

Ma
Prod
Apta

Read
polym
activa
using
FastS

Read
cDNA
targe
throu
High

Choo
Expa
optim
highe
PCR

Conta
cond
sensi
supp
PCR

For ru
of DN
buffe
conta
PCR

2x co
up to
Conta
pipet
Pwo

Read
dNTP
Taq.
cloni
Opt
Prod
MgC

MgC
MgC
for a
any P
PCR

For o
chain
a 25
mM T
PCR

For a
react
mM T
the M
PCR

Conv
vary
incre
optim
Strip

Strip
therm
cDNA
Caps

CR/RT-PC
roche-applied-sc
aster Mixes a
duct Name
aTaq Fast PCR M
dy-to-use master b
merase with aptam
ation. Use one-for-
g GC-RICH templat
Start PCR Maste
dy-to-use 2x maste
A targets up to 2 k
ets, with high spec
ughput, and direct
h Fidelity PCR Ma
ose this convenient
nd High Fidelity PC
mized reaction buff
Core Kit
ains everything for
itions for basic PC
itivity/specificity us
lied Mg-free buffe
Core Kit
PLUS

unning PCR using
NA contamination
er without Mg2+, a
aminating DNA.
Master
oncentrated, ready
o 2 kb. Use in place
ains everything ex
tting steps.
Master
dy-to-use 2x conce
Ps, and buffer. Hig
Use for high fidelit
ng, and gene expr
timization o
duct Name
Cl
2
Stock Solutio
l
2
Stock Solution (
l
2
, when optimizin
particular templat
PCR type: hot start
Buffer Set
optimizing the mag
n reaction using Ta
mM magnesium s
Tris-HCl, 500 mM
Buffer Without M
amplification of spe
tion. The buffer is a
Tris-HCl and 500 m
MgCl
2
Stock Soluti
Optimization Kit
venient, reliable rea
buffer pH, and ma
ease yield and spec
mize conditions in m
p PCR Tubes and
PCR Tubes and C
mal cyclers; design
A synthesis, and se
s are DNase- and R
CR
cience.com
and Kits for
aster
based on thermosta
mer mediated, reve
-all < 30 min proto
tes.
er
er mix for the ampl
kb long, or longer f
ificity, sensitivity, a
colony PCRs.
aster
t, 2x-concentrated
CR System with PC
fer. Delivers two tim
q DNA Polymerase
r PCR except temp
CRs using Taq. Opt
sing non-standard
er.
non-standard buf
from prior amplific
and Uracil-DNA Gl
-to-use mix for rou
e of Taq or the PC
cept template DNA
entrated mix of Pw
her yield and 18-fo
ty PCR up to 3 kb,
ression.
of PCR
n
(25 mM) for supple
ng the magnesium
te or target. Use w
t, high fidelity, long
gnesium chloride c
aq DNA Polymeras
solution and a PCR
KCl; pH 8.3).
MgCl
2
, 10x conc
ecific DNA fragme
a tenfold concentr
mM KCl, and shou
ion.
t
ady-to-use solutio
agnesium, DMSO, g
cificity. Use with Fa
multiplex PCR.
Caps
aps, either 8 or 12
ned for rapid, optim
equencing and cyc
RNase-free.
r PCR
able recombinant T
rsible hot start & im
ocol for superb res
lification of genom
fragments on plasm
and yield. Use in ho
d, ready-to-use mix
CR-Grade dNTPs, M
mes the yield and
e alone.
plate and primers.
timize assays for g
Mg-concentration
ffer conditions with
cations. Includes M
lycosylase for deg
utine genomic and
R Core Kit for rout
A and primers. Req
wo SuperYield DNA
old higher fidelity c
site-directed muta
ementing PCR buf
concentration of a
ith other PCR buff
g PCR.
concentration in th
se. This PCR Buffe
R buffer (10x conce
.
ents using the poly
rated solution cont
ld be used in com
ns to optimize PCR
glycerol concentra
astStart High Fidel
tubes per strip, ar
mal heat transfer in
cle sequencing. PC
Taq
mmediate
sults even
mic DNA and
mid DNA
ot start, high-
x, combining
MgCl
2
, and an
three times
Determine
reater
ns using the
h samples free
MgCl
2
solution,
grading
d cDNA targets
tine PCRs.
quires only 2
A Polymerase,
compared to
agenesis,
ffers without
a standard PCR
fers to optimize
e polymerase
r Set contains
entrate; 100
ymerase chain
taining 100
bination with
R setup. Easily
ations to
ity System to
re used in
n PCR, RT-PCR,
CR Tubes and

Cat. No.
06 879 080 001
06 879 101 001
04 710 436 001
04 710 444 001
04 710 452 001
12 140 314 001
11 578 553 001
11 585 541 001
11 636 103 001
03 789 403 001
Cat. No.
11 699 113 001
11 699 121 001
11 699 105 001
11 636 138 001
11 667 009 001

2 x 1.25 ml for
8 x 1.25 ml for u
10 x 5 ml for u
1 kit for up to 5
1 kit for up to 1
volume eac
1 kit for up to 5
volume, ea
1 kit for up to
reaction volume
2.5 ml (10 x 25
l final reacti
PWO Su
2 x 2 ml
1 kit for up to 1
optimization
125
Pack Size
100 reactions
1,000 reactions

up to 250 reaction
reaction volume
up to 1,000 reactio
reaction volume
up to 5,000 reaction
reaction volume
00 reactions of 20
volume

00 reactions of 50
ch containing 2.5 U
Polymerase

50 reactions of 50
ch containing 2.5
Polymerase

o 200 PCR reaction
e each containing
Polymerase

0 l) for up to 100
on volume each co
uperYield DNA Pol

Pack Size
3 x 1 ml

(2 x 1 ml of each

3 x 1 ml

100 one-step or up
n assays of 100 l f
volume

5 strips (8 tubes/st

ns of 20 l final
ons of 20 l final
ns of 20 l final
l final reaction
l final reaction
U Taq DNA
l final reaction
U Taq DNA
s of 50 l final
2.5 U Taq DNA-
reactions of 50
ontainig 2.5 U
lymerase
solution)
p to 50 two-step
final reaction
trip)

Price in
56,00
475,00
178,40
624,10
2.675,00
575,10
292,60
214,40
271,10
295,60
Price in
40,30
49,70
40,30
256,40
187,60

PC

T4 G

Singl
stimu
DNA
and t
Urac

Cleav
incre
labele
carry
Urac

Prima
heat-
react
deoxy
Wate

Spec
endp
highe
ampl
Prim
Prod
Prim

Rand
ensu
struc
Prim

This
a cDN
synth
qP
Lig
Ligh
Prod
Light

For a
Achie
using
use a
quan
resol
Ligh
Prod
Light

Use t
to ea
endp
Inclu

CR/RT-PC
Gene 32 Protein
e-strand-specific
ulate in vitro DNA
or RNA. It is also
to help RE digests
cil-DNA Glycosyla
ves DNA where a d
ease efficiency of s
ed oligonucleotide
yover contaminatio
cil-DNA Glycosyla
arily used to preve
-labile, is easily ina
tion by heating to +
yuridylate (dUTP)
er, PCR Grade
ially tested and qu
point and real-time
est quality water is
ification systems c
mer for PCR
duct Name
mer "random"
dom hexamer prim
ring reverse transc
cture. It is a primer
mer for cDNA Syn
primer will bind th
NA copy, for use in
hesis of first-strand
PCR System
htCycler
9
htCycler
96
duct Name
tCycler
96 Instr
accurate, consisten
eve the rigorous pe
g intuitive large tou
accessible data an
tification, endpoin
ution melting and
htCycler
96
duct Name
tCycler
8-Tube
these optimized re
sily set up and per
point genotyping, a
des both tube strip
CR
DNA-binding prot
synthesis, and stab
used in site-specif
go to completion.
ase
deoxyuridylate res
site-directed mutag
e probes, and, with
on.
ase, heat-labile
ent PCR product ca
activated at the be
+95C. DNA is cle
residue has incorp
ualified for use in a
e PCR assays, sequ
s required. All Ligh
contain this PCR g
R and RT-PC
ers bind througho
cription of all RNA
for cDNA synthes
thesis
e 3'-poly A tail of
n RT-PCR, generat
d cDNA.
ms and As
96 System
System - Ins
rument
nt real-time PCR re
erformance standa
uchscreen-based s
alysis. Application
nt and melting curv
qualitative detecti
System - Dis
Strips (white)
eaction vessels for
rform gene detecti
and high-resolution
ps and cap strips.
tein used to optimi
bilize single-strand
fic mutagenesis ex
idue has incorpora
genesis, to produc
h dUTP, to eliminat
arryover contamina
ginning of the am
aved at any site w
porated.
all PCR or RT-PCR.
uencing, and when
htCycler
kits and
rade water.
CR Reaction
out the entire lengt
A sequences due to
sis.
an mRNA to initiat
tion of cDNA libra
ssociated
strument
esults in your resea
ard of the LightCyc
software for power
s include absolute
ve-based genotypi
on.
sposables
the LightCycler
9
ion, gene quantific
n melting analysis
ize PCR,
ded regions of
xperiments,
ated. Used to
e highly
te PCR product
ation. UNG,
plification
where a
. Use with
never the
other Roche
s
th of RNA,
o their random
te synthesis of
ries, and
Products
arch lab.
cler
Systems,
rful easy-to-
e and relative
ng, high
96 Instrument
cation,
assays.

10 972 983 001
10 972 991 001
11 444 646 001
11 775 367 001
11 775 375 001
03 315 843 001
03 315 932 001
03 315 959 001
Cat. No.
11 034 731 001
10 814 270 001
Cat. No.
05 815 916 001
Cat. No.
06 612 601 001

100
25
25
2 mg (Random
units, 1 mo
40
1 instrument (
for the use of
120 x 8-tube-s
(Optimized rea
96 and the L
LightCycle
combination w
100 g
500 g

100 U

100 U
500 U

0 ml (4 vials of 25
5 ml (25 vials of 1 m
5 ml (1 vial of 25 m
Pack Size
m pd(N)
6
Potassiu
ol for up to 400 rea
primers)

g (1 A
260
unit, 8 n

Pack Size
(96-well realtime P
96-well plates and

Pack Size
strips white and 8-t
action device for th
LightCycler
480. N
er
480 it can only

with the LightCycle
Adapter Plate)

www.roche
ml)
ml)
ml)
um Salt, 50 A
260

ctions 5 ng
mol)
PCR instrument
d 8-tube strips)
tube caps clear
he LightCycler

Note: For the
y be used in
er
Tube Strip
e-applied-science

189,20
755,80
148,40
143,80
534,50
310,70
155,30
123,90
Price in
258,50
75,30
Price in
inquire
Price in
inquire

4
67

e.com
4

4

4
PC
68

www.r

Lig
Ligh
Prod
Light

Fast,
gene
footp
for ev
Light

Comp
Instru
each
sensi
quan
Light

Comp
Instru
each
sensi
Ligh
Prod
Light

Use f
(gene
resol
strips
Lig
Ligh
Prod
Light

Obta
high-
an ex
inter-
Ligh
Prod
Light

Impro
1536
LIMS
detec
Ligh
Prod
Light

Incre
this h
the L
costs
Lig
Ligh
Prod
Light

Achie
throu
work
and t
Light

Silver
480 I
by th

CR/RT-PC
roche-applied-sc
htCycler
N
htCycler

Na
duct Name
tCycler
Nano In
32-sample real-tim
tic variation analys
print, and weight, a
veryday use.
tCycler
Nano D
plete system, inclu
ument with real-tim
and 480 tube stri
itive, specific hot s
tification.
tCycler
Nano D
plete system, inclu
ument with real-tim
and 480 tube stri
htCycler
Na
duct Name
tCycler
8-Tube
for SYBR Green I, R
e detection, gene q
ution melting anal
s and cap strips ar
htCycler
1
htCycler
153
duct Name
tCycler
1536 In
in 1,536 data point
-throughput therm
xceptional range o
-assay errors.
htCycler
153
duct Name
tCycler
1536 So
ove PCR efficiency
Instrument. Ideal
S data managemen
ction of pipetting e
htCycler
153
duct Name
tCycler
1536 M
ease PCR throughp
high-performance
LightCycler
1536
s and minimizes as
htCycler

4
htCycler
48
duct Name
tCycler
480 Ins
eve fast, sensitive,
ughput platform. A
kflows, this cutting-
temperature homo
tCycler
480 Blo
r block cycler acce
nstrument. The blo
e instrument. Inclu
CR
cience.com
Nano System
no System -
nstrument
me PCR instrumen
sis in mono- and d
and easy reaction s
DNA Green Starte
uding LightCycler

me PCR Master rea
ips & caps, using S
start PCR assays fo
DNA Probes Start
uding LightCycler

me PCR Master rea
ips & caps, using U
start PCR for gene
ano System -
Strips (clear)
ResoLight dye, and
quantification, end
ysis) on the LightC
re provided togethe
536 System
36 System -
nstrument
ts in a single PCR
mal block cycler fea
f assay types while
36 System - S
oftware, Version
y using this dedica
for automated hig
nt. Use with RealTi
errors.
36 System -
Multiwell Plate
put fourfold compa
1,536-well reactio
Instrument. Precis
ssay errors.
80 System
0 System - In
strument II
and consistent PC
Adaptable for 96- o
-edge instrument o
ogeneity.
ock Kit 96 Silver
essory for 96-well
ock cycler is autom
udes block lid and
m
Instrument
nt for gene express
dual-color. Minima
setup and software
er Pack
Nano Real-Time
agents for 4,000 re
SYBR Green I dete
or gene detection a
ter Pack
Nano Real-Time
agents for 4,000 re
UPL or hydrolysis p
expression quanti
Disposables
d hydrolysis probe
dpoint genotyping,
Cycler
Nano Instr
er.
m
Instrument
run of less than 50
atures proven optic
e reducing sample
Software
1.1
ated software for th
h-throughput wor
me ready reagents
Disposables
ared to a 384-well
n plate specifically
sion miniaturization
nstrument
CR results using a
or 348-well plates a
offers exceptional
plates using the Li
matically detected
storage box.
sion and
al noise,
e make it ideal
PCR
eactions - 20 l
ection. Ideal for
and
PCR
eactions - 20 l
probes. For
fication.
e-based assays
high
rument. Tube
0 minutes. This
cs facilitating
e volumes and
he LightCycler

rkflows and
s for easy
plate using
y designed for
n reduces
versatile high-
and automated
reproducibility
ightCycler

and calibrated

Cat. No.
06 407 773 001
06 444 199 001
06 444 202 001
Cat. No.
06 327 672 001
Cat. No.
05 334 276 001
Cat. No.
06 569 382 001
Cat. No.
05 358 639 001
Cat. No.
05 015 243 001
05 015 278 001
05 015 219 001

1 inst
1 instrument an
20 l each an
1 instrument an
20 l each an
120 clea
1
1 instr
1 instr
1 block kit (bl
Pack Size
rument plus acces

nd 8 kits for up to
d 480 strips/caps f
reactions

nd 8 kits for up to
d 480 strips/caps f
reactions

Pack Size
r tube strips and c
(10 unit pack)

Pack Size
1 instrument

Pack Size
1 software packag

Pack Size
10 x 10 plates

Pack Size
rument (384-well v
rument (96-well ve

ock kit for 96-well
plates)

ssories
4,000 reactions,
for up to 3,840
4,000 reactions,
for up to 3,840
cap strips
e
version)
ersion)
PCR multiwell

Price in
inquire
inquire
inquire
Price in
inquire
Price in
inquire
Price in
inquire
Price in
inquire
Price in
inquire
inquire
inquire

PC

Light

Silver
Instru
the in
Ligh
Prod
Light

Analy
this a
PCR
meth
Light

Use t
intern
easy-
PCR
Light

Comp
quan
PCR
samp
Ligh
Prod
Light

This
melti
The w
Light

This
melti
Instru
track
Light

This
SYBR
Instru
labele
Light

Clear
based
on Li
recom
Light

Preve
assay
clear)
evapo
Ligh
Prod
Light

Track
Instru
scans
direc
Light

The L
Light
user
Light

The L
480 I
differ
inten

CR/RT-PC
tCycler
480 Blo
r block cycler for 3
ument. The block c
nstrument. Include
htCycler
48
duct Name
tCycler
480 Ge
yze melting curve
accessory software
fragments for gen
hylation.
tCycler
480 LIM
this module to inte
nal Laboratory Info
-to-install software
workflow efficienc
tCycler
480 Sof
prehensive suite o
tification and geno
Systems. Provides
ple editing, templat
htCycler
48
duct Name
tCycler
480 Mu
high performance
ng curve analysis
white, polypropylen
tCycler
480 Mu
high performance
ng curve analysis
uments.The white,
king.
tCycler
480 Mu
high performance
R Green I and hydr
uments. The clear,
ed for easy trackin
tCycler
480 Mu
r plates for high pe
d assays using the
ghtCycler
480 In
mmended for use w
tCycler
480 Sea
ent evaporation an
ys in LightCycler

) using the LightC
oration during cyc
htCycler
48
duct Name
tCycler
480 Bar
k and manage sam
ument using this h
s data from the ba
ctly into the LightCy
tCycler
480 Ven
LightCycler
480 V
tCycler
480 Instru
within a few minu
tCycler
480 Xen
LightCycler
480 X
nstruments. It is ea
rence between a X
sity, which differs
CR
ock Kit 384 Silver
384-well plates, for
cycler is automatic
es block lid and sto
0 System - S
ne Scanning Sof
data from the Ligh
e module for the L
etic variations suc
MS Interface Mod
egrate the LightCyc
ormation Managem
e package for impr
cy.
ftware, Version 1
f tools for setup, ru
otyping assays on
all functionalities
tes, macros).
0 System - D
ultiwell Plate 96 w
96-well reaction p
applications using
ne plate is barcode
ultiwell Plate 384
384-well reaction
applications using
polypropylene pla
ultiwell Plate 96,
96-well reaction p
rolysis probe-base
half-skirted, polyp
ng.
ultiwell Plate 384
erformance SYBR
e LightCycler
480
struments and 480
with FRET HybPro
aling Foil
nd contamination w
480 Multiwell Plat
Cycler
480 Instrum
cling or storage.
0 System- Ad
r-Code Scanner
mple information fo
handheld barcode
arcodes on LightCy
ycler
Software.
ntilation Dust Filt
Ventilation Dust Fi
ument. The dust fil
tes.
non Lamp
Xenon Lamp is a re
asily replaced with
Xenon and a Halog
at least by factor 1
r
r use with the Ligh
cally detected and
orage box.
oftware
ftware
htCycler
480 Instr
ightCycler
480 So
ch as SNPs, mutatio
dule
cler
480 System
ment System (LIMS
roved data manage
1.5
un, and analysis of
LightCycler
480
(user-friendly prog
Disposables
white
plate is specifically
g LightCycler
480
e-labeled for easy
4, white
plate is specificall
g LightCycler
480
ate is barcode-labe
clear
ed assays using Lig
propylene plate is
4, clear
Green I and hydro
0 Instrument, 384-w
0 Software, Version
be probes or HRM
when running real-
tes (96 or 384 well
ment. Strong adhes
dditional Prod
or the LightCycler
scanner. This optio

ycler
480 Multiwe
ter
lter is a replaceme
lter can be easily r
eplacement part fo
hin a few minutes.
gen lamp is the lum
10.
htCycler
480
calibrated by
rument using
oftware. Scan
ons, and
into your
S) using this
ement and
f real-time PCR
Real-Time
gramming,
y designed for
0 Instruments.
tracking.
ly designed for
0
eled for easy
y designed for
ghtCycler
480
barcode-
olysis probes-
well. Use only
n 1.5. Not
M.
-time PCR
ls, white or
sion prevents
ducts
480
onal accessory
ell Plates
ent part for the
replaced by the
or LightCycler

The main
minous

05 015 197 001
Cat. No.
05 103 908 001
05 066 310 001
04 994 884 001
Cat. No.
04 729 692 001
04 729 749 001
05 102 413 001
05 102 430 001
04 729 757 001
Cat. No.
04 710 606 001
04 686 128 001
04 686 136 001

1 block kit (blo
1
1
1
5 x 10
5 x 10
5 x 10
5 x 10
ock kit for 384-wel
plates)

Pack Size
1 software packag

1 software packag

1 software packag

Pack Size
plates (with sealin

plates (with sealin

plates (with sealin

plates (with sealin

50 foils

Pack Size
1 scanner

4 filters

1 lamp

www.roche
l PCR multiwell
e
e
e
ng foils)
ng foils)
ng foils)
ng foils)
e-applied-science

inquire
Price in
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire

4
69

e.com
4

4

4
PC
70

www.r

Light

The a
Light
to 12
times
the L
96-w
Instru
Lig
Ligh
Prod
Light

Perfo
Capil
wide
expe
Ligh
Prod
Light

Versi
Instru
modu
Light

Fully
and S
analy
mono
Ligh
Prod
Light

Use w
20 l
Light
maxim
Light

For L
highl
with
requi
medi
Ligh
Prod
LC C

Effici
comp
Comp
buck
LC C

This
versio
This s
LC C

Desig
adap
carou
rotor
Light

Perfo
Light
acces

CR/RT-PC
roche-applied-sc
tCycler
8-Tube
adapter plate is for
tCycler 8-Tube Stri
LightCycler
8-Tu
s. The LightCycler
LightCycler
480 In
well version. The pla
uments.
htCycler
C
htCycler
Ca
duct Name
tCycler
2.0 Inst
orm fast and sensit
llary-based techno
selection of fluore
rimental design an
htCycler
Ca
duct Name
tCycler
Softwar
on 4.1 is the up-to
uments. Allows use
ules for performing
tCycler
Probe D
automated design
SimpleProbe probe
ysis, or mutation de
oplex or multiplex
htCycler
Ca
duct Name
tCycler
Capillar
with LightCycler

and are compatib
tCycler
2.0 Samp
mizes fluorescent
tCycler
Capillar
LightCycler
2.0 In
y sensitive bacteri
LightCycler
2.0 S
irements of the Eu
cal devices.
htCycler
Ca
duct Name
Carousel Centrifu
ently centrifuge PC
pact benchtop dev
patible with LightC
ket, sold separately
Carousel Centrifu
bucket enables co
ons when using th
silver rotor bucket
Carousel Centrifu
gned for use with e
ter accessories en
usels used with Lig
and two rotor buc
tCycler
2.0 Cap
orm easy unloading
tCycler
Sample C
ssory.
CR
cience.com
Strip Adapter Pl
r use with the Ligh
ips (white or clear)
ube Strips in one r
8-Tube Strip Ada

nstrument I and Li
ate is not suitable
Carousel-Ba
arousel-Based
trument
tive real-time PCR
ology provides fast
escence formats m
nd analysis.
arousel-Based
re 4.1
o-date LightCycler
e with Windows X
g and analyzing re
Design Software
n of primers or pro
es. For easy qualita
etection using Ligh
assays with up to
arousel-Based
ries (20 l)
Carousel-Based In
ble with the LightC
le Carousel (20 l)
signal transmissio
ries (100 l) MG
struments if using
al, fungal nucleic a
Sample Carousel (1
ropean Directive 9
arousel-Based
uge 2.0
CR samples in Ligh
vice. For use with t
Cycler
1.5 and old

y).
uge 2.0 Bucket 2.
ompatibility with Li
he LC Carousel Cen
t replaces the buck
uge 2.0 Rotor Set
earlier model LC C
nable compatibility
ghtCycler
Carous
ckets.
pillary Releaser
g of the LightCycle
Carousel in one sim
late
htCycler
480 Syst
). The adapter plat
run and is re-usab
apter Plate can on
ghtCycler
480 In
for the use in Ligh
ased System
d System - In
on this proven ins
t, reproducible resu
maximizes flexibility
d System - So
Software for Lig

P. Integrates all so
eal-time PCR exper
2.0
obes, such as HybP
ative and gene exp
htCycler
Instrum
four different targe
d System - D
nstruments. Capilla
Cycler
Carousel a
). High quality boro
on.
RADE
g large reaction vol
acid detection. Co
100 l). This produ
98/79/EC for in vitr
d System - Ad
htCycler
carouse
he LightCycler
2
der versions (requ
.1
ghtCycler
1.5 and
ntrifuge to prepare
ket included with t
t
Carousel Centrifug
y with all types of s
sel-Based Instrume
er
Capillaries from
mple step, using th
tem and the
te can hold up
ble multiple
ly be used in
strument II ,
htCycler
96
m
nstrument
strument.
ults, and a
y in
oftware
ghtCycler
2.0
oftware
riments.
Probe probes
pression
ents in
ets at once.
isposables
aries hold 10 to
nd
osilicate glass
lumes. For
mpatible only
uct fulfills the
ro diagnostic
dditional Pro
els using this
.0 instrument.
ires different
d older
e PCR samples.
the centrifuge.
es. These
sample
ents. Includes
m the
is convenient

06 612 598 001
Cat. No.
03 531 414 001
Cat. No.
04 898 915 001
04 342 054 001
Cat. No.
04 929 292 001
03 612 066 001
ducts
Cat. No.
03 709 507 001
03 709 582 001
03 724 689 001
03 724 697 001
03 603 920 001

1 instrument
station (de
1
1
1 pack (con
cap
1 pack (con
cap
1 centrifuge p
1 centrifuge p
1 rotor bucke
1 rotor plus
LC
1 piece

Pack Size
(plus related prod
esktop or noteboo

Pack Size
1 software packag

1 software packag

Pack Size
ntaining 5 boxes, e
pillaries and stopp

ntaining 8 boxes, e
pillaries and stopp

Pack Size
plus rotor and buc
plus rotor and buc

et for LC Carousel

2 buckets for the e
C Carousel Centrifu

1 capillary release

ducts and data
k version))
e
e
each with 96
ers)
each with 96
ers)
cket (115 Volt)
cket (230 Volt)
Centrifuge 2.0
earlier model
uge
er

inquire
Price in
inquire
Price in
inquire
inquire
Price in
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire

PC

Light

Perfo
l) fo
preci
code
Light

Perfo
(100
ensu
uniqu
Light

Simp
remo
onto
all Lig
Light

Simp
Capil
stand
8-we
Light

The L
achie
32 po
Light

For re
(pack
versio
Capil
qP
Rea
qPC
HRM
Prod
Light

Save
Light
Reso
or PC
Hyb
Prod
Light

Easy-
Base
RNAs
minim
Light

Read
using
in PC
PCR
Light

Easy-
Light
detec
MgC

CR/RT-PC
tCycler
2.0 Sam
orm up to 32 simult
or the LightCycler
se positioning and
for easy identifica
tCycler
2.0 Sam
orm up to 32 simult
l) for the LightCy
re precise position
ue bar code for ea
tCycler
Capping
plifies the process o
ove a cap from the
a capillary holding
ghtCycler
Capilla
tCycler
Centrifu
plify cooling, filling,
llaries. Adapter eas
dard centrifuges. C
ell multichannel pip
tCycler
Sample
LightCycler
Samp
evable with the Lig
ositions to hold Lig
tCycler
Sample
eplacement of wor
k size of 2). It is co
ons. Developed to
llaries in the LightC
PCR/qRT-P
agents for L
CR Master Mi
M
duct Name
tCycler
480 Hig
time using an opt
tCycler
480 Syste
Light, a novel dye
CR.
ridization Prob
duct Name
tCycler
RNA M
-to-use mix for one
d Instruments and
s. High temperatur
mizes mispriming d
tCycler
Multiple
dy-to-use 5x mix fo
g LightCycler
Cap
CR to genotype SN
using a multiplex a
tCycler
DNA M
-to-use mix for sen
tCycler
Carousel-
ction format. For q
l
2
is supplied for s
CR
mple Carousel (2
taneous PCR react
2.0 Instrument. H
d reproducible resu
ation.
mple Carousel (1
taneous PCR react
ycler
2.0 Instrume
ning and reproduc
sy identification.
g Tool
of closing LightCyc
LightCycler
Cap
g the reaction mixt
aries.
uge Adapters
, and centrifugatio
sily fits holes in rot
Cooling block hold
pettes.
e Carousel
ple Carousel is us
ghtCycler
1.5 Inst
ghtCycler
Capilla
e Carousel O-Rin
rn out LightCycler
ompatible with all L

ensure proper pos
Cycler
Sample Ca
PCR Reage
LightCycler

ixes
gh Resolution Me
timized ready-to-u
em. This highly stab
that does not inte
bes
aster HybProbe
e-step RT-PCR usi
d HybProbe probes
re overcomes seco
during the RT step
ex DNA Master H
or optimal perform
pillaries and the Li
Ps, analyze mutati
approach.
aster HybProbe
nsitive, robust PCR
-Based Systems, u
uantitative PCR, an
specific application
0 l)
tions in this sampl
Heat-resistant mate
ults. Labeled with
00 l)
tions in this sampl
ent. Heat-resistant
ible results. Labele
cler
Capillaries. U
pillary box and plac
ture. The tool is co
n of all types of Li
tors for Eppendorf
s 32 adapters in 4
ed to increase the
trument and older
ries (20 l).
g
Sample Carouse
LightCycler
Samp
sitioning of the Lig
arousels.
ents
Systems
elting Master
se PCR master mix
ble reaction mix co
erfere with amplific
ing LightCycler
C
s for detection. Ide
ondary structures,
p.
HybProbe
ance in multiplex r
ightCycler
2.0 Ins
ons, and perform t
R in LightCycler
C
using the HybProbe
nd SNP and mutat
ns.
le carousel (20
erials ensure
a unique bar
le carousel
t materials
ed with a
Use the tool to
ce it directly
ompatible with
ghtCycler

f tubes in
rows; use with
e throughput
versions. It has
el O-Rings
ple Carousel
ghtCycler

x for the
ontains
cation enzymes
Carousel-
eal for difficult
and hot start
real-time PCR
strument. Use
two-step RT-
Capillaries on
e probes
tion detection.

03 603 962 001
03 603 954 001
03 357 317 001
11 909 312 001
11 909 282 001
03 603 989 001
Cat. No.
04 909 631 001
Cat. No.
03 018 954 001
04 340 019 001
12 015 102 001
12 158 825 001

1 set (32 ada
5 x 1 ml (for
1 kit for up to 9
1 kit for up to 9
1 kit for up to 9
1 kit for up to 4
1 sample carouse

1 sample carouse

1 capping tool

apters in a dedicat
cooling block)

1 sample carouse

2 O-Rings

Pack Size
up to 500 reaction

Pack Size
96 reactions of 20
volume

96 reactions of 20
volume

96 reactions of 20
volume
80 reactions of 20
volume

www.roche
l
l
ted aluminum
l
ns, 20 l each)
l final reaction
l final reaction
l final reaction
l final reaction
e-applied-science

inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
Price in
inquire
inquire
inquire
inquire

4
71

e.com
4

4

4
PC
72

www.r

Light

Easy-
Capil
HybP
expre
Light

Easy-
Light
detec
PCR.
Light

Easy-
Light
detec
risk o
Light

Perfo
480 I
The s
probe
Hyd
Prod
FastS

Read
the L
gene
prime
Light

Read
PCR
Probe
are n
Light

Note
1536
1536
Ideal
endp
preve
Light

Save
PCR
FastS
forma
Light

Easy-
cyclin
Unive
Preve
Glyco
Light

Spec
mast
Instru
Light

Spec
mast
Instru
Light

Spec
and r
Instru
Light

Spec
and r
Instru
CR/RT-PC
roche-applied-sc
tCycler
FastSta
-to-use hot start re
llaries on LightCyc
Probe probes for de
ession analysis. Ad
tCycler
FastSta
-to-use hot start m
tCycler
Carousel-
ction. For qPCR, SN
MgCl
2
is supplied
tCycler
RNA Am
-to-use mix for one
tCycler
Carousel-
ction. Provides rep
of contamination. M
tCycler
480 Ge
orm easy real-time
nstrument using th
single-component
es.
rolysis Probes
duct Name
Start Essential D
dy-to-use reaction
LightCycler
Nano
quantification. Se
ers, and hydrolysis
tCycler
TaqMan
dy-to-use hot start
using LightCycler
eLibrary and hydro

not compatible with
tCycler 1536 D
: RealTime ready D
DNA Probes Mas
Instruments with
for fast hot start a
point genotyping. U
ent carryover conta
tCycler
480 Pro
time in gene quan
master mix for the
Start Taq DNA Poly
ation of nonspecif
tCycler
480 RN
-to-use hot start m
ng conditions of pl
ersal ProbeLibrary
ent PCR product ca
osylase.
tCycler 96 DNA
ial bundle combip
er for hydrolysis p
ument.
tCycler
96 DNA
ial bundle combip
er for hydrolysis p
ument.
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
CR
cience.com
art DNA MasterP
eaction mix for hig
cler
Carousel-Bas
etection. Use also
ddition of MgCl
2
is
art DNA Master H
mix for sensitive PC
-Based Systems w
NP and mutation d
d for specific appli
mplification Kit H
e-step RT-PCR in
-Based Instrument
roducibility, high p
MgCl
2
is supplied
notyping Master
PCR and genotyp
his convenient, rea
kit requires only t
NA Probes Mast
mix for the hydroly
Instrument. Ideal
etup only requires t
s probes.
n
Master
mix for high perfo
Carousel-Based
olysis probe assays
h melting curve an
DNA Probes Mast
DNA Probes Maste
terFor real-time PC
appropriate probe
assays for gene de
Use LightCycler
U
amination.
obes Master
ntification assays u
e LightCycler
480
ymerase for hot sta
ic amplification pro
NA Master Hydrol
mix for one-step RT
late-based LightCy
and hydrolysis pro
arryover using Lig
A Probes Value P
ack, including mu
robe assays perfor
A Probes Value P
ack, including mu
robe assays perfor
DNA Probes Value
ack, including rea
ster for hydrolysis p
DNA Probes Value
ack, including rea
ster for hydrolysis u
LUS HybProbe
ghly sensitive PCR
sed Systems when
in two-step RT-PC
s not necessary.
HybProbe
CR in LightCycler
when using HybPro

detection. Use in tw
cations.
HybProbe
LightCycler
Capi
ts and HybProbe p
performance, and
for optimization.
r
ping analysis on the
ady-to-use hot sta
he addition of DNA
ter
ysis probe detectio
for hot start PCR a
the addition of tem
ormance qPCR or t
Instruments with
s. Note that hydrol
nalysis.
ter
er was renamed to
CR using LightCyc
es and gene-specif
etection and quant
Uracil-DNA Glycos
using an optimized
0 System. The mix c
art PCR, which min
oducts.
lysis Probes
T-PCR with the rap
ycler
480 Instrum
obes as the detect
htCycler
Uracil-D
Pack S
ltiwell plates and r
rmed on the LightC
Pack L
rmed on the LightC
e Pack S
ction device, react
probes using Light
e Pack L
ction device, react
using LightCycler
in LightCycler

n using
CR for gene
Capillaries on
be probes for
wo-step RT-
illaries using
probes for
minimizes the
e LightCycler

rt master mix.
A, primers, and
on format on
assays for
mplate DNA,
two-step RT-
Universal
lysis probes
o LightCycler

cler
480 and
fic primers.
ification and
sylase to
d ready-to-use
contains
nimizes
pid, accurate
ments using
tion format.
DNA
real-time PCR
Cycler 96
real-time PCR
Cycler
96
tion vessels
tCycler
Nano
tion vessels
Nano

03 515 567 001
03 515 575 001
03 752 178 001
03 003 248 001
12 239 272 001
12 015 145 001
04 707 524 001
Cat. No.
06 402 682 001
04 535 286 001
04 735 536 001
05 502 381 001
04 707 494 001
04 887 301 001
04 902 343 001
04 991 885 001
06 713 076 001
06 713 122 001
06 444 164 001
06 444 156 001

1 kit for up to 4
1 kit for up to 9
1 kit for up to
reactions o
1 kit for up to 9
1 kit for up to 4
1 kit for up to 9
4 x 384 l ((
of 20
5 x 1 ml for u
1 kit for up to 9
1 kit for up to 4
5 x 1 ml for
5 x 1 ml (for u
10 x 5 ml ((2x c
20
1 x 50 ml (for u
1 kit (for up t
5 packs of F
Master (a total
Multiwell P
20 packs of F
Master (a
LightCycl
(
2 kits (1,000
strip
4 kits (2,000
strips
80 reactions of 20
volume
96 reactions of 20
volume
o 1,920 reactions o
of 100 l final react
96 reactions of 20
volume
80 reactions of 20
volume

96 reactions of 20
volume

(5x conc.) approx.3
l reaction volume

Pack Size
up to 500 reactions
volume

96 reactions of 20
volume
80 reactions of 20
volume

r up to 12,500 x 2

up to 500 reactions
volume)
conc.) for up to 5,0
up to 5,000 reactio
volume)
to 5x100 reactions
volume)

FastStart Essential
of 25 ml) 1 pack L
Plates 96 (a total o

FastStart Essential
a total of 100 ml); 2
ler
480 Multiwell
(total of 100 plates
reactions 20 l e
ps/caps (960 react

reactions 20 l e
s/caps (1,920 react

l final reaction
l final reaction
of 20 l or 384
tion volume
l final reaction
l final reaction
l final reaction
384 reactions
e each)
s of 20 l final
l final reaction
l final reaction
l reactions
s of 20 l final
000 reactions of
ume)
ns of 20 l final
s at 20 l final
DNA Probes
LightCycler
480
of 50 plates)
DNA Probes
2 packs of
Plates 96
s)
each) and 120
ions)
each) and 240
tions)

inquire
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

PC

Path
Prod
Real

Real-
mixes
strain
HA g
Real
Syste

Prem
huma
Set fo
extra
Real
Syste

Prem
gene
Detec
If Infl
Real

Fast,
using
allow
Optim
SYB
Prod
FastS

Read
on th
gene
addit
Light

Perfo
track
detec
1536
Light

Easy-
Light
forma
is sup
Light

Easy-
Light
detec
RT-P
Light

Easy-
Capil
Gree
analy
Light

Easy-
Light
detec
risk o
Light

Easy-
Base
RNAs
minim

CR/RT-PC
hogen Detectio
duct Name
Time ready Inf A
-Time PCR detectio
s. One targets Influ
ns, including 2012
gene of the H1N1 2
Time ready Influ
em
mixed primers/hydr
an samples. Use w
or multiplex detect
ction control for h
Time ready Influ
em
mixed primers and h
s in human sampl
ction Set for multip
luenza A is positive
Time ready RNA
highly sensitive, s
g 50-fold concentr
wing fast hot start R
mized for HybProb
BR Green
duct Name
Start Essential D
dy-to-use reaction
he LightCycler
Na
detection and qua
tion of template DN
tCycler
1536 D
orm easy hot start
king in automater w
ction and gene qua
System.
tCycler
DNA M
-to-use mix for sen
tCycler
Carousel-
at. Use for quantita
pplied for specific
tCycler
FastSta
-to-use hot start m
tCycler
Carousel-
ction. For qPCR, SN
CR. MgCl
2
is supp
tCycler
FastSta
llaries on LightCyc
n I for detection. U
ysis. Addition of M
tCycler
RNA Am
-to-use mix for one
tCycler
Carousel-
ction. Provides rep
of contamination. M
tCycler
RNA M
-to-use mix for one
d Instruments and
s. High temperatur
mizes mispriming d
CR
on
A/H1N1 Detection
on set containing 2
uenza A Matrix Pro
point mutation. Th
2009 strain.
enza B Detection
olysis probe detec
with RealTime read
tion/differentiation
uman nucleic acid
enza B Detection
hydrolysis probe fo
es. Use with RealT
plex detection/diff
e, the H1N1 test ca
Virus Master
pecific real-time o
ated mix of Transc
RT-PCR. No need t
e, hydrolysis and U
NA Green Maste
mix using the SYB
ano Instrument. Ide
antification. React
NA and primers.
NA Green Maste
PCR assays using
workflows. Ideal fo
antification assays
aster SYBR Gree
nsitive, robust PCR
-Based Systems, u
ative PCR, and SN
applications.
art DNA Master S
-Based Systems w
NP, and mutation d
plied for specific a
art DNA MasterP
eaction mix for hig
cler
Carousel-Bas
Use in two-step RT
gCl
2
is not necess
mplification Kit S
e-step RT-PCR in
-Based Instrument
MgCl
2
is supplied
aster SYBR Gree
e-step RT-PCR usi
d SYBR Green I dye
re overcomes seco
during the RT step
n Set
2 highly specific p
otein M2 to detect
he other targets He
n Set, LightCycle
ct Influenza B viral
y Influenza A/H1N
n of Influenza A an
d.
n Set, LightCycle
or detecting Influe
Time ready Influenz
ferentiation of Influ
an be run.
one-step RT-PCR o
criptor/Taq, and a
to heat preactivate
UPL probes.
er
BR Green I dye det
eal for hot start PC
ion setup only req
er
fast protocols and
or high-throughput
s. For use on the L
en I
R in LightCycler
C
using the SYBR Gre
P and mutation de
SYBR Green I
CR in LightCycler
when using SYBR G

detection. Use also
pplications.
LUS SYBR Green
ghly sensitive PCR
sed Systems when
T-PCR for gene exp
sary.
SYBR Green I
LightCycler
Capi
ts and SYBR Green
performance, and
for optimization.
en I
ing LightCycler
C
e for detection. Ide
ondary structures,
p.
rimer/probe
t all influenza A
emagglutinin
er
480
genes in
N1 Detection
nd B, with an
er
2.0
nza B viral
za A/H1N1
uenza A and B.
of viral RNA
unique buffer
e Taq.
tection format
CR assays for
uires the
d built-in error
t gene
ightCycler

Capillaries on
een I detection
etection. MgCl
2

Capillaries on
Green I for
o for two-step
n I
in LightCycler

n using SYBR
pression
illaries using
n I dye for
minimizes the
Carousel-
eal for difficult
and hot start

Cat. No.
05 640 393 001
06 480 560 001
06 480 543 001
05 619 416 001
05 992 877 001
06 754 155 001
Cat. No.
06 402 712 001
05 573 092 001
12 158 817 001
03 003 230 001
12 239 264 001
03 515 869 001
03 515 885 001
03 752 186 001
12 015 137 001
03 064 760 001

for up to 2
fo
fo
1 kit for up
1,0
5 x 1 ml for u
1 kit (for up
1 kit for up to 4
1 kit for up to 9
1 kit for up to 4
1 kit for up to 9
1 kit for up to 4
1 kit for up to
reactions o
1 kit for up to 9
1 kit for up to 9
Pack Size
2x 100 reactions (2

r up to 100 reactio

r up to 100 reactio

p to 100 reactions (
000 reactions 20
200 reactions
Pack Size
up to 500 reactions
volume

to 12,500 reaction

80 reactions of 20
volume

96 reactions of 20
volume
80 reactions of 20
volume

96 reactions of 20
volume
80 reactions of 20
volume
o 1,920 reactions o
96 reactions of 20
volume

96 reactions of 20
volume

www.roche
20 l each)
ons
ons
(20 l each)
0 l
s of 20 l final
ns, 2 l each)
l final reaction
l final reaction
l final reaction
l final reaction
l final reaction
of 20 l or 384
tion volume
l final reaction
l final reaction
e-applied-science

Price in
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

4
73

e.com
4

4

4
PC
74

www.r

Light

Read
Light
and q
minim
Light

Spec
mast
Instru
Light

Spec
mast
Instru
Light

Spec
and r
Instru
Light

Spec
and r
Instru
qPC
Cell
Prod
Real

For ra
in tw
minu
time
Colo
Prod
Light

Read
Light
prere
and C
Con
Prod
Light

Conf
Instru
and s
dual-
Light

Conf
Light
pre-d
Hou
Prod
Light

Read
and s
mRN
No p

CR/RT-PC
roche-applied-sc
tCycler
480 SY
dy-to-use hot start
tCycler
480 Instru
quantification. Elim
mize pipetting step
tCycler 96 DNA
ial bundle combip
er for SYBR Green
ument.
tCycler
96 DNA
ial bundle combip
er for SYBR Green
ument.
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
CR Suppleme
Lysis Kits
duct Name
Time ready Cell
apid, high-perform
o-step real-time R
tes. Use lysate dire
PCR experiments
or Compensati
duct Name
tCycler
Color C
dy-to-use solutions
tCycler
Carousel-
equisite for multipl
Cy5.5-labeled Hyb
ntrol Kits
duct Name
tCycler
Control
irms PCR system p
uments. Quality ch
specific primers an
-color experiments
tCycler
480 Co
irm real-time PCR
tCycler
480 Instru
diluted samples of
ueskeeping Gen
duct Name
tCycler
h-G6PD
dy-to-use mix of pr
standard RNA for d
A in RT-PCR assay
seudogenes or co
CR
cience.com
BR Green I Mast
mix for SYBR Gree
uments. Ideal for P
minate time-consum
ps; just add DNA, p
A Green Value Pa
ack, including mu
n I assays performe
A Green Value Pa
ack, including mu
n I assays performe
DNA Green Value
ack, including rea
ster mix for SYBR G
NA Green Value
ack, including rea
ster for SYBR Gree
entary Reagen
Lysis Kit
mance gene expres
RT-PCR. Lyse 3 to 3
ectly in cDNA synt
at any throughput
on Sets
Compensation Se
s generate color co
-Based Instrument
ex experiments wi
Probe probes in a
l Kit DNA
performance of Lig
heck of both huma
nd HybProbe probe
s and color compe
ntrol Kit
and melting curve
ument using this c
human target gen
ne Sets
DH Housekeeping
rimers and HybPro
detection/quantita
ys using LightCycl
ntaminating DNA
ter
en I-based real-tim
PCR assays for gen
ming MgCl
2
titrati
primers.
ack S
ed on the LightCyc
ack L
ed on the LightCyc
e Pack S
ction device, react
Green I using Ligh
Pack L
ction device, react
en I using LightCyc
nts
ssion studies using
30,000 cells in one
thesis and analyze
.
et
ompensation files o
ts. Generated files
th both LightCycle
single capillary.
ghtCycler
Carous
n DNA used in a s
es, and as a functi
nsation.
e analysis performa
convenient kit. The
nes and internal co
g Gene Set
obe probes specific
ative comparison o
ler
Carousel-Bas
are detected.
me PCR on
ne detection
on and
real-time PCR
cler
96
real-time PCR
cler 96
tion vessels
htCycler
Nano
tion vessels
cler
Nano
g cultured cells
e step in 5
e cDNA in real-
on
are a
er
Red 640-
sel-Based
specific assay
onal check of
ance of the
kit contains
ontrols.
c for h-G6PDH,
of G6PDH
ed Systems.

04 707 516 001
04 887 352 001
06 713 092 001
06 713 106 001
06 444 229 001
06 444 172 001
Cat. No.
05 943 523 001
06 366 821 001
Cat. No.
12 158 850 001
Cat. No.
12 158 833 001
04 710 924 001
Cat. No.
03 261 883 001

5 x 1 ml ((2x
20
10 x 5 ml ((2x c
20
5 packs FastSt
(a total of 25
Multiwell P
20 packs of
Master (a total
480 Multiwell
2 kits (1,000
strip
4 kits (2,000
strips
1 kit for up to
reacti
1 kit for up t
reacti
1 set (4
1 kit for up
1 kit (for u
1 set for up to 9
conc.) approx. 500

tart Essential DNA
ml); 2 packs of Lig

FastStart Essentia
of 100 ml); 2 pack
l Plates 96 (a total

reactions 20 l e
ps/caps (960 react

reactions 20 l e
s/caps (1,920 react

Pack Size
o 500 lysis reaction
on volume of 40
to 50 lysis reaction
on volume of 40

Pack Size
4 vials, 5 calibratio

Pack Size
to 50 reactions wit
reaction volume

up to 2 x 3 control

Pack Size
96 reactions of 20
volume

0 reactions of
ume)
000 reactions of
ume)
A Green Master
ghtCyler
480
of 50 plates)
l DNA Green
ks of LightCyler

of 100 plates)
each) and 120
ions)
each) and 240
tions)
ns with a final
l each
ns with a final
l each
on runs)
th 20 l final
reactions)
l final reaction

inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
Price in
inquire
Price in
inquire
inquire
Price in
inquire

PC

HRM
Prod
Light

Achie
inhib
Obta
evalu
Labe
Prod
Light

Use t
with
HybP
Light

Use t
comb
oligo
suffic
oligo
Light

Use t
comb
oligo
enou
minim
Simp

For in
muta
estab
flexib
Urac
Prod
Light

Use w
dUTP
produ
that o
Rea
Prod
Tran

Conv
Read
supp
assay
FastS

Read
temp
enab
ROX.
FastS

Read
temp
inclu
instru
FastS

Read
quan
use o
for us

CR/RT-PC
M Dye
duct Name
tCycler
480 Hig
eve highly homoge
ition using this flu
in enhanced fluore
uation of amplicon
eling Reagents
duct Name
tCycler
Fluores
this dye to label th
5'-LightCycler
Re
Probe probes on Li
tCycler
Red 640
bination with 3'-Lig
nucleotides when
cient amount of es
nucleotides.
tCycler
Red 610
nucleotides for de
gh LightCycler
R
mum of 5 50 nm
pleProbe 519 Lab
nternal labeling of
ation detection pro
blished methods, la
bility.
cil-DNA Glycos
duct Name
tCycler
Uracil-D
with LightCycler

P-containing ampli
uct carryover cont
only native dTTP-c
agents for n
duct Name
scriptor Universa
venient fast solutio
dy-to-use master m
lied in just two via
ys on all real-time
Start Universal P
dy-to-use 2x mix co
plate for quantitativ
les use on all real-
. Not for use on Lig
Start TaqMan
P
dy-to-use 2x mix co
plate for running qu
ding qPCR and tw
uments other than
Start Universal S
dy-to-use 2x mix co
titative, real-time D
on all real-time ins
se on LightCycler
CR
gh Resolution Me
eneous staining of
orescent double-s
escent signal shar
melting behavior.
s
scein CPG
e 3'-end of oligon
ed-labeled oligonu
ghtCycler
480 an
0-N-hydroxysucc
e 5'-amino end of
ghtCycler
Fluores
using HybProbe p
ster to label a minim
0-N-hydroxysucc
e 5'-amino end of
ghtCycler
Fluores
etection with HybP
Red 610-N hydroxy
ol oligonucleotide
beling Reagent
oligonucleotide p
bes using LightCy
abeling is done in
sylase
DNA Glycosylase
FastStart enzyme-
ified DNA produce
amination in newly
containing DNA is
non-Roche S
al cDNA Master
n for cDNA synthe
mix (primers, nucle
als, brings out the f
PCR systems.
Probe Master (Ro
ontains everything
ve, real-time detec
-time instruments
ghtCycler
Instrum
Probe Master
ontaining all reage
uantitative, real-tim
wo-step qRT-PCR. U
LightCycler
Inst
SYBR Master (Ro
ontains everything
DNA detection ass
truments requiring
Instruments.
elting Dye
f amplicons withou
stranded DNA-bind
pness and high re
ucleotides. Use in
ucleotides for dete
nd Carousel-Based
cinimide ester
oligonucleotides.
scein CPG -labeled
probes for detectio
mum of 5 50 nm
cinimide ester
oligonucleotides.
scein CPG -labeled
robe probes. One v
ysuccinimide ester
s.
robes detected at
ycler
Systems. Co
a single step with
e
-containing kits to
ed in previous PCR
y prepared mixes,
available for real-t
Systems
esis and real-time
eotides, buffer, enz
full potential of you
ox)
except primers, p
ction assays. Refere
requiring normaliz
ments.
ents except primers
me DNA detection
Use with real-time
truments.
ox)
except primers an
says. The reference
g normalization wit
ut PCR
ding dye.
solution
combination
ection with
d Systems.
Use in
d
n. One vial has
mol
Use in
d
vial has
r to label a
519 nm for
ompared to
greater
eliminate
Rs. Prevent PCR
and ensure
time PCR.
PCR analysis.
ymes),
ur qRT-PCR
robe, and
ence dye
zation with
s, probe, and
assays,
e qPCR
nd template for
e dye enables
th ROX. Not

Cat. No.
04 909 640 001
Cat. No.
03 113 906 001
03 138 178 001
12 015 161 001
03 561 488 001
04 687 132 001
Cat. No.
03 539 806 001
Cat. No.
05 893 151 001
04 913 949 001
04 913 957 001
04 914 058 001
04 673 409 001
04 673 417 001
04 673 433 001
04 913 850 001
04 913 914 001

1 ml (for up to
1 vial (for 5
1 vial (for 5
5
2 x 1.25 ml for
10 x 1.25 ml fo
fi
10 x 5 ml for u
2 x 1.25 ml for
10 x 1.25 ml for
10 x 5 ml fo
4 x 1.25 ml for
10 x 5 ml for u
Pack Size
o 1,000 reactions o
volume)

Pack Size
5 columns
1 g

5 x 50 nmol oligon

5 x 50 nmol oligon

100 mol

Pack Size
50 l (100 U, 2 U/

Pack Size
100 reactions

up to 250 reaction
reaction volume
or up to 12,500 rea
nal reaction volum
reaction volume
up to 100 reaction
reaction volume
r up to 500 reactio
reaction volume
or 2,000 reactions o
reaction volume
up to 500 reaction
reaction volume
reaction volume

www.roche
f 20 l reaction
nucleotides)
nucleotides)
l)
ns of 20 l final
actions of 20 l
me
ns of 20 l final
ns of 50 l final
ons of 50 l final
of 50 l final
ns of 20 l final
ns of 20 l final
e-applied-science

Price in
inquire
Price in
inquire
inquire
inquire
inquire
inquire
Price in
inquire
Price in
inquire
139,30
657,60
inquire
189,10
886,90
3.429,10
289,80
inquire

4
75

e.com
4

4

4
PC
76

www.r

FastS

Read
need
inclu
instru
Re
Rea
Prod
Real

Custo
assay
provi
Cat. N
Real

This 5
Taq D
dTTP
cDNA
Rea
Prod
Real

Read
gene
prime
hydro
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
with

CR/RT-PC
roche-applied-sc
Start SYBR Gree
dy-to-use 2x mix co
ed for running qua
ding qPCR and tw
uments other than
ealTime rea
alTime ready
duct Name
Time ready Pre-A
om 4x concentrate
y primer pairs, for
de RealTime ready
No. 06 725 309 001
Time ready cDNA
5x concentrated re
DNA Polymerase, r
P), for 40 pre-ampli
A (1 to 250 ng).
alTime ready
duct Name
Time ready Cata
dy-to-use qPCR ass
expression in rea
ers and a Universa
olysis probe contai
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
se, rat genes) for g
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
the online Configu
CR
cience.com
n Master
ontaining all reage
antitative, real-tim
wo-step qRT-PCR. U
the LightCycler

ady
y cDNA Pre
Amp Primer Poo
ed solution of 6-96
40 pre-amplificatio
y Custom Assay Co
1 when ordering.
A Pre-Amp Mast
eady-to-use hot-st
reaction buffer, dN
ification reactions
y Custom P
alog Assays
says for human, m
l-time PCR. Each a
al ProbeLibrary Pro
ining locked nucle
om Panel 96 - 96
s 96 contain ready
genes for gene exp
-plated in wells. Se
Configurator.
om Panel 96 - 96
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 48
s 96 contain ready
genes for gene exp
Configurator.
om Panel 384 - 1
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 48
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 32
s 96 contain ready
genes for gene exp
Configurator.
om Panel 96 - 32
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 24
s 96 contain ready
genes for gene exp
urator.
ents except primers
e DNA detection a
Use with real-time
Instruments.
eamplificatio
l
6 different designer
on reactions of 50
onfiguration Numb
ter
tart PCR Master M
NTP mix, (with dUT
of 50 l of small q
anels
mouse and rat gene
assay includes gen
obe, a short FAM-l
eic acid.
6
y-to-use single qPC
pression profiling. A
elect custom assay
6+
y-to-use qPCR ass
rofiling + error det
wells. Select custo
or.
8
y-to-use single qPC
elect custom assay
192+
dy-to-use qPCR as
rofiling +error dete
wells. Select custo
or.
8+
y-to-use qPCR ass
wells. Select custo
or.
2
y-to-use single qPC
elect custom assay
2+
y-to-use qPCR ass
wells. Select custo
or.
4
y-to-use single qPC
elect custom assay
s and template
assays,
e qPCR
on System
r-specific
l each;
ber with the
Mix contains
TP instead of
quantities of
es to quantify
ne-specific
abeled
CR assays for
Assays include
ys and plate
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys and plate
ssays (human,
ection . Assays
om assays and
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys and plate
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys/plate layout

04 673 484 001
04 673 492 001
Cat. No.
06 725 309 001
06 720 455 001
Cat. No.
05 532 957 001
05 583 055 001
05 532 949 001
05 582 563 001
05 532 914 001
05 582 822 001
05 582 571 001
05 532 906 001
05 582 598 001
05 532 884 001

5 ml (4 x 1.25 m
fi
50 ml (10 x 5
20
Catalo
Design
ml) for up to 500 re
nal reaction volum
ml) for up to 5,00

Pack Size
40 reactions

40 reactions

Pack Size
og Assays, 300 rea
ner Assays, 300 rea

10 plates

10 plates

10 plates

40 plates

10 plates

10 plates

10 plates

6 plates

eactions of 20 l
me
0 reactions of
lume
actions
actions

390,30
3.535,60
Price in
200,00
600,00
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

PC

Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou

CR/RT-PC
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
CR
om Panel 96 - 24
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 16
s 96 contain ready
genes for gene exp
Configurator.
om Panel 96 - 16
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 8
s 96 contain ready
genes for gene exp
Configurator.
om Panel 384 - 3
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 3
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 1
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 1
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 1
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 9
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 9
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 6
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 6
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 4
s 384 contain read
genes for gene exp
Configurator.
4+
y-to-use qPCR ass
wells. Select custo
or.
6
y-to-use single qPC
elect custom assay
6+
y-to-use qPCR ass
wells. Select custo
or.
y-to-use single qPC
elect custom assay
384
dy-to-use single qP
elect custom assay
384+
dy-to-use qPCR as
wells. Select custo
or.
192
dy-to-use single qP
elect custom assay
128
dy-to-use single qP
elect custom assay
128+
dy-to-use qPCR as
wells. Select custo
or.
96
dy-to-use single qP
elect custom assay
96+
dy-to-use qPCR as
wells. Select custo
or.
64
dy-to-use single qP
elect custom assay
64+
dy-to-use qPCR as
wells. Select custo
or.
48
dy-to-use single qP
elect custom assay
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys and plate
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys and plate
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate

05 582 610 001
05 532 868 001
05 582 628 001
05 532 850 001
05 532 833 001
05 582 644 001
05 582 652 001
05 582 849 001
05 582 865 001
05 582 873 001
05 582 881 001
05 582 890 001
05 582 903 001
05 582 911 001

6 plates

6 plates

6 plates

6 plates

40 plates

40 plates

40 plates

20 plates

20 plates

10 plates

10 plates

10 plates

10 plates

10 plates


inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

4
77

e.com
4

4

4
PC
78

www.r

Real

Light
mous
UPL
onlin
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Real

Light
huma
prime
layou
Real

Light
mous
inclu
plate
Rea
Prod
Real

Quan
pane
inclu
samp
Real

Quan
pane
inclu
samp
Real

Quan
supe
Pre-p
add s
Real

Quan
Assay
assay
addin
Real

Quan
gene
plate
requi
Un
Prod
Univ

Use t
for al
PCR
Desig
Univ

Use i
a com
quan
Probe

CR/RT-PC
roche-applied-sc
Time ready Cust
tCycler
480 Plate
Probe pre-plated i
e Configurator. (+
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
alTime ready
duct Name
Time ready Hum
ntify expression lev
ls directly using Li
de gene-specific p
ple cDNA and mas
Time ready Hum
de gene-specific p
ple cDNA and mas
Time ready Hum
rfamily. Assay pan
plated assays inclu
sample cDNA and
Time ready Hum
ntify the expression
y panels directly u
ys include gene-sp
ng sample cDNA a
Time ready Hum
s. Assay panels di
d assays include g
ire adding sample
niversal Pr
duct Name
versal ProbeLibra
this fluorescent pro
ll the human gene
with LightCycler

gn assays using th
versal ProbeLibra
n combination wit
mplete set of 165 U
tification of transc
eLibrary Assay De
CR
cience.com
om Panel 384 - 4
s 384 contain read
gene expression pr
n wells. Select cus
+ error detection)
om Panel 384 - 3
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 3
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 1
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 1
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
y Focus Pan
man Apoptosis Pa
vels of 372 human
ightCycler
480 In
primers and a UPL
ster mix.
man Apoptosis Pa
vels of 84 human a
ightCycler
480 In
primers and a UPL
ster mix.
man ABC Transpo
vels of 42 genes of
nels directly using
ude gene-specific p
master mix.
man Cell Cycle Re
n levels of 84 gene
sing LightCycler

pecific primers and
and master mix.
man Reference Ge
n levels of 19 hum
rectly using LightC
gene-specific prim
cDNA and master
robeLibrar
ary Set, Human
obe set to rapidly q
s in the NCBI Ref
Systems and othe
he free online Assa
ary Extension Set
th the Universal Pr
Universal ProbeLib
cripts of all organis
sign Center.
48+
dy-to-use qPCR as
rofiling. Assays inc
stom assays/plate
32
dy-to-use single qP
elect custom assay
32+
dy-to-use qPCR as
wells. Select custo
or.
16
dy-to-use single qP
elect custom assay
16+
dy-to-use qPCR as
wells. Select custo
or.
nels
anel, 384
apoptosis-related
nstruments. Pre-pla
L Probe, and only re
anel, 96
apoptosis-related g
nstruments. Pre-pla
orter Panel
f the human ABC t
LightCycler
480 I
primers and a UPL
egulation Panel
es in human cell cy
480 Instruments.
d a UPL Probe, and
ene Panel
an genes to use as
Cycler
480 Instru
ers and a UPL Pro
r mix.
ry
quantify gene exp
Seq Database, usi
er real-time PCR in
ay Design Center.
t, Probes #91 to #
robeLibrary Set, Hu
brary Probes. Enab
sms using the onlin
ssays (human,
clude primer,
layout with
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
genes. Assay
ated assays
equire adding
genes. Assay
ated assays
equire adding
transporter
Instruments.
L Probe. Just
ycle regulation.
Pre-plated
d only require
s reference
ments. Pre-
obe, and only
ression levels
ng real-time
nstruments.
#165
uman to obtain
les
ne Universal

05 582 938 001
05 582 962 001
05 582 989 001
05 583 004 001
05 583 039 001
Cat. No.
05 339 316 001
05 392 063 001
05 339 324 001
05 339 359 001
05 339 545 001
05 467 675 001
Cat. No.
04 683 633 001
04 869 877 001

2 plates (e
2 plates (
2 plates (
2 plates (
2 plates (
2 plates (e
1 set of 90 Univ
1 set of 75 Univ
10 plates

10 plates

10 plates

6 plates

6 plates

Pack Size
each containing 38

(each containing 9

(each containing 9

(each containing 9

(each containing 9
each containing 38

Pack Size
versal ProbeLibrary
10 M each.

versal ProbeLibrary
10 M each.

84 assays)
96 assays)
96 assays)
96 assays)
96 assays)
84 assays)
y probes, 125 l,
y Probes, 125 l,

inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
Price in
3.393,90
2.574,80

PC

Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Quan
endo
assay
softw
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin
Univ

Gene
expre
assay
onlin

CR/RT-PC
versal ProbeLibra
e-specific probe an
ession levels using
ys for your target g
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
ogenous reference
ys for target gene
ware at the Assay D
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
CR
ary Human ACTP
nd primer pair for h
g dual-color real-ti
gene and UPL Refe
tware at the Assay
ary Human G6PD
gene and UPL Refe
tware at the Assay
ary Human GAPD
gene and UPL Refe
tware at the Assay
ary Human GUSB
gene and UPL Refe
tware at the Assay
ary Human HPRT
gene and UPL Refe
tware at the Assay
ary Human PBGD
gene and UPL Refe
tware at the Assay
ary Human PGK1
gene and UPL Refe
tware at the Assay
ary Human PPIA G
gene and UPL Refe
tware at the Assay
ary Human TBP G
gene and UPL Refe
tware at the Assay
ary Human 2M
gene and UPL Refe
tware at the Assay
ary Set, Human R
vels of a human ge
gene in a dual-co
and UPL Referenc
Design Center.
ary Mouse ACTB
nd primer pair for m
gene and UPL Refe
tware at the Assay
ary Mouse GAPD
gene and UPL Refe
tware at the Assay
ary Rat GAPD Gen
nd primer pair for r
gene and UPL Refe
tware at the Assay
Gene Assay
human ACTP. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human G6PD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
D Gene Assay
human GAPD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
B Gene Assay
human GUSB. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human HPRT. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
D Gene Assay
human PBGD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human PGK1. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human PPIA. Quan
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human TBP. Quan
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human 2M. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Reference Gene A
ene of interest in re
olor assay. Design
ce Gene Assay with
Gene Assay
mouse ACTB. Qua
me PCR. Design m
erence Gene Assay
y Design Center.
Gene Assay
mouse GAPD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
ne Assay
rat GAPD. Quantify
me PCR. Design m
erence Gene Assa
y Design Center.
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
ntify gene
multiplex PCR
y using the
tify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
Assays
elation to an
multiplex PCR
h free online
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
y gene
multiplex PCR
y using the

05 046 165 001
05 046 246 001
05 190 541 001
05 190 525 001
05 046 157 001
05 046 149 001
05 046 173 001
05 189 268 001
05 189 284 001
05 189 390 001
05 046 114 001
05 046 190 001
05 046 211 001
05 046 220 001

1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
250 reactions
1 set for up to
50
1 set for up to
50
1 set for up to
50
200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

100 reactions of 5
of 20 l for each r

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

www.roche
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
reference gene
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
e-applied-science

491,60
491,60
491,60
491,60
491,60
491,60
491,60
491,60
491,60
491,60
1.111,90
491,60
491,60
491,60

4
79

e.com
4

4

4
PC
80

www.r

Univ

Gene
expre
assay
onlin
Univ

Rapid
speci
with
free o
CR/RT-PC
roche-applied-sc
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
dly quantify gene e
ies in the NCBI Re
standard reagents
online Assay Desig
CR
cience.com
ary Rat ACTB Gen
gene and UPL Refe
tware at the Assay
ary Probes
expression levels o
eference Seq Datab
s in real-time PCR
gn Center.
ne Assay
rat ACTB. Quantify
me PCR. Design m
erence Gene Assa
y Design Center.
of human, mouse,
base. Use fluoresc
assays. Design ass
y gene
multiplex PCR
y using the
rat and other
cent probes
says using the

05 046 203 001
04 684 974 001
04 684 982 001
04 685 008 001
04 685 016 001
04 685 024 001
04 685 032 001
04 685 059 001
04 685 067 001
04 685 075 001
04 685 091 001
04 685 105 001
04 685 113 001
04 685 121 001
04 685 130 001
04 685 148 001
04 686 896 001
04 686 900 001
04 686 918 001
04 686 926 001
04 686 934 001
04 686 942 001
04 686 969 001
04 686 977 001
04 686 985 001
04 686 993 001
04 687 574 001
04 687 582 001
04 687 604 001
04 687 612 001
04 687 639 001
04 687 647 001
04 687 655 001
04 687 663 001
04 687 671 001
04 687 680 001
04 687 949 001
04 687 957 001
04 687 965 001
04 687 973 001
04 687 990 001
04 688 007 001

1 set for up to
50
200 reactions of 5
00 reactions of 20

Probe #1
Probe #2
Probe #3
Probe #4
Probe #5
Probe #6
Probe #7
Probe #8
Probe #9
Probe #10
Probe #11
Probe #12
Probe #13
Probe #14
Probe #15
Probe #16
Probe #17
Probe #18
Probe #19
Probe #20
Probe #21
Probe #22
Probe #23
Probe #24
Probe #25
Probe #26
Probe #27
Probe #28
Probe #29
Probe #30
Probe #31
Probe #32
Probe #33
Probe #34
Probe #35
Probe #36
Probe #37
Probe #38
Probe #39
Probe #40
Probe #41
0 l or for up to
l

491,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

PC

CR/RT-PCCR

04 688 015 001
04 688 031 001
04 688 040 001
04 688 058 001
04 688 066 001
04 688 074 001
04 688 082 001
04 688 104 001
04 688 112 001
04 688 481 001
04 688 490 001
04 688 503 001
04 688 511 001
04 688 520 001
04 688 538 001
04 688 546 001
04 688 554 001
04 688 562 001
04 688 589 001
04 688 597 001
04 688 619 001
04 688 627 001
04 688 635 001
04 688 643 001
04 688 651 001
04 688 660 001
04 688 678 001
04 688 686 001
04 688 937 001
04 688 945 001
04 688 953 001
04 688 961 001
04 688 970 001
04 688 988 001
04 688 996 001
04 689 003 001
04 689 011 001
04 689 020 001
04 689 038 001
04 689 046 001
04 689 054 001
04 689 062 001
04 689 089 001
04 689 097 001

Probe #42
Probe #43
Probe #44
Probe #45
Probe #46
Probe #47
Probe #48
Probe #49
Probe #50
Probe #51
Probe #52
Probe #53
Probe #54
Probe #55
Probe #56
Probe #57
Probe #58
Probe #59
Probe #60
Probe #61
Probe #62
Probe #63
Probe #64
Probe #65
Probe #66
Probe #67
Probe #68
Probe #69
Probe #70
Probe #71
Probe #72
Probe #73
Probe #74
Probe #75
Probe #76
Probe #77
Probe #78
Probe #79
Probe #80
Probe #81
Probe #82
Probe #83
Probe #84
Probe #85

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

4
81

e.com
4

4

4
PC
82

www.r

CR/RT-PC
roche-applied-sc
CR
cience.com

04 689 119 001
04 689 127 001
04 689 135 001
04 689 143 001
04 689 151 001
04 692 080 001
04 692 098 001
04 692 101 001
04 692 110 001
04 692 128 001
04 692 136 001
04 692 144 001
04 692 152 001
04 692 179 001
04 692 187 001
04 692 195 001
04 692 209 001
04 692 217 001
04 692 225 001
04 692 241 001
04 692 250 001
04 692 268 001
04 692 276 001
04 692 284 001
04 692 306 001
04 693 442 001
04 693 469 001
04 693 477 001
04 693 485 001
04 693 493 001
04 693 507 001
04 693 515 001
04 693 523 001
04 693 531 001
04 693 540 001
04 693 558 001
04 693 566 001
04 693 574 001
04 693 582 001
04 693 604 001
04 693 612 001
04 693 639 001
04 693 647 001
04 693 655 001

Probe #86
Probe #87
Probe #88
Probe #89
Probe #90
Probe #91
Probe #92
Probe #93
Probe #94
Probe #95
Probe #96
Probe #97
Probe #98
Probe #99
Probe #100
Probe #101
Probe #102
Probe #103
Probe #104
Probe #105
Probe #106
Probe #107
Probe #108
Probe #109
Probe #110
Probe #111
Probe #112
Probe #113
Probe #114
Probe #115
Probe #116
Probe #117
Probe #118
Probe #119
Probe #120
Probe #121
Probe #122
Probe #123
Probe #124
Probe #125
Probe #126
Probe #127
Probe #128
Probe #129

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

PC

CR/RT-PCCR

04 693 663 001
04 694 155 001
04 694 163 001
04 694 171 001
04 694 180 001
04 694 198 001
04 694 201 001
04 694 210 001
04 694 228 001
04 694 236 001
04 694 244 001
04 694 279 001
04 694 287 001
04 694 295 001
04 694 309 001
04 694 317 001
04 694 325 001
04 694 333 001
04 694 341 001
04 694 350 001
04 694 368 001
04 694 376 001
04 694 384 001
04 694 392 001
04 694 406 001
04 694 414 001
04 694 422 001
04 694 449 001
04 694 457 001
04 694 465 001
04 694 473 001
04 694 481 001
04 694 490 001
04 694 503 001
04 694 511 001
04 694 520 001

Probe #130
Probe #131
Probe #132
Probe #133
Probe #134
Probe #135
Probe #136
Probe #137
Probe #138
Probe #139
Probe #140
Probe #141
Probe #142
Probe #143
Probe #144
Probe #145
Probe #146
Probe #147
Probe #148
Probe #149
Probe #150
Probe #151
Probe #152
Probe #153
Probe #154
Probe #155
Probe #156
Probe #157
Probe #158
Probe #159
Probe #160
Probe #161
Probe #162
Probe #163
Probe #164
Probe #165

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

4
83

e.com
4

5

5
Se
84

www.r

GS
GS
Prod
GS J

Bring
chem
for sm
(10 h
GS
Prod
GS J

Provi
librar
millio
Instru
GS J

Provi
single
copie
using
GS J

The G
Titan
deter
ampl
GS J

The G
Titan
nucle
librar
GS J

Stand
only
that g
acco
GS J

Use t
Junio
perio
subsy
GS J

GS Ju
for th
presc
Devic
GS J

The G
and F
Instru
repla
GS J

The G
Instru
Sequ

equencin
roche-applied-sc
S Junior Sy
Junior Instr
duct Name
unior Complete
gs proven performa
mistry to the bench
mall to medium siz
hours) and obtain 4
Junior Titan
duct Name
unior Titanium e
des reagents for a
ry from a single eff
ons of copies per b
ument and GS Jun
unior Titanium e
des reagents for th
e effective bead-b
es per bead, amen
g GS Junior Titaniu
unior Titanium S
GS Junior Titanium
ium PicoTiterPlate
rmine the nucleotid
ified DNA library,
unior Titanium P
GS Junior Titanium
ium Sequencing K
eotide sequence of
ry. Use with the GS
unior Titanium C
dard sequencing c
Control Beads are
give sequencing re
rding to specificat
unior Maintenta
to thoroughly clean
or Instrument when
od of time, or if con
ystem.
unior Preventativ
unior Preventative
he scheduled main
cribed schedule. Th
ce Centrifuge Adap
unior Sipper Ma
GS Junior Sipper M
Filters (10) to repla
ument as part of a
acement Buffer Tra
unior Titanium S
GS Titanium Seque
ument Test. It is a
encing Kit (05 996
ng Solutio
cience.com
ystem
rument
ance and long rea
htop. Small footprin
zed laboratories. S
400 bp read length
nium Kits
emPCR Kit (Lib-L
amplification of a s
fective bead-boun
bead, amenable to
nior Titanium kits.
emPCR Kit (Lib-A
he amplification of
ound copy of DNA
able to sequencing
um kits.
Sequencing Kit
m Sequencing Kit c
e Kit, provides reag
de sequence of an
using GS Junior Ti
PicoTiterPlate Kit
m PicoTiterPlate Kit
Kit, provides device
f an immobilized a
S Junior Instrumen
Control Bead Kit
control for the GS J
sequenced. The b
esults showing the
ions.
nce Wash Kit
n and sterilize the
n the instrument h
ntamination is obse
ve Maintenance
Maintenance Kit c
ntenance of a GS J
he kit also contain
ptors (A and B).
intenance Kit
Maintenance Kit co
ace all of the short
maintenance proc
ay.
Sequencing Buffe
encing Buffers Kit
subcomponent of
6 554 001) and can
ons
ds of the GS FLX T
nt and low entry co
equence >35 milli
hs.
L)
shotgun, paired en
d copy of DNA to
sequencing using
A)
f an amplicon libra
A template to tens
g using the GS Jun
combined with the
gents and consuma
n immobilized and
itanium kits.
t
t combined with th
es and reagents to
and clonally amplif
nt.
Junior System. Du
beads contain know
e GS Junior System
fluidics subsystem
has been left idle fo
erved or suspected
Kit
contains compone
unior Instrument,
ns two pairs of Bea
ontains enough Sip
t Sipper Tubes of a
cedure. The kit als
ers Kit
is used to run the
the GS FLX Titaniu
n be ordered separ
Titanium
osts are ideal
on bases/run
d, or cDNA
tens of
g the GS Junior
ary from a
of millions of
nior Instrument
GS Junior
ables to
clonally
he GS Junior
determine the
fied DNA
ring a test run,
wn sequences
m is performing
m of the GS
or an extended
d in the fluidics
ents required
following the
ad Deposition
pper Tubes
a GS Junior
so contains a
GS Junior
um
rately.

Cat. No.
05 922 160 001
Cat. No.
05 996 481 001
05 996 520 001
05 996 554 001
05 996 619 001
05 996 643 001
05 889 111 001
05 898 765 001
05 954 070 001
06 627 846 001

Pack Size
1 instrument

Pack Size
1 kit

1 kit

1 kit

1 kit

1 kit

1 kit

1 kit

1 kit

1 kit

Price in
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Se

GS
Prod
GS J

The G
PicoT
the w
supp
GS J

Use d
a seq
Devic
Supp
IKA T

Smal
Amp
confi
GS J

The G
caps
GS J

Evalu
Amp
GS Ju
MV e
GS
GS
Prod
GS F

Uniq
accu
proje
sequ
GS
Prod
GS F

Comb
reage
sequ
ampl
GS
Prod
GS F

The G
Instru
is pro
GS F

The G
used
Servi
three
GS
Prod
GS F

Comp
Suita
analy
hrs fo
GS F

The G
for us

equencin
Junior Titan
duct Name
unior Bead Depo
GS Junior bead de
TiterPlate device an
wells of the PicoTite
lied with the GS Ju
unior Bead Depo
during GS Junior B
quencing run, and
ce Centrifuge Adap
plied with the GS J
Turrax
l device used for g
lification procedur
gurations for 100V
unior Reagent D
GS Junior Reagent
from the reagent
unior emPCR Be
uate the amount of
lification procedur
unior Titanium em
emPCR Kits. Suppl
S FLX+ Sys
FLX+ Instru
duct Name
FLX+ Instrument
ue combination of
racy and high-thro
ects: whole genom
encing, and samp
FLX+ Titani
duct Name
FLX Titanium Seq
bined with the GS
ents and other con
ence (in extra-long
ified DNA library (
FLX+ Titani
duct Name
FLX+ Upgrade Kit
GS FLX+ Upgrade
ument to a GS FLX
ovided in the kit.
FLX+ CB Filters a
GS FLX+ CB Filters
for GS FLX+ Instr
ce Engineers must
e (3) months or afte
FLX+ Comp
duct Name
FLX+ Computing
puting solution for
able for pipeline pr
ysis, including map
or the XL+ and ~4
FLX+ Computing
GS FLX+ Computin
se with the GS FLX
ng Solutio
nium Access
osition Device
position device ho
nd gasket, enablin
erPlate device prio
unior Complete.
osition Device Co
Bead Deposition D
use along with the
ptors A and B to fi
unior Complete.
generating emulsio
re. The device ship
V, 120V, and 230 V
Decapping Tool
t Decapping Tool i
cassette in the GS
ead Counter V2
f enriched beads r
re. Bead Counter c
PCR Kits or multip
ied with GS Junior
stem
ument
f long sequencing
oughput, make this
e shotgun, multi-s
le multiplexing.
ium Series K
quencing Kit XL+
FLX Titanium Pico
nsumables require
g reads; up to 1 kb
(the sample).
ium Series A
t
Kit is used to upg
X+ Instrument. Eve
nd Pump Tubing
s and Pump Tubin
rument maintenanc
t change the CB F
er 25 runs.
puting Hardw
Station
r fast processing o
ocessing of GS FL
pping and de novo
4 hrs for the XLR70
Station Monitor
ng Station Monitor
X+ Computing Sta
ons
sories
olds one GS Junior
ng the deposition o
or to a sequencing
ounterweight Kit
Device centrifugatio
e GS Junior Bead D
it into a variety of c
ons in the GS Junio
ps with multiple co
V power inputs.
s used to convenie
S Junior Titanium S
recovered during e
can be used for sin
ple prep with GS FL
r Complete.
reads (up to 1 kb)
s system ideal for
span paired end, am
Kits

oTiterPlate Kit 70
d to determine the
b) of an immobilize
Accessories
rade an existing G
erything required fo
g Kit
g Kit contains the
ce. Instrument use
ilters and Pump Tu
ware
of GS FLX+ sequen
LX+ System data a
o assembly. Proces
0.
r with power cords
ation.
r Titanium
of beads into
Run. It is
on steps before
Deposition
centrifuges.
or emPCR
rd
ently remove
Sequencing Kit.
emPCR
ngle prep with
LX Titanium
) and very high
large genomic
mplicon/cDNA
75, it provides
e nucleotide
ed and clonally
s
GS FLX
or the upgrade
components
ers or Roche
ubing every
ncing data.
nd subsequent
ssing time: ~18
s is intended

Cat. No.
05 996 473 001
05 889 103 001
05 943 353 001
06 593 020 001
06 594 662 001
Cat. No.
06 372 279 001
Cat. No.
06 380 565 001
Cat. No.
05 872 430 001
06 397 417 001
Cat. No.
06 388 779 001
06 388 787 001

1 inst
1 ki
Pack Size
1 device

1 device

1 device

1 device

1 device

Pack Size
rument plus acces

Pack Size
t for 1 sequencing

Pack Size
1 accessory

1 kit

Pack Size
1 instrument

1 instrument

www.roche
ssories
g run
e-applied-science

Price in
inquire
inquire
inquire
inquire
inquire
Price in
inquire
Price in
inquire
Price in
inquire
inquire
Price in
inquire
inquire

5
85

e.com
5

5

5
Se
86

www.r

GS
GS
Prod
GS F

Stand
only
that y
speci
GS F

Creat
librar
span
and s
GS F

Subs
Kit du
Tagg
sequ
GS F

Prepa
inser
and s
Titan
GS F

For la
boun
amen
Titan
GS F

For m
bead
amen
Titan
GS F

Provi
single
copie
and T
GS F

For la
effec
per b
FLX T
GS F

For m
effec
per b
FLX T
GS F

Provi
from
millio
Instru
GS F

The G
for br
Titan
regio
GS F

Comb
deter
ampl
layers

equencin
roche-applied-sc
S FLX Syst
FLX Titaniu
duct Name
FLX Titanium Con
dard sequencing c
Control Beads are
yield sequencing r
ifications.
FLX Titanium Rap
te a library of fragm
ry is a set of single
of the sample seq
sequencing DNA a
FLX Titanium Rap
titute MID Adapto
uring preparation
ing multiple librari
enced together in
FLX Titanium Libr
are up to 10 assort
t lengths of 3, 8, o
sequencing using
ium Series kits.
FLX Titanium LV e
arge-volume ampl
nd copy of DNA tem
nable to sequencin
ium series kits.
FLX Titanium MV
medium-volume am
-bound copy of D
nable to sequencin
ium series kits.
FLX Titanium SV e
des reagents for s
e effective bead-b
es per bead, amen
Titanium series kits
FLX Titanium LV e
arge-volume ampl
tive, beadbound c
bead, amenable to
FLX Titanium MV
medium-volume am
tive, bead-bound c
bead, amenable to
Titanium kits.
FLX Titanium SV e
des reagents for s
a single effective
ons of copies per b
ument and GS FLX
FLX Titanium emP
GS FLX Titanium e
reaking large-volu
ium LV emPCR Kit
ons of a PicoTiterPl
FLX Titanium Pico
bine this kit with th
rmine the nucleotid
ified DNA library. T
s in the wells of a
ng Solutio
cience.com
em
m Series Ki
ntrol Bead Kit
control for the GS F
sequenced. They
results to show the
pid Library Prepa
ments from a DNA
e-stranded DNA fra
quence. Each fragm
adaptors.
pid Library MID A
ors for those in the
of DNA libraries fo
ies with MIDs allow
1 region of the pla
rary Paired End A
ted single-strande
r 20 kb from dsDN
the GS FLX Instrum
emPCR Kit (Lib-L
ification of a librar
mplate to tens of m
ng using the GS FL
emPCR Kit (Lib-
mplification of a lib
NA template to ten
ng using the GS FL
emPCR Kit (Lib-L
small-volume ampl
ound copy of DNA
able to sequencing
s.
emPCR Kit (Lib-A
ification of an amp
opy of DNA templ
sequencing using
s.
emPCR Kit (Lib-
mplification of an a
copy of DNA temp
sequencing using
emPCR Kit (Lib-A
small-volume ampl
bead-bound copy
bead, amenable to
X Titanium kits.
PCR Breaking Kit
emPCR Breaking K
ume (LV) emulsion
t (Lib-L) to prepar
late device.
oTiterPlate Kit 70
he GS FLX Titanium
de sequence of an
The DNA-carrying
PicoiterPlate devic
ons
its
FLX Instrument. In
contain known DN
e instrument is with
ration Kit
A sample to be seq
agments represent
ment is flanked by
Adaptors Kit
GS FLX Titanium
or sequencing (GS
ws them to be am
ate.
Adaptors
ed paired end DNA
NA input sample fo
ment with appropr
L)
millions of copies p
LX Instrument and
-L)
brary from a single
ns of millions of co
LX Instrument and
L)
lification of a librar
A template to tens
g using the GS FLX
A)
plicon library from
ate to tens of milli
g the GS FLX Instru
-A)
amplicon library fro
plate to tens of mil
g the GS FLX Instru
A)
lification of an amp
of DNA template
sequencing using
ts LV/MV 12pc
Kit LV 12pc provide
s prepared using t
e samples for load
0x75
m Sequencing Kit
n immobilized and
g beads and reage
ce.
a test run,
NA sequences
hin
quenced. The
ting the entire
amplification
Rapid Library
S FLX System).
plified and
A libraries with
or amplification
riate GS FLX
fective, bead-
per bead,
GS FLX
e effective,
opies per bead,
GS FLX
ry from a
of millions of
X Instrument
a single
ons of copies
ument and GS
om a single
lions of copies
ument and GS
plicon library
to tens of
g the GS FLX
es components
the GS FLX
ding into large
XLR70 to
clonally
nts deposit in

Cat. No.
05 470 129 001
05 608 228 001
05 619 211 001
05 463 343 001
05 618 428 001
05 618 436 001
05 618 444 001
05 619 114 001
05 619 149 001
05 619 165 001
05 233 658 001
05 233 682 001

1 kit for u
1 kit for u
1 k
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for 12
1 pl
Pack Size
1 kit

up to 12 library pre


kit for up to 10 ass

p to 2 large volume
mplification reactio

to 8 medium volum

p to 16 small volum

p to 2 large volume

to 8 medium volum

p to 32 small volum

LV emulsion-brea

late (with accesso

eparations
eparations
says
e emulsion
ons
me emulsion
ons
me emulsion
ons
e emulsion
ons
me emulsion
ons
me emulsion
ons
aking setups
ries)

Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Se

GS F

Comb
reage
sequ
clona
GS
Prod
70x7

This d
plate
For u
Titan
70x7

This d
plate
For u
Titan
70x7

This d
plate
For u
Titan
70x7

This d
plate
For u
Titan
GS F

Use f
FLX T
for lo
PicoT
Nebu

The N
Instru
a Ne
GS
Prod
REM

Provi
syste
hybri
Titan
As
GS
Prod
GS G

This s
sever
resea
GS F
GS G

GS G
DNA
leuke
assay

equencin
FLX Titanium Seq
bined with the GS
ents and other con
ence in extra-long
ally amplified DNA
FLX Titaniu
duct Name
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
FLX Titanium emP
for breaking small-
Titanium SV emPC
oading into medium
TiterPlate device.
ulizer Holder
Nebulizer Holder is
uments and is also
bulizer during DNA
Automation
duct Name
M e System
des subcomponen
ems to automate em
dization procedure
ium series emulsio
says
GType Exon
duct Name
GType TET2/CBL/
set forms the basis
ral exons of the TE
arch. This DNA seq
LX, GS FLX+ or GS
GType RUNX1 Pri
GType RUNX1 Prim
sequence of seve
emia research. This
y using the GS FLX
ng Solutio
quencing Kit XLR
FLX Titanium Pico
nsumables require
g reads (350 to 450
A library.
m Series Ac
ion Device (2 larg
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
ion Device (16 sm
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
ion Device (4 me
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
ion Device (8 M/
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
PCR Filters SV 64
-volume (SV) emu
CR Kit (Lib-L) to pr
m, medium-small,
s supplied with the
o available separat
A sample fragmen
n Accessorie
nts and software to
mPCR enrichment
es in the GS FLX w
on oil formats.
n Primer Set
/KRAS Primer Se
s for a test to dete
ET2, CBL, and KRA
quence-based mut
S Junior Systems.
imer Set
mer Set forms the b
eral exons of the RU
s is a DNA sequen
X, FLX+, or Junior
ons
R70
oTiterPlate Kit 70x7
d for determining
0 nt) of an immobil
ccessories
ge regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
mall regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
edium regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
/S Regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
4pc
lsions generated u
repare samples at s
or small regions of
e Genome Sequen
tely. The Nebulizer
ntation.
es
o install onto liquid
and sequencing p
workflow. Supports
ts
et
ermine the DNA se
AS genes, of interes
tation detection as
basis for a test to d
UNX1 gene, of inte
nce-based mutatio
Systems.
75, provides
the nucleotide
lized and
plate and top
erPlate device.
nd GS FLX
plate and top
erPlate device.
nd GS FLX
plate and top
erPlate device.
nd GS FLX
plate and top
erPlate device.
nd GS FLX
using the GS
smaller scales
f a
cer
r Holder holds
d handling
primer
s all GS FLX
equence of
st in leukemia
ssay uses the
determine the
erest in
on detection

05 233 526 001
Cat. No.
05 414 601 001
05 414 636 001
05 414 610 001
05 414 628 001
05 233 674 001
04 777 026 001
Cat. No.
05 976 120 001
Cat. No.
06 500 498 001
06 500 358 001

1 kit for one Ge
1 bott
1 bott
1 bott
1 bott
4 PCR pla
4 PCR pla
enome Sequener F
run

Pack Size
tom plate and 1 top

tom plate and 1 top

tom plate and 1 top

tom plate and 1 top

1 kit (64 filters)

1 nebulizer holder

Pack Size
1 system

Pack Size
tes with dried-dow

tes with dried-dow

www.roche
FLX sequencing
p plate
p plate
p plate
p plate
r
wn primers
wn primers
e-applied-science

inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
Price in
inquire
Price in
inquire
inquire

5
87

e.com
5

5

5
Se
88

www.r

GS
Prod
GS G

GS G
the b
majo
class
GS G

GS G
the b
majo
class
Se
Seq
Prod
SeqC

2.1 m
tube.
ident
popu
SeqC

For e
variat
sequ
and d
SeqC

Use t
solut
solut
Exom
SeqC

Custo
of cu
comp
captu
SeqC

High
custo
reseq
unifo
SeqC

High
custo
reseq
unifo

equencin
roche-applied-sc
GType HLA
duct Name
GType HLA HR Pr
GType HLA MR Prim
basis for an HLA te
r histocompatibilit
s I and II), using GS
GType HLA MR P
GType HLA MR Prim
basis for an HLA te
r histocompatibilit
quence C
quence Cap
duct Name
Cap EZ Human Ex
million stable in-sol
Optimization tool
tify mutations for g
ulation genetics an
Cap EZ Human Ex
exome resequencin
tions in the genom
encing. Allows res
detect more signifi
Cap EZ Exome+U
the most compreh
ion to discover mo
ions, with the supe
me 2.1M overlappin
Cap EZ Exome Pl
omize your target e
stom target region
pared to other targ
ure efficiency.
Cap EZ Choice Li
ly efficient, flexible
omer-defined disea
quencing studies. S
orm capture of targ
Cap EZ Choice XL
omer-defined disea
quencing studies. S
orm capture of targ
ng Solutio
cience.com
A Primer Sets
rimer Set
mer Set and GS GT
est that measures H
ty complex region o
S FLX or GS Junior
rimer Set
mer Set and GS GT
est that measures H
ty complex region o
S FLX or GS Junior
apture
ture EZ Libr
xome Library v2.
lution DNA probes
for next-gen work
genetic disorders a
d pharmacogenet
xome Library v3.
ng, a powerful tech
me at a fraction of t
searchers added fle
icant variations.
UTR Library
ensive cost-effecti
ore variants compa
erior capture effici
ng probes.
us Library
enrichment discov
ns to EZ Exome v3
get enrichment sol
ibrary
e design, and easy
ase related regions
Save on costs by a
get regions up to 7
L Library
e design, and easy
ase related regions
Save on costs by a
get regions up to 5
ons
s
Type HLA HR Prim
HLA allelic haploty
of the human geno
r Systems.
Type HLA HR Prim
HLA allelic haploty
of the human geno
r Systems.
rary
0
s to capture all Ref
kflows enables new
and discover varian
ics.
0
hnique to identify f
the cost of whole g
exibility to analyze
ive exome and UTR
ared to other targe
ency of SeqCap EZ
very tool by adding
to discover more
utions, for cost-eff
-to-use solution ca
s in the human ge
achieving highly sp
7 Mb.
-to-use solution ca
s in the human ge
achieving highly sp
50 Mb.
mer Set form
ypes at the
ome (MHC
mer Set form
ypes at the
ome (MHC
fSeq exons in 1
w discoveries:
nts in
functional
genome
e more samples
R enrichment
et enrichment
Z Human
g up to 50 Mb
variants
fective superior
aptures
enome for
pecific and
aptures
enome for
pecific and

Cat. No.
05 872 537 001
05 872 529 001
Cat. No.
05 860 482 001
05 860 504 001
06 465 684 001
06 465 692 001
06 740 294 001
06 740 308 001
06 740 189 001
06 740 235 001
06 740 243 001
06 740 251 001
06 266 282 001
06 266 304 001
06 266 312 001
06 266 339 001
06 266 347 001
06 266 355 001
06 740 260 001
06 266 363 001
06 266 371 001
06 266 380 001
06 266 398 001
06 266 401 001
06 266 517 001

4 PCR pla
4 PCR pla
Pack Size
tes with dried-dow

tes with dried-dow

Pack Size
4 reactions
48 reactions

4 reactions
48 reactions

4 reactions
48 reactions

12 reactions
48 reactions
96 reactions
4 reactions
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions
4 reactions
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions

wn primers
wn primers

Price in
inquire
inquire
Price in
3.360,00
20.160,00
3.360,00
20.160,00
2.500,00
24.000,00
6.780,00
24.000,00
38.000,00
4.900,00
10.080,00
15.120,00
20.160,00
21.773,00
58.061,00
80.640,00
5.200,00
12.096,00
18.144,00
30.240,00
48.384,00
129.024,00
241.920,00

Se

SeqC

Provi
huma
costs
50 M
Kits
Prod
SeqC

The N
for Se
steps
SeqC
SeqC

Use t
when
Reag
produ
SeqC

Conv
captu
ampl
for hi
SeqC

Kit A
secon
TruSe
barco
SeqC

Kit B
secon
TruSe
barco
SeqC

Comp
Libra
hybri
Grad
SeqC

Comp
sequ
every
Acce
SeqC

For o
equencin
Cap EZ Develope
des custom oligon
an genomes for cu
s by achieving high
Mb. Flexible design
s and Consu
duct Name
Cap EZ Hybridiza
NimbleGen SeqCa
eqCap EZ product
s are supplied in o
Cap EZ Exome.
Cap EZ Develope
this universal reag
n species-specific
gent is for use spec
ucts.
Cap EZ Pure Cap
venient set of captu
ure and to isolate a
ification. Use this
igh-quality sequen
Cap EZ HE-Oligo
is used to block li
ndary capture. For
eq Library Kit A. In
ode 1-12 samples
Cap EZ HE-Oligo
is used to block li
ndary capture. For
eq Library Kit B. In
ode 13-24 samples
Cap EZ Accessor
ponents for proces
aries; includes COT
dization and High
e Water for LM-PC
Cap EZ Reagent K
plete reagent start
ence capture usin
ything you need fo
essory Kit, and Hyb
Cap EZ Reagent K
ordering informatio
ng Solutio
er Library
nucleotide libraries
ustomer-developed
hly specific, uniform
captures regions i
umables
ation and Wash K
p EZ Hybridization
ts. All buffers for th
ne convenient kit,
er Reagent
ent to block repeti
Cot-1 DNA is not
cifically with Roche
pture Bead Kit
ure and purificatio
a DNA sample libr
sensitive and robu
ncing results.
Kit A
ibrary adapters in
r labs performing s
ncludes hybridizati
and PCR Grade W
Kit B
brary adapters in
r labs performing s
ncludes hybridizatio
s and PCR Grade W
ry Kit
ssing sequence ca
T DNA to block rep
Fidelity PCR Mast
CR during pre/pos
Kit
ter kit (24 reaction
g Illumina Sequen
r target enrichmen
bridization and Was
Kit Plus
on contact your loc

ons
s for target regions
d capture protocol
m capture of targe
in any genome.
Kit
n and Wash Kit is a
he hybridization an
configured specifi
itive regions in the
available. SeqCap
e SeqCap EZ Deve
on beads to preven
rary from contamin
ust method for clea
hybridization to pr
sequence capture w
on enhancing (HE
Water.
hybridization to pr
sequence capture w
on enhancing (HE
Water.
apture using SeqCa
petitive regions du
ter, TS-PCR Oligos
st capture amplifica
s) for customers p
ncing Systems. Eas
nt. Includes HE-Oli
sh Kit.
cal representative.
s in non-
s. Reduce
et regions up to
a reagent kit
nd washing
ically for the
e genome
EZ Developer
eloper
nt secondary
nants during
anup of DNA
revent
with Illumina
E) oligos to
revent
with Illumina
) oligos to
ap EZ
ring
s, and PCR
ation.
performing
sily order
igo Kit A,

06 740 278 001
06 471 684 001
06 471 706 001
06 471 714 001
06 471 722 001
06 471 749 001
06 471 757 001
Cat. No.
05 634 261 001
05 634 253 001
06 684 335 001
06 977 952 001
06 777 287 001
06 777 317 001
06 776 302 001
06 776 345 001
06 953 212 001
06 953 247 001

4 reactions
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions
Pack Size
24 reactions
96 reactions

1 ml

24 reactions

96 reactions

96 reactions

24 reactions
96 reactions

24 reactions

1 kit

5.200,00
12.096,00
18.144,00
30.240,00
48.384,00
129.024,00
241.920,00
Price in
126,00
269,00
270,00
460,00
1.150,00
1.200,00
600,00
2.400,00
1.530,00
inquire

5
89

e.com
5

6

6
Ce
90

www.r

Ce
Ima
Ced
Prod
Cede

Cede
Analy
imag
Ced
Prod
Cede

The C
using
cell d
diam
Ced
Prod
Cede

Cede
brigh
Cede

Cede
of Ce
availa
Reag
Cede

Cede
Cede
as a c
Cede

Cede
and C
comp
Cede

Cede
on th
meas
Solut
Cede

Cede
on th
meas
Solut
Cede

Cede
on th
meas
Solut
Cede

The r
main
reage
Cede

Trypa
deter
solut
HiRes
Cede

These
Cede
Syste
hardw

ell Biolog
roche-applied-sc
ell Counter
age based C
dex XS Analyz
duct Name
ex Smart Slides
ex Smart Slides are
yzers. Their materi
e based analysis o
dex HiRes An
duct Name
ex HiRes Analyze
Cedex HiRes Syste
g Trypan Blue stain
diameter, aggregat
eter and cell comp
dex HiRes An
duct Name
ex Calibration Be
ex Calibration Bead
htness adjustments
ex Cleaning Solu
ex Cleaning Solutio
edex and Cedex Hi
able as a compone
gent Kit and as a se
ex Detergent Sol
ex Detergent is req
ex and Cedex HiRe
component of the
ex Detergent Sol
ex Detergent is req
Cedex HiRes Syste
ponent of the Cede
ex HiRes Control
ex HiRes Control B
he Cedex HiRes Sys
surement results a
tion (510
5
/ml 1
ex HiRes Control
ex HiRes Control B
he Cedex HiRes Sys
surement results a
tion (110
6
/ml 1
ex HiRes Control
ex HiRes Control B
he Cedex HiRes Sys
surement results a
tion (510
6
/ml 1
ex HiRes Reagen
ready-to-use Cede
tenance routines o
ents for preparatio
ex Trypan Blue S
an Blue Solution is
rmination with Ced
ion is available as
s Reagent Kit, and
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
gy
cience.com
r and Ana
Cell Counter
zer Compone
e disposable slides
al properties, size
of cell cultures.
alyzer Compo
er
em is a fully autom
ning for measuring
tes, and morpholog
pactness.
alyzer Reage
eads
ds are used to perf
s of Cedex and Ce
ution Refill
on is required for c
Res Systems. This
ent of the Cedex R
eparate bottle.
ution
quired for cleaning
es Systems. This re
Cedex Reagent Ki
ution Refill
quired for cleaning
ems. This ready-to-
ex Reagent Kit and
Beads
eads are used to p
stem. Regular use
nd documentation
10%), in 20% ethan
Beads
eads are used to p
stem. Regular use
nd documentation
10%), in 20% ethan
Beads
eads are used to p
stem. Regular use
nd documentation
10%), in 20% ethan
nt Kit
ex HiRes Reagent K
of the Cedex HiRes
on, staining, and an
Solution Refill
s required as an ex
dex and Cedex HiR
a component of th
d as a separate bot
s (30%)
the 30% viability of
es Systems. They a
for quick and relia
lyzer
rs and Analy
ents
s for use with Cede
and volume are op
onents
ated image-based
g cell concentratio
gical parameters, s
ents
form automated fo
dex HiRes Analyze
cleaning of the cap
ready-to-use solu
Reagent Kit and Ce
the capillary syste
eady-to-use solutio
it and as a separat
the capillary syste
-use solution is av
d as a separate bot
perform System Su
allows monitoring
n of system integrit
nol (v/v).
perform System Su
allows monitoring
nol (v/v).
perform System Su
allows monitoring
nol (v/v).
Kit is used for clea
s Analyzers. Conta
nalysis of eukaryot
xclusion stain for v
Res Systems. This r
he Cedex Reagent
ttle.
f cell culture suspe
re used for the com
able status checks
yzers
ex XS
ptimal for
d cell analyzer
n, cell viability,
such as cell
ocus and
ers.
pillary system
ution is
edex HiRes
em of the
on is available
te bottle.
em of Cedex
ailable as a
ttle.
uitability Tests
g of
ty. Bead
uitability Tests
g of
ty. Bead
uitability Tests
g of
ty. Bead
aning and
ains all
tic cells.
viability
ready-to-use
Kit, Cedex
ensions using
mprehensive
of optical

Cat. No.
05 650 801 001
Cat. No.
05 650 216 001
Cat. No.
05 650 470 001
05 650 666 001
05 650 496 001
05 650 658 001
05 650 780 001
05 650 771 001
05 650 763 001
05 650 798 001
05 650 640 001
05 650 704 001

15 smart slid
1 instrument w
1 set for app
Pack Size
des for a total of 12
measurements

Pack Size
with PC, monitor, a

Pack Size
20 ml

4 x 60 ml

1,000 ml

4 x 60 ml

30 ml

30 ml

30 ml

proximately 100 me

4 x 60 ml

30 ml

20 cell culture
and accessories
easurements

Price in
inquire
Price in
inquire
Price in
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Ce

Cede

These
Cede
Syste
hardw
Cede

These
Cede
Syste
hardw
Cede

These
Cede
Syste
hardw
Dens

These
Cell A
size a
Cede
Ced
Prod
Cede

The C
HiRes
chara
Cede

Addit
Syste
in hig
Cede

Cede
Syste
cultu
desig
Ced
Prod
Cede

Cede
Cede
and d
in 20
Cede

Cede
Cede
and d
in 20
Cede

Cede
Cede
and d
in 20
Cede

Read
Analy
(Tryp
Ced
Prod
Cede

The C
to an
cell c

ell Biolog
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
sity Reference St
e beads are used t
Analyzers. They mi
and optical proper
ex Software.
dex HiRes An
duct Name
ex HiRes Control
Cedex HiRes Contr
s Analyzer to analy
acteristics of cell c
ex MS 20 Sample
tional tray for use
em. Suitable for pre
gher throughput m
ex Sample Cups
ex Sample Cups ar
ems. Their material
re sample prepara
gned for single use
dex Analyzer
duct Name
ex Control Beads
ex Control Beads a
ex System. Regular
documentation of
% ethanol (v/v).
ex Control Beads
ex Control Beads a
ex System. Regular
documentation of
% ethanol (v/v).
ex Control Beads
ex Control Beads a
ex System. Regular
documentation of
% ethanol (v/v).
ex Reagent Kit
dy-to-use kit for cle
yzer. The kit also c
pan Blue), and ana
dex Analyzer
duct Name
ex Control Unit
Cedex Control Unit
nalyze concentratio
cultures.
gy
s (60%)
es Systems. They a
for quick and relia
s (80%)
es Systems. They a
for quick and relia
s (100%)
the 100% viability o
es Systems. They a
for quick and relia
tandard Beads
to calibrate and ad
imic cell behavior
rties, they will be d
alyzer Acces
Unit
rol Unit is used in
yze concentration,
cultures.
e Tray
with the Multi Sam
eparation of additi
measurement work
e for use with auto
l properties, size, a
ation and measure
e only.
Reagents
s
re used to perform
r use allows monito
system integrity. B
s
re used to perform
r use allows monito
system integrity. B
s
re used to perform
r use allows monito
system integrity. B
eaning and mainte
contains all reagen
lysis of eukaryotic
Accessories
t is used in combin
on, viability, and m
re used for the com
able status checks
re used for the com
able status checks
of cell culture susp
re used for the com
able status checks
djust Cedex and Ce
in flow dynamics.
etected as dead ce
ssories
combination with
viability, and mor
mpler delivered wit
onal samples in pa
kflows.
omated Cedex and
and volume are ide
ment. Cedex Samp
m System Suitabilit
oring of measurem
Bead Solution (51
m System Suitabilit
oring of measurem
Bead Solution (11
m System Suitabilit
oring of measurem
Bead Solution (51
enance routines of
nts for preparation,
cells using the Ce
nation with the Ce
orphological chara
ensions using
mprehensive
of optical
ensions using
mprehensive
of optical
pensions using
mprehensive
of optical
edex HiRes
Due to their
ells by the
the Cedex
phological
th the Cedex
arallel for use
d Cedex HiRes
eal for cell
ple Cups are
ty Tests on the
ment results
0
6
/ml 10%),
ty Tests on the
ment results
0
6
/ml 10%),
ty Tests on the
ment results
0
5
/ml 10%),
f the Cedex
, staining
edex System.
edex Analyzer
acteristics of

05 650 712 001
05 650 739 001
05 650 747 001
06 422 659 001
06 422 667 001
Cat. No.
06 412 874 001
05 650 569 001
05 650 623 001
Cat. No.
05 650 526 001
05 650 534 001
05 650 542 001
05 650 615 001
Cat. No.
06 412 866 001

1 cont
1
1
1
1 set for app
1 cont
30 ml

30 ml

30 ml

1 x 10 ml batch A
1 x 10 ml batch B

Pack Size
trol unit with recov

1 sample tray

500 cups

Pack Size
100 ml (5 x 10
6
/m

100 ml (1 x 10
6
/m

100 ml (5 x 10
5
/m

proximately 100 me

Pack Size

www.roche
A
B
very CD
l)
l)
l)
easurements
very CD
e-applied-science

inquire
inquire
inquire
inquire
inquire
Price in
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
Price in
inquire

6
91

e.com
6

6

6
Ce
92

www.r

Ced
Prod
Cede

Provi
This
envir
21 CF
Cede

Cede
Cede
Ced
Prod
Cede

Provi
Analy
envir
21 CF
Cede

Cede
previ
versio
Cede

This
Cede
integ
HiRes
Elec
CAS
Prod
CASY

The C
Analy
capil
m.
CASY

The C
and A
150
0.7 to
CASY

The C
for qu
docu
3.2 to
CASY

The C
for qu
docu
size r
CAS
Prod
CASY

Regu
capil
reage
syste
CASY

CASY
Coun
of ce

ell Biolog
roche-applied-sc
dex Analyzer
duct Name
ex 2.3 Software P
des comprehensiv
new software is de
onments, featuring
FR part 11 complia
ex 2.x to 2.3 Upg
ex 2.x to 2.3 Upgrad
ex 2.x Software ver
dex HiRes An
duct Name
ex HiRes 2.3 Soft
des comprehensiv
yzer. This new soft
onments, featuring
FR part 11 complia
ex HiRes 2.x to 2
ex HiRes 2.x to 2.3
ous Cedex HiRes 2
on 2.3.
ex HiRes SW 2.3
is a software interf
ex HiRes Analyzers
ration into existing
s SW V 2.2 Remote
ctrical Curre
SY System Co
duct Name
Y Model TT 150
CASY Model TT 15
yzer for quality con
lary, it enables the
Y Model TT 45, 6
CASY Model TT 45
Analyzer for quality
m capillaries, it en
o 120 m.
Y Model TTC 150
CASY Model TTC i
uality control of ce
mentation. It uses
o 120 m.
Y Model TTC 45,
CASY Model TTC i
mentation. It uses
range of 0.7 to 120
SY System Re
duct Name
Y clean
ular use of CASY c
laries of CASY Sys
ent prevents block
em.
Y blue
Y blue is a highly s
nter and Analyzers
lls to guarantee ce
gy
cience.com
Software
Package
ve analysis tools fo
esigned for project
g User and Rights
ance.
rade Package
de Package enable
sions to Cedex Sof
alyzer Softwa
tware Package
tware is designed f
g User and Rights
ance.
.3 Upgrade Pack
Upgrade Package
2.x software versio
Remote Control
face for on-site rem
s. Enables easy rea
g data managemen
e Control.
ent Based C
omponents
m
50 m is a multi-pa
ntrol of cell culture
e analysis of object
60, 150 m
5, 60, 150 m is a m
y control of cell cu
nables the analysis
0 m
s a fast multi-para
ell cultures with int
a 150 m capillary
, 60, 150 m
s a fast multi-para
45, 60, and 150 m
0 m.
eagents
lean protects the i
stems from biologic
kages and encrusta
specific alcoholic d
for viability determ
ell identity.
or operating the Ce
ts in cGMP regulat
Management and
es the upgrade of
ftware version 2.3.
are
or operating the Ce
for projects in cGM
Management and
kage
enables the upgra
ons to Cedex HiRes
mote control of Ce
ad out of result dat
nt systems; succes
Cell Counter
arameter Cell Coun
es. Equipped with a
ts in the size range
multi-parameter Ce
ultures. Equipped w
s of objects in the
ameter Cell Counte
tegrated data evalu
y for analysis in th
ameter Cell Counte
tegrated data evalu
m capillaries for an
nstrument and me
cal deposits. By em
ations of the intern
dilution used with t
mination and for q
edex Analyzer.
ted
d Audit Trail for
all previous
.
edex HiRes
MP regulated
d Audit Trail for
ade of all
s Software
edex and
ta for flexible
ssor to Cedex
rs and Analy
nter and
a 150 m
e of 3.2 to 120
ell Counter
with 45, 60, and
size range of
er and Analyzer
uation and
e size range of
er and Analyzer
uation and
nalysis in the
easurement
mulsifying, this
nal liquid
the CASY Cell
uality control

Cat. No.
07 045 271 001
07 045 298 001
Cat. No.
07 045 280 001
07 045 301 001
07 045 344 001
yzers
Cat. No.
05 651 697 001
05 651 735 001
05 651 719 001
05 651 727 001
Cat. No.
05 651 786 001
05 651 760 001

1 binder w
1 binder w
1 binder w
1 binder w
1 en
Pack Size
with CD and Opera

with CD and Opera

Pack Size
with CD and Opera

with CD and Opera

nvelope with instal

Pack Size
1 instrument

1 instrument

1 instrument

1 instrument

Pack Size
3 x 500 ml

4 x 30 ml

ator's Guide
ator's Guide
ator's Guide
ator's Guide
ll CD

Price in
inquire
inquire
Price in
inquire
inquire
inquire
Price in
inquire
inquire
inquire
inquire
Price in
inquire
inquire

Ce

CASY

CASY
cell c
cond
pH a
CAS
Prod
CASY

The m
cell c
using
from
Disp

This C
liquid
using
in pu
CASY

CASY
CASY
and b
Ce
Hig
Cell
Prod
DNA

The D
assay
micro
Cell

Simp
viabil
cellu
appli
Phos

For fa
conju
divid
for ce
Tra
Non
Prod
X-tre

State
delive
trans
effec
X-tre

Non-
cytot
trans
Ideal
X-tre

Trans
(siRN
and h
there

ell Biolog
Y ton
Y ton is a ready-to
cultures for use wit
uctivity guarantee
nd osmolarity ensu
SY System Ac
duct Name
Y cups
material properties
culture sample pre
g CASY Cell Count
adhering to the cu
penser 2 - 10 ml
Ceramus Dispense
d volumes in increm
g CASY Cell Count
urity and volume pr
Y rack
Y racks are used fo
Y Cell Counters an
black in color, hold
ell Imaging
gh-Throughp
lavista Imagi
duct Name
A Fragmentation I
DNA Fragmentatio
y to detect apoptos
oplates. It is ideal f
Viability Imaging
ple, accurate and fa
lity using fluoresce
lar workflows, esp
cations. Optimized
spho-Histone H3
ast, accurate quan
ugated antibodies.
ing cells on 96-we
ell-based workflow
ansfection
n-Liposoma
duct Name
emeGENE HP DN
e-of-the-art high p
ery of DNA into a w
sfect cells. Free of a
ts.
emeGENE 9 DNA
-liposomal multi-co
oxicity, minimal ne
sfection efficiency
for all cellular ana
emeGENE siRNA
sfection reagent fo
NA) into many cell
hard-to-transfect c
efore does not requ
gy
-use, isotonic, and
th CASY Cell Coun
s constant measur
ure cell size preser
ccessories
s, size, and volume
paration. Use to d
ters and Analyzers
up walls.
er is used for high
ments of 0.25 ml o
ters and Analyzers
recision.
or easy sample ha
nd Analyzers. Each
ds up to 24 CASY c
g Systems
put Cell Ima
ng Reagents
Imaging Kit
on Imaging Kit prov
sis induction in ma
for high throughpu
g Kit
ast (35 minutes) on
ence detection and
ecially for medium
d for 96-well plates
3 Imaging Kit
ntification of mitotic
Ideal for accurate
ell microplates. Qui
ws.
n
al Transfecti
NA Transfection R
erformance transf
wide range of euk
animal-derived co
A Transfection Re
omponent transfec
eed for optimizatio
in many cell lines,
alysis applications.
Transfection Rea
or efficiently delive
types (HeLa, NIH
cell lines (HT29). F
uire media change
d isoosmotic dilutio
nters and Analyzer
rement results. Its
rvation.
e of CASY cups are
ilute and analyze c
s. Cup material pre
ly reproducible adj
of CASY ton for me
s. It guarantees opt
ndling when work
rack, made of pol
cups.
s
agine Platfor
vides a simple and
ammalian cells in 9
ut cellular workflow
ne-step assay to m
d for quality contro
m to high throughp
s.
c cells using Alexa
e and fast quantific
ickly determine ce
ion Reagent
Reagent
ection reagent for
karyotic cells, inclu
mponents and low
eagent
ction reagent with
on, and ability to pr
even in the presen
.
agent
ering short interferi
3T3, HEK-293, CH
Functions with or w
es.
on liquid for
rs. Its defined
physiological
e optimal for
cell samples
events cells
justment of
easurements
timum quality
king with the
lyoxymethylene
rm
d rapid TUNEL
96-well
ws.
meausre cell
ol of cells in
put
aFluor
488
cation of
ell cycle status
ts
efficient
ding hard-to-
w cytotoxic
very low
rovide high
nce of serum.
ing RNA
O-K1, COS-7),
without serum,

05 651 808 001
Cat. No.
05 651 794 001
05 651 751 001
05 651 743 001
Cat. No.
06 432 344 001
06 432 379 001
06 569 161 001
Cat. No.
06 366 244 001
06 366 236 001
06 366 546 001
06 365 779 001
06 365 787 001
06 365 809 001
04 476 093 001
04 476 115 001

1
1 kit f
fo
1 ml (1 mg/m
5 x 1 ml (2,000
10 l container

Pack Size
1,800 cups with lid

1 dispenser

1 rack for 24 cups

Pack Size
96 tests

for up to 5 x 96 rea

or up to 5 x 96 test

Pack Size
0.4 ml
1.0 ml
5 x 1 ml
0.4 ml
1.0 ml
5 x 1.0 ml
l) (400 transfection
plate)
0 transfections in a

www.roche
ds
s
actions
ts
ns in a 24-well
a 24-well plate)
e-applied-science

inquire
Price in
inquire
inquire
inquire
Price in
685,00
320,00
450,00
Price in
214,30
424,50
1.643,20
200,30
397,20
1.535,90
255,90
1.087,00

6
93

e.com
6

6

6
Ce
94

www.r

Lip
Prod
DOTA

High
for tr
charg
and p
Ce
Ant
Prod
Amp

Amp
medi
BM-

For th
obvio
been
spect
G-41

High
mem
the n
cells.
Hygr

Hygro
synth
phen
hygro
Kana

Amin
of gra
cultu
Mito

Poten
studi
crysta
filteri
Peni

Preve
inhib
Strep
inhib
Ser
Prod
Tran

Trans
formu
cells
Insul

Conta
free c
facto
facto

ell Biolog
roche-applied-sc
osomal Tran
duct Name
AP Liposomal Tr
ly efficient transfec
ransient or stable g
ged molecules, suc
proteins into mam
ell Culture
tibiotics
duct Name
picillin
icillin is ideal for g
a, it selects for pla
Cyclin
he elimination of m
ous marked cytotox
tested and compa
tinomycin, lincomy
18 Solution
ly pure, convenien
brane, selects for
neomycin resistanc
Eliminates contam
romycin B
omycin B is an am
hesis in prokaryote
otype of eukaryoti
omycin-resistance
amycin sulfate
noglycosidic antibio
am-positive, gram
re. Also used to st
omycin C
nt DNA crosslinke
es of cell-free prot
alline form. Biobur
ng (e.g., Millipore
cillin-Streptomyc
ent and eliminate b
its bacterial growt
ptomycin, aminogly
iting protein synth
rum-free Me
duct Name
sferrin
sferrin, like insulin
ulations. The main
by receptor-media
lin-Transferrin-S
ains the most esse
culture media in a
r supplement to w
rs are added.
gy
cience.com
nsfection Re
ransfection Reag
ction of DNA inclu
gene expression, a
ch as RNA, oligos,
malian cells.
Reagents
ene-cloning strate
asmid-bearing, dru
mycoplasma from i
xic side effects. Th
ared to other antib
ycin, gentamicin).
t, antibiotic, filtere
eukaryotic cells th
ce gene, and maint
minating fibroblast
minoglycosidic antib
es and eukaryotes.
ic cells that are sta
gene (hyg or hph
otic with broad sp
-negative bacteria
tudy cell-free prote
r. Inhibits DNA syn
tein biosynthesis. M
rden reduction in s
e).
cin
bacterial contamin
th by inhibiting pep
ycoside antibiotic,
hesis.
edia Supple
, is a component o
function of transf
ated endocytosis.
Sodium Selenite S
ential growth-prom
n optimized ratio.
which other cell typ
eagents
ent
uding YACs into eu
nd for transfer of n
nucleotides, RNP
s
egies. When prese
ug-resistant bacter
infected cell cultur
he efficiency of BM
biotics (kanamycin
ed through 0.2 m
hat are stably trans
tains the phenotyp
ts from mixed cultu
biotic that inhibits
Selects and maint
ably transfected wi
h ).
ectrum inhibition o
a and mycoplasmas
ein biosynthesis.
nthesis and is an in
Mitomycin is provi
solution is obtained
nants in cell culture
ptidoglycan synthe
inhibits bacterial
ements
of most serum-free
ferrin is to transpo
Supplement
moting components
It is used as a bas
pe-specific nutrien
ukaryotic cells
negatively
complexes,
nt in growth
rial colonies.
res without
M-Cyclin has
, tylosine,
m pore size
sfected with
pe of resistant
ures.
protein
tains the
ith the E. coli
of the growth
s in cell
nhibitor for
ided in a
d by 0.2 m
e. Penicillin G
esis.
growth by
e media
rt iron into
s of serum-
al growth-
ts and growth

Cat. No.
11 202 375 001
Cat. No.
10 835 242 001
10 835 269 001
10 799 050 001
04 727 878 001
04 727 894 001
10 843 555 001
10 106 801 001
10 107 409 001
11 074 440 001
Cat. No.
10 652 202 001
11 074 547 001

5
37.5 m
20 ml
100 ml
1 g
for 20 ml
20 ml (30 mg/
m
50
Pack Size
x 400 l (5 x 400

Pack Size
5 g
50 g

mg (for 2 x 2.5 l me

- equivalent to 1 g
- equivalent to 5 g

(20 ml sterile-filte

5 g

2 mg

((500x), lyophiliza

Pack Size
/ml; in IMDM, filter
pore size membra

0 mg (for 5 l mediu

g)
edium)
g G-418
g G-418
ered)
te, sterile)
red through 0.2
ane)
um)

Price in
327,80
Price in
43,40
260,20
113,10
98,50
424,20
304,10
215,30
50,50
67,10
Price in
496,70
168,80

Ce

Atta
Prod
Colla

Colla
for th
lyoph
Fibro

Prom
adhe
and p
dishe
Fibro

Prom
adhe
and p
coati
Lami

Coat
prom
huma
neuro
Mit
Prod
BM-

Supp
RPM
and c
cells
Colc

Colce
the p
Phyt

Cons
high-
High
lymp
Phyt

Phyto
phyto
prolif
Hyb
Kits
Prod
Mou

Easy,
mous
of all
type.
IsoSt

High
and l
comp
addit

ell Biolog
achment Fa
duct Name
agen
agen is used as a s
he coating of cultu
hilizate is cell cultu
onectin
motes attachment a
sion region (cell b
promotes their bin
es. Lyophilizate.
onectin (pure)
motes attachment a
sion region (cell b
promotes their bin
ng of culture dishe
inin
cell culture dishes
mote attachment an
an carcinoma, sarc
oblastoma and em
togens
duct Name
Condimed
plement (10%, v/v)
I 1640, DMEM), co
chorionic villi cells
and peripheral blo
cemid
emid inhibits the fo
percentage of meta
ohemagglutinin-
sists of only L-type
-efficiency inductio
ly purified and test
hocytes.
ohemagglutinin-
ohemagglutinin PH
ohemagglutinin. It
feration in lymphoc
bridoma Rea
s for Isotyping
duct Name
use IgG ELISA
, fast (2-4 hours), a
se IgG in hybridom
mouse IgG-subcla
No crossreactivity
trip Mouse Mono
ly specific, fast and
ight-chain types o
parable results to t
tional equipment a
gy
actors
substrate for cultur
re dishes and the
ure grade.
and subsequent sp
binding domain) int
ding and spreadin
and subsequent sp
binding domain) int
ding to and spread
es. Highly purified
s with this highly p
nd growth of a var
coma, and retinobl
mbryonic carcinoma
to normal culture
ontaining 10-20%
. Improves culture
ood leukocytes.
ormation of mitotic
aphase cells for ch
-L (PHA-L)
subunits (isolectin
on and functional
ted for high-efficie
-M (PHA-M)
HA-M is the mucop
is a potent mitoge
cyte cultures.
agents
g
and sensitive (10 n
ma supernatants, as
asses are detected
y with FBS.
oclonal Antibody
d easy kit for rapid
of mouse monoclon
the standard ELISA
and reagents.
ring a variety of ce
preparation of col
preading of cells. T
teracts with mamm
ng on plastic. Use t
teracts with mamm
ding on plastic. Us
lyophilizate.
pure attachment fa
iety of cell types, in
lastoma cells, and
a cells.
basal medium (e.g
FCS to cultivate hu
conditions for bon
c spindles. It is use
hromosome analys
n L4, leuko-agglut
analysis of T-lymp
ency stimulation of
protein form of
en used to stimulat
ng/ml) ELISA for de
scites, mouse sera
d independent of li
y Isotyping Kit
d identification of c
nal antibodies. Yie
A assay without the
ells. It is used
lagen gels. The
The cell
malian cells
to coat culture
The cell
malian cells
sed for the
actor to
ncluding
murine
g., F 10, M 199,
uman amniotic
ne marrow
ed to increase
is.
tinin). Ideal for
phocytes.
f human
te cell
etermining
a, etc. Presence
ight-chain
class, subclass,
elds
e need for

Cat. No.
11 179 179 001
10 838 039 001
11 051 407 001
11 080 938 001
11 243 217 001
Cat. No.
10 663 573 001
10 295 892 001
11 249 738 001
11 082 132 001
Cat. No.
11 333 151 001
11 493 027 001

20 ml ((10 g/
1 k
1
Pack Size
30 mg

5 mg

1 mg
5 mg

1 mg (2 ml)

Pack Size
100 ml

/ml), filtered throug
size membrane)

5 mg

20 mg

Pack Size
kit for up to 400 te

kit for up to 10 tes

www.roche
gh 0.2 m pore
ests
sts
e-applied-science

Price in
138,60
546,70
174,60
694,00
240,30
Price in
291,90
45,10
349,30
150,20
Price in
654,80
314,70

6
95

e.com
6

6

6
Ce
96

www.r

Med
Prod
BM C

BM C
the g
used
thaw
Hybr

Supp
cell h
cells
thaw
Nutr

Defin
grow
Optim
serum
Nutr

Serum
with
P3x63
and o
Polye

Cell f
soma
quali
aldeh
My
Prod
Myco

Photo
conta
cultu
detec
DAP

DAPI
and f
speci
fluore
BM-

For th
obvio
been
spect
Kana

Amin
of gra
cultu
Gro
Sin
Prod
Basi

Mitog
vascu
chon
and l
Basi

Mitog
vascu
chon
and l

ell Biolog
roche-applied-sc
dia Suppleme
duct Name
Condimed H1
Condimed H1 is a s
growth of B-cell hy
to replace feeder
ing cells stored in
ridoma Fusion an
plement to the norm
hybridomas after fu
and is also used to
ing of cells stored
idoma-CS
ned supplement re
wth of SP2/0-, P3x6
mizes growth of fre
m-free cell culture
idoma-SP
m-free media supp
an intact cholester
3Ag8.653, and lym
other cell types (ne
ethylene Glycol 1
fusion induced by
aticcell genetics an
ty PEG does not ne
hydes not detectab
ycoplasma
duct Name
oplasma PCR EL
ometric ELISA for t
aminating Mycopla
res or other samp
ction for fast (6 hrs
I
I is a fluorescent d
forms strongly fluo
ificity. It is commo
escence microscop
Cyclin
he elimination of m
ous marked cytotox
tested and compa
tinomycin, lincomy
amycin sulfate
am-positive, gram
re. Also used to st
owth Fact
gle Reagen
duct Name
c Fibroblast Grow
gen for mesoderm
ular and corneal en
drocytes, and oste
imb and lens rege
c Fibroblast Grow
gen for mesoderm
ular and corneal en
drocytes, and oste
imb and lens rege
gy
cience.com
ents
supplement to nor
ybridomas after fus
cells, and optimize
liquid nitrogen.
nd Cloning Suppl
mal culture mediu
usion and during c
o optimize the gro
in liquid nitrogen.
eplaces FBS in hyb
63Ag8.653-, and NS
eshly fused hybrido
without feeder ce
plement for murine
rol biosynthesis pa
mphoblastoid cell li
eural explants).
1500
polyethylene glyco
nd the production
eed to be tested p
ble; free from Ca
2+

a Detectio
LISA
the detection of PC
asma, Acholeplasm
le materials. Ready
s) and semi-autom
ye that binds selec
orescent DNA-DAP
nly used to detect
py.
mycoplasma from i
ared to other antib
ycin, gentamicin).
otic with broad sp
-negative bacteria
tors and C
ts
wth Factor (156 A
m- and neuroectode
ndothelial, muscle
eoblasts). Induces
eneration in vivo .
wth Factor, huma
m- and neuroectode
ndothelial, muscle
eoblasts). Induces
eneration in vivo .
rmal culture mediu
sion and during clo
es growth of hybri
lement
m to support the g
cloning. HFCS repl
owth of hybridomas
.
ridoma cell culture
S-1-derived hybrid
omas during selec
ells.
e myelomas and h
athway (derived fro
nes), primary lymp
ol is a standard me
of hybridoma cells
prior to use. Peroxid
.
on and Elim
CR-amplified DNA
ma, and Ureaplasm
y-to-use mix and E
matic sample proce
ctively to double-s
PI complexes with
Mycoplasma in ce
he efficiency of BM
biotics (kanamycin
ectrum inhibition o
a and mycoplasmas
ein biosynthesis.
Cytokines
Aa), bovine (bbF
erm-derived cells
e, and glial cells, m
vessel growth, wo
an (hbFGF)
erm-derived cells
vessel growth, wo
um to support
oning. It is
domas after
growth of B-
aces feeder
s after the
es. Supports
domas.
ction/cloning in
ybridomas
om SP2/0,
phoid cultures,
ethod in
s. This high
des and
mination
A of
ma in cell
ELISA
essing.
stranded DNA
high
ell culture via
res without
M-Cyclin has
, tylosine,
of the growth
s in cell
FGF)
(fibroblasts,
yoblasts,
und healing,
(fibroblasts,
yoblasts,
und healing,

Cat. No.
11 088 947 001
11 363 735 001
11 363 743 001
11 011 375 001
10 783 641 001
Cat. No.
11 663 925 910
10 236 276 001
10 799 050 001
10 106 801 001
Cat. No.
11 104 616 001
11 120 417 001
11 123 149 001

1
1 kit
37.5 m
Pack Size
100 ml (10x)

10 ml (50x)

10 ml (50x)

100 ml (100x) steri

10 x 4 ml

Pack Size

10 mg


5 g

Pack Size
10 g

25 g
10 g

le
tions
edium)

Price in
411,80
219,10
180,30
762,70
130,10
Price in
810,20
68,20
113,10
215,30
Price in
302,00
769,90
342,00

Ce

Endo

ECGF
stimu
has a
grow
Epide

Reco
prolif
and m
formu
Eryth

Eryth
differ
respo
and a
Insul

Insul
stimu
insul
prima
Inter

Reco
purifi
inves
Inter

Reco
purifi
the s
Inter

Reco
purifi
mono
for a
Inter

Allow
natur
lymp
thym
Inter

Supp
inhib
inhib
pharm
Inter

Reco
cells,
murin
stand
Tran

Trans
grow
Reco
stand
Tumo

Has c
activa
activi
Reco
Tumo

Has c
activa
activi
Reco
Tumo

TNF-
tumo
cytos
syner

ell Biolog
othelial Cell Grow
F and basic fibrobl
ulate the growth of
also been reported
wth of hybridomas a
ermal Growth Fa
ombinant, human E
feration and differe
mesodermal origin
ulations.
hropoietin, huma
hropoietin is a glyc
rentiation of erythr
onsive to EPO have
adult spleen.
lin, human
in has many activit
ulates growth and
in activity on sensi
ary cells and cell li
rferon-, human
ombinant Interferon
ied by standard ch
stigate IFN- activ
rferon-, mouse
ombinant, Interfero
ied by standard ch
tudy of IFN- (int
rleukin-1, huma
ombinant Interleuk
ied by standard ch
ocytes or macroph
variety of sensitive
rleukin-2, human
ws cultivation of hu
ral killer cell lines a
hocytes and natur
ocyte, splenocyte,
rleukin-2, mouse
ports growth of mu
its binding of reco
its binding to hum
macological/physio
rleukin-6, human
ombinant IL-6, hum
and can be used
ne and human hyb
dard chromatograp
sforming Growth
sforming Growth F
wth factor affecting
ombinant, human T
dard chromatograp
or Necrosis Fact
cytolytic, cytostatic
ating/growth stimu
ity on cell types in
ombinant (E. coli ),
or Necrosis Fact
ating/growth stimu
ombinant (yeast), 1
or Necrosis Fact
causes selectiv
or-bearing mice. In
static activity on ce
rgistically with inte
gy
wth Factor, bovin
ast growth factor a
f endothelial cells.
d to eliminate the n
and other cell type
actor, human (hEG
Epidermal Growth
entiation of a wide
n, and is a constitu
an (hEPO)
oprotein which sti
roid precursor cells
e been identified in
ties on somatic ce
proliferation of ce
itive cells. Compon
ines.
n (hIFN-)
n-, human (hIFN
hromatographic tec
vities in human ce
e (mIFN-)
on-, mouse (mlFN
hromatographic tec
terferon-) action
an (hIL-1)
in-1, human (hI
hromatographic tec
hages and other ce
e cells.
n (hIL-2)
uman/murine IL-2
and proliferation o
ral killer cells. Estab
or PBL derived T-
e (mIL-2)
urine CTLL cells, no
ombinant hIL-2 to m
man responder cells
ological IL-2 activi
n (hIL-6)
man is a growth fac
to replace feeder
bridomas. It is prod
phic techniques.
h Factor-1, hum
Factor-1, human (
many functions in
TGF- 1 is produce
phic techniques.
or-, human (hT
c activity on transfo
ulating activity on
vitro , and can cau
10 g/ml PBS, 1 m
or-, human (hT
ulating activity on
vitro , and can cau
0 g/ml PBS, 1 mg
or-, mouse (m
ve necrosis of muri
n vitro , human TNF
ertain transformed
erferon-.
ne (bECGF)
are the only mitog
ECGF, bovine (cul
need for feeder cel
es.
GF)
Factor (EGF) stimu
e variety of cells of
ent of many serum
mulates proliferati
s to mature erythro
n adult bone marro
ells. Recombinant h
lls and is used to i
nent of serum-free
N-), is produced
chniques. It can be
ll systems.
N-) is produced
chniques. It is a va
ns in mouse mode
L-1) is produced
chniques. Secreted
ell types, it is a plei
dependent T-cell
of mitogen-activate
blishes human/mu
cell lines.
ot human T-cells. S
murine responder
s. Study
ity in murine mode
ctor for murine and
cells in the prepar
duced in E. coli an
man (hTGF-1)
(hTGF-1), is a mu
n a variety of differ
ed in CHO cells an
TNF-)
ormed cell lines,
many normal cells
use tumor necrosis
mg/ml BSA.
TNF-)
ormed cell lines,
many normal cells
use tumor necrosis
g/ml BSA.
mTNF-)
ine tumors when i
F- has direct cyt
cells. In this conte
gens that
lture grade)
lls in the clonal
ulates the
ectodermal
m-free media
on and
ocytes. Cells
ow, fetal liver,
human insulin
nvestigate
e media for
in E. coli and
e used to
in E. coli and
aluable tool for
l systems.
d in E. coli and
d by activated
iotropic factor
lines and
ed T-
urine
Strongly
cells; weakly
els.
d human B-
ration of
nd purified by
ultifunctional
rent cells.
nd purified by
s, antiviral
s in vivo .
s, antiviral
s in vivo .
njected into
tolytic or
ext, it acts

11 033 484 001
11 376 454 001
11 120 166 001
11 376 497 001
11 040 596 001
11 276 905 001
11 457 756 001
10 799 068 001
11 011 456 001
11 147 528 001
11 271 164 001
11 138 600 001
11 412 272 001
11 371 843 001
11 088 939 001
11 271 156 001

2
10
10
10
10
1
50
1
20
10
10
5
75 mg

100 g

250 U (2.5 g, 1 m

100 mg

00,000 U (5 g, 1 m

00,000 U (20 g, 1

00,000 U (2 g, 1 m

0,000 U (5 g, 50 m
0,000 U (5 g, 1 m
0,000 U (25 g, 5 m
0,000 U (5 g, 1 m

00,000 U (2 g, 1 m

1 g (1 ml)

g (1,000,000 U, 1

g (1,000,000 U, 1

g (2,000,000 U, 1

www.roche
l)
ml)
ml)
ml)
ml)
ml)
ml)
ml)
ml)
ml)
ml)
ml)
e-applied-science

493,60
426,10
363,80
140,40
240,20
797,70
452,70
250,20
250,20
1.046,40
294,80
257,20
702,80
908,20
908,20
401,00

6
97

e.com
6

6

6
Ce
98

www.r

ELI
Prod
EPO

The E
scien
conc
proce
hGH

Fast,
cultu
conta
comp
Re
Pro
Prod
Anti-

Mono
immu
type
-Ga

Quan
with
prote
enco
-Ga

Quan
with
techn
extra
-Ga

Optim
sectio
produ
CAT

Nonr
euka
repor
the s
hGH

Fast,
cultu
conta
comp
Lucif

Chem
lucife
lumin
film.
rGFP

Use a
PAGE
expe
easily
SEAP

Simp
medi
easily
samp

ell Biolog
roche-applied-sc
SAs
duct Name
ELISA
EPO ELISA is a fast
nce research studie
entrations in plasm
edures.
ELISA
sensitive ELISA fo
re supernatants of
aining a reporter g
parison even if kits
eporter Ge
oducts for Re
duct Name
-GFP
oclonal antibody to
unoprecipitation an
and mutant forms
al ELISA
ntitatively measure
a plasmid bearing
eins produced by in
ding DNA constru
al Reporter Gene
ntify -Gal expres
the -Gal-encodi
nology to detect ap
cts.
al Staining Set
mized staining set
ons demonstrating
uct can be seen by
ELISA
radioactively and q
ryotic cells transfe
rter gene. Assay tim
ensitivity of the rad
ELISA
sensitive ELISA fo
re supernatants of
aining a reporter g
ferase Reporter G
miluminescent assa
erase activity in tra
nometers, micropla
More sensitive tha
P
as a positive contro
E and western blot
riments involving f
y detected using b
P Reporter Gene
ple, fast, sensitive a
um of transfected
y sampled and ass
pling of medium or
gy
cience.com
t, highly sensitive a
es as a method for
ma and serum. Not
or quantitatively me
f eukaryotic cells t
gene encoding for
s are from different
ne Detect
eporter Gen
o detect GFP or GF
nd western blottin
of GFP.
e -Gal expression
a -Gal-encodin
n-frame cloning in
uct.
e Assay, chemilum
ssion in eukaryotic
ing lacZ reporter g
pproximately 20 fg
for the histochem
g -galactosidase
y the naked eye or
quantitatively meas
ected with a plasm
me approximately
dioactive CAT assa
gene encoding for
Gene Assay, high
ay for quantitative
ansfected cells. Use
ate or tube format,
an isotopic CAT as
ol when detecting
t analysis. It can al
fluorescence micro
blue or UV light.
Assay, chemilum
assay measures se
cells. SEAP is sec
sayed. Eliminating
r other analysis.
and easy assay for
r the determination
t for use in diagno
easuring hGH expr
transfected with a
hGH. Allows direc
t lots.
tion
ne Detection
FP fusion proteins
g. Anti-GFP recog
n in eukaryotic cel
ng reporter gene. Q
nto an appropriate
minescent
cells transfected w
gene. Use chemilu
-galactosidase
ical staining of cel
e activity. The -g
r using light micros
sure CAT expressio
id bearing a CAT-
4 hours. Sensitivity
ay.
easuring hGH expr
transfected with a
hGH. Allows direc
t lots.
h sensitivity
determination of f
e in manual or aut
, and scintillation c
ssay.
GFP Fusion Protei
so be used as a st
oscopy. rGFP fluore
minescent
creted placental A
reted into the supe
cell lysis allows re
r use in life
n of EPO
ostic
ression level in
plasmid
t data
n
using
nizes both wild
ls transfected
Quantify fusion
-Gal
with a plasmid
uminescence
in cell
ls and tissue
al reaction
scopy.
on in
encoding
y equivalent to
ression level in
plasmid
t data
firefly
tomated
counters or
ins by SDS-
tandard for
escence is
AP in culture
ernatant and is
peated

Cat. No.
11 693 417 001
11 585 878 001
Cat. No.
11 814 460 001
11 539 426 001
11 758 241 001
11 828 673 001
11 363 727 001
11 585 878 001
11 669 893 001
11 814 036 001
11 814 524 001
11 779 842 001

1
1 k
1 k
1 kit for 500 as
1 set for up
1 k
1 k
1 k
1 kit
1 kit for 500 a
250
Pack Size


Pack Size
200 g


ssays (microplate),
(tube format)

p to 100 tests in 3.5



it for up to 200 ass
t for up to 1,000 as

50 g (1 mg/ml)

assays, microplate
0 assays, tube form

sts
ests
ests
, for 250 assays
5 cm dishes
ests
ests
says
ssays
formate, or for
mate

Price in
711,40
543,60
Price in
342,90
456,00
458,70
200,00
431,80
543,60
297,90
1.099,80
197,40
458,70

Ce

Ap
Me
Mea
Prod
M30

Detec
early
immu
both
Casp

Use t
analy
step,
resea
Hom

Spec
deter
throu
Anti-

PARP
recog
subst
immu
Mea
Prod
Cell

Fast
requi
ELISA
cytop
Cell

Fast
ELISA
deter
fracti
Cell

Fast
ELISA
deter
fracti
Apop

For ra
gel e
a qui
apop
Me
Mea
Prod
Anne

Anne
cytom
on ou
differ
Anne

Kit w
and q
single
cellu

ell Biolog
poptosis
ethods for St
asurement of
duct Name
0 CytoDEATH
ct a cytokeratin 18
marker of apopto
unocytochemistry,
cryostat and paraf
pase 3 Activity As
this assay to detec
yze caspase 1, 2, 3
and to perform in
arch of apoptosis.
mogeneous Caspa
ific, one-step fluor
rmination of caspa
ughput screening.
-Poly (ADP-Ribo
P is a zinc-depend
gnizes DNA strand
trate for apoptosis
unochemistry, imm
asurement of
duct Name
Death Detection
(5-6 hrs), sensitive
ires coating of the
A. For specific dete
plasmic fraction of
Death Detection
A supplied with pla
rmination of mono
ion of cell lysates.
Death Detection
A supplied with pla
rmination of mono
ptotic DNA-Ladd
apid isolation of D
lectrophoresis for
ck and documenta
ptosis and necrosis
ethods for St
asurement of
duct Name
exin-V-FLUOS
exin-V-FLUOS dete
metry or fluorescen
uter leaflets of cell
rentiates apoptotic
exin-V-FLUOS St
with FLUOS-conjug
quantification of ap
e-cell level. Secon
lar characterizatio
gy
tudying Apo
f Apoptosis-I
8 epitope produced
sis in cells and tiss
flow cytometry, an
ffin-embedded sec
ssay
ct and quantify cas
, or 7 activity by om
hibitor studies for
ases Assay, fluor
rimetric assay for t
ases activity in mic
se) Polymerase
ent, eukaryotic DN
d breaks produced
s-specific protease
munoprecipitation,
f DNA Fragm
n ELISA
e, nonradioactive 2
microplates with a
ermination of mon
cell lysates.
n ELISA
PLUS

e, nonradioactive 1
ates, pre-coated w
- and oligonucleos
n ELISA
PLUS
, 10x
e, nonradioactive 1
ates pre-coated w
- and oligonucleos
Contains 10x buffe
der Kit
NA, which can be
the determination
able form of data t
s.
tudying Apo
f Membrane A
ects apoptotic cells
nce microscopy by
membranes. Prop
c from necrotic cel
taining Kit
ated annexin-V an
poptosis and differ
dary labeling (phy
n.
optosis in Ce
nduced Prote
d after caspase cle
sues. Use the M30
nd immunohistoch
ctions.
spase 3 activity in c
mitting the capture
caspase 3 in life s
rimetric
the quantitative in
roplates. Ideally su
NA-binding protein
by genotoxic age
es from the ICE-fam
and western blotti
entation
2-step colorimetric
anti-histone antibo
o- and oligonucleo
-step photometric
with streptavidin. Fo
somes in the cytop
-step photometric
ith streptavidin. Fo
somes in the cytop
ers.
analyzed and cha
of apoptotic cell d
to differentiate bet
optosis in In
Alteration
s in suspension ce
y binding to phosp
pidium iodide label
ls.
nd propidium iodid
rentiaton from nec
ycoerythrin, TRITC)
ell Populatio
eases (Caspa
eavage, an
0 antibody in
hemistry with
cell lysates,
e-antibody
science
vitro
uited for high-
n that
nts. It is a
mily. For
ing.
ELISA
ody prior to the
osomes in the
c sandwich
or specific
plasmic
c sandwich
or specific
plasmic
aracterized by
death. Provides
tween
dividual Cel
ells using flow
hatidylserine
ling
de for detection
crosis at the
) is possible for

ons
ases)
Cat. No.
12 140 322 001
12 140 349 001
12 012 952 001
03 005 372 001
12 236 869 001
11 835 238 001
Cat. No.
11 544 675 001
11 774 425 001
11 920 685 001
11 835 246 001
lls
Cat. No.
11 828 681 001
11 858 777 001
11 988 549 001

1
1 kit for 100 tes
1 kit for 1,000
tes
100
1
1
1 kit
1
500
1
1 k
Pack Size
50 tests
250 tests


sts on 96-well plat
on 384-well plates
tests on 96-well p
sts on 384-well pla

0 l for up to 50 b

Pack Size


t for up to 10 x 96


Pack Size
0 l for up to 250 t


www.roche
sts
tes, for 400 tests
s
plates, for 4,000
ates
lots
sts
sts
tests
sts
ests
sts
ests
e-applied-science

Price in
224,20
620,30
940,20
466,10
2.762,20
372,40
Price in
428,10
541,70
951,50
329,40
Price in
663,60
280,80
855,20

6
99

e.com
6

6

6
Ce
100

www.r

Mea
Prod
In Si

Preci
apop
apop
sensi
In Si

Preci
apop
apop
sensi
In Si

Preci
apop
quan
and f
In Si

Preci
quan
and t
flow
Mea
Prod
TUN

TUNE
assay
antib
visua
TUN

TUNE
assay
is lab
subst
TUN

Use w
deoxy
appli
break
TUN

This e
trans
TUNE
death
TUN

TUNE
react
to lab
level.
Det
Prod
p53

Dete
homo
betw
type

ell Biolog
roche-applied-sc
asurement of
duct Name
itu Cell Death De
se, fast, and simpl
ptotic cell death at
ptotic cells in frozen
itivity to drug-indu
itu Cell Death De
se, fast, and simpl
itu Cell Death De
se, fast, and simpl
ptosis at the single-
titative detection b
formalin-fixed tissu
itu Cell Death De
se, fast, and simpl
titating apoptotic
tissues using a red
cytometry.
asurement of
duct Name
EL AP
EL AP is an antibo
ys into colorimetric
body is bound to FI
alized using Fast Re
EL POD
EL POD is an antib
beled with peroxida
trate such as DAB
EL Dilution Buffe
with In Situ Cell D
ynucleotidyl transf
cations. The result
ks to quantity apop
EL Enzyme
enzyme solution c
sferase for the TUN
EL reaction mix lab
h at single-cell leve
EL Label Mix
EL Mix contains flu
tion to detect apop
bel DNA strand bre
.
tection of Apo
duct Name
pan ELISA
rmine p53 (human
ogenates (tumor ti
een elevated p53 l
and mutant forms
gy
cience.com
f DNA Fragm
etection Kit, AP
e nonradioactive k
the single-cell leve
n or formalin-fixed
uced apoptosis.
etection Kit, POD
e nonradioactive k
n or formalin-fixed
uced apoptosis.
etection Kit, Fluo
e nonradioactive k
-cell level using flu
by flow cytometry.
ue sections.
etection Kit, TMR
e nonradioactive t
DNA fragmentatio
d fluorescent label
f DNA Fragm
dy that converts fl
c assays for light m
TC-dUTP, labeled
ed or NBT/BCIP.
body that converts
c assays suitable fo
ase and is visualize
Substrate.
er
Death Detection Kit
ferase for the TUN
ting reaction mix is
ontains recombina
NEL reaction to det
bels DNA strand b
el.
uorescein-dUTP an
ptosis in situ . Use t
eaks to quantity ap
optosis-Relat
n, mouse, rat) in se
ssue/cell lines). Us
levels and tumor d
of p53 protein.
entation - Kit
kit to detect and q
el using light micr
d tissue and determ
D
kit to detect and q
el using light micr
d tissue and determ
orescein
kit for qualitative d
uorescence micros
Detect apoptotic c
R red
technique for dete
on at a single-cell l
for fluorescence m
entation - Sin
uorescence-based
microscopy. Anti-fl
with alkaline phos
fluorescence-base
or light microscop
ed using a precipit
ts to dilute termina
EL reaction in spe
s used to label DN
t the single-cell lev
ant terminal deoxy
tect apoptosis in s
breaks to quantity a
nd -dNTPs for the
this mix with the T
poptotic cell death
ted Proteins
erum/plasma, or fro
sed to investigate
development by qu
ts
uantify
oscopy. Detect
mine cell
uantify
oscopy. Detect
mine cell
detection of
scopy or
cells in frozen
cting and
level in cells
microscopy or
ngle Reagent
d TUNEL
uorescein
sphatase, and
ed TUNEL
y. The antibody
tating
al
ecial
NA strand
vel.
ynucleotidyl
situ . The
apoptotic cell
TUNEL
TUNEL Enzyme
h at single-cell
om tissue
relationships
uantifying wild

Cat. No.
11 684 809 910
11 684 817 910
11 684 795 910
12 156 792 910
ts
Cat. No.
11 772 457 001
11 772 465 001
11 966 006 001
11 767 305 001
11 767 291 910
Cat. No.
11 828 789 001

1
1
1
1
3.5
3.5
2 x
3 x 5
1
Pack Size




Pack Size
5 ml for up to 70 te


2 x 10 ml

50 l for up to 20 t

550 l for up to 30

Pack Size

sts
sts
sts
sts
ests
ests
tests
tests
sts

Price in
651,70
651,70
591,40
591,40
Price in
115,60
122,20
216,30
181,00
141,80
Price in
785,50

Ce

Cy
Me
Prod
Cellu

Nonr
quan
durin
apop
Cyto

Fast a
meas
cell-m
cytot
Cyto

Fast a
cytot
cells.
fewe
Ce
Me
Prod
Cell

Nonr
in 96
Analy
antib
Cell

Nonr
in 96
Analy
antib
Cell

Nonr
in 96
Analy
antib
Me
Prod
Brom

The k
incor
forma
Cell

Preci
quan
incor
differ
Cell

Preci
assay
incor
differ

ell Biolog
totoxicity
easurement
duct Name
ular DNA Fragme
radioactive, fast (4.
tification of BrdU-
ng necrosis or cell-
ptotic cells.
otoxicity Detectio
and simple 6-well
suring LDH activity
mediated cytotoxic
oxic potential of co
otoxicity Detectio
and simple 96- or
oxicity/cytolysis by
Has all the benefi
r steps, plus it con
ell Prolifera
easurement
duct Name
Proliferation Kit
radioactive spectro
-well plates. Meas
yze cytotoxic/cytos
bodies. Requires so
Proliferation Kit
radioactive spectro
-well plates. Meas
yze cytotoxic/cytos
bodies. No solubiliz
Proliferation Rea
radioactive spectro
-well plates. Meas
yze cytotoxic/cytos
bodies. Ready-to-u
easurement
duct Name
mo-2'-deoxy-urid
kit is used for the n
rporated into cellul
at.
Proliferation ELIS
se, fast (1.5-3 hrs)
titate cell prolifera
rporation during D
rent in vitro cell sy
Proliferation ELIS
y to quantitate cell
rporation during D
gy
of Cytotoxic
entation ELISA
.5 - 5.5 hours), sen
-labeled DNA fragm
-mediated cytotoxi
on Kit (LDH)
plate method to q
y released from da
city, determine med
ompounds.
on Kit
PLUS
(LDH)
384-well plate me
y measuring LDH a
its of the Cytotoxic
ntains a stop soluti
ation
of Metaboli
I (MTT)
ophotometric quan
sure proliferation in
static compounds.
olubilization.
II (XTT)
ophotometric quan
static compounds.
zation step.
agent WST-1
ophotometric quan
static compounds.
se solution.
of DNA Syn
dine Labeling and
nonradioactive qua
lar DNA using a 96
SA, BrdU (colorim
), and simple nonra
ation based on the
NA synthesis in re
ystems.
SA, BrdU (chemi
), and simple nonra
l proliferation base
NA synthesis in re
ystems.
city
nsitive (1 x 10
3
cel
ments either relea
icity, or within the
quantify cytotoxicity
amaged cells. Dete
diator-induced cyt
ethod to quantify
activity released fr
city Detection Kit (
on.
ic Activity in
ntification of prolife
n response to grow
Assess growth-in
n response to grow
Assess growth-in
n response to grow
Assess growth-in
nthesis in Ce
d Detection Kit II
antitative determin
6-well microplate c
metric)
adioactive colorim
measurement of B
eplicating cells. Us
iluminescent)
adioactive chemilu
ed on the measure
ls/well)
sed from cells
cytoplasm of
y/cytolysis by
ect and quantify
tolysis, and
om damaged
(LDH) with
n Cell Popul
eration/viability
wth factors.
hibitory
eration/viability
wth factors.
hibitory
eration/viability
wth factors.
hibitory
ell Populatio
II
nation of BrdU
cell ELISA
etric assay to
BrdU
ed in many
uminescent
ement of BrdU
ed in many

Cat. No.
11 585 045 001
11 644 793 001
04 744 926 001
04 744 934 001
ations
Cat. No.
11 465 007 001
11 465 015 001
05 015 944 001
11 644 807 001
ons
Cat. No.
11 444 611 001
11 647 229 001
11 669 915 001

1 k
1 k
1 kit for
1 kit for u
1 k
1 k
8 m
25 m
1 k
1 k
1 k
Pack Size

kit for up to 2,000 te

up to 400 tests in
up to 2,000 tests in

Pack Size


ml for up to 800 te
ml for up to 2,500 t

Pack Size



www.roche
ests
ests
96 wells
n 96 wells
ests
ests
ests
tests
ests
ests
ests
e-applied-science

Price in
465,10
615,70
208,00
561,70
Price in
338,80
435,60
211,50
568,60
Price in
621,80
705,90
712,70

6
101

e.com
6

6

6
Ce
102

www.r

Me
Prod
Brom

Nonr
immu
or org
embe
Brom

Nonr
immu
alkali
adde
In Si

Seco
single
/in vi
prolif
Sin
Prod
Anti-

Anti-
blood
on a
cryos
Anti-

Anti-
in blo
single
cryos
Anti-

Anti-
in blo
single
and p
Me
Prod
ATP

High
micro
detec
ATP
ATP

Optim
a con
kinet
ATP
On
Prod
MIA

One-
mela
strep
T elo

Quali
tube
biotin
micro
T elo

Sens
activi
PCR
meas

ell Biolog
roche-applied-sc
easurement
duct Name
mo-2'-deoxy-urid
radioactively detec
unofluorescence. D
gan cultures, or by
edded tissue must
mo-2'-deoxy-urid
radioactively detec
unohistocytochem
ine phosphatase (A
d, then bound to t
itu Cell Proliferat
nd generation non
e-cell level using i
ivo systems. Detec
ferating cells in he
gle Reagen
duct Name
-Bromodeoxyurid
-Bromodeoxyuridin
d, tissues, and tum
single-cell level us
sections, and paraf
-Bromodeoxyurid
-Bromodeoxyuridin
ood, tissues, and tu
e-cell level using f
sections, and paraf
-Bromodeoxyurid
-Bromodeoxyuridin
e-cell level using E
paraffin sections.
easurement
duct Name
Bioluminescenc
ly sensitive/quantit
oplate-format lumi
ction of microbial c
Bioluminescence A
Bioluminescenc
mized for tube and
nstant light signal,
tic studies and ATP
Bioluminescence A
ncology Re
duct Name
ELISA
-step, 2 hour ELISA
noma inhibitory ac
ptavidin-coated mic
oTAGGG Telome
itative detection of
ready-to-use mix
nylated primer to im
oplate, and a DIG p
oTAGGG Telome
itive, nonradioactiv
ity in cell extracts.
ELISA, but also ha
sure amount of rea
gy
cience.com
of DNA Syn
dine Labeling and
ct BrdU incorporate
Detect DNA synthe
y in vivo labeling, i
be prepared befo
dine Labeling and
ct BrdU incorporate
istry. In the BrdU L
AP)-labeled antibo
the anti-BrdU antib
tion Kit, FLUOS
nradioactive kit for
mmunohistocytoc
ct and quantify cel
eterogeneous popu
ts for the M
dine
ne is used for mon
mors, as well as for
sing flow cytometr
ffin sections.
dine-Fluorescein
ne-Fluorescein is u
umors, and to dete
flow cytometry, imm
ffin sections.
dine-Peroxidase,
ne-Peroxidase is us
umors, and to dete
ELISA, immunohist
of ATP usin
e Assay Kit HS II
tative determinatio
inometers. Contain
contamination. For
Assay Kit CLS II.
e Assay Kit CLS
d microplate-forma
sustained for seve
P determinations. F
Assay Kit HS II.
esearch
A for the quantitati
ctivity (MIA) protei
croplates.
erase PCR ELISA
f telomerase activit
for elongation and
mmobilize TRAP p
probe for detection
erase PCR ELISA
P
ve photometric EIA
One-tube mix sim
as an optimized sta
action product.
nthesis in Ind
d Detection Kit I
ed into cellular DN
esis by in vitro lab
in which frozen/pa
re fixation.
d Detection Kit II
ed into cellular DN
Labeling and Dete
ody to mouse imm
body.
r detecting DNA sy
hemistry. Ideal for
ls in S phase, and
ulations.
Measuremen
itoring proliferatin
determining BrdU
ry, immunohistocyt
n
used to monitor pro
ermine BrdU incor
munohistocytoche
, Fab fragments
sed to monitor pro
ermine BrdU incor
tocytochemistry, c
ng Biolumine
I
on of ATP, for use
ns a cell lysis reage
r a constant light s
II
at luminometers. Th
eral minutes and is
For higher sensitiv
ive in vitro determ
in in serum and pl
ty in cell extracts.
d amplification. Us
products in a strept
n.
PLUS

A to detect/quantif
milar to TeloTAGGG
andard and contro
dividual Cel
NA by
eling of cells
araffin-
I
NA by
ction Kit II, an
unoglobulin is
ynthesis at the
many in vitro
detect
nt of DNA Sy
g cells in
U incorporation
tochemistry,
oliferating cells
poration on a
emistry,
oliferating cells
poration on a
ryosections,
escence
in tube and
ent for
signal, use the
he kit exhibits
s used for
vity, use the
ination of
asma within
One-step/one-
es a
tavidin-coated
fy telomerase
G Telomerase
l template to

lls
Cat. No.
11 296 736 001
11 299 964 001
11 810 740 001
ynthesis in In
Cat. No.
11 170 376 001
11 202 693 001
11 585 860 001
Cat. No.
11 699 709 001
11 699 695 001
Cat. No.
11 976 826 001
11 854 666 910
12 013 789 001

1 k
1 k
1 k
ndividual Ce
1 kit for 1,000 a
1 kit for 1,600 a
1
1 kit
1 kit
Pack Size



ells
Pack Size
50 g (500 l)

50 g (500 l)

15 U

Pack Size
assays (microplate)
(tube).

assays (microplate)
(tube).

Pack Size



ests
ests
ests
), for 500 assays
), for 800 assays
sts
tions
tions

Price in
621,80
621,80
671,50
Price in
432,90
542,90
448,50
Price in
566,70
566,70
Price in
972,30
1.026,60
1.085,40

Ce

T elo

Use i
telom
from
deter
p53

Dete
homo
betw
type
Vir
Prod
Reve

Rapid
cultu
retrov
scree
ell Biolog
oTAGGG Telome
n life science rese
meric DNA in cell c
a variety of organ
rmine the telomere
pan ELISA
rmine p53 (human
ogenates (tumor ti
een elevated p53 l
and mutant forms
rus Resear
duct Name
erse Transcriptas
d, sensitive ELISA
res and other biolo
viruses in infected
ening for RT inhibit
gy
ere Length Assay
earch applications
cultures and other
isms, including hu
e length of these s
levels and tumor d
of p53 protein.
rch
se Assay, colorim
for quantitative de
ogical samples. De
mammalian cells
tors.

for sensitive detec
biological researc
umans and mice. U
amples.
erum/plasma, or fro
sed to investigate
development by qu
metric
etermination of RT
etermine propagat
in culture. Also us
ction of
ch samples
Use to
om tissue
relationships
uantifying wild
activity in cell
tion of
sed for in vitro

12 209 136 001
11 828 789 001
Cat. No.
11 468 120 910

1 kit
1
1 k


Pack Size

www.roche
tions
sts
ests
e-applied-science

771,60
785,50
Price in
594,10

6
103

e.com
6

Alp
104

www.r

Prod

1-
2,3-D
2,3-D
dipho
scien
3-Hy
3-Hyd
hydro
5'/3'
Analy
Ends
3 en
react
5-Br
5-Bro
that c
studi
sister
70x7
This d
plate
For u
Titan
70x7
This d
plate
For u
Titan
70x7
This d
plate
For u
Titan
70x7
This d
plate
For u
Titan
7-De
7-De
termi
comp
stretc
2
-
2
-M
endo
speci
uroki
-A
Use
polys
enzym
A
Aat I
Aat I
with
recog
5230
ABTS
ABTS
(abso

lphabetic
roche-applied-sc
duct Name
9
Diphosphoglycer
Diphosphoglycerate
osphoglycerate in
nce research applic
ydroxybutyrate D
droxybutyrate Deh
oxymonocarboxylic
RACE Kit, 2nd G
yze mRNA structu
(RACE). Generate
ds from low-copy
tion products witho
romo-2'-deoxyuri
omo-2'-deoxyuridi
can be incorporate
es of DNA synthes
r chromatid exchan
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
75 Bead Depositi
device with loadin
. The top plate pre
use with GS FLX St
ium PicoTiterPlate
eaza-2'-deoxy-gu
aza-2'-deoxy-guan
ination sequencing
pression problems
ches of DNA.
Macroglobulin
Macroglobulin is a
oproteinases. Not a
ific for one or a lim
inase, factor XIIa, a
Amylase
-Amylase for the
saccharides contai
me produces -d
II
I recognizes the se
3-cohesive termin
gnition sequence a
I and Zra I.
S
S substrate is a per
orbance), chromat
cal Produ
cience.com
rate (2,3-DPG)
e (2,3-DPG) is use
blood in the range
cations.
Dehydrogenase (3
hydrogenase (3-HB
c acids, or the reve
Generation
re and expression
e full-length cDNA
RNA, amplify and
out cloning.
idine
ne is an immunoc
ed into DNA instea
sis, and to detect m
nge (SCE).
ion Device (16 sm
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
ion Device (2 larg
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
ion Device (4 me
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
ion Device (8 M/
g ports and air ven
esses the gasket ag
tandard PicoTiterP
e Kit 70x75.
uanosine-5'-triph
nosine-5'-triphosp
g methods, in plac
in gel electrophor
a protease inhibito
affected are endop
mited number of se
and endoproteinas
e hydrolyzation of
ning 3 or more
extrins.
equence GA*CGT
as indicated (*). Aa
roxidase substrate
ographically homo
uct Index
ed for the determin
e of 0.02 - 0.15 m
3-HBDH)
BDH) selectively ox
erse reaction.
by Rapid Amplific
As, isolate and char
clone rare mRNA
hemically detectab
ad of thymidine. Us
mutagenic substan
mall regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
ge regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
edium regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
/S Regions)
nts has a bottom p
gainst the PicoTite
late Kit (70x75) an
hosphate
phate is used in did
ce of dGTP to overc
resis when sequen
r that blocks most
proteinases that are
equences (tissue k
se Lys-C).
1,4-glycosidic b
1,4-linked D-Gluco
*C and generates
y 5-methylcytosine
at II is a neoschizo
e for ELISA. Purity:>
ogeneous.
x
nation of 2,3-
ol in life
xidizes (R)-3-
cation of cDNA
racterize 5or
, and sequence
ble nucleotide
sed for in vivo
nces using
plate and top
erPlate device.
nd GS FLX
plate and top
erPlate device.
nd GS FLX
plate and top
erPlate device.
nd GS FLX
plate and top
erPlate device.
nd GS FLX
deoxy-chain
come
ncing GC-rich
t
e highly
kallikrein,
bonds in
ose units. The
fragments
e in the
omer of Ssp
>98%

Cat. No.

10 148 334 001
10 127 833 001
10 127 841 001
03 353 621 001
10 280 879 001
05 414 636 001
05 414 601 001
05 414 610 001
05 414 628 001
10 988 537 001
10 602 442 001
10 102 814 001
10 775 207 001
10 102 946 001

1 kit fo
1 kit
1 bott
1 bott
1 bott
1 bott
20
Pack Size

or approximately 3

10 mg (2 ml)
25 mg (5 ml)


1 g

tom plate and 1 top

tom plate and 1 top

tom plate and 1 top

tom plate and 1 top

0 l (2 mol, 10 m

25 inhibitor units

50 mg (5 ml)

250 U (1 - 5 U/l)

2 g

30 tests
tions
p plate
p plate
p plate
p plate
mM)
)

Price in

352,10
134,40
294,90
478,50
70,00
inquire
inquire
inquire
inquire
95,70
108,30
127,20
53,30
57,90

Alp

Prod

ABTS
For p
perox
as a
phos
ABTS
Ideal
mark
displa
perbo
ABTS
ABTS
immu
solut
diluti
ABTS
Ideal
mark
subst
sodiu
ABTS
Ideal
mark
subst
sodiu
Acc
Acc I
fragm
meth
Acc I
Acet
Acety
using
group
Purity
Acid
Acid
phos
lyoph
+25
Actin
Actin
quan
hybri
huma
Aden
Aden
used
inosin
phos
Aden
Aden
used
inosin
appro
Afl II
Afl III
fragm
meth
III ha
Agar
The A
fragm
fragm
prime
Agar
Agar
prepa
analy
phag

lphabetic
duct Name
S Buffer
preparing the enzym
xidase as the mark
powder: sodium p
phate.
S Buffer
enzyme immunoa
ker enzyme. The re
ay "over" after sev
orate, citric acid, d
S Solution
S Solution is an ide
unoassays with ho
ion is supplied as
on.
S Tablets
substrate for enzy
ker enzyme. Each t
trate solution. The
S Tablets
substrate for enzy
ker enzyme. Each t
trate solution. The
I
I recognizes the se
ments with 5-cohe
hyladenine and 5-m
I is an isoschizome
tyl-Coenzyme A
yl-Coenzyme A is u
g radioisotopes. CA
ps from acetylcoen
y: 85% acetyl-CoA
Phosphatase
Phosphatase grad
phohydrolase [aci
hilizate. Specific ac
C with 4-nitrophen
n RNA Probe, DIG
n RNA Probe, DIG-
tity of various RNA
dization and north
an cell lines and tis
nosine Deaminas
nosine Deaminase
for the determina
ne analogs. Solutio
phate, pH approxi
nosine Deaminas
nosine Deaminase
for the deaminatio
ne analogs. Suspe
oximately 6.
II
I recognizes the se
ments with 5-cohe
s no known isosch
rose Gel DNA Ext
Agarose DNA Extra
ments from standa
ments are suitable
ed labeling, and se
rose LE
ose LE (low electro
arative gel electrop
ysis of PCR, examin
ge DNA, and separ
cal Produ
me immunoassay
ker enzyme for hig
erborate, citric aci
assay substrate usi
action's high sens
veral minutes. Supp
disodium hydrogen
eal chromogenic s
rseradish peroxida
one component re
yme immunoassay
ablet contains 50 m
buffer solution for
c acid, and disodiu
yme immunoassay
ablet contains 5 m
buffer solution for
c acid, and disodiu
equence GT(A,C)
esive termini. It is i
methylcytosine as i
er to Fbl I and Xmi
used to assay CAT
AT enzyme activity
nzyme A to chloram
A (enzymatic/absor
de II (orthophospho
d optimum]) from
ctivity is approxima
nyl phosphate as t
G-labeled
-labeled is ideal fo
A species. Applicat
hern blot analysis t
ssue samples.
se (ADA)
(adenosine amino
tion of adenosine
on in 50% glycerol
mately 6.
se (ADA)
(adenosine amino
on of adenosine an
ension in 3.2 M am
equence A*C(A,G
esive ends. Afl III is
site indicated (*) on
hizomers.
traction Kit
action Kit efficient
rd or low melting p
for ligation, transf
equencing.
oendosmosis) is id
phoresis of nucleic
nation of RE digest
ration of RNA.
uct Index
buffer when using
h reaction sensitiv
d, disodium hydro
ing horseradish pe
sitivity can cause a
plied in solution: s
n phosphate.
ubstrate for enzym
ase as a marker en
eagent, ready-to-u
ys with horseradish
mg ABTS substrate
r ABTS substrate c
um hydrogen phos
ys with horseradish
mg ABTS substrate
r ABTS substrate c
um hydrogen phos
(T,G)*A*C and gen
nhibited by the pre
indicated (*) on the
I.
T enzyme activity in
y catalyzes the tran
mphenicol.
rbance), 2% Li.
oric-monoester
potato is supplied
ately 2 U/mg lyoph
the substrate.
r evaluating the qu
tions include in sit
to evaluate RNA fr
ohydrolase) from c
analogs to the cor
l (v/v), 10 mM pota
ohydrolase) from c
nalogs to the corre
mmonium sulfate so
G)(T,C)GT and gene
n the recognition s
tly isolates small an
point agarose. Re
formation, RE diges
deal for routine ana
c acids. Applicatio
tsfrom plasmid, co
x
g horseradish
vity. Supplied
ogen
eroxidase as a
utoreaders to
odium
me
nzyme. ABTS
se at working
h peroxidase as
e, for a 50 ml
consists of
sphate.
h peroxidase as
, for a 5 ml
consists of
sphate.
nerates
esence of N6-
e sequence.
n cell extracts
nsfer of acetyl
d as a
hilizate at
uality and
tu
rom various
calf intestine is
rresponding
assium
calf intestine is
esponding
olution, pH
erates
presence of 5-
sequence. Afl
nd large DNA
covered DNA
sts, random
alytical and
ns include
osmid, and -

Cat. No.

11 112 597 001
11 204 530 001
11 684 302 001
11 112 422 001
11 204 521 001
10 728 438 001
10 101 893 001
10 101 907 001
11 585 371 001
10 108 227 001
11 498 045 910
10 102 105 001
10 102 121 001
11 209 183 001
11 696 505 001
11 685 660 001
11 685 678 001

3 x 100 ml (f
20 tablets (ea
20 tablets (e
1 kit
Pack Size

16.7 g (for 1 l)

125 ml

for 1,500 to 3,000 E

solution)

solution)

500 U (5 U/l)

10 mg
50 mg
200 mg
500 mg

2 g

10 mg (2 ml)

10 mg (1 ml)

100 U (5 U/l)

t for max. 100 reac

100 g
500 g

www.roche
ELISA assays)
0 ml substrate
ml substrate
ctions
e-applied-science

Price in

48,30
29,40
177,20
65,90
53,70
421,60
102,40
436,40
1.466,90
276,90
399,40
192,40
164,80
261,50
182,80
244,70
828,80

105

e.com

Alp
106

www.r

Prod

Agar
Agar
analy
of hig
Agar
Agar
bp). I
sizing
fragm
Alco
Alcoh
syste
Spec
ethan
Alde
Aldeh
NAD
prote
Alka
Calf I
phos
cloni
Highe
Alka
Use t
phos
enzym
conc
Alka
Calf I
its am
for co
Alka
Alkal
phos
selec
Poly(
Alka
Activ
prima
witho
rabbi
Alka
Alkal
amin
direc
ELISA
Alu I
Alu I
blunt
hydro
Isosc
Amp
Amp
medi
AMP
Comp
hydro
cleav
veno
Amy
Amyl
activi
termi
polys

lphabetic
roche-applied-sc
duct Name
rose MP
ose MP is a high s
ytical and preparat
gh molecular weig
rose MS
ose MS is ideal fo
It can be used in s
g, and STR analysi
ments that differ by
ohol Dehydrogena
hol Dehydrogenas
ems. Substrate spe
ific activity is appr
nol as the substrat
ehyde Dehydroge
hyde Dehydrogena
PH recycling syste
ein at +25C with a
aline Phosphatase
Intestinal Alkaline
phates from DNA
ng efficiency by pr
er conc. 20 U/l en
aline Phosphatase
this calf intestinal a
phates from DNA
me (20 U/l), conv
entration (1 U/l)
aline Phosphatase
Intestine Alkaline P
mino groups. This
onjugation without
aline Phosphatase
ine Phosphatase g
phohydrolase [alk
ctive cleavage of te
(U) is not cleaved.
aline Phosphatase
vated Alkaline Phos
ary amino groups
out pre-activation t
it, mouse, sheep, a
aline Phosphatase
ine Phosphatase r
o and carbohydrat
As, microarrays, an
I
recognizes the se
t termini. It is inhib
oxymethylcytosine,
chizomer: AluB I.
picillin
icillin is ideal for g
a, it selects for pla
P-PNP
petitive inhibitor of
olyzing between th
vage between the
m phosphodiester
yloglucosidase
oglucosidase is us
ity: approx. 6 U/mg
inal glucoses that
saccharide of mult
cal Produ
cience.com
strength, multipurp
tive electrophoresi
ht DNA via pulse f
r separation of sm
separation of PCR p
s. Agarose MS dis
y only 4 base pairs
ase (ADH)
e from yeast is a c
cificity is limited to
rox. 300 U/mg enzy
te.
enase
ase from yeast is a
ems. Specific activi
acetaldehyde as th
e
Phosphatase (1 U
or RNA in small-s
reventing self ligat
nzyme is also avai
e
alkaline phosphata
or RNA. This prep
venient for large-sc
is also available.
e
Phosphatase can b
ready-to-use enzy
t prior dialysis; EIA
e (AP)
grade I (orthophos
aline optimum]) fr
erminal phosphate
e (AP), activated
sphatase labels wa
(peptides/proteins
to label Ig, Ig Fab,
and goat.
e recombinant, h
recombinant can b
te groups. The en
nd western blot an
quence *AG*CT a
bited by 6-methylad
,or 4-methylcytosin
ene-cloning strate
asmid-bearing, dru
f ATP-dependent s
he a- and -phos
- and -phosph
rase and adenylate
sed for the determ
g lyo. at +25C wit
are 1,4- or 1,6
iple glucose units;
uct Index
pose agarose deve
s of nucleic acids
field gel electroph
all DNA fragments
products, genotyp
scriminates betwee
s.
component of NAD
o low molecular we
yme protein at +25
a component of NA
ity is approx. 20 U/
he substrate.
/l) removes 5'-te
scale experiments,
tion of linearized v
lable.
ase to remove 5'-te
p has a high conce
cale experiments. A
be coupled to othe
yme solution can b
A Grade, 10 mg/ml
sphoric-monoester
rom calf intestine i
groups from oligo
d
ater-soluble substa
s) with alkaline pho
and Ig F(ab')
2
frag
highly active
be coupled to prote
zyme solution can
ysis. Applications
nalysis.
and generates frag
denine, 5-methylcy
ne at the (*) in the
egies. When prese
ug-resistant bacter
systems. Substrate
phorus atom, yet r
horus atom. Subst
e cyclase.
th glycogen as sub
6-linked to an olig
supplied as lyoph
x
eloped for
and separation
oresis (PFGE).
s (50 to 1500
ing, allele
en DNA
DH recycling
eight alcohols.
5C with
ADH and
/mg enzyme
rminal
enhancing
vector DNA.
erminal
entration of
A lower
er proteins via
e used directly
solution.
r
s used for
onucleotides.
ances carrying
osphatase. Use
gments from
eins via its
be used
include
gments with
ytosine, 5-
e sequence.
nt in growth
rial colonies.
e for enzymes
resistant to
trate of snake
Specific
bstrate. Cleaves
o- or
hilizate.

Cat. No.

03 573 788 001
11 388 983 001
11 388 991 001
11 816 586 001
10 127 558 001
10 171 832 001
10 713 023 001
11 097 075 001
10 567 752 001
10 108 138 001
10 108 146 001
11 464 752 001
03 359 123 001
10 239 275 001
10 656 267 001
10 835 242 001
10 835 269 001
10 102 547 001
11 202 332 001
11 202 367 001

10 m
Pack Size

500 g bulk
100 g
500 g
100 g

1 g (34 ml)

250 U

1,000 U (1 U/l)

1,000 U (20 U/l)

15 mg (1.5 ml)

1,500 U
7,500 U

mg (approx. 40 mg

10 mg (500 l)

500 U (10 U/l)
2,000 U (10 U/l)

5 g
50 g

25 mg

500 U
3,500 U

lyo.)

Price in

inquire
219,10
768,50
595,00
492,30
211,00
88,70
103,40
647,10
63,80
256,00
542,40
440,80
78,80
228,50
43,40
260,20
203,70
98,30
364,10

Alp

Prod

Amy
Amyl
activi
termi
polys
Anne
Anne
cytom
on ou
differ
Anne
Kit w
and q
single
cellu
Anti-
Anti-
blood
on a
cryos
Anti-
Anti-
in blo
single
cryos
Anti-
Anti-
in blo
single
and p
Anti-
Anti-
native
that c
immu
Anti-
Use f
recom
dot b
need
Anti-
Use A
digox
in situ
Anti-
Use A
digox
in situ
Anti-
Anti-
using
weste
light-
Anti-
Detec
colon
immu
nonra
north
Anti-
Detec
in gly
immu
cann
Anti-
Detec
dot b
fragm
sensi
Anti-
Detec
Immu
Perox
lphabetic
duct Name
yloglucosidase
oglucosidase is us
ity: approx. 6 U/mg
inal glucoses that
saccharide of mult
exin-V-FLUOS
exin-V-FLUOS dete
metry or fluorescen
uter leaflets of cell
rentiates apoptotic
exin-V-FLUOS St
with FLUOS-conjug
quantification of ap
e-cell level. Secon
lar characterizatio
-Bromodeoxyurid
-Bromodeoxyuridin
d, tissues, and tum
single-cell level us
sections, and paraf
-Bromodeoxyurid
-Bromodeoxyuridin
e-cell level using f
sections, and paraf
-Bromodeoxyurid
-Bromodeoxyuridin
e-cell level using E
paraffin sections.
-c-myc
-c-myc (clone 9E10
e human c-myc pr
contain the c-myc
unocytochemistry,
-c-myc-Peroxida
for single-step det
mbinant epitope-ta
blots and western b
for a secondary d
-Digoxigenin
Anti-Digoxigenin a
xigenin-labeled co
u hybridization, an
-Digoxigenin
Anti-Digoxigenin a
xigenin-labeled co
u hybridization, an
-Digoxigenin, Fab
-Digoxigenin, FAB
g ELISA, immunoh
ern blotting. Prefer
-chain specific ant
-Digoxigenin-AP
ct digoxigenin-lab
ny/plaque hybridiza
unohistocytochem
adioactive DNA se
hern blotting.
-Digoxigenin-Flu
ct digoxigenin-lab
ycoconjugate resea
unohistocytochem
ot be used for me
-Digoxigenin-PO
ct digoxigenin-lab
blots. Obtain highe
ments conjugated t
itivity. Not evaluate
-Digoxigenin-PO
ct digoxigenin-lab
unohistocytochem
xidase substrates i
cal Produ
sed for the determ
g lyo. at +25C wit
are 1,4- or 1,6
iple glucose units;
ects apoptotic cells
nce microscopy by
membranes. Prop
c from necrotic cel
taining Kit
ated annexin-V an
poptosis and differ
dary labeling (phy
n.
dine
ne is used for mon
mors, as well as for
sing flow cytometr
ffin sections.
dine-Fluorescein
ne-Fluorescein is u
umors, and to dete
flow cytometry, imm
ffin sections.
dine-Peroxidase,
ne-Peroxidase is us
umors, and to dete
ELISA, immunohist
0) is used for the im
rotein and recomb
epitope in western
and immunopreci
ase
tection of native hu
agged proteins tha
blots. Use of Anti-c
detection step.
antibody (clone 1.7
mpounds using EL
nd western blotting
antibody from shee
mpounds using EL
nd western blotting
b fragments
Fragments detect
istocytochemistry,
rentially used for s
ti-sheep conjugate
P, Fab fragments
eled compounds u
ation, ELISA, gel s
equncing blots, and
uorescein, Fab fra
eled compounds u
mbrane applicatio
OD (poly), Fab fra
eled compounds i
r signal-to-noise v
to unpolymerized
ed in immunohisto
OD, Fab fragment
eled compounds u
include DAB and B
uct Index
th glycogen as sub
6-linked to an olig
supplied as suspe
s in suspension ce
y binding to phosp
pidium iodide label
ls.
nd propidium iodid
rentiaton from nec
ycoerythrin, TRITC)
itoring proliferatin
determining BrdU
ry, immunohistocyt
n
used to monitor pro
ermine BrdU incor
munohistocytoche
, Fab fragments
sed to monitor pro
ermine BrdU incor
tocytochemistry, c
mmunochemical d
binant epitope tag
n and dot blots,
pitation.
uman c-myc prote
at contain the c-my
c-myc-Peroxidase
71.256) for the dete
LISA, immunohisto
g.
ep for the detectio
LISA, immunohisto
g.
digoxigenin-labele
in situ hybridizati
secondary detectio
e.
using cDNA arrays
hift assays,
dization, RNase pro
d Southern, weste
agments
using digoxigenin-
ybridization. The a
ns.
agments
n ELISA, Southern
values compared to
HRP (ELISA). Use
ochemistry.
s
using dot blots, EL
dization, and weste
BM Blue.
x
Specific
bstrate. Cleaves
o- or
ension.
ells using flow
hatidylserine
ling
de for detection
crosis at the
) is possible for
g cells in
U incorporation
tochemistry,
oliferating cells
poration on a
emistry,
oliferating cells
poration on a
ryosections,
detection of
ged proteins
in and
yc epitope in
eliminates the
ection of
ocytochemistry,
n of
ocytochemistry,
ed compounds
on, and
on using a
s,
otection,
rn, and
-labeled sugars
n (FISH),
antibody
n, western, and
o Anti-Dig-Fab
for high
ISA,
ern blotting.

Cat. No.

10 102 857 001
11 828 681 001
11 858 777 001
11 988 549 001
11 170 376 001
11 202 693 001
11 585 860 001
11 667 149 001
11 667 203 001
11 814 150 001
11 333 062 910
11 333 089 001
11 214 667 001
11 093 274 910
11 207 741 910
11 633 716 001
11 207 733 910

500
1
1 k
2
Pack Size

100 mg (10 ml)

0 l for up to 250 t


50 g (500 l)

50 g (500 l)

15 U

200 g (lyophilizate
5 mg (1 ml)

500 g (500 l)

100 g

200 g

1 mg

150 U (200 l)

200 g

50 U

150 U

www.roche
ests
sts
ests
e)
e-applied-science

Price in

131,40
663,60
280,80
855,20
432,90
542,90
448,50
417,90
1.322,90
407,40
255,50
152,50
159,40
191,90
210,20
320,30
210,20

107

e.com

Alp
108

www.r

Prod

Anti-
Use A
comp
resea
immu
Anti-
Detec
immu
The a
antib
Anti-
Detec
immu
weste
immu
Anti-
Detec
immu
weste
immu
Anti-
Mono
immu
type
Anti-
Detec
tagge
immu
10-fo
Anti-
Easy
mam
of HA
weste
Anti-
Detec
conta
immu
Since
label
Anti-
Detec
tagge
strep
fold l
Anti-
Detec
weste
mono
mono
Anti-
Loca
sharp
using
Anti-
Anti-
Use A
recom
immu
used
Anti-
Singl
blotti
HA-P
need
Anti-
For s
blot a
Since
conju

lphabetic
roche-applied-sc
duct Name
-Digoxigenin-Rh
Anti-Digoxigenin-R
pounds using digo
unohistocytochem
-Fluorescein
ct fluorescein-labe
unohistocytochem
antibody is not sta
body in sandwich-E
-Fluorescein-AP,
ct fluorescein-labe
unohistocytochem
ern blots. Use the
unohistochemistry
-Fluorescein-POD
ct fluorescein-labe
unohistocytochem
ern blots. Conjuga
unohistochemistry
-GFP
oclonal antibody to
unoprecipitation an
and mutant forms
-HA (12CA5)
ct native influenza
ed protein contain
unoprecipitation, a
old lower conc., us
-HA Affinity Matr
method for immun
A-tagged proteins
ern blotting or silv
-HA High Affinity
ct native influenza
ain the HA epitope
unoprecipitation, a
e it is a rat monocl
ing.
-HA-Biotin
ct native influenza
ed protein in weste
ptavidin fluorescent
ower conc. using A
-HA-Biotin, High
ct HA-tagged reco
ern and dot blottin
oclonals for double
-HA-Fluorescein
lize recombinant H
per images with cle
g unlabeled Anti-H
-HA-Fluorescein, H
-HA-Fluorescein
Anti-HA-Fluoresce
mbinant HA-tagge
unofluorescence. S
with murine mono
-HA-Peroxidase
e-step detection o
ng. For higher sen
Peroxidase High Af
for a secondary d
-HA-Peroxidase,
ingle-step detectio
analysis and ELISA
e Anti-HA High Aff
unction with murin
cal Produ
cience.com
odamine, Fab fra
Rhodamine to dete
oxigenin-labeled su
n situ hybridization
eled compounds u
bilized with protein
ELISAs and labelin
, Fab fragments
eled compounds in
conjugate in ELISA
with an anti-mous
D, Fab fragments
eled compounds in
te only usable in E
using anti-mouse
o detect GFP or GF
nd western blottin
of GFP.
a hemagglutinin pr
ing the HA epitope
and western and do
e Anti-HA High Af
rix
noprecipitation of
and yeast extracts
from crude extrac
er staining.
y
a hemagglutinin an
e in ELISA, immuno
and western and do
onal, use with mur
a hemagglutinin pr
ern blots and imm
t or POD systems.
Anti-HA-Biotin, Hi
Affinity (3F10)
ombinant proteins
ng, and ELISA. Sinc
ble to use it in conj
e labeling.
HA-tagged protein
eaner background
HA. For higher sens
High Affinity.
, High Affinity
ein, High Affinity fo
ed proteins using f
Since the antibody
oclonals for double
of HA-tagged reco
nsitivity at 10-fold l
ffinity. Use of Anti-
detection step.
High Affinity
on of HA-tagged r
A.
finity is a rat mono
ne monoclonals for
uct Index
agments
ect digoxigenin-lab
ugars in glycoconju
n (FISH),
ybridization.
sing ELISA,
dization, and weste
n and is suitable a
ng procedures.
n ELISA,
dization, Southern,
A, immunoblotting
s
n ELISA,
dization, Southern,
ELISA, immunoblot
e Ig fluorescein, Fa
FP fusion proteins
g. Anti-GFP recog
rotein and recombi
e in immunocytoch
ot blots. For highe
ffinity.
HA-tagged protein
and column affini
cts. Analyze tagged
nd recombinant pro
ocytochemistry,
ot blots.
rine monoclonals f
rotein and recombi
unofluorescence w
Obtain higher sen
igh Affinity.
with high sensitivi
ce Anti-HA-High A
junction with muri
s by immunofluore
d compared to indi
sitivity at 10-fold lo
or direct detection
low cytometry and
y is a rat monoclon
e labeling.
mbinant proteins b
lower concentratio
-HA-Peroxidase el
recombinant protei
r double labeling.
x
beled
ugate
ern blotting.
as a coating
dot, and
g, and
Fab2 fragment.
dot, and
tting, and
b2 fragment.
using
nizes both wild
inant epitope-
hemistry,
r sensitivity at
ns from
ity purification
d proteins by
oteins that
for double
inant HA-
with
nsitivityat 10-
ity using
Affinity is a rat
ine
escence. Yields
rect methods
ower conc., use
of
d
al, it can be
by western
on, use Anti-
iminates the
ins by western
ble to use it in

Cat. No.

11 207 750 910
11 426 320 001
11 426 338 910
11 426 346 910
11 814 460 001
11 583 816 001
11 666 606 001
11 815 016 001
11 867 423 001
11 867 431 001
11 666 851 001
12 158 167 001
11 666 878 001
11 988 506 001
11 667 475 001
12 013 819 001

1 ml
100
50
Pack Size

200 g

100 g

150 U (200 l)

150 U

200 g

200 g (lyo.)
5 mg (5 mg/ml)


50 g
500 g

g (0.2 mg/ml; 50

50 g

100 g (500 l)

25 g

g (0.1 mg/ml; 500

25 U (25 g)

ume)
00l)
0 l)

Price in

210,20
320,90
223,90
189,60
342,90
466,50
1.322,90
852,30
347,10
2.945,40
350,80
524,30
352,10
326,80
408,60
408,60

Alp

Prod

Anti-
Spec
of ex
immu
Anti-
Spec
vecto
immu
tagge
Anti-
Singl
blotti
indep
epito
Anti-
For s
weste
effici
to C-
Antip
Antip
to a s
than
fold h
Anti-
PARP
recog
subst
immu
Anti-
Easy
mam
prote
prote
Apa
Apa
with
indic
120 I
Apop
For ra
gel e
a qui
apop
Apro
Prote
cultu
chym
quan
Apta
Reco
& imm
One-
range
Apta
Read
polym
activa
using
Asco
Remo
(asco
mate
oxalic
Asp7
Reco
with
meth
inhib

lphabetic
duct Name
-His
6

ific and sensitive d
pression vector us
unocytochemistry,
-His
6
(2)
ific, sensitive detec
or. For immunoblot
unofluorescence, E
ed proteins than C
-His
6
-Peroxidase
e-step detection o
ng and ELISA. Rea
pendent of epitope
pe with high sens
-His
6
-Peroxidase
ingle-step detectio
ern and dot blot an
ently recognizes N
-terminal tagged p
pain dihydrochlo
pain dihydrochlorid
small extent. Note:
leupeptin. The inh
higher than that of
-Poly (ADP-Ribo
P is a zinc-depend
gnizes DNA strand
trate for apoptosis
unochemistry, imm
-Protein C Affinit
method for immun
ein C-tagged prote
eins by western blo
I
I recognizes the se
3-cohesive termin
ated (*) in the reco
and Psp OMI.
ptotic DNA-Ladd
apid isolation of D
lectrophoresis for
ck and documenta
ptosis and necrosis
otinin
ect proteins during
re studies. Used fo
motrypsin on immo
tification of kallikr
aTaq Fast DNA Po
ombinant Taq polym
mediate activation
-for-all < 30 min p
e, including GC-RI
aTaq Fast PCR M
dy-to-use master b
merase with aptam
ation. Use one-for-
g GC-RICH templat
orbate Oxidase S
ove ascorbic acid f
orbate, vitamin C)
erial, such as detec
c acid in urine dur
700 I (Xmn I)
ognizes the sequen
blunt termini. Inhib
hyladenine at the o
it. Isoschizomers:
cal Produ
detection for histid
sed. For immunoblo
immunofluorescen
ction of histidine-t
tting, immunoprec
ELISA. More efficie
C-tagged proteins.
e
of His
6
-tagged rec
acts with native an
e-sequence locatio
itivity.
e (2)
on of His
6
-tagged
nalysis and ELISA.
N-terminal histidine
roteins.
oride
de inhibits papain
: Antipain is more
hibitory potency of
f elastatinal.
se) Polymerase
ent, eukaryotic DN
d breaks produced
s-specific protease
munoprecipitation,
ty Matrix
noprecipitation of
and yeast extracts
eins from crude ext
otting or silver stai
equence GGG*CC
ognition sequence
der Kit
NA, which can be
the determination
able form of data t
s.
g isolation/purificat
or purification of u
bilized aprotinin, p
rein activity.
olymerase
merase with aptam
. Comes with optim
rotocol for superb
CH templates.
aster
based on thermosta
mer mediated, reve
-all < 30 min proto
tes.
Spatula
from aqueous solu
interferes with the
ction of erythrocyte
ring research studi
nce G*AANNNN
bited by 6-methyla
other A() or presen
MroX I, Pdm I, Xm
uct Index
dine-tagged protein
otting, immunopre
nce, and ELISA.
tagged proteins re
ipitation, immunoc
ently recognizes N
ombinant proteins
nd denatured tagge
on. Recognizes the
recombinant prote
Anti-His
6
-Peroxid
e-tagged proteins
and trypsin. Plasm
specific for papain
antipain is approx
NA-binding protein
by genotoxic age
es from the ICE-fam
and western blotti
protein C-tagged
and affinity purific
tracts. For analyzin
ning.
*C and generates
y 5'-methylcytosine
e. Apa I is a neosch
analyzed and cha
of apoptotic cell d
to differentiate bet
tion, increasing ce
urokinase, trypsin, a
protein-folding stu
mer mediated, reve
mized buffer syste
results in a broad
able recombinant T
rsible hot start & im
ocol for superb res
utions where ascor
e investigation of s
es in urine or deter
ies.
TTC and generate
adenine at the (*).
nce of 5-methylcyt
mn I.
x
ns regardless
ecipitation,
gardless of
cytochemistry,
-terminal-
s by western
ed proteins
e C-terminal
6

eins by
dase (2) more
in comparison
min is inhibited
n and trypsin
ximately 100-
n that
nts. It is a
mily. For
ing.
proteins from
cation of
ng tagged
s fragments
e at the sites
hizomer to Bsp
aracterized by
death. Provides
tween
ell lifetime in
and
dies, and
ersible hot start
m for fast PCR.
template
Taq
mmediate
sults even
rbic acid
sample
rmination of
es fragments
6-
tosine does not

Cat. No.

11 922 416 001
04 905 318 001
11 965 085 001
04 905 270 001
11 004 646 001
11 835 238 001
11 815 024 001
10 703 753 001
10 899 208 001
11 835 246 001
10 236 624 001
10 981 532 001
11 583 794 001
06 879 110 001
06 879 128 001
06 879 080 001
06 879 101 001
10 736 619 001
10 835 277 001

100
1 ml
1
Pack Size

100 g

200 l

50 U

80 U

10 mg

0 l for up to 50 b


20,000 U (40 U/l)
5,000 U (10 U/l)


10 mg
50 mg
100 mg
100 units
1,000 units

100 reactions
1,000 reactions

25 spatulas

500 U (10 U/l)

www.roche
lots
ume)
)

sts
e-applied-science

Price in

334,90
355,30
388,40
414,60
185,70
372,40
473,20
317,90
97,90
329,40
69,70
275,40
488,00
43,00
286,00
56,00
475,00
72,40
73,90

109

e.com

Alp
110

www.r

Prod

Asp7
Reco
fragm
5-me
not in
ATP
Suita
prepa
salt s
ATP
Aden
form.
deter
ATP
ATP i
lumin
speci
tripho
ATP
Optim
a con
kinet
ATP
ATP
High
micro
detec
ATP
ATP-
ATP-
Hydro
thiop
Supp
ATP-
ATP-
Hydro
thiop
Supp
AttoP
AttoP
phos
sensi
subst
B
Bam
Reco
cohe
meth
resid
Basi
Mitog
vascu
chon
and l
Basi
Mitog
vascu
chon
and l
BbrP
Reco
blunt
recog
I, Pm
lphabetic
roche-applied-sc
duct Name
718 I
ognizes GGTAC*C
ments with 5 cohe
ethylcytosine as ind
nfluence activity()
solution, 100 mM, p
nosine-5'-triphosph
. It can be used for
rmination of Lucife
is supplied as the
nometric determina
ial quality preparat
osphate in crystal
Bioluminescenc
mized for tube and
nstant light signal,
tic studies and ATP
Bioluminescence A
Bioluminescenc
ly sensitive/quantit
oplate-format lumi
ction of microbial c
Bioluminescence A
--S
-S is a substrate
olyzed very slowly
phosphorylated, pro
plied as a lithium sa
--S
-S is a substrate
olyzed very slowly
phosphorylated, pro
plied as a tetralithiu
Phos
Phos is a highly se
phatase-conjugate
itive by a factor of
trate 4-methylumb
mH I
ognizes the sequen
sive termini. Bam
hylation, but is inhi
ue as indicated (*)
c Fibroblast Grow
gen for mesoderm
ular and corneal en
drocytes, and oste
imb and lens rege
c Fibroblast Grow
gen for mesoderm
ular and corneal en
drocytes, and oste
imb and lens rege
P I (PmaC I)
ognizes the sequen
t ends. The enzyme
gnition site as indic
aC I, Pml I, and Ps
cal Produ
cience.com
C; same sequence
sive ends, not 3 e
dicated (*). Methyl
). Neoschizomer: K
ns such as in vitro
or the absence of R
pH 7.
hate is supplied as
r applications, suc
erase activity in ce
disodium salt. Use
ation of Luciferase
tion contains high
form.
e Assay Kit CLS
d microplate-forma
sustained for seve
P determinations. F
Assay Kit HS II.
e Assay Kit HS II
tative determinatio
inometers. Contain
contamination. For
Assay Kit CLS II.
by phosphatases
oteins are resistan
alt, 100 mM solutio
by phosphatases
oteins are resistan
um salt powder.
nsitive substrate fo
ed secondary dete
100 than the most
belliferyl-phosphat
nce GGAT*CC a
H I is not inhibited
bited by 5- or 4-m
). Isoschizomer: Bs
wth Factor (156 A
m- and neuroectode
ndothelial, muscle
eoblasts). Induces
eneration in vivo .
wth Factor, huma
m- and neuroectode
ndothelial, muscle
eoblasts). Induces
eneration in vivo .
nce CA*CGTG and
e is inhibited by 5-
cated (*). BbrP I is
spC I.
uct Index
e as Kpn I but gene
nds as from Kpn I
lation of A and cen
Kpn I.
RNA transcription
RNases. Supplied a
s the disodium salt
h as the luminome
ll extracts.
e in applications, s
e activity in cell ext
ly purified adenos
II
at luminometers. Th
eral minutes and is
For higher sensitiv
I
on of ATP, for use
ns a cell lysis reage
r a constant light s
ATP-dependent en
and most ATPases
nt to protein phosp
on, pH 7.
ATP-dependent en
and most ATPases
nt to protein phosp
or ELISA using alk
ection systems. It is
t commonly used f
e (MUP).
and generates frag
d by overlapping da
methylcytosine at th
stI.
Aa), bovine (bbF
erm-derived cells
vessel growth, wo
an (hbFGF)
erm-derived cells
vessel growth, wo
d generates fragm
-methylcytosine wi
s an isoschizomer o
x
erates
. Inhibited by
ntral C does
n. The
as a lithium
t in crystal
etric
uch as the
tracts. This
ine-5'-
he kit exhibits
s used for
vity, use the
in tube and
ent for
signal, use the
nzyme systems.
s. Once
phatases.
nzyme systems.
s. Once
phatases.
kaline
s more
fluorescence
ments with 5'-
am
he internal C
FGF)
(fibroblasts,
yoblasts,
und healing,
(fibroblasts,
yoblasts,
und healing,
ments with
ithin the
of Acv I, Eco72

Cat. No.

10 814 245 001
10 814 253 001
11 175 050 001
11 140 965 001
10 127 523 001
10 127 531 001
10 519 979 001
10 519 987 001
11 699 695 001
11 699 709 001
11 162 306 001
10 102 342 001
11 681 982 001
10 220 612 001
10 567 604 001
10 656 275 001
10 798 975 001
11 274 031 001
11 104 616 001
11 120 417 001
11 123 149 001
11 168 860 001

400
1 kit for 1,600 a
1 kit for 1,000 a
1 set for u
Pack Size

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)
l (40 mol, 100 m

5 g
10 g

1 g
5 g

assays (microplate)
(tube).

assays (microplate)
(tube).

20 mol (200 l)

25 mg

up to 1,800 wells 1

1,000 U (10 U/l)
2,500 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
50,000 U (40 U/l)
10 g

25 g
10 g

500 U (10 U/l)

mM)
), for 800 assays
), for 500 assays
00 l each

)
)
)

Price in

68,20
284,20
284,20
108,40
56,60
92,60
50,50
199,40
566,70
566,70
469,10
410,50
542,40
29,50
57,90
199,10
199,10
807,70
302,00
769,90
342,00
91,40

Alp

Prod

BCIP
For a
South
is ins
disso
BCIP
Use B
immu
react
can b
Bcl I
Reco
cohe
posit
meth
Best
Besta
leuci
locat
carbo
Bfr I
Reco
cohe
meth
I, Ms
-G
-G
as a s
appro
32,00
-G
Susp
gene
fluore
galac
-G
Use f
be co
direc
chrom
-G
Use
Provi
crysta
Bgl I
Reco
cohe
but is
Bgl II
-G
For h
analy
prepa
immu
-G
Used
urine
prepa
drugs
Bioti
The k
such
Bioti
Labe
polym
north
and i

lphabetic
duct Name
P
alkaline phosphata
hern and western
soluble in water. Th
olved (50 mg/ml) in
P
BCIP for alkaline p
unohistocytochem
tion product has a
be visually detecte

ognizes the sequen
ion of adenine. Inh
hylcytosine. Isoschi
tatin
atin is an inhibitor
ne aminopeptidase
ed on the surface
oxypeptidases.
(Afl II)
ognizes the sequen
sive ends. The enz
pC I, and Vha464
Galactose Dehydr
alactose Dehydrog
suspension in 3.2
oximately 6. It is a
00 D).
Galactose Dehydr
ension in 3.2 M am
for -galactose D
escens strain BMT
ctosidase promote
Galactosidase
for labeling enzym
oupled to other pro
matography. Supp
Galactosidase
-Galactosidase t
ded as a suspensi
alline.
II
ognizes the sequen
sive termini. It is n
s sensitive to 5-me
I has no known iso
Glucuronidase
hydrolysis of steroid
ysis, and to detect
aration to cleave g
unoassays, or othe
Glucuronidase/Ar
d for simultaneous
e and other biologi
are protoplasts, in
s in urine.
in Protein Labelin
kit is suitable for th
as immunohistoch
in RNA Labeling
l RNA with Biotin-
merases (SP6, T3, a
hern, and dot blots
in situ and microa
cal Produ
se detection using
blotting. The react
he blue color can b
n dimethylformami
phosphatase detec
istry and Southern
blue color and is
d. Supplied as a p
nce TG*AT*CA, ge
ited by the dam ge
hibited by 5-hydrox
zomers: Fba I, Ksp
of aminopeptidase
e, tripeptide amino
of mammalian cel
nce *CTTAAG and
zyme is inhibited b
site indicated (*). Is
I.
rogenase
genase from Pseud
M ammonium sulf
dimer with subuni
rogenase S
mmonium sulfate,
Dehydrogenase S
TU 102, placed und
r in the plasmid pU
e immunoassay te
oteins via its SH-g
lied as lyophilizate
to produce a calib
on in 3.2 M ammo
nce AGAT*CT an
not inhibited by ove
ethyl and 5-hydrox
oschizomers.
d conjugates (gluc
benzodiazepine in
glucuronides prior
er analytical metho
rylsulfatase
hydrolysis of -glu
cal fluids. Use to r
enzyme immobiliz
ng Kit
he labeling of prote
hemistry, immunob
Mix
-16-UTP by in vitro
and T7). Labeled R
s, plaque and colon
rray hybridizations
uct Index
g immunohistocyto
tion product has a
be visually detecte
ide.
tion using
n and western blott
insoluble in water.
owder.
enerating fragmen
ene and methylate
xymethyl-cytosine
p22 I.
es, such as aminop
opeptidase, and am
ls. Does not inhibi
d generates fragm
by the presence of
soschizomers: Afl I
domonas fluoresce
fate, 1 mM EDTA,
its of equal size (s
1 mM EDTA, pH a
is from the Pseudo
der the control of a
UR 51.
echniques. -Galac
roups. Use recons
ysis or gel permea
e.
ration curve in enz
onium sulfate, pH a
nd generates fragm
erlapping dam met
xy-methylcytosine,
curonides) in urine
n small doses. Use
to GC-MS, HPLC,
ods.
ucuronides and su
remove cell walls f
zation studies, and
eins with biotin fo
blotting, and ELISA
o transcription usin
RNA can be used i
ny lifts, RNase prot
s.
x
ochemistry and
blue color and
ed. BCIP is
ting. The
. The blue color
nts with 5-
s the 6N-
, but not by 5-
peptidase B,
minopeptidases
it
ents with 5-
5-
II, BspT I, Bst98
ens is provided
pH
ubunit =
approx. 6. The
omonas
an E. coli -
ctosidase can
tituted solution
ation
zymatic assays.
approx. 6,
ments with 5-
thylation (),
as shown (*).
e, in doping
during sample
ulfate esters in
rom yeast to
to determine
r applications,
A.
ng RNA
n Southern,
tection assays,

Cat. No.

11 383 221 001
10 760 994 001
11 585 002 001
10 693 952 001
11 097 059 001
10 874 515 001
11 198 939 001
10 104 973 001
10 104 981 001
10 662 046 001
10 745 731 001
10 105 031 001
10 348 767 001
10 567 639 001
10 899 224 001
11 175 068 001
03 707 580 001
03 707 598 001
03 707 601 001
10 127 060 001
10 127 698 001
11 418 165 001
11 685 597 910

1 kit for
40 l for up
Pack Size

3 ml (150 mg)

250 mg
1 g

500 U (10 U/l)
2,500 U (40 U/l)

10 mg

500 U (10 U/l)

1 mg (1 ml)
5 mg (1 ml)

50 U

25 mg

1,500 U

500 U (10 U/l)
2,000 U (10 U/l)
2,000 U (40 U/l)
10,000 U (40 U/l)
1 ml
5 ml
15 ml
2 ml
10 ml



www.roche

)
reactions
on reactions
e-applied-science

Price in

86,20
123,50
434,20
68,20
175,10
183,30
64,80
59,20
209,70
264,60
657,00
185,00
68,20
181,90
181,90
534,30
49,90
181,80
491,90
66,70
245,90
282,90
184,80

111

e.com

Alp
112

www.r

Prod

Bioti
Subs
trans
with
conju
Bioti
Subs
rever
using
colon
Bioti
For n
trans
(Tran
color
Bioti
Nonr
can r
Detec
using
Bioti
Comp
probe
after
situ ,
Bioti
Enzym
Biotin
for fil
High
Bln I
Bln I
5-co
meth
Bloc
Block
filter
Block
Bloc
This
bindi
BM B
Read
appli
sensi
react
BM B
BM B
ELISA
phen
nonto
BM C
Chem
conve
ELISA
sourc
BM C
Subs
syste
ELISA
forma
BM C
Ideal
sensi
than
sensi

lphabetic
roche-applied-sc
duct Name
in-11-CTP
trate for RNA poly
scription in RNA la
Biotin-16-UTP. De
ugate or ELISA wit
in-16-ddUTP
trate for DNA poly
rse transcriptase (T
g TdT. Biotin-labele
ny/plaque screens,
in-16-dUTP
nonradioactive DNA
slation. Substrate fo
nscriptor). Detect u
r or chemiluminesc
in-16-UTP
radioactively label
replace UTP as a s
ct labeled RNA wit
g a Streptavidin-AP
in-High Prime
plete reaction mix
es. Biotin-labeled
overnight incubat
and colony and pl
in-Nick Translati
me nucleotide mix
n-16-dUTP for use
Prime.
I (Avr II)
recognizes the seq
ohesive termini. Th
hylation. Bln I is an
cking Reagent
king Reagent is us
hybridization and
king reagent does
cking Reagent
Blocking Reagent
ng sites in ELISA p
Blue POD Substr
dy-to-use colorime
cations, such as w
itive than DAB and
tions using alkaline
Blue POD Substr
Blue POD Substrat
A applications. The
ylendiamine (oPD)
oxic.
Chemiluminesce
miluminescent sub
enient and highly
A and SEAP report
ces, such as intest
Chemiluminesce
trate solution for p
ems for highly sens
A and use with a m
at) or tube-format
Chemiluminesce
chemiluminescen
itivity is required. O
colorimetric metho
itive as radioactivit
cal Produ
cience.com
ymerase (SP6/T3/T
beling. For higher
etect labeled RNA w
th Strepavidin-AP.
ymerase I, TdT, Taq
Transcriptor). Labe
ed oligo is used fo
, and in situ hybrid
A labeling by rand
or TdT, DNA polym
using streptavidin-
cent substrate (CS
RNA during in vitr
ubstrate for SP6, T
th a fluorescent st
P conjugate.
for efficient rando
probes are genera
ion. Use in Southe
laque lifts.
on Mix
xture for generating
e in in situ hybridiz
quence CCTAGG
e enzyme is not kn
isoschizomer of A
sed to decrease the
the detection of n
not contain BSA.
preparation is use
procedures. Suppl
rate, precipitating
tric peroxidase sub
western , northern,
d produces less ba
e phosphatase det
rate, soluble
te, soluble, is an id
e reagent shows h
) or ABTS substrat
ence ELISA Subst
strate system base
sensitive method t
ter gene assays. M
ine, placenta, milk
ence ELISA Subst
peroxidase-based
sitive, enhanced ch
microplate chemilu
luminometers.
ence Western Blo
nce system for wes
Obtain 1 to 3 order
ods. Chemilumine
ty with shorter exp
uct Index
T7). Replaces CTP i
more uniform labe
with fluorescent st
q, T4 DNA polymer
el the 3'-end of olig
or DNA/RNA transf
dization..
dom priming, PCR,
merase I, Taq, and
alkaline phosphat
PD, CDP-Star ).
ro transcription. Bi
T3, and T7 RNA po
treptavidin conjuga
om primed labeling
ated at high yield w
ern, dot, and northe
g sensitive probes
zation. The mix can
G and generates fra
nown to be affecte
Avr II, AspA2 I, and
e background in n
ucleic acid hybrids
ed for the blocking
ied as a yellowish
g
bstrate solution fo
and Southern blot
ackground staining
tection.
eal ready-to-use s
igher sensitivity th
tes and can be cla
trate (AP)
ed on CSPD provid
to detect alkaline p
Measures AP from v
k, and bacteria.
trate (POD)
(POD, HRP) secon
hemiluminescence
uminescence reade
otting Kit (Mouse
stern and dot blots
rs of magnitude hi
scence image is at
posure.
x
in in vitro
el density, use
treptavidin
rase, and
gonucleotides
fers,
or nick
RT
ase and a
iotin-16-UTP
olymerase.
ate or by ELISA
g of DNA
within 1 hour or
ern blotting, in
labeled with
n also be used
on, use Biotin-
agments with
ed by
d Xma I.
onradioactive
s. This Roche
g of nonspecific
powder.
r a variety of
tting. It is more
g than
solution for
han o-
assified as
des a
phosphatase in
various
ndary detection
e. Optimized for
er (96-well
e/Rabbit)
s where high
gher sensitivity
t least as

Cat. No.

04 739 205 001
11 427 598 910
11 093 070 910
11 388 908 910
11 585 649 910
11 745 824 910
11 558 161 001
11 558 170 001
11 096 176 001
11 112 589 001
11 442 066 001
11 484 281 001
11 759 779 001
11 582 950 001
11 520 709 001

25
25
50
25
100 l for up t
tem
160 l for
27 g for
250 ml for u
1 kit
Pack Size

l (250 nmol) (10 m

5 l (25 nmol) (1 m

0 l (50 nmol) (1 m

l (250 nmol) (10 m

o 25 labeling assay
mplate DNA per as

r up to 40 labeling

200 U (10 U/l)
1,000 U (10 U/l)

50 g

one liter blocking

100 ml

100 ml

150 ml


(2,000 cm
2
memb

mM)
mM)
mM)
mM)
ys, 0.01 to 3 g
ssay
reactions

solution
r 1.000 tubes
brane)

Price in

253,90
263,40
286,00
253,90
351,60
508,80
131,80
528,70
88,60
49,60
107,10
66,50
387,30
201,80
417,20

Alp

Prod

BM C
Ideal
<10 p
than
mem
BM C
BM C
the g
used
thaw
BM P
Color
north
situ
bottle
BM-
Supp
RPM
and c
cells
BM-
For th
obvio
been
spect
Bovi
Spec
chec
prote
Bovi
Stabi
when
prote
elect
Bovi
Highe
meta
ligan
in low
Brom
Nonr
immu
or org
embe
Brom
Nonr
immu
alkali
adde
Brom
The k
incor
forma
Bsm
Reco
3'-co
sequ
Isosc
BssH
Reco
overh
gene
indic
BstX
Reco
with
meth
enzym

lphabetic
duct Name
Chemiluminesce
substrate (POD) f
pg antigen in west
other nonradioact
branes.
Condimed H1
Condimed H1 is a s
growth of B-cell hy
to replace feeder
ing cells stored in
Purple
rimetric AP substra
hern, and Southern
hybridization. Use
e with no mixing o
Condimed
plement (10%, v/v)
I 1640, DMEM), co
chorionic villi cells
and peripheral blo
Cyclin
he elimination of m
ous marked cytotox
tested and compa
tinomycin, lincomy
ne Serum Album
ial BSA quality for
ked for the absenc
eases, and is used
ne Serum Album
lize enzymes to pr
n proteins are in lo
ein blocker, media
rophoresis and pro
ne Serum Album
est quality BSA. Us
bolism in biologica
d binding, and inv
w concentration.
mo-2'-deoxy-urid
radioactively detec
unofluorescence. D
gan cultures, or by
edded tissue must
mo-2'-deoxy-urid
radioactively detec
unohistocytochem
ine phosphatase (A
d, then bound to t
mo-2'-deoxy-urid
kit is used for the n
rporated into cellul
at.
I
ognizes the sequen
ohesive termini.Inh
ence as indicated
chizomers: BsaM I,
H II
ognizes the sequen
hanging ends. Belo
rate large fragmen
ated (*). Isoschizo
X I
ognizes the sequen
3-overhanging en
hylcytosine within t
me has no known
cal Produ
ence Western Blo
for protein and nuc
tern blots. Shows a
tive or radioactive
supplement to nor
ybridomas after fus
cells, and optimize
liquid nitrogen.
ate for immunohist
n blotting, colony a
stabilized substrat
or reconstitution.
to normal culture
ontaining 10-20%
. Improves culture
ood leukocytes.
mycoplasma from i
ared to other antib
ycin, gentamicin).
min
r molecular biology
ce of DNases, nick
to stabilize enzym
min Fraction V
revent proteolysis a
ow concentration. S
supplement, and a
otein determinatio
min Fraction V, fat
sed for fatty acid a
al systems, identify
vestigate ionic bind
dine Labeling and
ct BrdU incorporate
Detect DNA synthe
y in vivo labeling, i
be prepared befo
dine Labeling and
ct BrdU incorporate
istry. In the BrdU L
AP)-labeled antibo
the anti-BrdU antib
dine Labeling and
nonradioactive qua
lar DNA using a 96
nce G*AATGCNN
ibited by 6-methyl
(*). 5-methylcytos
Mva1269 I, Pct I.
nce G*CG*CGC an
ongs to a class of
nts of DNA. Inhibit
mers: BseP I, Pau
nce *CC*A(N)5NT
nds. BstX I is inhib
the recognition seq
isoschizomers.
uct Index
otting Substrate (
cleic acid detectio
at least 10-fold hig
detection systems
rmal culture mediu
sion and during clo
es growth of hybri
tocytochemistry, w
and plaque hybridi
te solution directly
basal medium (e.g
FCS to cultivate hu
conditions for bon
he efficiency of BM
biotics (kanamycin
y. This albumin pre
king activity, RNase
es.
and denaturation,
Suitable as a buffe
as a protein standa
ns.
tty acid free
and lipid research.
y transport mecha
ding. Ideal if protei
d Detection Kit I
ed into cellular DN
esis by in vitro lab
in which frozen/pa
re fixation.
d Detection Kit II
ed into cellular DN
Labeling and Dete
ody to mouse imm
body.
d Detection Kit II
antitative determin
6-well microplate c
N and generates fr
adenine within the
ine does not inhib
nd generates fragm
rare-cutter enzyme
ted by 5'-methylcyt
I.
TGG and generates
ited by 6-methylad
quence as indicate
x
(POD)
n. Sensitivity:
gher sensitivity
on PVDF
um to support
oning. It is
domas after
western,
zation, and in
y from the
g., F 10, M 199,
uman amniotic
ne marrow
res without
M-Cyclin has
, tylosine,
eparation is
es, and
especially
er component,
ard in
Study lipid
nisms, study
ns are present
NA by
eling of cells
araffin-
I
NA by
ction Kit II, an
unoglobulin is
II
nation of BrdU
cell ELISA
ragments with
e recognition
it ().
ments with 5-
es, which
tosine as
s fragments
denine and 5-
ed (*). The

Cat. No.

11 500 694 001
11 500 708 001
11 088 947 001
11 442 074 001
10 663 573 001
10 799 050 001
10 711 454 001
10 735 078 001
10 735 086 001
10 735 094 001
10 735 108 001
10 775 835 001
11 296 736 001
11 299 964 001
11 444 611 001
11 292 307 001
11 168 851 001
11 117 777 001
11 117 785 001

1 set
1 set
37.5 m
1 k
1 k
1 k
Pack Size

(4,000 cm
2
memb
(1,000 cm
2
memb

100 ml (10x)

100 ml

100 ml


20 mg (1 ml)

50 g
100 g
500 g
1 kg
50 g




200 U (10 U/l)

200 U (10 U/l)

250 U (10 U/l)
1,250 U (10 U/l)

www.roche
brane)
brane)
edium)
ests
ests
ests

e-applied-science

Price in

344,40
165,60
411,80
86,70
291,90
113,10
120,40
123,30
220,80
887,30
1.296,70
409,60
621,80
621,80
621,80
114,90
114,90
64,80
261,50

113

e.com

Alp
114

www.r

Prod

Buffe
Stabl
resist
for th
temp
Buffe
Stabl
resist
for th
temp
Buffe
Stabl
resist
for th
temp
Buffe
Stabl
resist
for th
temp
C
Calp
Stron
and I
prote
weig
Carb
Use C
succe
prote
argin
Carn
Key e
endo
from
acylC
Casp
Use t
analy
step,
resea
CASY
CASY
Coun
of ce
CASY
Regu
capil
reage
syste
CASY
The m
cell c
using
from
CASY
The C
Analy
capil
m.
CASY
The C
and A
150
0.7 to
CASY
The C
for qu
docu
3.2 to
lphabetic
roche-applied-sc
duct Name
ers in a Box, Prem
e 10x solution of P
tant to enzymatic a
he absence of nucl
perature.
ers in a Box, Prem
e 20x solution of S
tant to enzymatic a
he absence of nucl
perature.
ers in a Box, Prem
e 10x solution of T
tant to enzymatic a
he absence of nucl
perature.
ers in a Box, Prem
e 10x solution of T
tant to enzymatic a
he absence of nucl
perature.
pain Inhibitor I
ng inhibitor of Ca
2+
I. Inhibits calpain,
ein kinase C. Most
ht and lack of cha
boxypeptidase B
Carboxypeptidase
essive cleavage of
eins. Specific Activ
nine as the substra
nitine Acetyltrans
enzyme in the met
oplasmic reticulum
an acyl-CoA thioe
CoA/CoA in subcel
pase 3 Activity As
this assay to detec
yze caspase 1, 2, 3
and to perform in
arch of apoptosis.
Y blue
Y blue is a highly s
nter and Analyzers
lls to guarantee ce
Y clean
ular use of CASY c
laries of CASY Sys
ent prevents block
em.
Y cups
material properties
culture sample pre
g CASY Cell Count
adhering to the cu
Y Model TT 150
CASY Model TT 15
yzer for quality con
lary, it enables the
Y Model TT 45, 6
CASY Model TT 45
Analyzer for quality
m capillaries, it en
o 120 m.
Y Model TTC 150
CASY Model TTC i
mentation. It uses
o 120 m.
cal Produ
cience.com
mixed PBS Buffe
PBS, filtered throug
and nonenzymatic
lease or protease a
mixed SSC Buffe
SSC, filtered throug
and nonenzymatic
lease or protease a
mixed TAE Buffer
TAE, filtered throug
and nonenzymatic
lease or protease a
mixed TBE Buffer
TBE, filtered throug
and nonenzymatic
lease or protease a
+
-dependent neutr
which activates m
likely membrane p
rged residues.
B for the sequenc
f basic amino acids
ity - approx. 150 U
ate.
sferase
abolic pathway in
. Catalyzes the rev
ester to carnitine a
llular compartmen
ssay
ct and quantify cas
, or 7 activity by om
hibitor studies for
specific alcoholic d
for viability determ
ell identity.
lean protects the i
stems from biologic
kages and encrusta
s, size, and volume
paration. Use to d
ters and Analyzers
up walls.
m
50 m is a multi-pa
ntrol of cell culture
e analysis of object
60, 150 m
5, 60, 150 m is a m
y control of cell cu
nables the analysis
0 m
s a fast multi-para
a 150 m capillary
uct Index
er, 10x
gh 0.2 m pore siz
degradation. Each
er, 20x
gh 0.2 m pore siz
degradation. Each
r, 10x
gh 0.2 m pore siz
degradation. Each
r, 10x
gh 0.2 m pore siz
degradation. Each
ral cysteine protea
myosin light chain k
permeable due to
ce analysis of prote
s from the C-termi
U/mg at +25C with
mitochondria, per
versible transfer of
nd regulates the r
ts.
spase 3 activity in c
mitting the capture
caspase 3 in life s
dilution used with t
mination and for q
nstrument and me
cal deposits. By em
ations of the intern
e of CASY cups are
ilute and analyze c
s. Cup material pre
arameter Cell Coun
es. Equipped with a
ts in the size range
multi-parameter Ce
ultures. Equipped w
s of objects in the
ameter Cell Counte
tegrated data evalu
y for analysis in th
x
ze membrane,
h lot is tested
s easily at room
ze membrane,
h lot is tested
s easily at room
ze membrane,
h lot is tested
s easily at room
e membrane,
h lot is tested
s easily at room
ases calpain I
kinase and
low molecular
eins by
nus of
h hippuryl-L-
roxisomes, and
acyl groups
atio of
cell lysates,
e-antibody
science
the CASY Cell
uality control
easurement
mulsifying, this
nal liquid
e optimal for
cell samples
events cells
nter and
a 150 m
e of 3.2 to 120
ell Counter
with 45, 60, and
size range of
er and Analyzer
uation and
e size range of

Cat. No.

11 666 789 001
11 666 681 001
11 666 690 001
11 666 703 001
11 086 090 001
10 103 233 001
10 103 241 001
12 012 952 001
05 651 760 001
05 651 786 001
05 651 794 001
05 651 697 001
05 651 735 001
05 651 719 001

1
1
Pack Size

4 l

4 l

4 l

4 l

25 mg

5 mg (1 ml)

5 mg (1 ml)


4 x 30 ml

3 x 500 ml

1,800 cups with lid

1 instrument

1 instrument

1 instrument

sts
ds

Price in

114,30
127,20
127,20
116,60
224,80
182,70
172,00
940,20
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

CASY
The C
for qu
docu
size r
CASY
CASY
CASY
and b
CASY
CASY
cell c
cond
pH a
CAT
Nonr
euka
repor
the s
cDNA
Synth
librar
gene
for hy
CDP
Chem
ultra-
acids
and d
CDP
Read
Enab
labele
For S
Cede
Provi
This
envir
21 CF
Cede
Cede
Cede
Cede
Cede
brigh
Cede
Cede
of Ce
availa
Reag
Cede
Cede
Cede
and d
in 20
Cede
Cede
Cede
and d
in 20
Cede
Cede
Cede
and d
in 20
Cede
The C
to an
cell c

lphabetic
duct Name
Y Model TTC 45,
CASY Model TTC i
mentation. It uses
range of 0.7 to 120
Y rack
Y racks are used fo
Y Cell Counters an
black in color, hold
Y ton
Y ton is a ready-to
cultures for use wit
uctivity guarantee
nd osmolarity ensu
ELISA
radioactively and q
ryotic cells transfe
rter gene. Assay tim
ensitivity of the rad
A Synthesis Syst
hesize ready-to-us
ries, for substractiv
s, and to in vitro t
ybridization on mic
-Star
miluminescent sub
-sensitive visible li
s on film or lumine
dot blots, and gel s
-Star , ready-to-
dy-to-use chemilum
bles fast, ultra-sens
ed nucleic acids o
Southern, dot, and
ex 2.3 Software P
des comprehensiv
new software is de
onments, featuring
FR part 11 complia
ex 2.x to 2.3 Upg
ex 2.x to 2.3 Upgrad
ex 2.x Software ver
ex Calibration Be
ex Calibration Bead
htness adjustments
ex Cleaning Solu
ex Cleaning Solutio
edex and Cedex Hi
able as a compone
gent Kit and as a se
ex Control Beads
ex Control Beads a
ex System. Regular
documentation of
% ethanol (v/v).
ex Control Beads
ex Control Beads a
ex System. Regular
documentation of
% ethanol (v/v).
ex Control Beads
ex Control Beads a
ex System. Regular
documentation of
% ethanol (v/v).
ex Control Unit
Cedex Control Unit
nalyze concentratio
cultures.
cal Produ
, 60, 150 m
s a fast multi-para
45, 60, and 150 m
0 m.
or easy sample ha
nd Analyzers. Each
ds up to 24 CASY c
-use, isotonic, and
th CASY Cell Coun
s constant measur
ure cell size preser
quantitatively meas
ected with a plasm
me approximately
dioactive CAT assa
tem
se ds cDNA to con
ve hybridization to
ranscribe whole cD
croarrays.
strate for alkaline
ght detection of no
scence imager sys
shift assays.
use
minescent substrat
n film/luminescen
northern blots, ge
Package
esigned for project
g User and Rights
ance.
rade Package
de Package enable
sions to Cedex Sof
eads
ds are used to perf
s of Cedex and Ce
ution Refill
on is required for c
Res Systems. This
ent of the Cedex R
eparate bottle.
s
re used to perform
r use allows monito
system integrity. B
s
re used to perform
r use allows monito
system integrity. B
s
re used to perform
r use allows monito
system integrity. B
t is used in combin
on, viability, and m
uct Index
ameter Cell Counte
tegrated data evalu
m capillaries for an
ndling when work
rack, made of pol
cups.
d isoosmotic dilutio
nters and Analyzer
rement results. Its
rvation.
sure CAT expressio
id bearing a CAT-
4 hours. Sensitivity
ay.
struct non-directio
enrich differential
DNA to generate l
phosphatase, ena
onradioactively lab
stems. For Souther
te for alkaline pho
detection of nonrad
ce imagers.
l shift assays.
or operating the Ce
ts in cGMP regulat
Management and
es the upgrade of
ftware version 2.3.
form automated fo
dex HiRes Analyze
cleaning of the cap
ready-to-use solu
Reagent Kit and Ce
m System Suitabilit
oring of measurem
Bead Solution (51
m System Suitabilit
oring of measurem
Bead Solution (11
m System Suitabilit
oring of measurem
Bead Solution (51
nation with the Ce
orphological chara
x
er and Analyzer
uation and
nalysis in the
king with the
lyoxymethylene
on liquid for
rs. Its defined
physiological
on in
encoding
y equivalent to
onal cDNA
lly expressed
abeled cRNA
bling fast,
beled nucleic
rn, northern,
sphatase.
dioactively
edex Analyzer.
ted
d Audit Trail for
all previous
.
ocus and
ers.
pillary system
ution is
edex HiRes
ty Tests on the
ment results
0
6
/ml 10%),
ty Tests on the
ment results
0
6
/ml 10%),
ty Tests on the
ment results
0
5
/ml 10%),
edex Analyzer
acteristics of

Cat. No.

05 651 727 001
05 651 743 001
05 651 808 001
11 363 727 001
11 117 831 001
11 685 627 001
11 759 051 001
12 041 677 001
07 045 271 001
07 045 298 001
05 650 470 001
05 650 666 001
05 650 526 001
05 650 534 001
05 650 542 001
06 412 866 001

1 k
1 kit
1 binder w
1 binder w
1
1
1
1 cont
Pack Size

1 instrument

1 rack for 24 cups

10 l container



1 ml
2 x 1 ml

2 x 50 ml

with CD and Opera

with CD and Opera

20 ml

4 x 60 ml

100 ml (5 x 10
6
/m

100 ml (1 x 10
6
/m

100 ml (5 x 10
5
/m


www.roche
s
ests
tions
ator's Guide
ator's Guide
l)
l)
l)
very CD
e-applied-science

Price in

inquire
inquire
inquire
431,80
651,70
286,10
514,80
410,90
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

115

e.com

Alp
116

www.r

Prod

Cede
Cede
Cede
as a c
Cede
Cede
and C
comp
Cede
Provi
Analy
envir
21 CF
Cede
Cede
previ
versio
Cede
The C
using
cell d
diam
Cede
Cede
on th
meas
Solut
Cede
Cede
on th
meas
Solut
Cede
Cede
on th
meas
Solut
Cede
The C
HiRes
chara
Cede
The r
main
reage
Cede
This
Cede
integ
HiRes
Cede
Addit
Syste
in hig
Cede
Read
Analy
(Tryp
Cede
Cede
Syste
cultu
desig
Cede
Cede
Analy
imag
Cede
Trypa
deter
solut
HiRes
lphabetic
roche-applied-sc
duct Name
ex Detergent Sol
ex Detergent is req
ex and Cedex HiRe
component of the
ex Detergent Sol
ex Detergent is req
Cedex HiRes Syste
ponent of the Cede
ex HiRes 2.3 Soft
des comprehensiv
yzer. This new soft
onments, featuring
FR part 11 complia
ex HiRes 2.x to 2
ex HiRes 2.x to 2.3
ous Cedex HiRes 2
on 2.3.
ex HiRes Analyze
Cedex HiRes Syste
g Trypan Blue stain
diameter, aggregat
eter and cell comp
ex HiRes Control
ex HiRes Control B
he Cedex HiRes Sys
surement results a
tion (510
5
/ml 1
ex HiRes Control
ex HiRes Control B
he Cedex HiRes Sys
surement results a
tion (110
6
/ml 1
ex HiRes Control
ex HiRes Control B
he Cedex HiRes Sys
surement results a
tion (510
6
/ml 1
ex HiRes Control
Cedex HiRes Contr
s Analyzer to analy
acteristics of cell c
ex HiRes Reagen
ready-to-use Cede
tenance routines o
ents for preparatio
ex HiRes SW 2.3
is a software interf
ex HiRes Analyzers
ration into existing
s SW V 2.2 Remote
ex MS 20 Sample
tional tray for use
em. Suitable for pre
gher throughput m
ex Reagent Kit
dy-to-use kit for cle
yzer. The kit also c
pan Blue), and ana
ex Sample Cups
ex Sample Cups ar
ems. Their material
re sample prepara
gned for single use
ex Smart Slides
ex Smart Slides are
yzers. Their materi
e based analysis o
ex Trypan Blue S
an Blue Solution is
rmination with Ced
ion is available as
s Reagent Kit, and
cal Produ
cience.com
ution
quired for cleaning
es Systems. This re
Cedex Reagent Ki
ution Refill
quired for cleaning
ems. This ready-to-
ex Reagent Kit and
tware Package
tware is designed f
g User and Rights
ance.
.3 Upgrade Pack
Upgrade Package
2.x software versio
er
em is a fully autom
ning for measuring
tes, and morpholog
pactness.
Beads
eads are used to p
stem. Regular use
nd documentation
10%), in 20% ethan
Beads
eads are used to p
stem. Regular use
nd documentation
10%), in 20% ethan
Beads
eads are used to p
stem. Regular use
nd documentation
10%), in 20% ethan
Unit
rol Unit is used in
yze concentration,
cultures.
nt Kit
ex HiRes Reagent K
of the Cedex HiRes
on, staining, and an
Remote Control
face for on-site rem
s. Enables easy rea
g data managemen
e Control.
e Tray
with the Multi Sam
eparation of additi
measurement work
eaning and mainte
contains all reagen
lysis of eukaryotic
e for use with auto
l properties, size, a
ation and measure
e only.
e disposable slides
al properties, size
of cell cultures.
Solution Refill
s required as an ex
dex and Cedex HiR
a component of th
d as a separate bot
uct Index
the capillary syste
eady-to-use solutio
it and as a separat
the capillary syste
-use solution is av
d as a separate bot
or operating the Ce
for projects in cGM
Management and
kage
enables the upgra
ons to Cedex HiRes
ated image-based
g cell concentratio
gical parameters, s
perform System Su
allows monitoring
nol (v/v).
perform System Su
allows monitoring
nol (v/v).
perform System Su
allows monitoring
nol (v/v).
combination with
viability, and mor
Kit is used for clea
s Analyzers. Conta
nalysis of eukaryot
mote control of Ce
ad out of result dat
nt systems; succes
mpler delivered wit
onal samples in pa
kflows.
enance routines of
nts for preparation,
cells using the Ce
omated Cedex and
and volume are ide
ment. Cedex Samp
s for use with Cede
and volume are op
xclusion stain for v
Res Systems. This r
he Cedex Reagent
ttle.
x
em of the
on is available
te bottle.
em of Cedex
ailable as a
ttle.
edex HiRes
MP regulated
d Audit Trail for
ade of all
s Software
d cell analyzer
n, cell viability,
such as cell
uitability Tests
g of
ty. Bead
uitability Tests
g of
ty. Bead
uitability Tests
g of
ty. Bead
the Cedex
phological
aning and
ains all
tic cells.
edex and
ta for flexible
ssor to Cedex
th the Cedex
arallel for use
f the Cedex
, staining
edex System.
d Cedex HiRes
eal for cell
ple Cups are
ex XS
ptimal for
viability
ready-to-use
Kit, Cedex

Cat. No.

05 650 496 001
05 650 658 001
07 045 280 001
07 045 301 001
05 650 216 001
05 650 780 001
05 650 771 001
05 650 763 001
06 412 874 001
05 650 798 001
07 045 344 001
05 650 569 001
05 650 615 001
05 650 623 001
05 650 801 001
05 650 640 001

1 binder w
1 binder w
1 instrument w
1 cont
1 set for app
1 en
1 set for app
15 smart slid
Pack Size

1,000 ml

4 x 60 ml

with CD and Opera

with CD and Opera

with PC, monitor, a

30 ml

30 ml

30 ml


proximately 100 me

nvelope with instal

1 sample tray

proximately 100 me

500 cups

measurements

4 x 60 ml

ator's Guide
ator's Guide
and accessories
very CD
easurements
ll CD
easurements
20 cell culture

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

Cede
These
Cede
Syste
hardw
Cede
These
Cede
Syste
hardw
Cede
These
Cede
Syste
hardw
Cede
These
Cede
Syste
hardw
Cell
Fast
requi
ELISA
cytop
Cell
Fast
ELISA
deter
fracti
Cell
Fast
ELISA
deter
fracti
Cell
Preci
assay
incor
differ
Cell
Preci
quan
incor
differ
Cell
Nonr
in 96
Analy
antib
Cell
Nonr
in 96
Analy
antib
Cell
Nonr
in 96
Analy
antib
Cell
Simp
viabil
cellu
appli
Cellu
Nonr
quan
durin
apop

lphabetic
duct Name
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
ex Viability Bead
e beads simulate t
ex and Cedex HiRe
em Suitability Test
ware.
Death Detection
ires coating of the
A. For specific dete
plasmic fraction of
Death Detection
A supplied with pla
rmination of mono
Death Detection
A supplied with pla
rmination of mono
Proliferation ELIS
y to quantitate cell
rporation during D
Proliferation ELIS
titate cell prolifera
rporation during D
Proliferation Kit
radioactive spectro
-well plates. Meas
yze cytotoxic/cytos
bodies. Requires so
Proliferation Kit
radioactive spectro
-well plates. Meas
yze cytotoxic/cytos
bodies. No solubiliz
Proliferation Rea
radioactive spectro
-well plates. Meas
yze cytotoxic/cytos
bodies. Ready-to-u
Viability Imaging
ple, accurate and fa
lity using fluoresce
lar workflows, esp
cations. Optimized
ular DNA Fragme
radioactive, fast (4.
tification of BrdU-
ng necrosis or cell-
ptotic cells.
cal Produ
s (100%)
the 100% viability o
es Systems. They a
for quick and relia
s (30%)
es Systems. They a
for quick and relia
s (60%)
es Systems. They a
for quick and relia
s (80%)
es Systems. They a
for quick and relia
n ELISA
e, nonradioactive 2
microplates with a
ermination of mon
cell lysates.
n ELISA
PLUS

e, nonradioactive 1
ates, pre-coated w
- and oligonucleos
n ELISA
PLUS
, 10x
e, nonradioactive 1
ates pre-coated w
- and oligonucleos
Contains 10x buffe
SA, BrdU (chemi
), and simple nonra
l proliferation base
NA synthesis in re
ystems.
SA, BrdU (colorim
), and simple nonra
ation based on the
NA synthesis in re
ystems.
I (MTT)
ophotometric quan
static compounds.
olubilization.
II (XTT)
ophotometric quan
static compounds.
zation step.
agent WST-1
ophotometric quan
static compounds.
se solution.
g Kit
ast (35 minutes) on
ence detection and
ecially for medium
d for 96-well plates
entation ELISA
.5 - 5.5 hours), sen
-labeled DNA fragm
-mediated cytotoxi
uct Index
of cell culture susp
re used for the com
able status checks
re used for the com
able status checks
re used for the com
able status checks
re used for the com
able status checks
2-step colorimetric
anti-histone antibo
o- and oligonucleo
-step photometric
with streptavidin. Fo
somes in the cytop
-step photometric
ith streptavidin. Fo
somes in the cytop
ers.
iluminescent)
adioactive chemilu
ed on the measure
metric)
adioactive colorim
measurement of B
n response to grow
Assess growth-in
n response to grow
Assess growth-in
n response to grow
Assess growth-in
ne-step assay to m
d for quality contro
m to high throughp
s.
nsitive (1 x 10
3
cel
ments either relea
icity, or within the
x
pensions using
mprehensive
of optical
ensions using
mprehensive
of optical
ensions using
mprehensive
of optical
ensions using
mprehensive
of optical
ELISA
ody prior to the
osomes in the
c sandwich
or specific
plasmic
c sandwich
or specific
plasmic
uminescent
ement of BrdU
ed in many
etric assay to
BrdU
ed in many
eration/viability
wth factors.
hibitory
eration/viability
wth factors.
hibitory
eration/viability
wth factors.
hibitory
meausre cell
ol of cells in
put
ls/well)
sed from cells
cytoplasm of

Cat. No.

05 650 747 001
05 650 704 001
05 650 712 001
05 650 739 001
11 544 675 001
11 774 425 001
11 920 685 001
11 669 915 001
11 647 229 001
11 465 007 001
11 465 015 001
05 015 944 001
11 644 807 001
06 432 379 001
11 585 045 001

1
1
1 kit
1 k
1 k
1 k
1 k
8 m
25 m
1 kit f
1 k
Pack Size

30 ml

30 ml

30 ml

30 ml



t for up to 10 x 96





ml for up to 800 te



www.roche
sts
sts
tests
ests
ests
ests
ests
ests
tests
actions
ests
e-applied-science

Price in

inquire
inquire
inquire
inquire
428,10
541,70
951,50
712,70
705,90
338,80
435,60
211,50
568,60
320,00
465,10

117

e.com

Alp
118

www.r

Prod

Cfo I
Reco
cohe
simu
Isosc
CHA
For s
of bo
Chro
Use C
prote
Chro
Use C
prote
Chro
Use C
prote
Chro
Use C
in pu
used
Chym
Chym
inhib
Chym
Use C
chym
for pe
Citra
Catal
enzym
mole
Cla I
Reco
cohe
meth
I, Bsp
c-my
The s
C-ter
can b
chrom
Colc
Colce
the p
Colla
Colla
for th
lyoph
Colla
Disso
mam
suspe
viabil
Colla
Disso
mam
suspe
and v

lphabetic
roche-applied-sc
duct Name
I (Hha I)
ognizes the sequen
ltaneous presence
chizomers: AspLE I
APS
olubilization of me
oth the sulfobetaine
omozym PK
Chromozym PK as
omozym PL
Chromozym PL as
omozym TH
Chromozym TH as
eases, specifically t
omozym t-PA
Chromozym t-PA a
urified preparations
to evaluate the co
mostatin
mostatin is a mixtu
itor of -, -,
motrypsin Seque
Chymotrypsin Sequ
motrypsin alone or
eptide mapping, fi
ate Lyase (CL)
lyzes the cleavage
me complex that c
cular weights abo
I
ognizes the sequen
sive termini. It is in
hylcytosine as show
pD I, BspX I, Bsu15
yc peptide
synthetic peptide E
rminus of human c
be used in compet
matography of pro
cemid
emid inhibits the fo
percentage of meta
agen
agen is used as a s
he coating of cultu
hilizate is cell cultu
agenase A
mary gland, blood
ensions to establis
lity, and functional
agenase B
mary gland, blood
ensions to establis
viability are import
cal Produ
cience.com
nce G*CG*C and g
ited by 5-methylcy
e of 5-hydroxymeth
, BstHH I, Hha I.
embrane proteins.
e-type and bile-ac
a substrate for the
plasma kallikrein i
a substrate for the
plasmin in aqueou
a substrate for the
thrombin in aques
s and in cell cultur
ontent of one-chai
re of chymostatins
-, and -chymotr
encing Grade
uencing Grade for
in combination wit
ngerprinting, and
of citrate to aceta
consists of three di
ut 54,000, 32,000, a
nce *AT*CG*AT a
nhibited by overlap
wn (*). Isoschizome
5 I, BsuTU I.
EQKLISEEDL, comp
c-myc protein, is re
tition experiments,
oteins that contain
ormation of mitotic
aphase cells for ch
substrate for cultur
re dishes and the
ure grade.
, heart, muscle, bo
lity are important.
, heart, muscle, bo
tant.
uct Index
generates fragmen
ytosine, as shown (
hylcytosine at both
CHAPS combines
cid detergents. CM
e determination of
n citrated plasma.
e determination of
us solutions.
e determination of
ous solutions.
the determination
re supernatants. It
n and two-chain t-
s a, b and c and is
rypsin.
r the hydrolysis of
th other proteases
sequence analysis
ate and oxaloaceta
fferent polypeptide
and 10,000, respec
nd generates fragm
pping dam-methyla
ers: Ban III, Bsa29
prising 10-amino a
ecognized by Anti-
including affinity
this epitope.
c spindles. It is use
hromosome analys
ring a variety of ce
preparation of col
ture systems. Use
ture systems. Use
x
nts with 3-
(*). Inhibited by
h C residues.
the properties
MC: 4 mM.
f serine
f serine
f serine
of t-PA, both
can also be
-PA.
a specific
proteins by
s. It is suitable
s.
te, and is an
e chains with
ctively.
ments with 5'-
ation and 5-
I, BseC I, BshV
acids from the
-c-myc and
ed to increase
is.
ells. It is used
lagen gels. The
cartilage,
ngle-cell
when yield,
cartilage,
ngle-cell
when yield

Cat. No.

10 688 541 001
10 810 118 001
10 810 126 001
10 378 445 001
10 378 461 001
10 206 849 001
11 585 398 001
11 093 037 001
11 004 638 001
11 418 467 001
10 354 074 001
10 404 217 001
10 656 291 001
11 092 758 001
11 667 246 001
10 295 892 001
11 179 179 001
10 103 578 001
10 103 586 001
11 088 793 001
11 088 807 001
11 088 815 001
11 088 831 001

20 ml ((10 g/
Pack Size

1,000 U (10 U/l)

10 g
50 g

20 mg

20 mg

20 mg
100 mg

20 mg

10 mg

4 x 25 g

120 U

500 U (10 U/l)
2,500 U (10 U/l)
2,500 U (40 U/l)
5 mg

size membrane)

30 mg

100 mg
500 mg
2.5 g
100 mg
500 mg
2.5 g

gh 0.2 m pore

Price in

51,50
277,50
1.239,90
369,90
362,60
290,60
1.199,50
333,70
185,70
101,60
163,30
75,00
299,10
299,10
495,00
45,10
138,60
59,00
251,90
1.009,90
59,00
251,90
1.009,90

Alp

Prod

Colla
Disso
blood
estab
integ
Colla
Use t
hepa
such
adipo
Colla
Use t
high
and r
epidi
Colla
Colla
variet
Colla
deter
cOm
Rely
and m
New
Supp
cOm
Rely
and m
New
Supp
cOm
Prepa
above
cOm
High-
tagge
enab
cOm
Rapid
inhib
in ce
EDTA
cOm
Rapid
inhib
extra
IMAC
cOm
Rapid
inhib
extra
prepa
cOm
Supe
of se
bacte
cOm
Excel
prote
cOmp

lphabetic
duct Name
agenase D
d vessels, brain, et
blish primary cell c
rity of cell-surface
agenase H
tocytes from rat liv
as for large vesse
ocytes from epidid
agenase P
collagenase activi
rat. The preparatio
dymal fat pads of
agenase/Dispase
agenase/Dispase

ty of different tissu
agenase/Dispase

rmined empirically
mplete
on proven perform
metalloproteases i
for EDTA inhibitio
plied in glass vials.
mplete
on proven perform
metalloproteases i
for EDTA inhibitio
plied in EASYpacks
mplete His-Tag Pu
acked columns wit
e). Fully compatibl
mplete His-Tag Pu
-capacity IMAC m
ed proteins from ly
les compatibility w
mplete Lysis-B (2x
d, gentle bacterial
ition of protease a
ll extracts. Obtain
A-free preparation
mplete Lysis-M
d, gentle mammali
ition of protease a
cts. Produces high
C, use with cOmple
mplete Lysis-M ED
d, gentle mammali
ition of protease a
cts. Obtain higher
aration allows use
mplete ULTRA Tab
erb protein protect
rine, cysteine, and
erial, yeast, and ma
mplete ULTRA Tab
llent inhibition of s
plete His-Tag Purif
cal Produ
, heart, muscle, bo
c.), and prepare si
culture systems. Us
e proteins are impo
ver and for the pre
el endothelial cells,
ymal fat pads of ra
ty, you can isolate
n is also used to is
rats.
e

is used for the pre
ues and organs. Th
for preparation of
y.
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
s .
urification Colum
th cOmplete His-T
le with standard pu
urification Resin
atrix for convenien
ysates. Proprietary
with EDTA and DTT
x) EDTA-free
cell lysis in 10 min
higher yields of pr
allows use in IMA
her yields of protei
ete His-Tag Purific
DTA-free
yields of protein t
in IMAC.
blets, EDTA-free,
ion combined with
aspartic protease
ammalian cell type
blets, glass vials
serine, cysteine, me
uct Index
one, liver, mammar
ngle-cell suspensi
se when functiona
ortant.
mary cell cultures.
eparation of other t
, and for the isolati
ats.
mary cell cultures.
pancreatic islets f
solate adipocytes f
eparation of cells f
he suitability of
f a particular cell ty
pes as cOmplete U
mplete His-Tag Pur
pes as cOmplete U
mplete His-Tag Pur
mn
Tag Purification Re
urification systems
nt single-step purif
nickel-chelate che
T with minimal nic
nutes and simultan
teine, but not meta
rotein than using s
AC.
minutes and simult
teine, metalloprote
n than using sonic
cation Resin.
minutes and simult
teine, metalloprote
than using sonicat
glass vials
h ease of use: High
es for protein prote
es.
etallo- and asparti
d mammalian cell t
IMAC.
x
ry, kidney,
ions to
lity and
Isolate
types of cells,
ion of
Because of its
from mouse
from
from a wide
ype must be
ne, cysteine,
ULTRA Tablets.
rification Resin.
ne, cysteine,
ULTRA Tablets.
rification Resin.
sin (see
s.
fication of His-
emistry
kel leakage.
neous
alloproteases)
sonication.
aneous
eases) in cell
cation. For
aneous
eases) in cell
ion. EDTA-free
hest inhibition
ection in
ic proteases for
types. Use new

Cat. No.

11 088 858 001
11 088 866 001
11 088 882 001
11 074 032 001
11 074 059 001
11 087 789 001
11 213 857 001
11 213 865 001
11 213 873 001
10 269 638 001
11 097 113 001
11 697 498 001
11 836 145 001
04 693 116 001
06 781 543 001
06 781 535 001
05 893 682 001
05 893 801 001
04 719 948 001
04 719 956 001
04 719 964 001
05 892 953 001
06 538 282 001
05 892 988 001
06 538 304 001

20 tablets in a
for a volum
3 x 20 tablet
sufficient fo
20 tablets (in
packs, each ta
50 m
25 m
200 m
1 kit
1 kit for the ly
1 kit for the ly
2 glass via
6 glass via
2 glass via
6 glass via
Pack Size

100 mg
500 mg
2.5 g
100 mg
500 mg
2.5 g
100 mg
500 mg
2.5 g
100 mg
500 mg

me of 50 ml extract
or a volume of 50 m
solution

ndividually packed
ml extraction solut

5 x 1 ml
1 x 5 ml


for up to 20 extrac

ysis of up to 100 g
cells

ysis of up to 100 g
cells

ls each containing
EDTA-free
ls each containing
EDTA-free

als each containing
(with EDTA)
als each containing
(with EDTA)

www.roche
blet is sufficient
ion solution
each tablet is
ml extraction
d in foil blister
for a volume of
tion)
lume)
olume)
ctions
of mammalian
of mammalian
g 10 tablets,
g 10 tablets,
g 10 tablets
g 10 tablets
e-applied-science

Price in

59,00
251,90
1.009,90
59,00
250,90
1.009,90
80,80
326,40
1.296,50
130,80
454,20
257,20
692,90
257,20
179,00
130,00
290,40
1.583,60
234,20
314,90
314,90
262,40
630,40
262,40
707,30

119

e.com

Alp
120

www.r

Prod

cOm
High
prote
cOmp
cOm
Supe
serin
yeast
cOm
Rely
EDTA
types
cOm
Rely
EDTA
types
cOm
Rely
and m
New
Supp
cOm
Rely
and m
New
Supp
cOm
Rely
EDTA
types
cOm
Rely
EDTA
types
COT
Use C
repet
(CISS
hybri
COT
Supp
DNA
hybri
captu
CPRG
Color
The r
be ev
Crea
Enzym
of cre
dipho
Spec
lyoph
Crea
Subs
mole
phos
CSPD
Chem
extre
labele
shift
CSPD
Read
enab
nonra
For b

lphabetic
roche-applied-sc
duct Name
mplete ULTRA Tab
inhibition of serin
plete His-Tag Purif
mplete ULTRA Tab
erb protein protect
e, cysteine, and as
t, and mammalian
mplete, EDTA-free
on proven perform
A-free Tablets inhi
s as cOmplete ULT
mplete, EDTA-free
on proven perform
A-free Tablets inhi
s as cOmplete ULT
mplete, Mini
on proven perform
metalloproteases i
for EDTA inhibitio
plied in a glass vial
mplete, Mini
on proven perform
metalloproteases i
for EDTA inhibitio
plied in EASYpacks
mplete, Mini, EDTA
on proven perform
A-free Tablets inhi
s as cOmplete ULT
mplete, Mini, EDTA
on proven perform
A-free Tablets inhi
s as cOmplete ULT
Human DNA
COT Human DNA
titive DNA in in situ
S) hybridizations, h
dizations.
Human DNA, Flu
presses cross-hybr
probes are hybrid
dizations, such as
ure, and nucleic ac
G
rimetric determina
reaction product h
valuated photomet
atine Kinase (CK)
me expressed by v
eatine and consum
osphate.
ific Activity - appro
hilizate at +37C).
atine phosphate
trate for creatine k
cule that serves as
phates in skeletal
D
miluminescent sub
mely fast and sens
ed nucleic acids o
assays, and seque
D ready-to-use
dy-to-use chemilum
ling extremely fast
adioactively labele
blotting, gel shift as
cal Produ
cience.com
blets, Mini, EASY
e, cysteine, metallo
blets, Mini, EDTA
ion combined with
spartic proteases fo
cell types.
e
mance combined w
bit serine and cyst
TRA Tablets. Suppl
e
mance combined w
bit serine and cyst
TRA Tablets. Suppl
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
.
mance: cOmplete T
n the same cell typ
on: IMAC with cOm
s .
A-free
mance combined w
bit serine and cyst
TRA Tablets. Suppl
A-free
mance combined w
bit serine and cyst
TRA Tablets. Suppl
to suppress cross-
u hybridizations, c
hybridization to mic
uorometric Grade
ridization to human
dized in situ . Use in
comparative geno
cid labeling and de
tion of -Gal activ
as a dark red colo
trically at 574 or 57
)
various tissues and
mes ATP to create
ox. 350 U/mg lyop
kinase. The enzym
s a rapidly mobiliza
muscle and brain.
strate for alkaline
n film or luminesc
encing.
minescent substrat
t and sensitive visi
ed nucleic acids on
ssays, and sequen
uct Index
Ypack
o- and aspartic pro
d mammalian cell t
IMAC.
A-free, EASYpack
h ease of use: High
or protein protecti
with high convenie
teine proteases in
ied in glass vials.
with high convenie
teine proteases in
ied in EASYpacks
pes as cOmplete U
mplete His-Tag Pur
pes as cOmplete U
mplete His-Tag Pur
with high convenie
teine proteases in
ied in a glass vial.
with high convenie
teine proteases in
ied in EASYpacks
-hybridization to h
chromosome in situ
croarrays, and filte
e
n repetitive DNA w
n FISH and DNA m
ome hybridization,
etection.
vity in cell extracts
78 nm.
d cells. Catalyzes th
phosphocreatine a
hilizate at +25C (
e is a phosphoryla
able reserve of hig
.
phosphatase, ena
detection of nonra
cence imagers. For
te for alkaline pho
ble light detection
n film or luminesce
cing.
x
oteases for
types. Use new
k
h inhibition of
on in bacterial,
nce. cOmplete
the same cell
nce. cOmplete
the same cell
.
ne, cysteine,
ULTRA Tablets.
rification Resin.
ne, cysteine,
ULTRA Tablets.
rification Resin.
nce. cOmplete
the same cell
nce. cOmplete
the same cell
.
human
u suppression
er
when human
microarray
sequence
and ELISA.
water. It can
he conversion
and adenosine
(800 U/mg
ated creatine
gh-energy
bling
dioactively
r blotting, gel
sphatase,
n of
ence imagers.

Cat. No.

05 892 970 001
05 892 791 001
05 056 489 001
11 873 580 001
04 693 132 001
11 836 153 001
04 693 124 001
11 836 170 001
04 693 159 001
11 581 074 001
05 480 647 001
10 884 308 001
10 127 566 001
10 736 988 001
10 621 714 001
10 621 722 001
11 655 884 001
11 755 633 001

30 tablets (in
packs, each tab
m
30 tablets (in
packs, each tab
m
3 x 20 table
sufficient f
20 tablets in a
for a volum
20 tablets (in
packs; each ta
50 m
25 tablets in a
for a volum
30 tablets (in
packs, each ta
10 m
25 tablets in a
for a volum
30 tablets (in
packs, each ta
10 m
Pack Size

ndividually packed
blet is sufficient for
l extraction solutio

ndividually packed
for a volume of 50
me of 50 ml extract

ndividually packed
ml extraction solut
me of 10 ml extract

ndividually packed
ml extraction solut

me of 10 ml extract

ndividually packed
ml extraction solut
500 g (500 l)

1 ml (1 mg/ml)

250 mg

100 mg
500 mg

5 g
10 g

1 ml

2 x 50 ml

d in foil blister
r a volume of 10
on)
d in foil blister
r a volume of 10
on)
ach tablet is
ml solution
blet is sufficient
ion solution
d in foil blister
for a volume of
tion)
blet is sufficient
ion solution
d in foil blister
for a volume of
tion)
blet is sufficient
ion solution
d in foil blister
for a volume of
tion)

Price in

158,40
158,40
617,70
257,20
257,20
136,00
163,10
136,00
163,10
161,10
425,60
87,30
99,70
398,80
98,30
179,20
237,90
227,20

Alp

Prod

CTP
CTP,
such
is tes
Cyto
Fast a
meas
cell-m
cytot
Cyto
Fast a
cytot
cells.
fewe
D
D(-)
Use f
extra
toget
biolu
DAB
DAB
of ap
and w
DAP
DAPI
and f
speci
fluore
dATP
Use d
ampl
clear
dATP
Use d
reage
react
of the
dCTP
Use d
ampl
mM c
dCTP
Suita
as rev
sequ
solut
Dde
Dde
5-co
hydro
HpyF
Dens
These
Cell A
size a
Cede
Deox
PCR-
RT-P
sodiu
color

lphabetic
duct Name
a 100 mM solution
as in vitro RNA tr
sted for the absenc
otoxicity Detectio
and simple 6-well
suring LDH activity
mediated cytotoxic
oxic potential of co
otoxicity Detectio
and simple 96- or
oxicity/cytolysis by
Has all the benefi
r steps, plus it con
-Luciferin
for the luminometr
cts. It is a natural s
ther with firefly luc
minescence.
B Substrate
Substrate is a colo
pplications, such as
western and dot b
I
I is a fluorescent d
forms strongly fluo
ificity. It is commo
escence microscop
P
dATP, lithium salt,
ification reactions
, colorless solution
P
dATP, PCR Grade s
ents are required:
tions, and sequenc
e sodium salt (pH
P
dCTP, lithium salt,
ification reactions
P
verse transcription
encing/cycle sequ
ion of the sodium
I
I recognizes the se
ohesive termini. It i
oxymethylcytosine
F3 I.
sity Reference St
e beads are used t
Analyzers. They mi
and optical proper
ex Software.
xynucleoside Trip
-Grade set for app
CR, DNA labeling,
um salts of dATP, d
rless solutions in w
cal Produ
n of the lithium sa
ranscription. This s
ce of RNases.
on Kit (LDH)
plate method to q
y released from da
city, determine med
ompounds.
on Kit
PLUS
(LDH)
384-well plate me
y measuring LDH a
its of the Cytotoxic
ntains a stop soluti
ric determination o
substrate of lucife
ciferase for the det
or substrate for pe
s immunohistocyto
lotting.
ye that binds selec
orescent DNA-DAP
nly used to detect
py.
for DNA sequenci
or primer-extensio
n of the lithium sal
sodium salt for ap
reverse transcripti
cing. Supplied as 1
8.3).
for DNA sequenci
or primer-extensio
lution of the lithium
ns where high-qua
n, PCR, RT-PCR, D
salt (pH 8.3).
equence *CTNAG
s inhibited by the
at the site indicate
tandard Beads
to calibrate and ad
imic cell behavior
rties, they will be d
phosphate Set
lications requiring
sequencing. Cont
dCTP, dGTP, dTTP
water (pH 8.3).
uct Index
lt, is suitable for ap
special quality prep
quantify cytotoxicity
amaged cells. Dete
diator-induced cyt
ethod to quantify
activity released fr
city Detection Kit (
on.
of Luc gene activity
rase from firefly an
termination of ATP
eroxidase and is us
ochemistry, in situ
ctively to double-s
PI complexes with
Mycoplasma in ce
on reactions. dATP
t (pH 7).
plications where h
on, PCR, RT-PCR,
00 mM clear colo
on reactions. Supp
m salt (pH 7).
NA labeling reacti
t is a 100 mM clea
G and generates fr
presence of 5-me
ed (*). Isoschizome
djust Cedex and Ce
in flow dynamics.
etected as dead ce
high-quality reage
tains individual via
at 100 mM concen
x
pplications
paration of CTP
y/cytolysis by
ect and quantify
tolysis, and
om damaged
(LDH) with
y in cell
nd is used
P using
sed in a variety
hybridization,
stranded DNA
high
ell culture via
all types of
P is a 100 mM
high-quality
DNA labeling
rless solution
all types of
plied as a 100
equired, such
ons, and
r colorless
agments with
ethyl- or 5-
ers: BstDE I,
edex HiRes
Due to their
ells by the
ents: RT, PCR,
als of the
ntration. Clear,

Cat. No.

11 140 922 001
11 644 793 001
04 744 926 001
04 744 934 001
11 626 353 001
11 718 096 001
10 236 276 001
11 051 440 001
03 732 681 001
11 934 511 001
11 969 013 001
11 051 458 001
03 732 690 001
11 934 520 001
11 969 021 001
10 835 307 001
06 422 659 001
06 422 667 001
03 622 614 001
11 969 064 001

400
1 k
1 kit for
1 kit for u
250 l (25
standard
4 x 1,250
250 l (25
standard
1,250 l (125
31,250 stand
250 l (25 m
a
4 x 1,250
250 l (25 m
6,250 stand
1,250 l (125
standard
4 x 1,250 l (4 x
37,500 rea
4 x 250 l (4 x
6,250 rea
Pack Size

l (40 mol, 100 m


up to 400 tests in

50 mg

1 pack

10 mg

mol, 100 mM) for
d PCR assays of 20

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) 100
dard PCR assays o
assays of 20 l eac

l (4 x 125 mol, 4
mol, 100 mM) 100
dard PCR assays o
mol, 100 mM) fo
d PCR assays of 20
1,000 U (10 U/l)

1 x 10 ml batch A
1 x 10 ml batch B

x 125 mol, 4 x 100
actions at 20 l fin
x 25 mol, 4 x 100

www.roche
mM)
ests
96 wells
n 96 wells
r up to 6,250
0 l each
x 100 mM)
r up to 6,250
0 l each
0 mM, for up to
of 20 l each
standard PCR
ch
x 100 mM)
mM, for up to
f 20 l each
or up to 31,250
0 l each

A
B
0 mM) for up to
nal volume
mM) for up to
al volume
e-applied-science

Price in

108,40
615,70
208,00
561,70
716,80
184,50
68,20
68,80
1.029,80
89,10
328,70
68,80
1.029,80
89,10
328,70
171,70
inquire
inquire
1.061,20
235,50

121

e.com

Alp
122

www.r

Prod

Deox
Use f
prime
vials:
solut
dGTP
Use d
ampl
100 m
dGTP
Suita
as rev
sequ
solut
Dide
2',3'-
prime
Kleno
ddAT
the s
DIG
Nonr
dUTP
subst
dot b
DIG
Nonr
dUTP
detec
chrom
DIG
Easy-
11-dU
or in
0.65
DIG
Read
using
Hyb b
nonto
DIG
Block
labele
100 m
made
DIG
Nonr
prepa
comp
detec
DIG
Analy
of se
nitroc
tissue
DIG
High
South
chem
meth
DIG
Produ
chem
Desig
reage
DIG
Conta
acid
labele
and t

lphabetic
roche-applied-sc
duct Name
xynucleoside Trip
for sequencing/cyc
er extension, and a
dATP, dCTP, dGTP
P
dGTP, lithium salt,
ification reactions
mM clear, colorless
P
verse transcription
encing/cycle sequ
ion of the sodium
eoxynucleoside T
Dideoxynucleoside
er catalyzed by
ow enzyme and ar
TP, ddCTP, ddGTP,
odium salt (pH 8.3
DNA Labeling an
radioactive random
P, followed by colo
trates NBT and BC
blots, and colony a
DNA Labeling Ki
radioactive random
P. Used for in situ
ction. Detect labele
mogenic or chemil
DNA Labeling M
-to-use nonradioac
UTP. For Southern
situ hybridization;
mM dTTP, 0.35 mM
Easy Hyb
dy-to-use blocking
g nonradioactive, d
buffer cannot be u
oxic solution and d
Easy Hyb Granul
king buffer for mem
ed nucleic acid pro
ml of a 1x working
e solutions and lon
Gel Shift Kit, 2nd
radioactive detectio
aring 3'-end-labele
plexes in gel mobil
cts as little as 20 fm
Glycan Different
yze and characteri
lected lectins. In a
cellulose membran
e sections.
Luminescent Det
ly sensitive, specif
hern/northern blot
miluminescent subs
hods, with shorter e
Northern Starter
uce DIG-labeled R
miluminescent dete
gned for the novice
ents proven to pro
Nucleic Acid Det
ains all reagents to
hybrids. Used in S
ed nucleic acids a
the color substrate
cal Produ
cience.com
phosphate Set
cle sequencing, la
all types of amplific
P, dTTP; each cont
salt (pH 7).
for DNA sequenci
or primer-extensio
s solution of the lit
ns where high-qua
n, PCR, RT-PCR, D
salt (pH 8.3).
Triphosphate Set
e triphosphates inh
e used in Sanger s
ddTTP; each a 10
3).
nd Detection Kit
m primed labeling o
r detection using a
CIP. Use labeled pr
nd plaque screeni
it
m primed labeling o
and filter hybridiza
ed hybrids using a
luminescence AP s
Mix
ctive rapid random
, northern, and do
; 10x solution with
M DIG-11-dUTP.
buffer for all mem
digoxigenin-labeled
used for in situ hyb
does not contain fo
es
mbrane hybridizat
obes (not for ISH).
solution; 6 x 100 m
ng-term storage.
d generation
on of sequence-sp
ed oligonucleotide
lity shift assays. Co
mol of the control
iation Kit
ze carbohydrate st
addition to differen
nes, lectins can ide
tection Kit
ic detection of DIG
ts and plaque/colo
strate CSPD. Signa
exposure times.
r Kit
RNA probes to use
ection reagents for
e DIG system user
vide successful, re
tection Kit
o detect membran
Southern, northern,
re detected using
es NBT and BCIP.
uct Index
beling, reverse tra
cation reactions. S
tains 100 mM clea
on reactions. It is s
thium salt (pH 7).
NA labeling reacti
t is a 100 mM clea
hibit chain elongat
sequencing. Conta
mM clear colorles
of DNA probes usi
anti-DIG-AP conju
robes in Southern,
ng.
of DNA probes wit
ations and single-c
anti-DIG-AP conjug
substrates.
m primed labeling m
t blots, colony and
1 mM dATP, dCTP
mbrane hybridizatio
d nucleic acid pro
bridization. The bu
ormamide.
ion using nonradio
. Dissolve granules
ml portions allow f
pecific DNA bindin
e probes that detec
onvenient and sens
oligo.
tructures by the sp
tiating glycoprotei
entify carbohydrate
G-labeled nucleic a
ony lifts with anti-D
al is as sensitive as
with the supplied
r northern blotting
r. This Starter Kit c
eproducible results
e-blotted, DIG-lab
, and dot blots, and
anti-DIG-AP antib
x
nscription,
Set contains 4
ar, colorless
all types of
supplied as a
equired, such
ons, and
r colorless
tion of a
ains 4 vials:
ss solution of
ing DIG-11-
ugate and the
northern, and
th DIG-11-
copy gene
gate and
mix with Dig-
d plaque lifts,
P, dGTP (each),
on applications
bes. DIG Easy
ffer is a
oactive DIG-
s in water for
for freshly
ng proteins. For
ct DNA-protein
sitive kit
pecific binding
ins bound to
e structures on
acids in
DIG-AP and the
s radioactive
techniques.
ontains the
s.
beled nucleic
d ISH. DIG-
body conjugate

Cat. No.

11 277 049 001
11 922 505 001
11 051 466 001
03 732 703 001
11 934 538 001
11 969 030 001
03 732 738 001
11 093 657 910
11 175 033 910
11 277 065 910
11 603 558 001
11 796 895 001
03 353 591 910
11 210 238 001
11 363 514 910
12 039 672 910
11 175 041 910

4 x
40 x 100 l
250 l (25
standard
4 x 1,250
250 l (25
standard
1,250 l (125
standard
4 x 100
1 kit for up to 2
of 50 blots, 10
1 kit for up to 4
50 l for
gr
1 kit for up to 2
reactions wi
reactions, chem
for up to 20
oligonucleotid
1 kit for the de
1 kit for u
1 kit for up to 1
of 10 blots, blot
DNA, yielding
1 kit for up
Pack Size

x 10 mol (4 x 100
l (40 x 10 mol, 40

mol, 100 mM) for
d PCR assays of 20

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
l (4 x 1 mol; 10 m

5 labeling reaction
ng to 3 g per ass
cm
2

0 labeling reaction
DNA per assay

up to 25 standard

500 ml

ranules for 6 x 100

20 Oligonucleotide
ith DIG-11-ddUTP,
miluminescent det
blots, DNA binding
de for up to 20 con
etection on 25 blot
cm

up to 50 blots of 1

0 labeling reaction
ts of 10 x 10 cm
2
r
approx. 20 g labe

p to 40 blots of 10

l)
x 100 mM)
r up to 6,250
0 l each
x 100 mM)
r up to 6,250
0 l each
or up to 31,250
0 l each
mM each)
ns and detection
say, blots of 100
ns, 10 ng to 3 g
reactions
ml
e 3'-end labeling
, 200 binding
tection reaction
g protein and
ntrol reactions
ts, each 10 x 10
0 x 10 cm
ns and detection
reactions of 1g
eled RNA, each
cm x 10 cm

Price in

126,10
885,00
68,80
1.029,80
89,10
328,70
228,40
801,40
626,60
164,50
279,30
321,10
715,20
620,40
541,40
508,20
413,20

Alp

Prod

DIG
3'-en
using
oligo
mem
DIG
For fa
11-dU
with
blots
DIG
Comp
(SP6/
effici
and R
DIG
Mixtu
(SP6/
and R
(each
DIG W
The D
hybri
block
DIG-
Prem
Obta
incub
dot b
DIG-
Comp
dUTP
probe
and c
DIG-
Comp
chem
labele
South
DIG-
Estim
hybri
temp
DIG-
Estim
probe
of DI
temp
DIG-
Conv
labele
for fil
the D
Digo
Subs
rever
recom
DNA
Digo
Subs
Repla
Use t
South
Digo
Subs
trans
labele
and r

lphabetic
duct Name
Oligonucleotide
nd labeling of oligo
g DIG-11-ddUTP a
nucleotides are us
brane-blot applica
Oligonucleotide
ast and sensitive ta
UTP and recombin
DIG-dUTP are use
or in situ hybridiz
RNA Labeling Ki
plete kit for RNA la
/T7). DIG-labeled r
ency. Used in nort
RNase protection e
RNA Labeling M
ure for RNA labelin
/T7/T3). Used in no
RNase protection e
h), 6.5 mM UTP, 3.5
Wash and Block
DIG Wash and Blo
dization and DIG d
king solution and m
-High Prime
mixed solution for ra
in high yields of la
bation. Use labeled
blots, and colony/p
-High Prime DNA
plete, convenient k
P and color detecti
es in 1 hour to ove
colony/plaque hyb
-High Prime DNA
plete, convenient k
milumiluminescent
ed probe in 1 hour
hern/northern blot
-labeled Control
dization probe in S
plate DNA and app
-labeled Control
e in Southern and
G-labeled neo-RN
plate DNA (fragme
-Nick Translation
venient enzyme nu
ed using DIG-11-d
DIG-High Prime kit
oxigenin-11-ddUT
trate for E. coli DN
rse transcriptase. Id
mbinant TdT. DIG-
/RNA transfers, IS
oxigenin-11-dUTP
aces dTTP in nick t
this alkaline-labile
hern blots planned
oxigenin-11-dUTP
salation, random pr
ed DNA needs to
reprobing, use DIG
cal Produ
3'-End Labeling
onucleotides from
nd recombinant Te
sed as hybridizatio
ations and in situ h
Tailing Kit, 2nd g
ailing of oligonucle
nant Terminal Tran
ed for DNA or RNA
zation.
t (SP6/T7)
abeling using DIG-
run-off transcripts
thern/Southern blo
experiments.
ix
ng using DIG-11-U
orthern/Southern b
experiments; 10x s
5 mM DIG-11-UTP
Buffer Set
ck Buffer Set is us
detection. The set
maleic acid, washin
andom primed DN
abeled probes with
d probes in library
plaque hybridizatio
A Labeling and De
kit for random prim
on of labeled hybr
ernight incubation.
bridizations.
A Labeling and De
kit for random-prim
detection of labele
r to overnight incu
ts, colony/plaque h
DNA
IG-labeled nucleic
Southern blots. Th
prox. 250 ng synthe
RNA
IG-labeled RNA or
northern blots. Th
NA (760 bp length)
nts of 798 and 328
n Mix
cleotide mix to ge
dUTP for in situ hy
ts.
TP
NA polymerase, T4
deal for 3'-end lab
labeled oligos can
H, and colony/plaq
P, alkali-labile
oli DNA polymeras
transalation, rando
formulation when
d.
P, alkali-stable
oli polymerase, RT
rimed labeling, and
survive alkaline tre
G-11-dUTP, alkali-l
uct Index
Kit, 2nd generati
14 to 100 nucleotid
erminal Transferas
n probes in all typ
hybridization.
generation
eotides at the 3'-e
nsferase. Oligonucl
A hybridization in m
-11-UTP by in vitro
are synthesized w
ots, ISH, plaque or
blots, ISH, plaque
solution of 10 mM
P.
sed at various step
contains 10x prep
ng, and detection
NA labeling using D
hin one hour or ove
screening, Southe
ns.
etection Starter
med DNA labeling
rids. Obtain high y
. Use in Southern/
etection Starter
med DNA labeling
ed hybrids. Obtain
ubation. Use in
hybridization.
c acids or use as a
e solution contain
esized DIG-labeled
r use as a control h
he solution contain
and 0.5 g pSPT1
81 bp).
nerate highly sens
ybridization. The m
4 /T7 DNA polyme
beling of oligonucle
n be used as a prob
que screening.
se, RT, and termina
om primed labeling
n stripping and rep
T, and TdT. Replace
d PCR. Use when t
eatment. For memb
labile.
x
ion
des in length
se. DIG-labeled
pes of
nd using DIG-
leotides tailed
membrane
o transcription
with high
colony lifts,
nscription
or colony lifts,
ATP, CTP, GTP
s of DIG
arations of
buffers.
DIG-11-dUTP.
ernight
ern, northern,
Kit I
using DIG-11-
ields of labeled
northern blots,
Kit II
with DIG and
n high yield of
control
s 1 g
d DNA.
hybridization
ns approx. 5 g
8-neo
sitive probes
mix can be used
on probes, use
rase, Taq, and
eotides with
be for
al transferase.
g, and PCR.
probing of
es dTTP in nick
the DIG-
brane stripping

Cat. No.

03 353 575 910
03 353 583 910
11 175 025 910
11 277 073 910
11 585 762 001
11 585 606 910
11 745 832 910
11 585 614 910
11 585 738 910
11 585 746 910
11 745 816 910
11 363 905 910
11 573 152 910
11 573 179 910
11 093 088 910
11 558 706 910
11 570 013 910

1 kit for up to 2
oligonucleotide
of a
1 kit for up to
oligonucleotide
of a
1 kit for up
40
1
160 l for up t
tem
1 kit for up to 1
of 24 blots, 10 n
1 kit for up to 1
of 24 blots, 10
50 l (5 g/
50 l (10
160 l for
25
25
125
25
125
5 x 125
Pack Size

25 labeling reactio
s per assay corres
30-mer oligonucle

e per assay corresp
30-mer oligonucle


l for up to 20 reac


o 40 labeling assay
mplate DNA per as

2 labeling reaction
ng to 3 g DNA pe
100 cm
2

2 labeling reaction
ng to 3 g per ass
cm
2

/ml DIG-labeled pl

00 g/ml DIG-labe

r up to 40 labeling

5 l (25 nmol; 1 mM

5 l (25 nmol) (1 m
5 l (125 nmol) (1 m

5 l (25 nmol) (1 m
5 l (125 nmol) (1 m
l (5 x 125 nmol) (5

www.roche
ons, 100 pmol of
sponding to 1 g
eotide
ons, 100 pmol
ponding to 1 g
eotide
g reactions
ctions
ots
ys, 0.01 to 3 g
ssay
ns and detection
er assay, blots of
ns and detection
say, blots of 100
asmid DNA)
led RNA)
reactions
M)
mM)
mM)
mM)
mM)
5 x 1 mM)
e-applied-science

Price in

571,60
531,40
590,90
168,70
264,40
560,20
484,80
493,20
118,30
118,30
508,80
274,20
225,80
826,40
225,80
826,40
3.325,20

123

e.com

Alp
124

www.r

Prod

Digo
Subs
vitro
of 35
the D
Digo
hydr
For D
via am
with
group
Disp
Rapid
Relea
cultu
suspe
Disp
Rapid
Relea
cultu
suspe
Disp
This C
liquid
using
in pu
DNA
The D
assay
micro
DNA
Easily
South
Elimi
reage
DNA
Rapid
or bu
diges
purifi
DNA
For s
mole
gene
23.1
DNA
DNA
in So
label
DNA
For s
deter
restri
DNA
DNA
in So
label
DNA
For s
deter
restri
DNA
For s
deter
restri
DNA
For s
deter
restri
DNA
For s
deter
restri
lphabetic
roche-applied-sc
duct Name
oxigenin-11-UTP
transcription RNA
to 65. Detect labe
DIG Nucleic Acid D
oxigenin-3-O-me
oxysuccinimide e
DIG labeling of pro
mino groups (unde
NH
2
-groups of pro
p, digoxigenin, is b
pase
I (neutral p
re to transfer to a
ension.
pase
II (neutral
re to transfer to a
ension.
penser 2 - 10 ml
Ceramus Dispense
d volumes in increm
g CASY Cell Count
urity and volume pr
A Fragmentation I
DNA Fragmentatio
y to detect apoptos
oplates. It is ideal f
A Isolation Kit for
y and quickly isola
hern blots, restrict
nates organic extr
ents.
A Isolation Kit for
dly isolate DNA fro
uffy coat samples.
sts, and Southern b
ication steps, and
A Molecular Weig
ize distribution an
cular weight deter
rated by restriction
kbp.
A Molecular Weig
Molecular Weight
outhern blot analys
ing and detection.
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
outhern blot analys
ing and detection.
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
cal Produ
cience.com
and T7 RNA Polym
A labeling reaction
eled RNA using An
Detection (color or
ethylcarbonyl--
ester
teins and 5'-amino
er gentle condition
oteins or oligonuc
bound by Anti-Dig
protease, grade I
secondary culture
protease, grade
secondary culture
er is used for high
ments of 0.25 ml o
ters and Analyzers
recision.
Imaging Kit
on Imaging Kit prov
sis induction in ma
for high throughpu
Cells and Tissue
ates DNA from mos
ion digests, PCR/lo
actions, anion exc
Mammalian Blo
om 1 -10 ml mamm
Use in PCR or long
blots. Eliminate org
chaotropic reagen
ght Marker II
alysis using agaro
rmination of doubl
n digests, PCR, an
ght Marker II, DIG
t Marker II, DIG-la
sis when using the
Size range: 0.12 to
ght Marker III
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker III, DI
t Marker III, DIG-la
sis when using the
Size range: 0.12 to
ght Marker IV
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker IX
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker V
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker VI
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
uct Index
merases. Replaces U
using a percent D
nti-DIG-AP and ch
chemiluminescen
-aminocaproic ac
o-substituted oligo
ns). One reactive g
leotides. The other
oxigenin and dete
)
x in many tissues a
ure or harvesting c
II)
x in many tissues a
ure or harvesting c
ly reproducible adj
of CASY ton for me
s. It guarantees opt
vides a simple and
ammalian cells in 9
ut cellular workflow
es
st cells and tissues
ong PCR, and sequ
hange columns, a
ood
malian whole blood
g PCR, sequencing
ganic extractions,
nts.
se gels. Simplifies
e-stranded DNA f
d RT-PCR. Size ran
G-labeled
beled, is used as a
DIG System for nu
o 23.1 kbp.
plifies accurate mo
fragments generate
e range: 0.12 to 21
IG-labeled
abeled, is used as
DIG System for nu
o 21.2 kbp.
plifies accurate mo
fragments generate
e range: 0.07 to 19
plifies accurate mo
fragments generate
e range: 72 to 135
plifies accurate mo
fragments generate
e range: 8 to 587 b
plifies accurate mo
fragments generate
e range: 0.15 to 2.
x
UTP in the in
Dig-UTP ratio
oose one of
t) Kits.
cid-N-
onucleotides
group interacts
r functional
cted.
and organs.
cells already in
mping in
and organs.
cells already in
mping in
justment of
easurements
timum quality
d rapid TUNEL
96-well
ws.
s. Use for
uencing.
nd chaotropic
d, lymphocyte,
g, restriction
column
accurate
fragments
nge: 0.12 to
a size standard
ucleic acid
olecular weight
ed by
1.2 kbp.
a size standard
ucleic acid
olecular weight
ed by
9.3 kbp.
olecular weight
ed by
3 bp.
olecular weight
ed by
bp.
olecular weight
ed by
1 kbp.

Cat. No.

03 359 247 910
11 209 256 910
11 333 054 001
04 942 086 001
04 942 078 001
05 651 751 001
06 432 344 001
11 814 770 001
11 667 327 001
10 236 250 001
11 218 590 910
10 528 552 001
11 218 603 910
11 418 009 001
11 449 460 001
10 821 705 001
11 062 590 001

57
25
10 x approx. 2
5
1 kit (10 isola
or 5
1 kit for up to
50 g in 200 l
50
50 g in 200 l
50
50 g in 200 l
50 g in 200 l
50 g in 200 l
50 g in 200 l
Pack Size

l (200 nmol, 3.5 m
l (250 nmol, 10 m

5 mg

mg (filtered throu
size membrane)


1 dispenser

96 tests

ations of 400 mg e
5 x 10
7
cultured ce

25 purifications of

(1 A
260
unit) for up

00 l (5 g, 10 g/m

(1 A
260
unit) for up

00 l (5 g, 10 g/m

(1 A
260
unit) for up

(1 A
260
unit) for up

(1 A
260
unit) for up

(1 A
260
unit) for up

mM)
mM)
gh 0.2 m pore
e)
each for tissue
ells)
f 10 ml samples
p to 50 gel lanes
ml)
p to 50 gel lanes
ml)
p to 50 gel lanes
p to 50 gel lanes
p to 50 gel lanes
p to 50 gel lanes

Price in

196,10
260,60
190,90
753,70
435,30
inquire
685,00
234,80
242,60
100,10
205,30
111,00
205,30
161,70
190,70
152,00
152,00

Alp

Prod

DNA
DNA
stand
acid
DNA
For s
deter
restri
DNA
DNA
stand
acid
DNA
For s
deter
restri
DNA
DNA
stand
acid
DNA
For s
deter
restri
DNA
For s
deter
restri
DNA
For s
deter
restri
addit
DNA
Mark
Allow
Temp
cleav
agaro
DNA
For s
deter
restri
DNA
For s
deter
restri
DNA
This
conta
trans
DNA
This
diges
DNA
The r
preve
DNA
dena
DNa
DNas
endo
for is
as a
DNa
DNas
degra
DNA
this e

lphabetic
duct Name
A Molecular Weig
Molecular Weight
dard in Southern b
labeling and detec
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
dard in Southern b
labeling and detec
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
Molecular Weight
dard in Southern b
labeling and detec
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
tional band of 2642
A Molecular Weig
ker)
ws accurate sizing
plate PCR System o
ved with rare-cuttin
ose gels. Size rang
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Molecular Weig
ize distribution in
rmination of doubl
iction digests, PCR
A Polymerase I
recombinant DNA
ain DNase I). It can
slation (with added
A, lambda
high quality prepa
sts, amplification o
A, MB-grade
ready-to-use solut
ents nonspecific hy
hybridizations. Ad
turing are not requ
se I
se I, Grade II from
onuclease that requ
solation procedures
lyophilizate.
se I
se I (double-strand
ades DNA. During
which causes cell
extracellular DNA.
cal Produ
ght Marker VI, DI
t Marker VI, DIG-la
blot analysis when
ght Marker VII
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker VII, D
t Marker VII, DIG-l
blot analysis when
ght Marker VIII
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker VIII, D
t Marker VII, DIG-l
blot analysis when
ght Marker X
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker XIII (5
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker XIV (1
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
2 bp.
ght Marker XV (E
of DNA fragments
or restriction diges
ng restriction endo
ge: 2.3 to 48.5 kbp.
ght Marker XVI (2
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
ght Marker XVII (
agarose gels. Simp
e-stranded DNA f
R, and RT-PCR. Size
A Polymerase I is en
n therefore be use
d DNase I) and sec
ration of Lambda
of large DNA targe
ion is directly adde
ybridization in all t
ddition of NaCl, so
uired.
bovine pancreas i
uires bivalent catio
s for proteins (e.g
d specific endonuc
tissue dissociatio
l clumping. Adding
Lyophilized.
uct Index
IG-labeled
abeled, is used as
using the DIG Sys
0.15 to 2.1 kbp.
plifies accurate mo
fragments generate
e range: 0.081 to 8
DIG-labeled
labeled, is used as
using the DIG Sys
0.081 to 8.57 kbp.
plifies accurate mo
fragments generate
e range: 19 to 111
DIG-labeled
labeled, is used as
using the DIG Sys
19 - 1114 bp.
plifies accurate mo
fragments generate
e range: 100 bp to
50 bp ladder)
plifies accurate mo
fragments generate
e range: 50 to 750
100 bp ladder)
plifies accurate mo
fragments generate
e range: 100 to 15
Expand DNA Mole
s generated by the
st of high molecula
onucleases and se
250 bp ladder)
plifies accurate mo
fragments generate
e range: 0.25 to 3.0
(500 bp ladder)
plifies accurate mo
fragments generate
e range: 0.5 to 5.0
ndonuclease-free
d for labeling of D
cond-strand synthe
DNA is used for re
ets, and as a PCR c
ed to the hybridiza
types of membrane
nication or shearin
s a double-strand-
ons for maximal ac
., membrane prote
clease) from bovin
n, some cells are ly
g DNase I to the b
x
a size
stem for nucleic
olecular weight
ed by
8.57 kbp.
s a size
stem for nucleic
olecular weight
ed by
4 bp.
s a size
stem for nucleic
olecular weight
ed by
o 12.2 kbp.
olecular weight
ed by
bp.
olecular weight
ed by
00 bp and an
ecular Weight
e Expand Long
ar weight DNA
eparated on
olecular weight
ed by
0 kbp.
olecular weight
ed by
kbp.
(does not
DNA by nick
esis of cDNA.
estriction
control.
ation mix. It
e or in situ
ng, and
-specific
ctivity. It is used
eins). Supplied
e pancreas
ysed, releasing
uffer degrades

Cat. No.

11 218 611 910
11 209 264 001
11 669 940 910
11 336 045 001
11 449 451 910
11 498 037 001
11 721 925 001
11 721 933 001
11 721 615 001
11 855 638 001
11 855 646 001
10 642 711 001
10 642 720 001
10 745 782 001
11 467 140 001
10 104 159 001
11 284 932 001

50
50 g in 200 l
50
50 g in 200 l
500
100 g in 400
50 g (1 A
2
50 g in 200 l
50 g in 200 l
50 g in 200 l
Pack Size

00 l (5 g, 10 g/m

(1 A
260
unit) for up

00 l (5 g, 10 g/m

(1 A
260
unit) for up

0 l (10 g/ml) (5

l (2 A
260
units) fo
lanes

260
unit) for up to 5

(1 A
260
unit) for up

50 g (1 A
260
unit)

(1 A
260
unit) for up

(1 A
260
unit) for up

250 U
1,000 U

1 ml (5 A
260
units)

500 mg (50 ml)

100 mg

100 mg

www.roche
ml)
p to 50 gel lanes
ml)
p to 50 gel lanes
g)
or up to 50 gel
50 gel lanes
p to 50 gel lanes
)
p to 50 gel lanes
p to 50 gel lanes
)
e-applied-science

Price in

203,90
152,00
231,40
173,70
256,00
125,60
132,80
139,80
121,90
115,70
115,70
146,20
486,00
119,10
197,80
58,20
157,20

125

e.com

Alp
126

www.r

Prod

DNa
DNas
isolat
DNA
DNa
Degr
to rem
after
sensi
DOTA
High
for tr
charg
and p
Dpn
Reco
ends
at the
Mal I
Dra I
Dra I
blunt
the s
isosc
Dra I
Dra I
fragm
(*). Is
DTT
For lu
extra
prote
mono
dTTP
Use d
ampl
mM c
dTTP
Suita
as rev
sequ
solut
dUTP
For s
react
DNA
conta
dUTP
Use d
requi
conta
Supp
E
E-64
Stron
cathe
of pro
betw
EclX
Reco
cohe
show
BseX
Eco4
Eco 4
with
as ind
Aor5
lphabetic
roche-applied-sc
duct Name
se I recombinant
se I, recombinant,
tion procedures, a
during sample pre
se I recombinant
rades DNA in appl
move genomic DN
in vitro transcripti
itive regions in euk
AP Liposomal Tr
ly efficient transfec
ransient or stable g
ged molecules, suc
proteins into mam
I
ognizes the sequen
. The enzyme is on
e indicated site (*)
I.
I
recognizes the se
t ends. Dra I is not
ite indicated () on
chizomer of Aha III
III
II recognizes the s
ments with 3-cohe
soschizomer: Ade I
uminometric deter
cts. Superb protec
eins/enzymes (com
othiols in the reduc
P
dTTP, lithium salt, f
ification reactions
P
verse transcription
encing/cycle sequ
ion of the sodium
P
equencing, labelin
tions. DNA contain
glycosylase. This
amination; 100 mM
P
dUTP, PCR Grade f
ired: RT, PCR, RT-P
amination between
plied as 100 mM so
4
ng, irreversible inhi
epsin B and L, bro
oteins and enzyme
een the SH compo
I (Xma III)
ognizes the sequen
wn (*). 5-methylcyto
X3 I, BstZ I, Eag I, E
47 III
47 III recognizes th
blunt ends. Eco47
dicated (*). 6-mety
1H I.
cal Produ
cience.com
t
grade I is used for
nalysis of chromat
eparation.
t, RNase-free
ications sensitive t
NA from RNA prep
ion, perform nick t
karyotic DNA.
ransfection Reag
ction of DNA inclu
gene expression, a
ch as RNA, oligos,
malian cells.
nce GmAT*C and
nly inhibited by the
if no 6-methylade
equence TTTAAA
inhibited by the p
n the recognition s
.
sequence C*A*CNN
esive termini. It is m
I.
mination of Lucife
ctive reagent for su
mpared to -merc
ced state and qua
for DNA sequenci
or primer-extensio
lution of lithium sa
ns where high-qua
n, PCR, RT-PCR, D
uencing analysis. T
salt (pH 8.3).
ng, primer extensio
ning dUTP is susce
allows dUTP to be
M lithium salt solut
for applications wh
PCR, labeling, sequ
n PCRs to eliminat
olution of the sodiu
ibitor of papain an
melain, and ficin d
es. Inhibition of thi
onents.
nce *CGG*C*CG a
ited by 5-methylcy
osine in position 4
Eco52 I.
he sequence AG*C
III is inhibited by t
yladenine is not inh
uct Index
r eliminating DNA
tin structure, and e
to the presence of
arations, isolate D
translations, and to
ent
uding YACs into eu
nd for transfer of n
nucleotides, RNP
generates fragme
e occurrence of 5-
enine is present. Is
A and generates fr
presence of 6-meth
sequence. Dra I is
NNGTG and gene
methlation sensitiv
erase gene activity
ulfhydryl groups of
captoethanol). Mai
ntitatively reduces
ng, labeling, and a
on reactions. Supp
alt (pH 7).
NA labeling reacti
This is a 100 mM cl
on,and all types of
eptible to hydrolysi
e used to prevent c
tion.
here high-quality r
uencing. Avoid car
e a source of false
um salt.
nd cysteine proteas
during isolation and
ol proteases is non
and generates frag
ytosine in position
4 also inhibits. Isosc
CGCT and genera
the presence of 5-
hibiting.Isoschizom
x
during protein
eliminating
RNase. Used
NA-free RNA
o map DNase-
ukaryotic cells
negatively
complexes,
ents with blunt
methylcytosine
oschizomer:
ragments with
hyladenine at
an
erates
ve as indicated
in cell
f
ntains
s disulfides.
all types of
plied as a 100
equired, such
ons, and
lear colorless
amplification
is using uracil-
carryover
reagents are
rryover
e positives.
ses, such as
d purification
n-competitive
gments with 5-
1 and 5 as
chizomers:
ates fragments
-methylcytosine
mers: Afe I,

Cat. No.

04 536 282 001
04 716 728 001
11 202 375 001
10 742 970 001
10 742 988 001
10 827 754 001
10 843 547 001
10 197 777 001
10 708 984 001
11 583 786 001
11 051 482 001
03 732 711 001
11 934 546 001
11 969 048 001
11 420 470 001
03 732 720 001
11 934 554 001
11 969 056 001
10 874 523 001
11 585 681 001
11 131 397 001
11 167 103 001

10,000 U (pr
5
250 l (25 m
a
4 x 1,250
250 l (25
standard
1,250 l (125
standard
250 l (25
standard
4 x 1,250
250 l (25
standard
1,250 l (125
standard
Pack Size

2 x 10,000 U

rovided with incub

x 400 l (5 x 400

200 U (10 U/l)
1,000 U (10 U/l)

5,000 U (10 U/l)

500 U (1 - 5 U/l)

2 g
10 g
25 g
assays of 20 l eac

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
mol, 100 mM) for
d PCR assays of 20

l (4 x 125 mol, 4
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
10 mg
25 mg

1,000 U (10 U/l)

100 U (5 U/l)

bation buffer)
g)

)
standard PCR
ch
x 100 mM)
r up to 6,250
0 l each
or up to 31,250
0 l each
r up to 6,250
0 l each
x 100 mM)
r up to 6,250
0 l each
or up to 31,250
0 l each

Price in

119,20
213,30
327,80
85,30
338,80
143,30
274,00
inquire
183,80
417,60
68,80
1.029,80
89,10
328,70
94,30
1.029,80
89,10
328,70
270,20
542,80
490,00
189,80

Alp

Prod

EcoR
Eco R
with
or bo
isosc
EcoR
Reco
blunt
(*). It
Hydro
Endo
Use r
glyco
glyco
N-Gly
Endo
Endo
purifi
mapp
solut
Endo
Endo
speci
analy
Endo
Use E
and f
Endo
Endo
is a h
analy
Endo
Use E
sequ
Endo
Endo
is a h
sequ
polya
Endo
ECGF
stimu
has a
grow
Ente
Enter
used
activa
Epide
Reco
prolif
and m
formu
EPO
The E
scien
conc
proce
Eryth
Eryth
differ
respo
and a

lphabetic
duct Name
R I
RI recognizes the s
5-cohesive termin
oth A residues, and
chizomer to Rsr I.
R V
ognizes the sequen
is not inhibited by
oxymethylcytosine
oglycosidase H
recombinant Endo
oproteins. Endoglyc
opeptides and prot
ycosidase A to cle
oproteinase Arg-
oproteinase Arg-C
ied, specific cystei
ping, fingerprinting
ion, gels, or on me
oproteinase Asp-
oproteinase Asp-N
ific metalloproteas
ysis.
oproteinase Glu-C
Endoproteinase Gl
for sequence analy
oproteinase Glu-C
oproteinase Glu-C
highly purified and
ysis and for sequen
oproteinase Lys-C
Endoproteinase Ly
ence analysis.
oproteinase Lys-C
oproteinase Lys-C S
highly purified, spe
ence analysis. Suit
acrylamide gels, or
othelial Cell Grow
F and basic fibrobl
ulate the growth of
also been reported
wth of hybridomas a
rokinase
rokinase is a highly
for the cleavage o
ates trypsinogen to
ermal Growth Fa
ombinant, human E
feration and differe
mesodermal origin
ulations.
ELISA
EPO ELISA is a fast
nce research studie
entrations in plasm
edures.
hropoietin, huma
hropoietin is a glyc
rentiation of erythr
onsive to EPO have
adult spleen.
cal Produ
sequence G*A*AT
ni. EcoR I is inhibite
d by 5-methylcytos
nce G*ATATC an
y the presence of 6
y the presence of 5
e. Isoschizomer: Ec
glycosidase H for
cosidase H hydroly
teins. It cleaves on
eave glycopeptides
C Sequencing G
Sequencing Grade
ne protease to cle
g, and sequence a
embrane blots.
-N Sequencing G
Sequencing Grad
se used for protein
C (V8 Protease)
u-C (V8 Protease)
ysis.
C Sequencing Gr
Sequencing Grade
specific serine pr
nce analysis.
C
ys-C for protein str
C Sequencing Gr
Sequencing Grade
ecific serine protea
table to digest pro
r on blotting memb
wth Factor, bovin
ast growth factor a
f endothelial cells.
d to eliminate the n
and other cell type
y purified preparat
of fusion proteins a
o trypsin.
actor, human (hEG
Epidermal Growth
entiation of a wide
n, and is a constitu
t, highly sensitive a
es as a method for
ma and serum. Not
an (hEPO)
oprotein which sti
roid precursor cells
e been identified in
uct Index
TT*C and generate
ed by 6-methylade
sine as indicated (*
nd generates fragm
6-methyladenine, a
5-methylcytosine (
co 32I.
the deglycosylatio
yzes N-linked oligo
ly high mannose s
s.
rade
e from C. histolytic
ave proteins/pepti
nalysis, and to dig
Grade
e is a highly purifi
n structure and seq
for protein structu
rade
e from Staphylococ
otease used for pr
ructure analysis an
rade
e from Lysobacter
ase for protein stru
oteins in solution, in
branes.
ne (bECGF)
are the only mitog
ECGF, bovine (cul
need for feeder cel
es.
tion from calf intes
at definite cleavag
GF)
Factor (EGF) stimu
e variety of cells of
ent of many serum
and easy assay for
r the determination
t for use in diagno
mulates proliferati
s to mature erythro
n adult bone marro
x
es fragments
enine at either
*). Eco RI is an
ments with
as indicated
() or 5-
n of
osaccarides of
structures. Use
cum is a highly
ides for
est protein in
ed and
quence
ure analysis
ccus aureus V8
rotein structure
nd for
enzymogenes
ucture and
n
gens that
lture grade)
lls in the clonal
stine and is
e site;
ulates the
ectodermal
m-free media
r use in life
n of EPO
ostic
on and
ocytes. Cells
ow, fetal liver,

Cat. No.

10 200 310 001
10 606 189 001
10 703 737 001
11 175 084 001
10 667 145 001
10 667 153 001
11 040 197 001
11 088 726 001
11 643 053 001
11 370 529 001
11 054 589 001
11 420 488 001
10 791 156 001
11 047 817 001
11 420 399 001
10 476 986 001
11 047 825 001
11 420 429 001
11 033 484 001
11 334 115 001
11 351 311 001
11 376 454 001
11 693 417 001
11 120 166 001

1
2
Pack Size

10,000 U (40 U/l)
50,000 U (40 U/l)
5,000 U (10 U/l)
10,000 U (10 U/l)
2,000 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
1 U (200 l)
2.5 U (500 l)

3 x 5 g

3 x 2 g
2 g

2 mg

3 x 50 g
50 g

3 U

3 x 5 g
5 g

75 mg

3 x 30 g
3 x 250 g

100 g


250 U (2.5 g, 1 m

www.roche
)
)

)

)
)
sts
l)
e-applied-science

Price in

52,30
210,30
42,00
52,30
75,00
282,00
282,00
406,10
749,00
305,00
403,90
161,80
147,60
397,10
157,90
325,60
326,30
128,30
493,60
287,80
1.115,30
426,10
711,40
363,80

127

e.com

Alp
128

www.r

Prod

Expa
Amp
buffe
and D
large
Expa
Amp
enzym
produ
ampl
Expa
Expa
resul
to Ta
targe
Expa
Enzym
three
resul
ready
Expa
Enzym
outst
PCR,
ampl
Expa
Enzym
outst
PCR.
Conta
Expa
For c
Use t
mix, a
PCR,
Expa
A RN
ampl
RACE
Expa
huma
F
Fast
Used
with
organ
using
FastS
Read
on th
gene
addit
FastS
Read
the L
gene
prime

lphabetic
roche-applied-sc
duct Name
and 20 kb
PLUS
PCR
lify genomic DNA
er and enzyme blen
DNA produce frag
e-fragment amplific
and 20 kb
PLUS
PCR
lify genomic DNA
me blend amplify p
uce fragments 23
ification. Contains
and High Fidelity
nd High Fidelity Sy
ts with twofold hig
q. Choose this sys
ets up to 5 kb, in PC
and High Fidelity
me blend that deliv
efold greater fidelit
ts for genomic targ
y-to-use PCR nucl
and High Fidelity
P
me blend for robus
tanding yield, spec
primer extension,
ification assay or o
and High Fidelity
P
me blend for robus
tanding yield, spec
Develop a new am
ains ready-to-use
and Long Range d
consistent, accurate
the specially desig
and optimized blen
and large-fragme
and Reverse Tran
Nase H
-
reverse tr
ification of long RN
E. A two-step RT-P
nd Long Template
an dystrophin RNA
Red Tablets
d as a substrate in
alkaline phosphata
nic solvent, which
g organic solvent-c
Start Essential D
dy-to-use reaction
he LightCycler
Na
detection and qua
tion of template DN
Start Essential D
dy-to-use reaction
LightCycler
Nano
quantification. Se
ers, and hydrolysis
cal Produ
cience.com
R System
fragments up to 3
nd to amplify prod
ments of 23 kb in
cation.
R System, dNTPa
fragments up to 3
products >20 kb. C
kb long. Use in PC
ready-to-use PCR
PCR System
ystem is an enzym
gher yield and thre
stem for the most s
CR/RT-PCR.
PCR System, dN
vers superior resu
ty compared to Taq
gets up to 5 kb, in
eotide mix.
PLUS
PCR System
st amplification of
carryover prevent
optimize an existin
PLUS
PCR System,
st amplification of
mplification assay o
PCR Nucleotide M
dNTPack
e amplification of
ned buffer set, ult
nd of thermostable
ent amplification.
nscriptase
ranscriptase for tw
NA targets, genera
PCR using Expand
e was used to amp
A.
immunohistocytoc
ase. The Fast Red
may cause proble
containing mounti
NA Green Maste
mix using the SYB
ano Instrument. Ide
antification. React
NA and primers.
NA Probes Mast
mix for the hydroly
Instrument. Ideal
etup only requires t
s probes.
uct Index
35 kb. Includes an o
ucts over 20 kb. C
length. Use in PCR
ack
35 kb. Optimized bu
Control primers an
CR, RT-PCR, large-
R Nucleotide Mix.
e blend delivering
eefold greater fidel
sensitive PCR resu
NTPack
lts with twofold hig
q. Use for the mos
PCR and RT-PCR
fragments up to 5
and accuracy. Use
tion, to develop a n
ng one.
dNTPack
fragments up to 5
and accuracy. Use
or optimize an exis
Mix.
long, 5 to 20 kb PC
rapure PCR-grade
e DNA polymerase
wo-step RT-PCR, es
ation of cDNA libra
Reverse Transcrip
lify up to 13.5 kb c
chemistry and wes
reaction product i
ms for in situ hybr
ng media.
er
BR Green I dye det
eal for hot start PC
ion setup only req
ter
ysis probe detectio
for hot start PCR a
the addition of tem
x
optimized
Control primers
R, RT-PCR, and
uffer and
nd DNA
-fragment
superior
lity compared
lts for genomic
gher yield and
st sensitive PCR
. Contains
5 kb with
in PCR/RT-
new
5 kb with
in PCR/RT-
sting one.
CR products.
e nucleotide
es for PCR, RT-
specially
aries, and 5'/3'
ptase and
cDNA from
stern blotting
s soluble in
ridization when
tection format
CR assays for
uires the
on format on
assays for
mplate DNA,

Cat. No.

11 811 002 001
04 743 814 001
11 732 641 001
11 732 650 001
11 759 078 001
04 738 250 001
04 738 268 001
04 738 276 001
03 300 226 001
03 300 234 001
04 743 725 001
04 743 733 001
04 829 034 001
04 829 042 001
04 829 069 001
11 785 826 001
11 785 834 001
11 496 549 001
06 402 712 001
06 402 682 001

200 U for up to
each co
200 U for up to
each co
100 U for up to
each con
500 U (2 x 250
final volume ea
2,500 U (10 x 2
50 l final volum
100 U for up to
each con
500 U (2 x 250
final volume ea
2,500 U (10 x 2
50 l final volum
500 U (2 x 250
final volume ea
2,500 U (10 x 2
20 l final volu
125 U for up
volume each
500 U (2 x 250
final volume ea
175 U for up
volume each
700 U for up
volume each
3,500 U (5 x 70
20 l final volum
5 x 1 ml for u
5 x 1 ml for u
Pack Size

40 reactions of 50
ntaining 5 U enzym

40 reactions of 50
ntaining 5 U enzym

40 reactions of 50
ntaining 2.6 U enzy
U) for up to 200 re
ch containing 2.6
me each containin
blend
40 reactions of 50
ntaining 2.6 U enzy
U) for up to 200 re
ch containing 2.6
me each containin
blend
U) for up to 500 re
ach containing 1 U
ume each containi
blend

p to 125 reactions
h containing 1 U e
U) for up to 500 re
ach containing 1 U

p to 125 reactions
containing 1.4 U e
p to 500 reactions
containing 1.4 U e
00 U) for up to 2,5
me each containin
blend
1,000 U (20 l)
5,000 U (100 l)

20 tablets

up to 500 reactions
volume

up to 500 reactions
volume

0 l final volume
me blend
0 l final volume
me blend
0 l final volume
yme blend
eactions of 50 l
U enzyme blend
000 reactions of
ng 2.6 U enzyme
0 l final volume
yme blend
eactions of 50 l
U enzyme blend
000 reactions of
ng 2.6 U enzyme
eactions of 20 l
U enzyme blend
500 reactions of
ng 1 U enzyme
of 20 l final
enzyme blend
eactions of 20 l
U enzyme blend
of 20 l final
enzyme blend
of 20 l final
enzyme blend
00 reactions of
ng 1.4 U enzyme
s of 20 l final
s of 20 l final

Price in

204,30
199,40
123,10
492,10
1.969,60
123,10
492,10
1.969,60
517,30
2.072,30
131,30
517,30
172,30
591,20
2.239,00
99,80
377,70
85,40
inquire
inquire

Alp

Prod

FastS
Enzym
Polym
fragm
RICH
FastS
Enzym
fourfo
multi
Conta
FastS
Read
cDNA
targe
throu
FastS
Read
need
inclu
instru
FastS
Therm
supe
Ideal
prior
FastS
Therm
PCR
and o
setup
FastS
Read
temp
inclu
instru
FastS
Read
temp
enab
ROX.

lphabetic
duct Name
Start High Fidelit
me blend that com
merase with fourfo
ments up to 5 kb. U
H template amplific
Start High Fidelit
me blend with ben
old higher accurac
plex PCR, RT-PCR
ains ready-to-use
Start PCR Maste
dy-to-use 2x maste
A targets up to 2 k
ets, with high spec
ughput, and direct
Start SYBR Gree
dy-to-use 2x mix co
ed for running qua
ding qPCR and tw
uments other than
Start Taq DNA Po
mostable, chemica
rb results due to it
tool for hot start P
to initial denatura
Start Taq DNA Po
mostable modified
nucleotide mix. De
optimized buffer. Id
p and prior to initia
Start TaqMan
P
dy-to-use 2x mix co
plate for running qu
ding qPCR and tw
uments other than
Start Universal P
dy-to-use 2x mix co
plate for quantitativ
les use on all real-
. Not for use on Lig
cal Produ
ty PCR System
mbines the benefits
old higher accuracy
Use for multiplex P
cation, and difficult
ty PCR System, d
nefits of FastStart T
cy and ability to am
R, GC-RICH templa
PCR Nucleotide M
er
er mix for the ampl
kb long, or longer f
ificity, sensitivity, a
colony PCRs.
n Master
ontaining all reage
antitative, real-tim
wo-step qRT-PCR. U
the LightCycler

olymerase, 5 U/
ally modified recom
ts unique enzyme
PCR, since it stays
ation step.
olymerase, dNTP
recombinant Taq
elivers superb resu
deal for hot start; e
al denaturation.
Probe Master
ontaining all reage
wo-step qRT-PCR. U
LightCycler
Inst
Probe Master (Ro
ontains everything
ve, real-time detec
-time instruments
ghtCycler
Instrum
uct Index
s of FastStart Taq D
y with the abilty to
PCR, sequencing, R
t PCRs.
dNTPack
Taq DNA Polymera
mplify fragments u
te amplification, d
Mix.
lification of genom
fragments on plasm
and yield. Use in ho
ents except primers
e DNA detection a
Use with real-time
Instruments.
l
mbinant Taq polym
design and optimi
inactive during PC
Pack
polymerase with r
ults with unique en
enzyme stays inact
ents except primers
me DNA detection
Use with real-time
truments.
ox)
except primers, p
ction assays. Refere
requiring normaliz
ments.
x
DNA
o amplify
RT-PCR, GC-
ase with
p to 5 kb. For
ifficult PCRs.
mic DNA and
mid DNA
ot start, high-
s and template
assays,
e qPCR
merase. Delivers
zed buffer.
CR setup and
ready-to-use
nzyme design
tive during
s, probe, and
assays,
e qPCR
robe, and
ence dye
zation with

Cat. No.

03 553 361 001
03 553 400 001
04 738 284 001
04 738 292 001
04 710 436 001
04 710 444 001
04 710 452 001
04 673 484 001
04 673 492 001
12 032 902 001
12 032 929 001
12 032 937 001
12 032 945 001
12 032 953 001
04 738 314 001
04 738 357 001
04 738 381 001
04 738 403 001
04 738 420 001
04 673 409 001
04 673 417 001
04 673 433 001
04 913 949 001
04 913 957 001
04 914 058 001

2,500 U (10 x 2
50 l final v
FastSt
500 U (2 x 250
final volume ea
125 U for up to
each conta
500 U (2 x 250
final volume ea
2 x 1.25 ml for
8 x 1.25 ml for u
10 x 5 ml for u
5 ml (4 x 1.25 m
fi
50 ml (10 x 5
20
100 U for up to
each conta
500 U (2 x 250
final volume e
2,500 U (10 x 2
50 l final volu
Ta
5,000 U (20 x 2
50 l final volu
Ta
100 U for up to
each conta
500 U (2 x 250
final volume e
1,000 U (4 x 25
l final volume
2,500 U (10 x 2
50 l final volu
Ta
5,000 U (20 x 2
50 l final volu
Ta
2 x 1.25 ml for
10 x 1.25 ml for
10 x 5 ml fo
2 x 1.25 ml for
10 x 1.25 ml fo
fi
10 x 5 ml for u
Pack Size

volume each conta
tart Taq DNA Polym
U) for up to 200 re
ach containing 2.5
DNA Polymerase

50 reactions of 50
ining 2.5 U FastSta
Polymerase
U) for up to 200 re
ach containing 2.5
DNA Polymerase

up to 250 reaction
reaction volume
up to 1,000 reactio
reaction volume
reaction volume
nal reaction volum
ml) for up to 5,00

50 reactions of 50
aining 2 U FastStar
Polymerase
U) for up to 250 re
ach containing 2 U
DNA Polymerase
1,000 U (4 x 250 U
250 U) for up to 12
me each containin
aq DNA Polymeras
me each containin
aq DNA Polymeras
50 reactions of 50
aining 2 U FastStar
Polymerase
U) for up to 250 re
ach containing 2 U
DNA Polymerase
50 U) for up to 500
each containing 2
DNA Polymerase
me each containin
aq DNA Polymeras
me each containin
aq DNA Polymeras
up to 100 reaction
reaction volume
r up to 500 reactio
reaction volume
reaction volume
up to 250 reaction
reaction volume
or up to 12,500 rea
nal reaction volum
reaction volume

www.roche
000 reactions of
aining 2.5 U
merase
eactions of 50 l
U FastStart Taq
0 l final volume
art Taq DNA
eactions of 50 l
U FastStart Taq
ns of 20 l final
ons of 20 l final
ns of 20 l final
eactions of 20 l
me
0 reactions of
lume
0 l final volume
rt Taq DNA
eactions of 50 l
U FastStart Taq
U)
250 reactions of
ng 2 U FastStart
se
500 reactions of
ng 2 U FastStart
se
0 l final volume
rt Taq DNA
eactions of 50 l
U FastStart Taq
reactions of 50
U FastStart Taq
250 reactions of
ng 2 U FastStart
se
500 reactions of
ng 2 U FastStart
se
ns of 50 l final
ons of 50 l final
of 50 l final
ns of 20 l final
actions of 20 l
me
ns of 20 l final
e-applied-science

Price in

2.107,90
497,50
152,20
497,50
178,40
624,10
2.675,00
390,30
3.535,60
119,40
486,10
837,20
1.991,10
3.349,20
119,40
486,10
837,20
1.991,10
3.349,20
189,10
886,90
3.429,10
139,30
657,60
inquire

129

e.com

Alp
130

www.r

Prod

FastS
Read
quan
use o
for us
Fibro
Prom
adhe
and p
dishe
Fibro
Prom
adhe
and p
coati
First
Synth
sequ
gene
quan
FLOW
FLOW
FLOW
The F
(one
Hand
FLOW
The F
Pure
FLOW
The F
Light
FLOW
The F
FLOW
FLOW
The F
Light
FLOW
The F
used
FLOW
The F
used
FLOW
The F
Outp
FLOW
The F
of pri
Cartr
FLOW
The F
96 Pr
Instru
FLOW
The F
data
Mana
FLOW
The 2
FLOW
Setup
Fluor
RNA
T7, o
enzym
(Sout
lphabetic
roche-applied-sc
duct Name
Start Universal S
dy-to-use 2x mix co
titative, real-time D
on all real-time ins
se on LightCycler
onectin
motes attachment a
sion region (cell b
promotes their bin
es. Lyophilizate.
onectin (pure)
motes attachment a
sion region (cell b
promotes their bin
ng of culture dishe
Strand cDNA Sy
hesize 1st strand c
ence-specific prim
rate cDNA librarie
tify mRNA to mon
W 32 Vial Carrier
W 32 Vial Carrier w
W Control Unit in
FLOW Control Unit
Control Unit is nee
dling Instrument, P
W Output Plate C
FLOW Output Plate
96 Output Plates.
W PCR Setup Ins
FLOW PCR Setup I
tCycler
480 Instru
W PCR Setup Ins
FLOW PCR Setup I
W PCR Setup Instru
W PCR Setup LC4
FLOW PCR Setup L
tCycler
480 Multi
W PCR Setup LC4
FLOW PCR Setup L
for cooling the Lig
W PCR Setup LC4
FLOW PCR Setup L
for cooling the Lig
W PCR Setup Out
FLOW PCR Setup O
ut Plate.
W Primary Samp
FLOW Primary Sam
imary and/or seco
ridges.
W Processing Ca
FLOW Processing C
rocessing Cartridg
ument.
W Software 1.0
FLOW Software 1.0
exchange between
agement Systems.
W Tubes (2 ml)
2 ml Screw Cap Tu
W Primary Sample
p Instrument (PSU
rescein RNA Lab
labeling with Fluo
r T3 RNA polymera
me-conjugated an
therns, northerns,
cal Produ
cience.com
SYBR Master (Ro
ontains everything
DNA detection ass
truments requiring
Instruments.
and subsequent sp
binding domain) int
ding and spreadin
and subsequent sp
binding domain) int
ding to and spread
es. Highly purified
ynthesis Kit for R
cDNA as the startin
mers, poly(dT)
15
pri
es, first step in diffe
nitor expression.
r
with Adaptors for th
nclusive Monitor
t is used in conjun
eded for each of th
PCR Setup Unit, an
Carrier
e Carrier enables t
strument
Instrument is for a
ument.
strument 50 l Fil
Instrument 50 l F
ument.
480 Multiwell Pla
LC480 Multiwell Pl
iwell Plates.
480 Multiwell Pla
LC480 Multiwell Pl
ghtCycler
480 M
480 Multiwell Pla
LC480 Multiwell Pl
ghtCycler
480 M
tput Plate Coolin
Output Plate Cooli
le Handling Instr
mple Handling Inst
ndary samples into
artridge Carrier
Cartridge Carrier i
e on the FLOW Pri
0 controls the FLOW
n FLOW compone
ubes, can be used
Handling Instrume
).
beling Mix
orescein-12-UTP by
ases. Detect labele
ti-fluorescein, and
plaque lifts, ISH).
uct Index
ox)
except primers an
says. The reference
g normalization wit
teracts with mamm
ng on plastic. Use t
teracts with mamm
ding on plastic. Us
lyophilizate.
RT-PCR (AMV)
ng reaction for RT
imers, or random p
erential display of
he FLOW Instrume
nction with the FLO
he following: Prima
d System Control)
the placement of u
utomated PCR set
lter Tips
ilter Tips are used
ate Carrier
late Carrier is used
ate Cooling Bloc
late Cooling Block
ultiwell Plates 384
ate Cooling Bloc
late Cooling Block
ultiwell Plates 96.
ng Block
ng Block is used f
rument
trument is for auto
o MagNA Pure 96
s used to place a M
imary Sample Han
W process and ma
nts and Laboratory
as secondary tube
ent (PSH) and for t
ed RNA directly or
x
nd template for
e dye enables
th ROX. Not
The cell
malian cells
to coat culture
The cell
malian cells
sed for the
PCR. Use with
primers to
mRNA, or
ent.
OW System
ary Sample
).
up to 5 MagNA
tup on the
with the
d to hold the
ck (384 well)
k (384 well) is
.
ck (96 well)
k (96 well) is
or cooling the
mated transfer
Processing
MagNA Pure
dling
anages the
y Information
es for the
the FLOW PCR
ption using SP6,
r with an
on techniques

Cat. No.

04 913 850 001
04 913 914 001
10 838 039 001
11 051 407 001
11 080 938 001
11 483 188 001
07 127 014 001
07 101 929 001
07 102 062 001
07 101 996 001
07 102 127 001
07 102 020 001
07 102 054 001
07 102 046 001
07 162 367 001
07 101 937 001
07 101 970 001
07 102 097 001
07 128 894 001
11 685 619 910

4 x 1.25 ml for
10 x 5 ml for u
1 kit for up to
1 c
1 co
1
1 m
1 co
1 c
1 proc
1
40
Pack Size

up to 500 reaction
reaction volume
reaction volume

5 mg

1 mg
5 mg

30 reactions, inclu
reactions

carrier with adapto
ontrol unit with mo

1 plate carrier

1 instrument


multiwell plate car

ooling block (384 w

cooling block (96 w

1 cooling block

1 instrument

cessing cartrigde c

1 software packag

280 tubes per box

l for up to 20 reac

ns of 20 l final
ns of 20 l final
uding 5 control
ors
onitor
ps
rier
well)
well)
carrier
e
x
ctions

Price in

289,80
inquire
546,70
174,60
694,00
244,00
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
168,70

Alp

Prod

Fluor
Subs
trans
and P
or EL
Fluor
Subs
vitro
hybri
Fluor
Fluor
Conv
prime
at hig
lifts,
Fok I
Reco
5'-co
dista
Neos
Form
Color
hybri
elect
to sta
Form
Most
dehy
cyste
Free
Enzym
samp
resea
role o
G
G-41
High
mem
the n
cells.
GC-R
Blend
diffic
RICH
high
GC-R
Blend
temp
Solut
Conta
Geno
Conv
with
durin
numb
Geno
Prepa
using
can b
sequ
Geno
Prepa
using
can b
sequ

lphabetic
duct Name
rescein-12-dUTP
trate for terminal t
scriptase. Replaces
PCR. Use labeled p
LISA with Anti-Fluo
rescein-12-UTP
transcription for R
dization and direc
rescein-AP, or Anti
rescein-High Pri
venient enzyme an
ed labeling of DNA
gh yield for use in
ISH, and library sc
I
ognizes the sequen
ohesive termini. A C
nces from the seq
schizomers: BseG I
mamide
rless liquid suitable
dization. Formamid
rophoresis by deio
abilize single stran
mate Dehydrogen
t widely used in co
drogenase is a dim
eine residue which
Fatty Acids, Half
matic colorimetric
ples from serum an
arch tool to increas
of free fatty acids i
18 Solution
ly pure, convenien
brane, selects for
neomycin resistanc
Eliminates contam
RICH PCR System
d of Taq DNA Poly
ult templates up to
H Resolution Solutio
yield and accuracy
RICH PCR System
d of Taq Polymeras
plates up to 5 kb. E
tion deliver superb
ains ready-to-use
opure Buffer Set
venient, ready-to-u
the Genopure Plas
ng the isolation, pro
ber plasmids.
opure Plasmid M
are highly purified
be used in transfec
encing, and clonin
opure Plasmid M
are highly purified
be used in transfec
encing, and clonin
cal Produ
P
transferase, DNA p
s dTTP in random p
probes for ISH with
orescein-AP.
and T7 RNA Polym
RNA labeling. Dete
ct fluorescence or d
i-Fluorescein-POD
me
d nucleotide mix f
A with fluorescein-
Southern, norther
reening.
nce GG*ATG(N)9/1
Class II S enzyme w
uence. Inhibited b
I, BstF5 I, BtsC I.
e for denaturing g
de is used as an R
onizing RNA. In ca
ds of denatured D
nase
ofactor recycling sy
mer of two identica
is essential for ac
f Micro Test
assay to determin
nd plasma. The tes
se scientific knowl
in blood.
t, antibiotic, filtere
eukaryotic cells th
ce gene, and maint
minating fibroblast
m
ymerase and a pro
o 5 kb. Enhanced p
on deliver superb
y.
m, dNTPack
se and a proofread
Enhanced processiv
b performance in P
nucleotide mix.
for Low-Copy Nu
use, nuclease-free
smid Kits. Doubling
ovides better yield
Maxi Kit
plasmid DNA in la
ne lysis method. P
ng.
Midi Kit
plasmid DNA in m
ne lysis method. P
ng.
uct Index
polymerase I, Taq,
primed labeling, ni
h direct fluorescen
merase. Can replace
ect labeled RNA by
detection by ELISA
D.
or highly efficient
-dUTP. Generate la
n, and dot blots, co
13 and generates f
which cleaves dsD
y 6-methyladenine
els and nucleic ac
RNA stabilizer in ge
pillary electrophor
DNA.
ystems for NADH.
al subunits. The en
ctivity or structural
ne free fatty acids i
st combination is in
ledge about the ph
ed through 0.2 m
hat are stably trans
tains the phenotyp
ts from mixed cultu
ofreading polymer
processivity and th
performance in PC
ding polymerase a
vity and GC-RICH
PCR (high yield and
umber Plasmids
buffers for use in
g the volume of th
s of plasmid DNA
arge quantities (up
urified plasmid DN
tion digestion, Sou
medium quantities
urified plasmid DN
tion digestion, Sou
x
and reverse
ick translation,
nce detection
e UTP in in
y in situ
A using Anti-
random
abeled probes
olony/plaque
fragments with
DNA at precise
e as shown (*).
cid
el
resis, it is used
Formate
nzyme has a
integrity.
n research
ntended as a
hysiological
m pore size
sfected with
pe of resistant
ures.
rase amplify
he unique GC-
CR, providing
mplify difficult
Resolution
d accuracy).
combination
he buffers
from low-copy
p to 500 g)
NA from E. coli
thern blotting,
(up to 100 g)
NA from E. coli
thern blotting,

Cat. No.

11 373 242 910
11 427 857 910
11 585 622 910
11 004 816 001
11 814 320 001
10 244 678 001
10 837 016 001
11 383 175 001
04 727 878 001
04 727 894 001
12 140 306 001
04 743 784 001
04 634 772 001
03 143 422 001
03 143 414 001

25
25
100 l for up t
tem
app
20 ml
100 ml
100 U for up to
each co
100 U for up to
each co
1 set buffer fo
1 kit f
1 kit f
Pack Size

5 l (25 nmol) (1 m

l (250 nmol) (10 m

o 25 labeling assay
mplate DNA per as

100 U (1 - 5 U/l)

500 ml

80 U
250 U


- equivalent to 1 g
- equivalent to 5 g

50 reactions of 50
ntaining 2 U enzym

50 reactions of 50
ntaining 2 U enzym

or up to 20 maxi pr
preps

for up to 10 prepar

for up to 20 prepar

www.roche
mM)
mM)
ys, 0.01 to 3 g
ssay
)
tests
g G-418
g G-418
0 l final volume
me blend
0 l final volume
me blend
reps or 60 midi
rations
rations
e-applied-science

Price in

257,90
354,70
430,70
128,50
91,10
125,70
294,90
604,20
98,50
424,20
206,60
206,60
137,80
172,30
149,40

131

e.com

Alp
132

www.r

Prod

Gluc
Gluco
comp
enter
subst
Gluc
Gluco
cofac
3.2 M
Gluc
Gluco
cofac
phos
solut
Gluc
Gluco
mese
Addit
amm
Gluc
Fast,
deter
scien
is com
Gluta
Gluta
for N
BSA
Gluta
Gluta
nonn
ketog
and L
Gluta
Gluta
synth
Gluta
A cru
gluta
perox
to GS
Glyc
Glyce
provi
appro
subst
Glyc
Mole
preci
repla
picog
GS F
Stand
only
that y
speci
GS F
The G
for br
Titan
regio
GS F
Use f
FLX T
for lo
PicoT

lphabetic
roche-applied-sc
duct Name
cose-6-phosphat
ose-6-Phosphate i
pound is very com
ring a cell will beco
trate for glucose-6
cose-6-Phosphat
ose-6-Phosphate D
M ammonium sulfa
cose-6-Phosphat
ose-6-Phosphate D
phate. Grade I from
ion, pH approx. 6.
cose-6-Phosphat
ose-6-Phosphate D
enteroides is a com
tional reagent gluc
onium sulfate solu
cosidase Assay
sensitive, specific
rmination of neutra
nce research applic
mpatible with micr
amate Dehydrog
amate Dehydrogen
NAD(P) and NAD(P
as a stabilizer, and
amate-Oxaloace
amate-Oxaloacetat
natural L-amino ac
glutarate, catalyzes
L-glutamate.
amate-Pyruvate
amate-Pyruvate Tra
hesis of nonnatura
athione Reductas
ucial flavoenzyme i
athione is used by g
xide and is then co
SH by glutathione
erol-3-Phosphat
erol-3-Phosphate D
ded as a suspensi
ox. 6. Specific activ
trate (optimized co
ogen
ecular biology grad
pitation of nucleic
ace tRNAs or sonic
gram amounts of D
FLX Titanium Con
dard sequencing c
Control Beads are
yield sequencing r
ifications.
FLX Titanium emP
GS FLX Titanium e
reaking large-volu
ium LV emPCR Kit
ons of a PicoTiterPl
FLX Titanium emP
for breaking small-
Titanium SV emPC
oading into medium
TiterPlate device.
cal Produ
cience.com
e
s glucose sugar p
mon in cells, as th
ome phosphorylate
6-phosphatase.
te Dehydrogenas
Dehydrogenase (G
ems for NADPH. G
ate solution, pH ap
te Dehydrogenas
Dehydrogenase (G
ems for NADPH. A
m yeast. Suspensi
te Dehydrogenas
Dehydrogenase (G
mponent of cofacto
cose-6-phosphate
ution, pH approx. 6
colorimetric assay
al -glucosidase
cations. Cannot be
roplate and cuvette
enase (GlDH)
nase is a compone
P)H. The formulatio
d ADP as an activa
tate Transamina
te Transaminase (G
cids from -keto a
s the conversion o
Transaminase (G
ansaminase (GPT)
l L-amino acids fro
se (GR)
in the antioxidant d
glutathione peroxi
onverted to oxidize
reductase.
te Dehydrogenas
Dehydrogenase (G
on in 3.2 M ammo
vity: approx. 170 U
onditions).
de Glycogen is use
c acids (DNA or RN
cated DNAs; 20 g
DNA or RNA from
ntrol Bead Kit
control for the GS F
sequenced. They
results to show the
PCR Breaking Kit
emPCR Breaking K
ume (LV) emulsion
t (Lib-L) to prepar
late device.
PCR Filters SV 64
-volume (SV) emu
CR Kit (Lib-L) to pr
m, medium-small,
uct Index
hosphorylated on
e vast majority of g
ed in this way. It is
se (G6P-DH)
G6P-DH) is a comp
Grade II from yeast
prox. 6.
se (G6P-DH)
G6P-DH) is a comp
Additional reagent
ion in 3.2 M ammo
se (G6P-DH)
G6P-DH) from Leuc
or recycling system
. Suspension in 3.2
6.
y for the quantitati
in human semen s
e used in other spe
e formats.
ent of cofactor recy
on contains buffer
ator.
se (GOT)
GOT) is used for th
acids. In the presen
f L-aspartate to ox
GPT)
from pig heart is
om -keto acids.
defense system. R
dase to detoxify hy
ed glutathione whi
se (GDH)
GDH) from rabbit m
onium sulfate solut
U/mg at +25C with
ed as a carrier for t
NA). As an inert m
g (1 l solution) pre
a volume of 1 ml.
FLX Instrument. In
contain known DN
e instrument is with
ts LV/MV 12pc
Kit LV 12pc provide
s prepared using t
e samples for load
4pc
lsions generated u
repare samples at s
or small regions of
x
carbon 6. This
glucose
s used as a
ponent of
. Suspension in
ponent of
glucose-6-
onium sulfate
conostoc
ms for NADPH.
2 M
ve
samples in life
ecimens. Assay
ycling systems
substances,
he synthesis of
nce of a-
xaloacetate
used for the
Reduced
ydrogen
ch is recycled
muscle is
tion, pH
h DAP as the
the
aterial it may
ecipitates
a test run,
NA sequences
hin
es components
the GS FLX
ding into large
using the GS
smaller scales
f a

Cat. No.

10 127 647 001
10 127 671 001
10 737 232 001
10 127 655 001
10 165 875 001
11 742 027 001
10 197 734 001
10 105 554 001
10 737 046 001
10 105 589 001
10 737 127 001
10 105 678 001
10 127 752 001
10 127 779 001
10 901 393 001
05 470 129 001
05 233 658 001
05 233 674 001

1 kit fo
1 kit for 12
Pack Size

5 g

10 mg (2 ml)
25 mg (5 ml)

5 mg (1 ml)

1,000 U (1 ml)

or 30 tests and 10

3,000 U

10 mg (1 ml)
25 mg (2.5 ml)

10 mg (1 ml)
25 mg (2.5 ml)

5 mg (1 ml)

10 mg (1 ml)
100 mg (10 ml)

20 mg (1 ml)

1 kit

LV emulsion-brea

1 kit (64 filters)

blanks
aking setups

Price in

116,90
192,40
364,10
310,90
105,40
363,50
47,80
143,10
270,20
122,80
225,30
134,40
105,40
650,50
99,50
inquire
inquire
inquire

Alp

Prod

GS F
Prepa
inser
and s
Titan
GS F
For la
effec
per b
FLX T
GS F
For la
boun
amen
Titan
GS F
For m
effec
per b
FLX T
GS F
For m
bead
amen
Titan
GS F
Comb
deter
ampl
layers
GS F
Subs
Kit du
Tagg
sequ
GS F
Creat
librar
span
and s
GS F
Comb
reage
sequ
ampl
GS F
Comb
reage
sequ
clona
GS F
Provi
from
millio
Instru
GS F
Provi
single
copie
and T
GS F
The G
used
Servi
three
GS F
Comp
Suita
analy
hrs fo
GS F
The G
for us
lphabetic
duct Name
FLX Titanium Libr
are up to 10 assort
t lengths of 3, 8, o
sequencing using
ium Series kits.
FLX Titanium LV e
arge-volume ampl
tive, beadbound c
bead, amenable to
FLX Titanium LV e
arge-volume ampl
nd copy of DNA tem
nable to sequencin
ium series kits.
FLX Titanium MV
medium-volume am
tive, bead-bound c
bead, amenable to
Titanium kits.
FLX Titanium MV
medium-volume am
-bound copy of D
nable to sequencin
ium series kits.
FLX Titanium Pico
bine this kit with th
rmine the nucleotid
ified DNA library. T
s in the wells of a
FLX Titanium Rap
titute MID Adapto
uring preparation
ing multiple librari
enced together in
FLX Titanium Rap
te a library of fragm
ry is a set of single
of the sample seq
sequencing DNA a
FLX Titanium Seq
bined with the GS
ents and other con
ence (in extra-long
ified DNA library (
FLX Titanium Seq
bined with the GS
ents and other con
ence in extra-long
ally amplified DNA
FLX Titanium SV e
des reagents for s
a single effective
ons of copies per b
ument and GS FLX
FLX Titanium SV e
des reagents for s
e effective bead-b
es per bead, amen
FLX+ CB Filters a
GS FLX+ CB Filters
for GS FLX+ Instr
ce Engineers must
e (3) months or afte
FLX+ Computing
puting solution for
able for pipeline pr
ysis, including map
or the XL+ and ~4
FLX+ Computing
GS FLX+ Computin
se with the GS FLX
cal Produ
rary Paired End A
ted single-strande
r 20 kb from dsDN
the GS FLX Instrum
emPCR Kit (Lib-A
ification of an amp
opy of DNA templ
sequencing using
s.
emPCR Kit (Lib-L
ification of a librar
mplate to tens of m
ng using the GS FL
emPCR Kit (Lib-
mplification of an a
copy of DNA temp
sequencing using
emPCR Kit (Lib-
mplification of a lib
NA template to ten
ng using the GS FL
oTiterPlate Kit 70
he GS FLX Titanium
de sequence of an
The DNA-carrying
PicoiterPlate devic
pid Library MID A
ors for those in the
of DNA libraries fo
ies with MIDs allow
1 region of the pla
pid Library Prepa
ments from a DNA
e-stranded DNA fra
quence. Each fragm
adaptors.
quencing Kit XL+
FLX Titanium Pico
nsumables require
g reads; up to 1 kb
(the sample).
quencing Kit XLR
FLX Titanium Pico
nsumables require
g reads (350 to 450
A library.
emPCR Kit (Lib-A
small-volume ampl
bead-bound copy
bead, amenable to
X Titanium kits.
emPCR Kit (Lib-L
small-volume ampl
ound copy of DNA
able to sequencing
s.
nd Pump Tubing
s and Pump Tubin
rument maintenanc
t change the CB F
er 25 runs.
Station
r fast processing o
ocessing of GS FL
pping and de novo
4 hrs for the XLR70
Station Monitor
ng Station Monitor
X+ Computing Sta
uct Index
Adaptors
ed paired end DNA
NA input sample fo
ment with appropr
A)
plicon library from
ate to tens of milli
g the GS FLX Instru
L)
millions of copies p
LX Instrument and
-A)
amplicon library fro
plate to tens of mil
g the GS FLX Instru
-L)
brary from a single
ns of millions of co
LX Instrument and
0x75
m Sequencing Kit
n immobilized and
g beads and reage
ce.
Adaptors Kit
GS FLX Titanium
or sequencing (GS
ws them to be am
ate.
ration Kit
A sample to be seq
agments represent
ment is flanked by

oTiterPlate Kit 70
d to determine the
b) of an immobilize
R70
oTiterPlate Kit 70x7
d for determining
0 nt) of an immobil
A)
lification of an amp
of DNA template
sequencing using
L)
lification of a librar
A template to tens
g using the GS FLX
g Kit
g Kit contains the
ce. Instrument use
ilters and Pump Tu
of GS FLX+ sequen
LX+ System data a
o assembly. Proces
0.
r with power cords
ation.
x
A libraries with
or amplification
riate GS FLX
a single
ons of copies
ument and GS
fective, bead-
per bead,
GS FLX
om a single
lions of copies
ument and GS
e effective,
opies per bead,
GS FLX
XLR70 to
clonally
nts deposit in
Rapid Library
S FLX System).
plified and
quenced. The
ting the entire
amplification
75, it provides
e nucleotide
ed and clonally
75, provides
the nucleotide
lized and
plicon library
to tens of
g the GS FLX
ry from a
of millions of
X Instrument
components
ers or Roche
ubing every
ncing data.
nd subsequent
ssing time: ~18
s is intended

Cat. No.

05 463 343 001
05 619 114 001
05 618 428 001
05 619 149 001
05 618 436 001
05 233 682 001
05 619 211 001
05 608 228 001
06 380 565 001
05 233 526 001
05 619 165 001
05 618 444 001
06 397 417 001
06 388 779 001
06 388 787 001

1 k
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 pl
1 kit for u
1 kit for u
1 ki
1 kit for one Ge
1 kit for up
am
1 kit for up
am
Pack Size


p to 2 large volume

p to 2 large volume

to 8 medium volum

to 8 medium volum

late (with accesso



t for 1 sequencing

enome Sequener F
run

p to 32 small volum

p to 16 small volum

1 kit

1 instrument

1 instrument

www.roche
says
e emulsion
ons
e emulsion
ons
me emulsion
ons
me emulsion
ons
ries)
eparations
eparations
g run
FLX sequencing
me emulsion
ons
me emulsion
ons
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

133

e.com

Alp
134

www.r

Prod

GS F
Uniq
accu
proje
sequ
GS F
The G
Instru
is pro
GS G
GS G
the b
majo
class
GS G
GS G
the b
majo
class
GS G
GS G
DNA
leuke
assay
GS G
This s
sever
resea
GS F
GS J
The G
PicoT
the w
supp
GS J
Use d
a seq
Devic
Supp
GS J
Bring
chem
for sm
(10 h
GS J
Evalu
Amp
GS Ju
MV e
GS J
Use t
Junio
perio
subsy
GS J
GS Ju
for th
presc
Devic
GS J
The G
caps
GS J
The G
and F
Instru
repla
GS J
Stand
only
that g
acco
lphabetic
roche-applied-sc
duct Name
FLX+ Instrument
ue combination of
racy and high-thro
ects: whole genom
encing, and samp
FLX+ Upgrade Kit
GS FLX+ Upgrade
ument to a GS FLX
ovided in the kit.
GType HLA HR Pr
GType HLA MR Prim
basis for an HLA te
r histocompatibilit
GType HLA MR P
GType HLA MR Prim
basis for an HLA te
r histocompatibilit
GType RUNX1 Pri
GType RUNX1 Prim
sequence of seve
emia research. This
y using the GS FLX
GType TET2/CBL/
set forms the basis
ral exons of the TE
arch. This DNA seq
LX, GS FLX+ or GS
unior Bead Depo
GS Junior bead de
TiterPlate device an
wells of the PicoTite
lied with the GS Ju
unior Bead Depo
during GS Junior B
quencing run, and
ce Centrifuge Adap
plied with the GS J
unior Complete
gs proven performa
mistry to the bench
mall to medium siz
hours) and obtain 4
unior emPCR Be
uate the amount of
lification procedur
unior Titanium em
emPCR Kits. Suppl
unior Maintenta
to thoroughly clean
or Instrument when
od of time, or if con
ystem.
unior Preventativ
unior Preventative
he scheduled main
cribed schedule. Th
ce Centrifuge Adap
unior Reagent D
GS Junior Reagent
from the reagent
unior Sipper Ma
GS Junior Sipper M
Filters (10) to repla
ument as part of a
acement Buffer Tra
unior Titanium C
dard sequencing c
Control Beads are
give sequencing re
rding to specificat
cal Produ
cience.com
f long sequencing
oughput, make this
e shotgun, multi-s
le multiplexing.
t
Kit is used to upg
X+ Instrument. Eve
rimer Set
mer Set and GS GT
est that measures H
ty complex region o
S FLX or GS Junior
rimer Set
mer Set and GS GT
est that measures H
ty complex region o
S FLX or GS Junior
imer Set
mer Set forms the b
eral exons of the RU
s is a DNA sequen
X, FLX+, or Junior
/KRAS Primer Se
s for a test to dete
ET2, CBL, and KRA
quence-based mut
S Junior Systems.
osition Device
position device ho
nd gasket, enablin
erPlate device prio
unior Complete.
osition Device Co
Bead Deposition D
use along with the
ptors A and B to fi
unior Complete.
ance and long rea
htop. Small footprin
zed laboratories. S
400 bp read length
ead Counter V2
f enriched beads r
re. Bead Counter c
PCR Kits or multip
ied with GS Junior
nce Wash Kit
n and sterilize the
n the instrument h
ntamination is obse
ve Maintenance
Maintenance Kit c
ntenance of a GS J
he kit also contain
ptors (A and B).
Decapping Tool
t Decapping Tool i
cassette in the GS
intenance Kit
Maintenance Kit co
ace all of the short
maintenance proc
ay.
Control Bead Kit
control for the GS J
sequenced. The b
esults showing the
ions.
uct Index
reads (up to 1 kb)
s system ideal for
span paired end, am
rade an existing G
erything required fo
Type HLA HR Prim
HLA allelic haploty
of the human geno
r Systems.
Type HLA HR Prim
HLA allelic haploty
of the human geno
r Systems.
basis for a test to d
UNX1 gene, of inte
nce-based mutatio
Systems.
et
ermine the DNA se
AS genes, of interes
tation detection as
olds one GS Junior
ng the deposition o
or to a sequencing
ounterweight Kit
Device centrifugatio
e GS Junior Bead D
it into a variety of c
ds of the GS FLX T
nt and low entry co
equence >35 milli
hs.
recovered during e
can be used for sin
ple prep with GS FL
r Complete.
fluidics subsystem
has been left idle fo
erved or suspected
Kit
contains compone
unior Instrument,
ns two pairs of Bea
s used to convenie
S Junior Titanium S
ontains enough Sip
t Sipper Tubes of a
cedure. The kit als
Junior System. Du
beads contain know
e GS Junior System
x
) and very high
large genomic
mplicon/cDNA
GS FLX
or the upgrade
mer Set form
ypes at the
ome (MHC
mer Set form
ypes at the
ome (MHC
determine the
erest in
on detection
equence of
st in leukemia
ssay uses the
r Titanium
of beads into
Run. It is
on steps before
Deposition
centrifuges.
Titanium
osts are ideal
on bases/run
emPCR
ngle prep with
LX Titanium
m of the GS
or an extended
d in the fluidics
ents required
following the
ad Deposition
ently remove
Sequencing Kit.
pper Tubes
a GS Junior
so contains a
ring a test run,
wn sequences
m is performing

Cat. No.

06 372 279 001
05 872 430 001
05 872 537 001
05 872 529 001
06 500 358 001
06 500 498 001
05 996 473 001
05 889 103 001
05 922 160 001
06 594 662 001
05 889 111 001
05 898 765 001
06 593 020 001
05 954 070 001
05 996 643 001

1 inst
4 PCR pla
4 PCR pla
4 PCR pla
4 PCR pla
Pack Size

rument plus acces

1 accessory

tes with dried-dow

tes with dried-dow

tes with dried-dow

tes with dried-dow

1 device

1 device

1 instrument

1 device

1 kit

1 kit

1 device

1 kit

1 kit

ssories
wn primers
wn primers
wn primers
wn primers

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

GS J
Provi
single
copie
using
GS J
Provi
librar
millio
Instru
GS J
The G
Titan
nucle
librar
GS J
The G
Instru
Sequ
GS J
The G
Titan
deter
ampl
GTP
GTP,
a cel
GTP
Suita
prepa
salt s
GTP-
GTP-
hydro
the s
powd
Guan
Suita
stron
H
HA P
The s
gentl
contr
anti-H
Hae
Reco
ends
C*. In
Isosc
Hexa
This
prime
in ma
and n
Hexo
For th
biolo
sacch
assay
Hexo
Hexo
yeast
sulfat
G6P-

lphabetic
duct Name
unior Titanium e
des reagents for th
e effective bead-b
es per bead, amen
g GS Junior Titaniu
unior Titanium e
des reagents for a
ons of copies per b
ument and GS Jun
unior Titanium P
GS Junior Titanium
ium Sequencing K
eotide sequence of
ry. Use with the GS
unior Titanium S
GS Titanium Seque
ument Test. It is a
encing Kit (05 996
unior Titanium S
GS Junior Titanium
ium PicoTiterPlate
rmine the nucleotid
ified DNA library,
disodium salt, is r
l-free system.
solution, 100 mM, p
--S
--S activates gua
olyzed enzymatical
timulation of aden
der.
nidine thiocyanat
able as denaturing
nger denaturant tha
Peptide
synthetic HA Pepti
y elute tagged fus
rol to verify immun
HA and HA-tagged
III
ognizes the sequen
. Inhibited by 5-me
nhibited by 5-hydro
chizomers: BshF I,
anucleotide Mix
10x Hexanucleotid
ed DNA labeling. H
any hybridization t
northern blots, and
okinase (HK)
he determination o
gical research sam
harides which con
y of many glycosid
okinase/Glucose
okinase/Glucose-6-
t/Leuconostoc ove
te suspension, pH
-DH. Ratio of HK:G
cal Produ
emPCR Kit (Lib-A
he amplification of
ound copy of DNA
able to sequencing
um kits.
emPCR Kit (Lib-L
amplification of a s
fective bead-boun
bead, amenable to
nior Titanium kits.
PicoTiterPlate Kit
m PicoTiterPlate Kit
Kit, provides device
f an immobilized a
S Junior Instrumen
Sequencing Buffe
encing Buffers Kit
subcomponent of
6 554 001) and can
Sequencing Kit
m Sequencing Kit c
e Kit, provides reag
de sequence of an
using GS Junior Ti
equired as a coenz
ns such as in vitro
or the absence of R
pH 7.
anine-nucleotide-b
lly. It inhibits GTPa
nylate cyclase. Sup
te
agent for proteins
an guanidine hydr
de YPYDVPDYA is
sion proteins from
nospecificity, and in
d fusion proteins.
nce GG*CC, gene
ethyl and 5-hydrox
oxymethylcytosine
Bsn I ,BspAN I, Bs
de Mix has all poss
High specific activ
echniques for scre
of D-glucose, D-fru
mples. It may also b
vert to glucose or
des.
e-6-Phosphate De
-Phosphate Dehyd
erproducer. It is pr
approx. 6. Prepare
G6P-DH is approx. 2
uct Index
A)
f an amplicon libra
A template to tens
g using the GS Jun
L)
shotgun, paired en
d copy of DNA to
sequencing using
t
t combined with th
es and reagents to
and clonally amplif
nt.
ers Kit
is used to run the
the GS FLX Titaniu
n be ordered separ
combined with the
gents and consuma
n immobilized and
itanium kits.
zyme for protein b
RNA transcription
RNases. Supplied a
binding proteins, a
ases more potently
plied as a tetralith
s. Guanidine thiocy
rochloride.
s recognized by An
immunocomplexe
n competition expe
erating fragments
xymethylcytosine a
at the external C
uR I, Pho I.
sible sequences fo
ity labeled DNA pr
eening gene librari
tion.
uctose, and D-sorb
be used to assay o
fructose, making i
ehydrogenase (H
drogenase is from
rovided as a 3.2 M
ed by mixing hexo
2:1 (protein conten
x
ary from a
of millions of
nior Instrument
d, or cDNA
tens of
g the GS Junior
he GS Junior
determine the
fied DNA
GS Junior
um
rately.
GS Junior
ables to
clonally
biosynthesis in
n. The
as a lithium
and is slowly
y than GTP in
ium salt
yanate is a
nti-HA. Use to
s, as positive
eriments using
with blunt
at the internal
.
r random
robes are used
ies, Southern
bitol in food or
other
it useful in the
HK/G6P-DH)
ammonium
kinase and
nt).

Cat. No.

05 996 520 001
05 996 481 001
05 996 619 001
06 627 846 001
05 996 554 001
10 106 399 001
11 140 957 001
10 220 647 001
11 685 929 001
11 666 975 001
10 693 944 001
11 277 081 001
11 426 362 001
10 127 825 001
10 737 275 001

400
100
Pack Size

1 kit

1 kit

1 kit

1 kit

1 kit

250 mg

l (40 mol, 100 m

10 mg

500 g

5 mg

5,000 U (10 U/l)

l for up to 50 reac

1,500 U (1 ml)

15 mg (5 ml)
30 mg (10 ml)

www.roche
mM)

ctions
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
198,00
108,40
319,50
307,60
549,80
136,20
60,40
85,40
156,20
275,80

135

e.com

Alp
136

www.r

Prod

hGH
Fast,
cultu
conta
comp
High
Choo
Expa
optim
highe
High
Labe
prime
librar
50 to
High
Conv
solut
tripho
kit fo
High
Isolat
direc
of mR
Light
High
For fa
- 10
Isolat
array
High
For fa
m th
Macr
isolat
High
Purifi
inclu
RNA
quan
High
Use t
bp. Is
cDNA
mole
High
Purify
Use p
sequ
fragm
High
Purify
cultu
treatm
SNP
High
Quick
cultu
trans
High
Rapid
cells.
purifi
RNas
High
Isolat
fresh
sectio
Light

lphabetic
roche-applied-sc
duct Name
ELISA
sensitive ELISA fo
re supernatants of
aining a reporter g
h Fidelity PCR Ma
ose this convenient
nd High Fidelity PC
mized reaction buff
h Prime
l DNA with radioa
ers. Labeled probe
ry screening, and i
remove unincorpo
h Prime DNA Lab
venient, rapid rand
ions offer a choice
osphates (
32
P,
35
S,
or many different h
h Pure FFPE RNA
te total RNA from
ct use in RT-PCR. Is
RNA in RT-PCR us
tCycler
Carousel-
h Pure FFPET DNA
ast and convenien
m thick sections
ted DNA is suitabl
ys), and sequencin
h Pure FFPET RNA
ast convenient isol
hick sections of fo
rodissected sample
ted RNA for qRT-P
h Pure miRNA Iso
ies and enriches s
ding formalin-fixed
in northern blots,
tification with RT-
h Pure PCR Clean
this kit to selective
solate PCR produc
A, and concentrate
cular biology tech
h Pure PCR Produ
y and concentrate
purified DNA direc
encing, cloning, lig
ments that are >10
h Pure PCR Temp
y nucleic acids fro
red cells, and tissu
ment with lysozym
detection, blotting
h Pure Plasmid Is
kly prepare up to 1
res. Use directly fo
sfection, and to gen
h Pure RNA Isolat
dly isolate small am
Blood, yeast, and
ied and intact RNA
se protection, and
h Pure RNA Paraf
te total RNA from
-frozen tissue for
ons is ideal for rela
tCycler
Carousel-
cal Produ
cience.com
gene encoding for
aster
t, 2x-concentrated
CR System with PC
fer. Delivers two tim
q DNA Polymerase
ctive dCTP using r
es are used in Sout
orated nucleotides
eling Kit
om-primed DNA l
e in the selection o
,
3
H, digoxigenin, f
ybridization techn
Micro Kit
formalin-fixed, par
solated RNA is sui
sing real-time PCR
-Based and the 48
A Isolation Kit
t isolation and pur
of formalin-fixed,
e for qPCR, microa
g.
A Isolation Kit
lation and purifica
rmalin-fixed, paraf
es or biopsy mater
PCR and microarra
olation Kit
mall (micro) RNAs
d/FFPE sections, a
miRNA array hybr
PCR on the LightC
nup Micro Kit
ely isolate small DN
cts from amplificati
e dilute solutions.
niques.
uct Purification K
amplified DNA (o
ctly in downstream
gation, and PCR. E
00 bp in length.
plate Preparation
m different sample
ue. Bacteria and ye
me or lyticase. Use
g, etc.
solation Kit
15 g highly purifie
or PCR, sequencin
nerate labeled hyb
tion Kit
mounts of high qu
bacteria require a
A in RT-PCR, north
much more.
ffin Kit
formalin-fixed par
use in RT-PCR. Th
ative quantification
-Based System.
uct Index
easuring hGH expr
transfected with a
hGH. Allows direc
t lots.
d, ready-to-use mix
CR-Grade dNTPs, M
mes the yield and
e alone.
random oligonucle
thern northern, an
ons. Use Quick Spi
s.
abeling kit. Suppli
of modified deoxyr
fluorescein, biotin,
iques.
raffin-embedded t
itable for relative q
R systems such as t
80 Systems.
rification of genom
paraffin-embedde
array analysis (CG
tion of total RNA f
ffin-embedded tiss
rial can also be use
ay analysis.
s from animal cells
nd plant material.
ridization, and rela
Cycler
480 System
NA fragment sizes
ion and other reac
Use purified DNA
Kit
or DNA from other
m applications, suc
Efficiently recovers
Kit
e materials, such a
east require a spec
purified nucleic ac
ed plasmid DNA fr
g, cloning, in vitro
bridization probes.
ality total RNA from
a pre-lysis treatme
hern blotting, prime
raffin-embedded ti
he quality of RNA f
n of mRNA with RT
x
ression level in
plasmid
t data
x, combining
MgCl
2
, and an
three times
eotides as
d dot blots,
n Columns, G-
ed nucleotide
ibonucleoside
, etc). Use this
tissues for
quantification
the
mic DNA from 5
d tissue.
H, methylation
from 5 to 10
sue.
ed. Use
s and tissues,
Use purified
tive
m.
25 bp to 100
ctions, purify
in most
reactions).
h as labeling,
DNA
as whole blood,
cific prelysis
cids in PCR,
rom bacterial
transcription,
m cultured
nt. Use the
er extension,
ssue and
from paraffin
T-PCR on the

Cat. No.

11 585 878 001
12 140 314 001
11 585 592 001
11 585 584 001
04 823 125 001
06 650 767 001
06 650 775 001
05 080 576 001
04 983 912 001
11 732 668 001
11 732 676 001
11 796 828 001
11 754 777 001
11 754 785 001
11 828 665 001
03 270 289 001

1 k
1 kit for up to 5
200 l fo
1 kit for up
labeled nucleo
1 kit
1
1
1 kit for
1 kit fo
1 kit f
1 kit fo
1 kit fo
1 kit f
1 kit fo
1 kit
1 kit
Pack Size


00 reactions of 20
volume

or up to 50 labelin

to 50 labeling reac
per assay




up to 50 miRNA is






for up to 100 isola

ests
l final reaction
g assays
ctions with a
01 to 2 g DNA
tions
ns
ns
solations
cations
cations
cations
cations
cations
cations
tions
ations

Price in

543,60
575,10
382,80
505,10
308,00
258,00
inquire
324,80
280,10
109,00
458,50
279,90
102,60
448,30
238,70
477,20

Alp

Prod

High
Quick
liver,
north
const
High
Use t
Nucle
Viral
be pr
High
Quick
whol
inclu
PCR,
High
Purify
same
colum
direc
High
Quick
fluids
analy
Hind
Reco
blunt
inhib
recog
Hind
Reco
cohe
hydro
inhib
Hinf
Reco
cohe
meth
hydro
Histo
Natu
Histo
pack
the p
Histo
Lysin
kinas
exit s
forma
Histo
Histo
in the
globu
nucle
HNP
Comb
nonra
used
and c
Hom
Spec
deter
throu

lphabetic
duct Name
h Pure RNA Tissu
kly purify total inta
spleen, lung, and
hern blotting, RNas
truction, and in vit
h Pure Viral Nucle
this Buffer Set in c
eic Acid Kit, the H
Nucleic Acid Larg
rocessed.
h Pure Viral Nucle
kly purify viral nuc
e blood. When usi
ding viral nucleic a
directly after eluti
h Pure Viral Nucle
y viral nucleic acid
e principle as the H
mn assembly purif
ct use in PCR and R
h Pure Viral RNA
kly purify viral RNA
s, or cell culture su
ysis directly after e
d II
ognizes the sequen
ited by 5-hydroxym
gnition sequence.
d III
ognizes the sequen
oxymethylcytosine
it (). Isoschizome
I
ognizes the sequen
sive termini. Sensi
hylcytosine at 3pos
oxymethylcytosine
one
ral mixture of histo
ones are highly alk
age and order the
primary component
one H1
ne-rich preparation
ses. The linker hist
sites of the DNA, lo
ation of higher ord
one H3
one H3 from calf th
e structure of chro
ular domain and a
eosome "beads on
PP Fluorescent De
bined with Fast Re
adioactively labele
for nonradioactive
colony and plaque
mogeneous Caspa
ific, one-step fluor
rmination of caspa
ughput screening.
cal Produ
e Kit
act RNA from mam
heart. Use isolated
se protection, prim
tro translation.
eic Acid Buffer S
combination with th
igh Pure Viral Nuc
ge Volume Kit whe
eic Acid Kit
cleic acids (DNA, R
ng whole blood, to
acids. Use purified
on in water.
eic Acid Large Vo
ds from serum, plas
High Pure Viral Nu
ies larger sample v
RT-PCR.
Kit
A from mammalian
upernatants. Isolate
elution in PCR grad
nce GTPyPu*AC a
y 6-methyladenine
methylcytosine at t
Isoschizomer: Hinc
nce *AAG*CTT a
ited by 6-methylad
also inhibits. 6-me
rs: none known.
nce G*ANTC and
tive to 6-methylad
sition () does not
does. Isoschizome
ones H1, H2A, H2B
aline proteins foun
DNA into structur
t of chromatin.
n from calf thymus
tone H1 binds the
ocking the DNA in
der structure.
hymus is one of the
omatin in eukaryoti
long N-terminal ta
a string" structure
etection Set
ed, HNPP is used fo
ed probe in in situ
e blots: Southern,
hybridizations.
ases Assay, fluor
rimetric assay for t
ases activity in mic
uct Index
mmalian tissues, su
d RNA directly in R
mer extension, cDN
Set
he High Pure 16 Sy
cleic Acid Kit, or th
n larger sample vo
RNA) from serum,
otal nucleic acids a
d nucleic acids in P
olume Kit
sma, or whole bloo
cleic Acid Kit. An
volumes up to 2.5
n serum, plasma, o
ed viral RNA is use
de water.
and generates frag
e as indicated (*). H
the 3-C residue of
c II.
nd generates fragm
denine or 5-methyl
ethyladenine at A
d generates fragme
denine (*). Presenc
prevent cleavage,
ers: none known.
B, H3, and H4 from
nd in eukaryotic ce
ral units (nucleoso
s used as a substra
nucleosome and t
nto place and allow
e five histone prote
ic cells. Featuring
ail, H3 is involved
e.
or fluorescent dete
hybridization. HNP
northern, DNA seq
rimetric
the quantitative in
roplates. Ideally su
x
uch as mouse
RT-PCR,
NA library
ystem Viral
e High Pure
olumes must
plasma, or
are isolated
PCR and RT-
od, using the
innovative spin
ml. Ideal for
other body
ed for RT-PCR
gments with
Hind II is
f the
ments with 5-
lcytosine (*). 5-
does not
ents with 5-
ce of 5-
but 5-
m calf thymus.
ell nuclei that
omes). They are
ate for protein
he entry and
wing the
eins involved
a main
in the
ection of a
PP alone is
quencing blots,
vitro
uited for high-

Cat. No.

12 033 674 001
12 011 875 001
11 858 874 001
05 114 403 001
11 858 882 001
10 656 305 001
10 656 313 001
10 656 321 001
10 798 983 001
11 274 040 001
10 779 652 001
10 779 679 001
11 274 082 001
10 223 565 001
10 223 549 001
11 004 875 001
11 034 758 001
11 758 888 001
03 005 372 001
12 236 869 001

1 kit
1 set
1 kit fo
1 kit
1 kit fo
2
1 kit for 100 tes
1 kit for 1,000
tes
Pack Size


for up to 100 isola




2,500 U (3 - 10 U/

5,000 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
50,000 U (40 U/l)
1,000 U (10 U/l)
5,000 U (10 U/l)
20,000 U (40 U/l)
10 mg

1 mg
5 mg

1 mg

1 set

sts on 96-well plat
on 384-well plates
tests on 96-well p
sts on 384-well pla

www.roche
tions
ations
cations
tions
cations
l)

)
)
)

)
tes, for 400 tests
s
plates, for 4,000
ates
e-applied-science

Price in

238,70
146,30
335,70
259,70
363,50
475,30
55,80
98,80
98,80
359,00
69,40
275,10
814,10
193,80
200,10
707,10
200,10
441,40
466,10
2.762,20

137

e.com

Alp
138

www.r

Prod

Hpa
Reco
blunt
as ind
Isosc
Hum
Prepa
(buffy
const
Expa
Hybr
Use t
stand
proce
sequ
Hybr
Use i
ELISA
Hybr
Supp
cell h
cells
thaw
Hygr
Hygro
synth
phen
hygro
I
IKA T
Smal
Amp
confi
Imm
For th
Prote
solub
Imm
For th
Prote
solub
In Si
Preci
apop
apop
sensi
In Si
Preci
apop
quan
and f
In Si
Preci
apop
apop
sensi
In Si
Preci
quan
and t
flow
In Si
Seco
single
/in vi
prolif

lphabetic
roche-applied-sc
duct Name
I
ognizes the sequen
dicated (*). 5-meth
chizomers: KspA I.
man Genomic DNA
aration of high mo
y coat). Suitable fo
truction, and the re
nd System.
ridization Bags
these bags in nonr
dard radioactive pr
edures. All hybridiz
entially to the sam
ridization Buffer
n combination wit
As for application
ridoma Fusion an
plement to the norm
hybridomas after fu
and is also used to
ing of cells stored
romycin B
omycin B is an am
hesis in prokaryote
otype of eukaryoti
omycin-resistance
Turrax
l device used for g
lification procedur
gurations for 100V
unoprecipitation
he immunoprecipit
ein A Agarose. The
unoprecipitation
he immunoprecipit
ein-G-Agarose. The
itu Cell Death De
se, fast, and simpl
itu Cell Death De
se, fast, and simpl
ptosis at the single-
titative detection b
formalin-fixed tissu
itu Cell Death De
se, fast, and simpl
itu Cell Death De
se, fast, and simpl
titating apoptotic
tissues using a red
cytometry.
itu Cell Proliferat
nd generation non
e-cell level using i
ivo systems. Detec
ferating cells in he
cal Produ
cience.com
nce GTT*AAC an
y 6-methyladenine
hylcytosine does n
A
olecular weight DN
or Southern hybrid
eliable amplificatio
radioactive hybridi
robe hybridizations
zation solutions an
me bag.
th the PCR ELISA a
in nucleic-acid hyb
nd Cloning Suppl
mal culture mediu
usion and during c
o optimize the gro
in liquid nitrogen.
minoglycosidic antib
es and eukaryotes.
ic cells that are sta
gene (hyg or hph
generating emulsio
re. The device ship
V, 120V, and 230 V
n Kit (Protein A)
tion, and the immu
n Kit (Protein G)
tion, and the immu
etection Kit, AP
e nonradioactive k
n or formalin-fixed
uced apoptosis.
etection Kit, Fluo
e nonradioactive k
-cell level using flu
by flow cytometry.
ue sections.
etection Kit, POD
e nonradioactive k
n or formalin-fixed
uced apoptosis.
etection Kit, TMR
e nonradioactive t
DNA fragmentatio
d fluorescent label
tion Kit, FLUOS
nradioactive kit for
mmunohistocytoc
ct and quantify cel
eterogeneous popu
uct Index
nd generates fragm
e and 5-hydroxyme
ot influence the cl
NA isolated from hu
dization analysis, ge
on of large DNA ta
zation and detecti
s, and western blo
nd blocking buffer
and the series of D
bridization reactio
lement
m to support the g
cloning. HFCS repl
owth of hybridomas
.
biotic that inhibits
Selects and maint
ably transfected wi
h ).
ons in the GS Junio
ps with multiple co
V power inputs.
from cellular extra
eagents necessary
from cellular extra
eagents necessary
kit to detect and q
el using light micr
d tissue and determ
orescein
uorescence micros
Detect apoptotic c
D
kit to detect and q
el using light micr
d tissue and determ
R red
technique for dete
for fluorescence m
r detecting DNA sy
hemistry. Ideal for
ls in S phase, and
ulations.
x
ments with
ethylcytosine
leavage ().
uman blood
enomic library
argets by the
on procedures,
tting
can be added
DIG-detection
ns.
growth of B-
aces feeder
s after the
protein
tains the
ith the E. coli
or emPCR
rd
cts using
for cell lysis,
proteins.
cts using
y for cell lysis,
proteins.
uantify
oscopy. Detect
mine cell
detection of
scopy or
cells in frozen
uantify
oscopy. Detect
mine cell
cting and
level in cells
microscopy or
ynthesis at the
many in vitro
detect

Cat. No.

10 380 385 001
10 567 647 001
11 691 112 001
11 666 649 001
11 717 472 001
11 363 735 001
10 843 555 001
05 943 353 001
11 719 394 001
11 719 386 001
11 684 809 910
11 684 795 910
11 684 817 910
12 156 792 910
11 810 740 001

1 g
1 kit
1 kit
1
1
1
1
1 k
Pack Size

100 U (3 - 10 U/l
500 U (3 - 10 U/l

100 g

50 bags

100 ml

10 ml (50x)


1 device








)
)
ered)
tions
tions
sts
sts
sts
sts
ests

Price in

75,00
300,10
181,50
107,50
80,70
219,10
304,10
inquire
279,40
332,30
651,70
591,40
651,70
591,40
671,50

Alp

Prod

Insul
Insul
stimu
insul
prima
Insul
Conta
free c
facto
facto
INT/
Color
phos
blot,
Inter
Reco
purifi
inves
Inter
Reco
purifi
the s
Inter
Reco
purifi
mono
for a
Inter
Allow
natur
lymp
thym
Inter
Supp
inhib
inhib
pharm
Inter
Reco
cells,
murin
stand
Isopr
Isopr
lac o
analo
IsoSt
High
and l
comp
addit
K
Kana
Amin
of gra
cultu
Kit V
For in
Klen
Use t
techn
in rec
oligo
Klen
This s
Sang
be us
the e
lphabetic
duct Name
lin, human
in has many activit
ulates growth and
in activity on sensi
ary cells and cell li
lin-Transferrin-S
ains the most esse
culture media in a
r supplement to w
rs are added.
BCIP Stock Solu
rimetric substrate s
phatase (AP) in bl
and for application
rferon-, human
ombinant Interferon
ied by standard ch
stigate IFN- activ
rferon-, mouse
ombinant, Interfero
ied by standard ch
tudy of IFN- (int
rleukin-1, huma
ombinant Interleuk
ied by standard ch
ocytes or macroph
variety of sensitive
rleukin-2, human
ws cultivation of hu
ral killer cell lines a
hocytes and natur
ocyte, splenocyte,
rleukin-2, mouse
ports growth of mu
its binding of reco
its binding to hum
macological/physio
rleukin-6, human
ombinant IL-6, hum
and can be used
ne and human hyb
dard chromatograp
ropyl--D-thioga
ropyl--D-thiogal
operon. It binds an
og of galactose tha
trip Mouse Mono
ly specific, fast and
ight-chain types o
parable results to t
tional equipment a
amycin sulfate
am-positive, gram
re. Also used to st
VFV Consumables
nstallation purpose
ow Enzyme
this labeling-grade
niques, such as 3-
cessed DNA ends
nucleotides during
ow Enzyme
sequencing grade
ger DNA sequencin
sed in 3-end label
elongation of oligon
cal Produ
ties on somatic ce
proliferation of ce
itive cells. Compon
ines.
Sodium Selenite S
ential growth-prom
n optimized ratio.
which other cell typ
tion
solution for the se
otting protocols, in
ns in immunohisto
n (hIFN-)
n-, human (hIFN
hromatographic tec
vities in human ce
e (mIFN-)
on-, mouse (mlFN
hromatographic tec
terferon-) action
an (hIL-1)
in-1, human (hI
hromatographic tec
hages and other ce
e cells.
n (hIL-2)
uman/murine IL-2
and proliferation o
ral killer cells. Estab
or PBL derived T-
e (mIL-2)
urine CTLL cells, no
ombinant hIL-2 to m
man responder cells
ological IL-2 activi
n (hIL-6)
man is a growth fac
to replace feeder
bridomas. It is prod
phic techniques.
alactoside
actoside (IPTG) is
d inactivates the la
at cannot be cleave
oclonal Antibody
d easy kit for rapid
of mouse monoclon
the standard ELISA
and reagents.
otic with broad sp
-negative bacteria
s ML STAR
es only.
e enzyme from E. c
-end labeling, rand
to create blunt-en
g site-directed mut
enzyme is specific
ng (dideoxy-chain
ing, random DNA
nucleotides.
uct Index
ells. Recombinant h
lls and is used to i
nent of serum-free
Supplement
moting components
It is used as a bas
pe-specific nutrien
ensitive detection o
ncluding Southern
ocytochemistry.
N-), is produced
chniques. It can be
ll systems.
N-) is produced
chniques. It is a va
ns in mouse mode
L-1) is produced
chniques. Secreted
ell types, it is a plei
dependent T-cell
of mitogen-activate
blishes human/mu
cell lines.
ot human T-cells. S
murine responder
s. Study
ity in murine mode
ctor for murine and
cells in the prepar
duced in E. coli an
a very effective in
ac repressor. It is
ed by -galactosi
y Isotyping Kit
d identification of c
nal antibodies. Yie
A assay without the
ectrum inhibition o
a and mycoplasmas
ein biosynthesis.
coli in many molec
dom primed DNA l
nded DNA, and elo
tagenesis.
cally prepared and
termination metho
labeling, fill-in rea
x
human insulin
nvestigate
e media for
s of serum-
al growth-
ts and growth
of alkaline
blot, western
in E. coli and
e used to
in E. coli and
aluable tool for
l systems.
d in E. coli and
d by activated
iotropic factor
lines and
ed T-
urine
Strongly
cells; weakly
els.
d human B-
ration of
nd purified by
ducer of the
a chemical
idase.
class, subclass,
elds
e need for
of the growth
s in cell
cular biology
labeling, filling
ongation of
d tested for
od). It can also
actions, and

Cat. No.

11 376 497 001
11 074 547 001
11 681 460 001
11 040 596 001
11 276 905 001
11 457 756 001
10 799 068 001
11 011 456 001
11 147 528 001
11 271 164 001
11 138 600 001
10 724 815 001
11 411 446 001
11 493 027 001
10 106 801 001
04 639 626 001
11 008 404 001
11 008 412 001
10 104 531 001

50
10
10
10
10
1
50
1
20
1
2
Pack Size

100 mg

0 mg (for 5 l mediu

3 ml

00,000 U (5 g, 1 m

00,000 U (20 g, 1

00,000 U (2 g, 1 m

0,000 U (5 g, 50 m
0,000 U (5 g, 1 m
0,000 U (25 g, 5 m
0,000 U (5 g, 1 m

00,000 U (2 g, 1 m

1 g
5 g


5 g

1 kit
100 U
500 U

250 U (5 x 10
3
U/m

www.roche
um)
ml)
ml)
ml)
ml)
ml)
ml)
ml)
ml)
sts
ml)
e-applied-science

Price in

140,40
168,80
130,20
240,20
797,70
452,70
250,20
250,20
1.046,40
294,80
257,20
82,20
308,00
314,70
215,30
inquire
109,20
438,70
275,00

139

e.com

Alp
140

www.r

Prod

Kpn
Reco
cohe
both
Ksp
Belon
fragm
gene
of 5'-
L
Lami
Coat
prom
huma
neuro
LC C
Effici
comp
Comp
buck
LC C
This
versio
This s
LC C
Desig
adap
carou
rotor
L-Ca
Dete
enzym
the te
Leup
Prote
prote
alpha
the re
Liber
Maxi
conta
non-c
provi
Liber
Maxi
conta
non-c
prote
Liber
Dete
these
Blend
appli
Liber
Maxi
conta
a non
more
Liber
Maxi
conta
a non
ensu

lphabetic
roche-applied-sc
duct Name
I
ognizes the sequen
sive termini. Kpn I
C-residues or by 6
I (Sac II)
ngs to a class of ra
ments of genomic
rates fragments w
-methylcytosine. Is
inin
cell culture dishes
mote attachment an
an carcinoma, sarc
oblastoma and em
Carousel Centrifu
ently centrifuge PC
pact benchtop dev
patible with LightC
ket, sold separately
Carousel Centrifu
bucket enables co
ons when using th
silver rotor bucket
Carousel Centrifu
gned for use with e
ter accessories en
usels used with Lig
and two rotor buc
arnitine
rmine L-carnitine
matic UV test. Line
est solution. For us
peptin
ect proteins during
ease inhibitor. Leup
a-amino group. It i
eaction by dialysis
rase DH Researc
clostridial neutral
des high experime
rase DL Researc
clostridial neutral
ein) for delicate ap
rase Research G
rmine the optimal
e five 5 mg vials of
ds, each with diffe
cability.
rase TH Researc
e difficult targets.
rase TL Research
res experimental r
cal Produ
cience.com
nce GGTACC and
is not inhibited by
6-methyladenine. I
are-cutter enzymes
DNA. Recognizes
with 3'-cohesive en
soschizomers: Sac
s with this highly p
nd growth of a var
coma, and retinobl
mbryonic carcinoma
uge 2.0
CR samples in Ligh
vice. For use with t
Cycler
1.5 and old

y).
uge 2.0 Bucket 2.
ompatibility with Li
he LC Carousel Cen
t replaces the buck
uge 2.0 Rotor Set
earlier model LC C
nable compatibility
ghtCycler
Carous
ckets.
levels in seminal p
earity in the range
se in life science re
g isolation from tiss
peptin is a tripepti
s highly soluble in
s.
ch Grade
d collagenase isofo
protease. Exceptio
ental reproducibilit
h Grade
d collagenase isofo
protease. Gentle a
plications.
rade Selection K
collagenase produ
f highly pure Libera
rent levels of aggr
h Grade
d collagenase isofo
al protease. More a
h Grade
d collagenase isofo
al protease. Except
reproducibility.
uct Index
d generates fragme
y 5-methylcytosine
Isoschizomers:Asp
s which generate l
the sequence CCG
ds. Not sensitive to
II, Sst II.
pure attachment fa
iety of cell types, in
lastoma cells, and
a cells.
htCycler
carouse
he LightCycler
2
der versions (requ
.1
ghtCycler
1.5 and
ntrifuge to prepare
ket included with t
t
Carousel Centrifug
y with all types of s
sel-Based Instrume
plasma, serum, or u
of 5.6 - 112 M L-
esearch applicatio
sues or membrane
de derivative with
n water and can be
s new enzyme blen
orms blended with
onal lot-to-lot cons
ty.
s new enzyme blen
orms blended with
activity (low activity
Kit
uct for your applica
ase Research Grad
ressiveness, specif
s new enzyme blen
orms blended with
aggressive proteas
s new enzyme blen
orms blended with
tional lot-to-lot con
x
ents with 3-
e at either or
p718 II, Acc65 I.
large
GCGG and
o the presence
actor to
ncluding
murine
els using this
.0 instrument.
ires different
d older
e PCR samples.
the centrifuge.
es. These
sample
ents. Includes
urine using this
-carnitine in
ns.
es using this
an acetylated
e removed from
nd that
h Dispase
, a
sistency
nd that
h Dispase
, a
y per mg
ation using
de Enzyme
icity, and
nd that
h Thermolysin,
se activity for
nd that
h Thermolysin,
nsistency

Cat. No.

10 742 953 001
10 899 186 001
11 117 807 001
11 243 217 001
03 709 507 001
03 709 582 001
03 724 689 001
03 724 697 001
11 242 008 001
11 017 101 001
11 017 128 001
11 034 626 001
11 529 048 001
05 401 054 001
05 401 089 001
05 401 160 001
05 466 202 001
05 401 046 001
05 401 135 001
05 401 151 001
05 401 020 001

1 centrifuge p
1 centrifuge p
1 rotor bucke
1 rotor plus
LC
approximately
approxim
1
1
1
Pack Size

10,000 U (40 U/l)
5,000 U (10 U/l)

1,000 U (10 U/l)

1 mg (2 ml)

plus rotor and buc
plus rotor and buc

et for LC Carousel

2 buckets for the e
C Carousel Centrifu


5 mg
25 mg
50 mg
100 mg
10 mg (2 x 5 mg)
100 mg (2 x 50 mg

10 mg (2 x 5 mg)
100 mg (2 x 50 mg

1 kit (5 x 5 mg)

10 mg (2 x 5 mg)
100 mg (2 x 50 mg

10 mg (2 x 5 mg)

)

cket (115 Volt)
cket (230 Volt)
Centrifuge 2.0
earlier model
uge
combination for
minations)

g)

g)

g)

Price in

195,60
121,70
94,40
240,30
inquire
inquire
inquire
inquire
462,60
82,90
292,80
418,40
630,90
333,00
1.367,50
62,50
402,70
213,30
82,10
611,50
36,50

Alp

Prod

Liber
Maxi
conta
a non
disso
Light
Perfo
track
detec
1536
Light
Note
1536
1536
Ideal
endp
preve
Light
Obta
high-
an ex
inter-
Light
Incre
this h
the L
costs
Light
Impro
1536
LIMS
detec
Light
Perfo
Light
acces
Light
Perfo
Capil
wide
expe
Light
Perfo
(100
ensu
uniqu
Light
Perfo
l) fo
preci
code
Light
Track
Instru
scans
direc
Light
Silver
Instru
the in
Light
Silver
480 I
by th
Light
Conf
Light
pre-d
Light
Analy
this a
PCR
meth
lphabetic
duct Name
rase TM Researc
ociation application
tCycler
1536 D
orm easy hot start
king in automater w
ction and gene qua
System.
tCycler 1536 D
: RealTime ready D
DNA Probes Mas
Instruments with
for fast hot start a
point genotyping. U
ent carryover conta
tCycler
1536 In
in 1,536 data point
-throughput therm
xceptional range o
-assay errors.
tCycler
1536 M
ease PCR throughp
high-performance
LightCycler
1536
s and minimizes as
tCycler
1536 So
ove PCR efficiency
Instrument. Ideal
S data managemen
ction of pipetting e
tCycler
2.0 Cap
orm easy unloading
tCycler
Sample C
ssory.
tCycler
2.0 Inst
orm fast and sensit
llary-based techno
selection of fluore
rimental design an
tCycler
2.0 Sam
orm up to 32 simult
l) for the LightCy
re precise position
ue bar code for ea
tCycler
2.0 Sam
orm up to 32 simult
or the LightCycler
se positioning and
for easy identifica
tCycler
480 Bar
k and manage sam
ument using this h
s data from the ba
ctly into the LightCy
tCycler
480 Blo
r block cycler for 3
ument. The block c
nstrument. Include
tCycler
480 Blo
r block cycler acce
nstrument. The blo
e instrument. Inclu
tCycler
480 Co
irm real-time PCR
tCycler
480 Instru
diluted samples of
tCycler
480 Ge
yze melting curve
accessory software
fragments for gen
hylation.
cal Produ
ch Grade
d collagenase isofo
al protease. Excelle
ns.
NA Green Maste
PCR assays using
workflows. Ideal fo
antification assays
DNA Probes Mast
DNA Probes Maste
terFor real-time PC
appropriate probe
assays for gene de
Use LightCycler
U
amination.
nstrument
ts in a single PCR
mal block cycler fea
f assay types while
Multiwell Plate
put fourfold compa
1,536-well reactio
Instrument. Precis
ssay errors.
oftware, Version
y using this dedica
for automated hig
nt. Use with RealTi
errors.
pillary Releaser
g of the LightCycle
Carousel in one sim
trument
tive real-time PCR
ology provides fast
escence formats m
nd analysis.
mple Carousel (1
taneous PCR react
ycler
2.0 Instrume
ning and reproduc
sy identification.
mple Carousel (2
taneous PCR react
2.0 Instrument. H
d reproducible resu
ation.
r-Code Scanner
mple information fo
handheld barcode
arcodes on LightCy
ycler
Software.
ock Kit 384 Silver
384-well plates, for
cycler is automatic
es block lid and sto
ock Kit 96 Silver
essory for 96-well
ock cycler is autom
udes block lid and
ntrol Kit
and melting curve
ument using this c
human target gen
ne Scanning Sof
data from the Ligh
e module for the L
etic variations suc
uct Index
s new enzyme blen
orms blended with
ent overall applicab
er
fast protocols and
or high-throughput
s. For use on the L
ter
er was renamed to
CR using LightCyc
es and gene-specif
etection and quant
Uracil-DNA Glycos
run of less than 50
atures proven optic
e reducing sample
ared to a 384-well
n plate specifically
sion miniaturization
1.1
ated software for th
h-throughput wor
me ready reagents
er
Capillaries from
mple step, using th
on this proven ins
t, reproducible resu
maximizes flexibility
00 l)
tions in this sampl
ent. Heat-resistant
ible results. Labele
0 l)
tions in this sampl
Heat-resistant mate
ults. Labeled with
or the LightCycler
scanner. This optio

ycler
480 Multiwe
r
r use with the Ligh
cally detected and
orage box.
plates using the Li
matically detected
storage box.
e analysis performa
convenient kit. The
nes and internal co
ftware
htCycler
480 Instr
ightCycler
480 So
ch as SNPs, mutatio
x
nd that
h Thermolysin,
bility in
d built-in error
t gene
ightCycler

o LightCycler

cler
480 and
fic primers.
ification and
sylase to
0 minutes. This
cs facilitating
e volumes and
plate using
y designed for
n reduces
he LightCycler

rkflows and
s for easy
m the
is convenient
strument.
ults, and a
y in
le carousel
t materials
ed with a
le carousel (20
erials ensure
a unique bar
480
onal accessory
ell Plates
htCycler
480
calibrated by
ightCycler

and calibrated
ance of the
kit contains
ontrols.
rument using
oftware. Scan
ons, and

Cat. No.

05 401 119 001
05 401 127 001
05 573 092 001
05 502 381 001
05 334 276 001
05 358 639 001
06 569 382 001
03 603 920 001
03 531 414 001
03 603 954 001
03 603 962 001
04 710 606 001
05 015 197 001
05 015 219 001
04 710 924 001
05 103 908 001

1
1 kit (for up
5 x 1 ml for
1
1 instrument
station (de
1 block kit (blo
1 block kit (bl
1 kit (for u
1
Pack Size

10 mg (2 x 5 mg)
100 mg (2 x 50 mg

to 12,500 reaction

r up to 12,500 x 2

1 instrument

10 x 10 plates

1 software packag

1 capillary release

(plus related prod
esktop or noteboo

1 sample carouse

1 sample carouse

1 scanner

ock kit for 384-wel
plates)

ock kit for 96-well
plates)

up to 2 x 3 control

1 software packag

www.roche

g)
ns, 2 l each)
l reactions
e
er
ducts and data
k version))
l
l
l PCR multiwell
PCR multiwell
reactions)
e
e-applied-science

Price in

108,50
642,40
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

141

e.com

Alp
142

www.r

Prod

Light
Perfo
480 I
The s
probe
Light
Achie
inhib
Obta
evalu
Light
Save
Light
Reso
or PC
Light
Achie
throu
work
and t
Light
Use t
intern
easy-
PCR
Light
High-
Instru
for re
Light
Light
Clear
based
on Li
recom
Light
This
melti
Instru
track
Light
This
melti
The w
Light
This
SYBR
Instru
labele
Light
High-
Instru
used
Light
Light
Save
PCR
FastS
forma
Light
Easy-
cyclin
Unive
Preve
Glyco
Light
Preve
assay
clear)
evapo

lphabetic
roche-applied-sc
duct Name
tCycler
480 Ge
orm easy real-time
nstrument using th
single-component
es.
tCycler
480 Hig
eve highly homoge
ition using this flu
in enhanced fluore
uation of amplicon
tCycler
480 Hig
time using an opt
tCycler
480 Syste
Light, a novel dye
CR.
tCycler
480 Ins
eve fast, sensitive,
ughput platform. A
kflows, this cutting-
temperature homo
tCycler
480 LIM
this module to inte
nal Laboratory Info
-to-install software
workflow efficienc
tCycler
480 Mu
-performance reac
uments, 384-well v
eal-time PCR and m
tCycler
480 Instru
tCycler
480 Mu
r plates for high pe
d assays using the
ghtCycler
480 In
mmended for use w
tCycler
480 Mu
high performance
ng curve analysis
uments.The white,
king.
tCycler
480 Mu
high performance
ng curve analysis
white, polypropylen
tCycler
480 Mu
high performance
R Green I and hydr
uments. The clear,
ed for easy trackin
tCycler
480 Mu
-performance reac
uments, 96-well ve
for real-time PCR
tCycler
480 Instru
tCycler
480 Pro
time in gene quan
master mix for the
Start Taq DNA Poly
ation of nonspecif
tCycler
480 RN
-to-use hot start m
ng conditions of pl
ersal ProbeLibrary
ent PCR product ca
osylase.
tCycler
480 Sea
ent evaporation an
ys in LightCycler

) using the LightC
oration during cyc
cal Produ
cience.com
notyping Master
PCR and genotyp
his convenient, rea
kit requires only t
gh Resolution Me
eneous staining of
orescent double-s
escent signal shar
melting behavior.
gh Resolution Me
timized ready-to-u
em. This highly stab
that does not inte
strument II
and consistent PC
Adaptable for 96- o
-edge instrument o
ogeneity.
MS Interface Mod
egrate the LightCyc
ormation Managem
e package for impr
cy.
ultiwell Plate 384
version.Use LightC
melting curve anal
ument, 384-well ve
ultiwell Plate 384
erformance SYBR
e LightCycler
480
struments and 480
with FRET HybPro
ultiwell Plate 384
384-well reaction
applications using
polypropylene pla
ultiwell Plate 96 w
96-well reaction p
applications using
ne plate is barcode
ultiwell Plate 96,
96-well reaction p
rolysis probe-base
half-skirted, polyp
ng.
ultiwell Plate 96,
ersion.LightCycler
and melting curve

ument, 96-well ver
obes Master
ntification assays u
e LightCycler
480
ymerase for hot sta
ic amplification pro
NA Master Hydrol
mix for one-step RT
late-based LightCy
and hydrolysis pro
arryover using Lig
aling Foil
nd contamination w
480 Multiwell Plat
Cycler
480 Instrum
cling or storage.
uct Index
r
ping analysis on the
ady-to-use hot sta
he addition of DNA
elting Dye
f amplicons withou
stranded DNA-bind
pness and high re
elting Master
se PCR master mix
ble reaction mix co
erfere with amplific
CR results using a
or 348-well plates a
offers exceptional
dule
cler
480 System
ment System (LIMS
roved data manage
4 white, 4 barcod
-made for the Ligh
Cycler
480 Multiw
lysis applications w
ersion.
4, clear
Green I and hydro
0 Instrument, 384-w
0 Software, Version
be probes or HRM
4, white
plate is specificall
g LightCycler
480
ate is barcode-labe
white
g LightCycler
480
e-labeled for easy
clear
ed assays using Lig
propylene plate is
white, 4 barcode
-made for the Ligh
480 Multiwell Pla

e analysis applicat
rsion.
using an optimized
0 System. The mix c
art PCR, which min
oducts.
lysis Probes
T-PCR with the rap
ycler
480 Instrum
obes as the detect
htCycler
Uracil-D
when running real-
tes (96 or 384 well
ment. Strong adhes
x
e LightCycler

rt master mix.
A, primers, and
ut PCR
ding dye.
solution
x for the
ontains
cation enzymes
versatile high-
and automated
reproducibility
into your
S) using this
ement and
des
htCycler
480
well Plates 384
with the
olysis probes-
well. Use only
n 1.5. Not
M.
ly designed for
0
eled for easy
y designed for
0 Instruments.
tracking.
y designed for
ghtCycler
480
barcode-
es
htCycler
480
ates 96 are
tions with the
d ready-to-use
contains
nimizes
pid, accurate
ments using
tion format.
DNA
-time PCR
ls, white or
sion prevents

Cat. No.

04 707 524 001
04 909 640 001
04 909 631 001
05 015 243 001
05 015 278 001
05 066 310 001
05 217 555 001
05 102 430 001
04 729 749 001
04 729 692 001
05 102 413 001
05 220 319 001
04 707 494 001
04 887 301 001
04 902 343 001
04 991 885 001
04 729 757 001

4 x 384 l ((
of 20
1 ml (for up to
5 x 1 ml (for
1 instr
1 instr
1
5 x 10 p
5 x 10
5 x 10
5 x 10
5 x 10
5 x 10 p
5 x 1 ml (for u
10 x 5 ml ((2x c
20
1 x 50 ml (for u
1 kit (for up t
Pack Size

(5x conc.) approx.3
l reaction volume

o 1,000 reactions o
volume)

up to 500 reaction

rument (384-well v
rument (96-well ve

1 software packag

plates without seal

plates (with sealin

plates (with sealin

plates (with sealin

plates (with sealin

plates without seal

up to 500 reactions
volume)
up to 5,000 reactio
volume)
to 5x100 reactions
volume)

50 foils

384 reactions
e each)
f 20 l reaction
ns, 20 l each)
version)
ersion)
e
ling foils
ng foils)
ng foils)
ng foils)
ng foils)
ling foils
s of 20 l final
000 reactions of
ume)
ns of 20 l final
s at 20 l final

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

Light
Comp
quan
PCR
samp
Light
Read
Light
and q
minim
Light
The L
Light
user
Light
The L
480 I
differ
inten
Light
The a
Light
to 12
times
the L
96-w
Instru
Light
Use f
(gene
resol
strips
Light
Use t
to ea
endp
Inclu
Light
Spec
mast
Instru
Light
Spec
mast
Instru
Light
Spec
mast
Instru
Light
Spec
mast
Instru
Light
For a
Achie
using
use a
quan
resol
Light
For L
highl
with
requi
medi
Light
Use w
20 l
Light
maxim
lphabetic
duct Name
tCycler
480 Sof
prehensive suite o
tification and geno
Systems. Provides
ple editing, templat
tCycler
480 SY
dy-to-use hot start
tCycler
480 Instru
quantification. Elim
mize pipetting step
tCycler
480 Ven
LightCycler
480 V
tCycler
480 Instru
within a few minu
tCycler
480 Xen
LightCycler
480 X
nstruments. It is ea
rence between a X
sity, which differs
tCycler
8-Tube
adapter plate is for
tCycler 8-Tube Stri
LightCycler
8-Tu
s. The LightCycler
LightCycler
480 In
well version. The pla
uments.
tCycler
8-Tube
for SYBR Green I, R
e detection, gene q
ution melting anal
s and cap strips ar
tCycler
8-Tube
these optimized re
sily set up and per
point genotyping, a
des both tube strip
tCycler
96 DNA
ial bundle combip
er for SYBR Green
ument.
tCycler 96 DNA
ial bundle combip
er for SYBR Green
ument.
tCycler
96 DNA
ial bundle combip
er for hydrolysis p
ument.
tCycler 96 DNA
ial bundle combip
er for hydrolysis p
ument.
tCycler
96 Instr
accurate, consisten
eve the rigorous pe
g intuitive large tou
accessible data an
tification, endpoin
ution melting and
tCycler
Capillar
LightCycler
2.0 In
y sensitive bacteri
LightCycler
2.0 S
irements of the Eu
cal devices.
tCycler
Capillar
with LightCycler

and are compatib
tCycler
2.0 Samp
mizes fluorescent
cal Produ
ftware, Version 1
f tools for setup, ru
otyping assays on
all functionalities
tes, macros).
BR Green I Mast
mix for SYBR Gree
uments. Ideal for P
minate time-consum
ps; just add DNA, p
ntilation Dust Filt
Ventilation Dust Fi
ument. The dust fil
tes.
non Lamp
Xenon Lamp is a re
asily replaced with
Xenon and a Halog
at least by factor 1
Strip Adapter Pl
r use with the Ligh
ips (white or clear)
ube Strips in one r
8-Tube Strip Ada

nstrument I and Li
ate is not suitable
Strips (clear)
ResoLight dye, and
quantification, end
ysis) on the LightC
re provided togethe
Strips (white)
eaction vessels for
rform gene detecti
and high-resolution
ps and cap strips.
A Green Value Pa
ack, including mu
n I assays performe
A Green Value Pa
ack, including mu
n I assays performe
A Probes Value P
ack, including mu
robe assays perfor
A Probes Value P
ack, including mu
robe assays perfor
rument
nt real-time PCR re
erformance standa
uchscreen-based s
alysis. Application
nt and melting curv
qualitative detecti
ries (100 l) MG
struments if using
al, fungal nucleic a
Sample Carousel (1
ropean Directive 9
ries (20 l)
Carousel-Based In
ble with the LightC
le Carousel (20 l)
signal transmissio
uct Index
1.5
un, and analysis of
LightCycler
480
(user-friendly prog
ter
en I-based real-tim
PCR assays for gen
ming MgCl
2
titrati
primers.
ter
lter is a replaceme
lter can be easily r
eplacement part fo
hin a few minutes.
gen lamp is the lum
10.
late
htCycler
480 Syst
). The adapter plat
run and is re-usab
apter Plate can on
ghtCycler
480 In
for the use in Ligh
d hydrolysis probe
dpoint genotyping,
Cycler
Nano Instr
er.
the LightCycler
9
ion, gene quantific
n melting analysis
ack L
ed on the LightCyc
ack S
ed on the LightCyc
Pack L
rmed on the LightC
Pack S
rmed on the LightC
esults in your resea
ard of the LightCyc
software for power
s include absolute
ve-based genotypi
on.
RADE
g large reaction vol
acid detection. Co
100 l). This produ
98/79/EC for in vitr
nstruments. Capilla
Cycler
Carousel a
). High quality boro
on.
x
f real-time PCR
Real-Time
gramming,
me PCR on
ne detection
on and
ent part for the
replaced by the
or LightCycler

The main
minous
tem and the
te can hold up
ble multiple
ly be used in
strument II ,
htCycler
96
e-based assays
high
rument. Tube
96 Instrument
cation,
assays.
real-time PCR
cler 96
real-time PCR
cler
96
real-time PCR
Cycler
96
real-time PCR
Cycler 96
arch lab.
cler
Systems,
rful easy-to-
e and relative
ng, high
lumes. For
mpatible only
uct fulfills the
ro diagnostic
aries hold 10 to
nd
osilicate glass

Cat. No.

04 994 884 001
04 707 516 001
04 887 352 001
04 686 128 001
04 686 136 001
06 612 598 001
06 327 672 001
06 612 601 001
06 713 106 001
06 713 092 001
06 713 122 001
06 713 076 001
05 815 916 001
03 612 066 001
04 929 292 001

1
5 x 1 ml ((2x
20
10 x 5 ml ((2x c
20
120 clea
120 x 8-tube-s
(Optimized rea
96 and the L
LightCycle
combination w
20 packs of
Master (a total
480 Multiwell
5 packs FastSt
(a total of 25
Multiwell P
20 packs of F
Master (a
LightCycl
(
5 packs of F
Master (a total
Multiwell P
1 instrument (
for the use of
1 pack (con
cap
1 pack (con
cap
Pack Size

1 software packag

conc.) approx. 500

4 filters

1 lamp

1 piece

r tube strips and c
(10 unit pack)

LightCycler
480. N
er
480 it can only

with the LightCycle
Adapter Plate)
FastStart Essentia
of 100 ml); 2 pack
tart Essential DNA
ml); 2 packs of Lig
FastStart Essential
ler
480 Multiwell
FastStart Essential
of 25 ml) 1 pack L
(96-well realtime P
96-well plates and

ntaining 8 boxes, e
pillaries and stopp

ntaining 5 boxes, e
pillaries and stopp

www.roche
e
0 reactions of
ume)
000 reactions of
ume)
cap strips
tube caps clear
he LightCycler

Note: For the
y be used in
er
Tube Strip
l DNA Green
ks of LightCyler

of 100 plates)
A Green Master
ghtCyler
480
of 50 plates)
DNA Probes
2 packs of
Plates 96
s)
DNA Probes
LightCycler
480
of 50 plates)
PCR instrument
d 8-tube strips)
each with 96
ers)
each with 96
ers)
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

143

e.com

Alp
144

www.r

Prod

Light
Simp
remo
onto
all Lig
Light
Simp
Capil
stand
8-we
Light
Read
Light
prere
and C
Light
Conf
Instru
and s
dual-
Light
Easy-
Light
detec
MgC
Light
Easy-
Light
forma
is sup
Light
Easy-
Light
detec
PCR.
Light
Easy-
Light
detec
RT-P
Light
Easy-
Capil
HybP
expre
Light
Easy-
Capil
Gree
analy
Light
Use t
with
HybP
Light
Read
and s
mRN
No p
Light
Read
using
in PC
PCR

lphabetic
roche-applied-sc
duct Name
tCycler
Capping
plifies the process o
ove a cap from the
a capillary holding
ghtCycler
Capilla
tCycler
Centrifu
plify cooling, filling,
llaries. Adapter eas
dard centrifuges. C
ell multichannel pip
tCycler
Color C
dy-to-use solutions
tCycler
Carousel-
equisite for multipl
Cy5.5-labeled Hyb
tCycler
Control
irms PCR system p
uments. Quality ch
specific primers an
-color experiments
tCycler
DNA M
-to-use mix for sen
tCycler
Carousel-
ction format. For q
l
2
is supplied for s
tCycler
DNA M
-to-use mix for sen
tCycler
Carousel-
at. Use for quantita
pplied for specific
tCycler
FastSta
-to-use hot start m
tCycler
Carousel-
ction. For qPCR, SN
MgCl
2
is supplied
tCycler
FastSta
-to-use hot start m
tCycler
Carousel-
ction. For qPCR, SN
CR. MgCl
2
is supp
tCycler
FastSta
llaries on LightCyc
Probe probes for de
ession analysis. Ad
tCycler
FastSta
llaries on LightCyc
n I for detection. U
ysis. Addition of M
tCycler
Fluores
5'-LightCycler
Re
Probe probes on Li
tCycler
h-G6PD
dy-to-use mix of pr
standard RNA for d
A in RT-PCR assay
seudogenes or co
tCycler
Multiple
dy-to-use 5x mix fo
g LightCycler
Cap
CR to genotype SN
using a multiplex a
cal Produ
cience.com
g Tool
of closing LightCyc
LightCycler
Cap
g the reaction mixt
aries.
uge Adapters
, and centrifugatio
sily fits holes in rot
Cooling block hold
pettes.
Compensation Se
s generate color co
-Based Instrument
ex experiments wi
Probe probes in a
l Kit DNA
performance of Lig
heck of both huma
nd HybProbe probe
s and color compe
aster HybProbe
nsitive, robust PCR
-Based Systems, u
uantitative PCR, an
specific application
aster SYBR Gree
nsitive, robust PCR
-Based Systems, u
ative PCR, and SN
applications.
art DNA Master H
-Based Systems w
NP and mutation d
d for specific appli
art DNA Master S
-Based Systems w
NP, and mutation d
plied for specific a
art DNA MasterP
eaction mix for hig
cler
Carousel-Bas
etection. Use also
ddition of MgCl
2
is
art DNA MasterP
eaction mix for hig
cler
Carousel-Bas
Use in two-step RT
gCl
2
is not necess
scein CPG
e 3'-end of oligon
ed-labeled oligonu
ghtCycler
480 an
DH Housekeeping
rimers and HybPro
detection/quantita
ys using LightCycl
ntaminating DNA
ex DNA Master H
or optimal perform
pillaries and the Li
Ps, analyze mutati
approach.
uct Index
cler
Capillaries. U
pillary box and plac
ture. The tool is co
n of all types of Li
tors for Eppendorf
s 32 adapters in 4
et
ompensation files o
ts. Generated files
th both LightCycle
single capillary.
ghtCycler
Carous
n DNA used in a s
es, and as a functi
nsation.
R in LightCycler
C
using the HybProbe
nd SNP and mutat
ns.
en I
R in LightCycler
C
using the SYBR Gre
P and mutation de
HybProbe
CR in LightCycler
when using HybPro

detection. Use in tw
cations.
SYBR Green I
CR in LightCycler
when using SYBR G

detection. Use also
pplications.
LUS HybProbe
ghly sensitive PCR
sed Systems when
in two-step RT-PC
s not necessary.
LUS SYBR Green
ghly sensitive PCR
sed Systems when
T-PCR for gene exp
sary.
ucleotides. Use in
ucleotides for dete
nd Carousel-Based
g Gene Set
obe probes specific
ative comparison o
ler
Carousel-Bas
are detected.
HybProbe
ance in multiplex r
ightCycler
2.0 Ins
ons, and perform t
x
Use the tool to
ce it directly
ompatible with
ghtCycler

f tubes in
rows; use with
on
are a
er
Red 640-
sel-Based
specific assay
onal check of
Capillaries on
e probes
tion detection.
Capillaries on
een I detection
etection. MgCl
2

Capillaries on
be probes for
wo-step RT-
Capillaries on
Green I for
o for two-step
in LightCycler

n using
CR for gene
n I
in LightCycler

n using SYBR
pression
combination
ection with
d Systems.
c for h-G6PDH,
of G6PDH
ed Systems.
real-time PCR
strument. Use
two-step RT-

Cat. No.

03 357 317 001
11 909 312 001
12 158 850 001
12 158 833 001
12 015 102 001
12 158 825 001
12 158 817 001
03 003 248 001
12 239 272 001
03 003 230 001
12 239 264 001
03 515 567 001
03 515 575 001
03 752 178 001
03 515 869 001
03 515 885 001
03 752 186 001
03 113 906 001
03 138 178 001
03 261 883 001
04 340 019 001

1 set (32 ada
1 set (4
1 kit for up
1 kit for up to 9
1 kit for up to 4
1 kit for up to 4
1 kit for up to 9
1 kit for up to 4
1 kit for up to 9
1 kit for up to 4
1 kit for up to 4
1 kit for up to 9
1 kit for up to
reactions o
1 kit for up to 9
1 kit for up to 4
1 kit for up to
reactions o
1 set for up to 9
1 kit for up to 9
Pack Size

1 capping tool

apters in a dedicat
cooling block)


to 50 reactions wit
reaction volume

96 reactions of 20
volume
80 reactions of 20
volume

80 reactions of 20
volume

96 reactions of 20
volume
80 reactions of 20
volume

96 reactions of 20
volume
80 reactions of 20
volume

80 reactions of 20
volume
96 reactions of 20
volume
o 1,920 reactions o
96 reactions of 20
volume
80 reactions of 20
volume
o 1,920 reactions o
5 columns
1 g

96 reactions of 20
volume

96 reactions of 20
volume

ted aluminum
on runs)
th 20 l final
l final reaction
l final reaction
l final reaction
l final reaction
l final reaction
l final reaction
l final reaction
l final reaction
l final reaction
of 20 l or 384
tion volume
l final reaction
l final reaction
of 20 l or 384
tion volume
l final reaction
l final reaction

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

Light
Comp
Instru
each
sensi
quan
Light
Spec
and r
Instru
Light
Spec
and r
Instru
Light
Comp
Instru
each
sensi
Light
Spec
and r
Instru
Light
Spec
and r
Instru
Light
Fast,
gene
footp
for ev
Light
Fully
and S
analy
mono
Light
Use t
comb
oligo
enou
minim
Light
Use t
comb
oligo
suffic
oligo
Light
Easy-
Light
detec
risk o
Light
Easy-
Light
detec
risk o
Light
Easy-
Base
RNAs
minim
Light
Easy-
Base
RNAs
minim
Light
The L
achie
32 po
lphabetic
duct Name
tCycler
Nano D
plete system, inclu
ument with real-tim
and 480 tube stri
tification.
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
tCycler
Nano D
plete system, inclu
ument with real-tim
and 480 tube stri
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
tCycler
Nano D
ial bundle combip
real-time PCR mas
uments.
tCycler
Nano In
32-sample real-tim
tic variation analys
print, and weight, a
veryday use.
tCycler
Probe D
automated design
SimpleProbe probe
ysis, or mutation de
oplex or multiplex
tCycler
Red 610
nucleotides for de
gh LightCycler
R
mum of 5 50 nm
tCycler
Red 640
nucleotides when
cient amount of es
nucleotides.
tCycler
RNA Am
-to-use mix for one
tCycler
Carousel-
ction. Provides rep
of contamination. M
tCycler
RNA Am
-to-use mix for one
tCycler
Carousel-
ction. Provides rep
of contamination. M
tCycler
RNA M
-to-use mix for one
d Instruments and
s. High temperatur
mizes mispriming d
tCycler
RNA M
-to-use mix for one
d Instruments and
s. High temperatur
mizes mispriming d
tCycler
Sample
LightCycler
Samp
evable with the Lig
ositions to hold Lig
cal Produ
DNA Green Starte
uding LightCycler

me PCR Master rea
ips & caps, using S
start PCR assays fo
NA Green Value
ack, including rea
ster for SYBR Gree
DNA Green Value
ack, including rea
ster mix for SYBR G
DNA Probes Start
uding LightCycler

me PCR Master rea
ips & caps, using U
start PCR for gene
DNA Probes Value
ack, including rea
ster for hydrolysis u
DNA Probes Value
ack, including rea
ster for hydrolysis p
nstrument
me PCR instrumen
sis in mono- and d
and easy reaction s
Design Software
n of primers or pro
es. For easy qualita
etection using Ligh
assays with up to
0-N-hydroxysucc
e 5'-amino end of
ghtCycler
Fluores
etection with HybP
Red 610-N hydroxy
ol oligonucleotide
0-N-hydroxysucc
e 5'-amino end of
ghtCycler
Fluores
using HybProbe p
ster to label a minim
mplification Kit H
e-step RT-PCR in
-Based Instrument
MgCl
2
is supplied
mplification Kit S
e-step RT-PCR in
-Based Instrument
MgCl
2
is supplied
aster HybProbe
e-step RT-PCR usi
d HybProbe probes
re overcomes seco
during the RT step
aster SYBR Gree
e-step RT-PCR usi
d SYBR Green I dye
re overcomes seco
during the RT step
e Carousel
ple Carousel is us
ghtCycler
1.5 Inst
ghtCycler
Capilla
uct Index
er Pack
Nano Real-Time
agents for 4,000 re
SYBR Green I dete
or gene detection a
Pack L
ction device, react
en I using LightCyc
e Pack S
ction device, react
Green I using Ligh
ter Pack
Nano Real-Time
agents for 4,000 re
UPL or hydrolysis p
expression quanti
e Pack L
ction device, react
using LightCycler
e Pack S
ction device, react
probes using Light
nt for gene express
dual-color. Minima
setup and software
2.0
obes, such as HybP
ative and gene exp
htCycler
Instrum
four different targe
cinimide ester
oligonucleotides.
scein CPG -labeled
robe probes. One v
ysuccinimide ester
s.
cinimide ester
oligonucleotides.
scein CPG -labeled
probes for detectio
mum of 5 50 nm
HybProbe
LightCycler
Capi
ts and HybProbe p
performance, and
for optimization.
SYBR Green I
LightCycler
Capi
ts and SYBR Green
performance, and
for optimization.
ing LightCycler
C
s for detection. Ide
ondary structures,
p.
en I
ing LightCycler
C
e for detection. Ide
ondary structures,
p.
ed to increase the
trument and older
ries (20 l).
x
PCR
eactions - 20 l
ection. Ideal for
and
tion vessels
cler
Nano
tion vessels
htCycler
Nano
PCR
eactions - 20 l
probes. For
fication.
tion vessels
Nano
tion vessels
tCycler
Nano
sion and
al noise,
e make it ideal
Probe probes
pression
ents in
ets at once.
Use in
d
vial has
r to label a
Use in
d
n. One vial has
mol
illaries using
probes for
minimizes the
illaries using
n I dye for
minimizes the
Carousel-
eal for difficult
and hot start
Carousel-
eal for difficult
and hot start
e throughput
versions. It has

Cat. No.

06 444 199 001
06 444 172 001
06 444 229 001
06 444 202 001
06 444 156 001
06 444 164 001
06 407 773 001
04 342 054 001
03 561 488 001
12 015 161 001
12 015 145 001
12 015 137 001
03 018 954 001
03 064 760 001
11 909 282 001

1 instrument an
20 l each an
4 kits (2,000
strips
2 kits (1,000
strip
1 instrument an
20 l each an
4 kits (2,000
strips
2 kits (1,000
strip
1 inst
1
1 vial (for 5
1 vial (for 5
1 kit for up to 9
1 kit for up to 9
1 kit for up to 9
1 kit for up to 9
Pack Size

nd 8 kits for up to
d 480 strips/caps f
reactions

reactions 20 l e
s/caps (1,920 react

reactions 20 l e
ps/caps (960 react

nd 8 kits for up to
d 480 strips/caps f
reactions

reactions 20 l e
s/caps (1,920 react

reactions 20 l e
ps/caps (960 react

rument plus acces

1 software packag

5 x 50 nmol oligon

5 x 50 nmol oligon

96 reactions of 20
volume

96 reactions of 20
volume

96 reactions of 20
volume

96 reactions of 20
volume

1 sample carouse

www.roche
4,000 reactions,
for up to 3,840
each) and 240
tions)
each) and 120
ions)
4,000 reactions,
for up to 3,840
each) and 240
tions)
each) and 120
ions)
ssories
e
nucleotides)
nucleotides)
l final reaction
l final reaction
l final reaction
l final reaction
l
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

145

e.com

Alp
146

www.r

Prod

Light
For re
(pack
versio
Capil
Light
Versi
Instru
modu
Light
Read
PCR
Probe
are n
Light
Use w
dUTP
produ
that o
L-La
L-Lac
-ke
in su
L-La
L-Lac
-ke
in su
L-Ma
L-Ma
enzym
using
glyce
L-Ma
L-Ma
enzym
using
amm
Lucif
Dete
activi
relea
suffic
Lucif
Bacte
the d
forme
Lucif
Chem
lucife
lumin
film.
Lum
Lumi
is ide
chem
techn
Lum
Lumi
is ide
chem
techn
Lum
Chem
PVDF
espec
for m
Lum
Chem
PVDF
high
hours
lphabetic
roche-applied-sc
duct Name
tCycler
Sample
eplacement of wor
k size of 2). It is co
ons. Developed to
llaries in the LightC
tCycler
Softwar
on 4.1 is the up-to
uments. Allows use
ules for performing
tCycler
TaqMan
dy-to-use hot start
using LightCycler
eLibrary and hydro

not compatible with
tCycler
Uracil-D
with LightCycler

P-containing ampli
uct carryover cont
only native dTTP-c
actate Dehydroge
ctate Dehydrogena
etoacids to -hyd
spension in 3.2 M
actate Dehydroge
ctate Dehydrogena
etoacids to -hyd
spension in 3.2 M
alate Dehydroge
alate Dehydrogena
me that reversibly
g the reduction of
erol (v/v), pH appro
alate Dehydroge
alate Dehydrogena
me that reversibly
g the reduction of
onium sulfate solu
ferase
rmine ATP in ATP
ity of enzymes suc
sed per molecule A
cient for 5,000 ATP
ferase
erial luciferase use
determination of NA
ed or consumed. F
ferase Reporter G
miluminescent assa
erase activity in tra
nometers, micropla
More sensitive tha
i-Film Chemilum
-Film Chemilumin
eal for detecting th
miluminescent subs
niques.
i-Film Chemilum
-Film Chemilumin
eal for the detectio
miluminescent subs
niques.
i-Light Western B
miluminescent POD
F or nitrocellulose
cially when quanti
multiple exposures.
i-Light
PLUS
Weste
miluminescent POD
F or nitrocellulose
sensitivity western
s, allowing for mul
cal Produ
cience.com
e Carousel O-Rin
rn out LightCycler
ompatible with all L

ensure proper pos
Cycler
Sample Ca
re 4.1
o-date LightCycler
e with Windows X
g and analyzing re
n
Master
mix for high perfo
Carousel-Based
olysis probe assays
h melting curve an
DNA Glycosylase
FastStart enzyme-
ified DNA produce
amination in newly
containing DNA is
enase (L-LDH)
ase from hog mus
droxycarboxylic aci
ammonium sulfat
enase (L-LDH)
ase from rabbit mu
droxycarboxylic aci
ammonium sulfat
nase (L-MDH)
ase (L-MDH) from
catalyzes the oxid
NAD
+
to NADH. S
oximately 7.
nase (L-MDH)
ase (L-MDH) from
catalyzes the oxid
NAD
+
to NADH. S
ution, pH approx. 6
generating or ATP
ch as creatine kina
ATP in biolumines
P determinations in
ed together with N
AD(P)H, and for re
From Photobacteriu
Gene Assay, high
ay for quantitative
ansfected cells. Use
ate or tube format,
an isotopic CAT as
minescent Detecti
escent Detection F
he signals from alk
strates (e.g ., CSPD
minescent Detecti
escent Detection F
on of signals from a
strates (e.g., CSPD
Blotting Substrat
D substrate detect
membranes. For h
fication is required
ern Blotting Kit (M
D substrate detect
membranes using
n blotting requiring
ltiple exposures.
uct Index
g
Sample Carouse
LightCycler
Samp
sitioning of the Lig
arousels.
Software for Lig

P. Integrates all so
eal-time PCR exper
ormance qPCR or t
Instruments with
s. Note that hydrol
nalysis.
e
-containing kits to
ed in previous PCR
y prepared mixes,
available for real-t
cle is used for the
ds, or reverse reac
e solution, pH app
ds, or reverse reac
e solution, pH app
pig heart (mitocho
ation of malate to
Supplied in solutio
pig heart (mitocho
ation of malate to
Supplied in suspen
6
P consuming react
se/ATPases. One p
scence assays. One
n concentration 0.1
AD(P)H:FMN oxid
eactions in which N
um fischeri .
h sensitivity
determination of f
e in manual or aut
, and scintillation c
ssay.
ion Film
Film 7.1 x 9.4 inche
kaline phosphatase
D) in membrane hy
ion Film
Film 8 x 10 inches,
alkaline phosphata
D) in membrane hy
te
s 10-50 pg antigen
high-sensitivity wes
d. Signal lasts >3 h
Mouse/Rabbit)
s 1-5 pg antigen b
mouse/rabbit ant
g quantification. Si
x
el O-Rings
ple Carousel
ghtCycler

ghtCycler
2.0
oftware
riments.
two-step RT-
Universal
lysis probes
eliminate
Rs. Prevent PCR
and ensure
time PCR.
reduction of
ction. Provided
prox. 6.5.
he reduction of
ction. Provided
prox. 7.
ondrial) is an
oxaloacetate
n in 50%
ondrial) is an
oxaloacetate
nsion in 3.2 M
tions, and
photon is
e milligram is
1 nM to 1 M.
doreductase for
NAD(P)H is
firefly
tomated
counters or
es, 18 x 24 cm
e
ybridization
20.3 x 25.4 cm
ase
ybridization
n blotted onto
stern blotting,
hours, allowing
blotted onto
tibodies. For
gnal lasts >9

Cat. No.

03 603 989 001
04 898 915 001
04 535 286 001
04 735 536 001
03 539 806 001
10 107 085 001
10 127 230 001
10 127 876 001
10 127 884 001
10 127 248 001
10 127 256 001
10 127 914 001
10 411 523 001
10 476 498 001
11 669 893 001
11 814 036 001
11 666 916 001
11 666 657 001
12 015 200 001
12 015 218 001

1
1 kit for up to 9
1 kit for up to 4
5
1 k
1 kit
100 films (
100 films (
400 m
1 kit
Pack Size

2 O-Rings

1 software packag

96 reactions of 20
volume
80 reactions of 20
volume

50 l (100 U, 2 U/

100 mg (10 ml)

10 mg (2 ml)
25 mg (5 ml)
100 mg (10 ml)
5 mg (1 ml)

5 mg (1 ml)
25 mg (5 ml)

1 mg protein

2 mg protein


(7.1 x 9.4 inches, 1

(8 x 10 inches, 20.3

ml (4,000 cm
2
mem

(1,000 cm
2
memb

e
l final reaction
l final reaction
l)
says
ssays
8 x 24 cm)
3 x 25.4 cm)
mbrane)
brane)

Price in

inquire
inquire
inquire
inquire
inquire
251,10
43,40
86,80
293,50
56,60
56,60
159,10
148,90
152,90
297,90
1.099,80
305,40
298,10
230,80
812,50

Alp

Prod

Lum
Chem
PVDF
sensi
allow
Lyso
Use L
of pro
heali
to iso
M
M30
Detec
early
immu
both
m7G
Use t
Polym
Mae
Reco
cohe
inform
FspB
Mae
Reco
cohe
by th
HpyC
Mae
Reco
cohe
not k
Mag
2.0 m
Use i
biolo
and M
Mag
Quick
appli
lysis
kits. E
Mag
Addit
samp
one s
MagN
Mag
One a
temp
Lyser
Lyser
Mag
This a
., mat
plate
Mag
Use t
purifi
for in
lysate
Mag
MagN
Mag
MagN
lphabetic
duct Name
i-Light
PLUS
Weste
miluminescent POD
F or nitrocellulose
itivity western blott
wing multiple expos
ozyme
Lysozyme from hen
otoplasts, bacterio
ng), food and drin
olation of nucleic a
0 CytoDEATH
ct a cytokeratin 18
marker of apopto
unocytochemistry,
cryostat and paraf
G(5')ppp(5')G
the nucleotide, m7
merase promoter s
e I
ognizes the sequen
sive termini. Supp
mation is available
I, Bfa I, Xsp I.
e II
ognizes the sequen
sive termini. Supp
e presence of 5-m
CH4 IV.
e III
ognizes the sequen
sive termini. Supp
known to be inhibit
gNA Lyser Green
ml sample tubes wi
n the MagNA Lyse
gical materials usi
MagNA Pure Com
gNA Lyser Instrum
kly and completely
cations. Use in com
buffers from the M
Easily integrates in
gNA Lyser Rotor
tional MagNA Lyse
ple tubes for tissue
shipped with the M
NA Lyser Rotor Co
gNA Lyser Rotor C
additional MagNA
perature of up to 16
r Rotor at +2 to +8
r Instrument. Use w
gNA Pure 96 Arch
adapter is used to
trix storage tubes,
is placed on top o
gNA Pure 96 Bact
this reagent with t
es.
gNA Pure 96 Barc
NA Pure 96 Barcod
gNA Pure 96 Bott
NA Pure 96 Bottle
cal Produ
ern Blotting Subs
D substrate detect
membranes using
ting, requiring qua
sures.
n egg white for ce
olysis, pharmacolog
ks (flavor enhance
acids.
8 epitope produced
sis in cells and tiss
flow cytometry, an
ffin-embedded sec
7G(5')ppp(5')G, tog
systems to initiate i
nce CTAG and ge
lied with the speci
e concerning meth
nce A*CGT and g
lied with the speci
nce GTNAC and g
lied with the speci
ted by methylation
Beads
th ceramic beads
er Instrument to d
ng lysis buffers su
pact isolation kits.
ment
y homogenize tissu
mbination with Ma
MagNA Pure LC or
nto your laboratory
er Rotors. Each Ma
e homogenization.
MagNA Lyser Instr
ooling Blocks to inc
Cooling Block
A Lyser Rotor Cooli
6 sample tubes be
8C. Identical to th
with additional roto
hive Plate Adapte
fix 96-well plates
in MagNA Pure 9
of the 96-well plate
terial Lysis Buffe
he MagNA Pure 9
cleic acids (DNA/R
purposes, and for s
code Scanner
de Scanner for rep
tle Rack
Rack for replacem
uct Index
strate
s 1-5 pg antigen b
secondary antibo
antification. Signal
ell wall degradation
gy (anti-inflammat
er), and sample pre
d after caspase cle
sues. Use the M30
nd immunohistoch
ctions.
gether with the SP
in vitro RNA synth
enerates fragments
ial 2x incubation b
ylation sensitivity.
enerates fragment
ial 2x incubation b
ndicated (*). Isosch
generates fragmen
ial 2x incubation b
n. Isoschizomers: n
to purify RNA, mR
isrupt cells, tissues
upplied with the M

ue for many extrac
agNA Lyser Green
r MagNA Pure Com
y workflow.
agNA Lyser Rotor
These rotors are id
ument. Use with a
crease throughput
ing Block for main
eing loaded onto th
e one shipped wit
ors to increase thr
er 4S
with no snap-lock
6 Instruments. The
es with non-snap-
er
6 System for the is
RNA) from biologic
placement.
ment.
x
blotted onto
dies. For high
lasts >9 hrs,
n, preparation
tory, tissue
eparation prior
eavage, an
0 antibody in
hemistry with
P6 and T7 RNA
hesis.
s with 5-
uffer. No
Isoschizomers:
ts with 5-
uffer. Inhibited
hizomers:
nts with 5-
uffer. Mae III is
none known.
RNA, and DNA.
s, and other
agNA Pure LC
ction
Beads and
mpact isolation
holds up to 16
dentical to the
additional
t.
taining the
he MagNA
h the MagNA
roughput.
k for tubes, e.g
e perforated
-lock tubes
solation and
cal specimens
cleic acids with

Cat. No.

12 015 196 001
10 837 059 001
12 140 322 001
12 140 349 001
10 904 988 001
10 822 221 001
10 862 495 001
10 822 230 001
10 822 248 001
03 358 941 001
03 358 968 001
03 358 976 001
03 359 093 001
03 359 085 001
06 639 003 001
06 374 921 001
06 541 143 001
06 541 178 001

100 m
100 tubes (
1 instrume
1 instrume
Pack Size

ml (1,000 cm
2
mem

10 g

50 tests
250 tests

5 U (at 260 nm)

250 U (1 - 5 U/l)

50 U (1 - 5 U/l)

50 U (1 - 5 U/l)
250 U (1 - 5 U/l)


ent (110 V, plus ac
ent (220 V, plus ac

2 rotors

1 cooling block

1 adapter

1 bottle (20 ml)

1 barcode scanne
1 bottle rack

www.roche
mbrane)
)
)
amic beads)
ccessories)
ccessories)
r
e-applied-science

Price in

497,50
245,90
224,20
620,30
170,90
369,50
347,90
90,90
369,50
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

147

e.com

Alp
148

www.r

Prod

Mag
Read
RNA
blood
Mag
Read
acids
Instru
Mag
Read
acids
Instru
Mag
Use t
purifi
for in
lysate
Mag
Drop
and c
Mag
Use t
purifi
for in
lysate
Mag
Dispo
by M
Quali
eleva
Mag
Auto
using
ready
stand
Mag
Barco
Instru
intern
Mag
MagN
Mag
This a
in the
of the
Mag
Need
Instru
Mag
Plate
for co
to mi
Mag
Holde
Mag
Deep
Pure
proce
Mag
MagN
Mag
Reag
of Ma
Mag
Use a
tande
Mag
Use t
use. T
pierc
lphabetic
roche-applied-sc
duct Name
gNA Pure 96 Cellu
dy-to-use reagents
using the MagNA
d, up to 1x10
6
cult
gNA Pure 96 DNA
dy-to-use reagents
s from up to 1,000
ument. External lys
gNA Pure 96 DNA
dy-to-use reagents
s from up to 200 l
ument. External lys
gNA Pure 96 DNA
this reagent with t
es.
gNA Pure 96 Drop
catcher and attac
cleaning MagNA P
gNA Pure 96 Exte
this reagent with t
es.
gNA Pure 96 Filte
osable pipetting tip
MagNA Pure 96 Inst
ity Control procedu
ated temperatures.
gNA Pure 96 Instr
mated high-throug
g flexible software-
y-to-use reagents.
dard volume samp
gNA Pure 96 Inter
oded tubes for pre
uments. These tub
nal controls during
gNA Pure 96 Inter
NA Pure 96 Interna
gNA Pure 96 Ligh
adapter is used to
e MagNA Pure 96
e LightCycler
480
gNA Pure 96 Nee
dle set for user rep
ument reagent pip
gNA Pure 96 Outp
for collecting elua
ooling by maximizi
nimize the risk of
gNA Pure 96 Plate
er for custom plate
gNA Pure 96 Proc
p well plates with 9
96 Instruments; nu
edures; inert to ch
gNA Pure 96 Purif
NA Pure 96 Purific
gNA Pure 96 Reag
gent loop unit for u
agNA Pure 96 Inst
gNA Pure 96 Reag
as replacement rac
em after the first k
gNA Pure 96 Seal
to reseal MagNA P
There is no need t
ced when removing
cal Produ
cience.com
ular RNA Large V
A Pure 96 Instrume
tured cells, up to 2
A and Viral NA La
l sample volume
sis is optional.
A and Viral NA Sm
l sample volumes u
sis is optional.
A Tissue Lysis Bu
he MagNA Pure 9
cleic acids (DNA/R
purposes, and for s
p Catcher
ched Drop Catcher
Pure 96 Instrument
ernal Lysis Buffer
he MagNA Pure 9
cleic acids (DNA/R
purposes, and for s
er Tips (1,000 l)
ps for 1,000 l volu
truments; nuclease
ures; inert to chem

rument
ghput instrument f
-driven protocols a
Typical run takes
les.
rnal Control Tube
eparing internal co
es are ideal for the
g a run.
rnal Waste Conta
al Waste Containe
htCycler 480 Ada
fix the 96-well Lig
Instrument. This p
0 Multiwell Plate 9
dle Set of 4
placement of the ne
petting heads.
put Plate
ates containing pu
ing contact with co
dead volume that
e Holder
es in the MagNA P
cessing Cartridge
96 wells for sample
uclease free accor
emical leaching at
fication Rack
cation Rack for rep
gent Loop Unit
user replacement o
truments.
gent Rack
ck or for storing a
kit.
ling Foil
Pure 96 reagent tra
o remove the seal
g reagent to minim
uct Index
Volume Kit
ealed trays for pur
ent from 400/800
0 mg tissue, or eq
arge Volume Kit
ealed trays for pur
using the MagNA
mall Volume Kit
ealed trays for pur
using the MagNA
uffer
6 System for the is
RNA) from biologic
stabilization of DN
r Fleece for runnin
ts.
r
6 System for the is
RNA) from biologic
ume with aerosol f
e free according to
mical leaching at lo
for nucleic acid pu
and barcoded, pref
less than one hou
e
ontrols using MagN
e automated proce
ainer
er for replacement.
pter
ghtCycler
480 Mu
perforated plate is
96 for access to ea
eedles on MagNA
urified nucleic acid
ooling block; wells
cannot be pipetted
Pure 96 Instrument
e
e processing steps
rding to current Qu
t low and elevated
placement.
onto the reagent p
second purificatio
ays and output pla
ing foil prior to nex
mize risk of cross-c
x
ifying total
l lysed whole
uivalent.
ifying nucleic
A Pure 96
ifying nucleic
Pure 96
solation and
cal specimens
NA in tissue
g, maintaining
solation and
cal specimens
cleic acids with
filters for use
o current
ow and
urification
filled trays with
ur for 96
NA Pure 96
essing of

ultiwell Plate 96
placed on top
ch well.
A Pure 96
s; optimized
s are v-shaped
d.
t.
s using MagNA
uality Control
temperatures.
ipetting head
on kit used in
ates for later
xt use. Foil is
contamination.

Cat. No.

05 467 535 001
06 374 891 001
06 543 588 001
06 640 702 001
06 541 119 001
06 374 913 001
06 241 620 001
06 541 089 001
06 374 905 001
06 541 267 001
06 638 996 001
06 541 194 001
06 241 611 001
06 541 283 001
06 241 603 001
06 541 208 001
06 541 127 001
06 541 224 001
06 241 638 001

3 set
3 set
3 sets
3,8
1 instrumen
1 in
Pack Size




1 bottle (100ml)

1 drop catcher

1 bottle (100 ml)



150 tubes (15x10)

ternal waste conta
1 adapter

1 set of 4 needles

60 plates

1 plate holder
36 cartridges

1 purification rack
1 reagent loop uni

1 reagent rack

100 foils

each
each
s each
96)
d accessories
)
ainer
s
k
it

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

Mag
For ri
purifi
confi
conta
Mag
For ri
purifi
confi
Mag
MagN
Mag
MagN
Mag
MagN
Mag
Use w
Kit I t
cultu
MagN
Mag
One a
Instru
Mag
One a
Instru
Mag
One a
Instru
Mag
One a
Instru
Mag
Benc
samp
purifi
stand
Mag
Read
from
using
PCR
PCR
Mag
Read
from
using
PCR
PCR
Mag
Read
from
MagN
Light
Mag
This a
MagN
for lo
one n
Mag
One a
Instru
Mag
One a
Instru
Mag
Use t
Isolat
from
stand
lphabetic
duct Name
gNA Pure 96 Syst
insing the MagNA
ication run. Using
guration, the instr
ainers.
gNA Pure 96 Syst
insing the MagNA
ication run. Using
guration, the instr
gNA Pure 96 Tip R
NA Pure 96 Tip Ra
gNA Pure 96 Was
NA Pure 96 Waste
gNA Pure 96 Was
NA Pure 96 Waste
gNA Pure Bacteri
with the MagNA P
to isolate bacterial
res. For automatio
NA Lyser Instrume
gNA Pure Compa
additional Cartridg
ument.
gNA Pure Compa
additional Drip Tra
ument.
gNA Pure Compa
additional Drop Ca
ument.
gNA Pure Compa
additional Elution
ument.
gNA Pure Compa
chtop instrument fo
ples, such as blood
ied nucleic acid in
dard cyclers, and d
gNA Pure Compa
dy-to-use reagents
mammalian cells
g MagNA Pure Com
with LightCycler

instruments.
gNA Pure Compa
dy-to-use reagents
mammalian cells
g MagNA Pure Com
with LightCycler

instruments.
gNA Pure Compa
dy-to-use reagents
tissue, blood cells
NA Pure Compact
tCycler
Systems,
gNA Pure Compa
accessory is requir
NA Pure Compact
ost or contaminated
nucleic acid extrac
gNA Pure Compa
additional Tube Ra
ument.
gNA Pure Compa
additional Waste T
ument.
gNA Pure DNA Tis
the MagNA Pure C
tion Kit I - Large V
mammalian tissue
dard cyclers, and in
cal Produ
tem Fluid (Extern
A Pure 96 Instrume
the external system
ument is on a tabl
tem Fluid (Interna
A Pure 96 Instrume
the internal system
ument can be run
Rack
ack for replacemen
ste Cover
e Cover for replace
ste Rack
e Rack for replacem
a Lysis Buffer
Pure Compact and
DNA from urine,
on and convenienc
ent and Green Bea
ct Cartridge Rac
ge Rack for use wi
ct Drip Tray
ay for use with the
ct Drop Catcher
atcher for use with
ct Elution Tube R
Tube Rack for use
ct Instrument
or automated nucl
d, serum, plasma, o
PCR, RT-PCR on
downstream applic
ct Nucleic Acid I
and viral nucleic a
mpact Instruments
Systems, standard
ct Nucleic Acid I
and viral nucleic a
mpact Instruments
Systems, standard
ct RNA Isolation
s, and whole blood
Instruments. Use
microarrays, and g
ct Tip Tray Kit
red when perform
Instrument. The T
d tip trays. One tip
ction.
ct Tube Rack
ack for use with th
ct Waste Tank
Tank for use with t
ssue Lysis Buffer
Compact Instrumen
Volume, and its rea
e. Use purified DN
n downstream app
uct Index
nal)
nt reagent head d
m fluid and liquid
e that also holds t
al)
nt reagent head d
m fluid and liquid w
as a tabletop instr
nt.
ement.
ment.
MagNA Pure Com
BAL, sputum, CSF
ce, combine lysis b
ads.
ck
th the MagNA Pur
e MagNA Pure Com
h the MagNA Pure
Rack
e with the MagNA
eic acid purificatio
or cells in 1540 m
LightCycler
Instr
cations.
Isolation Kit I
d cartridges for pu
acids in a volume u
s. Use purified DN
d cyclers and othe
Isolation Kit I - La
d cartridges for pu
acids in a volume u
s. Use purified DN
d cyclers and othe
Kit
d cartridges for pu
d in a volume up to
RNA for RT-PCR w
gene expression sy
ing the Leakage T
Tip Tray Kit is also a
p tray contains all d
he MagNA Pure Co
the MagNA Pure C
r
nt, MagNA Pure C
ady-to-use buffer t
A with LightCycler
plications.
x
uring a
waste
the external
uring a
waste
rument.
mpact Isolation
F, swabs, and
uffer with the
re Compact
mpact
e Compact
Pure Compact
on from 1-8
minutes. Use
uments,
urifying DNA
up to 400 l
A for PCR/RT-
er real-time
arge Volume
urifying DNA
up to 1 ml
A for PCR/RT-
er real-time
urifying RNA
o 200 l using
with
ystems.
Test using the
a replacement
disposables for
ompact
Compact
Compact
to isolate DNA
r
Systems,

Cat. No.

06 640 729 001
06 430 112 001
06 541 151 001
06 541 275 001
06 541 259 001
04 659 180 001
03 788 237 001
04 347 005 001
03 788 270 001
03 788 288 001
03 731 146 001
03 730 964 001
03 730 972 001
04 802 993 001
03 753 166 001
03 788 296 001
03 788 300 001
04 805 160 001

1 instrument w
moni
1 kit
1 kit
1 kit
Pack Size

1 container

2 containers

1 tip rack
1 waste cover
1 waste rack
20 ml lysis buffer

1 cartridge rack

1 drip tray

1 drop catcher

1 tube rack

with integrated PC
itor and barcode re




10 tip trays

1 tube rack

1 waste tank

100 ml lysis buffer

www.roche
C, touchscreen
eader
tions
tions
tions
r
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

149

e.com

Alp
150

www.r

Prod

Mag
Table
samp
Light
tubes
Mag
One a
Plate
adap
Light
Mag
This
MagN
Wast
Mag
These
Box o
tips f
Instru
Mag
One a
Bags
tips a
bag i
Mag
One a
a Ma
2.0 W
Instru
Mag
Barco
2844
area
Mag
One
Printe
Labe
Mag
One
docu
prints
MagN
Mag
These
purifi
Remo
using
Mag
Cooli
(0.2 m
vials.
post-
Mag
Cooli
Elutio
A-Rin
trans
Mag
Cooli
conta
using
posit
Mag
Cooli
Light
the p
sixtee
reage
Mag
Cooli
elutio
Block
Caro
lphabetic
roche-applied-sc
duct Name
gNA Pure LC 2.0 I
etop instrument bo
ple material and fo
tCycler
Capillarie
s. Process up to 32
gNA Pure LC 2.0 L
adapter for approp
96 in the MagNA
ter is placed onto
tCycler
480 Multi
gNA Pure LC 2.0 T
is a replacement w
NA Pure LC 2.0 Ins
te Slide into the M
gNA Pure LC 2.0 W
e Waste Bags are
of MagNA Pure LC
from 5 to 7 runs. Th
ument.
gNA Pure LC 2.0 W
additional Waste B
s are fixed to the M
are discarded by th
n the waste box.
gNA Pure LC 2.0 W
additional Waste B
agNA Pure LC 2.0 W
Waste Box Lid. Use
ument into the was
gNA Pure LC Barc
ode labels for use
. These barcode la
of the MagNA Pur
gNA Pure LC Barc
Barcode Printer Ri
er TLP 2844 to pro
ls.
gNA Pure LC Barc
Barcode Printer TL
mentation during
s barcodes created
NA Pure LC Samp
gNA Pure LC Cart
e adhesive films se
ied nucleic acids. T
ove a sample by pe
g a new Cartridge
gNA Pure LC Coo
ing Block for holdi
ml, 96-well plate),
It fits directly onto
-elution pipetting o
gNA Pure LC Coo
ing Block for holdi
on Module of the M
ngs with purified n
sferred to an instru
gNA Pure LC Coo
ing Block for holdi
aining LightCycler
g MagNA Pure LC
ions for 1.5 ml rea
gNA Pure LC Coo
ing Block for holdi
tCycler
Capillarie
post-elution progra
en 1.5 ml reaction
ents.
gNA Pure LC Coo
ing Block for holdi
on pipetting by Ma
k as required with
usel, LC Centrifuge
cal Produ
cience.com
Instrument
oth for automated
or pipetting into PC
es, 96-well plate, PC
2 samples in one ru
LightCycler
480
priate orientation o
Pure LC Cooling B
the 96-well PCR P
iwell Plate 96 is the
Tip Waste Slide
waste slide. Used r
strument through t
agNA Pure LC 2.0
Waste Bags
only for use with t
C 2.0 Instruments. T
hey cannot be use
Waste Box
Box for holding Ma
MagNA Pure LC 2.0
he MagNA Pure LC
Waste Box Lid
Box Lid. The MagN
Waste Bag which i
d tips are discarde
ste bag in the was
code Labels
with the MagNA P
abels are suitable f
re LC Sample Cart
code Printer Ribb
ibbon for use with
oduce barcodes on
code Printer TLP
LP 2844 for sample
MagNA Pure LC p
d by MagNA Pure
le Cartridges and/
tridge Seal
eal the MagNA Pu
They prevent evap
erforating the seal
Seal.
ling Block, 96-w
ng either one Ligh
or 0.2 ml 8-strip vi
o block cyclers, an
of master mixes by
ling Block, A-Rin
ng 1 or 2 A-Rings
MagNA Pure LC S
nucleic acids and P
ument platform for
ling Block, LC Ce
ng 32 LightCycler
Capillaries for au
Instruments. This
ction tubes for ma
ling Block, LC Sa
ng the LightCycler
es for robotic pipet
am of MagNA Pure
tube positions for
ling Block, Reac
ng thirty-two 1.5 m
agNA Pure LC Inst
the MagNA Pure
e Adapters, or 96-
uct Index
nucleic acid isolat
CR reaction vessel
CR tubes, and 1.5
un in 16-180 min.
0 Plate Adapter
of the LightCycler
Block, 96-well PCR

Plate Cooling Block
en positioned corr
reaction tips are di
the MagNA Pure L
Waste Box.
the MagNA Pure L
They can receive u
ed with the MagNA
agNA Pure LC 2.0
0 Waste Box Lid. U
C 2.0 Instrument in
NA Pure LC 2.0 Wa
is fixed to the Mag
ed by the MagNA
ste box.
Pure LC Barcode P
for the new barcod
tridge.
bon
the MagNA Pure
n the MagNA Pure
2844
e identification, tra
LC Software Versi
/or non-barcode-la
ure Cartridge when
poration and conta
l of the well, and th
well PCR Plate
htCycler
480 Mul
ials, or 0.2 ml singl
d can be used for
y MagNA Pure LC
ng
with barcodes. Us
oftware for autom
PCR reagents. A-R
testing.
entrifuge Adapte
Centrifuge Adap
utomated post-elu
Cooling Block also
aster mixes and oth
ample Carousel
r
Sample Carous
tting of up to 32 ca
e LC Instruments. I
master mixes and
ction Tubes
ml reaction tubes f
truments. Combine
Cooling Blocks for
well PCR Plate.
x
tion from crude
s, such as
ml reaction
480 Multiwell
R Plate. The
k. The
rectly.
scarded by the
LC 2.0 Tip
LC 2.0 Waste
used reaction
A Pure LC 1.0
Waste Bags.
Used reaction
nto the waste
aste Box holds
gNA Pure LC
Pure LC 2.0
Printer TLP
de labeling
LC Barcode
LC Barcode
acking, and
This device
ion 3.0 for the
abeled tubes.
n storing
mination.
hen reseal
tiwell Plate
le reaction
automated
Instruments.
se the Post
ated filling of
Rings are then
ers
pters
ution pipetting
o has fifteen
her reagents.
sel with
apillaries using
It also has
d other
for use in post-
e this Cooling
r either the LC

Cat. No.

05 197 686 001
05 323 983 001
05 324 122 001
05 324 157 001
05 323 991 001
05 324 114 001
03 531 520 001
03 531 538 001
03 576 094 001
03 118 827 001
12 189 674 001
03 201 287 001
12 190 664 001
12 189 704 001
12 189 666 001

1 instrument w
mo
25 b
1,000
1 cooling bloc
Pack Size

with integrated PC
nitor, and accesso

1 adapter

1 slide

bags (for 5 runs ea

1 box

1 lid

labels (10 mm x 6

1 ribbon

1 barcode printer

200 seals

1 cooling block

1 cooling block

ck (with 32 LightCy
adapters)

1 cooling block

1 cooling block

C, touchscreen
ories
ach)
0 mm)
r
ycler centrifuge

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

Mag
Isolat
blood
Resu
block
Mag
Isolat
1x10
3
Instru
Syste
Mag
Addit
Isolat
lysis
stabi
Mag
Isolat
Instru
lysate
with
instru
Mag
Isolat
types
purifi
Exter
Mag
Greas
servic
greas
Softw
Mag
The M
MagN
liquid
MagN
Mag
Reag
on th
MagN
Mag
Reag
on th
buffe
Tub L
Mag
Isolat
oligo
LC In
Syste
Mag
Use t
cultu
be im
LC In
mRN
Mag
Kit w
nozzl
pipet
MagN
Mag
Reac
MagN
nucle
with
Mag
Large
Instru
head

lphabetic
duct Name
gNA Pure LC DNA
te high-purity geno
d, blood cells, or cu
lting DNA is ideal
k cyclers and other
gNA Pure LC DNA
te high quality DN
3
to 1x10
6
blood o
uments. Resulting
ems, standard bloc
gNA Pure LC DNA
tional Lysis/Bindin
tion Kit I and Mag
of mammalian blo
lization of nucleic
gNA Pure LC DNA
te high-purity DNA
uments. External ly
es and difficult to h
LightCycler
Syste
uments.
gNA Pure LC DNA
te high-purity bact
s, up to 100 l volu
ied DNA for PCR w
rnal lysis protocols
gNA Pure LC Grea
sing station, pads,
cing of MagNA Pu
sing, the greasing
ware greasing prog
gNA Pure LC Liqu
MagNA Pure LC L
NA Pure LC Instru
ds from the reagen
NA Pure LC Waste
gNA Pure LC Med
gent containers for
he stage of MagNA
NA Pure LC Tub L
gNA Pure LC Med
gent containers for
he stage of MagNA
er volume and V-sh
Lids (small, mediu
gNA Pure LC mRN
te high-quality mR
(dT) and streptavid
nstruments. Use pu
ems and block cyc
gNA Pure LC mRN
this optimized buff
red cells, and to st
mmediately process
nstruments. Use bu
A HS Kit.
gNA Pure LC O-R
with a vial of grease
le head O-rings an
tting accuracy of th
NA Pure Compact
gNA Pure LC Proc
ction vessels for sa
NA Pure LC Instru
eic acids. Each pro
8 wells each.
gNA Pure LC Rea
e (50 - 1000 l volu
uments. With integ
nozzles when dis
cal Produ
A Isolation Kit - L
omic DNA from 20
ultured cells using
for qPCR using Li
r real-time PCR ins
A Isolation Kit I
A from 20 to 200
r cultured cells us
DNA is eluted in 1
ck cyclers and othe
A Isolation Kit I
ng Buffer for use w
NA Pure LC DNA
od, blood cells, or
acids.
A Isolation Kit II (
A from 1 to 10 mg
ysis protocols allow
homogenize samp
ems, block cyclers
A Isolation Kit III
terial and fungal D
ume, using MagNA
with LightCycler
S
for BAL, sputum,
asing Set
O-rings and grea
ure LC nozzlehead
station is placed o
gram performs the
uid Waste Funnel
iquid Waste Funne
ments. The robotic
nt/sample stage th
e Bottle.
dium Reagent Tu
A Pure LC Instrume
ids (small, medium
dium Reagent Tu
A Pure LC Instrum
haped bottom min
m).
NA HS Kit
RNA from 1 x 10
7
m
din-coated magne
urified mRNA for q
lers for gene expre
NA Isolation Kit I
fer to lyse mamma
tabilize mRNA. Lys
sed or after long-t
uffer in combinatio
Ring Maintenance
e and 12 sets of 8 O
nd for periodic rep
he nozzle head of
Instruments.
cessing Cartridge
mples and purifica
ment when purifyi
ocessing cartridge
ction Tip (large)
ume) reaction tips
grated filters to pre
pensing reagents
uct Index
Large Volume
0 l to 1 ml of mam
g MagNA Pure LC
ghtCycler
System
struments.
l mammalian who
ing MagNA Pure L
100 l. Ideal for Lig
er real-time PCR in
Lysis/Binding B
with the MagNA Pu
Isolation Kit Larg
cultured cells, and
(Tissue)
tissue with MagN
w DNA purification
ples. Use purified D
s and other real-tim
(Bacteria, Fungi
DNA from many dif
A Pure LC Instrume
Systems and block
CSF, and urine.
ase for automated
O-Rings. For auto
on the Instrument s
e process.
l
el is a replacement
c nozzle head pipe
rough this funnel
ub 20
ml of MagNA Pure
ents. Tubs are sea
m).
ub 30
ml of MagNA Pure
ments. Tub marking
imizes dead volum
mammalian blood
etic particles with M
qRT-PCR with Ligh
ession analysis.
Lysis Buffer R
alian whole blood,
sed and stabilized
term storage using
on with the MagNA
e Kit
O-rings to prolong
lacement of O-ring
both MagNA Pure
e
ation reagents pipe
ing DNA, RNA, mR
has 64 wells, arran
s for MagNA Pure
event contaminatio
and separating ma
x
mmalian whole
Instruments.
ms, standard
ole blood or
LC
ghtCycler

nstruments.
Buffer - Refill
ure LC DNA
ge Volume. For
d the
A Pure LC
n from FFPE
DNA for PCR
me PCR
)
fferent sample
ents. Use
k cyclers.
or manual
omated
stage, and the
t accessory for
ets unused
into the
e LC reagents
led using
e LC reagents
gs estimate
me. Use with
cells using
MagNA Pure
htCycler

Refill
blood and
samples can
g MagNA Pure
A Pure LC
g the life of
gs, ensuring
e LC and
etted by the
RNA, and total
nged in 8 rows
LC
on of pipetting
agnetic bead.

Cat. No.

03 310 515 001
03 003 990 001
03 246 752 001
03 186 229 001
03 264 785 001
03 561 402 001
03 253 805 001
03 004 058 001
03 045 501 001
03 267 393 001
03 246 744 001
03 561 429 001
03 004 147 001
03 004 171 001

1 kit for up to 9
1 kit
1 kit
1 kit
1
1 kit
1 vial of
960 tips (30 pre
Pack Size

sample volume

for up to 192 isola

100 ml

for up to 192 isola

for up to 192 isola

1 set

liquid waste funn

150 tubs

50 tubs

for up to 192 isola

2 x 35 ml

grease and 12 x 8

160 cartridges

e-packed trays ea

www.roche
s, depending on
ations
ations
ations
el
ations
8 O-rings
ch with 32 tips)
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

151

e.com

Alp
152

www.r

Prod

Mag
Smal
With
when
Mag
The M
holdi
MagN
Mag
Reag
of Ma
and V
Pure
Mag
Reag
on th
MagN
Mag
For a
blood
purifi
north
Mag
Isolat
tissue
for RT
syste
Mag
Addit
III (Ti
inhib
RNA.
Mag
Samp
acids
Instru
Comp
Mag
Addit
conta
5 to 5
distin
Mag
Addit
conta
50 to
distin
Mag
The T
purifi
reduc
posit
Mag
Isolat
serum
Purifi
qPCR
Mag
Isolat
plasm
elute
Light
blood
Mag
Buffe
Addit
plasm
MagN
Nucle
Instru

lphabetic
roche-applied-sc
duct Name
gNA Pure LC Rea
l (5 - 50 l volume
integrated filters t
n eluting nucleic ac
gNA Pure LC Rea
MagNA Pure LC R
ng two large reage
NA Pure LC Instru
gNA Pure LC Rea
gent containers for
agNA Pure LC Inst
V-shaped bottom m
LC Tub Lids (large
gNA Pure LC Rea
gent containers for
he stage of MagNA
NA Pure LC Tub L
gNA Pure LC RNA
automated isolation
d cells or cultured
ied RNA in RT-PCR
hern blots, and for
gNA Pure LC RNA
te total RNA from
es using MagNA P
T-PCR using Light
ems.
gNA Pure LC RNA
ssue) and MagNA
its RNases during
. Use to homogeni
gNA Pure LC Sam
ple reaction plates
s from magnetic be
uments. Each cartr
patible with standa
gNA Pure LC Tip R
tional Tip Rack for
aining MagNA Pur
50 l. These Tip Ra
nguish them from t
gNA Pure LC Tip R
tional Tip Rack for
aining MagNA Pur
1000 l. These Tip
nguish them from t
gNA Pure LC Tip S
Tip Stand is for tem
ication runs using
ces the number of
ions, so that the n
gNA Pure LC Tota
te high-purity tota
m, plasma, or whol
ied nucleic acids a
R and qRT-PCR us
gNA Pure LC Tota
te total nucleic aci
ma using MagNA P
d in 50-100 l. Nu
tCycler
Systems a
d.
gNA Pure LC Tota
er Refill
ma, and to stabilize
NA Pure LC Total
eic Acid Isolation K
uments.
cal Produ
cience.com
ction Tip (small)
e) reaction tips for
to prevent contam
cids and during po
gent Reservoir R
Reagent Reservoir R
ent tubs and six m
ments.
gent Tub (large)
r 100 ml of MagNA
truments. Tub mar
minimizes dead vo
e).
gent Tub (small)
r storing up to 3.5 m
A Pure LC Instrume
ids (small, medium
A Isolation Kit - H
n of total RNA from
cells using MagNA
R with LightCycler
gene expression a
A Isolation Kit III
fresh-frozen or for
Pure LC Instrumen
tCycler
Instrumen
A Isolation Tissue
for use with the M
A Pure LC Instrume
cell lysis, releasin
ze tissue with Mag
mple Cartridge
for aliquoting prim
eads, and sample s
ridge has 32 (4 x 8
ard 8-well multich
Rack
r small reaction tip
re LC Reaction Tip
acks for small tips
the Tip Racks for l
Rack
r large reaction tips
re LC Reaction Tip
p Racks for large t
the Tip Racks for s
Stand
mporary storage of
MagNA Pure LC I
f tips required for a
ozzle head can bri
al Nucleic Acid Is
l nucleic acids (vir
le blood using Ma
are eluted in 50-10
ing LightCycler
S
al Nucleic Acid Is
ds (viral DNA/RNA
Pure LC Instrumen
cleic acids are ide
and block cyclers.
al Nucleic Acid Is
for the lysis of mam
e nucleic acids. Us
Nucleic Acid Isolat
Kit - Large Volume
uct Index

r MagNA Pure LC
ination of pipetting
ost-elution pipettin
Rack
Rack is an addition
medium/small reag
A Pure LC reagents
rkings estimate bu
olume. Seal tubs us
)
ml of MagNA Pure
ents. Tubs are sea
m).
High Performance
m up to 200 l who
A Pure LC Instrum
r
Systems, block
analysis.
(Tissue)
rmalin-fixed paraff
nts. Resulting RNA
nts and other real-
e Lysis Buffer - R
agNA Pure LC RN
ents. This reagent
g and stabilizing m
gNA Lyser Instrum
mary samples, elut
storage using Mag
8) wells, each with
annel pipettes.
ps for holding 3 tip
ps (small), each wit
are colored yellow
arge tips which ar
s for holding 3 tip
ps (large), each wit
tips are colored blu
small tips which ar
f tips for multiple u
Instruments. The T
a purification run.
iefly store small or
solation Kit
ral DNA/RNA) from
gNA Pure LC Instr
00 l. Nucleic acids
Systems and block
solation Kit - Larg
A) from up to 1 ml
nts. Purified nucleic
eal for qPCR and q
Do not use this ki
solation Kit - Lys
mmalian blood, ser
se in combination w
tion Kit, MagNA P
e on MagNA Pure
x
Instruments.
g head nozzles
ng.
nal rack for
ent tubs in
s on the stage
ffer volume
sing MagNA
e LC reagents
led using
e
ole blood or 10
6

ments. Use
cyclers,
fin-embedded
from is ideal
-time PCR
Refill
NA Isolation Kit
efficiently
mRNA and total
ment.
ting nucleic
gNA Pure LC
1.5 ml volume.
trays
th a capacity of
w to easily
re blue.
trays
th a capacity of
ue to easily
re yellow.
use during
Tip Stand
It has 8
r large tips.
m up to 200 l
ruments.
s are ideal for
k cyclers.
ge Volume
l serum and
c acids are
RT-PCR using
t for whole
is/Binding
rum, or
with the
Pure LC Total
LC

Cat. No.

03 004 180 001
03 253 767 001
03 004 040 001
03 004 066 001
03 542 394 001
03 330 591 001
03 604 721 001
03 004 112 001
03 253 783 001
03 253 775 001
03 004 155 001
03 038 505 001
03 264 793 001
03 246 779 001

960 tips (30 pre
1 kit
1 kit
1 kit
1 kit
Pack Size

e-packed trays ea

1 reagent rack

120 tubs

150 tubs

for up to 192 reac

for up to 192 isola

70 ml

120 cartridges

1 tip rack

1 tip rack

200 tip stands

for up to 192 isola

for up to 192 isola

100 ml

ch with 32 tips)
ctions
ations
ations
ations

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

Mag
Isolat
whol
high
high
Mag
Reag
lids r
receiv
remo
Mag
Reag
These
perfo
surfa
Mag
Tub L
medi
term
also c
Mag
Auto
waste
react
MagN
Mag
Repla
Bottle
the re
tray.
Mag
The W
LC pu
conta
salts
Meg
Very
large
episo
chrom
MgC
MgC
MgC
for a
any P
MIA
One-
mela
strep
mini
Read
quick
of ex
sequ
mini
Read
quick
from
mini
Read
quick
from
limit:
Mito
Poten
studi
crysta
filteri

lphabetic
duct Name
gNA Pure LC Tota
te high-purity tota
e blood using Mag
sensitivity in down
performance PCR
gNA Pure LC Tub
reduce evaporative
ving up to 8 reacti
oved as tips are ext
gNA Pure LC Tub
e lids reduce evap
orations for receivin
aces are removed a
gNA Pure LC Tub
Lid Seals are for us
um, large). They p
storage after purif
catch liquid drops
gNA Pure LC Was
clavable MagNA P
e slide of the Mag
tion tips discarded
NA Pure LC 2.0 Ins
gNA Pure LC Was
acement accessory
e of all MagNA Pu
eagent/sample sta
gNA Pure LC Was
Waste Bottle collec
urification runs. Th
act with potentially
in the lysis buffers
ganuclease I-Sce
rare-cutter endon
e DNA fragments, a
omal DNA, cloned
mosomal DNA isol
Cl
2
Stock Solutio
l
2
Stock Solution (
l
2
, when optimizin
particular templat
PCR type: hot start
ELISA
-step, 2 hour ELISA
noma inhibitory ac
ptavidin-coated mic
Quick Spin DNA
dy-to-use, microce
k, efficient purifica
cess dye-labeled d
encing. Exclusion
Quick Spin Oligo
dy-to-use, microce
k and efficient rem
end-labeled oligo
Quick Spin RNA
dy-to-use, microce
k and efficient rem
RNA labeled by p
= 20 bases
omycin C
nt DNA crosslinke
es of cell-free prot
alline form. Biobur
ng (e.g., Millipore
cal Produ
al Nucleic Acid K
l viral nucleic acid
gNA Pure LC Instr
nstream applicatio
with LightCycler

Lid (large)
he MagNA Pure LC
e reagent loss. Eac
ion tips, ensuring t
tracted.
Lid (small, medi
he MagNA Pure LC
porative reagent los
ng up to 8 reaction
as tips are extracte
Lid Seal
se with all MagNA
prevent evaporative
fication using Mag
during robotic arm
ste Bags
Pure LC Waste Bag
NA Pure LC 1.0 In
by the robot. They
strument.
ste Bottle Tray
y tray holding the
ure LC Instruments
age into the MagN
ste Bottles
cts up to 330 ml liq
hese autoclavable
y infectious materi
s.
e I
uclease. Use in ad
and for mapping b
mammalian DNA
lated from pulsed-
n
(25 mM) for supple
ng the magnesium
te or target. Use w
t, high fidelity, long
A for the quantitati
ctivity (MIA) protei
croplates.
A Columns
ntrifuge-compatib
tion of DNA from
dideoxynucleotide
limit: = 20 bp
o Columns
ntrifuge-compatib
moval of unincorpo
nucleotides. Exclu
A Columns
ntrifuge-compatib
moval of unincorpo
olymerase or end-
r. Inhibits DNA syn
tein biosynthesis. M
rden reduction in s
e).
uct Index
Kit - High Perform
s from 1 ml serum
uments. This kit ac
ns. Use purified nu
Systems and bloc
C Reagent Tubs (la
h Tub Lid has 8 pe
that liquid on tip s
um)
C Reagent Tubs (s
ss. Each Tub Lid h
n tips, ensuring tha
ed.
A Pure LC Tub Lids
e reagent loss and
gNA Pure LC Instru
m movements.
gs are only for use
strument. They co
y cannot be used w
MagNA Pure LC L
s. The robot pipets
A Pure LC Waste
quid waste during
Waste Bottles prev
al and the irritating
dapter cloning and
bacterial or yeast c
fragments, or mam
-field gels.
ementing PCR buf
concentration of a
ith other PCR buff
g PCR.
ive in vitro determ
in in serum and pl
le chromatography
labeling reactions,
terminators prior t
le chromatography
rated radiolabeled
sion limit: = 8 bp
le chromatography
rated radiolabeled
-labeling technique
nthesis and is an in
Mitomycin is provi
solution is obtained
x
mance
m, plasma, or
chieves very
ucleic acids for
ck cyclers.
arge). These
erforations for
urfaces are
small, medium).
as 8
at liquid on tip
s (small,
permit long-
uments. They
e with the tip
llect used
with the
Liquid Waste
liquids from
Bottle on this
MagNA Pure
vent user
g chaotropic
subcloning of
chromosomes,
mmalian
ffers without
a standard PCR
fers to optimize
ination of
asma within
y columns for
, and removal
to fluorescent
y columns for
nucleotides
y columns for
nucleotides
es. Exclusion
nhibitor for
ided in a
d by 0.2 m

Cat. No.

05 323 738 001
03 004 074 001
03 004 082 001
03 004 104 001
03 004 201 001
03 253 813 001
03 004 198 001
11 362 399 001
11 699 113 001
11 976 826 001
11 814 419 001
11 814 397 001
11 814 427 001
10 107 409 001

1 kit
1
Pack Size

for up to 288 isola

120 lids

300 lids

400 seals

200 bags

1 waste bottle tray

40 bottles

1,000 U

3 x 1 ml


50 columns

50 columns

50 columns

2 mg

www.roche
ations
y
sts
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
414,90
40,30
972,30
206,40
206,40
222,90
50,50

153

e.com

Alp
154

www.r

Prod

Mlu
Reco
cohe
sequ
meth
MluN
Reco
blunt
indic
Mou
Easy,
mous
of all
type.
mRN
Isolat
homo
Use i
and c
mRN
Isolat
cells,
north
Isolat
mRN
Isolat
with
yield
blotti
Mro
Reco
cohe
inhib
Aor13
Mun
Mun
5-co
recog
Mva
Reco
cohe
resid
meth
Mvn
Mvn
blunt
sequ
BstFN
Myco
Photo
conta
cultu
detec
N
N-Ac
Use N
(appr
gluco
N-Ac
Addit
life sc
Acety
N-Ac
Stand
resea
gluco
Hitac

lphabetic
roche-applied-sc
duct Name
I
ognizes the sequen
ence as indicated
hyladenine (). Isos
N I (Bal I)
ognizes the sequen
t ends. MluN I is in
ated (*). Isoschizo
use IgG ELISA
, fast (2-4 hours), a
se IgG in hybridom
mouse IgG-subcla
No crossreactivity
NA Capture Kit
te highly purified p
ogenization, and im
mmobilized mRNA
cDNA-AFLP.
NA Isolation Kit
te highly purified m
or tissue (without
hern blotting, cDNA
te at least 70 g of
NA Isolation Kit fo
te high-quality mR
RNA/DNA Stabiliz
of 50 to 200 ng m
ng, cDNA library p
I (Acc III)
ognizes the sequen
sive ends. Inhibite
ition by overlappin
3H I, BseA I, Bsp13
n I (Mfe I)
I recognizes the s
ohesive termini. Mu
gnition sequence a
I (BstN I)
ognizes sequence *
sive termini. Sensi
ues, and 4-methyl
hyladenine. Isoschi
I (FnuD II)
I recognizes the se
t ends. Mvn I is inh
ence, as indicated
N I, BstU I.
oplasma PCR EL
ometric ELISA for t
aminating Mycopla
res or other samp
ction for fast (6 hrs
cetyl--D-Glucos
N-Acetyl--D-Glu
rox. 50 tests) for th
osaminidase in urin
cetyl--D-Glucos
tional control solut
cience research sa
yl--D-glucosam
cetyl--D-Glucos
dard for the determ
arch samples with
osaminidase. It can
chi 705, 704, and E
cal Produ
cience.com
nce A*CGCGT an
ited by 5-methylcy
(*). It is not influen
schizomers: none k
nce TGGC*CA and
nhibited by overlap
mers: Mls I, Bal I, M
and sensitive (10 n
ma supernatants, as
asses are detected
y with FBS.
poly (A)
+
RNA from
mmobilize in strept
A directly for qualit
mature mRNA from
t isolation of total R
A synthesis, RT-PC
f poly (A)
+
RNA.
or Blood/Bone M
RNA from blood or
zation Reagent for
RNA/ml blood can
preparation, and m
nce T*CCGGA, g
d by 5-methylcyto
ng dam-methylatio
3 I, BspE I, Kpn2 I.
sequence CA*ATT
un I is inhibited by
as indicated. Isosc
*C*C(A,T) GG, ge
tive to simultaneo
cytosine at extena
zomers: BstN I, Bs
equence *CGCG
hibited by 5-methy
(*).Isoschizomers
LISA
the detection of PC
asma, Acholeplasm
le materials. Ready
s) and semi-autom
saminidase (NAG
ucosaminidase (NA
he determination o
ne in life science r
saminidase Cont
tion for the determ
amples with the aid
inidase on automa
saminidase Stan
mination of NAG a
the aid of the Test
n be used in autom
pos 5060.
uct Index
nd generates fragm
ytosine within the r
nced by the presen
known.
d generates fragm
pping dcm-methyla
Msc I, Msp20 I.
ng/ml) ELISA for de
scites, mouse sera
d independent of li
m cells and tissue
tavidin-coated 0.2
tative and quantita
m RNA preparation
RNA). Use isolated
CR, in vitro translat
Marrow
r bone marrow lysa
Blood/Bone Marro
n be used in RT-PC
more.
enerating fragmen
sine(*). In contrast
on(). Isoschizomer
TG and generates
y 6-methyladenine
hizomers: Mfe I.
enerating fragment
us 5-methylation a
al C. Inhibited by 6-
seBI, BstOI, Bst2UI.
and generates fra
ylcytosine within th
: Acc II, Bsh1236 I,
CR-amplified DNA
ma, and Ureaplasm
y-to-use mix and E
matic sample proce
G)
AG) in a colorimet
of N-Acetyl--D-
research applicatio
trol (NAG Contro
mination of NAG ac
d of the Test-Com
ated analyzers.
ndard (NAG Stand
ctivity in urine life
t-Combination N-A
mated analyzers, su
x
ments with 5-
recognition
nce of 6-
ments with
ation as
etermining
a, etc. Presence
ight-chain
after lysis and
ml PCR tubes.
ative RT-PCR
ns, cultured
d mRNA in
tion, etc.
ates preserved
ow. Resulting
CR, northern
nts with 5'-
t to BseA I, no
rs: Acc III,
fragments with
in the
ts with 5-
at both C
-
.
gments with
he recognition
, BspFN I,
A of
ma in cell
ELISA
essing.
tric assay
ons.
ol)
ctivity in urine
bination N-
dard)
science
Acetyl--D-
uch as the

Cat. No.

10 909 700 001
10 909 718 001
11 526 430 001
11 333 151 001
11 787 896 001
11 741 985 001
11 934 333 001
11 102 982 001
11 441 337 001
11 288 075 001
11 062 573 001
11 663 925 910
10 875 406 001
11 164 368 001
10 982 962 001

1 k
1 kit
1 kit (for isolat
1 kit (for up to
m
1 kit
ap
Pack Size

500 U (10 U/l)
2,500 U (10 U/l)

200 U (10 U/l)


for up to 192 reac

tion of at least 70
RNA)

30 (100) isolations
ml) sample volume

100 U (1 - 5 U/l)

200 U (10 U/l)

5,000 U (10 U/l)

200 U (10 U/l)


pproximately 50 tes

3 x 1 ml

5 x 3 ml

ests
ctions
g of poly (A)
+

s from 5 ml (1.5
s)

tions
sts

Price in

69,40
239,90
106,80
654,80
459,70
348,90
587,60
353,50
172,80
203,60
109,10
810,20
605,60
98,20
189,30

Alp

Prod

NAD
Nicot
It act
provi
NAD
Nicot
It act
provi
NAD
Use w
and f
activi
subst
NAD
NAD
This
NAD
NAD
This
NAD
Nicot
anab
requi
amor
NAD
NAD
provi
Nar I
Reco
cohe
meth
posit
NBT
For u
Solub
hybri
weste
NBT
For u
colon
north
Supp
NBT/
Read
colon
and w
nitroc
NBT/
Stock
color
and w
nitroc
Nco
Reco
cohe
of 6-
Bsp1
Nde
Nde
with
recog
Isosc

lphabetic
duct Name
D
tinamide adenine d
ts as a coenzyme i
ded as a lyophiliza
D
tinamide adenine d
ts as a coenzyme i
ded as a lyophiliza
D(P)H:FMN Oxido
with luciferase from
for reactions in wh
ity: approx. 7 U/mg
trate, and NADH a
DH
H is the reduced f
NADH Grade I, dis
DH
H is the reduced f
NADH Grade II, di
DP
tinamide adenine d
olic reactions, suc
ire NADPH as a re
rphous powder.
DPH
PH is the reduced
ded as an amorph
I
ognizes the sequen
sive ends. Inhibite
hylcytosine at the 3
ions. Isoschizomer
ble in water, aqueo
dization, immunoh
ern blots, and to d
ny/plaque hybridiza
hern, and western
plied as 100 mg/ml
/BCIP Ready-to-
dy-to-use tablets fo
ny/plaque lifts, imm
western blots, and
cellulose and nylon
/BCIP Stock Solu
k solution for sens
rimetric AP substra
western blots, and
cellulose and nylon
I
ognizes the sequen
methyladenine doe
9 I.
I
I recognizes the se
5-cohesive termin
gnition sequence a
chizomers: FauND
cal Produ
dinucleotide is a c
n redox reactions.
ate.
dinucleotide is a c
n redox reactions.
ate.
oreductase
m Photobacterium
hich NAD(P)H is fo
g lyophilizate at +2
as the coenzyme.
form of nicotinamid
sodium salt is prov
form of nicotinamid
sodium salt is sup
dinucleotide phosp
ch as lipid and nuc
educing agent. NAD
form of NADP
+
. N
hous powder bottle
nce GG*CGCC an
d by 5-methylcyto
3'-position and by 5
rs: Mly113 I.
ous buffer, and DM
histocytochemistry
etect proteins/glyc
ation, immunohisto
blots, and to detec
l solution in 70% D
-Use Tablets
or sensitive detecti
munohistocytochem
to detect proteins
n membranes.
ution
itive detection of a
ate is used in immu
to detect proteins
n membranes.
nce *CCATGG an
ited by 5-methylcy
es not influence th
equence CAT*AT
ni. Nde I is inhibite
as indicated (*), bu
I.
uct Index
coenzyme found in
This NAD Grade I
coenzyme found in
This NAD Grade I
fischeri to determ
ormed or consume
25C and pH 7.0 w
de adenine dinucle
vided as an amorph
de adenine dinucle
pplied as an amorp
phate is a coenzym
cleic acid synthesis
DP disodium is su
NADPH tetrasodiu
ed under nitrogen.
nd generates fragm
sine as shown (*).
5'-hydroxymethylc
line phosphatase u
MF. For colony/plaq
y, ISH, Southern, no
coconjugates. Crys
line phosphatase u
ocytochemistry, IS
ct proteins and gly
DMF.
ion of alkaline pho
mistry, ISH, Southe
s/glycoconjugates.
alkaline phosphata
unohistocytochem
s and glycoconjuga
nd generates fragm
ytosine as indicated
he cleavage (). Iso
TG and generates
ed by 6-methyladen
ut not by 5-methylc
x
all living cells.
, free acid is
all living cells.
I, free acid is
mine NAD(P)H,
d. Specific
with FMN as the
eotide (NAD).
hous powder.
eotide (NAD).
phous powder.
me used in
s, which
pplied as an
m salt is
ments with 5-
Inhibited by 4-
cytosine in all
using BCIP.
que
orthern,
stalline form.
using BCIP. For
SH, Southern,
ycoconjugates.
osphatase. For
ern, northern,
Use with
ase. The
mistry, Southern
ates. Use with
ments with 5-
d (*). Presence
oschizomers:
fragments
nine within the
cytosine ().

Cat. No.

10 127 965 001
10 127 973 001
10 127 981 001
10 127 990 001
10 621 650 001
10 476 480 001
10 107 735 001
10 128 023 001
10 128 031 001
10 128 040 001
10 128 058 001
10 240 354 001
10 107 824 001
10 621 692 001
10 621 706 001
11 103 024 001
11 585 029 001
11 383 213 001
11 697 471 001
11 681 451 001
10 835 315 001
10 835 323 001
11 047 698 001
11 040 219 001
11 040 227 001

Pack Size

1 g
5 g

1 g
5 g
10 g
20 U

500 mg

1 g

100 mg
500 mg
1 g
5 g
100 mg
500 mg
1 g
1,000 U (10 U/l)

5 g

3 ml (300 mg)

20 tablets

8 ml

200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (40 U/l)
200 U (10 U/l)
1,000 U (10 U/l)

www.roche

e-applied-science

Price in

84,10
284,60
59,20
241,50
433,50
232,70
159,10
147,30
66,40
262,70
396,10
1.549,00
199,40
791,80
1.462,40
251,10
551,90
108,40
146,40
110,00
104,60
393,40
393,40
86,40
344,50

155

e.com

Alp
156

www.r

Prod

Nde
Reco
cohe
No in
I, Bst
Nebu
The N
Instru
a Ne
Neur
From
(2,
glyco
hydro
Neur
From
acyln
muco
sialic
Neur
From
acids
etc).
2,8
N-Gl
N-Gly
glyca
core
solut
N-Gl
N-Gly
recom
glyco
fucos
N-Gl
N-Gly
recom
glyco
fucos
Nhe
Nhe
5-co
recog
Nick
Labe
of the
the n
DNA
Nick
Optim
hybri
to de
chrom
Nitra
Nitra
nitrat
prepa
Nitric
Dete
Nitra
nicot
of the
Nitrit
Semi
wate
and b
the p
n-Oc
n-Oc
solub
dialys
lphabetic
roche-applied-sc
duct Name
II (Mbo I)
ognizes the sequen
nhibition by 5-meth
tMB I, Dpn II, Kzo9
ulizer Holder
Nebulizer Holder is
uments and is also
bulizer during DNA
raminidase (Siali
m Vibrio cholerae ; h
3-, 2,6-, 2,8-li
oproteins, and glyc
olytic cleavage of s
raminidase (Siali
m Arthrobacter urea
neuraminic acids,
opolysaccharides,
c acids from glycoc
raminidase (Siali
m Clostridium perfrin
s (2,3-, 2,6-,
In contrast to othe
8 sialic acids are cl
lycosidase A
ycosidase A from s
an chains from glyc
fucose residues p
ion.
lycosidase F
ycosidase F PNGa
mbinant from E.col
opeptides and glyc
se residues presen
lycosidase F
ycosidase F PNGa
mbinant from E.col
opeptides and glyc
se residues presen
I
I recognizes the se
ohesive termini. Nh
gnition sequence a
k Translation Kit
l DNA with radioa
e helix, incorporati
nicked site. Use lab
/RNA transfer hyb
k Translation Mix
mized enzyme mix
dization. Designed
etect multicopy or v
msomes or interph
ate Reductase
te Reductase is us
te in culture media
aration is a crucial
c Oxide, Colorim
rmination of nitric
te present in the s
tinamide adenine d
e enzyme nitrate re
te/Nitrate, Color
-micro method for
r, plant material, fo
biological samples
presence of nitrate
ctylglucoside
ctylglucoside is a m
bilization and recon
sis. CMC: 14.5 mM
cal Produ
cience.com
nce G*ATC, gener
ited by overlapping
hylcytosine. Isosch
9 I, Mbo I, Sau3A I.
s supplied with the
o available separat
A sample fragmen
idase)
hydrolyzes termina
nked to oligo-, po
colipids). For glyco
sialic acid from bio
idase)
afaciens ; hydrolyze
2,3-, 2,6-, or
glycoproteins, and
conjugates of a wid
idase)
ingens ; hydroyzes
2,8-linked to oligo
er neuraminidases
leaved with similar
sweet almond mea
copeptides, even t
resent in insect an
se F of Flavobacter
coproteins unless t
se F of Flavobacter
coproteins unless t
equence GCTAG*
he I is inhibited by
ctive or modified d
ing labeled nucleo
beled probes in co
bridization, and ISH
x
generates sensitiv
d for direct fluorop
very large hybridiz
hase nuclei.
sed for nitrate dete
a, and determinatio
l step. Deproteinat
metric Assay
oxide via nitrite in
sample is reduced
dinucleotide phosp
eductase.
imetric Test
r determining nitrit
oodstuffs, drugs, c
s. Nitrate reduced t
reductase.
mild, nonionic, non
nstitution of memb
M at +25C.
uct Index
rating fragments w
g dam-methylation
hizomers: BfuC I, B
e Genome Sequen
tely. The Nebulizer
ntation.
al N- or 0-acylneur
ly-, mucopolysacc
conjugate structur
ological material.
es terminal N- or 0
2,8-linked to olig
d glycolipids. Comp
de variety of biolog
terminal N- or 0-a
o-, poly-, mucopol
, cleaves 2,3 fas
r velocity as 2,6.
al; hydrolyzes all ty
those carrying
nd plant glycoprote
rium meningosepti
ypes of N-glycan c
they carry -1-3
ant glycoproteins. I
rium meningosepti
ypes of N-glycan c
they carry -1-3
ant glycoproteins L
*C and generates f
5'-methylcytosine
oschizomers: AsuN
dNTPs. Enzymes n
otides as polymeras
lony/plaque hybrid
H.
ve probes for fluor
phore-labeling of in
zation targets on m
ermination: Assay o
on of NO
3
in serum
n biological fluids i
to nitrite by reduc
phate (NADPH) in
te and/or nitrate to
cosmetics, and env
to nitrite by reduce
-denaturing deterg
brane proteins. Eas
x
with 5-
n as shown (*).
Bsp143 I, BssM
cer
r Holder holds
raminic acids
harides,
ral studies and
0-
go-, poly-, and
pletely remove
gical materials.
acylneuraminic
lysaccharides,
ter than 2,6;
ypes of N-
1,3-bound
eins. In
icum ,
chains from
3 linked core
In solution.
icum ,
chains from
3 linked core
Lyophilizate.
fragments with
within the
NH I.
ick one strand
se proofreads
dization,
escence in situ
n situ probes,
metaphase
of nitrite and
m. Sample
r good results.
n a microplate.
ced
the presence
o investigate
vironmental
ed NADPH in
gent for the
sily removed by

Cat. No.

11 040 243 001
04 777 026 001
11 080 725 001
10 269 611 001
11 585 886 001
11 642 995 001
11 365 169 001
11 365 177 001
11 365 185 001
11 365 193 001
10 885 843 001
10 885 851 001
10 885 860 001
10 976 776 001
11 745 808 910
10 981 249 001
11 756 281 001
11 746 081 001
10 634 425 001

1 kit for up to
200 l for
1 test
1 test combina
Pack Size

1,000 U (5 U/l)

1 nebulizer holder

1 U

1 U (100 l)

5 U

5 mU (0.1 ml)

100 U (0.1 ml)
250 U (0.25 ml)

100 U
250 U

200 U (10 U/l)
1,000 U (10 U/l)
1,500 U (40 U/l)
o 50 standard labe

r up to 50 labeling

20 U

combination for 9

ation for approxim

10 g

r

eling reactions
reactions
6 wells
ately 64 assays

Price in

314,90
inquire
104,00
262,60
190,90
431,00
243,20
456,00
243,20
456,00
72,80
291,00
345,60
408,50
350,60
186,40
458,30
262,10
741,50

Alp

Prod

Noni
Solub
comp
stabi
0.25
Noni
Solub
comp
stabi
nitrog
Not I
Not I
GCG
by 5-
not in
Nru I
Reco
ends
meth
posit
Nsi I
Nsi I
3-co
5-me
Zsp2
Nucl
Endo
dsDN
yield
vitro
Nucl
Nucle
rever
produ
Nutr
Defin
grow
Optim
serum
Nutr
Serum
with
P3x63
and o
Nylo
Unch
phag
chem
biotin
Nylo
Matr
(DIG)
RNA,
Stron
hybri
O
O-Gl
Relea
threo
acid)
glyco

lphabetic
duct Name
idet P40 Substitu
bilize membrane p
plexes. Also includ
lize enzymes such
mM.
idet P40 Substitu
bilize membrane p
plexes. Also includ
lize enzymes such
gen in injection via
I
is a rare-cutter en
GG*C*CGC, gener
-methylcytosine as
nhibiting (). Isosch
I
ognizes the sequen
. Inhibited by over
hylcytosine is inhib
ion of the C. Isosc

recognizes the seq
ohesive termini. Ns
ethylcytosine is not
I.
lease S7
onuclease preferen
NA and RNA. Cleav
3'-mono- and olig
translation system
leoside Monopho
eoside Monophos
rsible transfer of a
ucing adenosine d
idoma-CS
ned supplement re
wth of SP2/0-, P3x6
mizes growth of fre
m-free cell culture
idoma-SP
m-free media supp
an intact cholester
3Ag8.653, and lym
other cell types (ne
on Membranes fo
harged microporou
ge/cosmid libraries
miluminescent/ chr
nylated or radioact
on Membranes, p
ix for hybridization
) and biotin, or rad
, or oligonucleotide
ngest signals and l
ds.
lycosidase
ases Gal-(1,3)-Ga
onine are hydrolyze
prevent hydrolysis
oproteins before pr
cal Produ
ute
roteins during isol
ed in buffers for m
as Taq. Supplied
ute
roteins during isol
ed in buffers for m
as Taq. Aqueous
als. CMC: 0.25 mM
nzyme and recogn
rating fragments w
s shown (*). 5-meth
hizomers: CciN I.
nce T*CGCG*A, g
lapping dam-meth
iting(*) or not inhi
hizomers: BtuM I,
quence ATGC*AT
si I is inhibited by 6
t inhibiting. Isosch
ntially cleaves sing
ves 5'-phosphodie
gonucleotides. Rem
ms and in RNA seq
osphate Kinase
phate Kinase is a l
phosphate group
diphosphate and a
eplaces FBS in hyb
63Ag8.653-, and NS
eshly fused hybrido
without feeder ce
plement for murine
rol biosynthesis pa
mphoblastoid cell li
eural explants).
or Colony and Pla
us nylon membran
s with DIG probes a
romogenic substra
tive probes. Pore s
positively charged
n with nonradioact
dioactive labeling u
e probes, for Sout
owest background
aINAc from O-glyc
ed. Substituents at
s and must be rem
rotein sequencing.
uct Index
lation of membran
microplate assays a
as a Gel under nitr
lation of membran
microplate assays a
solution, 10% (w/v
M.
izes the sequence
with 5-cohesive te
hylcytosine in the 5
generating fragme
hylation as shown(
biting(), dependin
Bsp68 I.
T and generates fr
6-methyladenine, a
izomers: EcoT22 I,
le-strand substrate
ester bonds of RNA
move endogenous
quencing.
liver enzyme that c
from adenosine tr
nucleoside diphos
ridoma cell culture
S-1-derived hybrid
omas during selec
ells.
e myelomas and h
athway (derived fro
nes), primary lymp
aque Hybridizatio
e for nonradioactiv
and detection with
ates. Use in hybridi
size: 1.2 m.
d
tive labeling using
using
32
P,
35
S,
3
H
thern, northern an
d obtained with DI
cans. Bindings to s
t the disaccharide
moved. For deglyco
.
x
e-protein
and used to
rogen. CMC:
e-protein
and used to
v), filled under

rmini. Inhibited
5'-C position is
ents with blunt
(*). 5-
ng on the
ragments with
as indicated (*).
Mph1103 I,
es, as well as
A and DNA to
RNA from in
catalyzes the
riphosphate,
sphate.
es. Supports
domas.
ction/cloning in
ybridomas
om SP2/0,
phoid cultures,
on
ve screening of
h
izations with
digoxigenin
with DNA,
d dot blotting.
G-labeled
serine and
(e.g., sialic
osylation of

Cat. No.

11 754 599 001
11 332 473 001
11 014 706 001
11 014 714 001
11 037 668 001
10 776 777 001
10 909 831 001
10 909 840 001
10 107 921 001
10 107 948 001
11 363 743 001
11 011 375 001
11 699 075 001
11 699 083 001
11 209 272 001
11 209 299 001
11 417 240 001
11 347 101 001

10 m
1
50 disc
50 discs
10
20
Pack Size

100 ml

5 x 10 ml

200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (40 U/l)
1,000 U (10 U/l)

200 U (10 U/l)
1,000 U (10 U/l)

15,000 U

mg (60 mg lyophiliz

10 ml (50x)

100 ml (100x) steri

cs (each 82 mm dia
s (each 132 mm d

0 sheets (20 x 30 c
0 sheets (10 x 15 c
1 roll (0.3 x 3 m)
25 mU

www.roche

zate)
le
ameter)
iameter)
cm)
cm)
e-applied-science

Price in

122,30
102,40
90,90
351,40
351,40
364,40
97,80
269,40
169,50
197,90
180,30
762,70
282,20
525,30
423,20
235,20
552,10
328,90

157

e.com

Alp
158

www.r

Prod

P
p53
Dete
homo
betw
type
Papa
For c
immu
prote
Requ
pBR3
Selec
cleav
sites
inact
PCR
For o
chain
a 25
mM T
PCR
For a
react
mM T
the M
PCR
Conta
cond
sensi
supp
PCR
For ru
of DN
buffe
conta
PCR
For d
PCR.
in PC
produ
PCR
Direc
PCR.
diges
Urac
PCR
Gene
low-c
Probe
remo
PCR
Conv
100 t
ELISA
sequ
PCR
Conv
produ
No. 1
paral
PCR
Conv
produ
conve
Micro
PCR
Add
hybri
when
ELISA
lphabetic
roche-applied-sc
duct Name
pan ELISA
rmine p53 (human
ogenates (tumor ti
een elevated p53 l
and mutant forms
ain
complete proteolyti
unoglobulins, and
eins and produces
uires 0.5% cysteine
322 DNA
ctable plasmid for
vage sites in the am
in the tetracycline
ivating these drug
Buffer Set
optimizing the mag
n reaction using Ta
mM magnesium s
Tris-HCl, 500 mM
Buffer Without M
amplification of spe
tion. The buffer is a
Tris-HCl and 500 m
MgCl
2
Stock Soluti
Core Kit
ains everything for
itions for basic PC
itivity/specificity us
lied Mg-free buffe
Core Kit
PLUS

unning PCR using
NA contamination
er without Mg2+, a
aminating DNA.
DIG Labeling Mi
direct labeling of am
The PCR DIG labe
CR. The nucleotide
uct combined with
DIG Labeling Mi
ct labeling of ampl
Prevent PCR carry
st contaminating P
il-DNA Glycosylas
DIG Probe Synth
erate highly sensiti
copy gene detectio
es labeled with alk
oval of digoxigenin
ELISA, DIG-Dete
venient, nonradioac
times more sensitiv
A format makes de
ence in large sam
ELISA, DIG-Dete
venient, nonradioac
ucts; 5-pack is the
1636111910), prov
lel testing of a larg
ELISA, DIG-Labe
venient nonradioac
ucts for detection
entional ethidium
oplate format is ide
Fluorescein Lab
mix directly to PCR
dization probes. P
n limited amounts
A, membrane hybr
cal Produ
cience.com
levels and tumor d
of p53 protein.
ic cleavage of prot
tissue dissociation
glycopeptides from
e for activity.
cloning of recomb
mpicillin gene, or C
e gene, allow foreig
resistance genes.
gnesium chloride c
aq DNA Polymeras
solution and a PCR
KCl; pH 8.3).
MgCl
2
, 10x conc
ecific DNA fragme
a tenfold concentr
mM KCl, and shou
ion.
r PCR except temp
CRs using Taq. Opt
sing non-standard
er.
non-standard buf
from prior amplific
and Uracil-DNA Gl
ix
mplification produ
eling mix can repla
concentration ens
h DIG detection.
ix
PLUS

ification products
yover by incorpora
PCR products from
e.
hesis Kit
ve hybridization pr
on of rare mRNA in
kaline-labile digoxi
label after detecti
ection
ctive method for la
ve than ethidium b
etermining presenc
ple numbers easy.
ection, 5-pack
ctive method for la
e high capacity ver
viding more reage
ge number of sam
eling
ctive method adds
using PCR ELISA;
bromide staining o
eal for automation
beling Mix
Rs to produce fluo
articularly useful f
of target DNA is a
ridization, or ISH.
uct Index
erum/plasma, or fro
sed to investigate
development by qu
teins, limited hydro
n. Solubilizes integ
m purified proteog
binant DNA. Pst I a
Cla I, Hind III, Bam
gn DNA to be inse
.
concentration in th
se. This PCR Buffe
R buffer (10x conce
.
ents using the poly
rated solution cont
ld be used in com
plate and primers.
timize assays for g
Mg-concentration
ffer conditions with
cations. Includes M
lycosylase for deg
cts using digoxige
ace the unlabeled
sures maximum yie
using digoxigenin
ating dUTP instead
previous amplifica
robes using PCR. S
n Southern and no
igenin (DIG)-dUTP
ion are stable for o
abeling and detect
bromide staining o
ce or absence of s

abeling and detect
rsion of the standa
nts, but lacking co
ples.
a DIG label to you
100 times more se
of products using
n.
rescein-labeled DN
for synthesizing DN
available. Use label
x
om tissue
relationships
uantifying wild
olysis of native
ral membrane
glycans.
and Pvu I
HI, and Sal I
erted for
e polymerase
r Set contains
entrate; 100
ymerase chain
taining 100
bination with
Determine
reater
ns using the
h samples free
MgCl
2
solution,
grading
enin-dUTP in
nucleotide mix
eld of PCR
(DIG)-dUTP in
of dTTP and
ations using
Suitable for
orthern blots.
P for easy
over one year.
t PCR products;
n agarose gels.
specific target
ting PCR
ard kit (see Cat.
ontrols. For
ur PCR
ensitive than
agarose gels.
NA
NA probes
led probes in

Cat. No.

11 828 789 001
10 108 014 001
10 481 238 001
11 699 121 001
11 699 105 001
11 578 553 001
11 585 541 001
11 585 550 910
11 835 289 910
11 636 090 910
11 636 111 910
11 965 409 910
11 636 120 910
11 636 154 910

1
2 x 2 ml
1 kit for up to 1
volume eac
1 kit for up to 5
volume, ea
500 l (2 x 250
reactions of 1
co
2 x 250 l for u
50
1 kit for up to 2
volume (one
labeled pro
1 kit for 1
microplates
detec
1 kit for 4
microplates), th
number of
standar
1 kit
100 l for up t
Pack Size


100 mg (10 ml)

200 l 1 A
260
unit

(2 x 1 ml of each

3 x 1 ml

00 reactions of 50
ch containing 2.5 U
Polymerase

50 reactions of 50
ch containing 2.5
Polymerase

00 l final reaction
oncentration 200


25 reactions of 50
e reaction can prod
obe to analyze 650
membrane)
192 detection react
ction of 50 PCR pro

480 detection reac
he number of tests
required sample d
rd and/or control r

to 10 PCR reaction
100 l

sts
t
solution)
l final reaction
U Taq DNA
l final reaction
U Taq DNA
25 PCR assays,
n volume, final
M
ons, reactions of
lume
l final reaction
duce enough
cm
2
of blot
tions (two
-quantitative
oducts
tions (five
depends on the
dilutions and
eactions
tions
ns, reactions of

Price in

785,50
130,70
212,30
49,70
40,30
292,60
214,40
414,40
414,40
457,50
527,20
911,30
576,00
338,80

Alp

Prod

PCR
2x co
up to
Conta
pipet
PCR
Conv
dCTP
Wate
cDNA
PCR
Read
each
react
dUTP
PCR
Conv
vary
incre
optim
Pefa
Spec
comp
value
block
Pefa
Spec
comp
attac
conc
Peni
Preve
inhib
Strep
inhib
Peps
Use P
medi
yield
from
Peps
Prote
inves
class
pharm
Pero
For o
Perox
moie
dialys
Pero
Perox
as we
used
a salt
Pero
Use P
solub
For c
shee
Pero
Comp
acces
antib
immu
Phos
Use P
pyruv

lphabetic
duct Name
Master
oncentrated, ready
o 2 kb. Use in place
ains everything ex
tting steps.
Nucleotide Mix
venient, easy-to-us
P, dGTP, and dTTP,
er. Optimized for di
A synthesis, and p
Nucleotide Mix
P
dy-to-use premixed
at 10 mM, and dU
tions. Prevent carry
P instead of dTTP b
Optimization Kit
venient, reliable rea
buffer pH, and ma
ease yield and spec
mize conditions in m
bloc
SC
ific, potent, irrever
pared to PMSF or D
es. Completely inac
ker of thrombin in
bloc
SC PLUS
ific, potent irrevers
pared to PMSF or D
hment of Pefabloc
entration for longe
cillin-Streptomyc
ent and eliminate b
its bacterial growt
ptomycin, aminogly
iting protein synth
sin
Pepsin for nonspec
a. Pepsin provides
biologically active
pig gastric mucos
statin
ect proteins and en
stigation of enzyme
sifications. For affin
macological, HIV, a
oxidase (POD)
oxidation of electro
xidase (POD) to pr
ty. Use reconstitut
sis. Grade I salt-fre
oxidase (POD)
xidase (POD) can
ell as its carbohyd
directly for conjug
t-free lyophilizate.
oxidase (POD), ac
Peroxidase (POD),
ble substances wit
coupling of Ig, Ig Fa
p, and goat with P
oxidase Labeling
plete kit for labelin
ssible primary ami
bodies with POD, a
unoblotting. All req
sphoenol-pyruva
Phosphoenol-pyru
vate kinase.
cal Produ
-to-use mix for rou
e of Taq or the PC
cept template DNA
se, clear colorless s
each at 10 mM co
irect use in all type
rimer-extension.
PLUS

d solution of sodiu
UTP at 30 mM. Opt
yover contaminatio
by pretreatment wi
t
ady-to-use solutio
agnesium, DMSO, g
cificity. Use with Fa
multiplex PCR.
rsible inhibitor of s
DFP with higher st
ctivates proteinase
serum and plasma
sible inhibitor of se
DFP. Pefabloc
SC
c
SC to proteins.
er incubation times
cin
bacterial contamin
th by inhibiting pep
ycoside antibiotic,
hesis.
cific hydrolysis of p
s a limited hydrolys
e fragments. Pepsin
sa.
nzymes during isol
e mechanisms, bio
nity chromatograph
and cancer researc
on donors by epoxi
roteins via its amin
ted solution directl
ee lyophilizate.
be coupled to othe
rate moiety. The re
gation without prio
ctivated
activated,without
h reactive and acc
ab, and Ig F(ab')
2

POD. Use in ELISA,
Kit
ng water-soluble b
no groups with PO
nd downstream us
quired reagents ar
ate
vate PEP, monopo
uct Index
utine genomic and
R Core Kit for rout
A and primers. Req
solution of sodium
oncentration in PC
es of amplification
m salts of dATP, d
timized for most am
on using PCR prod
ith Uracil-DNA Gly
ns to optimize PCR
glycerol concentra
astStart High Fidel
serine proteases. N
tability at physiolog
e K. Unlike PMSF, e
a.
erine proteases. N
C and the PLUS ad
They can be used
s at alkaline pH.
nants in cell culture
ptidoglycan synthe
inhibits bacterial
proteins and pepti
sis of native immun
n is an aspartic en
ation and purificat
ological function, a
hy, and structural,
ch.
idation of double b
no groups and its c
ly in conjugation w
er proteins via its a
econstituted solutio
or dialysis. EIA grad
pre-activation to l
cessible primary am
fragments from ra
IHC, and immuno
biomolecules with r
OD. Ideal for coupl
se in ELISA, IHC, a
e supplied.
otassium salt as a s
x
d cDNA targets
tine PCRs.
quires only 2
m salts of dATP,
CR Grade
reactions,
dGTP, dCTP,
mplification
ducts with
ycosylase.
R setup. Easily
ations to
ity System to
Nontoxic
gical pH
excellent
ontoxic
dditive prevent
at higher
e. Penicillin G
esis.
growth by
des in acidic
noglobulins to
doproteinase
tion. Facilitates
and protease
bonds. Couple
carbohydrate
without prior
amino groups,
on can be
de, supplied as
abel water-
mino groups.
abbit, mouse,
oblotting.
reactive and
ing of
and
substrate for

Cat. No.

11 636 103 001
11 581 295 001
11 814 362 001
11 888 412 001
11 636 138 001
11 429 868 001
11 429 876 001
11 585 916 001
11 873 601 001
11 873 628 001
11 074 440 001
10 108 057 001
10 253 286 001
11 359 053 001
11 524 488 001
10 108 090 001
10 814 407 001
11 428 861 001
11 829 696 001
10 108 294 001

1 kit for up to
reaction volume
200 l 10 mM, e
l
2,000 l (10 x
5,000 reaction
2 x 100 l f
reactions o
1 kit for up to 1
optimization
set I (100 mg P
set II (1 g Pefab
for 20 ml
app
1 kit for
Pack Size

o 200 PCR reaction
e each containing
Polymerase

each, for up to 500
final reaction volu
x 200 l) 10 mM, e

for up to 10 mM, e
of 20 l final react

100 one-step or up
n assays of 100 l f
volume

100 mg
1 g
500 mg
Pefabloc
SC; 5 m
solution)
bloc
SC; 2 x 25 m
solution)

((500x), lyophiliza

1 g

2 mg
10 mg
50 mg
25,000 U

100 mg

prox. 40 mg lyophil


1 g

www.roche
s of 50 l final
2.5 U Taq DNA-
0 reactions of 20
me
each, for up to
action volume
ach, for 500
ion volume
p to 50 two-step
final reaction
l PSC-Protector
ml PSC-Protector
te, sterile)
izate
reactions
e-applied-science

Price in

271,10
60,00
445,60
120,80
256,40
101,60
505,30
271,40
153,60
724,60
67,10
84,30
42,60
163,10
457,00
277,60
301,80
362,90
494,10
294,90

159

e.com

Alp
160

www.r

Prod

Phos
Phos
of ke
sulfat
Phos
For fa
conju
divid
for ce
Phos
Use n
Inhib
almo
deph
Phyt
Cons
high-
High
lymp
Phyt
Phyto
phyto
prolif
Plasm
Use P
used
resea
Plasm
Use P
used
resea
Plasm
Plasm
plasm
Plast
The P
on a
PMS
Inhib
prote
most
solub
Poly
Poly(
work
tail to
(mRN
Poly
Use a
activi
single
this l
Poly
Poly(
chain
Poly
Use a
bioph
It is a
the d
Polye
Cell f
soma
quali
aldeh

lphabetic
roche-applied-sc
duct Name
sphoglucose Isom
phoglucose Isome
etoses to aldoses. S
te, pH approximate
spho-Histone H3
ast, accurate quan
ugated antibodies.
ing cells on 96-we
ell-based workflow
sSTOP
non-toxic tablets to
bition of acid/alkali
st any tissue or ce
osphorylation in F
ohemagglutinin-
sists of only L-type
-efficiency inductio
ly purified and test
hocytes.
ohemagglutinin-
ohemagglutinin PH
ohemagglutinin. It
feration in lymphoc
min, bovine
Plasma, bovine in c
for protein structu
arch. The enzyme c
min, human
Plasmin, human in
for protein structu
arch. The enzyme c
minogen
minogen from hum
minogen activators
tic Chute
Plastic Chutes can
Hamilton Trolley.
SF
bits serine protease
ease papain [revers
t cysteine or aspart
ble, water-stable a
(A)
(A) has a chain len
king solution is 0.5
o an RNA molecule
NA) for translation
(A) x (dT)
15

as a primer for rev
ity of reverse trans
e strand of poly(A)
ong strand of poly
(dA)
(dA) was prepared
n length is 250-500
[d(I-C)]
as a template for R
hysical investigatio
also used as a prim
determination of sm
ethylene Glycol 1
fusion induced by
aticcell genetics an
ty PEG does not ne
hydes not detectab
cal Produ
cience.com
merase (PGI)
erase (PGI) from ye
Supplied as a susp
ely 6.
3 Imaging Kit
ntification of mitotic
Ideal for accurate
ell microplates. Qui
ws.
o protect your prot
ne, serine/threonin
ell type. PhosSTOP
FFPE tissue section
-L (PHA-L)
subunits (isolectin
on and functional
ted for high-efficie
-M (PHA-M)
HA-M is the mucop
is a potent mitoge
cyte cultures.
coagulation resear
ure analysis, seque
coagulation resea
ure analysis, seque
man serum is used
s; substrate of t-PA
be used in combi
es (chymotrypsin, t
sible by DTT treatm
tic proteases. Pefa
lternative.
ngth of 2,100 to 10,
mg/ml. Polyadeny
e. This process pro
.
verse transcriptase
sriptases. Consists
). Short (15 bp) se
y(A).
from dATP using
0 bases and varies
RNA polymerases a
ons.
mer template with
mall amounts of dIT
1500
polyethylene glyco
nd the production
eed to be tested p
ble; free from Ca
2+

uct Index
east is used for the
pension in 3.2 M am
c cells using Alexa
e and fast quantific
ickly determine ce
tein from dephosp
ne and tyrosine ph
Tablets prevent
ns.
n L4, leuko-agglut
analysis of T-lymp
ency stimulation of
protein form of
en used to stimulat
rch and in medica
ence analysis, and
o soluble products
arch and medical r
ence analysis, and
o soluble products
to determine the a
A.
nation with the So
trypsin, thrombin, c
ment]). Does not in
abloc
SC is a non
,000 nucleotides. T
ylation is the additi
oduces mature me
s and can be appl
of 1 long (at least
quences of dT are
terminal transfera
s by lot.
and as a DNA mod
Kornberg DNA po
TP, dGTP, and dCT
ol is a standard me
of hybridoma cells
prior to use. Peroxid
.
x
e isomerization
mmonium
aFluor
488
cation of
ell cycle status
phorylation.
hosphatases in
tinin). Ideal for
phocytes.
f human
te cell
l research. It is
biochemical
.
research. It is
biochemical
.
activity of
olid Waste Bag
cysteine
nhibit metallo-,
ntoxic, water-
The suggested
on of a poly(A)
essenger RNA
ied to test the
t 1,000 bp),
e hybridized to
se. Mean
del for
lymerase for
TP.
ethod in
s. This high
des and

Cat. No.

10 127 396 001
10 128 139 001
06 569 161 001
04 906 837 001
04 906 845 001
11 249 738 001
11 082 132 001
10 602 370 001
10 602 361 001
10 874 477 001
04 639 669 001
10 837 091 001
11 359 061 001
10 108 626 001
10 108 677 001
10 223 581 001
10 108 812 001
11 219 847 001
10 783 641 001

fo
20 tablets in EA
for 10
10 tablets in EA
for 10
Pack Size

2 mg (1 ml)
10 mg (1 ml)


ASYpacks (foil blist
ml cell extract or
ml cell extract or

5 mg

20 mg

5 U (1 ml)

5 U (0.5 ml)

20 U

1 set of 10 chutes

10 g
25 g

100 mg

5 A
260
units

5 A
260
units

10 A
260
units
50 A
260
units

10 x 4 ml

ts
ter) (each tablet
buffer)
ter) (each tablet
buffer)
s

Price in

40,40
137,20
450,00
190,00
101,10
349,30
150,20
216,90
201,00
234,20
inquire
97,70
184,40
130,10
141,20
193,20
139,80
523,30
130,10

Alp

Prod

Polyn
Use t
DNA
phos
witho
Prim
The P
MagN
Prim
Rand
ensu
struc
Prim
This
a cDN
synth
Pron
Mix o
single
tissue
of gly
Prote
Each
a wid
and s
resor
Prote
Inhib
trans
degra
PCR,
prepa
Prote
Affin
from
enter
cultu
Prote
Affin
for th
for th
mitog
Prote
Activ
grade
from
lyoph
Prote
Activ
grade
from
mg/m
Pst I
Pst I
3-co
and 6
pUC
Plasm
orien
many
coli b
PVD
Ideal
low b
color
Light

lphabetic
duct Name
nucleotide Kinas
to phosphorylate 5
or RNA using [
phate exchange, a
out altering their 5
mary Sample Hand
Primary Sample Ha
NA Pure lysis buffe
mer "random"
dom hexamer prim
ring reverse transc
cture. It is a primer
mer for cDNA Syn
primer will bind th
NA copy, for use in
hesis of first-strand
nase
of nonspecific end
e amino acids. Deg
e dissociation alon
ycopeptides from g
ease Inhibitors S
inhibitor in the se
de variety of protea
sensitively verified
rufin-labeled).
ector RNase Inhi
bits a wide spectru
scription reactions
adation. Use in ma
RNase protection
aration of RNase-f
ein A Agarose
ity chromatograph
many species. Tes
rotoxins. Use to pu
re supernatant.
ein G Agarose
ity chromatograph
he purification of Ig
he absence of stap
genic.
einase K, recomb
ve endopeptidase i
e enzyme isolates
tissues/cell lines,
hilizate. Also availa
einase K, recomb
ve endopeptidase i
e enzyme isolates
tissues/cell lines,
ml in 10 mM Tris. A
recognizes the seq
ohesive termini. Pst
6-methyladenine, a
18 DNA
mid for loning doub
ntation with respec
y unique sites for c
by transformation.
F Western Blottin
membrane for we
background bindin
rimetric and chemi
t Western-Blotting
cal Produ
se
5' ends of DNA or
-
32
P]-ATP either b
and to remove 3'-p
' ends (at low pH o
dling Reagent Ca
andling Reagent C
ers.
ers bind througho
cription of all RNA
for cDNA synthes
thesis
e 3'-poly A tail of
n RT-PCR, generat
d cDNA.
o- and exoproteas
grade protein duri
ng with collagenas
glycoproteins.
Set
et can be used sep
ases. Effectiveness
using the Univers
ibitor
m of RNases also
(up to +60C) to p
any techniques: cD
, in vitro virus repl
free antibodies.
hy using Protein A
sted for the absenc
urify mouse monoc
hy using Protein G
gG from many spe
phylococcal entero
binant, PCR Grad
nactivates endoge
nucleic acids for P
and promotes bac
able in solution.
binant, PCR Grad
nactivates endoge
nucleic acid for PC
and promotes bac
Available lyophilize
quence *CTGCA
t I is inhibited by th
ble-digested restri
ct to the lac promo
cloning of foreign

ng Membranes
estern and dot blot
ng generate excelle
iluminescent detec
Substrates.
uct Index
RNA, label 5'-hydr
by direct phosphor
phosphates from R
only).
arrier
Carrier is used for h
out the entire lengt
A sequences due to
sis.
an mRNA to initiat
tion of cDNA libra
ses that digest prot
ng DNA and RNA
se and trypsin. Use
parately or as cockt
s of protease inhib
sal Protease Substr
in in challenging
protect RNA samp
DNA synthesis, RT-
lication, transcripti
agarose is ideal fo
ce of staphylococc
clonal antibodies fr
agarose is the me
ecies. Recombinant
toxins that are kno
de
enous RNases and
PCR and native RN
cterial cell lysis. Su
de
enous RNases/DNa
CR and native RNA
cterial cell lysis. So
ed.
G and generates f
he presence of 5-m
oschizomers: BspM
iction fragments in
oter. Polylinker (MC
DNA. Easily introd
ts. Strong sample r
ent signal-to-noise
ction. Ideal for use
x
roxyl ends of
rylation or by
RNA or DNA
holding
th of RNA,
o their random
te synthesis of
ries, and
tein down to
A isolation. For
e in production
tails to inhibit
ition is quickly
rate (casein,
reverse
les from
-PCR, qRT-
ion/translation,
or purifying IgG
cal
rom ascites or
ethod of choice
t form is tested
own to be
DNases. PCR-
NA and DNA
pplied as a
ases. PCR-
A and DNA
olution: 14 to 22
fragments with
methylcytosine
MA I.
n either
CS) provides
duced into E.
retention and
e ratios in
e with Lumi-

Cat. No.

10 174 645 001
10 633 542 001
07 101 988 001
11 034 731 001
10 814 270 001
10 165 921 001
11 459 643 001
11 206 893 001
03 335 399 001
03 335 402 001
05 015 979 001
11 134 515 001
11 719 408 001
05 015 952 001
11 243 233 001
11 719 416 001
03 115 801 001
03 115 836 001
03 115 852 001
03 115 879 001
03 115 828 001
03 115 844 001
03 115 887 001
10 621 625 001
10 621 633 001
10 798 991 001
10 885 819 001
03 010 040 001

2 mg (Random
units, 1 mo
40
1 set (10 in
10
15 m
5 ml
2 ml
15 m
5 ml
2 ml
1
Pack Size

200 U
1,000 U

1 reagent carrier

m pd(N)
6
Potassiu
primers)
g (1 A
260
unit, 8 n

1 g
5 g

ndividual protease

2,000 U
0,000 U (5 x 2,000

2 x 250 mg
25 mg
4 x 250 mg
100 mg
5 ml
25 ml
1.25 ml
3,000 U (10 U/l)
10,000 U (10 U/l)
10,000 U (40 U/l)
50 g (200 l)

roll (30 cm x 3.00

www.roche
um Salt, 50 A
260

ctions 5 ng
mol)
e inhibitors)
U)
lume)
ume)
ume)
lume)
ume)
ume)

)
)
m)
e-applied-science

Price in

217,20
864,20
inquire
258,50
75,30
108,30
396,10
346,30
134,00
496,80
1.238,00
531,50
265,80
2.043,70
877,20
438,00
364,80
37,70
590,50
82,30
113,40
453,90
51,40
90,90
225,20
225,20
468,30
300,50

161

e.com

Alp
162

www.r

Prod

Pvu
Reco
cohe
Inhib
Isosc
Pvu
Pvu I
blunt
recog
Pwo
High
fold l
extre
chara
Pwo
Read
dNTP
Taq.
cloni
Pwo
For h
gene
RICH
Perfo
Pwo
High
Use f
yield
temp
Pyro
Inorg
pyrop
prote
amm
Pyru
Pyruv
Catal
mole
amm
Pyru
Pyruv
Catal
mole
(v/v),
Q
Quic
Read
uninc
react
dsDN
Quic
Read
uninc
react
dsDN
Quic
Read
unlab
react
RNA:

lphabetic
roche-applied-sc
duct Name
I
ognizes the sequen
sive termini. Not in
bited by 5-methylcy
chizomers: BpvU I,
II
I recognizes the se
t ends. Pvu II is inh
gnition sequence a
DNA Polymeras
thermal stability p
ower than Taq DN
mely accurate DN
acterization of rare
Master
dy-to-use 2x conce
Ps, and buffer. Hig
Use for high fidelit
ng, and gene expr
SuperYield DNA
high fidelity PCR up
expression. Highe
H Solution ensures
orm digests directly
SuperYield DNA
fidelity PCR up to
for site-directed m
and 18-fold highe
plates (GC RICH So
ophosphatase, ino
ganic pyrophospha
phosphate to form
ein, RNA, and DNA
onium sulfate, pH
vate Kinase (PK)
vate Kinase from ra
cule of pyruvate a
onium sulfate solu
vate Kinase (PK)
vate Kinase from ra
cule of pyruvate a
, pH approx. 6.
ck Spin Columns
dy-to-use disposab
corporated nucleot
tions. Use in low-s
NA: <10 base pairs
ck Spin Columns
dy-to-use disposab
corporated nucleot
tions. Use in low-s
NA: <72 base pairs
ck Spin Columns
dy-to-use disposab
beled or radioactiv
tions. Use in low-s
: <12 bases. Samp
cal Produ
cience.com
nce CGAT*CG, g
nhibited by overlap
ytosine as shown (
Mvr I, Ple19 I.
equence CAG*CT
hibited by 5'- and 4
e
polymerase with an
NA Polymerase). Id
A synthesis, such
e mutations.
entrated mix of Pw
her yield and 18-fo
ty PCR up to 3 kb,
ression.
A Polymerase
p to 3 kb, site-dire
er yield and 18-fold
high performance
y in PCR mix.
A Polymerase, dN
3 kb. Contains rea
mutagenesis, clonin
olution).
organic (PPase)
atase (PPase) catal
orthophosphate. I
A synthesis. Suppli
6.
)
abbit muscle is an
of a phosphate gro
nd 1 molecule of A
ution, pH approx. 6
)
abbit muscle is an
of a phosphate gro
nd 1 molecule of A
for radiolabeled
ble columns quickl
tides from DNA la
peed, swinging-bu
s. Sample size: up
for radiolabeled
ble columns quickl
tides from DNA la
peed, swinging-bu
s. Sample size: up
for radiolabeled
ble columns quickl
vely labeled RNA fr
peed swinging-bu
ple size: up to 50
uct Index
enerating fragmen
pping dam-methyl
(*) and 4-methylcy
TG and generates f
4'-methylcytosine w
oschizomers: none
n extremely low er
deal for application
as high fidelity PC
wo SuperYield DNA
old higher fidelity c
site-directed muta
cted mutagenesis,
d higher fidelity th
e using difficult tem
NTPack
ady-to-use PCR Nu
ng, and gene expre
. High performanc
lyzes the hydrolysi
It plays an importa
ed in suspension i
n enzyme involved
oup from PEP to A
ATP. Suspension in
6.
n enzyme involved
oup from PEP to A
ATP. Solution in 50
DNA purification
beling and polyme
ucket centrifuges.
to 50 l.
DNA purification
beling and polyme
ucket centrifuges.
to 100 l.
RNA purification
rom nucleotides an
l.
x
nts with 3-
ation ().
ytosine.
fragments with
within the
e known.
ror rate (18-
ns that require
CR and
A Polymerase,
compared to
agenesis,
, cloning, and
an Taq. GC-
mplates.
ucleotide Mix.
ession. Higher
ce with difficult
s of inorganic
ant role in
in 3.2 M
in glycolysis.
DP, yielding 1
n 3.2 M
in glycolysis.
DP, yielding 1
0% glycerol
n
emove
erization
Exclusion limit
n
emove
erization
Exclusion limit
n
rate small
nd labeling
Exclusion limit

Cat. No.

10 650 129 001
10 650 137 001
10 642 690 001
10 642 703 001
11 644 947 001
11 644 955 001
03 789 403 001
04 340 850 001
04 340 868 001
04 743 750 001
10 108 987 001
10 128 155 001
10 128 163 001
10 109 045 001
11 273 922 001
11 273 949 001
11 273 965 001
11 273 973 001
11 273 990 001

100 U for up
volume eac
500 U (2 x 250
l final volume
2.5 ml (10 x 25
l final reacti
PWO Su
500 U (2 x 250
final volum
Supe
100 U for up to
each contain
100 U for up to
each contain
Pack Size

500 U (5 U/l)
100 U (5 U/l)

1,000 U (10 U/l)
5,000 U (10 U/l)

p to 40 reactions o
ch containing 2.5 U
Polymerase
U) for up to 200 r
e each containing 2
Polymerase

0 l) for up to 100
on volume each co
uperYield DNA Pol

U) for up to 200 re
me each containing
erYield DNA Polym
40 reactions of 50
ning 2.5 U Pwo Sup
Polymerase

40 reactions of 50
ning 2.5 U Pwo Sup
Polymerase

1 mg (1 ml)

10 mg (1 ml)
100 mg (10 ml)

10 mg (1 ml)

20 columns
50 columns

20 columns
50 columns

20 columns

of 100 l final
U Pwo DNA
reactions of 100
2.5 U Pwo DNA
reactions of 50
ontainig 2.5 U
lymerase
eactions of 50 l
g 2.5 U Pwo
merase
0 l final volume
perYield DNA
0 l final volume
perYield DNA

Price in

331,90
84,20
51,10
213,80
136,60
547,10
295,60
467,30
118,40
118,40
109,70
84,10
333,70
79,40
188,00
420,50
188,00
420,50
280,60

Alp

Prod

Quic
Read
unlab
react
RNA:
R
Rack
The R
which
Rack
The R
holdi
Rack
The R
Rack
The R
Flow
Rand
Unifo
modi
many
South
rAPid
Rapid
inact
requi
deph
Rapi
Fast,
or blu
fragm
linea
Rapi
Cova
plasm
recirc
just 5
Real
Read
gene
prime
hydro
Real
This 5
Taq D
dTTP
cDNA
Real
For ra
in tw
minu
time
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate

lphabetic
duct Name
ck Spin Columns
dy-to-use disposab
beled or radioactiv
tions. Use in low-s
:<72 bases. Sampl
k Sample Carrier
Rack Sample Carri
h is used for holdi
k Sample Carrier
Rack Sample Carri
ng up to 32 prima
k Tip Carrier, TIP-
Rack Tip Carrier, is
k Tube Carrier Fil
Rack Tube carrier
32 Vial Carriers fo
dom Primed DNA
ormly label plasmid
fied dNTP. High sp
y hybridization tech
hern and northern
d Alkaline Phosp
d, efficient dephos
ivated at +75C fo
ired after restrictio
osphorylated DNA
d DNA Dephos &
efficient dephosph
unt-end DNA frag
ments into plasmid
r DNA, and library
d DNA Ligation K
lently joins sticky-
mid or phage vecto
cularizing linear D
5 minutes at room
Time ready Cata
dy-to-use qPCR ass
expression in rea
ers and a Universa
olysis probe contai
Time ready cDNA
5x concentrated re
DNA Polymerase, r
P), for 40 pre-ampli
A (1 to 250 ng).
Time ready Cell
apid, high-perform
o-step real-time R
tes. Use lysate dire
PCR experiments
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
cal Produ
for radiolabeled
ble columns quickl
vely labeled RNA fr
peed swinging-bu
le size: up to 100
r, SMP-CAR-24-A
er, SMP-CAR-24-A
ng up to 24 prima
r, SMP-CAR-32-A
er, comes in a set
ry sample tubes.
-CAR-480-A00, f
s used for holding
lling
Filling is used to s
or tube loading
A Labeling Kit
d or phage DNA w
pecific activity labe
hniques, including
blots, and in situ
phatase
sphorylation of 5 e
or 2 minutes. No ad
on and dephospho
A directly in ligatio
& Ligation Kit
horylation (10 min
ments. Minimizes
d and phage vector
y generation.
Kit
- or blunt-end DNA
ors, adding linkers
NA. Contains all re
temperature.
alog Assays
says for human, m
l-time PCR. Each a
al ProbeLibrary Pro
ining locked nucle
A Pre-Amp Mast
eady-to-use hot-st
reaction buffer, dN
ification reactions
Lysis Kit
mance gene expres
RT-PCR. Lyse 3 to 3
ectly in cDNA synt
at any throughput
om Panel 384 - 1
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 1
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
uct Index
RNA purification
rom nucleotides an
l.
A00, Set of 4
A00, comes in a se
ry sample tubes.
A00, Set of 3
of 3 each of which
for 480 tips
up to 5 tip trays (9
ecure Rack Sampl
with any [-
32
P]-d
eled DNA probes a
g gene library scree
hybridizations.
ends of DNA and R
dditional purificatio
rylation. Use the
n reactions.
) and ligation (5 m
application times w
rs, linker ligation, r
A fragments for clo
to plasmids or oth
eagents needed fo
mouse and rat gene
assay includes gen
obe, a short FAM-l
eic acid.
ter
tart PCR Master M
NTP mix, (with dUT
of 50 l of small q
ssion studies using
30,000 cells in one
thesis and analyze
.
128
dy-to-use single qP
elect custom assay
128+
dy-to-use qPCR as
wells. Select custo
or.
x
n
rate small
nd labeling
Exclusion limit
et of 4 each of
h is used for
96 tips each).
le Carriers and
dNTP or
are used in
ening,
RNA. Rapidly
on steps
min) of sticky-
when cloning
recircularizing
oning into
her DNAs, and
or ligation in
es to quantify
ne-specific
abeled
Mix contains
TP instead of
quantities of
g cultured cells
e step in 5
e cDNA in real-
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and

Cat. No.

11 274 015 001
04 639 502 001
04 639 529 001
04 639 545 001
04 639 618 001
11 004 760 001
04 898 133 001
04 898 141 001
04 898 117 001
04 898 125 001
11 635 379 001
05 532 957 001
05 583 055 001
06 720 455 001
05 943 523 001
06 366 821 001
05 582 849 001
05 582 865 001

1 rack
1 kit for
1 kit
1 kit
1 kit for up
Catalo
Design
1 kit for up to
reacti
1 kit for up t
reacti
Pack Size

20 columns

set of 4

set of 3

1 rack tip carrier


up to 50 labeling r

1,000 U (1 U/l)
5,000 U (1 U/l)

for up to 160 reac

p to 40 DNA ligatio

og Assays, 300 rea
ner Assays, 300 rea

40 reactions

on volume of 40
on volume of 40

20 plates

20 plates

www.roche
g rack
reactions
tions
ctions
on reactions
actions
actions
ns with a final
l each
ns with a final
l each
e-applied-science

Price in

280,60
inquire
inquire
inquire
inquire
452,70
90,70
363,80
174,60
499,50
286,10
inquire
inquire
600,00
inquire
inquire
inquire
inquire

163

e.com

Alp
164

www.r

Prod

Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
mous
UPL
onlin
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate

lphabetic
roche-applied-sc
duct Name
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
Probe pre-plated i
e Configurator. (+
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
cal Produ
cience.com
om Panel 384 - 1
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 1
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 1
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 1
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 3
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 3
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 3
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 3
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 4
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 4
s 384 contain read
gene expression pr
n wells. Select cus
+ error detection)
om Panel 384 - 6
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 6
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
om Panel 384 - 9
s 384 contain read
genes for gene exp
Configurator.
om Panel 384 - 9
s 384 contain read
gene expression pr
obe pre-plated in w
online Configurato
uct Index
16
dy-to-use single qP
elect custom assay
16+
dy-to-use qPCR as
wells. Select custo
or.
192
dy-to-use single qP
elect custom assay
192+
dy-to-use qPCR as
rofiling +error dete
wells. Select custo
or.
32
dy-to-use single qP
elect custom assay
32+
dy-to-use qPCR as
wells. Select custo
or.
384
dy-to-use single qP
elect custom assay
384+
dy-to-use qPCR as
wells. Select custo
or.
48
dy-to-use single qP
elect custom assay
48+
dy-to-use qPCR as
rofiling. Assays inc
stom assays/plate
64
dy-to-use single qP
elect custom assay
64+
dy-to-use qPCR as
wells. Select custo
or.
96
dy-to-use single qP
elect custom assay
96+
dy-to-use qPCR as
wells. Select custo
or.
x
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
ection . Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
clude primer,
layout with
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and
PCR assays for
Assays include
ys and plate
ssays (human,
tection. Assays
om assays and

Cat. No.

05 583 004 001
05 583 039 001
05 582 652 001
05 582 822 001
05 582 962 001
05 582 989 001
05 532 833 001
05 582 644 001
05 582 911 001
05 582 938 001
05 582 890 001
05 582 903 001
05 582 873 001
05 582 881 001

Pack Size

6 plates

6 plates

40 plates

40 plates

10 plates

10 plates

40 plates

40 plates

10 plates

10 plates

10 plates

10 plates

10 plates

10 plates

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Alp

Prod

Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
with
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Light
huma
prime
layou
Real
Light
huma
prime
layou
Real
Light
mous
inclu
plate
Real
Quan
supe
Pre-p
add s
Real
Quan
pane
inclu
samp
Real
Quan
pane
inclu
samp

lphabetic
duct Name
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
the online Configu
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
an, mouse, or rat g
er, UPL Probe pre-
ut using the online
Time ready Cust
tCycler
480 Plate
de primer, UPL Pro
layout using the o
Time ready Hum
rfamily. Assay pan
plated assays inclu
sample cDNA and
Time ready Hum
de gene-specific p
ple cDNA and mas
Time ready Hum
de gene-specific p
ple cDNA and mas
cal Produ
om Panel 96 - 16
s 96 contain ready
genes for gene exp
Configurator.
om Panel 96 - 16
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 24
s 96 contain ready
genes for gene exp
urator.
om Panel 96 - 24
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 32
s 96 contain ready
genes for gene exp
Configurator.
om Panel 96 - 32
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 48
s 96 contain ready
genes for gene exp
Configurator.
om Panel 96 - 48
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
om Panel 96 - 8
s 96 contain ready
genes for gene exp
Configurator.
om Panel 96 - 96
s 96 contain ready
genes for gene exp
Configurator.
om Panel 96 - 96
s 96 contain ready
gene expression pr
obe pre-plated in w
online Configurato
man ABC Transpo
vels of 42 genes of
nels directly using
ude gene-specific p
master mix.
man Apoptosis Pa
vels of 372 human
ightCycler
480 In
primers and a UPL
ster mix.
man Apoptosis Pa
vels of 84 human a
ightCycler
480 In
primers and a UPL
ster mix.
uct Index
6
y-to-use single qPC
elect custom assay
6+
y-to-use qPCR ass
wells. Select custo
or.
4
y-to-use single qPC
elect custom assay
4+
y-to-use qPCR ass
wells. Select custo
or.
2
y-to-use single qPC
elect custom assay
2+
y-to-use qPCR ass
wells. Select custo
or.
8
y-to-use single qPC
elect custom assay
8+
y-to-use qPCR ass
wells. Select custo
or.
y-to-use single qPC
elect custom assay
6
y-to-use single qPC
elect custom assay
6+
y-to-use qPCR ass
wells. Select custo
or.
orter Panel
f the human ABC t
LightCycler
480 I
primers and a UPL
anel, 384
apoptosis-related
nstruments. Pre-pla
anel, 96
apoptosis-related g
nstruments. Pre-pla
x
CR assays for
Assays include
ys and plate
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys/plate layout
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys and plate
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys and plate
ays (human,
tection. Assays
om assays and
CR assays for
Assays include
ys and plate
CR assays for
Assays include
ys and plate
ays (human,
tection. Assays
om assays and
transporter
Instruments.
L Probe. Just
genes. Assay
ated assays
equire adding
genes. Assay
ated assays
equire adding

Cat. No.

05 532 868 001
05 582 628 001
05 532 884 001
05 582 610 001
05 532 906 001
05 582 598 001
05 532 914 001
05 582 571 001
05 532 850 001
05 532 949 001
05 582 563 001
05 339 324 001
05 339 316 001
05 392 063 001

2 plates (
2 plates (e
2 plates (
Pack Size

6 plates

6 plates

6 plates

6 plates

10 plates

10 plates

10 plates

10 plates

6 plates

10 plates

10 plates

(each containing 9

each containing 38

(each containing 9

www.roche
96 assays)
84 assays)
96 assays)
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

165

e.com

Alp
166

www.r

Prod

Real
Quan
Assay
assay
addin
Real
Quan
gene
plate
requi
Real
Real-
mixes
strain
HA g
Real
Syste
Prem
gene
Detec
If Infl
Real
Syste
Prem
huma
Set fo
extra
Real
Custo
assay
provi
Cat. N
Real
Fast,
using
allow
Optim
Red
Used
lyses
cells
use w
REM
Provi
syste
hybri
Titan
Rest
High
acid
sequ
of rec
Reve
For u
DNA
end l
hybri
Reve
Rapid
cultu
retrov
scree
Reve
For tr
prepa
M-M
Full-l
rGFP
Use a
PAGE
expe
easily
lphabetic
roche-applied-sc
duct Name
Time ready Hum
y panels directly u
ys include gene-sp
ng sample cDNA a
Time ready Hum
s. Assay panels di
d assays include g
ire adding sample
Time ready Inf A
-Time PCR detectio
s. One targets Influ
ns, including 2012
gene of the H1N1 2
Time ready Influ
em
mixed primers and h
s in human sampl
ction Set for multip
luenza A is positive
Time ready Influ
em
mixed primers/hydr
an samples. Use w
or multiplex detect
ction control for h
Time ready Pre-A
om 4x concentrate
y primer pairs, for
de RealTime ready
No. 06 725 309 001
Time ready RNA
highly sensitive, s
g 50-fold concentr
wing fast hot start R
mized for HybProb
Blood Cell Lysis
d for isolate DNA a
red blood cells in
free of red blood c
with other species.
M e System
des subcomponen
ems to automate em
dization procedure
ium series emulsio
triction Protease
ly purified, special
sequence IleGlu
ence may also be
combinant fusion
erse Transcriptas
up to 12 kb first- an
sequencing. Also
abeling of DNA fra
dization, and geno
erse Transcriptas
d, sensitive ELISA
res and other biolo
viruses in infected
ening for RT inhibit
erse Transcriptas
ranscription of RN
aration and synthe
MuLV lacks endonu
ength copies of la
P
as a positive contro
E and western blot
riments involving f
y detected using b
cal Produ
cience.com
man Cell Cycle Re
n levels of 84 gene
sing LightCycler

pecific primers and
and master mix.
man Reference Ge
n levels of 19 hum
rectly using LightC
gene-specific prim
cDNA and master
A/H1N1 Detection
on set containing 2
uenza A Matrix Pro
point mutation. Th
2009 strain.
enza B Detection
hydrolysis probe fo
es. Use with RealT
plex detection/diff
e, the H1N1 test ca
enza B Detection
olysis probe detec
with RealTime read
tion/differentiation
uman nucleic acid
Amp Primer Poo
ed solution of 6-96
40 pre-amplificatio
y Custom Assay Co
1 when ordering.
Virus Master
pecific real-time o
ated mix of Transc
RT-PCR. No need t
e, hydrolysis and U
Buffer
and RNA, this read
human whole blo
cells, for use in do

nts and software to
mPCR enrichment
es in the GS FLX w
on oil formats.
Factor Xa
quality serine pro
GlyArg with a
used as a restricti
proteins.
se AMV
nd second-strand
used for primer ex
agments, generati
omic footprint expe
se Assay, colorim
for quantitative de
ogical samples. De
mammalian cells
tors.
se M-MuLV
A fragments up to
esis of 1st-strand c
uclease activity and
arge mRNA are obt
ol when detecting
t analysis. It can al
fluorescence micro
blue or UV light.
uct Index
egulation Panel
es in human cell cy
480 Instruments.
d a UPL Probe, and
ene Panel
an genes to use as
Cycler
480 Instru
ers and a UPL Pro
r mix.
n Set
2 highly specific p
otein M2 to detect
he other targets He
n Set, LightCycle
or detecting Influe
Time ready Influenz
ferentiation of Influ
an be run.
n Set, LightCycle
ct Influenza B viral
y Influenza A/H1N
n of Influenza A an
d.
l
6 different designer
on reactions of 50
onfiguration Numb
one-step RT-PCR o
criptor/Taq, and a
to heat preactivate
UPL probes.
y-to-use buffer pr
od, yielding intact
wnstream applicat
o install onto liquid
and sequencing p
workflow. Supports
otease, recognizing
a high degree of s
on cleavage site fo
cDNA synthesis a
xtension, RNA seq
on of single-strand
eriments.
metric
etermination of RT
etermine propagat
in culture. Also us
o 10 kb. Use in cDN
cDNA for RT-PCR.
d has lower RNase
tained.
GFP Fusion Protei
so be used as a st
oscopy. rGFP fluore
x
ycle regulation.
Pre-plated
d only require
s reference
ments. Pre-
obe, and only
rimer/probe
t all influenza A
emagglutinin
er
2.0
nza B viral
za A/H1N1
uenza A and B.
er
480
genes in
N1 Detection
nd B, with an
r-specific
l each;
ber with the
of viral RNA
unique buffer
e Taq.
referentially
white blood
tions. Not for
d handling
primer
s all GS FLX
g the amino
pecificity. This
or processing
nd dideoxy
quencing, 3'-
ded probes for
activity in cell
tion of
sed for in vitro
NA library
Unlike AMV,
e H activity.
ins by SDS-
tandard for
escence is

Cat. No.

05 339 359 001
05 339 545 001
05 467 675 001
05 640 393 001
06 480 543 001
06 480 560 001
06 725 309 001
05 619 416 001
05 992 877 001
06 754 155 001
11 814 389 001
05 976 120 001
11 179 896 001
11 585 924 001
10 109 118 001
11 468 120 910
11 062 603 001
11 814 524 001

2 plates (
2 plates (
2 plates (e
for up to 2
fo
fo
1 kit for up
1,0
100 ml (for 50
sam
1 k
Pack Size

(each containing 9

(each containing 9
each containing 38

2x 100 reactions (2

r up to 100 reactio

r up to 100 reactio

40 reactions

000 reactions 20
200 reactions
0 to 500 reactions,
mple size 1 to 500

1 system

3 x 250 g
3 x 100 g

1,000 U


500 U

50 g (1 mg/ml)

96 assays)
96 assays)
84 assays)
20 l each)
ons
ons
(20 l each)
0 l
depending on
l)
ests

Price in

inquire
inquire
inquire
inquire
inquire
inquire
200,00
inquire
inquire
inquire
51,00
inquire
1.064,70
765,50
490,40
594,10
231,50
197,40

Alp

Prod

Ribo
Suita
DNA
ATP,
solut
RNA
For s
synth
hybri
RNA
RNA
size s
nucle
RNA
RNA
size s
nucle
RNA
RNA
size s
nucle
RNA
16S-
gel e
struc
RNA
For s
prote
polyp
proce
RNA
Easy-
For s
bone
long-
RNas
RNas
RNA.
RNas
RNas
that a
isolat
RNas
Cleav
of DN
site-s
and r
RNas
Use R
RNA
solut
RNas
Effici
prepa
deoxy
a boi
Rsa
Reco
ends
howe
inhib

lphabetic
duct Name
onucleoside Triph
able for in vitro tra
sequencing. This
CTP, GTP, and TTP
A
tudies which use n
hesizing system. Th
dization.
A Molecular Weig
Molecular Weight
standard in northe
A Molecular Weig
Molecular Weight
standard in northe
A Molecular Weig
Molecular Weight
standard in northe
A, 16S- and 23S-r
and 23S-ribosoma
lectrophoresis and
cture and function
A, MS2
tructural/functiona
ein-synthesizing sy
peptide synthesis. A
edures.
A/DNA Stabilizati
-to-use reagent fo
imultaneous cell ly
e marrow samples.
-term storage.
se
se from bovine pan
. This is a crude m
se A
se A from bovine p
acts on single-stra
tion of DNA. For D
se H
ves RNA in RNA:D
NA synthesis, elim
specific cleavage o
removal of poly (A)
se T1
RNase T1 from Asp
fingerprinting; sup
ion, pH 6.
se, DNase-free
ently removes con
arations. Heteroge
yribonuclease. Use
ling step. Solution
I
ognizes the sequen
. Rsa I is not inhib
ever, the presence
iting as indicated
cal Produ
hosphate Set
nscription reaction
special quality set
P, each containing
salt (pH 7).
natural RNA in a in
he product is also
ght Marker I, DIG
t Marker I, digoxig
nd detection. Size
ght Marker II, DIG
t Marker II, digoxig
nd detection. Size
ght Marker III, DI
t Marker III, digoxi
nd detection. Size
ribosomal
al RNA is used as
d ultracentrifugatio
of ribosomes.
al studies using na
ystems, initiation, e
Also used as a car
on Reagent for B
r collection of sam
ysis and stabilizatio
Also ideal for nuc
ncreas is used for
ixture of RNases.
pancreas is a pyrim
anded RNA. For an
DNA isolation, RNa
DNA hybrids. Use in
ination of mRNA in
of RNA, detection o
) sequences of mR
pergillus oryzae fo
pplied as a supens
ntaminating RNA fr
eneous mixture of r
e directly in any D
: 500 g/ml.
nce GT*AC and g
ited by the presen
of 6-methyladenin
(*). Isoschizomers:
uct Index
ns and RNA polym
t consists of 4 sepa
g a 100 mM clear, c
n vivo and in vitro
used as a carrier R
G-labeled
enin (DIG)-labeled
hen the DIG System
range: 0.3 to 6.9 k
G-labeled
genin (DIG)-labele
hen the DIG System
range: 1.5 to 6.9 k
G-labeled
genin (DIG)-labele
hen the DIG System
range: 0.3 to 1.5 k
a molecular weigh
on; also used to stu
atural RNA in in viv
elongation, and ter
rrier in sensitive RN
Blood/Bone Marr
mples for nucleic ac
on of nucleic acids
cleic acid stabilizat
the removal and d
midine-specific end
nalytical purposes a
ase A needs to be b
n in vivo RNA-prim
n 2nd-strand cDN
of RNA:DNA regio
RNA.
or RNA sequence a
sion in 3.2 M amm
rom plasmid or ge
ribonucleases, pre
NA isolation techn
generates fragmen
ce of 5-methylcyto
ne or 4-methylcyto
: Afa I.
x
merase-directed
arate vials of
colorless
protein-
RNA in in situ
d is used as a
m is used for
kb.
d is used as a
m is used for
kb.
ed is used as a
m is used for
kb.
ht standard in
udy the
vo and in vitro
rmination of
NA purification
row
cid isolation.
s in blood and
tion during
degradation of
doribonuclease
and for
boiled.
med initiation
A synthesis,
ons in dsDNA,
analysis and
onium sulfate
enomic DNA
epared free of
nique, without
nts with blunt
osine (),
osine is

Cat. No.

11 277 057 001
10 109 223 001
11 526 529 910
11 526 537 910
11 373 099 910
10 206 938 001
10 165 948 001
11 934 317 001
10 109 134 001
10 109 142 001
10 109 169 001
10 786 357 001
10 109 193 001
11 119 915 001
10 729 124 001
10 729 132 001
11 047 671 001

4 x 200 l
1
5
500 ml (for
Pack Size

(4 x 20 mol, 100

100 g

4 g (200 l)

2 g (200 l)

2 g (200 l)

ml (100 A
260
units

500 l (10 A
260
unit

r up to 50 ml samp

500 mg

25 mg
100 mg

100 U

100,000 U

500 g (1 ml)

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)

www.roche
mM, each)
s)
ts)
ple material)

e-applied-science

Price in

222,30
66,60
355,50
392,50
322,50
129,20
123,10
96,10
128,50
37,70
101,40
388,00
60,70
154,00
72,80
291,00
291,00

167

e.com

Alp
168

www.r

Prod

S
Sac
Reco
cohe
meth
(). Is
Sal I
Sal I
5-co
meth
Isosc
Sau3
Reco
termi
5- an
Isosc
Sca
Sca I
blunt
indic
SEAP
Simp
medi
easily
samp
SeqC
Comp
Libra
hybri
Grad
SeqC
High
custo
reseq
unifo
SeqC
High
custo
reseq
unifo
SeqC
Provi
huma
costs
50 M

lphabetic
roche-applied-sc
duct Name
I (Sst I)
ognizes the sequen
hylcytosine at the o
soschizomers: Psp1
recognizes the seq
ohesive termini. Sa
hyladenine within t
chizomers: none kn
3A I
ognizes sequence
ini. No inhibition b
nd 4-methylcytosin
chizomers: Mbo I, N
I
recognizes the se
t ends. Sca I is not
ated (). Isoschizo
P Reporter Gene
ple, fast, sensitive a
um of transfected
y sampled and ass
pling of medium or
Cap EZ Accessor
ponents for proces
aries; includes COT
dization and High
e Water for LM-PC
Cap EZ Choice Li
omer-defined disea
quencing studies. S
orm capture of targ
Cap EZ Choice XL
omer-defined disea
quencing studies. S
orm capture of targ
Cap EZ Develope
des custom oligon
an genomes for cu
s by achieving high
Mb. Flexible design
cal Produ
cience.com
nce GAG*CTC an
ited by 5-methylcy
other C does not in
124B I, Sst I.
quence GT*CG*A
l I is inhibited by 5
he recognition seq
nown.
GAT*C. Generate
by dam gene which
ne, 5-hydroxymethy
Nde II, Dpn II and
equence AGTAC
inhibited by the p
mers: Ass I, BmcA
Assay, chemilum
assay measures se
cells. SEAP is sec
sayed. Eliminating
r other analysis.
ry Kit
ssing sequence ca
T DNA to block rep
Fidelity PCR Mast
CR during pre/pos
ibrary
e design, and easy
ase related regions
Save on costs by a
get regions up to 7
L Library
e design, and easy
ase related regions
Save on costs by a
get regions up to 5
er Library
nucleotide libraries
ustomer-developed
hly specific, uniform
captures regions i
uct Index
nd generates fragm
ytosine at the centr
nhibit, nor does 6-m
AC and generates f
5-methylcytosine a
quence as indicate
es fragments with
h methylates N6 of
ylcytosine inhibit a
others.
CT and generates fr
presence of 5-meth
A I, Zrm I.
minescent
creted placental A
reted into the supe
cell lysis allows re
apture using SeqCa
petitive regions du
ter, TS-PCR Oligos
st capture amplifica
-to-use solution ca
s in the human ge
achieving highly sp
7 Mb.
-to-use solution ca
s in the human ge
achieving highly sp
50 Mb.
s for target regions
d capture protocol
m capture of targe
in any genome.
x
ments with 3-
ral C (*). 5-
methyladenine
fragments with
and N6-
ed (*).
5-cohesive
f adenine ().
at C(*).
ragments with
hylcytosine, as
AP in culture
ernatant and is
peated
ap EZ
ring
s, and PCR
ation.
aptures
enome for
pecific and
aptures
enome for
pecific and
s in non-
s. Reduce
et regions up to

Cat. No.

10 669 792 001
10 669 806 001
11 047 655 001
10 348 783 001
10 567 663 001
11 047 612 001
10 709 751 001
10 775 266 001
11 779 842 001
06 776 302 001
06 776 345 001
06 740 251 001
06 266 282 001
06 266 304 001
06 266 312 001
06 266 339 001
06 266 347 001
06 266 355 001
06 740 260 001
06 266 363 001
06 266 371 001
06 266 380 001
06 266 398 001
06 266 401 001
06 266 517 001
06 740 278 001
06 471 684 001
06 471 706 001
06 471 714 001
06 471 722 001
06 471 749 001
06 471 757 001

1 kit for 500 a
250
Pack Size

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)
500 U (10 U/l)
2,500 U (10 U/l)
2,500 U (40 U/l)
500 U (1 - 5 U/l)

2,500 U (10 U/l)

assays, microplate
0 assays, tube form

24 reactions
96 reactions

4 reactions
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions
4 reactions
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions
4 reactions
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions

)

formate, or for
mate

Price in

90,90
340,00
340,00
53,40
203,60
203,60
185,40
261,90
458,70
600,00
2.400,00
4.900,00
10.080,00
15.120,00
20.160,00
21.773,00
58.061,00
80.640,00
5.200,00
12.096,00
18.144,00
30.240,00
48.384,00
129.024,00
241.920,00
5.200,00
12.096,00
18.144,00
30.240,00
48.384,00
129.024,00
241.920,00

Alp

Prod

SeqC
Use t
when
Reag
produ
SeqC
Custo
of cu
comp
captu
SeqC
Use t
solut
solut
Exom
SeqC
Kit A
secon
TruSe
barco
SeqC
Kit B
secon
TruSe
barco
SeqC
2.1 m
tube.
ident
popu
SeqC
For e
variat
sequ
and d
SeqC
The N
for Se
steps
SeqC
SeqC
Conv
captu
ampl
for hi
SeqC
Comp
sequ
every
Acce
SeqC
For o
SexA
SexA
with
(*). Is
Sfi I
Analy
GGC
Inhib
Cs is
Sfu I
Reco
cohe
insen
BspT
Simp
For in
muta
estab
flexib
lphabetic
duct Name
Cap EZ Develope
this universal reag
n species-specific
gent is for use spec
ucts.
Cap EZ Exome Pl
omize your target e
stom target region
pared to other targ
ure efficiency.
Cap EZ Exome+U
the most compreh
ion to discover mo
ions, with the supe
me 2.1M overlappin
Cap EZ HE-Oligo
is used to block li
ndary capture. For
eq Library Kit A. In
ode 1-12 samples
Cap EZ HE-Oligo
is used to block li
ndary capture. For
eq Library Kit B. In
ode 13-24 samples
Cap EZ Human Ex
million stable in-sol
Optimization tool
tify mutations for g
ulation genetics an
Cap EZ Human Ex
exome resequencin
tions in the genom
encing. Allows res
detect more signifi
Cap EZ Hybridiza
NimbleGen SeqCa
eqCap EZ product
s are supplied in o
Cap EZ Exome.
Cap EZ Pure Cap
venient set of captu
ure and to isolate a
ification. Use this
igh-quality sequen
Cap EZ Reagent K
plete reagent start
ence capture usin
ything you need fo
essory Kit, and Hyb
Cap EZ Reagent K
ordering informatio
A I
AI recognizes the se
5'-cohesive termin
soschizomers: Mab
yze and clone larg
C*CNNNNNGGC
bited by 5-methylcy
not inhibiting ().
I (Asu II)
ognizes the sequen
nsitive to 5-methylc
T104 I, BstB I, Csp4
pleProbe 519 Lab
nternal labeling of
ation detection pro
blished methods, la
bility.
cal Produ
er Reagent
ent to block repeti
Cot-1 DNA is not
cifically with Roche
us Library
enrichment discov
ns to EZ Exome v3
get enrichment sol
UTR Library
ensive cost-effecti
ore variants compa
erior capture effici
ng probes.
Kit A
ibrary adapters in
r labs performing s
ncludes hybridizati
and PCR Grade W
Kit B
brary adapters in
r labs performing s
ncludes hybridizatio
s and PCR Grade W
xome Library v2.
lution DNA probes
for next-gen work
genetic disorders a
d pharmacogenet
xome Library v3.
ng, a powerful tech
me at a fraction of t
searchers added fle
icant variations.
ation and Wash K
p EZ Hybridization
ts. All buffers for th
ne convenient kit,
pture Bead Kit
ure and purificatio
a DNA sample libr
sensitive and robu
ncing results.
Kit
ter kit (24 reaction
g Illumina Sequen
r target enrichmen
bridization and Was
Kit Plus
on contact your loc
equence AC*C(T
ni. SexA I is dcm m
b I.
e DNA fragments.
CC. Generates frag
ytosine at central C
Isoschizomers: no
nce TTCG*AA an
ited by 6-methylad
cytosine (). Isosch
45 I, Nsp V.
beling Reagent
oligonucleotide p
bes using LightCy
abeling is done in
uct Index
itive regions in the
available. SeqCap
e SeqCap EZ Deve
very tool by adding
to discover more
utions, for cost-eff
ive exome and UTR
ared to other targe
ency of SeqCap EZ
hybridization to pr
sequence capture w
on enhancing (HE
Water.
hybridization to pr
sequence capture w
on enhancing (HE
Water.
0
s to capture all Ref
kflows enables new
and discover varian
ics.
0
hnique to identify f
the cost of whole g
exibility to analyze
Kit
n and Wash Kit is a
he hybridization an
configured specifi
on beads to preven
rary from contamin
ust method for clea
s) for customers p
ncing Systems. Eas
nt. Includes HE-Oli
sh Kit.
cal representative.
T,A)GGT and gener
methylation sensitiv
. Recognizes the se
gments with 3-co
C (*). 5-methylcyto
one.
nd generates fragm
denine as indicated
hizomers: Bpu14 I,
robes detected at
ycler
Systems. Co
a single step with
x
e genome
EZ Developer
eloper
g up to 50 Mb
variants
fective superior
R enrichment
et enrichment
Z Human
revent
with Illumina
E) oligos to
revent
with Illumina
) oligos to
fSeq exons in 1
w discoveries:
nts in
functional
genome
e more samples
a reagent kit
nd washing
ically for the
nt secondary
nants during
anup of DNA
performing
sily order
igo Kit A,
rates fragments
ve as indicated
equence
hesive termini.
osine at other
ments with 5-
d (*), but is
Bsp119 I,
519 nm for
ompared to
greater

Cat. No.

06 684 335 001
06 740 189 001
06 740 235 001
06 740 243 001
06 740 294 001
06 740 308 001
06 777 287 001
06 777 317 001
05 860 482 001
05 860 504 001
06 465 684 001
06 465 692 001
05 634 261 001
05 634 253 001
06 977 952 001
06 953 212 001
06 953 247 001
11 497 995 001
11 288 024 001
11 288 059 001
11 243 497 001
04 687 132 001

Pack Size

1 ml

12 reactions
48 reactions
96 reactions
4 reactions
48 reactions

96 reactions

96 reactions

4 reactions
48 reactions

4 reactions
48 reactions

24 reactions
96 reactions

24 reactions

24 reactions

1 kit
200 U (10 U/l)

1,250 U (10 U/l)
5,000 U (40 U/l)

2,000 U (10 U/l)

100 mol

www.roche

e-applied-science

Price in

270,00
6.780,00
24.000,00
38.000,00
2.500,00
24.000,00
1.150,00
1.200,00
3.360,00
20.160,00
3.360,00
20.160,00
126,00
269,00
460,00
1.530,00
inquire
152,30
240,90
792,40
103,40
inquire

169

e.com

Alp
170

www.r

Prod

Sma
Reco
Not i
other
Neos
Sodi
Pure
appli
Solid
The S
Samp
Sorb
Redu
relate
SP6
Trans
prom
Use l
prote
SP6/
For in
SP6 o
nonra
hybri
Spe
Reco
cohe
and 5
I, Ahl
Sph
Reco
cohe
meth
hydro
-Ga
Quan
with
prote
enco
-Ga
Quan
with
techn
extra
-Ga
Optim
sectio
produ
Ssp
Ssp I
blunt
as ind
Stau
Most
depe
effec
, diac
Stora
Box w
stora
Strep
Polyd
biotin
partic
succe

lphabetic
roche-applied-sc
duct Name
I
ognizes sequence*C
nhibited by 5-meth
r positions or 4-me
schizomers: Cfr9 I,
um Dodecyl Sulf
quality preparatio
cations as a denat
d Waste Bag
Solid Waste Bag ho
ple Handling Instru
bitol Dehydrogen
uces L-iditol to L-s
ed sugar alcohols.
RNA Polymerase
scribe RNA from c
moter. Perform synt
abeled RNA in DN
ection, and synthes
/T7 Transcription
n vitro transcriptio
or T7 promoter. Sy
adioactively labele
dizations, genomic
I
ognizes the sequen
sive termini. Spe I
5-methylcytosine
l I.
I
ognizes the sequen
hylcytosine at 3'-C(
oxymethylcytosine
al ELISA
ntitatively measure
a plasmid bearing
eins produced by in
ding DNA constru
al Reporter Gene
ntify -Gal expres
the -Gal-encodi
nology to detect ap
cts.
al Staining Set
mized staining set
ons demonstrating
uct can be seen by
I
recognizes the se
t ends. The enzyme
dicated (*). Isosch
urosporine
t potent PKC inhib
ndent protein kina
tively than with er
cylglycerol, or phos
age Box
with removable sty
ge of 50 microcen
ptavidin Magneti
disperse paramagn
n-labeled molecule
cles/ml. Magnetic
essfully used in ma
cal Produ
cience.com
CC*CGGG. Gene
hylcytosine at mid
ethylcytosine in eit
TspM I, Xma I, Xm
fate (SDS)
n, suitable in most
turing agent for pr
olds the waste pro
ument.
ase (SDH)
orbose. Also acts o
Allows the reduct
e
cloned DNA templa
thesis with labeled
NA/RNA blots, in s
sis of capped RNA
n Kit
on of DNA sequenc
ynthesize labeled R
ed ribonucleotides.
c sequencing, and
nce *A*CTAGT an
is inhibited by the
( mA?m CTAGT) a
nce GC*ATG?C. G
ited by 6-methylad
() or simultaneous
at both Cs. Isosch
e -Gal expression
a -Gal-encodin
n-frame cloning in
uct.
e Assay, chemilum
ssion in eukaryotic
ing lacZ reporter g
pproximately 20 fg
for the histochem
g -galactosidase
y the naked eye or
equence AAT*ATT
e is inhibited by th
izomers: none kno
itor known. Also in
ases. Protein tyrosi
bstatin and genist
spholipids.
yrofoam insert (0.5
ntrifuge tubes. Tem
ic Particles
netic particles for f
es. Supplied in sus
separation of biot
any applications.
uct Index
erates fragments w
dle C(). 5-methylc
ther position inhibi
maC I.
t routine electroph
roteins.
oducts of the FLOW
on D-glucitol and
tion of ketones to p
ates downstream f
d NTPs to generate
situ hybridization, R
A in vitro .
ces cloned downst
RNA using radioact
. Use in DNA/RNA
S1 nuclease stud
nd generates fragm
e presence of N6-m
as shown (*) . Isosc
enerates fragment
denine(*). No inhib
s presence of 5-
hizomers: Bbu I, Pa
n in eukaryotic cel
ng reporter gene. Q
nto an appropriate
minescent
cells transfected w
gene. Use chemilu
-galactosidase
ical staining of cel
e activity. The -g
r using light micros
T and generates fr
he presence of 6-m
own.
nhibits cAMP- and
ine kinases are blo
ein. Does not com
to 2.0 ml capacity
mperature-resistant
fast separation of a
spension, containin
in-labeled molecu
x
with blunt ends.
cytosine at
its(*).
horetic
W Primary
other closely
polyols.
from an SP6
e labeled RNA.
RNase
tream of the
tive or
A
ies.
ments with 5'-
methyladenine
chizomers: Bcu
ts with 3-
bition by 5-
ae I
ls transfected
Quantify fusion
-Gal
with a plasmid
uminescence
in cell
ls and tissue
al reaction
scopy.
ragments with
methyladenine
d cGMP-
ocked more
mpete with Ca
2+

y) for the
t to -70C.
a variety of
ng 10 mg
les is

Cat. No.

10 220 566 001
10 656 348 001
11 047 639 001
11 667 289 001
05 530 873 001
10 109 339 001
10 810 274 001
11 487 671 001
10 999 644 001
11 008 943 001
11 008 951 001
11 207 644 001
10 606 120 001
11 026 534 001
11 026 542 001
11 026 950 001
11 539 426 001
11 758 241 001
11 828 673 001
10 972 975 001
11 055 682 001
10 800 058 001
11 641 778 001
11 641 786 001

10 m
1 kit for up t
1 k
1 kit for 500 as
1 set for up
Pack Size

1,000 U (10 U/l)
5,000 U (10 U/l)
5,000 U (40 U/l)
1 kg

25 per roll

mg (60 mg lyophiliz

1,000 U
5,000 U


200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (40 U/l)
500 U (10 U/l)
2,500 U (10 U/l)
2,500 U (40 U/l)
200 U (10 U/l)

ssays (microplate),
(tube format)


1,000 U (10 U/l)

500 g

1 box

2 ml
10 ml

zate)
tion reactions

ests
, for 250 assays
5 cm dishes

Price in

104,60
365,00
365,00
359,50
inquire
312,10
111,90
433,40
587,00
90,90
351,40
351,40
268,20
931,20
931,20
121,70
456,00
458,70
200,00
269,40
426,00
7,40
189,80
719,10

Alp

Prod

Strep
Ideal
vitro
High
the m
Strep
Use S
solid
hapte
detec
Strep
Use S
immu
and w
phos
Strep
Use S
immu
and w
phos
Strep
Use S
immu
coval
Strep
Use S
immu
Strep
Strep
Strep
and f
steril
for ce
Strep
Strep
for co
steril
suita
Strep
Strep
bindi
immu
Not s
Strep
Strep
are u
Plate
coati
Strip
Strip
therm
cDNA
Caps
Stu I
Stu I
blunt
indic
SuRE
10x o
selec
Tris-a
mM d
SuRE
10x o
deter
diges
merc

lphabetic
duct Name
ptavidin Mutein M
for gentle purifica
expressed biotiny
binding capacity a
matrix.
ptavidin, recomb
Streptavidin, recom
phases (e.g., micr
ens and antibodies
ction systems.
ptavidin-AP
Streptavidin-AP to
unohistocytochem
western blotting. S
phatase. Supplied
ptavidin-AP
Streptavidin-AP to
unohistocytochem
western blotting. S
phatase. Supplied
ptavidin--Gal
Streptavidin--Ga
unohistocytochem
lently coupled to
ptavidin-POD
Streptavidin-POD t
unohistocytochem
ptavidin is covalent
ptaWell (transpa
fluorescent protein
ization procedure
ell culture purpose
ptaWell (transpa
olorimetric and flu
e as sterilization p
ble for cell culture
ptaWell, High Bin
ng capacity are us
unoassays. Not ste
suitable in cell cult
ptaWell, High Bin
used in colorimetric
s are not sterile as
ng. Not suitable fo
p PCR Tubes and
PCR Tubes and C
mal cyclers; design
A synthesis, and se
s are DNase- and R
I
recognizes the seq
t ends. Stu I is inhi
ated (*). Isoschizo
E/Cut Buffer A
optimized incubatio
ct 100% activity or
acetate, 660 mM p
dithiothreitol, pH 7
E/Cut Buffer B
optimized incubatio
rmined to select 10
sts. 100 mM Tris-H
captoethanol, pH 8
cal Produ
Matrix
ation of biotinylate
ylated proteins usin
and multiple reuse
binant
mbinant from Strep
roplates, beads etc
s in universal imm
detect biotinylate
istry,
as clear, colorless
detect biotinylate
istry, ISH,
as a clear, colorle
al to detect biotiny
istry, and western
-galactosidase fr
tly coupled to hors
arent 96-well)
in-coated micropla
n immunoassays. T
would impair the s
es.
arent, 12 x 8-well
in-coated micropla
orescent protein im
rocedures impair t
e.
nd (transparent,
in-coated micropla
sed in colorimetric
erile as sterilization
ture.
nd (transparent,
in-coated micropla
c and fluorescent n
s sterilization proce
or cell culture.
Caps
aps, either 8 or 12
ned for rapid, optim
equencing and cyc
RNase-free.
quence AGG*C*C
bited by the prese
mers: Aat I, Eco14
on buffer for RE di
to calculate activit
potassium-acetate,
7.9 (at +37C).
HCl, 1 M NaCl, 50 m
.0 (at +37C).
uct Index
d proteins. Tested
ng RTS AviTag Bio
e permits cost-effe
ptomyces avidinii f
c.), as well with bio
unological streptav
d compounds usin
s solution.
d nucleic acids in
ess solution.
ylated compounds
blotting. Streptavid
rom E. coli .
ted compounds in
dization, and weste
seradish peroxidas
ates can be used f
The plates are not
streptavidin coatin
l strips)
mmunoassays. The
the streptavidin co
12 x 8-well strips
c and fluorescent n
n impairs streptavid
96-well)
ates with high bind
nucleic acid immu
edures impair stre
tubes per strip, ar
mal heat transfer in
cle sequencing. PC
CT and generates f
ence of 5-methylcy
7 I, Pce I, SseB I.
igests. Activity dete
ty in double-digest
, 100 mM magnesi
cition digests. Act
mM MgCl
2
, 10 mM
x
for use with in
otinylation Kits.
ective use of
for coating of
otin-labeled
vidin/biotin
ng ELISA,
alkaline
ELISA,
alkaline
in ELISA,
din is
ELISA,
ern blotting.
se.
or colorimetric
sterile as any
ng. Not suitable
trips) are used
e plates are not
oating. Not
s)
trips) with high
nucleic acid
din coating.
ding capacity
unoassays.
ptavidin
re used in
n PCR, RT-PCR,
CR Tubes and
fragments with
ytosine as
ermined to
ts. 330 mM
ium acetate, 5
tivity
n double-
M 2-

Cat. No.

03 708 152 001
11 721 666 001
11 721 674 001
11 089 161 001
11 093 266 910
11 112 481 001
11 089 153 001
11 734 776 001
11 664 778 001
11 645 692 001
11 989 685 001
11 667 009 001
10 753 351 001
11 047 680 001
11 417 959 001
11 417 967 001

5 m
1
5 plates (
5 plates (
1
125
Pack Size


1 mg
5 mg

1,000 U (1 ml)

150 U (200 l)

500 U

500 U

15 plates (96 wells



15 plates (96 wells


500 U (10 U/l)
2,500 U (40 U/l)

5 x 1 ml

5 x 1 ml

www.roche
ume
s)
and frame)
and frame)
s)
trip)

e-applied-science

Price in

445,60
155,40
569,20
336,20
139,90
279,20
239,40
745,00
317,00
229,20
657,00
187,60
78,50
314,90
25,80
25,80

171

e.com

Alp
172

www.r

Prod

SuRE
10x o
deter
diges
dithio
SuRE
10x o
deter
diges
(at +
SuRE
10x o
deter
diges
dithio
SuRE
One s
and H
been
activi
Swa
Swa
with
geno
Isosc
T
T3 R
Trans
prom
Use l
synth
T4 D
Use T
Catal
hydro
nicks
T4 D
Labe
hybri
must
Gene
T4 G
Singl
stimu
DNA
and t
T4 P
Phos
RNA
CMP
label
T7 R
Trans
prom
Use R
synth
Taq D
Taq D
rigoro
ready
prime

lphabetic
roche-applied-sc
duct Name
E/Cut Buffer H
optimized incubatio
rmined to select 10
sts. 500 mM Tris-H
oerythritol, pH 7.5
E/Cut Buffer L
optimized incubatio
rmined to select 10
sts. 100 mM Tris-H
37C).
E/Cut Buffer M
optimized incubatio
rmined to select 10
sts. 100 mM Tris-H
oerythritol, pH 7.5
E/Cut Buffer Set
set containing 1 m
H for DNA restricti
determined in eac
ity in double-diges
I
I recognizes the se
blunt ends. The en
omes. No informati
chizomers: Smi I.
RNA Polymerase
scribe RNA from c
moter. Perform synt
abeled RNA in RN
hesis of capped RN
DNA Ligase
T4 DNA ligase to jo
lyzes formation of
oxyl- and 5'-phosp
s in dsDNA are als
DNA Polymerase
l 3'-termini of DNA
dization probe. DN
t have 5-protrudin
e 32 Protein in site-
Gene 32 Protein
e-strand-specific
ulate in vitro DNA
or RNA. It is also
to help RE digests
olynucleotide Kin
phorylate 5'-hydro
and DNA, 3' ends
, forming 5'[
32
P]pC
ing of RNA with T4
RNA Polymerase
scribe RNA from c
moter. Perform synt
RNA in RNA/DNA
hesis, and synthesi
DNA Polymerase
DNA Polymerase, d
ously tested prepa
y-to-use PCR Nucl
er-extension react
cal Produ
cience.com
HCl, 1 M NaCl, 100
(at +37C).
HCl, 100 mM MgCl
HCl, 500 mM NaCl,
(at +37C).
for Restriction E
ml 10x solutions ea
ion digests. Activit
ch buffer to select
sts.
equence ATTTAA
nzyme is very usefu
on is available con
cloned DNA templa
thesis with labeled
NA/DNA blots, ISH
NA in vitro with m7
oin sticky- or blun
phosphodiester bo
phate ends in doub
o closed by T4 DN
A, producing highl
NA labeled with re
ng ends. Blunt-end
-directed mutagen
DNA-binding prot
synthesis, and stab
used in site-specif
go to completion.
nase, 3'-phospha
oxyl ends of oligon
s of RNA, and add
Cp. This substrate
4 RNA ligase.
cloned DNA templa
thesis with labeled
blots, ISH, RNase
s of capped RNA
e (1 U/l), dNTPa
dNTPack combine
aration (1U/l) of r
leotide Mix. Use fo
ions (sequencing,
uct Index
cition digests. Act
mM MgCl
2
, 10 m
cition digests. Act
2
, 10 mM dithioery
cition digests. Act
100 mM MgCl
2
, 1
nzymes
ch of SuRE/Cut Bu
ty of all restriction
t 100% activity or to
AAT and generates
ul for digesting GC
ncerning methylati
ate downstream fr
d NTPs, generating
, RNase protection
7GpppG or m7Gpp
t-ended DNA frag
onds between neig
ble-stranded DNA.
NA Ligase.
ly labeled DNA for
ecombinant T4 DNA
d DNA will not wor
nesis.
tein used to optimi
bilize single-strand
fic mutagenesis ex
atase free
ucleotides and link
a 5'[
32
P]-terminal
is commonly used
ate downstream fr
d NTPs, generating
protection, microa
in vitro .
ack
es our low concent
ecombinant Taq w
or PCR, RT-PCR, an
labeling).
x
tivity
n double-
mM
tivity
n double-
ythritol, pH 7.5
tivity
n double-
10 mM
uffer A, B, L, M,
enzymes has
o calculate
s fragments
C-rich bacterial
on sensitivity.
rom a T3
g labeled RNA.
n, and
ppA.
gments.
ghboring 3'-
. Single-strand
r use as
A Polymerase
rk. Use with T4
ize PCR,
ded regions of
xperiments,
kers, 5' ends of
label to 3'-
d for 3'-end
rom a T7
g labeled RNA.
array target
tration,
with convenient,
nd other

Cat. No.

11 417 991 001
11 417 975 001
11 417 983 001
11 082 035 001
11 371 517 001
11 031 163 001
11 031 171 001
10 481 220 001
10 716 359 001
10 799 009 001
11 004 786 001
11 004 794 001
10 972 983 001
10 972 991 001
10 709 557 001
10 838 292 001
10 881 767 001
10 881 775 001
04 738 225 001
04 738 241 001

250 U for up
volume eac
1,000 U (4 x 25
20 l final vo
Pack Size

5 x 1 ml

5 x 1 ml

5 x 1 ml

1 set

200 U (10 U/l)

1,000 U
5,000 U

100 U (1 U/l)
500 U (1 U/l)
500 U (5 U/l)
100 U
500 U

100 g
500 g

200 U
1,000 U

1,000 U
5,000 U

p to 500 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase

of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq

Price in

25,80
25,80
25,80
23,40
103,40
111,90
433,40
87,20
275,50
275,50
204,10
771,90
189,20
755,80
306,80
947,10
111,90
433,40
202,60
640,50

Alp

Prod

Taq D
Lowe
conve
conc
exten
Taq D
Taq D
produ
PCR,
label
Taq D
Taq D
prepa
PCR
react
Taq D
Manu
docu
in ph
prime
.
Taq I
Taq l
cohe
indic
T elo
Quali
tube
biotin
micro
T elo
Sens
activi
PCR
meas
T elo
Use i
telom
from
deter
Term
Add
fragm
and 3
ddNT

lphabetic
duct Name
DNA Polymerase
er concentration of
enient pipetting of
entration (5 U/l)
nsion reactions (se
DNA Polymerase
DNA Polymerase (
uced using rigorou
and other primer-
ing.
DNA Polymerase
DNA Polymerase, d
aration (5 U/l) of
Nucleotide Mix. U
tions, such as sequ
DNA Polymerase
ufactured under G
mentation require
harmaceutical and
er-extension react
I
recognizes the se
sive termini. Taq I
ated (*). Isoschizo
oTAGGG Telome
itative detection of
ready-to-use mix
nylated primer to im
oplate, and a DIG p
oTAGGG Telome
itive, nonradioactiv
ity in cell extracts.
ELISA, but also ha
sure amount of rea
oTAGGG Telome
n life science rese
meric DNA in cell c
a variety of organ
rmine the telomere
minal Transferase
nucleotides to the
ments, such as for
3-end labeling wit
TPs (e.g ., DIG-ddU
cal Produ
e, 1 U/l
f recombinant Taq
f small amounts of
Taq. Use in PCR, R
equencing, labeling
e, 5 U/l
(5 U/l) is ideal for
us purity and quali
-extension reaction
e, dNTPack
dNTPack combine
recombinant Taq
se for PCR, RT-PC
uencing and labeli
e, GMP Grade
GMP regulations. M
ments of research
biotechnology ind
ions (sequencing,
equence TCG*A a
is inhibited by ove
mers: Tth HB8 I.
erase PCR ELISA
f telomerase activit
for elongation and
mmobilize TRAP p
probe for detection
erase PCR ELISA
P
ve photometric EIA
One-tube mix sim
as an optimized sta
action product.
ere Length Assay
earch applications
cultures and other
isms, including hu
e length of these s
e
3-OH ends of do
homopolymeric ta
th either radioactiv
UTP).
uct Index
allows more accu
f enzyme. Identical
RT-PCR, and other
g).
r routine PCR. The
ity standards for us
ns, such as sequen
es our standard, rig
with convenient, r
CR, and other prime
ng.
Meets high quality
h and development
dustry. Use in PCR,
labeling).
and generates frag
erlapping dam-met
ty in cell extracts.
d amplification. Us
products in a strept
n.
PLUS

A to detect/quantif
milar to TeloTAGGG
andard and contro
for sensitive detec
biological researc
umans and mice. U
amples.
uble- or single-str
ailing or end-labeli
ve or chemically m
x
urate and
l to our higher
r primer-
enzyme is
se in PCR, RT-
ncing and
gorously tested
ready-to-use
er-extension
and
t laboratories
RT-PCR, and
gments with 5'-
thylation, as
One-step/one-
es a
tavidin-coated
fy telomerase
G Telomerase
l template to
ction of
ch samples
Use to
randed DNA
ng with dNTPs,
modified

Cat. No.

11 647 679 001
11 647 687 001
11 146 165 001
11 146 173 001
11 418 432 001
11 435 094 001
11 596 594 001
04 728 858 001
04 728 866 001
04 728 874 001
04 728 882 001
04 728 904 001
03 734 927 001
10 567 671 001
11 175 114 001
11 854 666 910
12 013 789 001
12 209 136 001
03 333 566 001
03 333 574 001

250 U for up
volume eac
1,000 U (4 x 25
20 l final vo
100 U for up
volume eac
500 U for up
volume eac
1,000 U (4 x 25
20 l final vo
5,000 U (20 x 25
20 l final vo
2,500 U (10 x 2
50 l final vo
5,000 U (20 x 25
20 l final vo
100 U for up
volume eac
500 U (2 x 250
l final volume
1,000 U (4 x 25
20 l final vo
2,500 U (10 x 2
20 l final vo
1,000 U for up
volume eac
1 kit
1 kit
1 kit
8,000 U (fo
reacti
24,000 U (fo
reacti
Pack Size

p to 500 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase

p to 200 reactions
ch containing 0.5 U
Polymerase
to 1,000 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase
50 U) for up to 10,
lume each contain
DNA Polymerase
lume each contain
DNA Polymerase
50 U) for up to 10,
lume each contain
DNA Polymerase
p to 200 reactions
ch containing 0.5 U
Polymerase
U) for up to 1,000
e each containing
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase
lume each contain
DNA Polymerase
p to 2,000 reaction
ch containing 0.5 U
Polymerase

2,500 U (10 U/l)
10,000 U (10 U/l)




ons, 400 U per rea
ons, 400 U per rea

www.roche
of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq
of 20 l final
U Taq DNA
s of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
of 20 l final
U Taq DNA
reactions of 20
0.5 U Taq DNA
00 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
s of 20 l final
U Taq DNA

)
tions
tions
tions
end labeling
action)
end labeling
action)
e-applied-science

Price in

202,60
640,50
89,00
356,00
640,50
2.703,80
1.480,10
2.703,80
89,00
356,00
640,50
1.480,10
690,90
104,60
309,10
1.026,60
1.085,40
771,60
100,10
225,20

173

e.com

Alp
174

www.r

Prod

Tetra
Used
trans
Labe
hybri
Thro
Use T
prote
Throm
Tip H
The T
with
Instru
Titan
Analy
up to
inhib
reliab
Titan
Sens
tube
ampl
enzym
Tran
Reve
reage
time
Light
Tran
Reve
trans
intere
quan
Tran
Sens
gene
impro
ampl
Tran
Reco
fragm
and L
end l
Tran
Conv
Read
supp
assay
Tran
Trans
formu
cells
Tran
Trans
grow
Reco
stand
TriPu
Prepa
DNA
synth
dena

lphabetic
roche-applied-sc
duct Name
amethyl-Rhodam
d in nonradioactive
slation, random-pri
led probes show r
dization for direct
ombin
Thrombin in coagu
ein-structure analy
mbin contains EDT
High Vol, 1 ml wit
Tip High Vol tips co
the FLOW Primary
ument.
n One Tube RT-P
yze RNA from man
o 6 kb. Includes rea
itor, and PCR-grad
ble analysis of RNA
n One Tube RT-P
itive, quick and rep
system reverse tra
ifies cDNA with a
me blend from the
scriptor First Str
rse transcribe all t
ents for first-strand
instruments, inclu
tCycler
480 Syste
scriptor High Fid
rse transcribe RNA
scriptases. Optimiz
est and sequence
titative RT-PCR wi
scriptor One-Ste
itive and specific o
-specific primers.
oved performance
ification, including
scriptor Reverse
ombinant reverse tr
ments up to 14 kb.
LightCycler
and o
abeling, first stran
scriptor Universa
venient fast solutio
dy-to-use master m
lied in just two via
ys on all real-time
sferrin
sferrin, like insulin
ulations. The main
by receptor-media
sforming Growth
sforming Growth F
wth factor affecting
ombinant, human T
dard chromatograp
ure Isolation Rea
are total RNA, gen
-free RNA in north
hesis, RT-PCR. Use
tured protein in SD
cal Produ
cience.com
mine-5-dUTP
e labeling of DNA.
imed labeling, PCR
red fluorescence a
fluorescence dete
ulation, biochemica
ysis. The enzyme co
TA and additional s
th Filter
ome in a set of 3.8
y Sample Handling
CR Kit
ny sources (animal
agents, control prim
de water to perform
A with high fidelity
CR System
producible analysi
anscribes RNA into
thermal cycling re
e Expand High Fide
and cDNA Synth
types of RNA from
d cDNA synthesis
ding LightCycler

ems.
delity cDNA Synth
A with increased fi
ed for two-step RT
transcriptomes. St
ith LightCycler
Sy
ep RT-PCR Kit
one-step endpoint
Combines high-yie
of a hot start syst
g GC-rich RNA.
e Transcriptase
ranscriptase for ro
Used in two-step
other real-time PC
d cDNA synthesis
al cDNA Master
n for cDNA synthe
mix (primers, nucle
als, brings out the f
PCR systems.
, is a component o
function of transf
ated endocytosis.
h Factor-1, hum
Factor-1, human (
many functions in
TGF- 1 is produce
phic techniques.
agent
nomic DNA, and pr
herns, in vitro tran
e RNA-free DNA in
DS-PAGE and wes
uct Index
Replaces dTTP in
R, 3-tailing, and cD
nd are suitable for
ection.
al and medical res
onverts fibrinogen
stabilizing agents.
840 1 ml filter tips a
and the FLOW PC
l, plant, human, vir
mers, nucleotides,
m RT-PCR. For qui
y.
s of RNA with high
o cDNA (AMV) up
eaction using an op
elity PCR System.
hesis Kit
a variety of source
reactions up to 14
Carousel-Based
hesis Kit
idelity compared to
T-PCR. Use to clon
tudy gene express
ystems.
RT-PCR analysis o
eld reverse transcr
em for high-fidelit
obust transcription
RT-PCR using the
CR systems. Ideal fo
s, RACE, and more.
esis and real-time
eotides, buffer, enz
full potential of you
of most serum-free
ferrin is to transpo
man (hTGF-1)
(hTGF-1), is a mu
n a variety of differ
ed in CHO cells an
rotein from a singl
slation, RNase pro
n PCR and cloning
stern blots.
x
nick
DNA synthesis.
r in situ
search, and
to fibrin.
and are used
CR Setup
ral, bacterial)
RNase
ick, sensitive,
h fidelity. One-
to 6 kb and
ptimized
es. Includes all
4 kb on all real-
and
o other reverse
ne genes of
ion using
of RNA using
ription and
ty, high-yield
of RNA
ermal cyclers
or sequencing,
.
PCR analysis.
ymes),
ur qRT-PCR
e media
rt iron into
ultifunctional
rent cells.
nd purified by
e sample. Use
otection, cDNA
g. Use

Cat. No.

11 534 378 910
10 602 400 001
04 639 642 001
11 939 823 001
11 855 476 001
04 379 012 001
04 896 866 001
04 897 030 001
05 081 955 001
05 081 963 001
05 091 284 001
04 655 877 001
04 655 885 001
03 531 287 001
03 531 295 001
03 531 317 001
05 893 151 001
10 652 202 001
11 412 272 001
11 667 157 001
11 667 165 001

25
50 reactions
1 kit for up to 5
1 kit
1 kit
1 kit for up
1 kit
1 kit
1 kit for up to 5
1 kit for
2,000 U (4 x
of 50 l fina
Transcri
500 U for up to
each contain
250 U for up to
each contain
20 ml (30 mg/
m
Pack Size

5 l (25 nmol) (1 m

20 U

1 set of 3.840

, including 10 cont

100 reactions

50 reactions, inclu
reactions
for up to 100 reac
for up to 200 reac
to 50 reactions an
reaction
for up to 200 reac
for up to 100 reac
50 reactions of 50
control reactions
up to 150 reaction

l volume each con
ptor Reverse Trans
50 reactions of 50
ning 10 U Transcri
Transcriptase
25 reactions of 50
ning 10 U Transcri
Transcriptase
100 reactions

pore size membra

1 g (1 ml)

50 ml
200 ml

mM)
trol reactions
ding 10 control
ctions
ctions
nd 10 control
ctions
ctions
l including 10
s of 50 l
200 reactions
ntaining 10 U
scriptase
0 l final volume
iptor Reverse
0 l final volume
iptor Reverse
red through 0.2
ane)

Price in

241,80
125,70
inquire
530,90
576,50
332,40
484,00
869,90
413,20
1.087,40
598,10
326,30
717,70
946,00
266,10
162,70
inquire
496,70
702,80
160,20
530,90

Alp

Prod

Tris b
Tris B
comp
prepa
Tris h
Tris H
biolo
comb
Trito
Comm
durin
elect
inject
Trito
Comm
isolat
elect
CMC
tRNA
tRNA
preve
nega
tRNA
tRNA
preve
to im
a lyop
tRNA
tRNA
preve
to im
lyoph
Tru9
Tru9
cohe
availa
Tryps
Use t
Inhib
cultu
tissue
Tryps
Use t
Inhib
medi
kallik
Tryps
Spec
chrom
spect
chym
Tryps
Diges
prote
analy
prote
Tryps
Use t
struc
and t
to cro
Tth D
Perfo
temp
cloni
ampl

lphabetic
duct Name
base
Base is extensively
ponent of buffer so
aration is free of p
hydrochloride
Hydrochloride is ex
gy as a buffering a
bination with Tris B
on X-100
monly used non-io
ng isolation of mem
rophoresis. Aqueo
tion vials. CMC: ap
on X-100
monly used non-io
tion of membrane-
rophoresis. Suppli
C: approx. 0.2 mM a
A
A is used as a com
ent nonspecific bin
tive); supplied as a
A
A is used as a com
ent nonspecific bin
prove recovery of
philizate.
A
A is used as a com
ent nonspecific bin
prove recovery of
hilizate.
I
I recognizes the se
sive termini. No in
able. Isoschizomer
sin Inhibitor
to terminate tissue
bits trypsin, factor X
re media. Does no
e kallikrein. From s
sin Inhibitor
to terminate tissue
bits trypsin, plasmin
a. Does not inhibit
krein. From chicken
sin recombinant,
ifically digests pro
matographic meth
trometry. Tested fo
motrypsin, and othe
sin Sequencing G
st proteins in solut
ein-structure elucid
ysis, and translocat
eins in polyacrylam
sin Sequencing G
to generate glycop
cture elucidation, tr
translocation studi
oss-linking.
DNA Polymerase
orm reverse transc
peratures, allowing
ng, and analysis o
ification of RNA at
cal Produ
y used in biochemi
olutions, especially
roteases, DNases
xtensively used in
agent in incubation
Base for preparatio
onic detergent solu
mbrane-protein co
ous solution, 10% (
pprox. 0.2 mM at +
onic detergent for
-protein complexes
ed as a viscous liq
at +25C
petitor in pre- and
nding of the probe
a lyophilizate.
petitor in pre- and
nding of the probe
diluted samples. F
petitor in pre- and
nding of the probe
diluted samples. F
equence TTAA a
formation concern
rs: Mse I, Tru1 I.
e disaggregation an
Xa, plasmin, and p
ot inhibit metallo-,
soybean.
e disaggregation an
n, and plasma kall
t metallo-, cysteine
n egg white.
, Proteomics Gra
oteins separated by
ods during sample
or the absence of p
er contaminating p
Grade
tion, in gels, or on
dation, tryptic map
tion studies. It is s
mide gels.
Grade, modified
peptides from purif
ryptic mapping, fin
es. Enzyme resista

ription and DNA a
its use in RT-PCR
f gene expression
t least 1 kb length
uct Index
stry and molecular
y for nucleic acid s
and RNases.
biochemistry and
n mixtures. It is us
on of Tris-HCl buff
ubilizes membrane
mplexes. Used for
(w/v), filled under n
+25C.
solubilizing memb
s. It is also used fo
quid.
e. From E. coli MRE
From brewer's yeas
From baker's yeast
nd generates frag
ning methylation se
nd for subcultivati
lasma kallikrein in
cysteine, aspartic
nd for subcultivati
ikrein activity in se
e, aspartic proteas
ade
y 2D gel electroph
e preparation for m
porcine trypsin (se
proteases.
blotting membran
uitable for the dige
fied glycoproteins
ngerprinting, seque
ance to autolysis is
amplification at ele
R for detection, qua
at the RNA level.
.
x
r biology as a
solutions. This
molecular
ed in
fers.
e proteins
r native gel
nitrogen in
branes during
or native gel
utions to
E 600 (RNase
utions to
ed as a carrier
st, supplied as
utions to
ed as a carrier
t, supplied as a
ments with 5-
ensitivity is
on procedures.
n serum-free
proteases, or
on procedures.
erum-free
es, or tissue
oresis or liquid
mass
erine protease),
nes. Use for
ng, sequence
estion of
in protein-
ence analysis,
s increased due
evated
antification,
For RT-PCR

Cat. No.

10 708 976 001
11 814 273 001
10 812 846 001
11 332 481 001
10 789 704 001
10 109 541 001
10 109 550 001
10 109 517 001
10 109 525 001
10 109 495 001
10 109 509 001
11 464 825 001
10 109 886 001
10 109 878 001
03 708 969 001
03 708 985 001
11 047 841 001
11 418 475 001
11 418 025 001
11 418 033 001
11 480 022 001

500 U (2 x 250
final volume
Pack Size

1 kg
5 kg

500 g

5 x 10 ml

100 ml

100 mg
500 mg

100 mg
500 mg

100 mg
500 mg

1,000 U (10 U/l)

50 mg

1 g

4 x 100 g
4 x 25 g

4 x 100 g
4 x 25 g

4 x 25 g
4 x 100 g

U) for up to 200 re
each containing 2
Polymerase

www.roche

eactions of 50 l
2.5 U Tth DNA
e-applied-science

Price in

171,40
588,20
170,50
83,50
53,40
249,20
992,50
127,50
447,80
155,10
609,30
251,10
50,90
128,20
287,20
94,30
278,10
76,20
112,30
379,80
322,00

175

e.com

Alp
176

www.r

Prod

Tumo
Has c
activa
activi
Reco
Tumo
Has c
activa
activi
Reco
Tumo
TNF-
tumo
cytos
syner
TUN
TUNE
assay
antib
visua
TUN
Use w
deoxy
appli
break
TUN
This e
trans
TUNE
death
TUN
TUNE
react
to lab
level.
TUN
TUNE
assay
is lab
subst
Twee
Use T
mem
for a
and i
U
Univ
Use i
a com
quan
Probe
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin

lphabetic
roche-applied-sc
duct Name
or Necrosis Fact
ating/growth stimu
ombinant (E. coli ),
or Necrosis Fact
ating/growth stimu
ombinant (yeast), 1
or Necrosis Fact
causes selectiv
or-bearing mice. In
static activity on ce
rgistically with inte
EL AP
EL AP is an antibo
body is bound to FI
alized using Fast Re
EL Dilution Buffe
with In Situ Cell D
ynucleotidyl transf
cations. The result
ks to quantity apop
EL Enzyme
enzyme solution c
sferase for the TUN
EL reaction mix lab
h at single-cell leve
EL Label Mix
EL Mix contains flu
tion to detect apop
bel DNA strand bre
.
EL POD
EL POD is an antib
beled with peroxida
trate such as DAB
en 20
Tween 20 to solub
brane-protein com
subsequent prote
mmunoblotting. C
versal ProbeLibra
n combination wit
mplete set of 165 U
tification of transc
eLibrary Assay De
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
cal Produ
cience.com
or-, human (hT
ulating activity on
vitro , and can cau
10 g/ml PBS, 1 m
or-, human (hT
ulating activity on
vitro , and can cau
0 g/ml PBS, 1 mg
or-, mouse (m
ve necrosis of muri
n vitro , human TNF
ertain transformed
erferon-.
dy that converts fl
c assays for light m
TC-dUTP, labeled
ed or NBT/BCIP.
er
Death Detection Kit
ferase for the TUN
ting reaction mix is
ontains recombina
NEL reaction to det
bels DNA strand b
el.
uorescein-dUTP an
ptosis in situ . Use t
eaks to quantity ap
body that converts
c assays suitable fo
ase and is visualize
Substrate.
ilize membrane pr
mplexes. Due to its
in detection by UV
CMC: approx. 0.06 m
ary Extension Set
th the Universal Pr
Universal ProbeLib
cripts of all organis
sign Center.
ary Human ACTP
gene and UPL Refe
tware at the Assay
ary Human 2M
gene and UPL Refe
tware at the Assay
ary Human G6PD
gene and UPL Refe
tware at the Assay
uct Index
TNF-)
ormed cell lines,
many normal cells
use tumor necrosis
mg/ml BSA.
TNF-)
ormed cell lines,
many normal cells
use tumor necrosis
g/ml BSA.
mTNF-)
ine tumors when i
F- has direct cyt
cells. In this conte
uorescence-based
microscopy. Anti-fl
with alkaline phos
ts to dilute termina
EL reaction in spe
s used to label DN
t the single-cell lev
ant terminal deoxy
tect apoptosis in s
breaks to quantity a
nd -dNTPs for the
this mix with the T
poptotic cell death
fluorescence-base
or light microscop
ed using a precipit
roteins during isola
s low UV absorban
V light absorption.
mM.
t, Probes #91 to #
robeLibrary Set, Hu
brary Probes. Enab
sms using the onlin
Gene Assay
human ACTP. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human 2M. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human G6PD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
x
s, antiviral
s in vivo .
s, antiviral
s in vivo .
njected into
tolytic or
ext, it acts
d TUNEL
uorescein
sphatase, and
al
ecial
NA strand
vel.
ynucleotidyl
situ . The
apoptotic cell
TUNEL
TUNEL Enzyme
h at single-cell
ed TUNEL
y. The antibody
tating
ation of
ce, it is ideal
Used in ELISA
#165
uman to obtain
les
ne Universal
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the

Cat. No.

11 371 843 001
11 088 939 001
11 271 156 001
11 772 457 001
11 966 006 001
11 767 305 001
11 767 291 910
11 772 465 001
11 332 465 001
04 869 877 001
05 046 165 001
05 189 390 001
05 046 246 001

10
10
5
3.5
2 x
3 x 5
3.5
1 set of 75 Univ
1 set for up to
50
1 set for up to
50
1 set for up to
50
Pack Size

g (1,000,000 U, 1

g (1,000,000 U, 1

g (2,000,000 U, 1


2 x 10 ml

50 l for up to 20 t

550 l for up to 30


5 x 10 ml

versal ProbeLibrary
10 M each.

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

ml)
ml)
ml)
ests
tests
tests
ests
y Probes, 125 l,
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l

Price in

908,20
908,20
401,00
115,60
216,30
181,00
141,80
122,20
116,70
2.574,80
491,60
491,60
491,60

Alp

Prod

Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin
Univ
Gene
expre
assay
onlin

lphabetic
duct Name
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
cal Produ
ary Human GAPD
gene and UPL Refe
tware at the Assay
ary Human GUSB
gene and UPL Refe
tware at the Assay
ary Human HPRT
gene and UPL Refe
tware at the Assay
ary Human PBGD
gene and UPL Refe
tware at the Assay
ary Human PGK1
gene and UPL Refe
tware at the Assay
ary Human PPIA G
gene and UPL Refe
tware at the Assay
ary Human TBP G
gene and UPL Refe
tware at the Assay
ary Mouse ACTB
gene and UPL Refe
tware at the Assay
ary Mouse GAPD
gene and UPL Refe
tware at the Assay
uct Index
D Gene Assay
human GAPD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
B Gene Assay
human GUSB. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human HPRT. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
D Gene Assay
human PBGD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human PGK1. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human PPIA. Quan
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
human TBP. Quan
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
mouse ACTB. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
Gene Assay
mouse GAPD. Qua
me PCR. Design m
erence Gene Assa
y Design Center.
x
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
ntify gene
multiplex PCR
y using the
tify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the
antify gene
multiplex PCR
y using the

Cat. No.

05 190 541 001
05 190 525 001
05 046 157 001
05 046 149 001
05 046 173 001
05 189 268 001
05 189 284 001
05 046 190 001
05 046 211 001

1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
Pack Size

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

200 reactions of 5
00 reactions of 20

www.roche
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
e-applied-science

Price in

491,60
491,60
491,60
491,60
491,60
491,60
491,60
491,60
491,60

177

e.com

Alp
178

www.r

Prod

Univ
Rapid
speci
with
free o
lphabetic
roche-applied-sc
duct Name
versal ProbeLibra
dly quantify gene e
ies in the NCBI Re
standard reagents
online Assay Desig
cal Produ
cience.com
ary Probes
expression levels o
eference Seq Datab
s in real-time PCR
gn Center.
uct Index
of human, mouse,
base. Use fluoresc
assays. Design ass
x
rat and other
cent probes
says using the

Cat. No.

04 684 974 001
04 684 982 001
04 685 008 001
04 685 016 001
04 685 024 001
04 685 032 001
04 685 059 001
04 685 067 001
04 685 075 001
04 685 091 001
04 685 105 001
04 685 113 001
04 685 121 001
04 685 130 001
04 685 148 001
04 686 896 001
04 686 900 001
04 686 918 001
04 686 926 001
04 686 934 001
04 686 942 001
04 686 969 001
04 686 977 001
04 686 985 001
04 686 993 001
04 687 574 001
04 687 582 001
04 687 604 001
04 687 612 001
04 687 639 001
04 687 647 001
04 687 655 001
04 687 663 001
04 687 671 001
04 687 680 001
04 687 949 001
04 687 957 001
04 687 965 001
04 687 973 001
04 687 990 001
04 688 007 001
04 688 015 001

Pack Size

Probe #1
Probe #2
Probe #3
Probe #4
Probe #5
Probe #6
Probe #7
Probe #8
Probe #9
Probe #10
Probe #11
Probe #12
Probe #13
Probe #14
Probe #15
Probe #16
Probe #17
Probe #18
Probe #19
Probe #20
Probe #21
Probe #22
Probe #23
Probe #24
Probe #25
Probe #26
Probe #27
Probe #28
Probe #29
Probe #30
Probe #31
Probe #32
Probe #33
Probe #34
Probe #35
Probe #36
Probe #37
Probe #38
Probe #39
Probe #40
Probe #41
Probe #42

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

Alp

Prod

lphabetic
duct Name
cal Produuct Indexx

Cat. No.

04 688 031 001
04 688 040 001
04 688 058 001
04 688 066 001
04 688 074 001
04 688 082 001
04 688 104 001
04 688 112 001
04 688 481 001
04 688 490 001
04 688 503 001
04 688 511 001
04 688 520 001
04 688 538 001
04 688 546 001
04 688 554 001
04 688 562 001
04 688 589 001
04 688 597 001
04 688 619 001
04 688 627 001
04 688 635 001
04 688 643 001
04 688 651 001
04 688 660 001
04 688 678 001
04 688 686 001
04 688 937 001
04 688 945 001
04 688 953 001
04 688 961 001
04 688 970 001
04 688 988 001
04 688 996 001
04 689 003 001
04 689 011 001
04 689 020 001
04 689 038 001
04 689 046 001
04 689 054 001
04 689 062 001
04 689 089 001

Pack Size

Probe #43
Probe #44
Probe #45
Probe #46
Probe #47
Probe #48
Probe #49
Probe #50
Probe #51
Probe #52
Probe #53
Probe #54
Probe #55
Probe #56
Probe #57
Probe #58
Probe #59
Probe #60
Probe #61
Probe #62
Probe #63
Probe #64
Probe #65
Probe #66
Probe #67
Probe #68
Probe #69
Probe #70
Probe #71
Probe #72
Probe #73
Probe #74
Probe #75
Probe #76
Probe #77
Probe #78
Probe #79
Probe #80
Probe #81
Probe #82
Probe #83
Probe #84

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

179

e.com

Alp
180

www.r

Prod

lphabetic
roche-applied-sc
duct Name
cal Produ
cience.com
uct Indexx

Cat. No.

04 689 097 001
04 689 119 001
04 689 127 001
04 689 135 001
04 689 143 001
04 689 151 001
04 692 080 001
04 692 098 001
04 692 101 001
04 692 110 001
04 692 128 001
04 692 136 001
04 692 144 001
04 692 152 001
04 692 179 001
04 692 187 001
04 692 195 001
04 692 209 001
04 692 217 001
04 692 225 001
04 692 241 001
04 692 250 001
04 692 268 001
04 692 276 001
04 692 284 001
04 692 306 001
04 693 442 001
04 693 469 001
04 693 477 001
04 693 485 001
04 693 493 001
04 693 507 001
04 693 515 001
04 693 523 001
04 693 531 001
04 693 540 001
04 693 558 001
04 693 566 001
04 693 574 001
04 693 582 001
04 693 604 001
04 693 612 001

Pack Size

Probe #85
Probe #86
Probe #87
Probe #88
Probe #89
Probe #90
Probe #91
Probe #92
Probe #93
Probe #94
Probe #95
Probe #96
Probe #97
Probe #98
Probe #99
Probe #100
Probe #101
Probe #102
Probe #103
Probe #104
Probe #105
Probe #106
Probe #107
Probe #108
Probe #109
Probe #110
Probe #111
Probe #112
Probe #113
Probe #114
Probe #115
Probe #116
Probe #117
Probe #118
Probe #119
Probe #120
Probe #121
Probe #122
Probe #123
Probe #124
Probe #125
Probe #126

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

Alp

Prod

Univ
Gene
expre
assay
onlin
lphabetic
duct Name
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
cal Produ
ary Rat ACTB Gen
gene and UPL Refe
tware at the Assay
uct Index
ne Assay
rat ACTB. Quantify
me PCR. Design m
erence Gene Assa
y Design Center.
x
y gene
multiplex PCR
y using the

Cat. No.

04 693 639 001
04 693 647 001
04 693 655 001
04 693 663 001
04 694 155 001
04 694 163 001
04 694 171 001
04 694 180 001
04 694 198 001
04 694 201 001
04 694 210 001
04 694 228 001
04 694 236 001
04 694 244 001
04 694 279 001
04 694 287 001
04 694 295 001
04 694 309 001
04 694 317 001
04 694 325 001
04 694 333 001
04 694 341 001
04 694 350 001
04 694 368 001
04 694 376 001
04 694 384 001
04 694 392 001
04 694 406 001
04 694 414 001
04 694 422 001
04 694 449 001
04 694 457 001
04 694 465 001
04 694 473 001
04 694 481 001
04 694 490 001
04 694 503 001
04 694 511 001
04 694 520 001
05 046 203 001

1 set for up to
50
Pack Size

Probe #127
Probe #128
Probe #129
Probe #130
Probe #131
Probe #132
Probe #133
Probe #134
Probe #135
Probe #136
Probe #137
Probe #138
Probe #139
Probe #140
Probe #141
Probe #142
Probe #143
Probe #144
Probe #145
Probe #146
Probe #147
Probe #148
Probe #149
Probe #150
Probe #151
Probe #152
Probe #153
Probe #154
Probe #155
Probe #156
Probe #157
Probe #158
Probe #159
Probe #160
Probe #161
Probe #162
Probe #163
Probe #164
Probe #165
200 reactions of 5
00 reactions of 20

www.roche
0 l or for up to
l
e-applied-science

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
491,60

181

e.com

Alp
182

www.r

Prod

Univ
Gene
expre
assay
onlin
Univ
Use t
for al
PCR
Desig
Univ
Quan
endo
assay
softw
Univ
Use a
activi
Prote
fluori
Urac
Cleav
incre
labele
carry
Urac
Prima
heat-
react
deoxy
UTP
This s
trans
mM s
W
Wate
Spec
endp
highe
ampl
West
10x s
expe
mem
X
Xant
Catal
oxida
purin
EDTA
Xba
Reco
termi
gene
hydro
X-Ga
Use X
produ
meth
detec

lphabetic
roche-applied-sc
duct Name
versal ProbeLibra
e-specific probe an
ession levels using
e ProbeFinder soft
versal ProbeLibra
this fluorescent pro
ll the human gene
with LightCycler

gn assays using th
versal ProbeLibra
ogenous reference
ys for target gene
ware at the Assay D
versal Protease S
as a general subst
ities, such as conta
ease Substrate can
imetrically in a hom
cil-DNA Glycosyla
ves DNA where a d
ease efficiency of s
ed oligonucleotide
yover contaminatio
cil-DNA Glycosyla
arily used to preve
-labile, is easily ina
tion by heating to +
yuridylate (dUTP)
special quality pre
scription since it is
solution of the lith
er, PCR Grade
ially tested and qu
point and real-time
est quality water is
ification systems c
tern Blocking Re
solution used as a
riments. The reage
brane, membrane
thine Oxidase (XO
lyzes oxidation of h
ation of xanthine to
nes in some specie
A, pH approx. 8.
I
ognizes sequence T
ini. Requires at lea
which methylates
oxymethylcytosine
al
X-Gal for immunoh
uct has a blue colo
hanol. It is not solu
cted.
cal Produ
cience.com
ary Rat GAPD Gen
gene and UPL Refe
tware at the Assay
ary Set, Human
obe set to rapidly q
s in the NCBI Ref
Systems and othe
he free online Assa
ary Set, Human R
vels of a human ge
gene in a dual-co
and UPL Referenc
Design Center.
Substrate
rate for proteases
amination in enzym
n be measured spe
mogeneous assay.
ase
deoxyuridylate res
site-directed mutag
e probes, and, with
on.
ase, heat-labile
ent PCR product ca
activated at the be
+95C. DNA is cle
residue has incorp
eparation of UTP is
tested for the abs
ium salt (pH 7).
ualified for use in a
e PCR assays, sequ
s required. All Ligh
contain this PCR g
eagent, Solution
general blocking a
ent is used in steps
washing steps, an
OD)
hypoxanthine to xa
o uric acid. Plays a
es. Suspension in 3
T*CTAGA. Genera
ast two nucleotide
s 6N of adenine inh
inhibit at (*). Isosc
histocytochemistry
ble in water. The b
uct Index
ne Assay
rat GAPD. Quantify
me PCR. Design m
erence Gene Assa
y Design Center.
quantify gene exp
Seq Database, usi
er real-time PCR in
ay Design Center.
Reference Gene A
ene of interest in re
olor assay. Design
ce Gene Assay with
and to detect trac
me preparations. T
ectrophotometrical
idue has incorpora
genesis, to produc
h dUTP, to eliminat
arryover contamina
ginning of the am
aved at any site w
porated.
s suitable for in vitr
sence of RNases. U
all PCR or RT-PCR.
uencing, and when
htCycler
kits and
rade water.
agent during weste
s such as blocking
nd diluting detectio
anthine and can fu
an important role in
3.2 M ammonium s
ates fragments wit
es around target se
hibits; 5-methylcyt
chizomers: none.
y applications. The
n dimethylformami
blue color can be v
x
y gene
multiplex PCR
y using the
ression levels
ng real-time
nstruments.
Assays
elation to an
multiplex PCR
h free online
ce protease
The Universal
ly and
ated. Used to
e highly
te PCR product
ation. UNG,
plification
where a
ro RNA
UTP is a 100
. Use with
never the
other Roche
ern blotting
g the
on antibodies.
urther catalyze
n catabolism of
sulfate, 10 mM
th 5-cohesive
equence; dam
tosine and 5-
reaction
ide and
visually

Cat. No.

05 046 220 001
04 683 633 001
05 046 114 001
11 734 334 001
11 444 646 001
11 775 367 001
11 775 375 001
11 140 949 001
03 315 843 001
03 315 932 001
03 315 959 001
11 921 673 001
11 921 681 001
10 110 434 001
10 674 257 001
10 674 265 001
10 674 273 001
11 047 663 001
10 651 745 001
10 703 729 001
10 745 740 001
11 680 293 001

1 set for up to
50
1 set of 90 Univ
1 set for up to
250 reactions
400
100
25
25
100
6 x 10
Pack Size

200 reactions of 5
00 reactions of 20

versal ProbeLibrary
10 M each.

100 reactions of 5
of 20 l for each r

40 mg

100 U

100 U
500 U

l (40 mol, 100 m

0 ml (4 vials of 25
ml (10 blots, 100 c
00 ml (60 blots, 100

20 U (1 ml)

1,000 U (10 U/l)
5,000 U (10 U/l)
20,000 U (10 U/l)
20,000 U (40 U/l)
250 mg
2.5 g
1 g
100 mg

0 l or for up to
l
y probes, 125 l,
0 l or for up to
reference gene
mM)
ml)
ml)
ml)
cm
2
)
0 cm
2
)

)
)

Price in

491,60
3.393,90
1.111,90
565,00
148,40
143,80
534,50
108,40
310,70
155,30
123,90
91,40
321,90
99,70
45,50
105,80
400,20
400,20
148,00
1.122,10
492,50
91,90

Alp

Prod

Xho
Xho I
with
meth
PaeR
X-tre
Non-
cytot
trans
Ideal
X-tre
State
delive
trans
effec
X-tre
Trans
(siRN
and h
there
lphabetic
duct Name
I
I recognizes the se
5-cohesive termin
hyladenine and 5-m
R7 I, Sfr274 I, Sla I,
emeGENE 9 DNA
-liposomal multi-co
oxicity, minimal ne
sfection efficiency
for all cellular ana
emeGENE HP DN
e-of-the-art high p
ery of DNA into a w
sfect cells. Free of a
ts.
emeGENE siRNA
sfection reagent fo
NA) into many cell
hard-to-transfect c
efore does not requ
cal Produ
equence *CT*CG*
ni. Xho I is inhibited
methylcytosine as i
Str I, Tli I.
A Transfection Re
omponent transfec
eed for optimizatio
in many cell lines,
alysis applications.
NA Transfection R
erformance transf
wide range of euk
animal-derived co
Transfection Rea
or efficiently delive
types (HeLa, NIH
cell lines (HT29). F
uire media change
uct Index
*AG and generates
d by the presence
indicated (*). Isosc
eagent
ction reagent with
on, and ability to pr
even in the presen
.
Reagent
ection reagent for
karyotic cells, inclu
mponents and low
agent
ering short interferi
3T3, HEK-293, CH
Functions with or w
es.
x
s fragments
of 6-
chizomers:
very low
rovide high
nce of serum.
efficient
ding hard-to-
w cytotoxic
ing RNA
O-K1, COS-7),
without serum,

Cat. No.

10 703 770 001
10 703 788 001
10 899 194 001
06 365 779 001
06 365 787 001
06 365 809 001
06 366 244 001
06 366 236 001
06 366 546 001
04 476 093 001
04 476 115 001

1 ml (1 mg/m
5 x 1 ml (2,000
Pack Size

2,500 U (40 U/l)
12,500 U (40 U/l)
5,000 U (10 U/l)
0.4 ml
1.0 ml
5 x 1.0 ml
0.4 ml
1.0 ml
5 x 1 ml
plate)

www.roche

)

ns in a 24-well
a 24-well plate)
e-applied-science

Price in

53,40
216,00
102,30
200,30
397,20
1.535,90
214,30
424,50
1.643,20
255,90
1.087,00

183

e.com

Pr
184

www.r

Cat.

03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
03 00
roducts b
roche-applied-sc

No.
03 230 001 Lig
Eas
Ligh
dete
RT-
03 248 001 Lig
Eas
Ligh
dete
PCR
03 990 001 Ma
Isol
1x1
Inst
Syst
04 040 001 Ma
Rea
of M
and
Pur
04 058 001 Ma
Rea
on t
Mag
04 066 001 Ma
Rea
on t
Mag
04 074 001 Ma
Rea
lids
rece
rem
04 082 001 Ma
Rea
The
perf
surf
04 104 001 Ma
Tub
med
term
also
04 112 001 Ma
Sam
acid
Inst
Com
04 147 001 Ma
Rea
Mag
nuc
with
04 155 001 Ma
The
pur
red
pos
04 171 001 Ma
Larg
Inst
hea
04 180 001 Ma
Sma
Wit
whe
04 198 001 Ma
The
LC
con
salt

by Catalo
cience.com
htCycler
FastSt
y-to-use hot start
htCycler
Carouse
ection. For qPCR, S
-PCR. MgCl
2
is sup
htCycler
FastSt
y-to-use hot start
htCycler
Carouse
ection. For qPCR, S
R. MgCl
2
is supplie
agNA Pure LC DN
ate high quality D
0
3
to 1x10
6
blood
truments. Resulting
tems, standard blo
agNA Pure LC Re
agent containers fo
MagNA Pure LC In
d V-shaped bottom
e LC Tub Lids (larg
agNA Pure LC Me
agent containers fo
the stage of MagN
gNA Pure LC Tub
agNA Pure LC Re
agent containers fo
the stage of MagN
gNA Pure LC Tub
agNA Pure LC Tub
agent Tub Lids for
reduce evaporativ
eiving up to 8 reac
moved as tips are e
agNA Pure LC Tub
agent Tub Lids for
ese lids reduce eva
forations for receiv
faces are removed
agNA Pure LC Tub
b Lid Seals are for
dium, large). They
m storage after pu
o catch liquid drop
agNA Pure LC Sa
mple reaction plate
ds from magnetic b
truments. Each car
mpatible with stand
agNA Pure LC Pro
action vessels for s
gNA Pure LC Instr
cleic acids. Each pr
h 8 wells each.
agNA Pure LC Tip
e Tip Stand is for te
ification runs using
uces the number o
sitions, so that the
agNA Pure LC Re
ge (50 - 1000 l vo
truments. With inte
ad nozzles when di
agNA Pure LC Re
all (5 - 50 l volum
h integrated filters
en eluting nucleic
agNA Pure LC Wa
e Waste Bottle colle
ntact with potential
ts in the lysis buffe
og Numb
Product N

tart DNA Master
mix for sensitive P
el-Based Systems w
SNP, and mutation
pplied for specific
tart DNA Master
mix for sensitive P
el-Based Systems w
SNP and mutation
ed for specific app
NA Isolation Kit I
NA from 20 to 200
or cultured cells u
g DNA is eluted in
ock cyclers and oth
eagent Tub (large
or 100 ml of MagN
nstruments. Tub ma
m minimizes dead v
ge).
edium Reagent T
or storing up to 20
NA Pure LC Instrum
Lids (small, mediu
eagent Tub (smal
or storing up to 3.5
NA Pure LC Instrum
Lids (small, mediu
b Lid (large)
the MagNA Pure
ve reagent loss. Ea
ction tips, ensuring
extracted.
b Lid (small, med
the MagNA Pure
aporative reagent l
ving up to 8 reactio
d as tips are extrac
b Lid Seal
use with all MagN
prevent evaporativ
rification using Ma
ps during robotic a
mple Cartridge
es for aliquoting pr
beads, and sample
rtridge has 32 (4 x
dard 8-well multic
ocessing Cartridg
samples and purific
rument when purif
rocessing cartridge
p Stand
emporary storage o
g MagNA Pure LC
of tips required for
nozzle head can b
eaction Tip (large
olume) reaction tip
egrated filters to p
ispensing reagents
eaction Tip (smal
me) reaction tips fo
s to prevent contam
acids and during p
aste Bottles
ects up to 330 ml l
These autoclavable
lly infectious mate
ers.
ber
Name
SYBR Green I
PCR in LightCycler
when using SYBR

n detection. Use al
applications.
HybProbe
PCR in LightCycler
when using HybPr

detection. Use in
plications.
0 l mammalian wh
using MagNA Pure
n 100 l. Ideal for L
her real-time PCR
e)
NA Pure LC reagen
arkings estimate b
volume. Seal tubs
Tub 20
ml of MagNA Pur
ments. Tubs are se
um).
l)
5 ml of MagNA Pu
ments. Tubs are se
um).
LC Reagent Tubs
ach Tub Lid has 8 p
g that liquid on tip
dium)
LC Reagent Tubs
oss. Each Tub Lid
on tips, ensuring t
cted.
NA Pure LC Tub Lid
ve reagent loss an
agNA Pure LC Inst
arm movements.
rimary samples, elu
e storage using Ma
8) wells, each wit
channel pipettes.
ge
cation reagents pi
fying DNA, RNA, m
e has 64 wells, arr
of tips for multiple
C Instruments. The
r a purification run
briefly store small o
e)
ps for MagNA Pure
revent contaminat
s and separating m
l)
or MagNA Pure LC
mination of pipettin
post-elution pipett
liquid waste during
e Waste Bottles pr
rial and the irritati
Capillaries on
Green I for
so for two-step
Capillaries on
robe probes for
two-step RT-
hole blood or
e LC
LightCycler

instruments.
nts on the stage
buffer volume
using MagNA
re LC reagents
ealed using
re LC reagents
ealed using
(large). These
perforations for
surfaces are
(small, medium).
has 8
hat liquid on tip
ds (small,
d permit long-
truments. They
uting nucleic
agNA Pure LC
h 1.5 ml volume.
petted by the
mRNA, and total
anged in 8 rows
e use during
Tip Stand
n. It has 8
or large tips.
e LC
tion of pipetting
magnetic bead.
C Instruments.
ng head nozzles
ting.
g MagNA Pure
revent user
ng chaotropic

1 kit for up to 9
1 kit for up to 9
1 kit
960 tips (30 pre
960 tips (30 pre

Pack Size

96 reactions of 20
volume
96 reactions of 20
volume
for up to 192 isola
120 tubs
150 tubs
150 tubs
120 lids
300 lids
400 seals
120 cartridges
160 cartridges
200 tip stands
e-packed trays ea
e-packed trays ea
40 bottles
l final reaction
l final reaction
ations
ch with 32 tips)
ch with 32 tips)

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Pr

Cat.

03 00
03 00
03 01
03 01
03 03
03 04
03 06
03 11
03 11
03 11
03 11
03 11
03 11
03 11
03 11
roducts b

No.
04 201 001 Ma
Aut
was
reac
Mag
05 372 001 Hom
Spe
dete
thro
10 040 001 PVD
Idea
low
colo
Ligh
18 954 001 Lig
Eas
Bas
RNA
min
38 505 001 Ma
Isol
seru
Pur
qPC
45 501 001 Ma
Rea
on t
buff
Tub
64 760 001 Lig
Eas
Bas
RNA
min
13 906 001 Lig
Use
with
Hyb
15 801 001 Pro
Act
grad
from
lyop
15 828 001 Pro
Act
grad
from
mg/
15 836 001 Pro
Act
grad
from
lyop
15 844 001 Pro
Act
grad
from
mg/
15 852 001 Pro
Act
grad
from
lyop
15 879 001 Pro
Act
grad
from
lyop
15 887 001 Pro
Act
grad
from
mg/
by Catalo
agNA Pure LC Wa
toclavable MagNA
ste slide of the Ma
ction tips discarde
gNA Pure LC 2.0 I
mogeneous Casp
ecific, one-step fluo
ermination of casp
oughput screening
DF Western Blott
al membrane for w
w background bind
orimetric and chem
ht Western-Blottin
htCycler
RNA M
y-to-use mix for o
sed Instruments an
As. High temperat
nimizes mispriming
agNA Pure LC Tot
ate high-purity tot
um, plasma, or wh
ified nucleic acids
CR and qRT-PCR u
agNA Pure LC Me
agent containers fo
the stage of MagN
fer volume and V-
b Lids (small, medi
htCycler
RNA M
y-to-use mix for o
sed Instruments an
As. High temperat
nimizes mispriming
htCycler
Fluore
e this dye to label t
h 5'-LightCycler
R
bProbe probes on
oteinase K, recom
ive endopeptidase
de enzyme isolates
m tissues/cell lines
philizate. Also ava
oteinase K, recom
ive endopeptidase
de enzyme isolates
/ml in 10 mM Tris.
oteinase K, recom
ive endopeptidase
de enzyme isolates
philizate. Also ava
oteinase K, recom
ive endopeptidase
de enzyme isolates
/ml in 10 mM Tris.
oteinase K, recom
ive endopeptidase
de enzyme isolates
philizate. Also ava
oteinase K, recom
ive endopeptidase
de enzyme isolates
philizate. Also ava
oteinase K, recom
ive endopeptidase
de enzyme isolates
/ml in 10 mM Tris.
og Numb
Product N

aste Bags
A Pure LC Waste Ba
agNA Pure LC 1.0 I
ed by the robot. Th
nstrument.
pases Assay, fluo
orimetric assay for
pases activity in mi
g.
ting Membranes
western and dot blo
ing generate exce
miluminescent dete
g Substrates.
Master HybProbe
ne-step RT-PCR u
nd HybProbe probe
ure overcomes sec
g during the RT ste
tal Nucleic Acid
tal nucleic acids (v
ole blood using M
s are eluted in 50-1
using LightCycler
edium Reagent T
or storing up to 30
NA Pure LC Instru
shaped bottom mi
um).
Master SYBR Gre
ne-step RT-PCR u
nd SYBR Green I d
ure overcomes sec
g during the RT ste
escein CPG
the 3'-end of oligo
Red-labeled oligon
LightCycler
480 a
mbinant, PCR Gra
e inactivates endog
s nucleic acids for
s, and promotes ba
ailable in solution.
mbinant, PCR Gra
e inactivates endog
s nucleic acid for P
s, and promotes ba
Available lyophiliz
mbinant, PCR Gra
e inactivates endog
s nucleic acids for
s, and promotes ba
mbinant, PCR Gra
e inactivates endog
s, and promotes ba
Available lyophiliz
mbinant, PCR Gra
e inactivates endog
s nucleic acids for
s, and promotes ba
mbinant, PCR Gra
e inactivates endog
s nucleic acids for
s, and promotes ba
mbinant, PCR Gra
e inactivates endog
s, and promotes ba
Available lyophiliz
ber
Name
ags are only for us
Instrument. They c
ey cannot be used
orimetric
r the quantitative in
icroplates. Ideally s
ots. Strong sample
llent signal-to-nois
ection. Ideal for us
e
using LightCycler
es for detection. Id
condary structures
ep.
Isolation Kit
viral DNA/RNA) fro
MagNA Pure LC Ins
100 l. Nucleic acid
Systems and bloc
Tub 30
ml of MagNA Pur
ments. Tub markin
inimizes dead volu
een I
using LightCycler
ye for detection. Id
condary structures
ep.
onucleotides. Use i
nucleotides for det
and Carousel-Base
ade
genous RNases an
r PCR and native R
acterial cell lysis. S
ade
genous RNases/DN
PCR and native RN
zed.
ade
genous RNases an
r PCR and native R
ade
genous RNases/DN
PCR and native RN
zed.
ade
genous RNases an
r PCR and native R
ade
genous RNases an
r PCR and native R
ade
genous RNases/DN
PCR and native RN
zed.
se with the tip
collect used
d with the
n vitro
suited for high-
e retention and
se ratios in
se with Lumi-
Carousel-
deal for difficult
s, and hot start
om up to 200 l
struments.
ds are ideal for
ck cyclers.
re LC reagents
ngs estimate
ume. Use with
Carousel-
deal for difficult
s, and hot start
n combination
tection with
ed Systems.
nd DNases. PCR-
RNA and DNA
Supplied as a
Nases. PCR-
NA and DNA
Solution: 14 to 22
nd DNases. PCR-
RNA and DNA
Supplied as a
Nases. PCR-
NA and DNA
Solution: 14 to 22
nd DNases. PCR-
RNA and DNA
Supplied as a
nd DNases. PCR-
RNA and DNA
Supplied as a
Nases. PCR-
NA and DNA
Solution: 14 to 22

1 kit for 100 tes
1
1 kit for up to 9
1 kit
1 kit for up to 9
Pack Size

200 bags
sts on 96-well plat
on 384-well plates
roll (30 cm x 3.00
96 reactions of 20
volume
for up to 192 isola
50 tubs
96 reactions of 20
volume
5 columns
2 x 250 mg
5 ml
25 mg
25 ml
4 x 250 mg
100 mg
1.25 ml
www.roche
tes, for 400 tests
s
m)
l final reaction
ations
l final reaction
e-applied-science

Price in

inquire
466,10
300,50
inquire
inquire
inquire
inquire
inquire
364,80
113,40
37,70
453,90
590,50
82,30
51,40

185

e.com

Pr
186

www.r

Cat.

03 11
03 13
03 14
03 14
03 18
03 20
03 24
03 24
03 24
03 25
03 25
03 25
03 25
03 25
roducts b
roche-applied-sc

No.
18 827 001 Ma
The
pur
Rem
usin
38 178 001 Lig
Use
with
Hyb
43 414 001 Gen
Pre
usin
can
seq
43 422 001 Gen
Pre
usin
can
seq
86 229 001 Ma
Isol
Inst
lysa
with
inst
01 287 001 Ma
Coo
Elut
A-R
tran
46 744 001 Ma
Use
cult
be i
LC
mR
46 752 001 Ma
Add
Isol
lysis
stab
46 779 001 Ma
Buf
Add
plas
Mag
Nuc
Inst
53 767 001 Ma
The
hold
Mag
53 775 001 Ma
Add
con
50 t
dist
53 783 001 Ma
Add
con
5 to
dist
53 805 001 Ma
The
Mag
liqu
Mag
53 813 001 Ma
Rep
Bott
the
tray
by Catalo
cience.com
agNA Pure LC Ca
ese adhesive films
ified nucleic acids
move a sample by
ng a new Cartridge
htCycler
Fluore
h 5'-LightCycler
R
bProbe probes on
nopure Plasmid M
pare highly purifie
ng a modified alka
n be used in transfe
uencing, and clon
nopure Plasmid M
pare highly purifie
ng a modified alka
n be used in transfe
uencing, and clon
agNA Pure LC DN
ate high-purity DN
truments. External
ates and difficult to
h LightCycler
Sys
truments.
agNA Pure LC Co
oling Block for hold
tion Module of the
Rings with purified
nsferred to an instr
agNA Pure LC mR
e this optimized bu
tured cells, and to
immediately proce
Instruments. Use b
NA HS Kit.
agNA Pure LC DN
ditional Lysis/Bind
ation Kit I and Ma
s of mammalian bl
bilization of nucleic
agNA Pure LC Tot
ffer Refill
ditional lysis buffer
sma, and to stabiliz
gNA Pure LC Tota
cleic Acid Isolation
truments.
agNA Pure LC Re
e MagNA Pure LC
ding two large rea
gNA Pure LC Instr
agNA Pure LC Tip
ditional Tip Rack fo
ntaining MagNA Pu
to 1000 l. These T
tinguish them from
agNA Pure LC Tip
ditional Tip Rack fo
ntaining MagNA Pu
o 50 l. These Tip R
tinguish them from
agNA Pure LC Liq
e MagNA Pure LC
gNA Pure LC Instr
uids from the reage
gNA Pure LC Was
agNA Pure LC Wa
placement accesso
tle of all MagNA P
reagent/sample st
y.
og Numb
Product N

artridge Seal
seal the MagNA P
s. They prevent eva
perforating the sea
e Seal.
escein CPG
the 3'-end of oligo
Red-labeled oligon
LightCycler
480 a
Midi Kit
ed plasmid DNA in
aline lysis method.
ection, PCR, restric
ing.
Maxi Kit
ed plasmid DNA in
aline lysis method.
ection, PCR, restric
ing.
NA Isolation Kit II
NA from 1 to 10 mg
lysis protocols allo
o homogenize sam
stems, block cycler
ooling Block, A-R
ding 1 or 2 A-Ring
e MagNA Pure LC
nucleic acids and
rument platform fo
RNA Isolation Kit
uffer to lyse mamm
stabilize mRNA. L
essed or after long-
buffer in combinat
NA Isolation Kit I
ing Buffer for use
gNA Pure LC DNA
lood, blood cells, o
c acids.
tal Nucleic Acid
r for the lysis of ma
ze nucleic acids. U
al Nucleic Acid Isol
n Kit - Large Volum
eagent Reservoir
Reagent Reservoir
gent tubs and six
ruments.
p Rack
or large reaction ti
ure LC Reaction Ti
Tip Racks for large
m the Tip Racks for
p Rack
or small reaction ti
ure LC Reaction Ti
Racks for small tip
m the Tip Racks for
quid Waste Funne
Liquid Waste Funn
ruments. The robot
ent/sample stage t
ste Bottle.
aste Bottle Tray
ory tray holding the
Pure LC Instrumen
tage into the Mag
ber
Name
Pure Cartridge whe
aporation and cont
al of the well, and
onucleotides. Use i
nucleotides for det
and Carousel-Base
medium quantitie
Purified plasmid D
ction digestion, So
large quantities (u
Purified plasmid D
ction digestion, So
I (Tissue)
g tissue with Mag
ow DNA purificatio
mples. Use purified
rs and other real-t
Ring
gs with barcodes. U
Software for autom
d PCR reagents. A-
or testing.
t I Lysis Buffer
malian whole blood
Lysed and stabilized
-term storage usin
tion with the MagN
Lysis/Binding
with the MagNA P
A Isolation Kit La
or cultured cells, an
Isolation Kit - Ly
ammalian blood, s
Use in combination
lation Kit, MagNA
me on MagNA Pur
Rack
r Rack is an additio
medium/small rea
ps for holding 3 ti
ips (large), each w
e tips are colored b
r small tips which a
ips for holding 3 ti
ips (small), each w
s are colored yello
r large tips which a
el
nel is a replaceme
tic nozzle head pip
through this funne
e MagNA Pure LC
ts. The robot pipet
NA Pure LC Waste
en storing
tamination.
then reseal
n combination
tection with
ed Systems.
es (up to 100 g)
DNA from E. coli
outhern blotting,
up to 500 g)
DNA from E. coli
outhern blotting,
NA Pure LC
on from FFPE
DNA for PCR
time PCR
Use the Post
mated filling of
-Rings are then
Refill
d, blood and
d samples can
ng MagNA Pure
NA Pure LC
Buffer - Refill
Pure LC DNA
arge Volume. For
nd the
ysis/Binding
erum, or
n with the
Pure LC Total
e LC
onal rack for
gent tubs in
p trays
with a capacity of
blue to easily
are yellow.
p trays
with a capacity of
ow to easily
are blue.
nt accessory for
pets unused
el into the
Liquid Waste
ts liquids from
e Bottle on this

1 kit f
1 kit f
1 kit
1
Pack Size

200 seals
1 g
for up to 20 prepar
for up to 10 prepar
for up to 192 isola
1 cooling block
2 x 35 ml
100 ml
100 ml
1 reagent rack
1 tip rack
1 tip rack
liquid waste funn
1 waste bottle tray
rations
rations
ations
el
y

Price in

inquire
inquire
149,40
172,30
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Pr

Cat.

03 26
03 26
03 26
03 26
03 27
03 30
03 30
03 31
03 31
03 31
03 31
03 33
03 33
03 33
roducts b

No.
61 883 001 Lig
Rea
and
mR
No
64 785 001 Ma
Isol
type
pur
Exte
64 793 001 Ma
Isol
plas
elut
Ligh
bloo
67 393 001 Ma
Isol
olig
LC
Syst
70 289 001 Hig
Isol
fres
sect
Ligh
00 226 001 Exp
Enz
outs
PCR
amp
00 234 001 Exp
Enz
outs
PCR
amp
10 515 001 Ma
Isol
bloo
Res
bloc
15 843 001 Wa
Spe
end
high
amp
15 932 001 Wa
Spe
end
high
amp
15 959 001 Wa
Spe
end
high
amp
30 591 001 Ma
Isol
tiss
for
syst
33 566 001 Ter
Add
frag
and
ddN
33 574 001 Ter
Add
frag
and
ddN

by Catalo
htCycler
h-G6P
ady-to-use mix of p
d standard RNA fo
NA in RT-PCR ass
pseudogenes or c
agNA Pure LC DN
ate high-purity ba
es, up to 100 l vo
ified DNA for PCR
ernal lysis protoco
agNA Pure LC Tot
ate total nucleic ac
sma using MagNA
ted in 50-100 l. N
htCycler
Systems
od.
agNA Pure LC mR
ate high-quality m
go(dT) and streptav
Instruments. Use p
tems and block cy
gh Pure RNA Para
ate total RNA from
sh-frozen tissue fo
tions is ideal for re
htCycler
Carouse
pand High Fidelity
zyme blend for rob
standing yield, spe
R, primer extension
plification assay or
pand High Fidelity
zyme blend for rob
standing yield, spe
R, primer extension
plification assay or
agNA Pure LC DN
ate high-purity ge
od, blood cells, or
sulting DNA is idea
ck cyclers and oth
ater, PCR Grade
ecially tested and q
dpoint and real-tim
hest quality water
plification systems
ater, PCR Grade
dpoint and real-tim
hest quality water
plification systems
ater, PCR Grade
dpoint and real-tim
hest quality water
plification systems
agNA Pure LC RN
ate total RNA from
ues using MagNA
RT-PCR using Ligh
tems.
rminal Transferas
d nucleotides to th
gments, such as fo
d 3-end labeling w
NTPs (e.g ., DIG-dd
rminal Transferas
d nucleotides to th
gments, such as fo
d 3-end labeling w
NTPs (e.g ., DIG-dd
og Numb
Product N

PDH Housekeepin
primers and HybPr
r detection/quantit
says using LightCy
contaminating DNA
NA Isolation Kit II
cterial and fungal
lume, using MagN
R with LightCycler
ls for BAL, sputum

tal Nucleic Acid
cids (viral DNA/RN
A Pure LC Instrume
Nucleic acids are id
s and block cyclers
RNA HS Kit
mRNA from 1 x 10
7
vidin-coated magn
purified mRNA for
yclers for gene exp
affin Kit
m formalin-fixed pa
r use in RT-PCR. T
elative quantificatio
el-Based System.
y
PLUS
PCR System
ust amplification o
ecificity, sensitivity
n, carryover preven
r optimize an exist
y
PLUS
PCR System
ust amplification o
n, carryover preven
r optimize an exist
NA Isolation Kit -
nomic DNA from 2
cultured cells usin
al for qPCR using L
er real-time PCR i
qualified for use in
me PCR assays, seq
is required. All Lig
s contain this PCR
me PCR assays, seq
s contain this PCR
me PCR assays, seq
s contain this PCR
NA Isolation Kit II
m fresh-frozen or fo
A Pure LC Instrume
htCycler
Instrum
se
he 3-OH ends of d
or homopolymeric t
with either radioact
dUTP).
se
he 3-OH ends of d
or homopolymeric t
with either radioact
dUTP).
ber
Name
ng Gene Set
robe probes specif
tative comparison
cler
Carousel-Ba
A are detected.
II (Bacteria, Fung
DNA from many d
NA Pure LC Instrum
Systems and blo

m, CSF, and urine.
Isolation Kit - La
NA) from up to 1 m
ents. Purified nucle
deal for qPCR and
s. Do not use this k
mammalian blood
netic particles with
qRT-PCR with Lig
pression analysis.
araffin-embedded
The quality of RNA
on of mRNA with R
m
of fragments up to
, and accuracy. Us
ntion, to develop a
ing one.
m
of fragments up to
, and accuracy. Us
ntion, to develop a
ing one.
Large Volume
20 l to 1 ml of m
ng MagNA Pure LC
LightCycler
Syste
nstruments.
n all PCR or RT-PC
quencing, and whe
ghtCycler
kits and
grade water.
n all PCR or RT-PC
quencing, and whe
ghtCycler
kits and
grade water.
n all PCR or RT-PC
quencing, and whe
ghtCycler
kits and
grade water.
II (Tissue)
ormalin-fixed para
ents. Resulting RNA
ents and other rea
double- or single-s
tailing or end-labe
tive or chemically
double- or single-s
tailing or end-labe
tive or chemically
fic for h-G6PDH,
of G6PDH
ased Systems.
gi)
different sample
ments. Use
ck cyclers.
arge Volume
ml serum and
eic acids are
qRT-PCR using
kit for whole
d cells using
h MagNA Pure
ghtCycler

tissue and
A from paraffin
RT-PCR on the
5 kb with
se in PCR/RT-
new
5 kb with
se in PCR/RT-
new
ammalian whole
C Instruments.
ems, standard
R. Use with
enever the
d other Roche
R. Use with
enever the
d other Roche
R. Use with
enever the
d other Roche
affin-embedded
A from is ideal
al-time PCR
tranded DNA
eling with dNTPs,
modified
tranded DNA
eling with dNTPs,
modified

1 set for up to 9
1 kit
1 kit
1 kit
1 kit
500 U (2 x 250
final volume ea
2,500 U (10 x 2
20 l final volu
1 kit for up to 9
100
25
25
1 kit
8,000 U (fo
reacti
24,000 U (fo
reacti

Pack Size

96 reactions of 20
volume
for up to 192 isola
for up to 192 isola
for up to 192 isola
for up to 100 isola
U) for up to 500 re
ach containing 1 U
ume each containi
blend
sample volume
0 ml (4 vials of 25
for up to 192 isola
ons, 400 U per rea
ons, 400 U per rea
www.roche
l final reaction
ations
ations
ations
ations
eactions of 20 l
U enzyme blend
500 reactions of
ng 1 U enzyme
s, depending on
ml)
ml)
ml)
ations
end labeling
action)
end labeling
action)
e-applied-science

Price in

inquire
inquire
inquire
inquire
477,20
517,30
2.072,30
inquire
310,70
155,30
123,90
inquire
100,10
225,20

187

e.com

Pr
188

www.r

Cat.

03 33
03 33
03 35
03 35
03 35
03 35
03 35
03 35
03 35
03 35
03 35
03 35
03 35
03 35
roducts b
roche-applied-sc

No.
35 399 001 Pro
Inhi
tran
deg
PCR
pre
35 402 001 Pro
Inhi
tran
deg
PCR
pre
53 575 910 DIG
3'-e
usin
olig
mem
53 583 910 DIG
For
11-d
with
blot
53 591 910 DIG
Non
pre
com
dete
53 621 001 5'/3
Ana
End
3 e
reac
57 317 001 Lig
Sim
rem
onto
all L
58 941 001 Ma
2.0
Use
biol
and
58 968 001 Ma
Qui
app
lysis
kits
58 976 001 Ma
Qui
app
lysis
kits
59 085 001 Ma
One
tem
Lys
Lys
59 093 001 Ma
Add
sam
one
Mag
59 123 001 Alk
Alka
ami
dire
ELIS
59 247 910 Dig
Sub
vitro
of 3
the
by Catalo
cience.com
otector RNase Inh
ibits a wide spectr
nscription reaction
gradation. Use in m
R, RNase protectio
paration of RNase
otector RNase Inh
ibits a wide spectr
nscription reaction
gradation. Use in m
R, RNase protectio
paration of RNase
G Oligonucleotide
end labeling of olig
ng DIG-11-ddUTP
gonucleotides are u
mbrane-blot applic
G Oligonucleotide
fast and sensitive
dUTP and recomb
h DIG-dUTP are us
ts or in situ hybrid
G Gel Shift Kit, 2n
nradioactive detec
paring 3'-end-labe
mplexes in gel mob
ects as little as 20
3' RACE Kit, 2nd
alyze mRNA struct
ds (RACE). Generat
ends from low-cop
ction products wit
htCycler
Cappi
mplifies the process
move a cap from th
o a capillary holdin
LightCycler
Capil
agNA Lyser Green
ml sample tubes w
e in the MagNA Ly
logical materials u
d MagNA Pure Com
agNA Lyser Instru
ckly and complete
plications. Use in c
s buffers from the
. Easily integrates
agNA Lyser Instru
ckly and complete
plications. Use in c
s buffers from the
. Easily integrates
agNA Lyser Rotor
e additional MagN
mperature of up to
er Rotor at +2 to +
er Instrument. Use
agNA Lyser Rotor
ditional MagNA Ly
mple tubes for tissu
e shipped with the
gNA Lyser Rotor C
kaline Phosphata
aline Phosphatase
ino and carbohydr
ectly for conjugatio
SAs, microarrays, a
goxigenin-11-UTP
bstrate for SP6, T3,
o transcription RN
35 to 65. Detect lab
DIG Nucleic Acid
og Numb
Product N

hibitor
rum of RNases also
s (up to +60C) to
many techniques: c
on, in vitro virus re
-free antibodies.
hibitor
rum of RNases also
s (up to +60C) to
many techniques: c
on, in vitro virus re
-free antibodies.
e 3'-End Labeling
gonucleotides from
and recombinant
used as hybridizati
cations and in situ
e Tailing Kit, 2nd
tailing of oligonuc
inant Terminal Tra
sed for DNA or RN
dization.
nd generation
tion of sequence-s
eled oligonucleotid
bility shift assays. C
fmol of the contro
Generation
ture and expressio
te full-length cDN
y RNA, amplify an
hout cloning.
ng Tool
s of closing LightC
e LightCycler
Ca
ng the reaction mix
llaries.
n Beads
with ceramic beads
yser Instrument to
sing lysis buffers s
mpact isolation kit
ument
ely homogenize tis
ombination with M
MagNA Pure LC o
into your laborato
ument
ely homogenize tis
ombination with M
MagNA Pure LC o
into your laborato
r Cooling Block
NA Lyser Rotor Coo
16 sample tubes b
+8C. Identical to t
e with additional ro
r
yser Rotors. Each M
ue homogenization
MagNA Lyser Inst
Cooling Blocks to i
ase recombinant,
e recombinant can
rate groups. The e
on without prior dia
and western blot a
P
and T7 RNA Polym
NA labeling reactio
beled RNA using A
Detection (color o
ber
Name
o in in challenging
o protect RNA sam
cDNA synthesis, RT
plication, transcrip
o in in challenging
o protect RNA sam
cDNA synthesis, RT
plication, transcrip
g Kit, 2nd genera
m 14 to 100 nucleo
Terminal Transfera
ion probes in all ty
hybridization.
d generation
cleotides at the 3'-
ansferase. Oligonu
NA hybridization in
specific DNA bind
de probes that dete
Convenient and se
ol oligo.
n by Rapid Amplif
As, isolate and ch
d clone rare mRNA
Cycler
Capillaries.
apillary box and pla
xture. The tool is c
s to purify RNA, m
disrupt cells, tissu
supplied with the M
ts.
sue for many extra
MagNA Lyser Gree
or MagNA Pure Co
ry workflow.
sue for many extra
MagNA Lyser Gree
or MagNA Pure Co
ry workflow.
oling Block for mai
being loaded onto
the one shipped w
otors to increase th
MagNA Lyser Roto
n. These rotors are
trument. Use with
ncrease throughp
highly active
be coupled to pro
enzyme solution ca
alysis. Application
analysis.
merases. Replaces
on using a percent
Anti-DIG-AP and c
or chemiluminesce
g reverse
ples from
T-PCR, qRT-
ption/translation,
g reverse
ples from
T-PCR, qRT-
ption/translation,
ation
tides in length
ase. DIG-labeled
ypes of
end using DIG-
cleotides tailed
membrane
ing proteins. For
ect DNA-protein
nsitive kit
ication of cDNA
aracterize 5or
A, and sequence
. Use the tool to
ace it directly
compatible with
mRNA, and DNA.
es, and other
MagNA Pure LC
action
en Beads and
ompact isolation
action
en Beads and
ompact isolation
intaining the
the MagNA
with the MagNA
hroughput.
or holds up to 16
e identical to the
additional
ut.
oteins via its
an be used
s include
s UTP in the in
Dig-UTP ratio
choose one of
ent) Kits.

10
1 kit for up to 2
oligonucleotide
of a
1 kit for up to
oligonucleotide
of a
1 kit for up to 2
reactions wi
reactions, chem
for up to 20
oligonucleotid
1 kit
100 tubes (
1 instrume
1 instrume
57
Pack Size

2,000 U
0,000 U (5 x 2,000
25 labeling reactio
s per assay corres
30-mer oligonucle
e per assay corresp
30-mer oligonucle
20 Oligonucleotide
ith DIG-11-ddUTP,
miluminescent det
blots, DNA binding
de for up to 20 con
1 capping tool
ent (110 V, plus ac
ent (220 V, plus ac
1 cooling block
2 rotors
10 mg (500 l)
l (200 nmol, 3.5 m
U)
ons, 100 pmol of
sponding to 1 g
eotide
ons, 100 pmol
ponding to 1 g
eotide
e 3'-end labeling
, 200 binding
tection reaction
g protein and
ntrol reactions
tions
amic beads)
ccessories)
ccessories)
mM)

Price in

134,00
496,80
571,60
531,40
715,20
478,50
inquire
inquire
inquire
inquire
inquire
inquire
440,80
196,10

Pr

Cat.

03 51
03 51
03 51
03 51
03 53
03 53
03 53
03 53
03 53
03 53
03 53
03 54
03 55
03 55
03 56
roducts b

No.
15 567 001 Lig
Eas
Cap
Hyb
exp
15 575 001 Lig
Eas
Cap
Hyb
exp
15 869 001 Lig
Eas
Cap
Gre
ana
15 885 001 Lig
Eas
Cap
Gre
ana
31 287 001 Tra
Rec
frag
and
end
31 295 001 Tra
Rec
frag
and
end
31 317 001 Tra
Rec
frag
and
end
31 414 001 Lig
Perf
Cap
wid
exp
31 520 001 Ma
Bar
284
area
31 538 001 Ma
One
Prin
Lab
39 806 001 Lig
Use
dUT
pro
that
42 394 001 Ma
For
bloo
pur
nort
53 361 001 Fas
Enz
Poly
frag
RIC
53 400 001 Fas
Enz
Poly
frag
RIC
61 402 001 Ma
Gre
serv
grea
Soft
by Catalo
htCycler
FastSt
y-to-use hot start
pillaries on LightCy
bProbe probes for
pression analysis. A
htCycler
FastSt
y-to-use hot start
bProbe probes for
htCycler
FastSt
y-to-use hot start
een I for detection.
alysis. Addition of M
htCycler
FastSt
y-to-use hot start
anscriptor Revers
combinant reverse
gments up to 14 kb
d LightCycler
and
d labeling, first stra
anscriptor Revers
combinant reverse
gments up to 14 kb
d LightCycler
and
anscriptor Revers
combinant reverse
gments up to 14 kb
d LightCycler
and
htCycler
2.0 Ins
form fast and sens
pillary-based techn
e selection of fluo
perimental design a
agNA Pure LC Ba
rcode labels for use
44. These barcode
a of the MagNA P
agNA Pure LC Ba
e Barcode Printer R
nter TLP 2844 to pr
bels.
htCycler
Uracil
e with LightCycler
TP-containing amp
duct carryover con
t only native dTTP-
agNA Pure LC RN
automated isolatio
od cells or cultured
ified RNA in RT-PC
thern blots, and fo
stStart High Fidel
zyme blend that co
ymerase with fourf
gments up to 5 kb.
CH template amplif
stStart High Fidel
zyme blend that co
ymerase with fourf
gments up to 5 kb.
CH template amplif
agNA Pure LC Gre
easing station, pad
vicing of MagNA P
asing, the greasing
tware greasing pro
og Numb
Product N

tart DNA Master
reaction mix for h
ycler
Carousel-Ba
detection. Use also
Addition of MgCl
2

tart DNA Master
reaction mix for h
ycler
Carousel-Ba
detection. Use also
Addition of MgCl
2

tart DNA Master
reaction mix for h
ycler
Carousel-Ba
Use in two-step R
MgCl
2
is not neces
tart DNA Master
reaction mix for h
ycler
Carousel-Ba
Use in two-step R
MgCl
2
is not neces
se Transcriptase
transcriptase for r
b. Used in two-ste
d other real-time P
and cDNA synthes
se Transcriptase
transcriptase for r
b. Used in two-ste
d other real-time P
and cDNA synthes
se Transcriptase
transcriptase for r
b. Used in two-ste
d other real-time P
and cDNA synthes
strument
sitive real-time PCR
nology provides fas
rescence formats
and analysis.
arcode Labels
e with the MagNA
labels are suitable
ure LC Sample Ca
arcode Printer Rib
Ribbon for use wit
roduce barcodes o
-DNA Glycosylas
FastStart enzyme
plified DNA produc
ntamination in new
-containing DNA i
NA Isolation Kit -
on of total RNA fro
d cells using MagN
CR with LightCycle
or gene expression
lity PCR System
ombines the benefi
fold higher accura
. Use for multiplex
fication, and difficu
lity PCR System
ombines the benefi
fold higher accura
. Use for multiplex
fication, and difficu
easing Set
s, O-rings and gre
Pure LC nozzlehea
g station is placed
ogram performs th
ber
Name
PLUS HybProbe
ighly sensitive PCR
ased Systems whe
o in two-step RT-P
is not necessary.
PLUS HybProbe
ighly sensitive PCR
ased Systems whe
o in two-step RT-P
is not necessary.
PLUS SYBR Gree
ighly sensitive PCR
ased Systems whe
RT-PCR for gene ex
ssary.
PLUS SYBR Gree
ighly sensitive PCR
ased Systems whe
RT-PCR for gene ex
ssary.
robust transcriptio
p RT-PCR using th
PCR systems. Ideal
is, RACE, and mor
robust transcriptio
p RT-PCR using th
PCR systems. Ideal
is, RACE, and mor
robust transcriptio
p RT-PCR using th
PCR systems. Ideal
is, RACE, and mor
R on this proven in
st, reproducible re
maximizes flexibili
A Pure LC Barcode
e for the new barco
artridge.
bbon
th the MagNA Pure
on the MagNA Pur
se
e-containing kits t
ced in previous PC
wly prepared mixes
s available for real
High Performan
om up to 200 l wh
NA Pure LC Instru
er
Systems, block
n analysis.
its of FastStart Taq
acy with the abilty t
PCR, sequencing,
ult PCRs.
its of FastStart Taq
acy with the abilty t
PCR, sequencing,
ult PCRs.
ease for automated
d O-Rings. For aut
on the Instrument
he process.
R in LightCycler

en using
PCR for gene
R in LightCycler

en using
PCR for gene
en I
R in LightCycler

en using SYBR
xpression
en I
R in LightCycler

en using SYBR
xpression
n of RNA
hermal cyclers
for sequencing,
re.
n of RNA
hermal cyclers
for sequencing,
re.
n of RNA
hermal cyclers
for sequencing,
re.
nstrument.
sults, and a
ty in
Printer TLP
ode labeling
e LC Barcode
re LC Barcode
o eliminate
CRs. Prevent PCR
s, and ensure
l-time PCR.
ce
hole blood or 10
6

ments. Use
k cyclers,
q DNA
to amplify
RT-PCR, GC-
q DNA
to amplify
RT-PCR, GC-
d or manual
tomated
t stage, and the

1 kit for up to 4
1 kit for up to 9
1 kit for up to 9
1 kit for up to 4
2,000 U (4 x
of 50 l fina
Transcri
500 U for up to
each contain
250 U for up to
each contain
1 instrument
station (de
1,000
5
1 kit
2,500 U (10 x 2
50 l final v
FastSt
500 U (2 x 250
final volume ea
Pack Size

80 reactions of 20
volume
96 reactions of 20
volume
96 reactions of 20
volume
80 reactions of 20
volume
l volume each con
ptor Reverse Trans
50 reactions of 50
ning 10 U Transcri
Transcriptase
25 reactions of 50
ning 10 U Transcri
Transcriptase
(plus related prod
esktop or noteboo
labels (10 mm x 6
1 ribbon
50 l (100 U, 2 U/
for up to 192 reac
volume each conta
tart Taq DNA Polym
U) for up to 200 re
ach containing 2.5
DNA Polymerase
1 set
www.roche
l final reaction
l final reaction
l final reaction
l final reaction
200 reactions
ntaining 10 U
scriptase
0 l final volume
iptor Reverse
0 l final volume
iptor Reverse
ducts and data
k version))
0 mm)
l)
ctions
000 reactions of
aining 2.5 U
merase
eactions of 50 l
U FastStart Taq
e-applied-science

Price in

inquire
inquire
inquire
inquire
946,00
266,10
162,70
inquire
inquire
inquire
inquire
inquire
2.107,90
497,50
inquire

189

e.com

Pr
190

www.r

Cat.

03 56
03 56
03 57
03 57
03 60
03 60
03 60
03 60
03 60
03 61
03 62
03 70
03 70
03 70
roducts b
roche-applied-sc

No.
61 429 001 Ma
Kit w
noz
pipe
Mag
61 488 001 Lig
Use
com
olig
eno
min
73 788 001 Aga
Aga
ana
of h
76 094 001 Ma
One
doc
prin
Mag
03 920 001 Lig
Perf
Ligh
acc
03 954 001 Lig
Perf
(100
ens
uniq
03 962 001 Lig
Perf
l) f
prec
cod
03 989 001 Lig
For
(pac
vers
Cap
04 721 001 Ma
Add
III (T
inhi
RNA
12 066 001 Lig
For
high
with
req
med
22 614 001 Deo
PCR
RT-
sod
colo
07 580 001 -
For
ana
pre
imm
07 598 001 -
For
ana
pre
imm
07 601 001 -
For
ana
pre
imm

by Catalo
cience.com
agNA Pure LC O-
with a vial of greas
zzle head O-rings a
etting accuracy of
gNA Pure Compac
htCycler
Red 6
mbination with 3'-L
gonucleotides for d
ough LightCycler

nimum of 5 50 nm
arose MP
arose MP is a high
alytical and prepara
high molecular wei
agNA Pure LC Ba
e Barcode Printer T
cumentation during
nts barcodes create
gNA Pure LC Sam
htCycler
2.0 Ca
form easy unloadin
htCycler
Sample
cessory.
htCycler
2.0 Sa
form up to 32 simu
0 l) for the LightC
sure precise positio
que bar code for e
htCycler
2.0 Sa
form up to 32 simu
for the LightCycler
cise positioning an
de for easy identific
htCycler
Sampl
replacement of w
ck size of 2). It is c
sions. Developed t
pillaries in the Ligh
agNA Pure LC RN
ditional lysis buffer
Tissue) and MagN
ibits RNases durin
A. Use to homogen
htCycler
Capilla
LightCycler
2.0 I
hly sensitive bacte
h LightCycler
2.0
uirements of the E
dical devices.
oxynucleoside Tr
R-Grade set for ap
-PCR, DNA labeling
ium salts of dATP,
orless solutions in
Glucuronidase
hydrolysis of stero
alysis, and to detec
paration to cleave
munoassays, or oth
Glucuronidase
hydrolysis of stero
paration to cleave
munoassays, or oth
Glucuronidase
hydrolysis of stero
paration to cleave
munoassays, or oth
og Numb
Product N

Ring Maintenanc
se and 12 sets of 8
and for periodic re
the nozzle head o
ct Instruments.
10-N-hydroxysuc
the 5'-amino end o
LightCycler
Fluor
detection with Hyb
Red 610-N hydrox
mol oligonucleotid
h strength, multipu
ative electrophores
ight DNA via pulse
arcode Printer TL
TLP 2844 for samp
g MagNA Pure LC
ed by MagNA Pur
mple Cartridges and
apillary Releaser
ng of the LightCyc
Carousel in one s
ample Carousel (
ultaneous PCR rea
Cycler
2.0 Instrum
oning and reprodu
easy identification.
ample Carousel (
ultaneous PCR rea
r
2.0 Instrument.
nd reproducible re
cation.
le Carousel O-Ri
orn out LightCycle
compatible with all
to ensure proper p
htCycler
Sample C
NA Isolation Tissu
r for use with the M
NA Pure LC Instrum
g cell lysis, releasi
nize tissue with M
aries (100 l) MG
Instruments if usin
erial, fungal nucleic
Sample Carousel
European Directive
riphosphate Set
plications requirin
g, sequencing. Co
, dCTP, dGTP, dTTP
water (pH 8.3).
oid conjugates (glu
ct benzodiazepine
glucuronides prio
her analytical meth
oid conjugates (glu
ct benzodiazepine
glucuronides prio
her analytical meth
oid conjugates (glu
ct benzodiazepine
glucuronides prio
her analytical meth
ber
Name
ce Kit
8 O-rings to prolon
eplacement of O-ri
of both MagNA Pu
ccinimide ester
of oligonucleotides
rescein CPG -label
Probe probes. One
xysuccinimide este
des.
rpose agarose dev
sis of nucleic acids
e field gel electrop
P 2844
ple identification, tr
C purification runs.
re LC Software Ver
d/or non-barcode-
cler
Capillaries fro
imple step, using t
(100 l)
actions in this sam
ment. Heat-resistan
ucible results. Labe
(20 l)
actions in this sam
Heat-resistant ma
esults. Labeled with
ing
er
Sample Carous
l LightCycler
Sam
positioning of the L
Carousels.
ue Lysis Buffer -
MagNA Pure LC R
ments. This reagen
ng and stabilizing
agNA Lyser Instru
GRADE
ng large reaction v
c acid detection. C
(100 l). This prod
e 98/79/EC for in vi
ng high-quality rea
ntains individual v
P at 100 mM conc
ucuronides) in urin
in small doses. Us
or to GC-MS, HPLC
hods.
ucuronides) in urin
in small doses. Us
or to GC-MS, HPLC
hods.
ucuronides) in urin
in small doses. Us
or to GC-MS, HPLC
hods.
ng the life of
ngs, ensuring
re LC and
s. Use in
ed
e vial has
er to label a
veloped for
s and separation
phoresis (PFGE).
racking, and
This device
rsion 3.0 for the
-labeled tubes.
om the
this convenient
ple carousel
nt materials
eled with a
ple carousel (20
aterials ensure
h a unique bar
sel O-Rings
mple Carousel
LightCycler

Refill
RNA Isolation Kit
t efficiently
mRNA and total
ment.
olumes. For
Compatible only
duct fulfills the
itro diagnostic
gents: RT, PCR,
ials of the
entration. Clear,
ne, in doping
e during sample
C,
ne, in doping
e during sample
C,
ne, in doping
e during sample
C,

1 vial of
1 vial (for 5
1 pack (con
cap
4 x 1,250 l (4 x
37,500 rea

Pack Size

grease and 12 x 8
5 x 50 nmol oligon
500 g bulk
1 barcode printer
1 capillary release
1 sample carouse
1 sample carouse
2 O-Rings
70 ml
ntaining 8 boxes, e
pillaries and stopp
x 125 mol, 4 x 100
actions at 20 l fin
1 ml
5 ml
15 ml
8 O-rings
nucleotides)
r
er
l
l
each with 96
ers)
0 mM) for up to
nal volume

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
1.061,20
49,90
181,80
491,90

Pr

Cat.

03 70
03 70
03 70
03 70
03 70
03 72
03 72
03 73
03 73
03 73
03 73
03 73
03 73
03 73
roducts b

No.
08 152 001 Stre
Idea
vitro
Hig
the
08 969 001 Try
Spe
chro
spe
chy
08 985 001 Try
Spe
chro
spe
chy
09 507 001 LC
Effic
com
Com
buc
09 582 001 LC
Effic
com
Com
buc
24 689 001 LC
This
vers
This
24 697 001 LC
Des
ada
caro
roto
30 964 001 Ma
Rea
from
usin
PCR
PCR
30 972 001 Ma
Rea
from
usin
PCR
PCR
31 146 001 Ma
Ben
sam
pur
stan
32 681 001 dAT
Use
reag
reac
of t
32 690 001 dCT
Suit
as r
seq
solu
32 703 001 dGT
Suit
as r
seq
solu
32 711 001 dTT
Suit
as r
seq
solu

by Catalo
eptavidin Mutein
al for gentle purific
o expressed biotin
h binding capacity
matrix.
psin recombinan
ecifically digests pr
omatographic met
ectrometry. Tested
ymotrypsin, and oth
psin recombinan
ecifically digests pr
omatographic met
ectrometry. Tested
ymotrypsin, and oth
Carousel Centrif
ciently centrifuge
mpact benchtop de
mpatible with Ligh
cket, sold separate
Carousel Centrif
ciently centrifuge
mpact benchtop de
mpatible with Ligh
cket, sold separate
Carousel Centrif
s bucket enables c
sions when using t
s silver rotor bucke
Carousel Centrif
signed for use with
apter accessories e
ousels used with L
or and two rotor bu
agNA Pure Comp
ady-to-use reagent
m mammalian cells
ng MagNA Pure C
R with LightCycler
R instruments.
agNA Pure Comp
ady-to-use reagent
m mammalian cells
ng MagNA Pure C
R with LightCycler
R instruments.
agNA Pure Comp
nchtop instrument
mples, such as bloo
ified nucleic acid i
ndard cyclers, and
TP
e dATP, PCR Grade
gents are required
ctions, and sequen
he sodium salt (pH
TP
table for applicatio
reverse transcriptio
uencing/cycle seq
ution of the sodium
TP
uencing/cycle seq
ution of the sodium
TP
uencing/cycle seq
ution of the sodium
og Numb
Product N

n Matrix
cation of biotinylat
nylated proteins us
y and multiple reus
nt, Proteomics Gr
roteins separated b
thods during samp
for the absence of
her contaminating
nt, Proteomics Gr
roteins separated b
thods during samp
for the absence of
her contaminating
fuge 2.0
PCR samples in Li
evice. For use with
tCycler
1.5 and o
ly).
fuge 2.0
PCR samples in Li
evice. For use with
tCycler
1.5 and o
ly).
fuge 2.0 Bucket 2
compatibility with L
the LC Carousel C
et replaces the buc
fuge 2.0 Rotor Se
h earlier model LC
enable compatibilit
LightCycler
Carou
uckets.
act Nucleic Acid
ts in prefilled, seal
s and viral nucleic
ompact Instrumen
Systems, standa
act Nucleic Acid
s and viral nucleic
ompact Instrumen
Systems, standa
act Instrument
for automated nuc
od, serum, plasma,
in PCR, RT-PCR on
downstream appl
e sodium salt for a
d: reverse transcrip
ncing. Supplied as
H 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
ber
Name
ted proteins. Teste
sing RTS AviTag Bi
se permits cost-eff
rade
by 2D gel electrop
ple preparation for
f porcine trypsin (s
proteases.
rade
by 2D gel electrop
ple preparation for
f porcine trypsin (s
proteases.
ghtCycler
carous
the LightCycler

older versions (req
ghtCycler
carous
the LightCycler

older versions (req
2.1
LightCycler
1.5 a
Centrifuge to prepa
cket included with
et
Carousel Centrifu
ty with all types of
usel-Based Instrum
d Isolation Kit I
ed cartridges for p
acids in a volume
nts. Use purified D
ard cyclers and oth
d Isolation Kit I -
ed cartridges for p
acids in a volume
nts. Use purified D
ard cyclers and oth
cleic acid purificat
, or cells in 1540
n LightCycler
Inst
ications.
pplications where
ption, PCR, RT-PCR
100 mM clear col
uality reagents are
DNA labeling reac
It is a 100 mM cle
uality reagents are
DNA labeling reac
It is a 100 mM cle
uality reagents are
DNA labeling reac
This is a 100 mM
d for use with in
iotinylation Kits.
fective use of
horesis or liquid
mass
serine protease),
horesis or liquid
mass
serine protease),
sels using this
2.0 instrument.
uires different
sels using this
2.0 instrument.
uires different
nd older
are PCR samples.
h the centrifuge.
ges. These
sample
ments. Includes
purifying DNA
up to 400 l
NA for PCR/RT-
her real-time
Large Volume
purifying DNA
up to 1 ml
NA for PCR/RT-
her real-time
tion from 1-8
minutes. Use
truments,
high-quality
R, DNA labeling
orless solution
required, such
ctions, and
ear colorless
required, such
ctions, and
ear colorless
required, such
ctions, and
clear colorless

5 m
1 centrifuge p
1 centrifuge p
1 rotor bucke
1 rotor plus
LC
1 kit
1 kit
1 instrument w
moni
4 x 1,250
4 x 1,250
4 x 1,250
4 x 1,250

Pack Size

4 x 100 g
4 x 25 g
plus rotor and buc
plus rotor and buc
et for LC Carousel
2 buckets for the e
C Carousel Centrifu
with integrated PC
itor and barcode re
l (4 x 125 mol, 4
l (4 x 125 mol, 4
l (4 x 125 mol, 4
l (4 x 125 mol, 4
www.roche
ume
cket (115 Volt)
cket (230 Volt)
Centrifuge 2.0
earlier model
uge
tions
tions
C, touchscreen
eader
x 100 mM)
x 100 mM)
x 100 mM)
x 100 mM)
e-applied-science

Price in

445,60
287,20
94,30
inquire
inquire
inquire
inquire
inquire
inquire
inquire
1.029,80
1.029,80
1.029,80
1.029,80

191

e.com

Pr
192

www.r

Cat.

03 73
03 73
03 73
03 75
03 75
03 75
03 78
03 78
03 78
03 78
03 78
03 78
04 34
04 34
04 34
04 34
roducts b
roche-applied-sc

No.
32 720 001 dUT
Use
req
con
Sup
32 738 001 Did
2',3
prim
Klen
ddA
the
34 927 001 Taq
Ma
doc
in p
prim
.
52 178 001 Lig
Eas
Cap
Hyb
exp
52 186 001 Lig
Eas
Cap
Gre
ana
53 166 001 Ma
This
Mag
for
one
88 237 001 Ma
One
Inst
88 270 001 Ma
One
Inst
88 288 001 Ma
One
Inst
88 296 001 Ma
One
Inst
88 300 001 Ma
One
Inst
89 403 001 Pw
Rea
dNT
Taq
clon
40 019 001 Lig
Rea
usin
in P
PCR
40 850 001 Pw
For
gen
RIC
Perf
40 868 001 Pw
For
gen
RIC
Perf
42 054 001 Lig
Full
and
ana
mon
by Catalo
cience.com
TP
e dUTP, PCR Grade
uired: RT, PCR, RT
ntamination betwee
pplied as 100 mM s
deoxynucleoside
'-Dideoxynucleosid
mer catalyzed by
now enzyme and a
ATP, ddCTP, ddGTP
sodium salt (pH 8
q DNA Polymeras
nufactured under
cumentation requir
pharmaceutical and
mer-extension reac
htCycler
FastSt
y-to-use hot start
bProbe probes for
htCycler
FastSt
y-to-use hot start
agNA Pure Comp
s accessory is requ
gNA Pure Compac
lost or contaminat
e nucleic acid extra
agNA Pure Comp
e additional Cartrid
trument.
agNA Pure Comp
e additional Drop C
trument.
agNA Pure Comp
e additional Elution
trument.
agNA Pure Comp
e additional Tube R
trument.
agNA Pure Comp
e additional Waste
trument.
o Master
ady-to-use 2x conc
TPs, and buffer. Hi
q. Use for high fide
ning, and gene exp
htCycler
Multip
ady-to-use 5x mix f
ng LightCycler
Ca
PCR to genotype S
R using a multiplex
o SuperYield DN
high fidelity PCR u
ne expression. High
CH Solution ensure
form digests direc
o SuperYield DN
high fidelity PCR u
ne expression. High
CH Solution ensure
form digests direc
htCycler
Probe
y automated desig
d SimpleProbe prob
alysis, or mutation
noplex or multiplex
og Numb
Product N

e for applications w
T-PCR, labeling, seq
en PCRs to elimina
solution of the sod
Triphosphate Se
de triphosphates i
are used in Sanger
P, ddTTP; each a 1
8.3).
se, GMP Grade
GMP regulations.
rements of researc
d biotechnology in
ctions (sequencing
tart DNA Master
reaction mix for h
ycler
Carousel-Ba
detection. Use also
Addition of MgCl
2

tart DNA Master
reaction mix for h
ycler
Carousel-Ba
Use in two-step R
MgCl
2
is not neces
act Tip Tray Kit
uired when perform
ct Instrument. The
ted tip trays. One t
action.
act Cartridge Ra
dge Rack for use w
act Drop Catche
Catcher for use wi
act Elution Tube
n Tube Rack for us
act Tube Rack
Rack for use with t
act Waste Tank
e Tank for use with
centrated mix of Pw
gher yield and 18-
elity PCR up to 3 kb
pression.
plex DNA Master
for optimal perform
apillaries and the
NPs, analyze muta
x approach.
NA Polymerase
up to 3 kb, site-dir
her yield and 18-fo
es high performanc
tly in PCR mix.
NA Polymerase
up to 3 kb, site-dir
her yield and 18-fo
es high performanc
tly in PCR mix.
e Design Software
gn of primers or pr
bes. For easy quali
detection using Li
x assays with up to
ber
Name
where high-quality
quencing. Avoid c
ate a source of fals
dium salt.
et
nhibit chain elong
r sequencing. Con
0 mM clear colorle
Meets high quality
ch and developmen
ndustry. Use in PCR
g, labeling).
PLUS HybProbe
ighly sensitive PCR
ased Systems whe
o in two-step RT-P
is not necessary.
PLUS SYBR Gree
ighly sensitive PCR
ased Systems whe
RT-PCR for gene ex
ssary.
ming the Leakage
Tip Tray Kit is also
tip tray contains al
ack
with the MagNA P
er
th the MagNA Pur
Rack
se with the MagNA
the MagNA Pure C
h the MagNA Pure
wo SuperYield DN
-fold higher fidelity
b, site-directed mu
r HybProbe
mance in multiplex
LightCycler
2.0 In
ations, and perform
rected mutagenesi
old higher fidelity t
ce using difficult te
rected mutagenesi
old higher fidelity t
ce using difficult te
e 2.0
robes, such as Hyb
itative and gene ex
ghtCycler
Instrum
o four different tar
y reagents are
arryover
se positives.
ation of a
tains 4 vials:
ess solution of
y and
nt laboratories
R, RT-PCR, and
R in LightCycler

en using
PCR for gene
en I
R in LightCycler

en using SYBR
xpression
Test using the
o a replacement
l disposables for
ure Compact
re Compact
A Pure Compact
Compact
Compact
NA Polymerase,
y compared to
utagenesis,
x real-time PCR
nstrument. Use
m two-step RT-
s, cloning, and
than Taq. GC-
emplates.
s, cloning, and
than Taq. GC-
emplates.
bProbe probes
xpression
ments in
rgets at once.

4 x 1,250
4 x 100
1,000 U for up
volume eac
1 kit for up to
reactions o
1 kit for up to
reactions o
2.5 ml (10 x 25
l final reacti
PWO Su
1 kit for up to 9
500 U (2 x 250
final volum
Supe
100 U for up to
each contain
1
Pack Size

l (4 x 125 mol, 4
l (4 x 1 mol; 10 m
p to 2,000 reaction
ch containing 0.5 U
Polymerase
o 1,920 reactions o
o 1,920 reactions o
10 tip trays
1 cartridge rack
1 drop catcher
1 tube rack
1 tube rack
1 waste tank
0 l) for up to 100
on volume each co
uperYield DNA Pol
96 reactions of 20
volume
U) for up to 200 re
me each containing
erYield DNA Polym
40 reactions of 50
ning 2.5 U Pwo Sup
Polymerase
1 software packag
x 100 mM)
mM each)
s of 20 l final
U Taq DNA
of 20 l or 384
tion volume
of 20 l or 384
tion volume
reactions of 50
ontainig 2.5 U
lymerase
l final reaction
eactions of 50 l
g 2.5 U Pwo
merase
0 l final volume
perYield DNA
e

Price in

1.029,80
228,40
690,90
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
295,60
inquire
467,30
118,40
inquire

Pr

Cat.

04 34
04 37
04 47
04 47
04 53
04 53
04 63
04 63
04 63
04 63
04 63
04 63
04 63
04 63
04 65
04 65
04 65
04 67
roducts b

No.
47 005 001 Ma
One
Inst
79 012 001 Tra
Rev
reag
time
Ligh
76 093 001 X-t
Tran
(siR
and
ther
76 115 001 X-t
Tran
(siR
and
ther
35 286 001 Lig
Rea
PCR
Pro
are
36 282 001 DN
DN
isol
DNA
34 772 001 Gen
Con
with
dur
num
39 502 001 Rac
The
whi
39 529 001 Rac
The
hold
39 545 001 Rac
The
39 618 001 Rac
The
Flow
39 626 001 Kit
For
39 642 001 Tip
The
with
Inst
39 669 001 Pla
The
on a
55 877 001 Tra
Sen
gen
imp
amp
55 885 001 Tra
Sen
gen
imp
amp
59 180 001 Ma
Use
Kit
cult
Mag
73 409 001 Fas
Rea
tem
incl
inst
by Catalo
agNA Pure Comp
e additional Drip T
trument.
anscriptor First St
verse transcribe all
gents for first-stra
e instruments, incl
htCycler
480 Syst
remeGENE siRNA
nsfection reagent
RNA) into many ce
d hard-to-transfect
refore does not req
remeGENE siRNA
nsfection reagent
RNA) into many ce
d hard-to-transfect
refore does not req
htCycler
TaqMa
ady-to-use hot star
R using LightCycle
beLibrary and hyd
not compatible wi
ase I recombina
ase I, recombinant
ation procedures,
A during sample p
nopure Buffer Se
nvenient, ready-to-
h the Genopure Pla
ing the isolation, p
mber plasmids.
ck Sample Carrie
e Rack Sample Car
ch is used for hold
ck Sample Carrie
e Rack Sample Car
ding up to 32 prim
ck Tip Carrier, TI
e Rack Tip Carrier,
ck Tube Carrier F
e Rack Tube carrie
w 32 Vial Carriers f
VFV Consumable
installation purpo
High Vol, 1 ml w
e Tip High Vol tips
h the FLOW Prima
trument.
astic Chute
e Plastic Chutes ca
a Hamilton Trolley
anscriptor One-St
nsitive and specific
ne-specific primers
proved performanc
plification, includin
anscriptor One-St
nsitive and specific
ne-specific primers
proved performanc
plification, includin
agNA Pure Bacte
e with the MagNA
I to isolate bacteria
tures. For automat
gNA Lyser Instrum
stStart TaqMan

ady-to-use 2x mix
mplate for running
uding qPCR and tw
truments other tha
og Numb
Product N

act Drip Tray
Tray for use with th
trand cDNA Synt
l types of RNA from
nd cDNA synthesi
luding LightCycler
tems.
A Transfection R
for efficiently deliv
ll types (HeLa, NIH
t cell lines (HT29).
quire media chang
A Transfection R
for efficiently deliv
ll types (HeLa, NIH
t cell lines (HT29).
quire media chang
an
Master
rt mix for high perf
er
Carousel-Base
rolysis probe assa
ith melting curve a
nt
t, grade I is used fo
analysis of chroma
preparation.
et for Low-Copy N
-use, nuclease-free
asmid Kits. Doubli
provides better yiel
er, SMP-CAR-24
rrier, SMP-CAR-24
ding up to 24 prim
er, SMP-CAR-32
rrier, comes in a se
mary sample tubes.
P-CAR-480-A00
is used for holding
Filling
r Filling is used to
for tube loading
es ML STAR
ses only.
with Filter
come in a set of 3
ry Sample Handlin
an be used in comb
.
tep RT-PCR Kit
c one-step endpoin
s. Combines high-y
ce of a hot start sys
ng GC-rich RNA.
tep RT-PCR Kit
c one-step endpoin
s. Combines high-y
ce of a hot start sys
ng GC-rich RNA.
ria Lysis Buffer
Pure Compact and
al DNA from urine
ion and convenien
ment and Green Be
Probe Master
containing all reag
quantitative, real-t
wo-step qRT-PCR
an LightCycler
Ins
ber
Name
he MagNA Pure Co
thesis Kit
m a variety of sour
s reactions up to 1
Carousel-Based
Reagent
vering short interfe
H 3T3, HEK-293, C
Functions with or
ges.
Reagent
vering short interfe
H 3T3, HEK-293, C
Functions with or
ges.
formance qPCR or
d Instruments with
ays. Note that hydr
analysis.
or eliminating DNA
atin structure, and
Number Plasmid
e buffers for use in
ng the volume of t
lds of plasmid DNA
-A00, Set of 4
4-A00, comes in a s
ary sample tubes.
-A00, Set of 3
et of 3 each of whi
0, for 480 tips
g up to 5 tip trays
secure Rack Sam
3.840 1 ml filter tips
ng and the FLOW P
bination with the S
nt RT-PCR analysis
yield reverse trans
stem for high-fidel
nt RT-PCR analysis
yield reverse trans
stem for high-fidel
d MagNA Pure Co
e, BAL, sputum, CS
nce, combine lysis
eads.
gents except prime
time DNA detectio
. Use with real-tim
struments.
ompact
rces. Includes all
14 kb on all real-
d and
ering RNA
HO-K1, COS-7),
without serum,
ering RNA
HO-K1, COS-7),
without serum,
r two-step RT-
h Universal
olysis probes
A during protein
eliminating
s
n combination
the buffers
A from low-copy
set of 4 each of
ch is used for
(96 tips each).
ple Carriers and
s and are used
PCR Setup
Solid Waste Bag
s of RNA using
cription and
lity, high-yield
s of RNA using
cription and
lity, high-yield
ompact Isolation
SF, swabs, and
buffer with the
ers, probe, and
on assays,
me qPCR

1 kit for up to 5
1 ml (1 mg/m
5 x 1 ml (2,000
1 kit for up to 9
1 set buffer fo
1 rack
1 kit for up to 5
1 kit for
2 x 1.25 ml for
Pack Size

1 drip tray
50 reactions, inclu
reactions
plate)
96 reactions of 20
volume
2 x 10,000 U
or up to 20 maxi pr
preps
set of 4
set of 3
1 rack tip carrier
1 kit
1 set of 3.840
1 set of 10 chutes
50 reactions of 50
control reactions
up to 150 reaction
20 ml lysis buffer
up to 100 reaction
reaction volume
www.roche
ding 10 control
ns in a 24-well
a 24-well plate)
l final reaction
reps or 60 midi
g rack
s
l including 10
s of 50 l
ns of 50 l final
e-applied-science

Price in

inquire
332,40
255,90
1.087,00
inquire
119,20
137,80
inquire
inquire
inquire
inquire
inquire
inquire
inquire
326,30
717,70
inquire
189,10

193

e.com

Pr
194

www.r

Cat.

04 67
04 67
04 67
04 67
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
roducts b
roche-applied-sc

No.
73 417 001 Fas
Rea
tem
incl
inst
73 433 001 Fas
Rea
tem
incl
inst
73 484 001 Fas
Rea
nee
incl
inst
73 492 001 Fas
Rea
nee
incl
inst
83 633 001 Uni
Use
for
PCR
Des
84 974 001 Uni
Rap
spe
with
free
84 982 001 Uni
Rap
spe
with
free
85 008 001 Uni
Rap
spe
with
free
85 016 001 Uni
Rap
spe
with
free
85 024 001 Uni
Rap
spe
with
free
85 032 001 Uni
Rap
spe
with
free
85 059 001 Uni
Rap
spe
with
free
85 067 001 Uni
Rap
spe
with
free
85 075 001 Uni
Rap
spe
with
free

by Catalo
cience.com
stStart TaqMan

ady-to-use 2x mix
mplate for running
uding qPCR and tw
truments other tha
stStart TaqMan

ady-to-use 2x mix
mplate for running
uding qPCR and tw
truments other tha
stStart SYBR Gre
ady-to-use 2x mix
eded for running q
uding qPCR and tw
truments other tha
stStart SYBR Gre
ady-to-use 2x mix
eded for running q
uding qPCR and tw
truments other tha
iversal ProbeLibr
e this fluorescent p
all the human gen
R with LightCycler
sign assays using

iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

Probe Master
containing all reag
wo-step qRT-PCR
an LightCycler
Ins
Probe Master
containing all reag
wo-step qRT-PCR
an LightCycler
Ins
een Master
containing all reag
wo-step qRT-PCR
an the LightCycler
een Master
containing all reag
wo-step qRT-PCR
an the LightCycler
rary Set, Human

probe set to rapidly
nes in the NCBI Re
Systems and oth

the free online As
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
gents except prime
time DNA detectio
. Use with real-tim
struments.
gents except prime
time DNA detectio
. Use with real-tim
struments.
gents except prime
me DNA detection
. Use with real-tim
Instruments.
gents except prime
me DNA detection
. Use with real-tim
Instruments.
y quantify gene ex
ef Seq Database, us
her real-time PCR
ssay Design Center
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
ers, probe, and
on assays,
me qPCR
ers, probe, and
on assays,
me qPCR
ers and template
n assays,
me qPCR
ers and template
n assays,
me qPCR
pression levels
sing real-time
instruments.
r.
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

10 x 1.25 ml for
10 x 5 ml fo
5 ml (4 x 1.25 m
fi
50 ml (10 x 5
20
1 set of 90 Univ

Pack Size

r up to 500 reactio
reaction volume
reaction volume
nal reaction volum
ml) for up to 5,00
versal ProbeLibrary
10 M each.
Probe #1
Probe #2
Probe #3
Probe #4
Probe #5
Probe #6
Probe #7
Probe #8
Probe #9
ons of 50 l final
of 50 l final
eactions of 20 l
me
0 reactions of
lume
y probes, 125 l,

Price in

886,90
3.429,10
390,30
3.535,60
3.393,90
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

Pr

Cat.

04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
roducts b

No.
85 091 001 Uni
Rap
spe
with
free
85 105 001 Uni
Rap
spe
with
free
85 113 001 Uni
Rap
spe
with
free
85 121 001 Uni
Rap
spe
with
free
85 130 001 Uni
Rap
spe
with
free
85 148 001 Uni
Rap
spe
with
free
86 128 001 Lig
The
Ligh
use
86 136 001 Lig
The
480
diffe
inte
86 896 001 Uni
Rap
spe
with
free
86 900 001 Uni
Rap
spe
with
free
86 918 001 Uni
Rap
spe
with
free
86 926 001 Uni
Rap
spe
with
free
86 934 001 Uni
Rap
spe
with
free
86 942 001 Uni
Rap
spe
with
free

by Catalo
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
htCycler
480 V
e LightCycler
480
htCycler
480 Inst
er within a few min
htCycler
480 X
e LightCycler
480
0 Instruments. It is
erence between a
ensity, which differ
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
entilation Dust F
0 Ventilation Dust F
trument. The dust f
nutes.
enon Lamp
0 Xenon Lamp is a
easily replaced wi
Xenon and a Halo
rs at least by factor
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
Filter
Filter is a replacem
filter can be easily
replacement part
thin a few minutes
ogen lamp is the lu
r 10.
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
ment part for the
y replaced by the
for LightCycler

s. The main
uminous
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #10
Probe #11
Probe #12
Probe #13
Probe #14
Probe #15
4 filters
1 lamp
Probe #16
Probe #17
Probe #18
Probe #19
Probe #20
Probe #21

Price in

210,60
210,60
210,60
210,60
210,60
210,60
inquire
inquire
210,60
210,60
210,60
210,60
210,60
210,60

195

e.com

Pr
196

www.r

Cat.

04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
roducts b
roche-applied-sc

No.
86 969 001 Uni
Rap
spe
with
free
86 977 001 Uni
Rap
spe
with
free
86 985 001 Uni
Rap
spe
with
free
86 993 001 Uni
Rap
spe
with
free
87 132 001 Sim
For
mut
esta
flex
87 574 001 Uni
Rap
spe
with
free
87 582 001 Uni
Rap
spe
with
free
87 604 001 Uni
Rap
spe
with
free
87 612 001 Uni
Rap
spe
with
free
87 639 001 Uni
Rap
spe
with
free
87 647 001 Uni
Rap
spe
with
free
87 655 001 Uni
Rap
spe
with
free
87 663 001 Uni
Rap
spe
with
free
87 671 001 Uni
Rap
spe
with
free

by Catalo
cience.com
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
mpleProbe 519 La
internal labeling o
tation detection pr
ablished methods,
xibility.
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
abeling Reagent
of oligonucleotide
robes using LightC
labeling is done in
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
probes detected a
Cycler
Systems. C
n a single step wit
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
t 519 nm for
Compared to
h greater
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #22
Probe #23
Probe #24
Probe #25
100 mol
Probe #26
Probe #27
Probe #28
Probe #29
Probe #30
Probe #31
Probe #32
Probe #33
Probe #34

Price in

210,60
210,60
210,60
210,60
inquire
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

Pr

Cat.

04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
roducts b

No.
87 680 001 Uni
Rap
spe
with
free
87 949 001 Uni
Rap
spe
with
free
87 957 001 Uni
Rap
spe
with
free
87 965 001 Uni
Rap
spe
with
free
87 973 001 Uni
Rap
spe
with
free
87 990 001 Uni
Rap
spe
with
free
88 007 001 Uni
Rap
spe
with
free
88 015 001 Uni
Rap
spe
with
free
88 031 001 Uni
Rap
spe
with
free
88 040 001 Uni
Rap
spe
with
free
88 058 001 Uni
Rap
spe
with
free
88 066 001 Uni
Rap
spe
with
free
88 074 001 Uni
Rap
spe
with
free
88 082 001 Uni
Rap
spe
with
free

by Catalo
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #35
Probe #36
Probe #37
Probe #38
Probe #39
Probe #40
Probe #41
Probe #42
Probe #43
Probe #44
Probe #45
Probe #46
Probe #47
Probe #48

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

197

e.com

Pr
198

www.r

Cat.

04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
roducts b
roche-applied-sc

No.
88 104 001 Uni
Rap
spe
with
free
88 112 001 Uni
Rap
spe
with
free
88 481 001 Uni
Rap
spe
with
free
88 490 001 Uni
Rap
spe
with
free
88 503 001 Uni
Rap
spe
with
free
88 511 001 Uni
Rap
spe
with
free
88 520 001 Uni
Rap
spe
with
free
88 538 001 Uni
Rap
spe
with
free
88 546 001 Uni
Rap
spe
with
free
88 554 001 Uni
Rap
spe
with
free
88 562 001 Uni
Rap
spe
with
free
88 589 001 Uni
Rap
spe
with
free
88 597 001 Uni
Rap
spe
with
free
88 619 001 Uni
Rap
spe
with
free

by Catalo
cience.com
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #49
Probe #50
Probe #51
Probe #52
Probe #53
Probe #54
Probe #55
Probe #56
Probe #57
Probe #58
Probe #59
Probe #60
Probe #61
Probe #62

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

Pr

Cat.

04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
roducts b

No.
88 627 001 Uni
Rap
spe
with
free
88 635 001 Uni
Rap
spe
with
free
88 643 001 Uni
Rap
spe
with
free
88 651 001 Uni
Rap
spe
with
free
88 660 001 Uni
Rap
spe
with
free
88 678 001 Uni
Rap
spe
with
free
88 686 001 Uni
Rap
spe
with
free
88 937 001 Uni
Rap
spe
with
free
88 945 001 Uni
Rap
spe
with
free
88 953 001 Uni
Rap
spe
with
free
88 961 001 Uni
Rap
spe
with
free
88 970 001 Uni
Rap
spe
with
free
88 988 001 Uni
Rap
spe
with
free
88 996 001 Uni
Rap
spe
with
free

by Catalo
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #63
Probe #64
Probe #65
Probe #66
Probe #67
Probe #68
Probe #69
Probe #70
Probe #71
Probe #72
Probe #73
Probe #74
Probe #75
Probe #76

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

199

e.com

Pr
200

www.r

Cat.

04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
04 68
roducts b
roche-applied-sc

No.
89 003 001 Uni
Rap
spe
with
free
89 011 001 Uni
Rap
spe
with
free
89 020 001 Uni
Rap
spe
with
free
89 038 001 Uni
Rap
spe
with
free
89 046 001 Uni
Rap
spe
with
free
89 054 001 Uni
Rap
spe
with
free
89 062 001 Uni
Rap
spe
with
free
89 089 001 Uni
Rap
spe
with
free
89 097 001 Uni
Rap
spe
with
free
89 119 001 Uni
Rap
spe
with
free
89 127 001 Uni
Rap
spe
with
free
89 135 001 Uni
Rap
spe
with
free
89 143 001 Uni
Rap
spe
with
free
89 151 001 Uni
Rap
spe
with
free

by Catalo
cience.com
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #77
Probe #78
Probe #79
Probe #80
Probe #81
Probe #82
Probe #83
Probe #84
Probe #85
Probe #86
Probe #87
Probe #88
Probe #89
Probe #90

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

Pr

Cat.

04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
roducts b

No.
92 080 001 Uni
Rap
spe
with
free
92 098 001 Uni
Rap
spe
with
free
92 101 001 Uni
Rap
spe
with
free
92 110 001 Uni
Rap
spe
with
free
92 128 001 Uni
Rap
spe
with
free
92 136 001 Uni
Rap
spe
with
free
92 144 001 Uni
Rap
spe
with
free
92 152 001 Uni
Rap
spe
with
free
92 179 001 Uni
Rap
spe
with
free
92 187 001 Uni
Rap
spe
with
free
92 195 001 Uni
Rap
spe
with
free
92 209 001 Uni
Rap
spe
with
free
92 217 001 Uni
Rap
spe
with
free
92 225 001 Uni
Rap
spe
with
free

by Catalo
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #91
Probe #92
Probe #93
Probe #94
Probe #95
Probe #96
Probe #97
Probe #98
Probe #99
Probe #100
Probe #101
Probe #102
Probe #103
Probe #104

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

201

e.com

Pr
202

www.r

Cat.

04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
roducts b
roche-applied-sc

No.
92 241 001 Uni
Rap
spe
with
free
92 250 001 Uni
Rap
spe
with
free
92 268 001 Uni
Rap
spe
with
free
92 276 001 Uni
Rap
spe
with
free
92 284 001 Uni
Rap
spe
with
free
92 306 001 Uni
Rap
spe
with
free
93 116 001 cOm
Rely
and
New
Sup
93 124 001 cOm
Rely
and
New
Sup
93 132 001 cOm
Rely
EDT
type
93 159 001 cOm
Rely
EDT
type
93 442 001 Uni
Rap
spe
with
free
93 469 001 Uni
Rap
spe
with
free
93 477 001 Uni
Rap
spe
with
free
93 485 001 Uni
Rap
spe
with
free
93 493 001 Uni
Rap
spe
with
free
by Catalo
cience.com
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
mplete
y on proven perfor
d metalloproteases
w for EDTA inhibiti
pplied in EASYpack
mplete, Mini
y on proven perfor
d metalloproteases
w for EDTA inhibiti
pplied in EASYpack
mplete, EDTA-fre
y on proven perfor
TA-free Tablets inh
es as cOmplete UL
mplete, Mini, EDT
y on proven perfor
TA-free Tablets inh
es as cOmplete UL
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rmance: cOmplete
s in the same cell t
ion: IMAC with cO
ks .
rmance: cOmplete
ion: IMAC with cO
ks .
ee
rmance combined
hibit serine and cy
LTRA Tablets. Supp
TA-free
rmance combined
hibit serine and cy
LTRA Tablets. Supp
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
Tablets inhibit ser
types as cOmplete
Omplete His-Tag Pu
Tablets inhibit ser
types as cOmplete
Omplete His-Tag Pu
with high conveni
steine proteases in
plied in EASYpack
with high conveni
steine proteases in
plied in EASYpack
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
rine, cysteine,
ULTRA Tablets.
urification Resin.
rine, cysteine,
ULTRA Tablets.
urification Resin.
ence. cOmplete
n the same cell
ks .
ence. cOmplete
n the same cell
ks .
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

20 tablets (in
packs, each ta
50 m
30 tablets (in
packs, each ta
10 m
20 tablets (in
packs; each ta
50 m
30 tablets (in
packs, each ta
10 m
Pack Size

Probe #105
Probe #106
Probe #107
Probe #108
Probe #109
Probe #110
ndividually packed
ml extraction solut
ndividually packed
ml extraction solut
ndividually packed
ml extraction solut
ndividually packed
ml extraction solut
Probe #111
Probe #112
Probe #113
Probe #114
Probe #115
d in foil blister
for a volume of
tion)
d in foil blister
for a volume of
tion)
d in foil blister
for a volume of
tion)
d in foil blister
for a volume of
tion)

Price in

210,60
210,60
210,60
210,60
210,60
210,60
257,20
163,10
257,20
163,10
210,60
210,60
210,60
210,60
210,60

Pr

Cat.

04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
roducts b

No.
93 507 001 Uni
Rap
spe
with
free
93 515 001 Uni
Rap
spe
with
free
93 523 001 Uni
Rap
spe
with
free
93 531 001 Uni
Rap
spe
with
free
93 540 001 Uni
Rap
spe
with
free
93 558 001 Uni
Rap
spe
with
free
93 566 001 Uni
Rap
spe
with
free
93 574 001 Uni
Rap
spe
with
free
93 582 001 Uni
Rap
spe
with
free
93 604 001 Uni
Rap
spe
with
free
93 612 001 Uni
Rap
spe
with
free
93 639 001 Uni
Rap
spe
with
free
93 647 001 Uni
Rap
spe
with
free
93 655 001 Uni
Rap
spe
with
free

by Catalo
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #116
Probe #117
Probe #118
Probe #119
Probe #120
Probe #121
Probe #122
Probe #123
Probe #124
Probe #125
Probe #126
Probe #127
Probe #128
Probe #129

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

203

e.com

Pr
204

www.r

Cat.

04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
roducts b
roche-applied-sc

No.
93 663 001 Uni
Rap
spe
with
free
94 155 001 Uni
Rap
spe
with
free
94 163 001 Uni
Rap
spe
with
free
94 171 001 Uni
Rap
spe
with
free
94 180 001 Uni
Rap
spe
with
free
94 198 001 Uni
Rap
spe
with
free
94 201 001 Uni
Rap
spe
with
free
94 210 001 Uni
Rap
spe
with
free
94 228 001 Uni
Rap
spe
with
free
94 236 001 Uni
Rap
spe
with
free
94 244 001 Uni
Rap
spe
with
free
94 279 001 Uni
Rap
spe
with
free
94 287 001 Uni
Rap
spe
with
free
94 295 001 Uni
Rap
spe
with
free

by Catalo
cience.com
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #130
Probe #131
Probe #132
Probe #133
Probe #134
Probe #135
Probe #136
Probe #137
Probe #138
Probe #139
Probe #140
Probe #141
Probe #142
Probe #143

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

Pr

Cat.

04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
roducts b

No.
94 309 001 Uni
Rap
spe
with
free
94 317 001 Uni
Rap
spe
with
free
94 325 001 Uni
Rap
spe
with
free
94 333 001 Uni
Rap
spe
with
free
94 341 001 Uni
Rap
spe
with
free
94 350 001 Uni
Rap
spe
with
free
94 368 001 Uni
Rap
spe
with
free
94 376 001 Uni
Rap
spe
with
free
94 384 001 Uni
Rap
spe
with
free
94 392 001 Uni
Rap
spe
with
free
94 406 001 Uni
Rap
spe
with
free
94 414 001 Uni
Rap
spe
with
free
94 422 001 Uni
Rap
spe
with
free
94 449 001 Uni
Rap
spe
with
free

by Catalo
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the

Pack Size

Probe #144
Probe #145
Probe #146
Probe #147
Probe #148
Probe #149
Probe #150
Probe #151
Probe #152
Probe #153
Probe #154
Probe #155
Probe #156
Probe #157

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60

205

e.com

Pr
206

www.r

Cat.

04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 69
04 70
04 70
04 70
04 71
04 71
04 71
roducts b
roche-applied-sc

No.
94 457 001 Uni
Rap
spe
with
free
94 465 001 Uni
Rap
spe
with
free
94 473 001 Uni
Rap
spe
with
free
94 481 001 Uni
Rap
spe
with
free
94 490 001 Uni
Rap
spe
with
free
94 503 001 Uni
Rap
spe
with
free
94 511 001 Uni
Rap
spe
with
free
94 520 001 Uni
Rap
spe
with
free
07 494 001 Lig
Sav
PCR
Fast
form
07 516 001 Lig
Rea
Ligh
and
min
07 524 001 Lig
Perf
480
The
pro
10 436 001 Fas
Rea
cDN
targ
thro
10 444 001 Fas
Rea
cDN
targ
thro
10 452 001 Fas
Rea
cDN
targ
thro

by Catalo
cience.com
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
iversal ProbeLibr
pidly quantify gene
ecies in the NCBI R
h standard reagen
e online Assay Des
htCycler
480 Pr
ve time in gene qua
R master mix for th
tStart Taq DNA Po
mation of nonspec
htCycler
480 SY
ady-to-use hot star
htCycler
480 Inst
d quantification. Eli
nimize pipetting ste
htCycler
480 G
form easy real-tim
0 Instrument using
e single-componen
bes.
stStart PCR Mast
ady-to-use 2x mast
NA targets up to 2
gets, with high spe
oughput, and direc
stStart PCR Mast
ady-to-use 2x mast
NA targets up to 2
gets, with high spe
oughput, and direc
stStart PCR Mast
ady-to-use 2x mast
NA targets up to 2
gets, with high spe
oughput, and direc
og Numb
Product N

rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
rary Probes
e expression levels
Reference Seq Data
ts in real-time PCR
sign Center.
robes Master
antification assays
he LightCycler
48
olymerase for hot s
cific amplification p
YBR Green I Mas
rt mix for SYBR Gr
truments. Ideal for
iminate time-cons
eps; just add DNA
enotyping Maste
me PCR and genoty
this convenient, re
nt kit requires only
ter
ter mix for the amp
kb long, or longer
ecificity, sensitivity,
ct colony PCRs.
ter
ter mix for the amp
kb long, or longer
ct colony PCRs.
ter
ter mix for the amp
kb long, or longer
ct colony PCRs.
ber
Name
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s of human, mouse
abase. Use fluores
R assays. Design a
s using an optimize
80 System. The mix
start PCR, which m
products.
ster
reen I-based real-t
PCR assays for ge
uming MgCl
2
titra
, primers.
er
yping analysis on t
eady-to-use hot st
y the addition of DN
plification of geno
r fragments on pla
, and yield. Use in
plification of geno
r fragments on pla
, and yield. Use in
plification of geno
r fragments on pla
, and yield. Use in
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
e, rat and other
scent probes
assays using the
ed ready-to-use
x contains
minimizes
time PCR on
ene detection
ation and
he LightCycler

tart master mix.
NA, primers, and
mic DNA and
asmid DNA
hot start, high-
mic DNA and
asmid DNA
hot start, high-
mic DNA and
asmid DNA
hot start, high-

5 x 1 ml (for u
5 x 1 ml ((2
of 20
4 x 384 l ((
of 20
2 x 1.25 ml for
8 x 1.25 ml for u
10 x 5 ml for u

Pack Size

Probe #158
Probe #159
Probe #160
Probe #161
Probe #162
Probe #163
Probe #164
Probe #165
up to 500 reactions
volume)
x conc.) approx. 50
l final reaction vo
(5x conc.) approx.3
l reaction volume
up to 250 reaction
reaction volume
up to 1,000 reactio
reaction volume
reaction volume
s of 20 l final
00 reactions
olume)
384 reactions
e each)
ns of 20 l final
ons of 20 l final
ns of 20 l final

Price in

210,60
210,60
210,60
210,60
210,60
210,60
210,60
210,60
inquire
inquire
inquire
178,40
624,10
2.675,00

Pr

Cat.

04 71
04 71
04 71
04 71
04 71
04 71
04 72
04 72
04 72
04 72
04 72
04 72
04 72
04 72
04 72
roducts b

No.
10 606 001 Lig
Trac
Inst
sca
dire
10 924 001 Lig
Con
Ligh
pre-
16 728 001 DN
Deg
to r
afte
sen
19 948 001 cOm
Rap
inhi
in c
EDT
19 956 001 cOm
Rap
inhi
extr
IMA
19 964 001 cOm
Rap
inhi
extr
pre
27 878 001 G-4
Hig
mem
the
cell
27 894 001 G-4
Hig
mem
the
cell
28 858 001 Taq
Taq
pre
PCR
reac
28 866 001 Taq
Taq
pre
PCR
reac
28 874 001 Taq
Taq
pre
PCR
reac
28 882 001 Taq
Taq
pre
PCR
reac
28 904 001 Taq
Taq
pre
PCR
reac
29 692 001 Lig
This
mel
The
29 749 001 Lig
This
mel
Inst
trac
by Catalo
htCycler
480 B
ck and manage sa
trument using this
ns data from the b
ectly into the Light
htCycler
480 C
nfirm real-time PCR
htCycler
480 Inst
-diluted samples o
ase I recombina
grades DNA in app
emove genomic D
er in vitro transcrip
sitive regions in eu
mplete Lysis-B (2
pid, gentle bacteria
ibition of protease
cell extracts. Obtain
TA-free preparatio
mplete Lysis-M
pid, gentle mamma
ibition of protease
racts. Produces hig
AC, use with cOmp
mplete Lysis-M E
pid, gentle mamma
ibition of protease
racts. Obtain highe
paration allows us
418 Solution
hly pure, convenie
mbrane, selects fo
neomycin resistan
s. Eliminates conta
418 Solution
hly pure, convenie
mbrane, selects fo
neomycin resistan
s. Eliminates conta
q DNA Polymeras
q DNA Polymerase
paration (5 U/l) o
R Nucleotide Mix.
ctions, such as seq
q DNA Polymeras
q DNA Polymerase
paration (5 U/l) o
R Nucleotide Mix.
ctions, such as seq
q DNA Polymeras
q DNA Polymerase
paration (5 U/l) o
R Nucleotide Mix.
ctions, such as seq
q DNA Polymeras
q DNA Polymerase
paration (5 U/l) o
R Nucleotide Mix.
ctions, such as seq
q DNA Polymeras
q DNA Polymerase
paration (5 U/l) o
R Nucleotide Mix.
ctions, such as seq
htCycler
480 M
s high performanc
lting curve analysis
e white, polypropyl
htCycler
480 M
s high performanc
lting curve analysis
truments.The white
cking.
og Numb
Product N

ar-Code Scanne
ample information
handheld barcode
barcodes on LightC
Cycler
Software.
ontrol Kit
R and melting curv
trument using this
of human target ge
nt, RNase-free
plications sensitive
DNA from RNA pre
ption, perform nick
ukaryotic DNA.
2x) EDTA-free
al cell lysis in 10 m
activity (serine, cy
n higher yields of p
n allows use in IM
alian cell lysis in 5
gher yields of prote
plete His-Tag Purif
EDTA-free
alian cell lysis in 5
er yields of protein
se in IMAC.
ent, antibiotic, filter
r eukaryotic cells t
nce gene, and mai
aminating fibroblas
ent, antibiotic, filter
r eukaryotic cells t
nce gene, and mai
aminating fibroblas
se, dNTPack
, dNTPack combin
of recombinant Taq
Use for PCR, RT-P
quencing and labe
se, dNTPack
, dNTPack combin
of recombinant Taq
Use for PCR, RT-P
quencing and labe
se, dNTPack
, dNTPack combin
of recombinant Taq
Use for PCR, RT-P
quencing and labe
se, dNTPack
, dNTPack combin
of recombinant Taq
Use for PCR, RT-P
quencing and labe
se, dNTPack
, dNTPack combin
of recombinant Taq
Use for PCR, RT-P
quencing and labe
Multiwell Plate 96
ce 96-well reaction
s applications usin
ene plate is barcod
Multiwell Plate 38
ce 384-well reactio
s applications usin
e, polypropylene p
ber
Name
er
for the LightCycle
e scanner. This op
Cycler
480 Multiw
ve analysis perform
convenient kit. Th
enes and internal c
e to the presence o
eparations, isolate D
k translations, and
minutes and simulta
ysteine, but not me
protein than using
MAC.
minutes and simu
ysteine, metallopro
ein than using son
fication Resin.
minutes and simu
ysteine, metallopro
n than using sonica
red through 0.2
that are stably tran
ntains the phenoty
sts from mixed cul
red through 0.2
that are stably tran
ntains the phenoty
sts from mixed cul
nes our standard, r
q with convenient,
PCR, and other prim
eling.
nes our standard, r
q with convenient,
PCR, and other prim
eling.
nes our standard, r
q with convenient,
PCR, and other prim
eling.
nes our standard, r
q with convenient,
PCR, and other prim
eling.
nes our standard, r
q with convenient,
PCR, and other prim
eling.
6 white
plate is specifical
ng LightCycler
48
de-labeled for eas
84, white
n plate is specifica
ng LightCycler
48
late is barcode-lab
r
480
tional accessory
well Plates
mance of the
e kit contains
controls.
of RNase. Used
DNA-free RNA
to map DNase-
aneous
etalloproteases)
sonication.
ltaneous
oteases) in cell
nication. For
ltaneous
oteases) in cell
ation. EDTA-free
m pore size
nsfected with
ype of resistant
ltures.
m pore size
nsfected with
ype of resistant
ltures.
rigorously tested
ready-to-use
mer-extension
rigorously tested
ready-to-use
mer-extension
rigorously tested
ready-to-use
mer-extension
rigorously tested
ready-to-use
mer-extension
rigorously tested
ready-to-use
mer-extension
ly designed for
80 Instruments.
sy tracking.
ally designed for
80
beled for easy

1 kit (for u
10,000 U (pr
1 kit
1 kit for the ly
1 kit for the ly
20 ml
100 ml
5,000 U (20 x 25
20 l final vo
100 U for up
volume eac
500 U (2 x 250
l final volume
1,000 U (4 x 25
20 l final vo
2,500 U (10 x 2
20 l final vo
5 x 10
5 x 10
Pack Size

1 scanner
up to 2 x 3 control
rovided with incub
for up to 20 extrac
ysis of up to 100 g
cells
ysis of up to 100 g
cells
- equivalent to 1 g
- equivalent to 5 g
50 U) for up to 10,
lume each contain
DNA Polymerase
p to 200 reactions
ch containing 0.5 U
Polymerase
U) for up to 1,000
e each containing
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase
lume each contain
DNA Polymerase
plates (with sealin
plates (with sealin
www.roche
reactions)
bation buffer)
ctions
of mammalian
of mammalian
g G-418
g G-418
000 reactions of
ning 0.5 U Taq
of 20 l final
U Taq DNA
reactions of 20
0.5 U Taq DNA
00 reactions of
ning 0.5 U Taq
000 reactions of
ning 0.5 U Taq
ng foils)
ng foils)
e-applied-science

Price in

inquire
inquire
213,30
234,20
314,90
314,90
98,50
424,20
2.703,80
89,00
356,00
640,50
1.480,10
inquire
inquire

207

e.com

Pr
208

www.r

Cat.

04 72
04 73
04 73
04 73
04 73
04 73
04 73
04 73
04 73
04 73
04 73
04 73
04 73
04 73
roducts b
roche-applied-sc

No.
29 757 001 Lig
Prev
assa
clea
eva
35 536 001 Lig
Rea
PCR
Pro
are
38 225 001 Taq
Taq
rigo
read
prim
38 241 001 Taq
Taq
rigo
read
prim
38 250 001 Exp
Enz
thre
resu
read
38 268 001 Exp
Enz
thre
resu
read
38 276 001 Exp
Enz
thre
resu
read
38 284 001 Fas
Enz
four
mul
Con
38 292 001 Fas
Enz
four
mul
Con
38 314 001 Fas
The
PCR
and
setu
38 357 001 Fas
The
PCR
and
setu
38 381 001 Fas
The
PCR
and
setu
38 403 001 Fas
The
PCR
and
setu
38 420 001 Fas
The
PCR
and
setu

by Catalo
cience.com
htCycler
480 Se
vent evaporation a
ays in LightCycler
ar) using the Light

poration during cy
htCycler
TaqMa
ady-to-use hot star
R using LightCycle
beLibrary and hyd
not compatible wi
q DNA Polymeras
q DNA Polymerase
orously tested prep
dy-to-use PCR Nu
mer-extension reac
q DNA Polymeras
q DNA Polymerase
orously tested prep
dy-to-use PCR Nu
mer-extension reac
pand High Fidelity
zyme blend that de
eefold greater fide
ults for genomic ta
dy-to-use PCR nuc
pand High Fidelity
zyme blend that de
eefold greater fide
ults for genomic ta
dy-to-use PCR nuc
pand High Fidelity
zyme blend that de
eefold greater fide
ults for genomic ta
dy-to-use PCR nuc
stStart High Fidel
zyme blend with be
rfold higher accura
ltiplex PCR, RT-PC
ntains ready-to-use
stStart High Fidel
zyme blend with be
rfold higher accura
ltiplex PCR, RT-PC
ntains ready-to-use
stStart Taq DNA P
ermostable modifie
R nucleotide mix. D
d optimized buffer.
up and prior to init
stStart Taq DNA P
ermostable modifie
R nucleotide mix. D
d optimized buffer.
stStart Taq DNA P
ermostable modifie
R nucleotide mix. D
d optimized buffer.
stStart Taq DNA P
ermostable modifie
R nucleotide mix. D
d optimized buffer.
stStart Taq DNA P
ermostable modifie
R nucleotide mix. D
d optimized buffer.
og Numb
Product N

ealing Foil
and contamination
480 Multiwell Pl
tCycler
480 Instru
ycling or storage.
an
Master
rt mix for high perf
er
Carousel-Base
rolysis probe assa
ith melting curve a
se (1 U/l), dNTP
, dNTPack combin
paration (1U/l) of
cleotide Mix. Use
ctions (sequencing
se (1 U/l), dNTP
, dNTPack combin
paration (1U/l) of
cleotide Mix. Use
ctions (sequencing
y PCR System, d
elivers superior res
lity compared to T
argets up to 5 kb, i
cleotide mix.
y PCR System, d
lity compared to T
cleotide mix.
y PCR System, d
lity compared to T
cleotide mix.
lity PCR System,
enefits of FastStart
acy and ability to a
CR, GC-RICH templ
e PCR Nucleotide
lity PCR System,
enefits of FastStart
acy and ability to a
CR, GC-RICH templ
e PCR Nucleotide
Polymerase, dNT
ed recombinant Ta
Delivers superb res
Ideal for hot start
tial denaturation.
Polymerase, dNT
ed recombinant Ta
Delivers superb res
Ideal for hot start
tial denaturation.
Polymerase, dNT
ed recombinant Ta
Delivers superb res
Ideal for hot start
tial denaturation.
Polymerase, dNT
ed recombinant Ta
Delivers superb res
Ideal for hot start
tial denaturation.
Polymerase, dNT
ed recombinant Ta
Delivers superb res
Ideal for hot start
tial denaturation.
ber
Name
when running rea
ates (96 or 384 we
ument. Strong adh
formance qPCR or
d Instruments with
ays. Note that hydr
analysis.
Pack
nes our low concen
f recombinant Taq
for PCR, RT-PCR,
g, labeling).
Pack
nes our low concen
f recombinant Taq
for PCR, RT-PCR,
g, labeling).
NTPack
sults with twofold h
aq. Use for the mo
n PCR and RT-PC
NTPack
aq. Use for the mo
n PCR and RT-PC
NTPack
aq. Use for the mo
n PCR and RT-PC
dNTPack
t Taq DNA Polyme
amplify fragments
late amplification,
Mix.
dNTPack
t Taq DNA Polyme
amplify fragments
late amplification,
Mix.
TPack
q polymerase with
sults with unique e
; enzyme stays ina
TPack
q polymerase with
sults with unique e
; enzyme stays ina
TPack
q polymerase with
sults with unique e
; enzyme stays ina
TPack
q polymerase with
sults with unique e
; enzyme stays ina
TPack
q polymerase with
sults with unique e
; enzyme stays ina
al-time PCR
ells, white or
esion prevents
r two-step RT-
h Universal
olysis probes
ntration,
with convenient,
and other
ntration,
with convenient,
and other
higher yield and
ost sensitive PCR
R. Contains
higher yield and
ost sensitive PCR
R. Contains
higher yield and
ost sensitive PCR
R. Contains
rase with
up to 5 kb. For
difficult PCRs.
rase with
up to 5 kb. For
difficult PCRs.
h ready-to-use
enzyme design
active during
h ready-to-use
enzyme design
active during
h ready-to-use
enzyme design
active during
h ready-to-use
enzyme design
active during
h ready-to-use
enzyme design
active during

1 kit for up to 4
250 U for up
volume eac
1,000 U (4 x 25
20 l final vo
100 U for up to
each con
500 U (2 x 250
final volume ea
2,500 U (10 x 2
50 l final volum
125 U for up to
each conta
500 U (2 x 250
final volume ea
100 U for up to
each conta
500 U (2 x 250
final volume e
1,000 U (4 x 25
l final volume
2,500 U (10 x 2
50 l final volu
Ta
5,000 U (20 x 2
50 l final volu
Ta

Pack Size

50 foils
80 reactions of 20
volume
p to 500 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase
40 reactions of 50
ntaining 2.6 U enzy
U) for up to 200 re
ch containing 2.6
me each containin
blend
50 reactions of 50
ining 2.5 U FastSta
Polymerase
U) for up to 200 re
ach containing 2.5
DNA Polymerase
50 reactions of 50
aining 2 U FastStar
Polymerase
U) for up to 250 re
ach containing 2 U
DNA Polymerase
50 U) for up to 500
each containing 2
DNA Polymerase
me each containin
aq DNA Polymeras
me each containin
aq DNA Polymeras
l final reaction
of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq
0 l final volume
yme blend
eactions of 50 l
U enzyme blend
000 reactions of
ng 2.6 U enzyme
0 l final volume
art Taq DNA
eactions of 50 l
U FastStart Taq
0 l final volume
rt Taq DNA
eactions of 50 l
U FastStart Taq
reactions of 50
U FastStart Taq
250 reactions of
ng 2 U FastStart
se
500 reactions of
ng 2 U FastStart
se

Price in

inquire
inquire
202,60
640,50
123,10
492,10
1.969,60
152,20
497,50
119,40
486,10
837,20
1.991,10
3.349,20

Pr

Cat.

04 73
04 74
04 74
04 74
04 74
04 74
04 74
04 74
04 77
04 80
04 80
04 82
04 82
04 82
roducts b

No.
39 205 001 Bio
Sub
tran
with
con
43 725 001 Exp
Enz
outs
PCR
Con
43 733 001 Exp
Enz
outs
PCR
Con
43 750 001 Pw
Hig
Use
yiel
tem
43 784 001 GC
Blen
tem
Solu
Con
43 814 001 Exp
Am
enz
pro
amp
44 926 001 Cyt
Fast
cyto
cell
few
44 934 001 Cyt
Fast
cyto
cell
few
77 026 001 Neb
The
Inst
a N
02 993 001 Ma
Rea
from
Mag
Ligh
05 160 001 Ma
Use
Isol
from
stan
23 125 001 Hig
Isol
dire
of m
Ligh
29 034 001 Exp
For
Use
mix
PCR
29 042 001 Exp
For
Use
mix
PCR

by Catalo
otin-11-CTP
bstrate for RNA po
nscription in RNA l
h Biotin-16-UTP. D
njugate or ELISA w
pand High Fidelity
zyme blend for rob
standing yield, spe
R. Develop a new a
ntains ready-to-use
pand High Fidelity
zyme blend for rob
standing yield, spe
R. Develop a new a
ntains ready-to-use
o SuperYield DN
h fidelity PCR up t
e for site-directed m
d and 18-fold high
mplates (GC RICH S
-RICH PCR Syste
nd of Taq Polymer
mplates up to 5 kb.
ution deliver super
ntains ready-to-use
pand 20 kb
PLUS
PC
plify genomic DNA
zyme blend amplify
duce fragments 23
plification. Contain
totoxicity Detecti
t and simple 96- o
otoxicity/cytolysis b
s. Has all the bene
wer steps, plus it co
totoxicity Detecti
t and simple 96- o
otoxicity/cytolysis b
s. Has all the bene
wer steps, plus it co
bulizer Holder
e Nebulizer Holder
truments and is als
ebulizer during DN
agNA Pure Comp
ady-to-use reagent
m tissue, blood cel
gNA Pure Compac
htCycler
Systems
agNA Pure DNA T
e the MagNA Pure
ation Kit I - Large
m mammalian tissu
ndard cyclers, and
gh Pure FFPE RNA
ate total RNA from
ect use in RT-PCR.
mRNA in RT-PCR u
htCycler
Carouse
pand Long Range
consistent, accura
e the specially desi
x, and optimized bl
R, and large-fragm
pand Long Range
consistent, accura
x, and optimized bl
R, and large-fragm
og Numb
Product N

olymerase (SP6/T3/
labeling. For highe
Detect labeled RNA
with Strepavidin-AP
y
PLUS
PCR System
ust amplification o
amplification assay
e PCR Nucleotide
y
PLUS
PCR System
ust amplification o
amplification assay
e PCR Nucleotide
NA Polymerase, d
to 3 kb. Contains re
mutagenesis, clon
her fidelity than Ta
Solution).
em, dNTPack
rase and a proofrea
Enhanced process
rb performance in
e nucleotide mix.
CR System, dNTP
A fragments up to
y products >20 kb.
3 kb long. Use in P
ns ready-to-use PC
ion Kit
PLUS
(LDH)
or 384-well plate m
by measuring LDH
efits of the Cytotox
ontains a stop solu
ion Kit
PLUS
(LDH)
or 384-well plate m
by measuring LDH
efits of the Cytotox
ontains a stop solu
is supplied with th
so available separa
NA sample fragme
act RNA Isolatio
ls, and whole bloo
ct Instruments. Use
s, microarrays, and
Tissue Lysis Buffe
Compact Instrum
Volume, and its re
ue. Use purified DN
in downstream ap
A Micro Kit
m formalin-fixed, p
Isolated RNA is s
using real-time PC
el-Based and the 4
e dNTPack
ate amplification o
igned buffer set, u
end of thermostab
ment amplification.
e dNTPack
ate amplification o
igned buffer set, u
end of thermostab
ment amplification.
ber
Name
/T7). Replaces CTP
er more uniform la
A with fluorescent
P.
m, dNTPack
of fragments up to
, and accuracy. Us
y or optimize an ex
Mix.
m, dNTPack
of fragments up to
, and accuracy. Us
y or optimize an ex
Mix.
dNTPack
eady-to-use PCR N
ing, and gene exp
q. High performan
ading polymerase
sivity and GC-RICH
PCR (high yield an
Pack
35 kb. Optimized
. Control primers a
PCR, RT-PCR, large
CR Nucleotide Mix
method to quantify
H activity released f
xicity Detection Kit
ution.
method to quantify
H activity released f
xicity Detection Kit
ution.
he Genome Seque
ately. The Nebuliz
entation.
n Kit
ed cartridges for p
od in a volume up t
e RNA for RT-PCR
d gene expression
er
ent, MagNA Pure
eady-to-use buffer
NA with LightCycl
pplications.
araffin-embedded
uitable for relative
CR systems such as
480 Systems.
f long, 5 to 20 kb P
ltrapure PCR-grad
ble DNA polymeras
ltrapure PCR-grad
ble DNA polymeras
P in in vitro
bel density, use
streptavidin
5 kb with
se in PCR/RT-
xisting one.
5 kb with
se in PCR/RT-
xisting one.
Nucleotide Mix.
ression. Higher
nce with difficult
amplify difficult
H Resolution
nd accuracy).
buffer and
and DNA
e-fragment
.
from damaged
(LDH) with
from damaged
(LDH) with
encer
er Holder holds
purifying RNA
to 200 l using
R with
systems.
Compact
r to isolate DNA
er
Systems,
tissues for
quantification
s the
PCR products.
de nucleotide
ses for PCR, RT-
PCR products.
de nucleotide
ses for PCR, RT-

25
125 U for up
volume each
500 U (2 x 250
final volume ea
100 U for up to
each contain
100 U for up to
each co
200 U for up to
each co
1 kit for
1 kit for u
1 kit
1 kit
175 U for up
volume each
700 U for up
volume each

Pack Size

l (250 nmol) (10 m
p to 125 reactions
h containing 1 U e
U) for up to 500 re
ach containing 1 U
40 reactions of 50
ning 2.5 U Pwo Sup
Polymerase
50 reactions of 50
ntaining 2 U enzym
40 reactions of 50
ntaining 5 U enzym
up to 400 tests in
1 nebulizer holder
100 ml lysis buffer
p to 125 reactions
containing 1.4 U e
p to 500 reactions
containing 1.4 U e
www.roche
mM)
of 20 l final
enzyme blend
eactions of 20 l
U enzyme blend
0 l final volume
perYield DNA
0 l final volume
me blend
0 l final volume
me blend
96 wells
n 96 wells
r
tions
r
tions
of 20 l final
enzyme blend
of 20 l final
enzyme blend
e-applied-science

Price in

253,90
131,30
517,30
118,40
206,60
199,40
208,00
561,70
inquire
inquire
inquire
308,00
172,30
591,20

209

e.com

Pr
210

www.r

Cat.

04 82
04 86
04 88
04 88
04 89
04 89
04 89
04 89
04 89
04 89
04 89
04 90
04 90
04 90
roducts b
roche-applied-sc

No.
29 069 001 Exp
For
Use
mix
PCR
69 877 001 Uni
Use
a co
qua
Pro
87 301 001 Lig
Sav
PCR
Fast
form
87 352 001 Lig
Rea
Ligh
and
min
96 866 001 Tra
Rev
reag
time
Ligh
97 030 001 Tra
Rev
reag
time
Ligh
98 117 001 Rap
Fast
or b
frag
line
98 125 001 Rap
Fast
or b
frag
line
98 133 001 rAP
Rap
inac
req
dep
98 141 001 rAP
Rap
inac
req
dep
98 915 001 Lig
Ver
Inst
mod
02 343 001 Lig
Sav
PCR
Fast
form
05 270 001 Ant
For
wes
effic
to C
05 318 001 Ant
Spe
vect
imm
tagg

by Catalo
cience.com
pand Long Range
consistent, accura
x, and optimized bl
R, and large-fragm
iversal ProbeLibr
e in combination w
omplete set of 165
antification of trans
beLibrary Assay D
htCycler
480 Pr
ve time in gene qua
R master mix for th
tStart Taq DNA Po
mation of nonspec
htCycler
480 SY
ady-to-use hot star
htCycler
480 Inst
d quantification. Eli
nimize pipetting ste
anscriptor First St
e instruments, incl
htCycler
480 Syst
anscriptor First St
e instruments, incl
htCycler
480 Syst
pid DNA Dephos
t, efficient dephos
blunt-end DNA fra
gments into plasm
ear DNA, and librar
pid DNA Dephos
t, efficient dephos
blunt-end DNA fra
gments into plasm
ear DNA, and librar
Pid Alkaline Phos
pid, efficient depho
ctivated at +75C f
uired after restrict
phosphorylated DN
Pid Alkaline Phos
pid, efficient depho
ctivated at +75C f
uired after restrict
phosphorylated DN
htCycler
Softwa
sion 4.1 is the up-
truments. Allows u
dules for performin
htCycler
480 Pr
ve time in gene qua
R master mix for th
tStart Taq DNA Po
mation of nonspec
ti-His
6
-Peroxidas
single-step detect
stern and dot blot
ciently recognizes
C-terminal tagged
ti-His
6
(2)
ecific, sensitive det
tor. For immunoblo
munofluorescence,
ged proteins than
og Numb
Product N

e dNTPack
ate amplification o
igned buffer set, u
end of thermostab
ment amplification.
rary Extension Se
with the Universal P
5 Universal ProbeL
scripts of all organ
Design Center.
robes Master
antification assays
he LightCycler
48
olymerase for hot s
YBR Green I Mas
rt mix for SYBR Gr
truments. Ideal for
iminate time-cons
eps; just add DNA
trand cDNA Synt
l types of RNA from
nd cDNA synthesi
luding LightCycler
tems.
trand cDNA Synt
l types of RNA from
nd cDNA synthesi
luding LightCycler
tems.
& Ligation Kit
phorylation (10 mi
agments. Minimizes
id and phage vect
ry generation.
& Ligation Kit
phorylation (10 mi
agments. Minimizes
id and phage vect
ry generation.
sphatase
osphorylation of 5
for 2 minutes. No a
ion and dephosph
NA directly in ligati
sphatase
osphorylation of 5
for 2 minutes. No a
ion and dephosph
NA directly in ligati
are 4.1
to-date LightCycle
use with Windows X
ng and analyzing r
robes Master
antification assays
he LightCycler
48
olymerase for hot s
se (2)
tion of His
6
-tagge
analysis and ELISA
N-terminal histidi
proteins.
tection of histidine
otting, immunopre
, ELISA. More effic
C-tagged proteins
ber
Name
ltrapure PCR-grad
ble DNA polymeras
et, Probes #91 to
ProbeLibrary Set, H
ibrary Probes. Ena
nisms using the on
s using an optimize
80 System. The mix
start PCR, which m
products.
ster
reen I-based real-t
PCR assays for ge
uming MgCl
2
titra
, primers.
thesis Kit
m a variety of sour
s reactions up to 1
Carousel-Based
thesis Kit
m a variety of sour
s reactions up to 1
Carousel-Based
in) and ligation (5
s application times
ors, linker ligation
in) and ligation (5
s application times
ors, linker ligation
ends of DNA and
additional purificat
orylation. Use the
ion reactions.
ends of DNA and
additional purificat
orylation. Use the
ion reactions.
er
Software for L
XP. Integrates all s
real-time PCR expe
s using an optimize
80 System. The mix
start PCR, which m
products.
d recombinant pro
A. Anti-His
6
-Perox
ne-tagged protein
e-tagged proteins r
ecipitation, immuno
ciently recognizes N
s.
PCR products.
de nucleotide
ses for PCR, RT-
o #165
Human to obtain
bles
line Universal
ed ready-to-use
x contains
minimizes
time PCR on
ene detection
ation and
rces. Includes all
14 kb on all real-
d and
rces. Includes all
14 kb on all real-
d and
min) of sticky-
s when cloning
, recircularizing
min) of sticky-
s when cloning
, recircularizing
RNA. Rapidly
tion steps
RNA. Rapidly
tion steps
ightCycler
2.0
software
eriments.
ed ready-to-use
x contains
minimizes
oteins by
xidase (2) more
s in comparison
regardless of
ocytochemistry,
N-terminal-

3,500 U (5 x 70
20 l final volum
1 set of 75 Univ
10 x 5 ml ((2x c
20
10 x 5 ml ((2x c
20
1 kit
1 kit
1 kit
1 kit
1
1 x 50 ml (for u

Pack Size

00 U) for up to 2,5
me each containin
blend
versal ProbeLibrary
10 M each.
for up to 100 reac
for up to 200 reac
for up to 160 reac
1,000 U (1 U/l)
5,000 U (1 U/l)
1 software packag
up to 5,000 reactio
volume)
80 U
200 l
00 reactions of
ng 1.4 U enzyme
y Probes, 125 l,
000 reactions of
ume)
000 reactions of
ume)
ctions
ctions
tions
ctions
e
ns of 20 l final

Price in

2.239,00
2.574,80
inquire
inquire
484,00
869,90
174,60
499,50
90,70
363,80
inquire
inquire
414,60
355,30

Pr

Cat.

04 90
04 90
04 90
04 90
04 91
04 91
04 91
04 91
04 91
04 92
04 94
04 94
04 98
04 99
roducts b

No.
06 837 001 Pho
Use
Inhi
alm
dep
06 845 001 Pho
Use
Inhi
alm
dep
09 631 001 Lig
Sav
Ligh
Res
or P
09 640 001 Lig
Ach
inhi
Obt
eva
13 850 001 Fas
Rea
qua
use
for
13 914 001 Fas
Rea
qua
use
for
13 949 001 Fas
Rea
tem
ena
ROX
13 957 001 Fas
Rea
tem
ena
ROX
14 058 001 Fas
Rea
tem
ena
ROX
29 292 001 Lig
Use
20
Ligh
max
42 078 001 Dis
Rap
Rele
cult
sus
42 086 001 Dis
Rap
Rele
cult
sus
83 912 001 Hig
Use
bp.
cDN
mol
91 885 001 Lig
Eas
cyc
Uni
Prev
Glyc

by Catalo
osSTOP
e non-toxic tablets
ibition of acid/alka
most any tissue or c
phosphorylation in
osSTOP
e non-toxic tablets
ibition of acid/alka
most any tissue or c
phosphorylation in
htCycler
480 H
ve time using an op
htCycler
480 Syst
soLight, a novel dy
PCR.
htCycler
480 H
hieve highly homog
ibition using this fl
tain enhanced fluo
luation of amplico
stStart Universal
ady-to-use 2x mix
antitative, real-time
e on all real-time in
use on LightCycle
stStart Universal
ady-to-use 2x mix
antitative, real-time
e on all real-time in
use on LightCycle
stStart Universal
ady-to-use 2x mix
mplate for quantitat
ables use on all rea
X. Not for use on L
stStart Universal
ady-to-use 2x mix
X. Not for use on L
stStart Universal
ady-to-use 2x mix
X. Not for use on L
htCycler
Capilla
e with LightCycler
l and are compat

htCycler
2.0 Sam
ximizes fluorescen
spase
II (neutra
pid, gentle disrupti
eases single cells f
ture to transfer to a
pension.
spase
I (neutral
pid, gentle disrupti
eases single cells f
ture to transfer to a
pension.
gh Pure PCR Clea
e this kit to selectiv
Isolate PCR produ
NA, and concentra
lecular biology tec
htCycler
480 R
y-to-use hot start
ling conditions of
versal ProbeLibrar
vent PCR product
cosylase.
og Numb
Product N

to protect your pr
aline, serine/threon
cell type. PhosSTO
FFPE tissue sectio
to protect your pr
aline, serine/threon
cell type. PhosSTO
FFPE tissue sectio
igh Resolution M
ptimized ready-to-
tem. This highly st
ye that does not int
igh Resolution M
geneous staining o
luorescent double-
orescent signal sha
n melting behavio
SYBR Master (R
contains everythin
e DNA detection a
nstruments requirin
r
Instruments.
SYBR Master (R
contains everythin
e DNA detection a
nstruments requirin
r
Instruments.
Probe Master (R
contains everythin
tive, real-time dete
al-time instrument
LightCycler
Instru
Probe Master (R
contains everythin
al-time instrument
LightCycler
Instru
Probe Master (R
contains everythin
al-time instrument
LightCycler
Instru
aries (20 l)
Carousel-Based
ible with the Light
mple Carousel (20
t signal transmissi
al protease, grade
on of cellular matr
for primary cell cu
a secondary cultur
protease, grade
on of cellular matr
for primary cell cu
a secondary cultur
anup Micro Kit
vely isolate small D
ucts from amplifica
ate dilute solutions
chniques.
NA Master Hydro
mix for one-step R
plate-based LightC
ry and hydrolysis p
carryover using Li
ber
Name
rotein from dephos
nine and tyrosine p
P Tablets prevent
ons.
rotein from dephos
nine and tyrosine p
P Tablets prevent
ons.
Melting Master
-use PCR master m
table reaction mix
terfere with amplif
Melting Dye
of amplicons witho
-stranded DNA-bi
arpness and high r
r.
Rox)
ng except primers a
ssays. The referen
ng normalization w
Rox)
ng except primers a
ssays. The referen
ng normalization w
Rox)
ng except primers,
ection assays. Refe
s requiring norma
uments.
Rox)
ng except primers,
ection assays. Refe
s requiring norma
uments.
Rox)
ng except primers,
ection assays. Refe
s requiring norma
uments.
Instruments. Capi
tCycler
Carousel
l). High quality bo
ion.
e II)
rix in many tissues
lture or harvesting
re. Prevents cell cl
e I)
rix in many tissues
lture or harvesting
re. Prevents cell cl
DNA fragment size
ation and other rea
s. Use purified DNA
olysis Probes
RT-PCR with the ra
Cycler
480 Instru
probes as the detec
ghtCycler
Uracil-
sphorylation.
phosphatases in
sphorylation.
phosphatases in
mix for the
contains
fication enzymes
out PCR
nding dye.
resolution
and template for
ce dye enables
with ROX. Not
and template for
ce dye enables
with ROX. Not
probe, and
erence dye
lization with
probe, and
erence dye
lization with
probe, and
erence dye
lization with
llaries hold 10 to
and
orosilicate glass
s and organs.
g cells already in
umping in
s and organs.
g cells already in
umping in
es 25 bp to 100
actions, purify
A in most
apid, accurate
uments using
ction format.
-DNA

20 tablets in EA
for 10
10 tablets in EA
for 10
5 x 1 ml (for
1 ml (for up to
4 x 1.25 ml for
10 x 5 ml for u
2 x 1.25 ml for
10 x 1.25 ml fo
fi
10 x 5 ml for u
1 pack (con
cap
5
10 x approx. 2
1 kit fo
1 kit (for up t

Pack Size

ml cell extract or
ml cell extract or
up to 500 reaction
o 1,000 reactions o
volume)
up to 500 reaction
reaction volume
reaction volume
up to 250 reaction
reaction volume
or up to 12,500 rea
nal reaction volum
reaction volume
ntaining 5 boxes, e
pillaries and stopp
mg (filtered throu
size membrane)
to 5x100 reactions
volume)
www.roche
ter) (each tablet
buffer)
ter) (each tablet
buffer)
ns, 20 l each)
f 20 l reaction
ns of 20 l final
ns of 20 l final
ns of 20 l final
actions of 20 l
me
ns of 20 l final
each with 96
ers)
e)
gh 0.2 m pore
cations
s at 20 l final
e-applied-science

Price in

190,00
101,10
inquire
inquire
289,80
inquire
139,30
657,60
inquire
inquire
435,30
753,70
280,10
inquire

211

e.com

Pr
212

www.r

Cat.

04 99
05 01
05 01
05 01
05 01
05 01
05 01
05 01
05 04
05 04
05 04
05 04
05 04
05 04
05 04
roducts b
roche-applied-sc

No.
94 884 001 Lig
Com
qua
PCR
sam
15 197 001 Lig
Silv
Inst
the
15 219 001 Lig
Silv
480
by t
15 243 001 Lig
Ach
thro
wor
and
15 278 001 Lig
Ach
thro
wor
and
15 944 001 Cel
Non
in 9
Ana
anti
15 952 001 Pro
Affi
for t
for t
mito
15 979 001 Pro
Affi
from
ente
cult
46 114 001 Uni
Qua
end
assa
soft
46 149 001 Uni
Gen
exp
assa
onli
46 157 001 Uni
Gen
exp
assa
onli
46 165 001 Uni
Gen
exp
assa
onli
46 173 001 Uni
Gen
exp
assa
onli
46 190 001 Uni
Gen
exp
assa
onli
46 203 001 Uni
Gen
exp
assa
onli
by Catalo
cience.com
htCycler
480 So
mprehensive suite
antification and ge
R Systems. Provide
mple editing, templ
htCycler
480 B
ver block cycler for
trument. The block
instrument. Includ
htCycler
480 B
ver block cycler acc
0 Instrument. The b
the instrument. Inc
htCycler
480 In
hieve fast, sensitive
oughput platform.
rkflows, this cutting
d temperature hom
htCycler
480 In
hieve fast, sensitive
oughput platform.
rkflows, this cutting
d temperature hom
ll Proliferation Re
nradioactive spect
96-well plates. Mea
alyze cytotoxic/cyto
ibodies. Ready-to-
otein G Agarose
nity chromatograp
the purification of
the absence of sta
ogenic.
otein A Agarose
nity chromatograp
m many species. Te
erotoxins. Use to p
ture supernatant.
iversal ProbeLibr
antify expression le
dogenous referenc
ays for target gene
tware at the Assay
iversal ProbeLibr
ne-specific probe a
pression levels usin
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
og Numb
Product N

oftware, Version
of tools for setup,
notyping assays o
es all functionalitie
lates, macros).
lock Kit 384 Silve
r 384-well plates, fo
k cycler is automat
des block lid and s
lock Kit 96 Silver
cessory for 96-wel
block cycler is auto
cludes block lid an
nstrument II
e, and consistent P
Adaptable for 96-
g-edge instrument
mogeneity.
nstrument II
e, and consistent P
Adaptable for 96-
g-edge instrument
mogeneity.
eagent WST-1
rophotometric qua
asure proliferation
ostatic compounds
-use solution.
phy using Protein G
IgG from many sp
aphylococcal enter
phy using Protein A
ested for the abse
purify mouse mono
rary Set, Human
evels of a human g
ce gene in a dual-c
e and UPL Referen
y Design Center.
rary Human PBG
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Human HPRT
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Human ACTP
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Human PGK
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Mouse ACTB
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Rat ACTB Ge
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
ber
Name
1.5
run, and analysis
n LightCycler
48
es (user-friendly pr
er
or use with the Lig
tically detected and
storage box.
r
ll plates using the
omatically detected
nd storage box.
PCR results using a
or 348-well plates
t offers exceptiona
PCR results using a
or 348-well plates
t offers exceptiona
antification of proli
in response to gro
s. Assess growth-i
G agarose is the m
pecies. Recombina
rotoxins that are kn
A agarose is ideal
nce of staphylococ
oclonal antibodies
Reference Gene
gene of interest in
color assay. Design
nce Gene Assay w
D Gene Assay
r human PBGD. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
RT Gene Assay
r human HPRT. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
P Gene Assay
r human ACTP. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
K1 Gene Assay
r human PGK1. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
B Gene Assay
r mouse ACTB. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
ene Assay
r rat ACTB. Quanti
-time PCR. Design
eference Gene Ass
ay Design Center.
of real-time PCR
0 Real-Time
rogramming,
ghtCycler
480
d calibrated by
LightCycler

d and calibrated
a versatile high-
s and automated
al reproducibility
a versatile high-
s and automated
al reproducibility
feration/viability
owth factors.
nhibitory
method of choice
nt form is tested
nown to be
for purifying IgG
ccal
from ascites or
Assays
relation to an
n multiplex PCR
ith free online
uantify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
fy gene
multiplex PCR
say using the

1
1 block kit (blo
1 block kit (bl
1 instr
1 instr
8 m
15 m
15 m
1 set for up to
250 reactions
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
Pack Size

1 software packag
ock kit for 384-wel
plates)
ock kit for 96-well
plates)
rument (384-well v
rument (96-well ve
ml for up to 800 te
100 reactions of 5
of 20 l for each r
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
e
l PCR multiwell
PCR multiwell
version)
ersion)
ests
lume)
lume)
0 l or for up to
reference gene
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l

Price in

inquire
inquire
inquire
inquire
inquire
211,50
2.043,70
1.238,00
1.111,90
491,60
491,60
491,60
491,60
491,60
491,60

Pr

Cat.

05 04
05 04
05 04
05 05
05 06
05 08
05 08
05 08
05 09
05 10
05 10
05 10
05 11
05 18
roducts b

No.
46 211 001 Uni
Gen
exp
assa
onli
46 220 001 Uni
Gen
exp
assa
onli
46 246 001 Uni
Gen
exp
assa
onli
56 489 001 cOm
Rely
EDT
type
66 310 001 Lig
Use
inte
easy
PCR
80 576 001 Hig
Pur
incl
RNA
qua
81 955 001 Tra
Rev
tran
inte
qua
81 963 001 Tra
Rev
tran
inte
qua
91 284 001 Tra
Rev
tran
inte
qua
02 413 001 Lig
This
SYB
Inst
labe
02 430 001 Lig
Clea
bas
on L
reco
03 908 001 Lig
Ana
this
PCR
met
14 403 001 Hig
Pur
sam
colu
dire
89 268 001 Uni
Gen
exp
assa
onli

by Catalo
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
mplete, EDTA-fre
y on proven perfor
TA-free Tablets inh
es as cOmplete UL
htCycler
480 LI
e this module to int
ernal Laboratory In
y-to-install softwa
R workflow efficien
gh Pure miRNA Is
ifies and enriches
uding formalin-fix
A in northern blots
antification with RT
anscriptor High Fi
verse transcribe RN
nscriptases. Optim
erest and sequence
antitative RT-PCR w
anscriptor High Fi
verse transcribe RN
nscriptases. Optim
erest and sequence
antitative RT-PCR w
anscriptor High Fi
verse transcribe RN
nscriptases. Optim
erest and sequence
antitative RT-PCR w
htCycler
480 M
s high performanc
BR Green I and hyd
truments. The clea
eled for easy track
htCycler
480 M
ar plates for high p
sed assays using th
LightCycler
480 I
ommended for use
htCycler
480 G
alyze melting curve
s accessory softwa
R fragments for ge
thylation.
gh Pure Viral Nuc
ify viral nucleic ac
me principle as the
umn assembly pur
ect use in PCR and
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
og Numb
Product N

rary Mouse GAPD
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Rat GAPD G
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Human G6PD
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
ee
rmance combined
hibit serine and cy
LTRA Tablets. Supp
IMS Interface Mo
tegrate the LightC
nformation Manage
are package for im
ncy.
solation Kit
small (micro) RNA
xed/FFPE sections,
s, miRNA array hyb
T-PCR on the Light
idelity cDNA Syn
NA with increased
ized for two-step R
e transcriptomes. S
with LightCycler

idelity cDNA Syn
NA with increased
ized for two-step R
e transcriptomes. S
with LightCycler

idelity cDNA Syn
NA with increased
ized for two-step R
e transcriptomes. S
with LightCycler

Multiwell Plate 96
ce 96-well reaction
drolysis probe-bas
ar, half-skirted, poly
king.
Multiwell Plate 38
performance SYBR
he LightCycler
48
Instruments and 4
e with FRET HybPr
ene Scanning So
e data from the Lig
re module for the
enetic variations su
cleic Acid Large V
ids from serum, pl
High Pure Viral N
rifies larger sample
d RT-PCR.
rary Human PPIA
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
ber
Name
D Gene Assay
r mouse GAPD. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
ene Assay
r rat GAPD. Quant
-time PCR. Design
eference Gene Ass
ay Design Center.
D Gene Assay
r human G6PD. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
with high conveni
steine proteases in
plied in glass vials
odule
Cycler
480 System
ement System (LIM
proved data mana
As from animal cel
and plant materia
bridization, and rel
tCycler
480 Syste
nthesis Kit
fidelity compared
RT-PCR. Use to clo
Study gene expres
Systems.
nthesis Kit
fidelity compared
RT-PCR. Use to clo
Study gene expres
Systems.
nthesis Kit
fidelity compared
RT-PCR. Use to clo
Study gene expres
Systems.
6, clear
plate is specifical
sed assays using L
ypropylene plate is
84, clear
R Green I and hydr
80 Instrument, 384
80 Software, Versi
robe probes or HRM
oftware
ghtCycler
480 Ins
LightCycler
480
uch as SNPs, muta
Volume Kit
asma, or whole blo
Nucleic Acid Kit. An
e volumes up to 2.5
A Gene Assay
r human PPIA. Qua
-time PCR. Design
eference Gene Ass
ay Design Center.
uantify gene
multiplex PCR
say using the
ify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
ence. cOmplete
n the same cell
.
m into your
MS) using this
gement and
ls and tissues,
l. Use purified
lative
em.
to other reverse
one genes of
ssion using
to other reverse
one genes of
ssion using
to other reverse
one genes of
ssion using
ly designed for
LightCycler
480
s barcode-
rolysis probes-
-well. Use only
on 1.5. Not
M.
strument using
Software. Scan
tions, and
ood, using the
n innovative spin
5 ml. Ideal for
antify gene
multiplex PCR
say using the

1 set for up to
50
1 set for up to
50
1 set for up to
50
3 x 20 table
sufficient f
1
1 kit for
1 kit for up
1 kit
1 kit
5 x 10
5 x 10
1
1 kit
1 set for up to
50

Pack Size

200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
for a volume of 50
1 software packag
up to 50 miRNA is
to 50 reactions an
reaction
for up to 200 reac
for up to 100 reac
plates (with sealin
plates (with sealin
1 software packag
200 reactions of 5
00 reactions of 20
www.roche
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
ach tablet is
ml solution
e
solations
nd 10 control
ctions
ctions
ng foils)
ng foils)
e
tions
0 l or for up to
l
e-applied-science

Price in

491,60
491,60
491,60
617,70
inquire
324,80
413,20
1.087,40
598,10
inquire
inquire
inquire
259,70
491,60

213

e.com

Pr
214

www.r

Cat.

05 18
05 18
05 19
05 19
05 19
05 21
05 22
05 23
05 23
05 23
05 23
05 32
05 32
05 32
roducts b
roche-applied-sc

No.
89 284 001 Uni
Gen
exp
assa
onli
89 390 001 Uni
Gen
exp
assa
onli
90 525 001 Uni
Gen
exp
assa
onli
90 541 001 Uni
Gen
exp
assa
onli
97 686 001 Ma
Tab
sam
Ligh
tube
17 555 001 Lig
Hig
Inst
for
Ligh
20 319 001 Lig
Hig
Inst
use
Ligh
33 526 001 GS
Com
reag
seq
clon
33 658 001 GS
The
for
Tita
reg
33 674 001 GS
Use
FLX
for
Pico
33 682 001 GS
Com
dete
amp
laye
23 738 001 Ma
Isol
who
high
high
23 983 001 Ma
One
Plat
ada
Ligh
23 991 001 Ma
One
Bag
tips
bag

by Catalo
cience.com
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
iversal ProbeLibr
ne-specific probe a
ays for your target
ine ProbeFinder so
agNA Pure LC 2.0
bletop instrument b
mple material and f
htCycler
Capillar
es. Process up to 3
htCycler
480 M
h-performance rea
truments, 384-well
real-time PCR and
htCycler
480 Inst
htCycler
480 M
h-performance rea
truments, 96-well v
ed for real-time PC
htCycler
480 Inst
FLX Titanium Se
mbined with the GS
gents and other co
uence in extra-lon
nally amplified DN
FLX Titanium em
e GS FLX Titanium
breaking large-vol
anium LV emPCR K
ions of a PicoTiter
FLX Titanium em
e for breaking sma
X Titanium SV emP
loading into mediu
oTiterPlate device.
FLX Titanium Pic
mbine this kit with
ermine the nucleo
plified DNA library
ers in the wells of a
agNA Pure LC Tot
ate high-purity tot
ole blood using Ma
h sensitivity in dow
h performance PC
agNA Pure LC 2.0
e adapter for appro
te 96 in the MagNA
apter is placed onto
htCycler
480 Mu
agNA Pure LC 2.0
e additional Waste
gs are fixed to the
s are discarded by
g in the waste box.
og Numb
Product N

rary Human TBP
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Human 2M
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Human GUS
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
rary Human GAP
and primer pair for
ng dual-color real-
t gene and UPL Re
oftware at the Assa
0 Instrument
both for automated
for pipetting into P
ies, 96-well plate,
32 samples in one
Multiwell Plate 38
action device tailo
l version.Use Light
d melting curve an
trument, 384-well v
Multiwell Plate 96
action device tailo
version.LightCycle
R and melting cur
trument, 96-well ve
equencing Kit XL
S FLX Titanium Pic
onsumables requir
ng reads (350 to 45
A library.
mPCR Breaking K
emPCR Breaking
lume (LV) emulsio
Kit (Lib-L) to prepa
Plate device.
mPCR Filters SV 6
all-volume (SV) em
PCR Kit (Lib-L) to p
um, medium-small
coTiterPlate Kit 7
the GS FLX Titani
tide sequence of a
y. The DNA-carryin
a PicoiterPlate dev
tal Nucleic Acid
tal viral nucleic aci
agNA Pure LC Inst
wnstream applicati
R with LightCycler
0 LightCycler
48
opriate orientation
A Pure LC Cooling
o the 96-well PCR
ltiwell Plate 96 is t
0 Waste Box
e Box for holding M
MagNA Pure LC 2
the MagNA Pure

ber
Name
Gene Assay
r human TBP. Qua
-time PCR. Design
eference Gene Ass
ay Design Center.
M Gene Assay
r human 2M. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
SB Gene Assay
r human GUSB. Qu
-time PCR. Design
eference Gene Ass
ay Design Center.
PD Gene Assay
r human GAPD. Q
-time PCR. Design
eference Gene Ass
ay Design Center.
d nucleic acid isola
PCR reaction vesse
PCR tubes, and 1.5
run in 16-180 min
84 white, 4 barco
r-made for the Lig
tCycler
480 Multi
alysis applications
version.
6, white, 4 barcod
r-made for the Lig
r
480 Multiwell P
rve analysis applica
ersion.
R70
coTiterPlate Kit 70x
red for determining
50 nt) of an immob
Kits LV/MV 12pc
Kit LV 12pc provid
ons prepared using
are samples for loa
64pc
mulsions generated
prepare samples at
l, or small regions
70x75
um Sequencing K
an immobilized and
ng beads and reag
vice.
Kit - High Perfor
ids from 1 ml seru
truments. This kit a
ions. Use purified
r
Systems and bl
80 Plate Adapter
n of the LightCycle
g Block, 96-well PC
Plate Cooling Bloc
then positioned co
MagNA Pure LC 2.0
2.0 Waste Box Lid.
LC 2.0 Instrument
antify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
uantify gene
multiplex PCR
say using the
ation from crude
els, such as
5 ml reaction
n.
odes
ghtCycler
480
well Plates 384
s with the
des
ghtCycler
480
Plates 96 are
ations with the
x75, provides
g the nucleotide
bilized and
des components
g the GS FLX
ading into large
using the GS
t smaller scales
of a
it XLR70 to
d clonally
ents deposit in
mance
m, plasma, or
achieves very
nucleic acids for
ock cyclers.
r
r
480 Multiwell
CR Plate. The
ck. The
rrectly.
0 Waste Bags.
Used reaction
into the waste

1 set for up to
50
1 set for up to
50
1 set for up to
50
1 set for up to
50
1 instrument w
mo
5 x 10 p
5 x 10 p
1 kit for one Ge
1 kit for 12
1 pl
1 kit

Pack Size

200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
200 reactions of 5
00 reactions of 20
with integrated PC
nitor, and accesso
plates without seal
plates without seal
enome Sequener F
run
LV emulsion-brea
1 kit (64 filters)
late (with accesso
for up to 288 isola
1 adapter
1 box
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
0 l or for up to
l
C, touchscreen
ories
ling foils
ling foils
FLX sequencing
aking setups
ries)
ations

Price in

491,60
491,60
491,60
491,60
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Pr

Cat.

05 32
05 32
05 32
05 33
05 33
05 33
05 33
05 33
05 35
05 39
05 40
05 40
05 40
05 40
roducts b

No.
24 114 001 Ma
One
a M
2.0
Inst
24 122 001 Ma
This
Mag
Was
24 157 001 Ma
The
Box
tips
Inst
34 276 001 Lig
Obt
high
an e
inte
39 316 001 Rea
Qua
pan
incl
sam
39 324 001 Rea
Qua
sup
Pre-
add
39 359 001 Rea
Qua
Ass
assa
add
39 545 001 Rea
Qua
gen
plat
req
58 639 001 Lig
Incr
this
the
cos
92 063 001 Rea
Qua
pan
incl
sam
01 020 001 Lib
Max
con
a no
ens
01 046 001 Lib
Det
thes
Blen
app
01 054 001 Lib
Max
con
non
prov
01 089 001 Lib
Max
con
non
prov

by Catalo
agNA Pure LC 2.0
e additional Waste
MagNA Pure LC 2.0
Waste Box Lid. Us
trument into the w
agNA Pure LC 2.0
s is a replacement
gNA Pure LC 2.0 I
ste Slide into the M
agNA Pure LC 2.0
ese Waste Bags are
x of MagNA Pure L
s from 5 to 7 runs.
trument.
htCycler
1536 I
tain 1,536 data poi
h-throughput ther
exceptional range
er-assay errors.
alTime ready Hum
nels directly using
ude gene-specific
mple cDNA and ma
alTime ready Hum
perfamily. Assay pa
-plated assays inc
d sample cDNA an
alTime ready Hum
antify the expressio
say panels directly
ays include gene-s
ding sample cDNA
alTime ready Hum
nes. Assay panels d
ted assays include
uire adding sampl
htCycler
1536 M
rease PCR through
s high-performance
LightCycler
1536
ts and minimizes a
alTime ready Hum
nels directly using
ude gene-specific
mple cDNA and ma
erase TL Researc
ximize yield of isol
ntains highly purifie
on-clostridial neut
sures experimental
erase Research G
termine the optima
se five 5 mg vials o
nds, each with diff
plicability.
erase DH Resear
vides high experim
erase DH Resear
vides high experim
og Numb
Product N

0 Waste Box Lid
e Box Lid. The Mag
0 Waste Bag which
sed tips are discard
waste bag in the wa
0 Tip Waste Slide
waste slide. Used
nstrument through
MagNA Pure LC 2.
0 Waste Bags
e only for use with
LC 2.0 Instruments
They cannot be us
Instrument
nts in a single PCR
mal block cycler fe
of assay types wh
man Apoptosis P
evels of 372 huma
LightCycler
480
c primers and a UP
aster mix.
man ABC Transp
evels of 42 genes o
anels directly using
lude gene-specific
d master mix.
man Cell Cycle R
on levels of 84 gen
using LightCycler
specific primers an
A and master mix.
man Reference G
on levels of 19 hum
directly using Ligh
e gene-specific prim
e cDNA and mast
Multiwell Plate
hput fourfold comp
e 1,536-well reacti
6 Instrument. Prec
assay errors.
man Apoptosis P
evels of 84 human
LightCycler
480
c primers and a UP
aster mix.
ch Grade
ated cells using th
ed collagenase iso
tral protease. Excep
reproducibility.
Grade Selection
al collagenase prod
of highly pure Libe
ferent levels of agg
rch Grade
ated cells using th
ed collagenase iso
al protease. Except
mental reproducibi
rch Grade
ated cells using th
ed collagenase iso
al protease. Except
mental reproducibi
ber
Name
gNA Pure LC 2.0 W
h is fixed to the Ma
ded by the MagNA
aste box.
e
reaction tips are d
h the MagNA Pure
.0 Waste Box.
h the MagNA Pure
s. They can receive
sed with the MagN
R run of less than
eatures proven opt
ile reducing samp
Panel, 384
n apoptosis-relate
Instruments. Pre-p
PL Probe, and only
porter Panel
of the human ABC
g LightCycler
480
c primers and a UP
Regulation Panel
nes in human cell
480 Instruments
nd a UPL Probe, an
Gene Panel
man genes to use
htCycler
480 Instr
mers and a UPL Pr
er mix.
pared to a 384-wel
ion plate specifica
ision miniaturizatio
Panel, 96
apoptosis-related
Instruments. Pre-p
PL Probe, and only
his new enzyme ble
oforms blended wit
ptional lot-to-lot c
Kit
duct for your appli
erase Research Gra
gressiveness, spec
his new enzyme ble
oforms blended wit
ional lot-to-lot con
lity.
his new enzyme ble
oforms blended wit
ional lot-to-lot con
lity.
Waste Box holds
agNA Pure LC
A Pure LC 2.0
discarded by the
e LC 2.0 Tip
LC 2.0 Waste
e used reaction
NA Pure LC 1.0
50 minutes. This
tics facilitating
le volumes and
ed genes. Assay
plated assays
require adding
C transporter
0 Instruments.
PL Probe. Just
cycle regulation.
s. Pre-plated
nd only require
as reference
ruments. Pre-
robe, and only
ll plate using
lly designed for
on reduces
d genes. Assay
plated assays
require adding
end that
th Thermolysin,
onsistency
cation using
ade Enzyme
cificity, and
end that
th Dispase
, a
nsistency
end that
th Dispase
, a
nsistency

25 b
2 plates (e
2 plates (
2 plates (
2 plates (
2 plates (
1

Pack Size

1 lid
1 slide
bags (for 5 runs ea
1 instrument
each containing 38
(each containing 9
(each containing 9
(each containing 9
10 x 10 plates
(each containing 9
10 mg (2 x 5 mg)
1 kit (5 x 5 mg)
10 mg (2 x 5 mg)
100 mg (2 x 50 mg
www.roche
ach)
84 assays)
96 assays)
96 assays)
96 assays)
96 assays)

g)
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
36,50
213,30
333,00
1.367,50

215

e.com

Pr
216

www.r

Cat.

05 40
05 40
05 40
05 40
05 40
05 41
05 41
05 41
05 41
05 46
05 46
05 46
05 46
05 47
roducts b
roche-applied-sc

No.
01 119 001 Lib
Max
con
a no
diss
01 127 001 Lib
Max
con
a no
diss
01 135 001 Lib
Max
con
a no
mor
01 151 001 Lib
Max
con
a no
mor
01 160 001 Lib
Max
con
non
prot
14 601 001 70x
This
plat
For
Tita
14 610 001 70x
This
plat
For
Tita
14 628 001 70x
This
plat
For
Tita
14 636 001 70x
This
plat
For
Tita
63 343 001 GS
Pre
inse
and
Tita
66 202 001 Lib
Max
con
non
prot
67 535 001 Ma
Rea
RNA
bloo
67 675 001 Rea
Qua
gen
plat
req
70 129 001 GS
Stan
only
that
spe

by Catalo
cience.com
erase TM Resear
on-clostridial neut
sociation applicatio
erase TM Resear
on-clostridial neut
sociation applicatio
erase TH Resear
on-clostridial neut
re difficult targets.
erase TH Resear
on-clostridial neut
re difficult targets.
erase DL Resear
tein) for delicate a
x75 Bead Deposi
s device with loadi
te. The top plate p
use with GS FLX S
anium PicoTiterPlat
x75 Bead Deposi
s device with loadi
te. The top plate p
use with GS FLX S
anium PicoTiterPlat
x75 Bead Deposi
s device with loadi
te. The top plate p
use with GS FLX S
anium PicoTiterPlat
x75 Bead Deposi
s device with loadi
te. The top plate p
use with GS FLX S
anium PicoTiterPlat
FLX Titanium Lib
pare up to 10 asso
ert lengths of 3, 8,
d sequencing using
anium Series kits.
erase DL Resear
tein) for delicate a
agNA Pure 96 Ce
ady-to-use reagent
A using the MagN
od, up to 1x10
6
cu
alTime ready Hum
nes. Assay panels d
ted assays include
uire adding sampl
FLX Titanium Co
ndard sequencing
y Control Beads ar
t yield sequencing
ecifications.
og Numb
Product N

rch Grade
ated cells using th
ed collagenase iso
tral protease. Excel
ons.
rch Grade
ated cells using th
ed collagenase iso
tral protease. Excel
ons.
rch Grade
ated cells using th
ed collagenase iso
tral protease. More

rch Grade
ated cells using th
ed collagenase iso
tral protease. More

rch Grade
ated cells using th
ed collagenase iso
al protease. Gentle
applications.
ition Device (2 la
ing ports and air v
resses the gasket
Standard PicoTiter
te Kit 70x75.
ition Device (4 m
ing ports and air v
resses the gasket
Standard PicoTiter
te Kit 70x75.
ition Device (8 M
ing ports and air v
resses the gasket
Standard PicoTiter
te Kit 70x75.
ition Device (16 s
ing ports and air v
resses the gasket
Standard PicoTiter
te Kit 70x75.
brary Paired End
orted single-strand
or 20 kb from dsD
g the GS FLX Instr
rch Grade
ated cells using th
ed collagenase iso
al protease. Gentle
applications.
llular RNA Large
ts in two prefilled s
NA Pure 96 Instrum
ultured cells, up to
man Reference G
on levels of 19 hum
directly using Ligh
e gene-specific prim
e cDNA and mast
ontrol Bead Kit
control for the GS
re sequenced. They
results to show th
ber
Name
his new enzyme ble
oforms blended wit
llent overall applic
his new enzyme ble
oforms blended wit
llent overall applic
his new enzyme ble
oforms blended wit
e aggressive protea
his new enzyme ble
oforms blended wit
e aggressive protea
his new enzyme ble
oforms blended wit
activity (low activi
arge regions)
ents has a bottom
against the PicoTit
rPlate Kit (70x75) a
medium regions)
ents has a bottom
against the PicoTit
M/S Regions)
ents has a bottom
against the PicoTit
small regions)
ents has a bottom
against the PicoTit
Adaptors
ded paired end DN
DNA input sample
ument with approp
his new enzyme ble
oforms blended wit
activity (low activi
e Volume Kit
sealed trays for pu
ment from 400/800
20 mg tissue, or e
Gene Panel
man genes to use
htCycler
480 Instr
mers and a UPL Pr
er mix.
S FLX Instrument. I
y contain known D
he instrument is w
end that
th Thermolysin,
ability in
end that
th Thermolysin,
ability in
end that
th Thermolysin,
ase activity for
end that
th Thermolysin,
ase activity for
end that
th Dispase
, a
ity per mg
plate and top
terPlate device.
and GS FLX
plate and top
terPlate device.
and GS FLX
plate and top
terPlate device.
and GS FLX
plate and top
terPlate device.
and GS FLX
NA libraries with
for amplification
priate GS FLX
end that
th Dispase
, a
ity per mg
urifying total
l lysed whole
equivalent.
as reference
ruments. Pre-
robe, and only
In a test run,
DNA sequences
ithin

1
1
1 bott
1 bott
1 bott
1 bott
1 k
1
3 set
2 plates (e

Pack Size

10 mg (2 x 5 mg)
100 mg (2 x 50 mg
10 mg (2 x 5 mg)
100 mg (2 x 50 mg
10 mg (2 x 5 mg)
tom plate and 1 top
tom plate and 1 top
tom plate and 1 top
tom plate and 1 top
100 mg (2 x 50 mg
each containing 38
1 kit

g)

g)

p plate
p plate
p plate
p plate
says
g)
each
84 assays)

Price in

108,50
642,40
82,10
611,50
62,50
inquire
inquire
inquire
inquire
inquire
402,70
inquire
inquire
inquire

Pr

Cat.

05 48
05 50
05 53
05 53
05 53
05 53
05 53
05 53
05 53
05 53
05 53
05 57
05 58
05 58
roducts b

No.
80 647 001 COT
Sup
DNA
hyb
cap
02 381 001 Lig
Not
153
153
Idea
end
prev
30 873 001 Sol
The
Sam
32 833 001 Rea
Ligh
hum
prim
layo
32 850 001 Rea
Ligh
hum
prim
layo
32 868 001 Rea
Ligh
hum
prim
layo
32 884 001 Rea
Ligh
hum
prim
with
32 906 001 Rea
Ligh
hum
prim
layo
32 914 001 Rea
Ligh
hum
prim
layo
32 949 001 Rea
Ligh
hum
prim
layo
32 957 001 Rea
Rea
gen
prim
hyd
73 092 001 Lig
Perf
trac
dete
153
82 563 001 Rea
Ligh
mou
incl
plat
82 571 001 Rea
Ligh
mou
incl
plat

by Catalo
T Human DNA, F
ppresses cross-hyb
A probes are hybr
bridizations, such a
pture, and nucleic a
htCycler 1536
te: RealTime ready
36 DNA Probes Ma
36 Instruments with
al for fast hot start
dpoint genotyping.
vent carryover con
id Waste Bag
e Solid Waste Bag
mple Handling Inst
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
h the online Config
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cat
ady-to-use qPCR a
ne expression in re
mers and a Univers
drolysis probe cont
htCycler
1536 D
form easy hot star
cking in automater
ection and gene q
36 System.
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
og Numb
Product N

Fluorometric Grad
bridization to huma
ridized in situ . Use
as comparative gen
acid labeling and d
DNA Probes Ma
y DNA Probes Mas
asterFor real-time P
h appropriate prob
t assays for gene d
Use LightCycler
ntamination.
holds the waste pr
trument.
stom Panel 384 -
tes 384 contain rea
t genes for gene ex
e-plated in wells. S
ne Configurator.
stom Panel 96 - 8
tes 96 contain read
t genes for gene ex
ne Configurator.
stom Panel 96 - 1
tes 96 contain read
t genes for gene ex
ne Configurator.
stom Panel 96 - 2
tes 96 contain read
t genes for gene ex
gurator.
stom Panel 96 - 3
tes 96 contain read
t genes for gene ex
ne Configurator.
stom Panel 96 - 4
tes 96 contain read
t genes for gene ex
ne Configurator.
stom Panel 96 - 9
tes 96 contain read
t genes for gene ex
ne Configurator.
talog Assays
assays for human,
eal-time PCR. Each
sal ProbeLibrary P
taining locked nuc
DNA Green Mast
rt PCR assays using
r workflows. Ideal f
uantification assay
stom Panel 96 - 9
tes 96 contain read
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 96 - 4
tes 96 contain read
r gene expression p
Probe pre-plated in
e online Configurat
ber
Name
de
an repetitive DNA
e in FISH and DNA
nome hybridization
detection.
ster
ster was renamed t
PCR using LightCy
bes and gene-spec
detection and quan
Uracil-DNA Glyco
roducts of the FLO
- 384
ady-to-use single q
xpression profiling
Select custom assa
8
dy-to-use single q
xpression profiling
Select custom assa
16
dy-to-use single q
xpression profiling
Select custom assa
24
dy-to-use single q
xpression profiling
Select custom assa
32
dy-to-use single q
xpression profiling
Select custom assa
48
dy-to-use single q
xpression profiling
Select custom assa
96
dy-to-use single q
xpression profiling
Select custom assa
mouse and rat gen
h assay includes ge
robe, a short FAM
cleic acid.
ter
g fast protocols an
for high-throughpu
ys. For use on the
96+
dy-to-use qPCR as
profiling + error de
n wells. Select cust
tor.
48+
dy-to-use qPCR as
tor.
when human
microarray
n, sequence
to LightCycler

ycler
480 and
cific primers.
ntification and
osylase to
OW Primary
qPCR assays for
. Assays include
ays and plate
PCR assays for
. Assays include
ays and plate
PCR assays for
. Assays include
ays and plate
PCR assays for
. Assays include
ays/plate layout
PCR assays for
. Assays include
ays and plate
PCR assays for
. Assays include
ays and plate
PCR assays for
. Assays include
ays and plate
nes to quantify
ene-specific
-labeled
nd built-in error
ut gene
LightCycler

ssays (human,
etection. Assays
tom assays and
ssays (human,
etection. Assays
tom assays and

5 x 1 ml for
Catalo
1 kit (for up

Pack Size

1 ml (1 mg/ml)
r up to 12,500 x 2
25 per roll
40 plates
6 plates
6 plates
6 plates
10 plates
10 plates
10 plates
og Assays, 300 rea
to 12,500 reaction
10 plates
10 plates
www.roche
l reactions
actions
ns, 2 l each)
e-applied-science

Price in

425,60
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

217

e.com

Pr
218

www.r

Cat.

05 58
05 58
05 58
05 58
05 58
05 58
05 58
05 58
05 58
05 58
05 58
05 58
05 58
05 58
roducts b
roche-applied-sc

No.
82 598 001 Rea
Ligh
mou
incl
plat
82 610 001 Rea
Ligh
mou
incl
plat
82 628 001 Rea
Ligh
mou
incl
plat
82 644 001 Rea
Ligh
mou
incl
plat
82 652 001 Rea
Ligh
hum
prim
layo
82 822 001 Rea
Ligh
mou
incl
plat
82 849 001 Rea
Ligh
hum
prim
layo
82 865 001 Rea
Ligh
mou
incl
plat
82 873 001 Rea
Ligh
hum
prim
layo
82 881 001 Rea
Ligh
mou
incl
plat
82 890 001 Rea
Ligh
hum
prim
layo
82 903 001 Rea
Ligh
mou
incl
plat
82 911 001 Rea
Ligh
hum
prim
layo
82 938 001 Rea
Ligh
mou
UPL
onli

by Catalo
cience.com
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
L Probe pre-plated
ine Configurator. (
og Numb
Product N

stom Panel 96 - 3
tes 96 contain read
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 96 - 2
tes 96 contain read
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 96 - 1
tes 96 contain read
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 384 -
tes 384 contain rea
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 384 -
tes 384 contain rea
t genes for gene ex
ne Configurator.
stom Panel 384 -
tes 384 contain rea
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 384 -
tes 384 contain rea
t genes for gene ex
ne Configurator.
stom Panel 384 -
tes 384 contain rea
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 384 -
tes 384 contain rea
t genes for gene ex
ne Configurator.
stom Panel 384 -
tes 384 contain rea
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 384 -
tes 384 contain rea
t genes for gene ex
ne Configurator.
stom Panel 384 -
tes 384 contain rea
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 384 -
tes 384 contain rea
t genes for gene ex
ne Configurator.
stom Panel 384 -
tes 384 contain rea
r gene expression p
d in wells. Select cu
(+ error detection)
ber
Name
32+
dy-to-use qPCR as
tor.
24+
dy-to-use qPCR as
tor.
16+
dy-to-use qPCR as
tor.
- 384+
ady-to-use qPCR a
tor.
- 192
ady-to-use single q
xpression profiling
Select custom assa
- 192+
ady-to-use qPCR a
profiling +error de
tor.
- 128
ady-to-use single q
xpression profiling
Select custom assa
- 128+
ady-to-use qPCR a
tor.
- 96
ady-to-use single q
xpression profiling
Select custom assa
- 96+
ady-to-use qPCR a
tor.
- 64
ady-to-use single q
xpression profiling
Select custom assa
- 64+
ady-to-use qPCR a
tor.
- 48
ady-to-use single q
xpression profiling
Select custom assa
- 48+
ady-to-use qPCR a
profiling. Assays in
ustom assays/plate
ssays (human,
etection. Assays
tom assays and
ssays (human,
etection. Assays
tom assays and
ssays (human,
etection. Assays
tom assays and
assays (human,
etection. Assays
tom assays and
qPCR assays for
. Assays include
ays and plate
assays (human,
etection . Assays
tom assays and
qPCR assays for
. Assays include
ays and plate
assays (human,
etection. Assays
tom assays and
qPCR assays for
. Assays include
ays and plate
assays (human,
etection. Assays
tom assays and
qPCR assays for
. Assays include
ays and plate
assays (human,
etection. Assays
tom assays and
qPCR assays for
. Assays include
ays and plate
assays (human,
nclude primer,
e layout with

Pack Size

10 plates
6 plates
6 plates
40 plates
40 plates
40 plates
20 plates
20 plates
10 plates
10 plates
10 plates
10 plates
10 plates
10 plates

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Pr

Cat.

05 58
05 58
05 58
05 58
05 58
05 60
05 61
05 61
05 61
05 61
05 61
05 61
05 61
05 61
roducts b

No.
82 962 001 Rea
Ligh
hum
prim
layo
82 989 001 Rea
Ligh
mou
incl
plat
83 004 001 Rea
Ligh
hum
prim
layo
83 039 001 Rea
Ligh
mou
incl
plat
83 055 001 Rea
Rea
gen
prim
hyd
08 228 001 GS
Cre
libra
spa
and
18 428 001 GS
For
bou
ame
Tita
18 436 001 GS
For
bea
ame
Tita
18 444 001 GS
Prov
sing
cop
and
19 114 001 GS
For
effe
per
FLX
19 149 001 GS
For
effe
per
FLX
19 165 001 GS
Prov
from
mill
Inst
19 211 001 GS
Sub
Kit
Tag
seq
19 416 001 Rea
Fast
usin
allo
Opt

by Catalo
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cus
htCycler
480 Plat
man, mouse, or rat
mer, UPL Probe pre
out using the onlin
alTime ready Cus
htCycler
480 Plat
use, rat genes) for
ude primer, UPL P
te layout using the
alTime ready Cat
ady-to-use qPCR a
ne expression in re
mers and a Univers
drolysis probe cont
FLX Titanium Ra
ate a library of frag
ary is a set of sing
n of the sample se
d sequencing DNA
FLX Titanium LV
large-volume amp
und copy of DNA t
enable to sequenc
anium series kits.
FLX Titanium MV
medium-volume a
ad-bound copy of D
enable to sequenc
anium series kits.
FLX Titanium SV
vides reagents for
gle effective bead-
pies per bead, ame
d Titanium series k
FLX Titanium LV
large-volume amp
ective, beadbound
bead, amenable t
X Titanium series k
FLX Titanium MV
medium-volume a
ective, bead-bound
bead, amenable t
X Titanium kits.
FLX Titanium SV
vides reagents for
m a single effective
ions of copies per
trument and GS FL
FLX Titanium Ra
bstitute MID Adapt
during preparation
gging multiple libra
uenced together i
alTime ready RNA
t, highly sensitive,
ng 50-fold concent
owing fast hot start
timized for HybPro
og Numb
Product N

stom Panel 384 -
tes 384 contain rea
t genes for gene ex
ne Configurator.
stom Panel 384 -
tes 384 contain rea
r gene expression p
Probe pre-plated in
e online Configurat
stom Panel 384 -
tes 384 contain rea
t genes for gene ex
ne Configurator.
stom Panel 384 -
tes 384 contain rea
r gene expression p
Probe pre-plated in
e online Configurat
talog Assays
assays for human,
eal-time PCR. Each
sal ProbeLibrary P
taining locked nuc
apid Library Prep
gments from a DN
le-stranded DNA f
equence. Each frag
A adaptors.
V emPCR Kit (Lib
plification of a libra
emplate to tens of
cing using the GS F
V emPCR Kit (Lib
amplification of a l
DNA template to t
cing using the GS F
V emPCR Kit (Lib
small-volume am
-bound copy of DN
enable to sequenci
kits.
V emPCR Kit (Lib
plification of an am
copy of DNA temp
o sequencing usin
kits.
V emPCR Kit (Lib
amplification of an
d copy of DNA tem
o sequencing usin
V emPCR Kit (Lib
small-volume am
e bead-bound cop
r bead, amenable t
LX Titanium kits.
apid Library MID
tors for those in th
n of DNA libraries
aries with MIDs all
n 1 region of the p
A Virus Master
specific real-time
trated mix of Trans
t RT-PCR. No need
obe, hydrolysis and
ber
Name
- 32
ady-to-use single q
xpression profiling
Select custom assa
- 32+
ady-to-use qPCR a
tor.
- 16
ady-to-use single q
xpression profiling
Select custom assa
- 16+
ady-to-use qPCR a
tor.
mouse and rat gen
h assay includes ge
robe, a short FAM
cleic acid.
paration Kit
NA sample to be se
fragments represe
gment is flanked b
-L)
ary from a single e
f millions of copies
FLX Instrument an
b-L)
ibrary from a sing
tens of millions of c
FLX Instrument an
b-L)
plification of a libr
NA template to ten
ng using the GS F
-A)
mplicon library from
plate to tens of mi
ng the GS FLX Inst
b-A)
n amplicon library f
mplate to tens of m
ng the GS FLX Inst
b-A)
plification of an am
py of DNA template
to sequencing usin
Adaptors Kit
he GS FLX Titanium
for sequencing (G
ows them to be am
plate.
one-step RT-PCR
scriptor/Taq, and a
d to heat preactiva
d UPL probes.
qPCR assays for
. Assays include
ays and plate
assays (human,
etection. Assays
tom assays and
qPCR assays for
. Assays include
ays and plate
assays (human,
etection. Assays
tom assays and
nes to quantify
ene-specific
-labeled
equenced. The
enting the entire
by amplification
effective, bead-
s per bead,
d GS FLX
le effective,
copies per bead,
d GS FLX
ary from a
s of millions of
LX Instrument
m a single
llions of copies
rument and GS
from a single
millions of copies
rument and GS
mplicon library
e to tens of
ng the GS FLX
m Rapid Library
GS FLX System).
mplified and
of viral RNA
a unique buffer
te Taq.

Design
1 kit for u
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for up
am
1 kit for u
1 kit for up

Pack Size

10 plates
10 plates
6 plates
6 plates
ner Assays, 300 rea
p to 2 large volume
to 8 medium volum
p to 16 small volum
p to 2 large volume
to 8 medium volum
p to 32 small volum
www.roche
actions
eparations
e emulsion
ons
me emulsion
ons
me emulsion
ons
e emulsion
ons
me emulsion
ons
me emulsion
ons
eparations
(20 l each)
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

219

e.com

Pr
220

www.r

Cat.

05 63
05 63
05 64
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
roducts b
roche-applied-sc

No.
34 253 001 Seq
The
for
step
Seq
34 261 001 Seq
The
for
step
Seq
40 393 001 Rea
Rea
mix
stra
HA
50 216 001 Ced
The
usin
cell
diam
50 470 001 Ced
Ced
brig
50 496 001 Ced
Ced
Ced
as a
50 526 001 Ced
Ced
Ced
and
in 2
50 534 001 Ced
Ced
Ced
and
in 2
50 542 001 Ced
Ced
Ced
and
in 2
50 569 001 Ced
Add
Syst
in h
50 615 001 Ced
Rea
Ana
(Try
50 623 001 Ced
Ced
Syst
cult
des
50 640 001 Ced
Tryp
dete
solu
HiR
50 658 001 Ced
Ced
and
com
50 666 001 Ced
Ced
of C
ava
Rea

by Catalo
cience.com
qCap EZ Hybridiz
e NimbleGen SeqC
SeqCap EZ produc
ps are supplied in
qCap EZ Exome.
qCap EZ Hybridiz
e NimbleGen SeqC
SeqCap EZ produc
ps are supplied in
qCap EZ Exome.
alTime ready Inf
al-Time PCR detect
xes. One targets Inf
ains, including 201
gene of the H1N1
dex HiRes Analyz
e Cedex HiRes Syst
ng Trypan Blue sta
diameter, aggrega
meter and cell com
dex Calibration B
dex Calibration Bea
ghtness adjustmen
dex Detergent So
dex Detergent is re
dex and Cedex HiR
a component of th
dex Control Bead
dex Control Beads
dex System. Regula
d documentation o
20% ethanol (v/v).
dex Control Bead
dex Control Beads
dex System. Regula
d documentation o
20% ethanol (v/v).
dex Control Bead
dex Control Beads
dex System. Regula
d documentation o
20% ethanol (v/v).
dex MS 20 Samp
ditional tray for use
tem. Suitable for p
higher throughput
dex Reagent Kit
ady-to-use kit for c
alyzer. The kit also
ypan Blue), and an
dex Sample Cups
dex Sample Cups a
tems. Their materi
ture sample prepa
signed for single us
dex Trypan Blue
pan Blue Solution
ermination with Ce
ution is available a
Res Reagent Kit, an
dex Detergent So
dex Detergent is re
d Cedex HiRes Syst
mponent of the Ced
dex Cleaning Sol
dex Cleaning Solut
Cedex and Cedex H
ilable as a compon
agent Kit and as a
og Numb
Product N

zation and Wash
Cap EZ Hybridizatio
cts. All buffers for
one convenient kit
zation and Wash
Cap EZ Hybridizatio
cts. All buffers for
one convenient kit
A/H1N1 Detectio
tion set containing
fluenza A Matrix P
2 point mutation. T
2009 strain.
zer
tem is a fully autom
aining for measurin
ates, and morphol
mpactness.
Beads
ads are used to pe
nts of Cedex and C
olution
equired for cleanin
Res Systems. This r
e Cedex Reagent K
ds
are used to perfor
ar use allows mon
f system integrity.
ds
are used to perfor
ar use allows mon
f system integrity.
ds
are used to perfor
ar use allows mon
f system integrity.
ple Tray
e with the Multi Sa
preparation of addi
measurement wor
cleaning and main
contains all reage
nalysis of eukaryoti
s
are for use with au
al properties, size,
ration and measur
se only.
Solution Refill
is required as an e
edex and Cedex H
as a component of
nd as a separate bo
olution Refill
equired for cleanin
tems. This ready-to
dex Reagent Kit an
lution Refill
HiRes Systems. Th
nent of the Cedex
separate bottle.
ber
Name
Kit
on and Wash Kit is
the hybridization a
t, configured spec
Kit
on and Wash Kit is
the hybridization a
t, configured spec
on Set
g 2 highly specific
Protein M2 to detec
The other targets H
mated image-base
ng cell concentrati
ogical parameters
erform automated
Cedex HiRes Analyz
ng the capillary sys
ready-to-use solut
Kit and as a separa
rm System Suitabil
itoring of measure
Bead Solution (5
rm System Suitabil
itoring of measure
Bead Solution (1
rm System Suitabil
itoring of measure
Bead Solution (5
ampler delivered w
itional samples in
rkflows.
tenance routines o
ents for preparatio
ic cells using the C
utomated Cedex an
, and volume are id
rement. Cedex Sam
exclusion stain for
iRes Systems. This
the Cedex Reagen
ottle.
ng the capillary sys
o-use solution is a
nd as a separate b
r cleaning of the ca
is ready-to-use so
Reagent Kit and C
s a reagent kit
and washing
ifically for the
s a reagent kit
and washing
ifically for the
primer/probe
ct all influenza A
Hemagglutinin
ed cell analyzer
on, cell viability,
, such as cell
focus and
zers.
stem of the
ion is available
ate bottle.
lity Tests on the
ement results
10
6
/ml 10%),
lity Tests on the
ement results
10
6
/ml 10%),
lity Tests on the
ement results
10
5
/ml 10%),
with the Cedex
parallel for use
of the Cedex
n, staining
Cedex System.
nd Cedex HiRes
deal for cell
mple Cups are
viability
s ready-to-use
nt Kit, Cedex
stem of Cedex
available as a
bottle.
apillary system
lution is
Cedex HiRes

for up to 2
1 instrument w
1
1
1
1 set for app

Pack Size

96 reactions
24 reactions
2x 100 reactions (2
with PC, monitor, a
20 ml
1,000 ml
100 ml (5 x 10
6
/m
100 ml (1 x 10
6
/m
100 ml (5 x 10
5
/m
1 sample tray
proximately 100 me
500 cups
4 x 60 ml
4 x 60 ml
4 x 60 ml
20 l each)
and accessories
l)
l)
l)
easurements

Price in

269,00
126,00
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

Pr

Cat.

05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
05 65
roducts b

No.
50 704 001 Ced
The
Ced
Syst
hard
50 712 001 Ced
The
Ced
Syst
hard
50 739 001 Ced
The
Ced
Syst
hard
50 747 001 Ced
The
Ced
Syst
hard
50 763 001 Ced
Ced
on t
mea
Solu
50 771 001 Ced
Ced
on t
mea
Solu
50 780 001 Ced
Ced
on t
mea
Solu
50 798 001 Ced
The
mai
reag
50 801 001 Ced
Ced
Ana
ima
51 697 001 CAS
The
Ana
cap
m.
51 719 001 CAS
The
for
doc
3.2
51 727 001 CAS
The
for
doc
size
51 735 001 CAS
The
and
150
0.7
51 743 001 CAS
CAS
CAS
and
51 751 001 Dis
This
liqu
usin
in p
by Catalo
dex Viability Bea
ese beads simulate
dex and Cedex HiR
tem Suitability Tes
dware.
dex Viability Bea
ese beads simulate
dex and Cedex HiR
tem Suitability Tes
dware.
dex Viability Bea
ese beads simulate
dex and Cedex HiR
tem Suitability Tes
dware.
dex Viability Bea
ese beads simulate
dex and Cedex HiR
tem Suitability Tes
dware.
dex HiRes Contro
dex HiRes Control
the Cedex HiRes S
asurement results
ution (510
6
/ml
dex HiRes Contro
dex HiRes Control
the Cedex HiRes S
asurement results
ution (110
6
/ml
dex HiRes Contro
dex HiRes Control
the Cedex HiRes S
asurement results
ution (510
5
/ml
dex HiRes Reage
e ready-to-use Ced
intenance routines
gents for preparat
dex Smart Slides
dex Smart Slides a
alyzers. Their mate
age based analysis
SY Model TT 150
e CASY Model TT 1
alyzer for quality co
pillary, it enables th
.
SY Model TTC 15
e CASY Model TTC
quality control of c
cumentation. It use
to 120 m.
SY Model TTC 45
e CASY Model TTC
quality control of c
cumentation. It use
e range of 0.7 to 12
SY Model TT 45,
e CASY Model TT 4
d Analyzer for qual
0 m capillaries, it e
to 120 m.
SY rack
SY racks are used
SY Cell Counters a
d black in color, ho
spenser 2 - 10 ml
s Ceramus Dispen
uid volumes in incr
ng CASY Cell Coun
purity and volume p
og Numb
Product N

ads (30%)
e the 30% viability
Res Systems. They
st for quick and rel
ads (60%)
e the 60% viability
Res Systems. They
ads (80%)
e the 80% viability
Res Systems. They
ads (100%)
e the 100% viability
Res Systems. They
ol Beads
Beads are used to
System. Regular us
and documentatio
10%), in 20% etha
ol Beads
Beads are used to
System. Regular us
and documentatio
10%), in 20% etha
ol Beads
Beads are used to
System. Regular us
and documentatio
10%), in 20% etha
ent Kit
dex HiRes Reagent
s of the Cedex HiR
ion, staining, and a
s
re disposable slide
erial properties, size
s of cell cultures.
0 m
150 m is a multi-p
ontrol of cell cultu
he analysis of objec
50 m
C is a fast multi-pa
cell cultures with i
es a 150 m capilla
5, 60, 150 m
C is a fast multi-pa
cell cultures with i
es 45, 60, and 150
20 m.
60, 150 m
45, 60, 150 m is a
ity control of cell c
enables the analys
for easy sample h
and Analyzers. Eac
olds up to 24 CASY
l
ser is used for hig
rements of 0.25 ml
nters and Analyzer
precision.
ber
Name
of cell culture sus
are used for the c
liable status check
of cell culture sus
are used for the c
liable status check
of cell culture sus
are used for the c
liable status check
y of cell culture su
are used for the c
liable status check
o perform System S
se allows monitorin
on of system integ
anol (v/v).
o perform System S
se allows monitorin
on of system integ
anol (v/v).
o perform System S
se allows monitorin
on of system integ
anol (v/v).
t Kit is used for cle
Res Analyzers. Cont
analysis of eukaryo
es for use with Ced
e and volume are
parameter Cell Co
res. Equipped with
cts in the size rang
rameter Cell Coun
ntegrated data eva
ary for analysis in t
rameter Cell Coun
ntegrated data eva
m capillaries for
a multi-parameter C
cultures. Equipped
sis of objects in the
handling when wor
ch rack, made of po
Y cups.
hly reproducible a
of CASY ton for m
rs. It guarantees o
pensions using
omprehensive
ks of optical
pensions using
omprehensive
ks of optical
pensions using
omprehensive
ks of optical
spensions using
omprehensive
ks of optical
Suitability Tests
ng of
rity. Bead
Suitability Tests
ng of
rity. Bead
Suitability Tests
ng of
rity. Bead
eaning and
tains all
otic cells.
dex XS
optimal for
unter and
h a 150 m
ge of 3.2 to 120
ter and Analyzer
aluation and
the size range of
ter and Analyzer
aluation and
analysis in the
Cell Counter
with 45, 60, and
e size range of
rking with the
olyoxymethylene
adjustment of
measurements
ptimum quality

1 set for app
15 smart slid
Pack Size

30 ml
30 ml
30 ml
30 ml
30 ml
30 ml
30 ml
proximately 100 me
measurements
1 instrument
1 instrument
1 instrument
1 instrument
1 rack for 24 cups
1 dispenser
www.roche
easurements
20 cell culture
s
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

221

e.com

Pr
222

www.r

Cat.

05 65
05 65
05 65
05 65
05 81
05 86
05 86
05 87
05 87
05 87
05 88
05 88
05 89
05 89
05 89
roducts b
roche-applied-sc

No.
51 760 001 CAS
CAS
Cou
of c
51 786 001 CAS
Reg
cap
reag
syst
51 794 001 CAS
The
cell
usin
from
51 808 001 CAS
CAS
cell
con
pH
15 916 001 Lig
For
Ach
usin
use
qua
reso
60 482 001 Seq
2.1
tube
iden
pop
60 504 001 Seq
2.1
tube
iden
pop
72 430 001 GS
The
Inst
is p
72 529 001 GS
GS
the
maj
clas
72 537 001 GS
GS
the
maj
clas
89 103 001 GS
Use
a se
Dev
Sup
89 111 001 GS
Use
Jun
per
sub
92 791 001 cOm
Sup
seri
yea
92 953 001 cOm
Sup
of s
bac
92 970 001 cOm
Hig
prot
cOm
by Catalo
cience.com
SY blue
SY blue is a highly
unter and Analyzer
cells to guarantee c
SY clean
gular use of CASY
pillaries of CASY Sy
gent prevents bloc
tem.
SY cups
e material propertie
culture sample pr
ng CASY Cell Coun
m adhering to the
SY ton
SY ton is a ready-t
cultures for use w
nductivity guarante
and osmolarity en
htCycler
96 Ins
accurate, consiste
hieve the rigorous
ng intuitive large to
e accessible data a
antification, endpo
olution melting and
qCap EZ Human
million stable in-s
e. Optimization too
ntify mutations for
pulation genetics a
qCap EZ Human
million stable in-s
e. Optimization too
ntify mutations for
pulation genetics a
FLX+ Upgrade K
e GS FLX+ Upgrad
trument to a GS FL
provided in the kit.
GType HLA MR
GType HLA MR Pr
basis for an HLA t
jor histocompatibil
ss I and II), using G
GType HLA HR P
GType HLA MR Pr
basis for an HLA t
jor histocompatibil
ss I and II), using G
Junior Bead Dep
e during GS Junior
equencing run, and
vice Centrifuge Ad
pplied with the GS
Junior Maintent
e to thoroughly cle
ior Instrument wh
iod of time, or if co
bsystem.
mplete ULTRA Ta
perb protein protec
ne, cysteine, and a
st, and mammalian
mplete ULTRA Ta
perb protein protec
serine, cysteine, an
cterial, yeast, and m
mplete ULTRA Ta
h inhibition of seri
tein protection in b
mplete His-Tag Pu
og Numb
Product N

y specific alcoholic
rs for viability dete
cell identity.
clean protects the
ystems from biolog
ckages and encrus
es, size, and volum
reparation. Use to
nters and Analyzer
cup walls.
to-use, isotonic, an
with CASY Cell Cou
ees constant meas
sure cell size pres
strument
ent real-time PCR
performance stand
ouchscreen-based
analysis. Applicatio
int and melting cu
d qualitative detec
Exome Library v2
olution DNA probe
ol for next-gen wo
genetic disorders
and pharmacogene
Exome Library v2
olution DNA probe
ol for next-gen wo
genetic disorders
and pharmacogene
Kit
e Kit is used to up
LX+ Instrument. Ev
Primer Set
rimer Set and GS G
test that measures
lity complex region
GS FLX or GS Junio
Primer Set
rimer Set and GS G
test that measures
lity complex region
GS FLX or GS Junio
position Device C
r Bead Deposition
d use along with t
aptors A and B to
Junior Complete.
ance Wash Kit
an and sterilize th
en the instrument
ontamination is ob
ablets, Mini, EDT
ction combined wit
aspartic proteases
n cell types.
ablets, EDTA-free
ction combined wit
nd aspartic proteas
mammalian cell typ
ablets, Mini, EAS
ine, cysteine, meta
bacterial, yeast, an
rification Resin for
ber
Name
c dilution used with
ermination and for
e instrument and m
gical deposits. By e
stations of the inte
me of CASY cups a
dilute and analyze
rs. Cup material pr
nd isoosmotic dilut
unters and Analyze
urement results. It
ervation.
results in your rese
dard of the LightC
d software for pow
ons include absolut
urve-based genotyp
ction.
2.0
es to capture all R
rkflows enables ne
and discover varia
etics.
2.0
es to capture all R
rkflows enables ne
and discover varia
etics.
pgrade an existing
verything required
GType HLA HR Pri
s HLA allelic haplo
n of the human ge
or Systems.
GType HLA HR Pri
s HLA allelic haplo
n of the human ge
or Systems.
Counterweight K
Device centrifugat
he GS Junior Bead
fit into a variety of
e fluidics subsyste
has been left idle
bserved or suspect
TA-free, EASYpac
th ease of use: Hig
for protein protec
e, glass vials
th ease of use: Hig
ses for protein prot
pes.
SYpack
allo- and aspartic p
nd mammalian cell
r IMAC.
h the CASY Cell
quality control
measurement
emulsifying, this
rnal liquid
re optimal for
e cell samples
revents cells
tion liquid for
ers. Its defined
ts physiological
earch lab.
Cycler
Systems,
werful easy-to-
te and relative
ping, high
efSeq exons in 1
ew discoveries:
ants in
efSeq exons in 1
ew discoveries:
ants in
GS FLX
for the upgrade
mer Set form
otypes at the
nome (MHC
mer Set form
otypes at the
nome (MHC
it
tion steps before
d Deposition
f centrifuges.
em of the GS
for an extended
ed in the fluidics
ck
gh inhibition of
ction in bacterial,
ghest inhibition
tection in
proteases for
types. Use new

1
1 instrument (
for the use of
4 PCR pla
4 PCR pla
30 tablets (in
packs, each tab
m
2 glass via
30 tablets (in
packs, each tab
m
Pack Size

4 x 30 ml
3 x 500 ml
1,800 cups with lid
10 l container
(96-well realtime P
96-well plates and
4 reactions
48 reactions
1 accessory
tes with dried-dow
tes with dried-dow
1 device
1 kit
ndividually packed
ls each containing
EDTA-free
ndividually packed
ds
PCR instrument
d 8-tube strips)
wn primers
wn primers
d in foil blister
r a volume of 10
on)
g 10 tablets,
d in foil blister
r a volume of 10
on)

Price in

inquire
inquire
inquire
inquire
inquire
3.360,00
20.160,00
inquire
inquire
inquire
inquire
inquire
158,40
262,40
158,40

Pr

Cat.

05 89
05 89
05 89
05 89
05 89
05 92
05 94
05 94
05 95
05 97
05 99
05 99
05 99
05 99
05 99
roducts b

No.
92 988 001 cOm
Exc
prot
cOm
93 151 001 Tra
Con
Rea
sup
assa
93 682 001 cOm
Hig
tagg
ena
93 801 001 cOm
Hig
tagg
ena
98 765 001 GS
GS
for t
pres
Dev
22 160 001 GS
Brin
che
for
(10
43 353 001 IKA
Sma
Am
con
43 523 001 Rea
For
in tw
min
time
54 070 001 GS
The
and
Inst
rep
76 120 001 REM
Prov
syst
hyb
Tita
92 877 001 Rea
Fast
usin
allo
Opt
96 473 001 GS
The
Pico
the
sup
96 481 001 GS
Prov
libra
mill
Inst
96 520 001 GS
Prov
sing
cop
usin
96 554 001 GS
The
Tita
dete
amp

by Catalo
mplete ULTRA Ta
ellent inhibition of
mplete His-Tag Pu
anscriptor Univer
nvenient fast soluti
ady-to-use master
pplied in just two v
ays on all real-time
mplete His-Tag P
h-capacity IMAC m
ged proteins from
ables compatibility
mplete His-Tag P
h-capacity IMAC m
ged proteins from
ables compatibility
Junior Preventat
Junior Preventativ
the scheduled ma
scribed schedule.
vice Centrifuge Ad
Junior Complete
ngs proven perform
emistry to the benc
small to medium s
hours) and obtain
A Turrax
all device used for
plification procedu
nfigurations for 100
alTime ready Cel
rapid, high-perfor
wo-step real-time
nutes. Use lysate d
e PCR experiments
Junior Sipper M
e GS Junior Sipper
d Filters (10) to rep
trument as part of
lacement Buffer Tr
M e System
vides subcompone
tems to automate
bridization procedu
anium series emuls
alTime ready RNA
ng 50-fold concent
timized for HybPro
Junior Bead Dep
e GS Junior bead d
oTiterPlate device
wells of the PicoT
pplied with the GS
Junior Titanium
vides reagents for
ary from a single e
ions of copies per
trument and GS Ju
Junior Titanium
vides reagents for
gle effective bead-
pies per bead, ame
ng GS Junior Titan
Junior Titanium
e GS Junior Titaniu
anium PicoTiterPlat
ermine the nucleo
plified DNA library
og Numb
Product N

ablets, glass vials
f serine, cysteine, m
sal cDNA Maste
ion for cDNA synth
mix (primers, nuc
ials, brings out the
e PCR systems.
Purification Resin
matrix for convenie
lysates. Proprietar
with EDTA and DT
Purification Resin
matrix for convenie
lysates. Proprietar
with EDTA and DT
tive Maintenance
ve Maintenance Kit
intenance of a GS
The kit also conta
aptors (A and B).
e
mance and long re
chtop. Small footpr
sized laboratories.
n 400 bp read leng
r generating emuls
ure. The device shi
0V, 120V, and 230
l Lysis Kit
rmance gene expre
RT-PCR. Lyse 3 to
irectly in cDNA sy
s at any throughpu
aintenance Kit
Maintenance Kit c
place all of the sho
a maintenance pro
ray.
ents and software
emPCR enrichmen
ures in the GS FLX
sion oil formats.
A Virus Master
specific real-time
trated mix of Trans
t RT-PCR. No need
obe, hydrolysis and
position Device
deposition device h
and gasket, enabl
TiterPlate device pr
Junior Complete.
emPCR Kit (Lib-
amplification of a
effective bead-bou
r bead, amenable t
unior Titanium kits
emPCR Kit (Lib-
the amplification
-bound copy of DN
enable to sequenci
ium kits.
Sequencing Kit
um Sequencing Kit
te Kit, provides rea
tide sequence of a
y, using GS Junior
ber
Name
s
metallo- and aspar
nd mammalian cell
r IMAC.
r
hesis and real-tim
leotides, buffer, en
e full potential of y
n
ent single-step pu
ry nickel-chelate c
TT with minimal ni
n
ent single-step pu
ry nickel-chelate c
TT with minimal ni
e Kit
t contains compon
Junior Instrument
ins two pairs of Be
eads of the GS FLX
rint and low entry c
Sequence >35 mi
ths.
sions in the GS Jun
ips with multiple c
V power inputs.
ession studies usin
o 30,000 cells in on
ynthesis and analyz
ut.
contains enough S
rt Sipper Tubes of
ocedure. The kit a
to install onto liqu
nt and sequencing
workflow. Suppor
one-step RT-PCR
scriptor/Taq, and a
d to heat preactiva
d UPL probes.
holds one GS Junio
ing the deposition
rior to a sequencin
-L)
shotgun, paired e
und copy of DNA to
to sequencing usin
.
-A)
of an amplicon lib
NA template to ten
ng using the GS J
t combined with th
agents and consum
an immobilized and
Titanium kits.
rtic proteases for
types. Use new
e PCR analysis.
nzymes),
our qRT-PCR
rification of His-
hemistry
ickel leakage.
rification of His-
hemistry
ickel leakage.
nents required
t, following the
ead Deposition
X Titanium
costs are ideal
llion bases/run
nior emPCR
cord
ng cultured cells
ne step in 5
ze cDNA in real-
Sipper Tubes
a GS Junior
lso contains a
uid handling
primer
rts all GS FLX
of viral RNA
a unique buffer
te Taq.
or Titanium
of beads into
g Run. It is
end, or cDNA
o tens of
ng the GS Junior
rary from a
s of millions of
unior Instrument
e GS Junior
mables to
d clonally

2 glass via
25 m
200 m
1 kit for up to
reacti
1,0

Pack Size

als each containing
(with EDTA)
100 reactions
1 kit
1 instrument
1 device
on volume of 40
1 kit
1 system
000 reactions 20
1 device
1 kit
1 kit
1 kit
www.roche
g 10 tablets
lume)
olume)
ns with a final
l each
0 l
e-applied-science

Price in

262,40
inquire
290,40
1.583,60
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

223

e.com

Pr
224

www.r

Cat.

05 99
05 99
06 24
06 24
06 24
06 24
06 26
06 26
06 26
06 26
06 26
06 26
06 26
06 26
06 26
roducts b
roche-applied-sc

No.
96 619 001 GS
The
Tita
nuc
libra
96 643 001 GS
Stan
only
that
acc
41 603 001 Ma
Dee
Pur
pro
41 611 001 Ma
Plat
for
to m
41 620 001 Ma
Disp
by M
Qua
elev
41 638 001 Ma
Use
use
pier
66 282 001 Seq
Hig
cus
rese
unif
66 304 001 Seq
Hig
cus
rese
unif
66 312 001 Seq
Hig
cus
rese
unif
66 339 001 Seq
Hig
cus
rese
unif
66 347 001 Seq
Hig
cus
rese
unif
66 355 001 Seq
Hig
cus
rese
unif
66 363 001 Seq
Hig
cus
rese
unif
66 371 001 Seq
Hig
cus
rese
unif
66 380 001 Seq
Hig
cus
rese
unif
by Catalo
cience.com
Junior Titanium
e GS Junior Titaniu
anium Sequencing
cleotide sequence
ary. Use with the G
Junior Titanium
ndard sequencing
y Control Beads ar
t give sequencing
cording to specifica
agNA Pure 96 Pro
ep well plates with
e 96 Instruments;
cedures; inert to c
agNA Pure 96 Ou
te for collecting elu
cooling by maximi
minimize the risk o
agNA Pure 96 Filt
posable pipetting t
MagNA Pure 96 In
ality Control proce
vated temperature
agNA Pure 96 Sea
e to reseal MagNA
e. There is no need
rced when removin
qCap EZ Choice L
hly efficient, flexib
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice L
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice L
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice L
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice L
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice L
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice X
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice X
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice X
tomer-defined dis
equencing studies
form capture of ta
og Numb
Product N

PicoTiterPlate K
um PicoTiterPlate K
Kit, provides devic
of an immobilized
GS Junior Instrume
Control Bead Kit
control for the GS
re sequenced. The
results showing th
ations.
ocessing Cartridg
96 wells for samp
nuclease free acco
chemical leaching a
tput Plate
uates containing p
izing contact with
of dead volume tha
ter Tips (1,000 l
tips for 1,000 l vo
nstruments; nuclea
dures; inert to che
s.
aling Foil
A Pure 96 reagent t
to remove the sea
ng reagent to mini
Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
XL Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
XL Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
XL Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
ber
Name
Kit
Kit combined with
ces and reagents t
and clonally ampl
ent.
t
S Junior System. D
beads contain kn
he GS Junior Syste
ge
ple processing step
ording to current Q
at low and elevate
purified nucleic aci
cooling block; wel
at cannot be pipett
l)
olume with aerosol
ase free according
emical leaching at
trays and output p
aling foil prior to n
imize risk of cross-
sy-to-use solution
ns in the human g
y achieving highly s
7 Mb.
sy-to-use solution
ns in the human g
7 Mb.
sy-to-use solution
ns in the human g
7 Mb.
sy-to-use solution
ns in the human g
7 Mb.
sy-to-use solution
ns in the human g
7 Mb.
sy-to-use solution
ns in the human g
7 Mb.
sy-to-use solution
ns in the human g
50 Mb.
sy-to-use solution
ns in the human g
50 Mb.
sy-to-use solution
ns in the human g
50 Mb.
the GS Junior
to determine the
lified DNA
uring a test run,
own sequences
em is performing
ps using MagNA
Quality Control
d temperatures.
ids; optimized
ls are v-shaped
ted.
filters for use
to current
low and
lates for later
ext use. Foil is
-contamination.
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and

3,8
Pack Size

1 kit
1 kit
36 cartridges
60 plates
100 foils
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions
12 reactions
24 reactions
48 reactions
96)

Price in

inquire
inquire
inquire
inquire
inquire
inquire
10.080,00
15.120,00
20.160,00
21.773,00
58.061,00
80.640,00
12.096,00
18.144,00
30.240,00

Pr

Cat.

06 26
06 26
06 26
06 32
06 36
06 36
06 36
06 36
06 36
06 36
06 36
06 37
06 37
06 37
06 37
roducts b

No.
66 398 001 Seq
Hig
cus
rese
unif
66 401 001 Seq
Hig
cus
rese
unif
66 517 001 Seq
Hig
cus
rese
unif
27 672 001 Lig
Use
(ge
reso
strip
65 779 001 X-t
Non
cyto
tran
Idea
65 787 001 X-t
Non
cyto
tran
Idea
65 809 001 X-t
Non
cyto
tran
Idea
66 236 001 X-t
Stat
deli
tran
effe
66 244 001 X-t
Stat
deli
tran
effe
66 546 001 X-t
Stat
deli
tran
effe
66 821 001 Rea
For
in tw
min
time
72 279 001 GS
Uni
acc
proj
seq
74 891 001 Ma
Rea
acid
Inst
74 905 001 Ma
Bar
Inst
inte
74 913 001 Ma
Use
pur
for
lysa
by Catalo
qCap EZ Choice X
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice X
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice X
tomer-defined dis
equencing studies
form capture of ta
htCycler
8-Tub
e for SYBR Green I
ne detection, gene
olution melting ana
ps and cap strips a
remeGENE 9 DNA
n-liposomal multi-
otoxicity, minimal n
nsfection efficiency
al for all cellular an
remeGENE 9 DNA
n-liposomal multi-
remeGENE 9 DNA
n-liposomal multi-
remeGENE HP D
te-of-the-art high
very of DNA into a
nsfect cells. Free o
ects.
remeGENE HP D
te-of-the-art high
very of DNA into a
ects.
remeGENE HP D
te-of-the-art high
very of DNA into a
ects.
alTime ready Cel
rapid, high-perfor
wo-step real-time
nutes. Use lysate d
e PCR experiments
FLX+ Instrumen
que combination o
curacy and high-th
jects: whole genom
uencing, and sam
agNA Pure 96 DN
ady-to-use reagent
ds from up to 1,000
trument. External ly
agNA Pure 96 Inte
rcoded tubes for pr
truments. These tu
ernal controls durin
agNA Pure 96 Ext
e this reagent with
ification of total nu
in vitro diagnostic
ates.
og Numb
Product N

XL Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
XL Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
XL Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
be Strips (clear)
, ResoLight dye, a
e quantification, en
alysis) on the Ligh
are provided toget
A Transfection R
component transfe
need for optimizati
y in many cell lines
nalysis application
A Transfection R
component transfe
need for optimizati
nalysis application
A Transfection R
component transfe
need for optimizati
nalysis application
NA Transfection
performance trans
a wide range of eu
f animal-derived c
NA Transfection
performance trans
a wide range of eu
f animal-derived c
NA Transfection
performance trans
a wide range of eu
f animal-derived c
l Lysis Kit
rmance gene expre
RT-PCR. Lyse 3 to
irectly in cDNA sy
s at any throughpu
t
of long sequencing
roughput, make th
me shotgun, multi-
ple multiplexing.
NA and Viral NA L
0 l sample volum
ysis is optional.
ernal Control Tub
reparing internal c
ubes are ideal for t
ng a run.
ternal Lysis Buffe
the MagNA Pure
ucleic acids (DNA/
c purposes, and for
ber
Name
sy-to-use solution
ns in the human g
50 Mb.
sy-to-use solution
ns in the human g
50 Mb.
sy-to-use solution
ns in the human g
50 Mb.
nd hydrolysis prob
ndpoint genotyping
htCycler
Nano Ins
ther.
Reagent
ection reagent wit
ion, and ability to p
s, even in the pres
s.
Reagent
ection reagent wit
s, even in the pres
s.
Reagent
ection reagent wit
s, even in the pres
s.
Reagent
sfection reagent fo
ukaryotic cells, incl
components and lo
Reagent
sfection reagent fo
components and lo
Reagent
sfection reagent fo
components and lo
ession studies usin
o 30,000 cells in on
ynthesis and analyz
ut.
g reads (up to 1 kb
his system ideal fo
-span paired end,
Large Volume Kit
sealed trays for pu
e using the MagN
be
controls using Mag
he automated proc
er
96 System for the
/RNA) from biolog
r stabilization of nu
captures
genome for
specific and
captures
genome for
specific and
captures
genome for
specific and
be-based assays
g, high
strument. Tube
h very low
provide high
ence of serum.
h very low
provide high
ence of serum.
h very low
provide high
ence of serum.
or efficient
uding hard-to-
ow cytotoxic
or efficient
uding hard-to-
ow cytotoxic
or efficient
uding hard-to-
ow cytotoxic
ng cultured cells
ne step in 5
ze cDNA in real-
b) and very high
r large genomic
amplicon/cDNA
t
urifying nucleic
A Pure 96
gNA Pure 96
cessing of
isolation and
gical specimens
ucleic acids with

120 clea
1 kit for up t
reacti
1 inst
3 set
Pack Size

96 reactions
384 reactions
960 reactions
r tube strips and c
(10 unit pack)
0.4 ml
1.0 ml
5 x 1.0 ml
1.0 ml
0.4 ml
5 x 1 ml
on volume of 40
rument plus acces
150 tubes (15x10)
1 bottle (100 ml)
www.roche
cap strips
ns with a final
l each
ssories
each
)
e-applied-science

Price in

48.384,00
129.024,00
241.920,00
inquire
200,30
397,20
1.535,90
424,50
214,30
1.643,20
inquire
inquire
inquire
inquire
inquire

225

e.com

Pr
226

www.r

Cat.

06 37
06 38
06 38
06 38
06 39
06 40
06 40
06 40
06 41
06 41
06 42
06 42
06 43
06 43
06 43
06 44
roducts b
roche-applied-sc

No.
74 921 001 Ma
Use
pur
for
lysa
80 565 001 GS
Com
reag
seq
amp
88 779 001 GS
Com
Suit
ana
hrs
88 787 001 GS
The
for
97 417 001 GS
The
use
Serv
thre
02 682 001 Fas
Rea
the
gen
prim
02 712 001 Fas
Rea
on t
gen
add
07 773 001 Lig
Fast
gen
foot
for
12 866 001 Ced
The
to a
cell
12 874 001 Ced
The
HiR
cha
22 659 001 Den
The
Cell
size
Ced
22 667 001 Den
The
Cell
size
Ced
30 112 001 Ma
For
pur
con
32 344 001 DN
The
assa
mic
32 379 001 Cel
Sim
viab
cell
app
44 156 001 Lig
Spe
and
Inst
by Catalo
cience.com
agNA Pure 96 Ba
e this reagent with
in vitro diagnostic
ates.
FLX Titanium Se
mbined with the GS
gents and other co
uence (in extra-lo
plified DNA library
FLX+ Computing
mputing solution fo
table for pipeline p
alysis, including ma
for the XL+ and ~
FLX+ Computing
e GS FLX+ Comput
use with the GS FL
FLX+ CB Filters
e GS FLX+ CB Filte
ed for GS FLX+ Ins
vice Engineers mu
ee (3) months or a
stStart Essential D
ady-to-use reaction
LightCycler
Nan
ne quantification. S
mers, and hydrolys
stStart Essential D
ady-to-use reaction
the LightCycler
N
ne detection and q
dition of template D
htCycler
Nano
t, 32-sample real-t
netic variation anal
tprint, and weight,
everyday use.
dex Control Unit
e Cedex Control Un
analyze concentrat
cultures.
dex HiRes Contro
e Cedex HiRes Con
Res Analyzer to ana
aracteristics of cell
nsity Reference S
ese beads are used
l Analyzers. They m
e and optical prope
dex Software.
nsity Reference S
ese beads are used
l Analyzers. They m
e and optical prope
dex Software.
agNA Pure 96 Sys
rinsing the MagN
ification run. Using
nfiguration, the inst
A Fragmentation
e DNA Fragmentat
ay to detect apopt
croplates. It is idea
ll Viability Imagin
mple, accurate and
bility using fluoresc
ular workflows, es
plications. Optimize
htCycler
Nano
ecial bundle combi
d real-time PCR ma
truments.
og Numb
Product N

cterial Lysis Buff
the MagNA Pure
ucleic acids (DNA/
c purposes, and for
equencing Kit XL
S FLX Titanium Pic
onsumables requir
ng reads; up to 1 k
y (the sample).
g Station
or fast processing
processing of GS F
apping and de nov
~4 hrs for the XLR
g Station Monito
ting Station Monit
LX+ Computing St
and Pump Tubin
ers and Pump Tubi
strument maintena
ust change the CB
fter 25 runs.
DNA Probes Mas
n mix for the hydro
no Instrument. Idea
Setup only requires
sis probes.
DNA Green Mast
n mix using the SY
Nano Instrument. I
uantification. Reac
DNA and primers.
Instrument
time PCR instrume
lysis in mono- and
and easy reaction
nit is used in comb
tion, viability, and m
ol Unit
ntrol Unit is used in
alyze concentration
cultures.
Standard Beads
d to calibrate and a
mimic cell behavio
erties, they will be
Standard Beads
d to calibrate and a
mimic cell behavio
erties, they will be
stem Fluid (Inter
A Pure 96 Instrum
g the internal syste
trument can be ru
n Imaging Kit
ion Imaging Kit pr
tosis induction in m
l for high throughp
ng Kit
fast (35 minutes)
cence detection an
specially for mediu
ed for 96-well plate
DNA Probes Valu
ipack, including re
aster for hydrolysis
ber
Name
fer
96 System for the
/RNA) from biolog
r stabilization of nu
+
coTiterPlate Kit 70
red to determine th
kb) of an immobili
of GS FLX+ seque
FLX+ System data
vo assembly. Proce
70.
or
or with power cord
tation.
ng Kit
ng Kit contains th
nce. Instrument us
Filters and Pump T
ster
olysis probe detect
al for hot start PCR
s the addition of te
ter
YBR Green I dye de
deal for hot start P
ction setup only re
ent for gene expres
d dual-color. Minim
n setup and softwa
bination with the C
morphological cha
n combination with
n, viability, and mo
adjust Cedex and C
r in flow dynamics
detected as dead
adjust Cedex and C
r in flow dynamics
detected as dead
rnal)
ment reagent head
em fluid and liquid
n as a tabletop ins
rovides a simple an
mammalian cells in
put cellular workflo
one-step assay to
nd for quality cont
m to high through
es.
ue Pack L
eaction device, rea
s using LightCycle
isolation and
gical specimens
ucleic acids with
75, it provides
he nucleotide
zed and clonally
encing data.
and subsequent
essing time: ~18
ds is intended
e components
sers or Roche
Tubing every
tion format on
R assays for
emplate DNA,
etection format
PCR assays for
equires the
ssion and
mal noise,
are make it ideal
Cedex Analyzer
aracteristics of
h the Cedex
orphological
Cedex HiRes
s. Due to their
cells by the
Cedex HiRes
s. Due to their
cells by the
during a
d waste
strument.
nd rapid TUNEL
n 96-well
ows.
meausre cell
trol of cells in
hput
ction vessels
r
Nano

1 ki
5 x 1 ml for u
5 x 1 ml for u
1 inst
1 cont
1 cont
1 kit f
4 kits (2,000
strips
Pack Size

1 bottle (20 ml)
t for 1 sequencing
1 instrument
1 instrument
1 kit
up to 500 reactions
volume
up to 500 reactions
volume
rument plus acces
1 x 10 ml batch A
1 x 10 ml batch B
2 containers
96 tests
reactions 20 l e
s/caps (1,920 react
g run
s of 20 l final
s of 20 l final
ssories
very CD
very CD
A
B
actions
each) and 240
tions)

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
685,00
320,00
inquire

Pr

Cat.

06 44
06 44
06 44
06 44
06 44
06 46
06 46
06 47
06 47
06 47
06 47
06 47
06 47
06 48
roducts b

No.
44 164 001 Lig
Spe
and
Inst
44 172 001 Lig
Spe
and
Inst
44 199 001 Lig
Com
Inst
eac
sen
qua
44 202 001 Lig
Com
Inst
eac
sen
44 229 001 Lig
Spe
and
Inst
65 684 001 Seq
For
vari
seq
and
65 692 001 Seq
For
vari
seq
and
71 684 001 Seq
Prov
hum
cos
50 M
71 706 001 Seq
Prov
hum
cos
50 M
71 714 001 Seq
Prov
hum
cos
50 M
71 722 001 Seq
Prov
hum
cos
50 M
71 749 001 Seq
Prov
hum
cos
50 M
71 757 001 Seq
Prov
hum
cos
50 M
80 543 001 Rea
Sys
Pre
gen
Det
If In

by Catalo
htCycler
Nano
ecial bundle combi
d real-time PCR ma
truments.
htCycler
Nano D
ecial bundle combi
d real-time PCR ma
truments.
htCycler
Nano
mplete system, inc
trument with real-t
ch and 480 tube st
sitive, specific hot
antification.
htCycler
Nano
mplete system, inc
trument with real-t
ch and 480 tube st
sitive, specific hot
htCycler
Nano
ecial bundle combi
d real-time PCR ma
truments.
qCap EZ Human
exome resequenc
ations in the geno
uencing. Allows re
d detect more sign
qCap EZ Human
exome resequenc
ations in the geno
uencing. Allows re
d detect more sign
qCap EZ Develop
vides custom oligo
man genomes for c
ts by achieving hig
Mb. Flexible design
qCap EZ Develop
vides custom oligo
man genomes for c
ts by achieving hig
Mb. Flexible design
qCap EZ Develop
vides custom oligo
man genomes for c
ts by achieving hig
Mb. Flexible design
qCap EZ Develop
vides custom oligo
man genomes for c
ts by achieving hig
Mb. Flexible design
qCap EZ Develop
vides custom oligo
man genomes for c
ts by achieving hig
Mb. Flexible design
qCap EZ Develop
vides custom oligo
man genomes for c
ts by achieving hig
Mb. Flexible design
alTime ready Infl
stem
mixed primers and
nes in human samp
tection Set for mult
nfluenza A is positi
og Numb
Product N

DNA Probes Valu
ipack, including re
aster for hydrolysis
DNA Green Value
ipack, including re
aster for SYBR Gre
DNA Green Start
luding LightCycler
time PCR Master r
trips & caps, using
start PCR assays f
DNA Probes Sta
luding LightCycler
time PCR Master r
trips & caps, using
start PCR for gene
DNA Green Valu
ipack, including re
aster mix for SYBR
Exome Library v3
cing, a powerful tec
ome at a fraction o
esearchers added
ificant variations.
Exome Library v3
cing, a powerful tec
ome at a fraction o
esearchers added
ificant variations.
per Library
onucleotide librarie
customer-develope
ghly specific, unifo
n captures regions
per Library
customer-develope
n captures regions
per Library
customer-develope
n captures regions
per Library
customer-develope
n captures regions
per Library
customer-develope
n captures regions
per Library
customer-develope
n captures regions
uenza B Detectio
d hydrolysis probe
ples. Use with Rea
tiplex detection/di
ive, the H1N1 test
ber
Name
ue Pack S
eaction device, rea
s probes using Lig
e Pack L
eaction device, rea
een I using LightCy
ter Pack
r
Nano Real-Time
reagents for 4,000
g SYBR Green I det
for gene detection
rter Pack
r
Nano Real-Time
reagents for 4,000
g UPL or hydrolysis
e expression quan
ue Pack S
eaction device, rea
R Green I using Lig
3.0
chnique to identify
f the cost of whole
flexibility to analyz
3.0
chnique to identify
f the cost of whole
flexibility to analyz
es for target region
ed capture protoco
orm capture of targ
s in any genome.
ed capture protoco
orm capture of targ
s in any genome.
ed capture protoco
orm capture of targ
s in any genome.
ed capture protoco
orm capture of targ
s in any genome.
ed capture protoco
orm capture of targ
s in any genome.
ed capture protoco
orm capture of targ
s in any genome.
on Set, LightCycl
for detecting Influ
alTime ready Influe
fferentiation of Inf
can be run.
ction vessels
htCycler
Nano
ction vessels
ycler
Nano
e PCR
reactions - 20 l
tection. Ideal for
n and
e PCR
reactions - 20 l
s probes. For
tification.
ction vessels
ghtCycler
Nano
y functional
e genome
ze more samples
y functional
e genome
ze more samples
ns in non-
ols. Reduce
get regions up to
ns in non-
ols. Reduce
get regions up to
ns in non-
ols. Reduce
get regions up to
ns in non-
ols. Reduce
get regions up to
ns in non-
ols. Reduce
get regions up to
ns in non-
ols. Reduce
get regions up to
ler
2.0
uenza B viral
nza A/H1N1
fluenza A and B.

2 kits (1,000
strip
4 kits (2,000
strips
1 instrument an
20 l each an
1 instrument an
20 l each an
2 kits (1,000
strip
fo

Pack Size

reactions 20 l e
ps/caps (960 react
reactions 20 l e
s/caps (1,920 react
nd 8 kits for up to
d 480 strips/caps f
reactions
nd 8 kits for up to
d 480 strips/caps f
reactions
reactions 20 l e
ps/caps (960 react
4 reactions
48 reactions
12 reactions
24 reactions
48 reactions
96 reactions
384 reactions
960 reactions
r up to 100 reactio
www.roche
each) and 120
ions)
each) and 240
tions)
4,000 reactions,
for up to 3,840
4,000 reactions,
for up to 3,840
each) and 120
ions)
ons
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
3.360,00
20.160,00
12.096,00
18.144,00
30.240,00
48.384,00
129.024,00
241.920,00
inquire

227

e.com

Pr
228

www.r

Cat.

06 48
06 50
06 50
06 53
06 53
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 54
06 56
06 56
roducts b
roche-applied-sc

No.
80 560 001 Rea
Sys
Pre
hum
Set
extr
00 358 001 GS
GS
DNA
leuk
assa
00 498 001 GS
This
seve
rese
GS
38 282 001 cOm
Sup
of s
bac
38 304 001 cOm
Exc
prot
cOm
41 089 001 Ma
Aut
usin
read
stan
41 119 001 Ma
Dro
and
41 127 001 Ma
Rea
of M
41 143 001 Ma
Mag
41 151 001 Ma
Mag
41 178 001 Ma
Mag
41 194 001 Ma
Nee
Inst
41 208 001 Ma
Mag
41 224 001 Ma
Use
tand
41 259 001 Ma
Mag
41 267 001 Ma
Mag
41 275 001 Ma
Mag
41 283 001 Ma
Hol
43 588 001 Ma
Rea
acid
Inst
69 161 001 Pho
For
con
divi
for
69 382 001 Lig
Imp
153
LIM
dete

by Catalo
cience.com
alTime ready Infl
stem
mixed primers/hyd
man samples. Use
for multiplex dete
raction control for
GType RUNX1 P
GType RUNX1 Pri
A sequence of sev
kemia research. Th
ay using the GS FL
GType TET2/CBL
s set forms the bas
eral exons of the T
earch. This DNA se
FLX, GS FLX+ or G
mplete ULTRA Ta
perb protein protec
serine, cysteine, an
cterial, yeast, and m
mplete ULTRA Ta
ellent inhibition of
mplete His-Tag Pu
agNA Pure 96 Ins
tomated high-throu
ng flexible software
dy-to-use reagents
ndard volume sam
agNA Pure 96 Dro
op catcher and atta
d cleaning MagNA
agNA Pure 96 Rea
agent loop unit for
MagNA Pure 96 Ins
agNA Pure 96 Ba
gNA Pure 96 Barc
agNA Pure 96 Tip
gNA Pure 96 Tip R
agNA Pure 96 Bot
gNA Pure 96 Bottl
agNA Pure 96 Ne
edle set for user re
trument reagent pi
agNA Pure 96 Pur
gNA Pure 96 Purif
agNA Pure 96 Rea
e as replacement r
dem after the first
agNA Pure 96 Wa
gNA Pure 96 Wast
agNA Pure 96 Inte
gNA Pure 96 Inter
agNA Pure 96 Wa
gNA Pure 96 Wast
agNA Pure 96 Pla
der for custom pla
agNA Pure 96 DN
ady-to-use reagent
ds from up to 200
trument. External ly
ospho-Histone H
fast, accurate qua
njugated antibodies
ding cells on 96-w
cell-based workflo
htCycler
1536 S
prove PCR efficienc
36 Instrument. Idea
MS data manageme
ection of pipetting
og Numb
Product N

uenza B Detectio
drolysis probe dete
with RealTime rea
ction/differentiatio
human nucleic ac
Primer Set
mer Set forms the
veral exons of the R
his is a DNA seque
LX, FLX+, or Junio
L/KRAS Primer S
sis for a test to det
TET2, CBL, and KR
equence-based m
GS Junior Systems
ablets, EDTA-free
ction combined wit
nd aspartic proteas
mammalian cell typ
ablets, glass vials
f serine, cysteine, m
strument
ughput instrument
e-driven protocols
s. Typical run take
mples.
op Catcher
ached Drop Catche
A Pure 96 Instrume
agent Loop Unit
user replacement
struments.
rcode Scanner
ode Scanner for re
p Rack
Rack for replaceme
ttle Rack
e Rack for replace
eedle Set of 4
eplacement of the
ipetting heads.
rification Rack
fication Rack for re
agent Rack
ack or for storing
kit.
aste Rack
te Rack for replace
ernal Waste Con
rnal Waste Contain
aste Cover
te Cover for replac
ate Holder
ates in the MagNA
NA and Viral NA S
l sample volumes
ysis is optional.
H3 Imaging Kit
antification of mito
s. Ideal for accurat
well microplates. Q
ows.
Software, Versio
cy using this dedic
al for automated hi
ent. Use with RealT
errors.
ber
Name
on Set, LightCycl
ect Influenza B vira
ady Influenza A/H1
on of Influenza A a
cid.
basis for a test to
RUNX1 gene, of in
ence-based mutat
or Systems.
Set
termine the DNA s
RAS genes, of intere
utation detection a
s.
e, glass vials
th ease of use: Hig
ses for protein prot
pes.
s
metallo- and aspar
nd mammalian cell
r IMAC.
t for nucleic acid p
s and barcoded, pr
es less than one ho
er Fleece for runni
nts.
t onto the reagent
eplacement.
ent.
ement.
needles on MagN
eplacement.
a second purificat
ement.
ntainer
ner for replacemen
cement.
A Pure 96 Instrume
Small Volume Kit
sealed trays for pu
s using the MagNA
tic cells using Alex
te and fast quantif
Quickly determine c
on 1.1
cated software for
igh-throughput wo
Time ready reagen
ler
480
al genes in
N1 Detection
and B, with an
determine the
nterest in
ion detection
sequence of
est in leukemia
assay uses the
ghest inhibition
tection in
rtic proteases for
types. Use new
purification
refilled trays with
our for 96
ing, maintaining
pipetting head
A Pure 96
ion kit used in
nt.
nt.
t
urifying nucleic
A Pure 96
xaFluor
488
fication of
cell cycle status
the LightCycler

orkflows and
nts for easy

fo
4 PCR pla
4 PCR pla
6 glass via
6 glass via
1 instrumen
1 in
3 sets
fo
1

Pack Size

r up to 100 reactio
tes with dried-dow
tes with dried-dow
ls each containing
EDTA-free
als each containing
(with EDTA)
1 drop catcher
1 reagent loop uni
1 barcode scanne
1 tip rack
1 bottle rack
1 set of 4 needles
1 purification rack
1 reagent rack
1 waste rack
ternal waste conta
1 waste cover
1 plate holder
1 software packag
ons
wn primers
wn primers
g 10 tablets,
g 10 tablets
d accessories
it
r
s
k
ainer
s each
ts
e

Price in

inquire
inquire
inquire
630,40
707,30
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
450,00
inquire

Pr

Cat.

06 59
06 59
06 61
06 61
06 62
06 63
06 63
06 64
06 64
06 65
06 65
06 68
06 71
06 71
06 71
roducts b

No.
93 020 001 GS
The
cap
94 662 001 GS
Eva
Am
GS
MV
12 598 001 Lig
The
Ligh
to 1
time
the
96-w
Inst
12 601 001 Lig
Use
to e
end
Incl
27 846 001 GS
The
Inst
Seq
38 996 001 Ma
This
in th
of t
39 003 001 Ma
This
., m
plat
40 702 001 Ma
Use
pur
for
lysa
40 729 001 Ma
For
pur
con
con
50 767 001 Hig
For
- 10
Isol
arra
50 775 001 Hig
For
m
Mac
isol
84 335 001 Seq
Use
whe
Rea
pro
13 076 001 Lig
Spe
mas
Inst
13 092 001 Lig
Spe
mas
Inst
13 106 001 Lig
Spe
mas
Inst

by Catalo
Junior Reagent
e GS Junior Reagen
ps from the reagen
Junior emPCR B
luate the amount o
plification procedu
Junior Titanium em
V emPCR Kits. Supp
htCycler
8-Tub
e adapter plate is fo
htCycler 8-Tube St
2 LightCycler
8-
es. The LightCycle
LightCycler
480
well version. The p
truments.
htCycler
8-Tub
e these optimized r
easily set up and p
dpoint genotyping,
udes both tube str
Junior Titanium
e GS Titanium Sequ
trument Test. It is a
quencing Kit (05 99
agNA Pure 96 Lig
s adapter is used t
he MagNA Pure 9
he LightCycler
48
agNA Pure 96 Arc
s adapter is used t
atrix storage tubes
te is placed on top
agNA Pure 96 DN
e this reagent with
in vitro diagnostic
ates.
agNA Pure 96 Sys
rinsing the MagN
ification run. Using
nfiguration, the inst
ntainers.
gh Pure FFPET DN
fast and convenie
0 m thick sections
ated DNA is suitab
ays), and sequenci
gh Pure FFPET RN
fast convenient is
thick sections of f
crodissected samp
ated RNA for qRT-
qCap EZ Develop
e this universal rea
en species-specific
agent is for use spe
ducts.
htCycler 96 DN
ecial bundle combi
ster for hydrolysis
trument.
htCycler 96 DN
ecial bundle combi
ster for SYBR Gree
trument.
htCycler
96 DN
ecial bundle combi
ster for SYBR Gree
trument.
og Numb
Product N

Decapping Tool
nt Decapping Tool
t cassette in the G
Bead Counter V2
of enriched beads
ure. Bead Counter
mPCR Kits or mult
plied with GS Junio
be Strip Adapter P
or use with the Lig
trips (white or clea
Tube Strips in one
r
8-Tube Strip Ad
Instrument I and L
plate is not suitable
be Strips (white)
reaction vessels fo
erform gene detec
and high-resolutio
rips and cap strips
Sequencing Buff
uencing Buffers Ki
a subcomponent o
96 554 001) and ca
ghtCycler 480 Ad
to fix the 96-well L
6 Instrument. This
80 Multiwell Plate
chive Plate Adap
to fix 96-well plate
s, in MagNA Pure
p of the 96-well pla
NA Tissue Lysis B
the MagNA Pure
ucleic acids (DNA/
c purposes, and for
stem Fluid (Exter
A Pure 96 Instrum
g the external syst
trument is on a tab
NA Isolation Kit
ent isolation and pu
s of formalin-fixed
ble for qPCR, micr
ing.
NA Isolation Kit
olation and purific
formalin-fixed, par
ples or biopsy mate
-PCR and microarr
per Reagent
agent to block repe
c Cot-1 DNA is no
ecifically with Roc
NA Probes Value
ipack, including m
probe assays perfo
NA Green Value P
ipack, including m
en I assays perform
NA Green Value P
ipack, including m
en I assays perform
ber
Name
l is used to conven
GS Junior Titanium
recovered during
can be used for s
tiple prep with GS
or Complete.
Plate
ghtCycler
480 Sys
ar). The adapter pla
e run and is re-usa
dapter Plate can o
LightCycler
480 I
e for the use in Lig
or the LightCycler
ction, gene quantif

on melting analysi
s.
fers Kit
it is used to run th
of the GS FLX Titan
an be ordered sep
dapter
LightCycler
480 M
perforated plate is
96 for access to e
pter 4S
s with no snap-loc
96 Instruments. Th
ates with non-snap
Buffer
96 System for the
/RNA) from biolog
r stabilization of D
rnal)
ment reagent head
tem fluid and liquid
ble that also holds
urification of geno
d, paraffin-embedd
oarray analysis (CG
cation of total RNA
raffin-embedded ti
erial can also be u
ray analysis.
etitive regions in th
ot available. SeqCa
he SeqCap EZ Dev
Pack S
multiwell plates and
ormed on the Ligh
Pack S
med on the LightCy
Pack L
med on the LightCy
niently remove
Sequencing Kit.
emPCR
ingle prep with
FLX Titanium
stem and the
ate can hold up
able multiple
only be used in
nstrument II ,
ghtCycler
96
96 Instrument
fication,
s assays.
e GS Junior
nium
arately.
Multiwell Plate 96
s placed on top
each well.
ck for tubes, e.g
he perforated
p-lock tubes
isolation and
gical specimens
NA in tissue
during a
d waste
the external
mic DNA from 5
ded tissue.
GH, methylation
A from 5 to 10
ssue.
used. Use
he genome
p EZ Developer
veloper
d real-time PCR
htCycler 96
d real-time PCR
ycler
96
d real-time PCR
ycler 96

120 x 8-tube-s
(Optimized rea
96 and the L
LightCycle
combination w
1
1
5 packs of F
Master (a total
Multiwell P
5 packs FastSt
(a total of 25
Multiwell P
20 packs of
Master (a total
480 Multiwell

Pack Size

1 device
1 device
1 piece
LightCycler
480. N
er
480 it can only

with the LightCycle
Adapter Plate)
1 kit
1 adapter
1 adapter
1 bottle (100ml)
1 container
1 ml
FastStart Essential
of 25 ml) 1 pack L
tart Essential DNA
ml); 2 packs of Lig
FastStart Essentia
of 100 ml); 2 pack
www.roche
tube caps clear
he LightCycler

Note: For the
y be used in
er
Tube Strip
ns
ns
DNA Probes
LightCycler
480
of 50 plates)
A Green Master
ghtCyler
480
of 50 plates)
l DNA Green
ks of LightCyler

of 100 plates)
e-applied-science

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
258,00
inquire
270,00
inquire
inquire
inquire

229

e.com

Pr
230

www.r

Cat.

06 71
06 72
06 72
06 74
06 74
06 74
06 74
06 74
06 74
06 74
06 74
06 75
06 77
06 77
roducts b
roche-applied-sc

No.
13 122 001 Lig
Spe
mas
Inst
20 455 001 Rea
This
Taq
dTT
cDN
25 309 001 Rea
Cus
assa
prov
Cat
40 189 001 Seq
Cus
of c
com
cap
40 235 001 Seq
Cus
of c
com
cap
40 243 001 Seq
Cus
of c
com
cap
40 251 001 Seq
Hig
cus
rese
unif
40 260 001 Seq
Hig
cus
rese
unif
40 278 001 Seq
Prov
hum
cos
50 M
40 294 001 Seq
Use
solu
solu
Exo
40 308 001 Seq
Use
solu
solu
Exo
54 155 001 Rea
Fast
usin
allo
Opt
76 302 001 Seq
Com
Libr
hyb
Gra
76 345 001 Seq
Com
Libr
hyb
Gra

by Catalo
cience.com
htCycler
96 DN
ecial bundle combi
ster for hydrolysis
trument.
alTime ready cDN
s 5x concentrated
q DNA Polymerase
TP), for 40 pre-amp
NA (1 to 250 ng).
alTime ready Pre
stom 4x concentrat
ay primer pairs, fo
vide RealTime read
. No. 06 725 309 0
qCap EZ Exome P
stomize your target
custom target regio
mpared to other tar
pture efficiency.
qCap EZ Exome P
stomize your target
custom target regio
mpared to other tar
pture efficiency.
qCap EZ Exome P
stomize your target
custom target regio
mpared to other tar
pture efficiency.
qCap EZ Choice L
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Choice X
tomer-defined dis
equencing studies
form capture of ta
qCap EZ Develop
vides custom oligo
man genomes for c
ts by achieving hig
Mb. Flexible design
qCap EZ Exome+
e the most compre
ution to discover m
utions, with the su
ome 2.1M overlapp
qCap EZ Exome+
e the most compre
ution to discover m
utions, with the su
ome 2.1M overlapp
alTime ready RNA
ng 50-fold concent
timized for HybPro
qCap EZ Accesso
mponents for proc
raries; includes CO
bridization and Hig
ade Water for LM-P
qCap EZ Accesso
mponents for proc
raries; includes CO
bridization and Hig
ade Water for LM-P
og Numb
Product N

NA Probes Value
ipack, including m
probe assays perfo
NA Pre-Amp Mas
ready-to-use hot-
, reaction buffer, d
plification reaction
e-Amp Primer Po
ted solution of 6-9
r 40 pre-amplificat
dy Custom Assay C
01 when ordering.
Plus Library
t enrichment disco
ons to EZ Exome v
rget enrichment so
Plus Library
t enrichment disco
ons to EZ Exome v
rget enrichment so
Plus Library
t enrichment disco
ons to EZ Exome v
rget enrichment so
Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
XL Library
ble design, and eas
ease related regio
s. Save on costs by
rget regions up to
per Library
customer-develope
n captures regions
+UTR Library
ehensive cost-effec
more variants comp
perior capture effic
ping probes.
+UTR Library
ehensive cost-effec
more variants comp
perior capture effic
ping probes.
A Virus Master
specific real-time
trated mix of Trans
t RT-PCR. No need
obe, hydrolysis and
ory Kit
essing sequence c
OT DNA to block re
h Fidelity PCR Mas
PCR during pre/po
ory Kit
essing sequence c
OT DNA to block re
h Fidelity PCR Mas
PCR during pre/po
ber
Name
Pack L
ormed on the Ligh
ster
start PCR Master M
dNTP mix, (with dU
s of 50 l of small
ool
96 different design
tion reactions of 5
Configuration Num
.
overy tool by addin
v3 to discover more
olutions, for cost-e
overy tool by addin
v3 to discover more
overy tool by addin
v3 to discover more
sy-to-use solution
ns in the human g
7 Mb.
sy-to-use solution
ns in the human g
50 Mb.
ed capture protoco
orm capture of targ
s in any genome.
ctive exome and U
pared to other targ
ciency of SeqCap
ctive exome and U
pared to other targ
ciency of SeqCap
one-step RT-PCR
scriptor/Taq, and a
d to heat preactiva
d UPL probes.
capture using SeqC
epetitive regions d
ster, TS-PCR Oligo
ost capture amplifi
capture using SeqC
epetitive regions d
ster, TS-PCR Oligo
ost capture amplifi
d real-time PCR
htCycler
96
Mix contains
UTP instead of
quantities of
er-specific
0 l each;
mber with the
ng up to 50 Mb
e variants
effective superior
ng up to 50 Mb
e variants
effective superior
ng up to 50 Mb
e variants
effective superior
captures
genome for
specific and
captures
genome for
specific and
ns in non-
ols. Reduce
get regions up to
TR enrichment
get enrichment
EZ Human
TR enrichment
get enrichment
EZ Human
of viral RNA
a unique buffer
te Taq.
Cap EZ
uring
os, and PCR
cation.
Cap EZ
uring
os, and PCR
cation.

20 packs of F
Master (a
LightCycl
(

Pack Size

FastStart Essential
ler
480 Multiwell
40 reactions
40 reactions
12 reactions
48 reactions
96 reactions
4 reactions
4 reactions
4 reactions
4 reactions
48 reactions
200 reactions
24 reactions
96 reactions
DNA Probes
2 packs of
Plates 96
s)

Price in

inquire
600,00
200,00
6.780,00
24.000,00
38.000,00
4.900,00
5.200,00
5.200,00
2.500,00
24.000,00
inquire
600,00
2.400,00

Pr

Cat.

06 77
06 77
06 78
06 78
06 87
06 87
06 87
06 87
06 95
06 95
06 97
07 04
07 04
07 04
07 04
07 04
roducts b

No.
77 287 001 Seq
Kit A
sec
TruS
barc
77 317 001 Seq
Kit
sec
TruS
barc
81 535 001 cOm
Pre
abo
81 543 001 cOm
Pre
abo
79 080 001 Apt
Rea
poly
acti
usin
79 101 001 Apt
Rea
poly
acti
usin
79 110 001 Apt
Rec
& im
One
rang
79 128 001 Apt
Rec
& im
One
rang
53 212 001 Seq
Com
seq
eve
Acc
53 247 001 Seq
For
77 952 001 Seq
Con
cap
amp
for
45 271 001 Ced
Prov
This
env
21 C
45 280 001 Ced
Prov
Ana
env
21 C
45 298 001 Ced
Ced
Ced
45 301 001 Ced
Ced
prev
vers
45 344 001 Ced
This
Ced
inte
HiR

by Catalo
qCap EZ HE-Oligo
A is used to block
ondary capture. Fo
Seq Library Kit A.
code 1-12 samples
qCap EZ HE-Oligo
B is used to block
ondary capture. Fo
Seq Library Kit B.
code 13-24 sample
mplete His-Tag P
packed columns w
ove). Fully compati
mplete His-Tag P
packed columns w
ove). Fully compati
taTaq Fast PCR M
ady-to-use master
ymerase with apta
vation. Use one-fo
ng GC-RICH templ
taTaq Fast PCR M
ady-to-use master
ymerase with apta
vation. Use one-fo
ng GC-RICH templ
taTaq Fast DNA P
combinant Taq pol
mmediate activatio
e-for-all < 30 min
ge, including GC-R
taTaq Fast DNA P
combinant Taq pol
mmediate activatio
e-for-all < 30 min
ge, including GC-R
qCap EZ Reagent
mplete reagent sta
uence capture usi
rything you need f
cessory Kit, and Hy
qCap EZ Reagent
ordering informat
qCap EZ Pure Ca
nvenient set of cap
pture and to isolate
plification. Use this
high-quality seque
dex 2.3 Software
vides comprehens
s new software is d
vironments, featurin
CFR part 11 compl
dex HiRes 2.3 So
vides comprehens
alyzer. This new so
vironments, featurin
CFR part 11 compl
dex 2.x to 2.3 Up
dex 2.x to 2.3 Upgr
dex 2.x Software ve
dex HiRes 2.x to
dex HiRes 2.x to 2.3
vious Cedex HiRes
sion 2.3.
dex HiRes SW 2.3
s is a software inte
dex HiRes Analyze
egration into existin
Res SW V 2.2 Remo
og Numb
Product N

o Kit A
k library adapters in
or labs performing
Includes hybridiza
s and PCR Grade W
o Kit B
library adapters in
or labs performing
Includes hybridiza
es and PCR Grade
Purification Colum
with cOmplete His-
ble with standard
Purification Colum
with cOmplete His-
ble with standard
Master
based on thermos
mer mediated, rev
or-all < 30 min pro
lates.
Master
based on thermos
mer mediated, rev
or-all < 30 min pro
lates.
Polymerase
ymerase with apta
on. Comes with opt
protocol for super
RICH templates.
Polymerase
ymerase with apta
on. Comes with opt
protocol for super
RICH templates.
t Kit
arter kit (24 reactio
ing Illumina Seque
for target enrichme
ybridization and W
t Kit Plus
tion contact your lo
apture Bead Kit
pture and purificat
e a DNA sample lib
s sensitive and rob
encing results.
e Package
sive analysis tools f
designed for proje
ng User and Right
liance.
oftware Package
sive analysis tools f
oftware is designed
ng User and Right
liance.
grade Package
rade Package enab
ersions to Cedex S
2.3 Upgrade Pac
3 Upgrade Packag
s 2.x software vers
3 Remote Contro
erface for on-site r
rs. Enables easy re
ng data managem
ote Control.
ber
Name
n hybridization to p
sequence capture
ation enhancing (H
Water.
n hybridization to p
sequence capture
ation enhancing (H
e Water.
mn
-Tag Purification R
purification system
mn
-Tag Purification R
purification system
stable recombinan
versible hot start &
otocol for superb re
stable recombinan
versible hot start &
otocol for superb re
amer mediated, rev
timized buffer syst
rb results in a broa
amer mediated, rev
timized buffer syst
rb results in a broa
ons) for customers
encing Systems. Ea
ent. Includes HE-O
Wash Kit.
ocal representative
ion beads to preve
brary from contam
bust method for cle
for operating the C
ects in cGMP regul
ts Management an
for operating the C
d for projects in cG
ts Management an
bles the upgrade o
Software version 2.
ckage
ge enables the upg
ions to Cedex HiR
ol
remote control of C
ead out of result da
ent systems; succe
prevent
e with Illumina
HE) oligos to
prevent
e with Illumina
HE) oligos to
Resin (see
ms.
Resin (see
ms.
t Taq
& immediate
esults even
t Taq
& immediate
esults even
versible hot start
tem for fast PCR.
ad template
versible hot start
tem for fast PCR.
ad template
performing
asily order
Oligo Kit A,
e.
ent secondary
inants during
eanup of DNA
Cedex Analyzer.
ated
nd Audit Trail for
Cedex HiRes
GMP regulated
nd Audit Trail for
of all previous
3.
grade of all
es Software
Cedex and
ata for flexible
essor to Cedex

1 binder w
1 binder w
1 binder w
1 binder w
1 en

Pack Size

96 reactions
96 reactions
1 x 5 ml
5 x 1 ml
100 reactions
1,000 reactions
100 units
1,000 units
24 reactions
1 kit
24 reactions
with CD and Opera
with CD and Opera
with CD and Opera
with CD and Opera
nvelope with instal
www.roche
ator's Guide
ator's Guide
ator's Guide
ator's Guide
ll CD
e-applied-science

Price in

1.150,00
1.200,00
130,00
179,00
56,00
475,00
43,00
286,00
1.530,00
inquire
460,00
inquire
inquire
inquire
inquire
inquire

231

e.com

Pr
232

www.r

Cat.

07 10
07 10
07 10
07 10
07 10
07 10
07 10
07 10
07 10
07 10
07 10
07 12
07 12
07 16
10 10
10 10
10 10
10 10
10 10
roducts b
roche-applied-sc

No.
01 929 001 FLO
The
(on
Han
01 937 001 FLO
The
of p
Car
01 970 001 FLO
The
96 P
Inst
01 988 001 Prim
The
Mag
01 996 001 FLO
The
Ligh
02 020 001 FLO
The
Ligh
02 046 001 FLO
The
use
02 054 001 FLO
The
use
02 062 001 FLO
The
Pur
02 097 001 FLO
The
data
Ma
02 127 001 FLO
The
FLO
27 014 001 FLO
FLO
28 894 001 FLO
The
FLO
Setu
62 367 001 FLO
The
Out
01 893 001 Ace
Ace
usin
gro
Pur
01 907 001 Ace
Ace
usin
gro
Pur
02 105 001 Ade
Ade
use
inos
pho
02 121 001 Ade
Ade
use
inos
app
02 342 001 ATP
ATP
Hyd
thio
Sup

by Catalo
cience.com
OW Control Unit i
e FLOW Control Un
e Control Unit is n
ndling Instrument,
OW Primary Sam
e FLOW Primary Sa
primary and/or sec
rtridges.
OW Processing C
e FLOW Processing
Processing Cartrid
trument.
mary Sample Ha
e Primary Sample H
gNA Pure lysis buf
OW PCR Setup In
e FLOW PCR Setup
htCycler
480 Inst
OW PCR Setup LC
e FLOW PCR Setup
htCycler
480 Mu
OW PCR Setup LC
e FLOW PCR Setup
ed for cooling the L
OW PCR Setup LC
e FLOW PCR Setup
ed for cooling the L
OW Output Plate
e FLOW Output Pla
e 96 Output Plates
OW Software 1.0
e FLOW Software 1
a exchange betwe
nagement Systems
OW PCR Setup In
e FLOW PCR Setup
OW PCR Setup Inst
OW 32 Vial Carrie
OW 32 Vial Carrier
OW Tubes (2 ml)
e 2 ml Screw Cap T
OW Primary Sample
up Instrument (PS
OW PCR Setup O
e FLOW PCR Setup
tput Plate.
etyl-Coenzyme A
etyl-Coenzyme A is
ng radioisotopes. C
ups from acetylcoe
ity: 85% acetyl-Co
etyl-Coenzyme A
etyl-Coenzyme A is
ng radioisotopes. C
ups from acetylcoe
ity: 85% acetyl-Co
enosine Deamina
enosine Deaminas
ed for the determin
sine analogs. Solut
osphate, pH approx
enosine Deamina
enosine Deaminas
ed for the deamina
sine analogs. Susp
proximately 6.
P--S
P--S is a substra
drolyzed very slowl
ophosphorylated, p
pplied as a tetralith
og Numb
Product N

inclusive Monito
nit is used in conju
eeded for each of
PCR Setup Unit, a
ple Handling Ins
ample Handling Ins
condary samples in
Cartridge Carrier
g Cartridge Carrier
ge on the FLOW P
ndling Reagent C
Handling Reagent
ffers.
nstrument
p Instrument is for
trument.
C480 Multiwell P
p LC480 Multiwell
ltiwell Plates.
C480 Multiwell P
p LC480 Multiwell
LightCycler
480 M
C480 Multiwell P
p LC480 Multiwell
LightCycler
480 M
Carrier
ate Carrier enables
s.
1.0 controls the FLO
een FLOW compon
s.
nstrument 50 l F
p Instrument 50 l
trument.
er
with Adaptors for
Tubes, can be used
e Handling Instrum
U).
utput Plate Cool
p Output Plate Coo
A
s used to assay CA
CAT enzyme activit
enzyme A to chlor
A (enzymatic/abso
A
s used to assay CA
CAT enzyme activit
enzyme A to chlor
A (enzymatic/abso
ase (ADA)
e (adenosine amin
nation of adenosine
tion in 50% glycero
ximately 6.
ase (ADA)
e (adenosine amin
tion of adenosine
pension in 3.2 M am
ate and inhibitor of
ly by phosphatases
proteins are resista
hium salt powder.
ber
Name
or
unction with the FL
the following: Prim
and System Contro
trument
strument is for aut
nto MagNA Pure 9
r is used to place a
Primary Sample Ha
Carrier
Carrier is used for
automated PCR se
Plate Carrier
Plate Carrier is use
Plate Cooling Blo
Plate Cooling Bloc
Multiwell Plates 96
Plate Cooling Blo
Plate Cooling Bloc
Multiwell Plates 38
s the placement of
OW process and m
nents and Laborato
Filter Tips
Filter Tips are use
the FLOW Instrum
d as secondary tub
ment (PSH) and fo
ing Block
oling Block is used
AT enzyme activity
ty catalyzes the tra
ramphenicol.
orbance), 2% Li.
AT enzyme activity
ramphenicol.
orbance), 2% Li.
nohydrolase) from
e analogs to the co
ol (v/v), 10 mM po
nohydrolase) from
analogs to the cor
mmonium sulfate s
f ATP-dependent e
s and most ATPase
ant to protein phos
LOW System
mary Sample
ol).
tomated transfer
6 Processing
a MagNA Pure
andling
r holding
etup on the
ed to hold the
ock (96 well)
ck (96 well) is
6.
ock (384 well)
ck (384 well) is
84.
up to 5 MagNA
manages the
ory Information
d with the
ment.
bes for the
r the FLOW PCR
for cooling the
in cell extracts
ansfer of acetyl
in cell extracts
ansfer of acetyl
calf intestine is
orresponding
otassium
calf intestine is
rresponding
solution, pH
enzyme systems.
es. Once
sphatases.

1 co
1 proc
1 m
1 c
1 co
1
1
1 c

Pack Size

ontrol unit with mo
1 instrument
cessing cartrigde c
1 reagent carrier
1 instrument
multiwell plate car
cooling block (96 w
ooling block (384 w
1 plate carrier
1 software packag
carrier with adapto
280 tubes per box
1 cooling block
10 mg
50 mg
10 mg (2 ml)
10 mg (1 ml)
25 mg
onitor
carrier
rier
well)
well)
e
ps
ors
x

Price in

inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire
102,40
436,40
192,40
164,80
410,50

Pr

Cat.

10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
roducts b

No.
02 547 001 AM
Com
hyd
clea
ven
02 814 001 -
Use
poly
enz
02 857 001 Am
Am
acti
term
poly
02 946 001 ABT
ABT
(abs
03 233 001 Car
Use
suc
prot
arg
03 241 001 Car
Key
end
from
acy
03 578 001 Col
Diss
mam
sus
viab
03 586 001 Col
Diss
mam
sus
viab
04 159 001 DN
DN
end
for
as a
04 531 001 Kle
This
San
be u
the
04 973 001 -
-
as a
app
32,0
04 981 001 -
-
as a
app
32,0
05 031 001 -
Use
Prov
crys
05 554 001 Glu
Glu
non
keto
and
05 589 001 Glu
Glu
synt

by Catalo
MP-PNP
mpetitive inhibitor
drolyzing between t
avage between the
om phosphodieste
Amylase
e -Amylase for th
ysaccharides conta
zyme produces -
myloglucosidase
yloglucosidase is u
vity: approx. 6 U/m
minal glucoses tha
ysaccharide of mu
TS
TS substrate is a p
sorbance), chroma
rboxypeptidase B
e Carboxypeptidase
ccessive cleavage o
teins. Specific Act
inine as the substr
rnitine Acetyltran
y enzyme in the me
doplasmic reticulum
m an acyl-CoA thio
lCoA/CoA in subc
llagenase A
sociate tissue (lun
mmary gland, bloo
pensions to establ
bility, and function
llagenase A
sociate tissue (lun
mmary gland, bloo
pensions to establ
ase I
ase I, Grade II from
donuclease that req
isolation procedur
a lyophilizate.
enow Enzyme
s sequencing grad
nger DNA sequenc
used in 3-end labe
elongation of olig
Galactose Dehyd
Galactose Dehydro
a suspension in 3.2
proximately 6. It is a
000 D).
Galactose Dehyd
Galactose Dehydro
a suspension in 3.2
proximately 6. It is a
000 D).
Galactosidase
e -Galactosidase
vided as a suspen
stalline.
utamate-Oxaloac
tamate-Oxaloaceta
nnatural L-amino a
oglutarate, catalyz
d L-glutamate.
utamate-Pyruvate
tamate-Pyruvate T
thesis of nonnatur
og Numb
Product N

of ATP-dependent
the a- and -pho
e - and -phos
erase and adenylat
he hydrolyzation o
aining 3 or more
-dextrins.
used for the determ
mg lyo. at +25C w
at are 1,4- or 1
ltiple glucose unit
peroxidase substrat
atographically hom
B
e B for the sequen
of basic amino acid
ivity - approx. 150
rate.
nsferase
etabolic pathway in
m. Catalyzes the re
oester to carnitine
ellular compartme
g, heart, muscle, b
od vessels, brain, e
lish primary cell cu
ality are important
g, heart, muscle, b
ality are important
m bovine pancreas
quires bivalent cat
res for proteins (e.g
de enzyme is speci
cing (dideoxy-chai
eling, random DNA
onucleotides.
drogenase
ogenase from Pseu
2 M ammonium su
a dimer with subu
drogenase
ogenase from Pseu
2 M ammonium su
a dimer with subu
e to produce a cali
sion in 3.2 M amm
cetate Transamin
ate Transaminase
acids from -keto
es the conversion
e Transaminase (
Transaminase (GPT
ral L-amino acids f
ber
Name
t systems. Substra
osphorus atom, yet
phorus atom. Subs
te cyclase.
of 1,4-glycosidic
1,4-linked D-Glu
mination of starch
with glycogen as su
1,6-linked to an oli
s; supplied as susp
te for ELISA. Purity
mogeneous.
nce analysis of pro
ds from the C-term
U/mg at +25C w
n mitochondria, pe
eversible transfer o
and regulates the
ents.
bone, liver, kidney,
etc.), and prepare s
ulture systems. Use
t.
ulture systems. Use
t.
s is a double-stran
tions for maximal a
g ., membrane pro
fically prepared an
n termination met
A labeling, fill-in re
udomonas fluoresc
ulfate, 1 mM EDTA
nits of equal size (
udomonas fluoresc
ulfate, 1 mM EDTA
nits of equal size (
bration curve in en
monium sulfate, pH
nase (GOT)
(GOT) is used for
o acids. In the pres
of L-aspartate to o
(GPT)
T) from pig heart is
from -keto acids
te for enzymes
t resistant to
strate of snake
bonds in
cose units. The
. Specific
ubstrate. Cleaves
go- or
pension.
y:>98%
teins by
minus of
ith hippuryl-L-
eroxisomes, and
of acyl groups
ratio of
cartilage,
single-cell
e when yield,
cartilage,
single-cell
e when yield,
d-specific
activity. It is used
oteins). Supplied
nd tested for
hod). It can also
eactions, and
cens is provided
A, pH
(subunit =
cens is provided
A, pH
(subunit =
nzymatic assays.
H approx. 6,
the synthesis of
ence of a-
oxaloacetate
s used for the
s.

2

Pack Size

25 mg
50 mg (5 ml)
100 mg (10 ml)
2 g
5 mg (1 ml)
5 mg (1 ml)
100 mg
500 mg
100 mg
250 U (5 x 10
3
U/m
1 mg (1 ml)
5 mg (1 ml)
1,500 U
10 mg (1 ml)
10 mg (1 ml)
www.roche
ml)
e-applied-science

Price in

203,70
127,20
131,40
57,90
182,70
172,00
59,00
251,90
58,20
275,00
59,20
209,70
185,00
143,10
122,80

233

e.com

Pr
234

www.r

Cat.

10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
roducts b
roche-applied-sc

No.
05 678 001 Glu
A c
glut
pero
to G
06 399 001 GTP
GTP
a ce
06 801 001 Kan
Am
of g
cult
07 085 001 L-L
L-L
-
in s
07 409 001 Mit
Pote
stud
crys
filte
07 735 001 NA
NA
This
07 824 001 NA
NA
prov
07 921 001 Nuc
End
dsD
yiel
vitro
07 948 001 Nuc
Nuc
reve
pro
08 014 001 Pap
For
imm
prot
Req
08 057 001 Pep
Use
med
yiel
from
08 090 001 Per
For
Pero
moi
dial
08 138 001 Alk
Alka
pho
sele
Poly
08 146 001 Alk
Alka
pho
sele
Poly
08 227 001 Aci
Acid
pho
lyop
+25
08 294 001 Pho
Use
pyru

by Catalo
cience.com
utathione Reduct
rucial flavoenzyme
tathione is used by
oxide and is then c
GSH by glutathione
P
P, disodium salt, is
ell-free system.
namycin sulfate
inoglycosidic antib
gram-positive, gram
ture. Also used to s
Lactate Dehydrog
actate Dehydroge
ketoacids to -hy
suspension in 3.2 M
tomycin C
ent DNA crosslink
dies of cell-free pr
stalline form. Biobu
ering (e.g., Millipor
DH
DH is the reduced
s NADH Grade I, d
DPH
DPH is the reduce
vided as an amorp
clease S7
donuclease prefere
DNA and RNA. Cle
d 3'-mono- and ol
o translation syste
cleoside Monoph
cleoside Monopho
ersible transfer of
ducing adenosine
pain
complete proteoly
munoglobulins, and
teins and produce
quires 0.5% cystein
psin
e Pepsin for nonsp
dia. Pepsin provide
d biologically activ
m pig gastric muco
roxidase (POD)
oxidation of electr
oxidase (POD) to p
iety. Use reconstitu
ysis. Grade I salt-f
kaline Phosphata
aline Phosphatase
osphohydrolase [al
ective cleavage of
y(U) is not cleaved
kaline Phosphata
aline Phosphatase
osphohydrolase [al
ective cleavage of
y(U) is not cleaved
id Phosphatase
d Phosphatase gra
osphohydrolase [ac
philizate. Specific a
5C with 4-nitrophe
osphoenol-pyruv
e Phosphoenol-pyr
uvate kinase.
og Numb
Product N

ase (GR)
e in the antioxidan
y glutathione perox
converted to oxidiz
e reductase.
required as a coe
biotic with broad s
m-negative bacter
study cell-free pro
genase (L-LDH)
nase from hog mu
ydroxycarboxylic a
M ammonium sulfa
ker. Inhibits DNA sy
rotein biosynthesis
urden reduction in
re).
form of nicotinam
disodium salt is pro
ed form of NADP
+
.
phous powder bott
entially cleaves sin
aves 5'-phosphod
igonucleotides. Re
ems and in RNA se
hosphate Kinase
osphate Kinase is a
a phosphate group
diphosphate and
ytic cleavage of pro
d tissue dissociatio
es glycopeptides fr
ne for activity.
ecific hydrolysis of
es a limited hydroly
ve fragments. Peps
osa.
ron donors by epo
proteins via its am
uted solution direc
free lyophilizate.
ase (AP)
e grade I (orthopho
lkaline optimum])
terminal phosphat
d.
ase (AP)
e grade I (orthopho
lkaline optimum])
terminal phosphat
d.
ade II (orthophosp
cid optimum]) from
activity is approxim
enyl phosphate as
vate
ruvate PEP, monop
ber
Name
t defense system.
xidase to detoxify
zed glutathione wh
enzyme for protein
spectrum inhibition
ia and mycoplasm
otein biosynthesis.
cids, or reverse rea
ate solution, pH ap
ynthesis and is an
s. Mitomycin is pro
n solution is obtain
mide adenine dinuc
ovided as an amor
. NADPH tetrasodi
tled under nitrogen
gle-strand substra
iester bonds of RN
emove endogenou
equencing.
e
a liver enzyme that
p from adenosine
a nucleoside diph
oteins, limited hyd
on. Solubilizes inte
om purified proteo
f proteins and pep
ysis of native imm
sin is an aspartic e
xidation of double
ino groups and its
ctly in conjugation
osphoric-monoeste
from calf intestine
te groups from olig
osphoric-monoeste
from calf intestine
te groups from olig
horic-monoester
m potato is supplie
mately 2 U/mg lyop
s the substrate.
potassium salt as a
Reduced
hydrogen
hich is recycled
biosynthesis in
n of the growth
as in cell
e reduction of
action. Provided
pprox. 6.5.
inhibitor for
vided in a
ed by 0.2 m
cleotide (NAD).
phous powder.
um salt is
n.
ates, as well as
NA and DNA to
s RNA from in
t catalyzes the
triphosphate,
osphate.
rolysis of native
egral membrane
oglycans.
ptides in acidic
unoglobulins to
endoproteinase
e bonds. Couple
s carbohydrate
without prior
er
e is used for
gonucleotides.
er
e is used for
gonucleotides.
ed as a
philizate at
a substrate for

10 m

Pack Size

5 mg (1 ml)
250 mg
5 g
100 mg (10 ml)
2 mg
500 mg
100 mg
15,000 U
mg (60 mg lyophiliz
100 mg (10 ml)
1 g
25,000 U
1,500 U
7,500 U
500 mg
1 g
zate)

Price in

134,40
198,00
215,30
251,10
50,50
159,10
199,40
169,50
197,90
130,70
84,30
277,60
63,80
256,00
276,90
294,90

Pr

Cat.

10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
10 10
roducts b

No.
08 626 001 Pol
Poly
wor
tail
(mR
08 677 001 Pol
Use
acti
sing
this
08 812 001 Pol
Use
biop
It is
the
08 987 001 Pyr
Inor
pyro
prot
amm
09 045 001 Pyr
Pyru
Cat
mol
(v/v
09 118 001 Rev
For
DNA
end
hyb
09 134 001 RNa
RNa
RNA
09 142 001 RNa
RNa
that
isol
09 169 001 RNa
RNa
that
isol
09 193 001 RNa
Use
RNA
solu
09 223 001 RNA
For
synt
hyb
09 339 001 Sor
Red
rela
09 495 001 tRN
tRN
prev
to im
lyop
09 509 001 tRN
tRN
prev
to im
lyop
09 517 001 tRN
tRN
prev
to im
a ly
09 525 001 tRN
tRN
prev
to im
a ly
by Catalo
y(A)
y(A) has a chain le
rking solution is 0.
to an RNA molecu
RNA) for translatio
y(A) x (dT)
15

e as a primer for re
vity of reverse tran
gle strand of poly(A
s long strand of po
y[d(I-C)]
e as a template for
physical investigat
s also used as a pr
determination of s
rophosphatase, in
rganic pyrophosph
ophosphate to form
tein, RNA, and DN
monium sulfate, pH
ruvate Kinase (PK
uvate Kinase from
alyzes the transfer
lecule of pyruvate
v), pH approx. 6.
verse Transcripta
up to 12 kb first-
A sequencing. Als
d labeling of DNA f
bridization, and gen
ase
ase from bovine pa
A. This is a crude m
ase A
ase A from bovine
t acts on single-str
ation of DNA. For
ase A
ase A from bovine
t acts on single-str
ation of DNA. For
ase T1
e RNase T1 from A
A fingerprinting; s
ution, pH 6.
A
studies which use
thesizing system. T
bridization.
rbitol Dehydroge
duces L-iditol to L-
ated sugar alcohols
NA
NA is used as a com
vent nonspecific b
mprove recovery o
philizate.
NA
NA is used as a com
vent nonspecific b
mprove recovery o
philizate.
NA
NA is used as a com
vent nonspecific b
mprove recovery o
yophilizate.
NA
NA is used as a com
vent nonspecific b
mprove recovery o
yophilizate.
og Numb
Product N

ength of 2,100 to 1
5 mg/ml. Polyaden
ule. This process p
on.
everse transcriptas
nsriptases. Consist
A). Short (15 bp) s
ly(A).
r RNA polymerases
tions.
imer template with
small amounts of d
norganic (PPase
hatase (PPase) cat
m orthophosphate
NA synthesis. Supp
H 6.
K)
rabbit muscle is a
r of a phosphate g
and 1 molecule of
ase AMV
and second-strand
so used for primer
fragments, genera
nomic footprint ex
ancreas is used fo
mixture of RNases
pancreas is a pyri
randed RNA. For a
DNA isolation, RN
pancreas is a pyri
randed RNA. For a
DNA isolation, RN
Aspergillus oryzae f
upplied as a supen
e natural RNA in a
The product is also
enase (SDH)
-sorbose. Also acts
s. Allows the reduc
mpetitor in pre- an
binding of the prob
of diluted samples.
mpetitor in pre- an
binding of the prob
of diluted samples.
mpetitor in pre- an
binding of the prob
of diluted samples.
mpetitor in pre- an
binding of the prob
of diluted samples.
ber
Name
0,000 nucleotides.
nylation is the addi
produces mature m
ses and can be app
ts of 1 long (at leas
sequences of dT ar
s and as a DNA m
h Kornberg DNA p
dITP, dGTP, and dC
e)
talyzes the hydrolys
e. It plays an impor
plied in suspension
an enzyme involved
roup from PEP to A
f ATP. Solution in
d cDNA synthesis
extension, RNA se
ation of single-stra
periments.
r the removal and
s.
imidine-specific en
analytical purposes
Nase A needs to be
imidine-specific en
analytical purposes
Nase A needs to be
for RNA sequence
nsion in 3.2 M amm
in vivo and in vitro
o used as a carrier
s on D-glucitol and
ction of ketones to
nd hybridization so
be. It can also be u
From baker's yeas
nd hybridization so
From baker's yeas
nd hybridization so
From brewer's ye
nd hybridization so
From brewer's ye
The suggested
ition of a poly(A)
messenger RNA
plied to test the
st 1,000 bp),
re hybridized to
odel for
polymerase for
CTP.
sis of inorganic
tant role in
n in 3.2 M
d in glycolysis.
ADP, yielding 1
50% glycerol
and dideoxy
equencing, 3'-
nded probes for
degradation of
ndoribonuclease
s and for
e boiled.
ndoribonuclease
s and for
e boiled.
e analysis and
monium sulfate
o protein-
r RNA in in situ
d other closely
o polyols.
olutions to
sed as a carrier
st, supplied as a
olutions to
sed as a carrier
st, supplied as a
olutions to
sed as a carrier
ast, supplied as
olutions to
sed as a carrier
ast, supplied as

10 m
Pack Size

100 mg
5 A
260
units
10 A
260
units
1 mg (1 ml)
10 mg (1 ml)
1,000 U
500 mg
25 mg
100 mg
100,000 U
100 g
mg (60 mg lyophiliz
100 mg
500 mg
100 mg
500 mg
www.roche
zate)
e-applied-science

Price in

130,10
141,20
139,80
109,70
79,40
490,40
128,50
37,70
101,40
60,70
66,60
312,10
155,10
609,30
127,50
447,80

235

e.com

Pr
236

www.r

Cat.

10 10
10 10
10 10
10 10
10 11
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
roducts b
roche-applied-sc

No.
09 541 001 tRN
tRN
prev
neg
09 550 001 tRN
tRN
prev
neg
09 878 001 Try
Use
Inhi
med
kall
09 886 001 Try
Use
Inhi
cult
tiss
10 434 001 Xan
Cat
oxid
pur
EDT
27 060 001 -
Use
urin
pre
dru
27 230 001 L-L
L-L
-
in s
27 248 001 L-M
L-M
enz
usin
glyc
27 256 001 L-M
L-M
enz
usin
amm
27 396 001 Pho
Pho
of k
sulf
27 523 001 ATP
Ade
form
dete
27 531 001 ATP
Ade
form
dete
27 558 001 Alc
Alco
syst
Spe
etha
27 566 001 Cre
Enz
of c
diph
Spe
lyop
27 647 001 Glu
Glu
com
ente
sub

by Catalo
cience.com
NA
NA is used as a com
vent nonspecific b
gative); supplied as
NA
NA is used as a com
vent nonspecific b
gative); supplied as
psin Inhibitor
e to terminate tissu
ibits trypsin, plasm
dia. Does not inhib
ikrein. From chick
psin Inhibitor
e to terminate tissu
ibits trypsin, factor
ture media. Does n
ue kallikrein. From
nthine Oxidase (X
alyzes oxidation of
dation of xanthine
ines in some spec
TA, pH approx. 8.
Glucuronidase/A
ed for simultaneou
ne and other biolog
pare protoplasts, i
gs in urine.
Lactate Dehydrog
actate Dehydroge
ketoacids to -hy
suspension in 3.2 M
Malate Dehydrog
Malate Dehydrogen
zyme that reversibly
ng the reduction o
cerol (v/v), pH app
Malate Dehydrog
Malate Dehydrogen
ng the reduction o
monium sulfate so
osphoglucose Iso
osphoglucose Isom
ketoses to aldoses.
fate, pH approxima
P
enosine-5'-triphos
m. It can be used f
ermination of Luci
P
enosine-5'-triphos
m. It can be used f
ermination of Luci
cohol Dehydrogen
ohol Dehydrogena
tems. Substrate sp
ecific activity is app
anol as the substra
eatine Kinase (CK
zyme expressed by
creatine and consu
hosphate.
ecific Activity - app
philizate at +37C)
ucose-6-phospha
cose-6-Phosphate
mpound is very com
ering a cell will be
bstrate for glucose-
og Numb
Product N

mpetitor in pre- an
binding of the prob
s a lyophilizate.
mpetitor in pre- an
binding of the prob
s a lyophilizate.
ue disaggregation
min, and plasma ka
bit metallo-, cystein
en egg white.
ue disaggregation
r Xa, plasmin, and
not inhibit metallo-
m soybean.
XOD)
f hypoxanthine to x
to uric acid. Plays
ies. Suspension in
Arylsulfatase
s hydrolysis of -g
gical fluids. Use to
n enzyme immobil
genase (L-LDH)
nase from rabbit m
ydroxycarboxylic a
M ammonium sulfa
genase (L-MDH)
nase (L-MDH) from
y catalyzes the oxi
f NAD
+
to NADH.
proximately 7.
genase (L-MDH)
nase (L-MDH) from
y catalyzes the oxi
f NAD
+
to NADH.
olution, pH approx.
omerase (PGI)
merase (PGI) from y
. Supplied as a sus
ately 6.
phate is supplied a
for applications, su
ferase activity in c
phate is supplied a
for applications, su
ferase activity in c
nase (ADH)
ase from yeast is a
pecificity is limited
prox. 300 U/mg en
ate.
K)
y various tissues an
umes ATP to create
prox. 350 U/mg lyo
).
ate
e is glucose sugar
mmon in cells, as t
come phosphoryla
-6-phosphatase.
ber
Name
nd hybridization so
be. From E. coli MR
nd hybridization so
be. From E. coli MR
and for subcultiva
allikrein activity in s
ne, aspartic protea
and for subcultiva
plasma kallikrein
-, cysteine, aspartic
xanthine and can
an important role
3.2 M ammonium
glucuronides and s
o remove cell walls
lization studies, an
muscle is used for
ate solution, pH ap
m pig heart (mitoc
idation of malate to
Supplied in soluti
m pig heart (mitoc
Supplied in suspe
6
yeast is used for th
spension in 3.2 M
as the disodium sa
uch as the luminom
cell extracts.
as the disodium sa
uch as the luminom
cell extracts.
component of NA
to low molecular w
zyme protein at +
nd cells. Catalyzes
e phosphocreatine
ophilizate at +25C
phosphorylated on
the vast majority o
ated in this way. It
olutions to
RE 600 (RNase
olutions to
RE 600 (RNase
tion procedures.
serum-free
ases, or tissue
tion procedures.
in serum-free
c proteases, or
further catalyze
in catabolism of
m sulfate, 10 mM
sulfate esters in
from yeast to
d to determine
the reduction of
action. Provided
pprox. 7.
hondrial) is an
o oxaloacetate
on in 50%
hondrial) is an
o oxaloacetate
ension in 3.2 M
he isomerization
ammonium
alt in crystal
metric
alt in crystal
metric
ADH recycling
weight alcohols.
25C with
the conversion
e and adenosine
C (800 U/mg
n carbon 6. This
f glucose
is used as a

Pack Size

100 mg
500 mg
1 g
50 mg
20 U (1 ml)
2 ml
10 mg (2 ml)
5 mg (1 ml)
5 mg (1 ml)
2 mg (1 ml)
5 g
10 g
1 g (34 ml)
100 mg
5 g

Price in

249,20
992,50
128,20
50,90
99,70
66,70
43,40
56,60
56,60
40,40
56,60
92,60
492,30
99,70
116,90

Pr

Cat.

10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
10 12
roducts b

No.
27 655 001 Glu
Glu
cofa
pho
solu
27 671 001 Glu
Glu
cofa
3.2
27 698 001 -
Use
urin
pre
dru
27 752 001 Gly
Glyc
prov
app
sub
27 779 001 Gly
Glyc
prov
app
sub
27 825 001 Hex
Hex
yea
sulf
G6P
27 833 001 3-H
3-H
hyd
27 841 001 3-H
3-H
hyd
27 876 001 L-L
L-L
-
in s
27 884 001 L-L
L-L
-
in s
27 914 001 L-M
L-M
enz
usin
amm
27 965 001 NA
Nic
It ac
prov
27 973 001 NA
Nic
It ac
prov
27 981 001 NA
Nic
It ac
prov
27 990 001 NA
Nic
It ac
prov
28 023 001 NA
NA
This
28 031 001 NA
Nic
ana
req
amo
by Catalo
ucose-6-Phospha
cose-6-Phosphate
actor recycling sys
osphate. Grade I fro
ution, pH approx. 6
ucose-6-Phospha
cose-6-Phosphate
actor recycling sys
M ammonium sulf
Glucuronidase/A
ed for simultaneou
ne and other biolog
pare protoplasts, i
gs in urine.
ycerol-3-Phospha
cerol-3-Phosphate
vided as a suspen
prox. 6. Specific act
bstrate (optimized c
ycerol-3-Phospha
cerol-3-Phosphate
vided as a suspen
prox. 6. Specific act
bstrate (optimized c
xokinase/Glucos
xokinase/Glucose-
st/Leuconostoc ov
fate suspension, pH
P-DH. Ratio of HK:
Hydroxybutyrate
Hydroxybutyrate De
droxymonocarboxy
Hydroxybutyrate
Hydroxybutyrate De
droxymonocarboxy
Lactate Dehydrog
actate Dehydroge
ketoacids to -hy
suspension in 3.2 M
Lactate Dehydrog
actate Dehydroge
ketoacids to -hy
suspension in 3.2 M
Malate Dehydrog
Malate Dehydrogen
ng the reduction o
monium sulfate so
D
otinamide adenine
cts as a coenzyme
vided as a lyophiliz
D
otinamide adenine
cts as a coenzyme
D
otinamide adenine
cts as a coenzyme
D
otinamide adenine
cts as a coenzyme
DH
DH is the reduced
s NADH Grade II, d
DP
otinamide adenine
abolic reactions, su
uire NADPH as a r
orphous powder.
og Numb
Product N

ate Dehydrogena
e Dehydrogenase (
stems for NADPH.
om yeast. Suspen
6.
ate Dehydrogena
e Dehydrogenase (
stems for NADPH.
fate solution, pH a
Arylsulfatase
s hydrolysis of -g
gical fluids. Use to
n enzyme immobil
ate Dehydrogena
e Dehydrogenase (
sion in 3.2 M amm
tivity: approx. 170
conditions).
ate Dehydrogena
e Dehydrogenase (
sion in 3.2 M amm
tivity: approx. 170
conditions).
se-6-Phosphate D
-6-Phosphate Dehy
verproducer. It is p
H approx. 6. Prepa
G6P-DH is approx
Dehydrogenase
ehydrogenase (3-H
lic acids, or the rev
Dehydrogenase
ehydrogenase (3-H
lic acids, or the rev
genase (L-LDH)
nase from rabbit m
ydroxycarboxylic a
M ammonium sulfa
genase (L-LDH)
nase from rabbit m
ydroxycarboxylic a
M ammonium sulfa
genase (L-MDH)
nase (L-MDH) from
y catalyzes the oxi
f NAD
+
to NADH.
olution, pH approx.
e dinucleotide is a
e in redox reactions
zate.
e dinucleotide is a
zate.
e dinucleotide is a
zate.
e dinucleotide is a
zate.
form of nicotinam
disodium salt is su
e dinucleotide pho
uch as lipid and nu
reducing agent. NA
ber
Name
ase (G6P-DH)
(G6P-DH) is a com
Additional reagen
sion in 3.2 M amm
ase (G6P-DH)
(G6P-DH) is a com
Grade II from yeas
approx. 6.
glucuronides and s
o remove cell walls
lization studies, an
ase (GDH)
(GDH) from rabbit
monium sulfate solu
U/mg at +25C wi
ase (GDH)
(GDH) from rabbit
monium sulfate solu
U/mg at +25C wi
Dehydrogenase (
ydrogenase is from
provided as a 3.2 M
ared by mixing hex
x. 2:1 (protein cont
(3-HBDH)
HBDH) selectively
verse reaction.
(3-HBDH)
HBDH) selectively
verse reaction.
muscle is used for
ate solution, pH ap
muscle is used for
ate solution, pH ap
m pig heart (mitoc
Supplied in suspe
6
coenzyme found i
s. This NAD Grade
coenzyme found i
s. This NAD Grade
coenzyme found i
s. This NAD Grade
coenzyme found i
s. This NAD Grade
mide adenine dinuc
upplied as an amor
osphate is a coenzy
ucleic acid synthes
ADP disodium is s
mponent of
t glucose-6-
monium sulfate
mponent of
st. Suspension in
sulfate esters in
from yeast to
d to determine
muscle is
ution, pH
th DAP as the
muscle is
ution, pH
th DAP as the
(HK/G6P-DH)
m
M ammonium
xokinase and
ent).
oxidizes (R)-3-
oxidizes (R)-3-
the reduction of
action. Provided
pprox. 7.
the reduction of
action. Provided
pprox. 7.
hondrial) is an
o oxaloacetate
ension in 3.2 M
in all living cells.
e I, free acid is
e I, free acid is
e II, free acid is
e II, free acid is
cleotide (NAD).
rphous powder.
yme used in
sis, which
upplied as an

Pack Size

5 mg (1 ml)
10 mg (2 ml)
10 ml
10 mg (1 ml)
100 mg (10 ml)
15 mg (5 ml)
10 mg (2 ml)
25 mg (5 ml)
25 mg (5 ml)
100 mg (10 ml)
25 mg (5 ml)
1 g
5 g
1 g
5 g
1 g
100 mg

Price in

310,90
192,40
245,90
105,40
650,50
156,20
134,40
294,90
86,80
293,50
159,10
84,10
284,60
59,20
241,50
147,30
66,40

237

e.com

Pr
238

www.r

Cat.

10 12
10 12
10 12
10 12
10 12
10 14
10 16
10 16
10 16
10 17
10 17
10 19
10 19
10 20
10 20
10 20
roducts b
roche-applied-sc

No.
28 040 001 NA
Nic
ana
req
amo
28 058 001 NA
Nic
ana
req
amo
28 139 001 Pho
Pho
of k
sulf
28 155 001 Pyr
Pyru
Cat
mol
amm
28 163 001 Pyr
Pyru
Cat
mol
amm
48 334 001 2,3
2,3-
diph
scie
65 875 001 Glu
Glu
mes
Add
amm
65 921 001 Pro
Mix
sing
tiss
of g
65 948 001 RNA
For
prot
poly
pro
71 832 001 Ald
Ald
NA
prot
74 645 001 Pol
Use
DNA
pho
with
97 734 001 Glu
Glu
for
BSA
97 777 001 DTT
For
extr
prot
mon
00 310 001 Eco
Eco
with
or b
isos
06 849 001 Chr
Use
prot
06 938 001 RNA
16S
gel
stru
by Catalo
cience.com
DP
otinamide adenine
uire NADPH as a r
orphous powder.
DP
otinamide adenine
uire NADPH as a r
orphous powder.
osphoglucose Iso
osphoglucose Isom
ketoses to aldoses.
fate, pH approxima
ruvate Kinase (PK
uvate Kinase from
alyzes the transfer
lecule of pyruvate
monium sulfate so
ruvate Kinase (PK
uvate Kinase from
alyzes the transfer
lecule of pyruvate
monium sulfate so
-Diphosphoglyce
-Diphosphoglycera
hosphoglycerate in
ence research app
ucose-6-Phospha
cose-6-Phosphate
senteroides is a co
ditional reagent glu
monium sulfate so
onase
x of nonspecific en
gle amino acids. D
ue dissociation alo
glycopeptides from
A, MS2
structural/function
tein-synthesizing s
ypeptide synthesis
cedures.
dehyde Dehydrog
ehyde Dehydrogen
DPH recycling syst
tein at +25C with
ynucleotide Kina
e to phosphorylate
A or RNA using [
osphate exchange,
hout altering their
utamate Dehydro
tamate Dehydroge
NAD(P) and NAD
A as a stabilizer, an
T
luminometric dete
racts. Superb prote
teins/enzymes (co
nothiols in the red
oR I
o RI recognizes the
h 5-cohesive term
both A residues, an
schizomer to Rsr I.
romozym TH
e Chromozym TH a
teases, specifically
A, 16S- and 23S
S- and 23S-ribosom
electrophoresis an
ucture and function
og Numb
Product N

e dinucleotide pho
uch as lipid and nu
reducing agent. NA
e dinucleotide pho
uch as lipid and nu
reducing agent. NA
omerase (PGI)
merase (PGI) from y
. Supplied as a sus
ately 6.
K)
rabbit muscle is a
r of a phosphate g
and 1 molecule of
olution, pH approx.
K)
rabbit muscle is a
r of a phosphate g
and 1 molecule of
olution, pH approx.
erate (2,3-DPG)
ate (2,3-DPG) is us
n blood in the rang
lications.
ate Dehydrogena
e Dehydrogenase (
omponent of cofac
ucose-6-phosphat
olution, pH approx.
ndo- and exoprotea
Degrade protein du
ong with collagena
m glycoproteins.
nal studies using n
systems, initiation,
s. Also used as a ca
genase
nase from yeast is
tems. Specific acti
acetaldehyde as t
ase
5' ends of DNA o
-
32
P]-ATP either
and to remove 3'-
5' ends (at low pH
ogenase (GlDH)
enase is a compon
(P)H. The formulat
nd ADP as an activ
ermination of Lucif
ective reagent for s
ompared to -mer
uced state and qu
e sequence G*A*A
mini. EcoR I is inhib
nd by 5-methylcyto
y thrombin in aque
-ribosomal
mal RNA is used as
nd ultracentrifugat
n of ribosomes.
ber
Name
osphate is a coenzy
ucleic acid synthes
ADP disodium is s
osphate is a coenzy
ucleic acid synthes
ADP disodium is s
yeast is used for th
spension in 3.2 M
an enzyme involved
roup from PEP to A
f ATP. Suspension
6.
an enzyme involved
roup from PEP to A
f ATP. Suspension
6.
sed for the determ
ge of 0.02 - 0.15 m
ase (G6P-DH)
(G6P-DH) from Le
te. Suspension in 3
6.
ases that digest pr
ring DNA and RNA
ase and trypsin. Us
natural RNA in in v
elongation, and te
arrier in sensitive R
a component of N
vity is approx. 20 U
the substrate.
r RNA, label 5'-hyd
by direct phospho
-phosphates from
H only).
nent of cofactor rec
tion contains buffe
vator.
ferase gene activit
sulfhydryl groups o
rcaptoethanol). Ma
uantitatively reduce
ATT*C and genera
bited by 6-methylad
osine as indicated
the determination o
esous solutions.
s a molecular weig
tion; also used to s
yme used in
sis, which
upplied as an
yme used in
sis, which
upplied as an
he isomerization
ammonium
d in glycolysis.
ADP, yielding 1
in 3.2 M
d in glycolysis.
ADP, yielding 1
in 3.2 M
ination of 2,3-
mol in life
uconostoc
ems for NADPH.
3.2 M
rotein down to
A isolation. For
se in production
vivo and in vitro
ermination of
RNA purification
NADH and
U/mg enzyme
droxyl ends of
orylation or by
RNA or DNA
cycling systems
er substances,
ty in cell
of
aintains
es disulfides.
tes fragments
denine at either
(*). Eco RI is an
of serine
ght standard in
study the

1 kit fo
5
1
Pack Size

500 mg
1 g
10 mg (1 ml)
10 mg (1 ml)
100 mg (10 ml)
or approximately 3
1,000 U (1 ml)
1 g
500 l (10 A
260
unit
250 U
200 U
3,000 U
2 g
10,000 U (40 U/l)
20 mg
ml (100 A
260
units
30 tests
ts)
)
s)

Price in

262,70
396,10
137,20
84,10
333,70
352,10
105,40
108,30
123,10
211,00
217,20
47,80
inquire
52,30
290,60
129,20

Pr

Cat.

10 22
10 22
10 22
10 22
10 22
10 22
10 23
10 23
10 23
10 23
10 24
10 24
10 25
10 26
10 26
roducts b

No.
20 566 001 Sm
Rec
Not
othe
Neo
20 612 001 Bam
Rec
coh
met
resi
20 647 001 GTP
GTP
hyd
the
pow
23 549 001 His
Lys
kina
exit
form
23 565 001 His
Nat
Hist
pac
the
23 581 001 Pol
Poly
cha
36 250 001 DN
For
mol
gen
23.1
36 276 001 DA
DAP
and
spe
fluo
36 624 001 Apr
Prot
cult
chy
qua
39 275 001 Alu
Alu
blun
hyd
Isos
40 354 001 NA
Nic
ana
req
amo
44 678 001 For
Mos
deh
cyst
53 286 001 Pep
Prot
inve
clas
pha
69 611 001 Neu
From
acy
muc
sial
69 638 001 Col
Col
vari
Col
dete
by Catalo
ma I
cognizes sequence
t inhibited by 5-me
er positions or 4-m
oschizomers: Cfr9
mH I
cognizes the seque
hesive termini. Bam
thylation, but is inh
due as indicated (
P--S
P--S activates gu
drolyzed enzymatic
stimulation of ade
wder.
stone H1
ine-rich preparatio
ases. The linker his
t sites of the DNA,
mation of higher o
stone
tural mixture of his
tones are highly al
ckage and order th
primary compone
y(dA)
y(dA) was prepare
ain length is 250-50
A Molecular We
size distribution a
lecular weight dete
nerated by restricti
1 kbp.
PI
PI is a fluorescent
d forms strongly flu
ecificity. It is comm
orescence microsc
rotinin
tect proteins durin
ture studies. Used
ymotrypsin on imm
antification of kallik
u I
I recognizes the s
nt termini. It is inh
droxymethylcytosin
schizomer: AluB I.
DP
otinamide adenine
uire NADPH as a r
orphous powder.
rmate Dehydroge
st widely used in c
hydrogenase is a d
teine residue whic
pstatin
tect proteins and e
estigation of enzym
ssifications. For aff
armacological, HIV
uraminidase (Sia
m Arthrobacter ure
lneuraminic acids,
copolysaccharides
ic acids from glyco
llagenase/Dispas
lagenase/Dispase
ety of different tiss

lagenase/Dispase
ermined empirical
og Numb
Product N

e*CC*CGGG. Gen
ethylcytosine at mi
methylcytosine in e
I, TspM I, Xma I, X
ence GGAT*CC
m H I is not inhibite
hibited by 5- or 4-m
(*). Isoschizomer: B
uanine-nucleotide
cally. It inhibits GTP
enylate cyclase. Su
on from calf thymu
stone H1 binds the
locking the DNA
rder structure.
stones H1, H2A, H2
lkaline proteins fou
he DNA into struct
nt of chromatin.
ed from dATP using
00 bases and varie
ight Marker II
analysis using agar
ermination of doub
on digests, PCR, a
dye that binds sel
uorescent DNA-DA
only used to detec
opy.
ng isolation/purific
for purification of
mobilized aprotinin,
krein activity.
sequence *AG*CT
ibited by 6-methyl
e,or 4-methylcytos
e dinucleotide pho
uch as lipid and nu
reducing agent. NA
enase
cofactor recycling
imer of two identic
ch is essential for a
enzymes during iso
me mechanisms, b
finity chromatogra
V, and cancer resea
alidase)
eafaciens ; hydrolyz
, 2,3-, 2,6-, or
s, glycoproteins, an
oconjugates of a w
se
is used for the p

sues and organs. T
for preparation o
ly.
ber
Name
nerates fragments
ddle C(). 5-methy
either position inhi
XmaC I.
and generates fra
ed by overlapping
methylcytosine at t
BstI.
-binding proteins,
Pases more potent
upplied as a tetralit
us used as a subst
e nucleosome and
into place and allo
2B, H3, and H4 fro
und in eukaryotic c
ural units (nucleos
g terminal transfer
es by lot.
rose gels. Simplifie
ble-stranded DNA
and RT-PCR. Size r
ectively to double-
API complexes wit
ct Mycoplasma in
ation, increasing c
urokinase, trypsin
protein-folding st
T and generates fra
adenine, 5-methyl
sine at the (*) in th
osphate is a coenzy
ucleic acid synthes
ADP disodium is s
systems for NADH
cal subunits. The e
activity or structura
olation and purific
iological function,
phy, and structura
arch.
zes terminal N- or
2,8-linked to ol
nd glycolipids. Com
wide variety of biolo
preparation of cells
The suitability of
of a particular cell
with blunt ends.
ylcytosine at
bits(*).
agments with 5'-
dam
the internal C
and is slowly
tly than GTP in
thium salt
rate for protein
the entry and
owing the
m calf thymus.
cell nuclei that
somes). They are
rase. Mean
es accurate
A fragments
ange: 0.12 to
-stranded DNA
h high
cell culture via
cell lifetime in
, and
tudies, and
agments with
cytosine, 5-
he sequence.
yme used in
sis, which
upplied as an
H. Formate
enzyme has a
al integrity.
ation. Facilitates
and protease
al,
r 0-
igo-, poly-, and
mpletely remove
ogical materials.
s from a wide
type must be

50 g in 200 l
Pack Size

1,000 U (10 U/l)
1,000 U (10 U/l)
10 mg
1 mg
10 mg
5 A
260
units
(1 A
260
unit) for up
10 mg
10 mg
500 U (10 U/l)
5 g
80 U
2 mg
1 U (100 l)
100 mg
www.roche

p to 50 gel lanes
e-applied-science

Price in

104,60
29,50
319,50
200,10
193,80
193,20
100,10
68,20
69,70
78,80
1.549,00
125,70
42,60
262,60
130,80

239

e.com

Pr
240

www.r

Cat.

10 28
10 29
10 34
10 34
10 35
10 37
10 37
10 38
10 40
10 41
10 47
10 47
10 47
10 48
10 48
10 51
roducts b
roche-applied-sc

No.
80 879 001 5-B
5-B
that
stud
sist
95 892 001 Col
Colc
the
48 767 001 Bgl
Rec
coh
but
Bgl
48 783 001 Sal
Sal
5-c
met
Isos
54 074 001 Citr
Cat
enz
mol
78 445 001 Chr
Use
prot
78 461 001 Chr
Use
prot
80 385 001 Hpa
Rec
blun
as i
Isos
04 217 001 Cla
Rec
coh
met
I, Bs
11 523 001 Luc
Det
acti
rele
suff
76 480 001 NA
Use
and
acti
sub
76 498 001 Luc
Bac
the
form
76 986 001 End
Use
seq
81 220 001 T4
Use
Cat
hyd
nick
81 238 001 pBR
Sele
clea
site
inac
19 979 001 ATP
ATP
lum
spe
trip

by Catalo
cience.com
Bromo-2'-deoxyu
Bromo-2'-deoxyurid
t can be incorpora
dies of DNA synth
er chromatid exch
lcemid
cemid inhibits the
percentage of me
l II
cognizes the seque
hesive termini. It is
is sensitive to 5-m
II has no known is
I
I recognizes the se
cohesive termini. S
thyladenine within
schizomers: none k
rate Lyase (CL)
alyzes the cleavag
zyme complex that
lecular weights ab
romozym PK
e Chromozym PK a
romozym PL
e Chromozym PL a
a I
cognizes the seque
nt ends. Inhibited
ndicated (*). 5-me
schizomers: KspA
a I
cognizes the seque
thylcytosine as sho
spD I, BspX I, Bsu1
ciferase
termine ATP in ATP
vity of enzymes su
eased per molecule
ficient for 5,000 AT
D(P)H:FMN Oxid
e with luciferase fro
d for reactions in w
vity: approx. 7 U/m
bstrate, and NADH
ciferase
cterial luciferase us
determination of N
med or consumed.
doproteinase Lys
e Endoproteinase L
uence analysis.
DNA Ligase
e T4 DNA ligase to
alyzes formation o
droxyl- and 5'-phos
ks in dsDNA are a
R322 DNA
ectable plasmid fo
avage sites in the a
s in the tetracyclin
ctivating these dru
P
P is supplied as the
minometric determi
ecial quality prepar
hosphate in crysta
og Numb
Product N

uridine
dine is an immuno
ated into DNA inste
esis, and to detect
ange (SCE).
formation of mitot
etaphase cells for c
ence AGAT*CT a
not inhibited by ov
methyl and 5-hydro
soschizomers.
equence GT*CG*
Sal I is inhibited by
the recognition se
known.
ge of citrate to acet
consists of three d
bout 54,000, 32,000
y plasma kallikrein
as a substrate for th
y plasmin in aqueo
ence GTT*AAC a
by 6-methyladenin
ethylcytosine does
I.
ence *AT*CG*AT
inhibited by overla
own (*). Isoschizom
15 I, BsuTU I.
P generating or AT
uch as creatine kin
e ATP in biolumine
TP determinations
doreductase
om Photobacterium
which NAD(P)H is f
mg lyophilizate at +
as the coenzyme.
sed together with
NAD(P)H, and for
From Photobacter
s-C
Lys-C for protein s
o join sticky- or blu
of phosphodiester
sphate ends in dou
lso closed by T4 D
r cloning of recom
ampicillin gene, or
ne gene, allow fore
ug resistance gene
e disodium salt. Us
nation of Luciferas
ration contains hig
al form.
ber
Name
ochemically detecta
ead of thymidine. U
t mutagenic substa
tic spindles. It is us
chromosome analy
and generates frag
verlapping dam m
oxy-methylcytosine
*AC and generates
5-methylcytosine
equence as indica
tate and oxaloacet
different polypepti
0, and 10,000, respe
he determination o
in citrated plasma
he determination o
ous solutions.
and generates frag
ne and 5-hydroxym
not influence the
and generates fra
apping dam-methy
mers: Ban III, Bsa29
TP consuming reac
nase/ATPases. One
escence assays. On
in concentration 0
m fischeri to deter
formed or consum
+25C and pH 7.0 w

NAD(P)H:FMN ox
reactions in which
rium fischeri .
structure analysis a
unt-ended DNA fra
bonds between ne
uble-stranded DNA
DNA Ligase.
mbinant DNA. Pst I
r Cla I, Hind III, Bam
eign DNA to be ins
es.
se in applications,
se activity in cell e
ghly purified adeno
able nucleotide
Used for in vivo
ances using
sed to increase
ysis.
gments with 5-
ethylation (),
e, as shown (*).
s fragments with
and N6-
ted (*).
tate, and is an
de chains with
ectively.
of serine
a.
of serine
gments with
methylcytosine
cleavage ().
gments with 5'-
ylation and 5-
9 I, BseC I, BshV
ctions, and
e photon is
ne milligram is
0.1 nM to 1 M.
rmine NAD(P)H,
med. Specific
with FMN as the
idoreductase for
h NAD(P)H is
and for
agments.
eighboring 3'-
A. Single-strand
and Pvu I
m HI, and Sal I
serted for
such as the
extracts. This
osine-5'-

20 ml ((10 g/

Pack Size

1 g
size membrane)
500 U (10 U/l)
500 U (10 U/l)
120 U
20 mg
20 mg
100 U (3 - 10 U/l
500 U (10 U/l)
1 mg protein
20 U
2 mg protein
3 U
100 U (1 U/l)
200 l 1 A
260
unit
1 g
gh 0.2 m pore
)
t

Price in

70,00
45,10
68,20
53,40
163,30
369,90
362,60
75,00
75,00
148,90
232,70
152,90
325,60
87,20
212,30
50,50

Pr

Cat.

10 51
10 52
10 56
10 56
10 56
10 56
10 56
10 56
10 60
10 60
10 60
10 60
10 60
10 60
10 62
10 62
roducts b

No.
19 987 001 ATP
ATP
lum
spe
trip
28 552 001 DN
For
dete
rest
67 604 001 Bam
Rec
coh
met
resi
67 639 001 Bgl
Rec
coh
but
Bgl
67 647 001 Hpa
Rec
blun
as i
Isos
67 663 001 Sal
Sal
5-c
met
Isos
67 671 001 Taq
Taq
coh
indi
67 752 001 Alk
Calf
its a
for
02 361 001 Pla
Use
use
rese
02 370 001 Pla
Use
use
rese
02 400 001 Thr
Use
prot
Thro
02 442 001
2

2

end
spe
uro
06 120 001 Sph
Rec
coh
met
hyd
06 189 001 Eco
Eco
with
or b
isos
21 625 001 Pst
Pst
3-c
and
21 633 001 Pst
Pst
3-c
and
by Catalo
P
P is supplied as the
minometric determi
ecial quality prepar
hosphate in crysta
A Molecular We
size distribution in
ermination of doub
triction digests, PC
mH I
cognizes the seque
hesive termini. Bam
due as indicated (
l II
cognizes the seque
is sensitive to 5-m
II has no known is
a I
cognizes the seque
nt ends. Inhibited
ndicated (*). 5-me
schizomers: KspA
I
I recognizes the se
cohesive termini. S
thyladenine within
schizomers: none k
q I
q l recognizes the s
hesive termini. Taq
icated (*). Isoschiz
kaline Phosphata
f Intestine Alkaline
amino groups. This
conjugation witho
asmin, human
e Plasmin, human i
ed for protein struc
earch. The enzyme
asmin, bovine
e Plasma, bovine in
ed for protein struc
earch. The enzyme
rombin
e Thrombin in coag
tein-structure ana
ombin contains ED
-Macroglobulin
-Macroglobulin is
doproteinases. Not
ecific for one or a li
kinase, factor XIIa
h I
cognizes the seque
hesive termini. Inhi
thylcytosine at 3'-C
droxymethylcytosin
oR I
o RI recognizes the
h 5-cohesive term
both A residues, an
schizomer to Rsr I.
t I
I recognizes the se
cohesive termini. P
d 6-methyladenine
t I
I recognizes the se
cohesive termini. P
d 6-methyladenine
og Numb
Product N

e disodium salt. Us
nation of Luciferas
ration contains hig
al form.
ight Marker III
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
ence GGAT*CC
ence AGAT*CT a
not inhibited by ov
methyl and 5-hydro
soschizomers.
ence GTT*AAC a
by 6-methyladenin
ethylcytosine does
I.
equence GT*CG*
the recognition se
known.
sequence TCG*A
I is inhibited by ov
zomers: Tth HB8 I.
ase
e Phosphatase can
s ready-to-use enz
ut prior dialysis; EI
in coagulation rese
cture analysis, sequ
e converts fibrin in
n coagulation rese
cture analysis, sequ
e converts fibrin in
gulation, biochemi
lysis. The enzyme
DTA and additiona
s a protease inhibit
t affected are endo
imited number of s
, and endoproteina
ence GC*ATG?C.
bited by 6-methyla
C() or simultaneou
e at both Cs. Isosc
e sequence G*A*A
nd by 5-methylcyto
equence *CTGCA
Pst I is inhibited by
, as indicated (*). I
equence *CTGCA
ber
Name
se in applications,
se activity in cell e
ghly purified adeno
mplifies accurate m
A fragments genera
ize range: 0.12 to 2
and generates fra
ed by overlapping
methylcytosine at t
BstI.
and generates frag
verlapping dam m
oxy-methylcytosine
and generates frag
ne and 5-hydroxym
not influence the
*AC and generates
5-methylcytosine
equence as indica
A and generates fra
verlapping dam-m
n be coupled to oth
zyme solution can
IA Grade, 10 mg/m
earch and medica
uence analysis, an
to soluble product
arch and in medic
uence analysis, an
to soluble product
cal and medical re
converts fibrinoge
al stabilizing agents
tor that blocks mos
oproteinases that a
sequences (tissue
ase Lys-C).
Generates fragme
adenine(*). No inh
us presence of 5-
chizomers: Bbu I, P
ATT*C and genera
bited by 6-methylad
osine as indicated
AG and generates
the presence of 5
soschizomers: Bsp
AG and generates
the presence of 5
soschizomers: Bsp
such as the
extracts. This
osine-5'-
molecular weight
ated by
21.2 kbp.
agments with 5'-
dam
the internal C
gments with 5-
ethylation (),
e, as shown (*).
gments with
methylcytosine
cleavage ().
s fragments with
and N6-
ted (*).
agments with 5'-
ethylation, as
her proteins via
be used directly
ml solution.
l research. It is
d biochemical
ts.
cal research. It is
d biochemical
ts.
esearch, and
en to fibrin.
s.
st
are highly
kallikrein,
nts with 3-
ibition by 5-
Pae I
tes fragments
denine at either
(*). Eco RI is an
s fragments with
-methylcytosine
pMA I.
s fragments with
-methylcytosine
pMA I.

50 g in 200 l
Pack Size

5 g
(1 A
260
unit) for up
2,500 U (10 U/l)
2,000 U (10 U/l)
500 U (3 - 10 U/l
2,500 U (10 U/l)
2,500 U (10 U/l)
15 mg (1.5 ml)
5 U (0.5 ml)
5 U (1 ml)
20 U
25 inhibitor units
500 U (10 U/l)
50,000 U (40 U/l)
3,000 U (10 U/l)
10,000 U (10 U/l)
www.roche
p to 50 gel lanes

)

)

)
e-applied-science

Price in

199,40
111,00
57,90
181,90
300,10
203,60
104,60
647,10
201,00
216,90
125,70
108,30
268,20
210,30
90,90
225,20

241

e.com

Pr
242

www.r

Cat.

10 62
10 62
10 62
10 62
10 62
10 63
10 63
10 64
10 64
10 64
10 64
10 65
10 65
10 65
10 65
10 65
10 65
roducts b
roche-applied-sc

No.
21 650 001 NA
Nic
It ac
prov
21 692 001 NA
NA
prov
21 706 001 NA
NA
prov
21 714 001 Cre
Sub
mol
pho
21 722 001 Cre
Sub
mol
pho
33 542 001 Pol
Use
DNA
pho
with
34 425 001 n-O
n-O
solu
dial
42 690 001 Pvu
Pvu
blun
reco
42 703 001 Pvu
Pvu
blun
reco
42 711 001 DN
This
con
tran
42 720 001 DN
This
con
tran
50 129 001 Pvu
Rec
coh
Inhi
Isos
50 137 001 Pvu
Rec
coh
Inhi
Isos
51 745 001 X-G
Use
pro
met
dete
52 202 001 Tra
Tran
form
cell
56 267 001 Alu
Alu
blun
hyd
Isos
56 275 001 Bam
Rec
coh
met
resi
by Catalo
cience.com
D
otinamide adenine
cts as a coenzyme
DPH
DPH is the reduce
vided as an amorp
DPH
DPH is the reduce
vided as an amorp
eatine phosphate
bstrate for creatine
lecule that serves
osphates in skeleta
eatine phosphate
bstrate for creatine
lecule that serves
osphates in skeleta
ynucleotide Kina
e to phosphorylate
A or RNA using [
osphate exchange,
hout altering their
Octylglucoside
Octylglucoside is a
ubilization and rec
ysis. CMC: 14.5 m
u II
u II recognizes the
nt ends. Pvu II is in
ognition sequence
u II
u II recognizes the
nt ends. Pvu II is in
ognition sequence
A Polymerase I
s recombinant DN
ntain DNase I). It ca
nslation (with adde
A Polymerase I
s recombinant DN
ntain DNase I). It ca
nslation (with adde
u I
cognizes the seque
hesive termini. Not
ibited by 5-methyl
schizomers: BpvU
u I
cognizes the seque
hesive termini. Not
ibited by 5-methyl
schizomers: BpvU
Gal
e X-Gal for immuno
duct has a blue co
thanol. It is not sol
ected.
ansferrin
nsferrin, like insuli
mulations. The mai
s by receptor-med
u I
I recognizes the s
nt termini. It is inh
droxymethylcytosin
schizomer: AluB I.
mH I
cognizes the seque
hesive termini. Bam
due as indicated (
og Numb
Product N

e dinucleotide is a
zate.
ed form of NADP
+
.
phous powder bott
ed form of NADP
+
.
phous powder bott
e
e kinase. The enzym
as a rapidly mobili
al muscle and brai
e
e kinase. The enzym
as a rapidly mobili
al muscle and brai
ase
5' ends of DNA o
-
32
P]-ATP either
and to remove 3'-
5' ends (at low pH
mild, nonionic, no
onstitution of mem
M at +25C.
sequence CAG*C
nhibited by 5'- and
e as indicated (*). I
sequence CAG*C
nhibited by 5'- and
A Polymerase I is
an therefore be us
ed DNase I) and se
A Polymerase I is
an therefore be us
ed DNase I) and se
ence CGAT*CG,
inhibited by overla
cytosine as shown
I, Mvr I, Ple19 I.
ence CGAT*CG,
inhibited by overla
cytosine as shown
I, Mvr I, Ple19 I.
ohistocytochemist
olor and is soluble
uble in water. The
n, is a component
in function of trans
diated endocytosis
sequence *AG*CT
ibited by 6-methyl
e,or 4-methylcytos
ence GGAT*CC
ber
Name
coenzyme found i
s. This NAD Grade
. NADPH tetrasodi
tled under nitrogen
. NADPH tetrasodi
tled under nitrogen
me is a phosphory
izable reserve of h
n.
me is a phosphory
izable reserve of h
n.
r RNA, label 5'-hyd
by direct phospho
-phosphates from
H only).
on-denaturing dete
mbrane proteins. E
CTG and generates
d 4'-methylcytosine
soschizomers: non
CTG and generates
d 4'-methylcytosine
soschizomers: non
endonuclease-free
sed for labeling of
econd-strand synt
endonuclease-free
sed for labeling of
econd-strand synt
generating fragme
apping dam-methy
n (*) and 4-methylc
generating fragme
apping dam-methy
n (*) and 4-methylc
try applications. Th
in dimethylformam
e blue color can be
t of most serum-fre
sferrin is to transp
.
T and generates fra
adenine, 5-methyl
sine at the (*) in th
and generates fra
ed by overlapping
methylcytosine at t
BstI.
e II, free acid is
um salt is
n.
um salt is
n.
ylated creatine
igh-energy
ylated creatine
igh-energy
droxyl ends of
orylation or by
RNA or DNA
ergent for the
asily removed by
s fragments with
e within the
ne known.
s fragments with
e within the
ne known.
e (does not
DNA by nick
hesis of cDNA.
e (does not
DNA by nick
hesis of cDNA.
ents with 3-
ylation ().
cytosine.
ents with 3-
ylation ().
cytosine.
he reaction
mide and
e visually
ee media
ort iron into
agments with
cytosine, 5-
he sequence.
agments with 5'-
dam
the internal C

20 ml (30 mg/
m
Pack Size

10 g
500 mg
1 g
5 g
10 g
1,000 U
10 g
1,000 U (10 U/l)
5,000 U (10 U/l)
250 U
1,000 U
500 U (5 U/l)
100 U (5 U/l)
250 mg
pore size membra
2,000 U (10 U/l)
10,000 U (10 U/l)

red through 0.2
ane)

)

Price in

433,50
791,80
1.462,40
98,30
179,20
864,20
741,50
51,10
213,80
146,20
486,00
331,90
84,20
148,00
496,70
228,50
199,10

Pr

Cat.

10 65
10 65
10 65
10 65
10 65
10 66
10 66
10 66
10 66
10 66
10 66
10 67
10 67
10 67
roducts b

No.
56 291 001 Cla
Rec
coh
met
I, Bs
56 305 001 Hin
Rec
blun
inhi
reco
56 313 001 Hin
Rec
coh
hyd
inhi
56 321 001 Hin
Rec
coh
hyd
inhi
56 348 001 Sm
Rec
Not
othe
Neo
62 046 001 -
Sus
gen
fluo
gala
63 573 001 BM
Sup
RPM
and
cell
67 145 001 Eco
Rec
blun
(*).
Hyd
67 153 001 Eco
Rec
blun
(*).
Hyd
69 792 001 Sac
Rec
coh
met
().
69 806 001 Sac
Rec
coh
met
().
74 257 001 Xba
Rec
term
gen
hyd
74 265 001 Xba
Rec
term
gen
hyd
74 273 001 Xba
Rec
term
gen
hyd

by Catalo
a I
cognizes the seque
thylcytosine as sho
spD I, BspX I, Bsu1
nd II
cognizes the seque
nt ends. Inhibited
ibited by 5-hydroxy
ognition sequence
nd III
cognizes the seque
droxymethylcytosin
ibit (). Isoschizom
nd III
cognizes the seque
droxymethylcytosin
ibit (). Isoschizom
ma I
cognizes sequence
t inhibited by 5-me
er positions or 4-m
oschizomers: Cfr9
Galactose Dehyd
spension in 3.2 M a
ne for -galactose
orescens strain BM
actosidase promot
M-Condimed
pplement (10%, v/v
MI 1640, DMEM), c
d chorionic villi cell
s and peripheral b
oR V
cognizes the seque
nt ends. Inhibited
It is not inhibited b
droxymethylcytosin
oR V
cognizes the seque
nt ends. Inhibited
droxymethylcytosin
c I (Sst I)
cognizes the seque
thylcytosine at the
Isoschizomers: Ps
c I (Sst I)
cognizes the seque
thylcytosine at the
Isoschizomers: Ps
a I
cognizes sequence
mini. Requires at l
ne which methylate
droxymethylcytosin
a I
cognizes sequence
mini. Requires at l
ne which methylate
droxymethylcytosin
a I
cognizes sequence
mini. Requires at l
ne which methylate
droxymethylcytosin
og Numb
Product N

ence *AT*CG*AT
inhibited by overla
own (*). Isoschizom
15 I, BsuTU I.
ence GTPyPu*AC
by 6-methyladenin
ymethylcytosine at
e. Isoschizomer: Hi
ence *AAG*CTT
bited by 6-methyla
e also inhibits. 6-m
mers: none known.
ence *AAG*CTT
bited by 6-methyla
mers: none known.
e*CC*CGGG. Gen
ethylcytosine at mi
methylcytosine in e
I, TspM I, Xma I, X
drogenase S
ammonium sulfate
e Dehydrogenase S
MTU 102, placed un
ter in the plasmid p
v) to normal cultur
containing 10-20%
ls. Improves cultur
blood leukocytes.
ence G*ATATC a
by the presence of
by the presence of
ne. Isoschizomer: E
ence G*ATATC a
by the presence of
by the presence of
ne. Isoschizomer: E
ence GAG*CTC a
bited by 5-methylc
other C does not
p124B I, Sst I.
ence GAG*CTC a
bited by 5-methylc
other C does not
p124B I, Sst I.
e T*CTAGA. Gene
east two nucleotid
es 6N of adenine i
e inhibit at (*). Iso
e T*CTAGA. Gene
east two nucleotid
es 6N of adenine i
e T*CTAGA. Gene
east two nucleotid
es 6N of adenine i
ber
Name
and generates fra
apping dam-methy
C and generates fra
ne as indicated (*).
t the 3-C residue o
nc II.
and generates fra
adenine or 5-meth
methyladenine at A
and generates fra
adenine or 5-meth
methyladenine at A
nerates fragments
ddle C(). 5-methy
XmaC I.
e, 1 mM EDTA, pH
S is from the Pseu
nder the control of
pUR 51.
re basal medium (e
% FCS to cultivate h
re conditions for bo
and generates frag
f 6-methyladenine
f 5-methylcytosine
Eco 32I.
and generates frag
f 6-methyladenine
f 5-methylcytosine
Eco 32I.
and generates frag
cytosine at the cen
inhibit, nor does 6
and generates frag
cytosine at the cen
inhibit, nor does 6
erates fragments w
des around target s
nhibits; 5-methylcy
schizomers: none.
erates fragments w
des around target s
nhibits; 5-methylcy
schizomers: none.
erates fragments w
des around target s
nhibits; 5-methylcy
schizomers: none.
gments with 5'-
ylation and 5-
9 I, BseC I, BshV
agments with
. Hind II is
of the
gments with 5-
ylcytosine (*). 5-
A does not
gments with 5-
ylcytosine (*). 5-
A does not
with blunt ends.
ylcytosine at
bits(*).
approx. 6. The
domonas
f an E. coli -
e.g., F 10, M 199,
human amniotic
one marrow
gments with
e, as indicated
e () or 5-
gments with
e, as indicated
e () or 5-
gments with 3-
ntral C (*). 5-
6-methyladenine
gments with 3-
ntral C (*). 5-
6-methyladenine
with 5-cohesive
sequence; dam
ytosine and 5-
with 5-cohesive
sequence; dam
ytosine and 5-
with 5-cohesive
sequence; dam
ytosine and 5-

2

Pack Size

2,500 U (10 U/l)
2,500 U (3 - 10 U/
5,000 U (10 U/l)
10,000 U (10 U/l)
5,000 U (10 U/l)
50 U
100 ml
2,000 U (10 U/l)
10,000 U (10 U/l)
1,000 U (10 U/l)
5,000 U (10 U/l)
1,000 U (10 U/l)
5,000 U (10 U/l)
20,000 U (10 U/l)
www.roche

l)

)

)

)
e-applied-science

Price in

299,10
475,30
55,80
98,80
365,00
264,60
291,90
75,00
282,00
90,90
340,00
45,50
105,80
400,20

243

e.com

Pr
244

www.r

Cat.

10 68
10 69
10 69
10 70
10 70
10 70
10 70
10 70
10 70
10 70
10 70
10 70
10 71
10 71
10 71
roducts b
roche-applied-sc

No.
88 541 001 Cfo
Rec
coh
sim
Isos
93 944 001 Hae
Rec
end
C*.
Isos
93 952 001 Bcl
Rec
coh
pos
met
03 729 001 X-G
Use
pro
met
dete
03 737 001 Eco
Eco
with
or b
isos
03 753 001 Apa
Apa
with
indi
120
03 770 001 Xho
Xho
with
met
Pae
03 788 001 Xho
Xho
with
met
Pae
08 976 001 Tris
Tris
com
pre
08 984 001 DTT
For
extr
prot
mon
09 557 001 T4
Pho
RNA
CM
labe
09 751 001 Sau
Rec
term
5- a
Isos
11 454 001 Bov
Spe
che
prot
13 023 001 Alk
Calf
pho
clon
Hig
16 359 001 T4
Use
Cat
hyd
nick
by Catalo
cience.com
o I (Hha I)
cognizes the seque
ultaneous presenc
schizomers: AspLE
e III
cognizes the seque
ds. Inhibited by 5-m
Inhibited by 5-hyd
schizomers: BshF I
I
cognizes the seque
sition of adenine. In
thylcytosine. Isosch
Gal
e X-Gal for immuno
duct has a blue co
ected.
oR I
o RI recognizes the
h 5-cohesive term
both A residues, an
schizomer to Rsr I.
a I
a I recognizes the s
h 3-cohesive term
icated (*) in the re
0 I and Psp OMI.
o I
o I recognizes the s
h 5-cohesive term
thyladenine and 5-
eR7 I, Sfr274 I, Sla
o I
h 5-cohesive term
thyladenine and 5-
s base
s Base is extensive
mponent of buffer s
paration is free of
T
luminometric dete
racts. Superb prote
teins/enzymes (co
nothiols in the red
Polynucleotide K
osphorylate 5'-hydr
A and DNA, 3' end
MP, forming 5'[
32
P]p
eling of RNA with
u3A I
cognizes sequence
mini. No inhibition
and 4-methylcytos
schizomers: Mbo I,
vine Serum Album
ecial BSA quality fo
ecked for the absen
teases, and is used
kaline Phosphata
f Intestinal Alkaline
osphates from DNA
ning efficiency by
her conc. 20 U/l
DNA Ligase
e T4 DNA ligase to
alyzes formation o
droxyl- and 5'-phos
ks in dsDNA are a
og Numb
Product N

ence G*CG*C and
bited by 5-methylc
ce of 5-hydroxyme
E I, BstHH I, Hha I.
ence GG*CC, ge
methyl and 5-hydro
droxymethylcytosin
, Bsn I ,BspAN I, B
ence TG*AT*CA, g
bited by the dam g
nhibited by 5-hydr
hizomers: Fba I, Ks
ohistocytochemist
olor and is soluble
uble in water. The
e sequence G*A*A
nd by 5-methylcyto
sequence GGG*CC
mini. It is inhibited b
cognition sequenc
sequence *CT*CG
mini. Xho I is inhibit
-methylcytosine as
I, Str I, Tli I.
sequence *CT*CG
-methylcytosine as
I, Str I, Tli I.
ly used in biochem
solutions, especial
proteases, DNase
ermination of Lucif
ompared to -mer
uced state and qu
Kinase, 3'-phosph
roxyl ends of oligo
ds of RNA, and add
pCp. This substrate
T4 RNA ligase.
e GAT*C. Genera
by dam gene whic
ine, 5-hydroxymet
, Nde II, Dpn II and
min
or molecular biolog
nce of DNases, nic
d to stabilize enzym
ase
e Phosphatase (1
A or RNA in small-
preventing self liga
enzyme is also ava
of phosphodiester
sphate ends in dou
lso closed by T4 D
ber
Name
d generates fragm
cytosine, as shown
ethylcytosine at bot
nerating fragment
oxymethylcytosine
ne at the external C
BsuR I, Pho I.
generating fragme
gene and methylat
roxymethyl-cytosin
sp22 I.
in dimethylformam
e blue color can be
ATT*C and genera
bited by 6-methylad
osine as indicated
C*C and generate
by 5'-methylcytosin
ce. Apa I is a neosc
G*AG and generat
ted by the presenc
s indicated (*). Isos
G*AG and generat
ted by the presenc
mistry and molecul
lly for nucleic acid
s and RNases.
ferase gene activit
sulfhydryl groups o
rcaptoethanol). Ma
hatase free
onucleotides and li
d a 5'[
32
P]-termina
e is commonly use
ates fragments wit
ch methylates N6 o
hylcytosine inhibit
d others.
gy. This albumin p
cking activity, RNa
mes.
U/l) removes 5'-t
-scale experiments
ation of linearized
ailable.
unt-ended DNA fra
bonds between ne
uble-stranded DNA
DNA Ligase.
ents with 3-
n (*). Inhibited by
th C residues.
ts with blunt
at the internal
C.
ents with 5-
tes the 6N-
e, but not by 5-
he reaction
mide and
e visually
tes fragments
denine at either
(*). Eco RI is an
es fragments
ne at the sites
chizomer to Bsp
es fragments
ce of 6-
schizomers:
es fragments
ce of 6-
schizomers:
ar biology as a
solutions. This
ty in cell
of
aintains
es disulfides.
nkers, 5' ends of
al label to 3'-
ed for 3'-end
h 5-cohesive
of adenine ().
at C(*).
reparation is
ases, and
terminal
s, enhancing
vector DNA.
agments.
eighboring 3'-
A. Single-strand

Pack Size

1,000 U (10 U/l)
5,000 U (10 U/l)
500 U (10 U/l)
2.5 g
5,000 U (10 U/l)
20,000 U (40 U/l)
2,500 U (40 U/l)
12,500 U (40 U/l)
1 kg
10 g
200 U
500 U (1 - 5 U/l)
20 mg (1 ml)
1,000 U (1 U/l)
500 U (1 U/l)

)

)
)

Price in

51,50
136,20
68,20
1.122,10
42,00
317,90
53,40
216,00
171,40
183,80
306,80
185,40
120,40
88,70
275,50

Pr

Cat.

10 72
10 72
10 72
10 72
10 73
10 73
10 73
10 73
10 73
10 73
10 73
10 73
10 73
10 73
10 74
roducts b

No.
24 815 001 Iso
Isop
lac
ana
28 438 001 Acc
Acc
frag
met
Acc
29 124 001 Rsa
Rec
end
how
inhi
29 132 001 Rsa
Rec
end
how
inhi
35 078 001 Bov
Stab
whe
prot
elec
35 086 001 Bov
Stab
whe
prot
elec
35 094 001 Bov
Stab
whe
prot
elec
35 108 001 Bov
Stab
whe
prot
elec
36 619 001 Asc
Rem
(asc
mat
oxa
36 988 001 Cre
Enz
of c
diph
Spe
lyop
37 046 001 Glu
Glu
non
keto
and
37 127 001 Glu
Glu
synt
37 232 001 Glu
Glu
cofa
3.2
37 275 001 Hex
Hex
yea
sulf
G6P
42 953 001 Kpn
Rec
coh
both

by Catalo
propyl--D-thiog
propyl--D-thioga
operon. It binds a
alog of galactose th
c I
c I recognizes the s
gments with 5-coh
thyladenine and 5-
c I is an isoschizom
a I
cognizes the seque
ds. Rsa I is not inhi
wever, the presenc
ibiting as indicated
a I
cognizes the seque
wever, the presenc
vine Serum Album
bilize enzymes to p
en proteins are in
tein blocker, medi
ctrophoresis and p
vine Serum Album
bilize enzymes to p
en proteins are in
tein blocker, medi
ctrophoresis and p
vine Serum Album
bilize enzymes to p
en proteins are in
tein blocker, medi
ctrophoresis and p
vine Serum Album
bilize enzymes to p
en proteins are in
tein blocker, medi
ctrophoresis and p
corbate Oxidase
move ascorbic acid
corbate, vitamin C)
terial, such as dete
lic acid in urine du
eatine Kinase (CK
zyme expressed by
creatine and consu
hosphate.
ecific Activity - app
philizate at +37C)
utamate-Oxaloac
tamate-Oxaloaceta
nnatural L-amino a
oglutarate, catalyz
d L-glutamate.
utamate-Pyruvate
tamate-Pyruvate T
thesis of nonnatur
ucose-6-Phospha
cose-6-Phosphate
actor recycling sys
M ammonium sulf
xokinase/Glucos
xokinase/Glucose-
st/Leuconostoc ov
fate suspension, pH
P-DH. Ratio of HK:
n I
cognizes the seque
hesive termini. Kpn
h C-residues or by
og Numb
Product N

galactoside
alactoside (IPTG) i
and inactivates the
hat cannot be clea
sequence GT(A,C
-methylcytosine as
mer to Fbl I and Xm
ence GT*AC and
bited by the prese
ce of 6-methyladen
d (*). Isoschizomer
ence GT*AC and
bited by the prese
ce of 6-methyladen
d (*). Isoschizomer
min Fraction V
prevent proteolysis
low concentration
a supplement, and
protein determinati
min Fraction V
prevent proteolysis
low concentration
a supplement, and
protein determinati
min Fraction V
prevent proteolysis
low concentration
a supplement, and
protein determinati
min Fraction V
prevent proteolysis
low concentration
a supplement, and
protein determinati
Spatula
d from aqueous so
) interferes with th
ection of erythrocy
uring research stud
K)
y various tissues an
umes ATP to create
prox. 350 U/mg lyo
).
cetate Transamin
ate Transaminase
acids from -keto
es the conversion
e Transaminase (
Transaminase (GPT
ral L-amino acids f
ate Dehydrogena
e Dehydrogenase (
stems for NADPH.
fate solution, pH a
se-6-Phosphate D
-6-Phosphate Dehy
verproducer. It is p
H approx. 6. Prepa
G6P-DH is approx
ence GGTACC an
n I is not inhibited b
y 6-methyladenine
ber
Name
s a very effective i
lac repressor. It i
aved by -galacto
C)(T,G)*A*C and ge
s indicated (*) on t
mi I.
d generates fragme
ence of 5-methylcy
nine or 4-methylcyt
rs: Afa I.
d generates fragme
ence of 5-methylcy
nine or 4-methylcyt
rs: Afa I.
s and denaturation
. Suitable as a buf
d as a protein stan
ions.
s and denaturation
. Suitable as a buf
d as a protein stan
ions.
s and denaturation
. Suitable as a buf
d as a protein stan
ions.
s and denaturation
. Suitable as a buf
d as a protein stan
ions.
olutions where asco
he investigation of
ytes in urine or det
dies.
nd cells. Catalyzes
e phosphocreatine
ophilizate at +25C
nase (GOT)
(GOT) is used for
o acids. In the pres
of L-aspartate to o
(GPT)
T) from pig heart is
from -keto acids
ase (G6P-DH)
(G6P-DH) is a com
Grade II from yeas
approx. 6.
Dehydrogenase (
ydrogenase is from
provided as a 3.2 M
ared by mixing hex
x. 2:1 (protein cont
nd generates fragm
by 5-methylcytosin
. Isoschizomers:As
nducer of the
s a chemical
osidase.
enerates
presence of N6-
the sequence.
ents with blunt
ytosine (),
tosine is
ents with blunt
ytosine (),
tosine is
n, especially
fer component,
dard in
n, especially
fer component,
dard in
n, especially
fer component,
dard in
n, especially
fer component,
dard in
orbic acid
f sample
ermination of
the conversion
e and adenosine
C (800 U/mg
the synthesis of
ence of a-
oxaloacetate
s used for the
s.
mponent of
st. Suspension in
(HK/G6P-DH)
m
M ammonium
xokinase and
ent).
ments with 3-
ne at either or
sp718 II, Acc65 I.

Pack Size

1 g
500 U (5 U/l)
1,000 U (10 U/l)
5,000 U (10 U/l)
50 g
100 g
500 g
1 kg
25 spatulas
500 mg
25 mg (2.5 ml)
25 mg (2.5 ml)
25 mg (5 ml)
30 mg (10 ml)
10,000 U (40 U/l)
www.roche

)
e-applied-science

Price in

82,20
421,60
72,80
291,00
123,30
220,80
887,30
1.296,70
72,40
398,80
270,20
225,30
364,10
275,80
195,60

245

e.com

Pr
246

www.r

Cat.

10 74
10 74
10 74
10 74
10 74
10 75
10 76
10 77
10 77
10 77
10 77
10 77
10 77
10 78
10 78
roducts b
roche-applied-sc

No.
42 970 001 Dpn
Rec
end
at th
Ma
42 988 001 Dpn
Rec
end
at th
Ma
45 731 001 -
Use
be c
dire
chro
45 740 001 X-G
Use
pro
met
dete
45 782 001 DN
This
dige
53 351 001 Stu
Stu
blun
indi
60 994 001 BCI
Use
imm
reac
can
75 207 001 Aat
Aat
with
reco
523
75 266 001 Sca
Sca
blun
indi
75 835 001 Bov
Hig
met
liga
in lo
76 777 001 Nru
Rec
end
met
pos
79 652 001 Hin
Rec
coh
met
hyd
79 679 001 Hin
Rec
coh
met
hyd
83 641 001 Pol
Cell
som
qua
alde
86 357 001 RNa
Clea
of D
site
and

by Catalo
cience.com
n I
cognizes the seque
ds. The enzyme is o
he indicated site (*
l I.
n I
cognizes the seque
ds. The enzyme is o
he indicated site (*
l I.
Galactosidase
e for labeling enzym
coupled to other p
ectly for conjugatio
omatography. Sup
Gal
e X-Gal for immuno
duct has a blue co
ected.
A, lambda
s high quality prep
ests, amplification
u I
I recognizes the s
nt ends. Stu I is inh
IP
e BCIP for alkaline
munohistocytochem
ction product has
n be visually detect
t II
t II recognizes the s
h 3-cohesive term
ognition sequence
30 I and Zra I.
a I
nt ends. Sca I is no
icated (). Isoschiz
vine Serum Album
hest quality BSA. U
tabolism in biologi
and binding, and in
ow concentration.
u I
cognizes the seque
ds. Inhibited by ove
thylcytosine is inhi
sition of the C. Isos
nf I
cognizes the seque
hesive termini. Sen
thylcytosine at 3po
droxymethylcytosin
nf I
cognizes the seque
hesive termini. Sen
thylcytosine at 3po
droxymethylcytosin
yethylene Glycol
l fusion induced by
maticcell genetics a
ality PEG does not
ehydes not detecta
ase H
aves RNA in RNA:
DNA synthesis, elim
-specific cleavage
d removal of poly (A
og Numb
Product N

ence GmAT*C an
only inhibited by th
*) if no 6-methylad
ence GmAT*C an
only inhibited by th
*) if no 6-methylad
me immunoassay t
proteins via its SH-
on without prior dia
pplied as lyophilizat
ohistocytochemist
olor and is soluble
uble in water. The
paration of Lambda
of large DNA targ
sequence AGG*C
hibited by the pres
zomers: Aat I, Eco1
phosphatase dete
mistry and Souther
a blue color and is
ted. Supplied as a
sequence GA*CGT
e as indicated (*). A
sequence AGTA
ot inhibited by the
zomers: Ass I, Bmc
min Fraction V, f
Used for fatty acid
cal systems, ident
nvestigate ionic bin
ence T*CGCG*A,
erlapping dam-me
ibiting(*) or not inh
schizomers: BtuM
ence G*ANTC an
sitive to 6-methyla
osition () does no
e does. Isoschizom
ence G*ANTC an
sitive to 6-methyla
osition () does no
e does. Isoschizom
l 1500
y polyethylene glyc
and the production
need to be tested
able; free from Ca
2
DNA hybrids. Use
mination of mRNA
e of RNA, detection
A) sequences of m
ber
Name
d generates fragm
he occurrence of 5
denine is present.
d generates fragm
he occurrence of 5
denine is present.
techniques. -Gala
groups. Use recon
alysis or gel perme
te.
in dimethylformam
e blue color can be
a DNA is used for
gets, and as a PCR
C*CT and generates
sence of 5-methylc
47 I, Pce I, SseB I.
ection using
rn and western blo
s insoluble in wate
powder.
T*C and generate
by 5-methylcytosin
Aat II is a neoschiz
CT and generates
presence of 5-me
cA I, Zrm I.
fatty acid free
d and lipid research
ify transport mech
nding. Ideal if prote
, generating fragm
thylation as shown
hibiting(), depend
I, Bsp68 I.
nd generates fragm
adenine (*). Presen
ot prevent cleavage
mers: none known.
nd generates fragm
adenine (*). Presen
ot prevent cleavage
mers: none known.
col is a standard m
n of hybridoma ce
prior to use. Perox
2+
.
in in vivo RNA-pr
A in 2nd-strand cD
n of RNA:DNA reg
mRNA.
ments with blunt
5-methylcytosine
Isoschizomer:
ments with blunt
5-methylcytosine
Isoschizomer:
actosidase can
nstituted solution
eation
he reaction
mide and
e visually
restriction
control.
s fragments with
cytosine as
otting. The
er. The blue color
es fragments
ne in the
zomer of Ssp
fragments with
ethylcytosine, as
h. Study lipid
anisms, study
eins are present
ments with blunt
n(*). 5-
ing on the
ments with 5-
nce of 5-
e, but 5-
.
ments with 5-
nce of 5-
e, but 5-
.
method in
lls. This high
xides and
rimed initiation
NA synthesis,
ions in dsDNA,

Pack Size

200 U (10 U/l)
1,000 U (10 U/l)
25 mg
1 g
1 ml (5 A
260
units)
500 U (10 U/l)
250 mg
250 U (1 - 5 U/l)
2,500 U (10 U/l)
50 g
1,000 U (10 U/l)
1,000 U (10 U/l)
5,000 U (10 U/l)
10 x 4 ml
100 U

)
)

Price in

85,30
338,80
657,00
492,50
119,10
78,50
123,50
53,30
261,90
409,60
364,40
69,40
275,10
130,10
388,00

Pr

Cat.

10 78
10 79
10 79
10 79
10 79
10 79
10 79
10 79
10 80
10 81
10 81
10 81
10 81
10 81
10 81
10 81
roducts b

No.
89 704 001 Trit
Com
isol
elec
CM
91 156 001 End
Use
and
98 975 001 Bam
Rec
coh
met
resi
98 983 001 Hin
Rec
coh
hyd
inhi
98 991 001 Pst
Pst
3-c
and
99 009 001 T4
Use
Cat
hyd
nick
99 050 001 BM
For
obv
bee
spe
99 068 001 Inte
Allo
natu
lym
thym
00 058 001 Sto
Box
stor
10 118 001 CHA
For
of b
10 126 001 CHA
For
of b
10 274 001 SP6
Tran
pro
Use
prot
12 846 001 Tris
Tris
biol
com
14 245 001 Asp
Rec
frag
5-m
not
14 253 001 Asp
Rec
frag
5-m
not
14 270 001 Prim
This
a cD
synt

by Catalo
ton X-100
mmonly used non-
ation of membrane
ctrophoresis. Supp
MC: approx. 0.2 mM
doproteinase Glu
e Endoproteinase G
d for sequence ana
mH I
cognizes the seque
hesive termini. Bam
due as indicated (
nd III
cognizes the seque
droxymethylcytosin
ibit (). Isoschizom
t I
I recognizes the se
cohesive termini. P
d 6-methyladenine
DNA Ligase
e T4 DNA ligase to
alyzes formation o
droxyl- and 5'-phos
ks in dsDNA are a
M-Cyclin
the elimination of
vious marked cytot
en tested and comp
ectinomycin, lincom
erleukin-2, huma
ows cultivation of h
ural killer cell lines
phocytes and natu
mocyte, splenocyte
orage Box
x with removable s
rage of 50 microce
APS
solubilization of m
both the sulfobetai
APS
solubilization of m
both the sulfobetai
6 RNA Polymeras
nscribe RNA from
moter. Perform syn
e labeled RNA in D
tection, and synthe
s hydrochloride
s Hydrochloride is e
logy as a buffering
mbination with Tris
p718 I
cognizes GGTAC
gments with 5 coh
influence activity(
p718 I
cognizes GGTAC
gments with 5 coh
influence activity(
mer for cDNA Sy
s primer will bind t
DNA copy, for use
thesis of first-stran
og Numb
Product N

-ionic detergent fo
e-protein complex
plied as a viscous l
M at +25C
u-C (V8 Protease
Glu-C (V8 Protease
alysis.
ence GGAT*CC
ence *AAG*CTT
bited by 6-methyla
mers: none known.
equence *CTGCA
of phosphodiester
sphate ends in dou
lso closed by T4 D
f mycoplasma from
toxic side effects. T
pared to other ant
mycin, gentamicin)
an (hIL-2)
human/murine IL-2
s and proliferation
ural killer cells. Est
e, or PBL derived T
styrofoam insert (0.
entrifuge tubes. Te
membrane proteins
ne-type and bile-a
membrane proteins
ne-type and bile-a
se
cloned DNA temp
nthesis with labele
DNA/RNA blots, in
esis of capped RN
extensively used in
g agent in incubati
s Base for preparat
C*C; same sequenc
hesive ends, not 3
ndicated (*). Meth
(). Neoschizomer:
C*C; same sequenc
hesive ends, not 3
ndicated (*). Meth
(). Neoschizomer:
ynthesis
the 3'-poly A tail o
in RT-PCR, gener
nd cDNA.
ber
Name
r solubilizing mem
xes. It is also used
iquid.
e)
e) for protein struc
and generates fra
ed by overlapping
methylcytosine at t
BstI.
and generates fra
adenine or 5-meth
methyladenine at A
AG and generates
the presence of 5
soschizomers: Bsp
unt-ended DNA fra
bonds between ne
uble-stranded DNA
DNA Ligase.
m infected cell cultu
The efficiency of B
tibiotics (kanamyci
).
2 dependent T-cel
of mitogen-activa
tablishes human/m
T-cell lines.
.5 to 2.0 ml capaci
mperature-resista
s. CHAPS combine
acid detergents. CM
s. CHAPS combine
acid detergents. CM
plates downstream
ed NTPs to generat
situ hybridization,
NA in vitro .
n biochemistry and
on mixtures. It is u
tion of Tris-HCl bu
ce as Kpn I but gen
ends as from Kpn
ylation of A and ce
Kpn I.
ce as Kpn I but gen
ends as from Kpn
ylation of A and ce
Kpn I.
of an mRNA to initi
ration of cDNA libr
mbranes during
for native gel
cture analysis
agments with 5'-
dam
the internal C
gments with 5-
ylcytosine (*). 5-
A does not
s fragments with
-methylcytosine
pMA I.
agments.
eighboring 3'-
A. Single-strand
ures without
M-Cyclin has
n, tylosine,
ll lines and
ted T-
murine
ty) for the
nt to -70C.
es the properties
MC: 4 mM.
es the properties
MC: 4 mM.
m from an SP6
te labeled RNA.
, RNase
d molecular
used in
ffers.
nerates
I. Inhibited by
entral C does
nerates
I. Inhibited by
entral C does
ate synthesis of
raries, and

37.5 m
10
40

Pack Size

100 ml
2 mg
10,000 U (40 U/l)
10,000 U (40 U/l)
10,000 U (40 U/l)
500 U (5 U/l)
0,000 U (5 g, 50 m
1 box
10 g
50 g
1,000 U
500 g
1,000 U (10 U/l)
5,000 U (10 U/l)
g (1 A
260
unit, 8 n
www.roche
)
)
)
edium)
ml)

mol)
e-applied-science

Price in

53,40
147,60
199,10
98,80
225,20
275,50
113,10
250,20
7,40
277,50
1.239,90
111,90
170,50
68,20
284,20
75,30

247

e.com

Pr
248

www.r

Cat.

10 81
10 82
10 82
10 82
10 82
10 82
10 83
10 83
10 83
10 83
10 83
10 83
10 83
10 83
10 83
10 83
roducts b
roche-applied-sc

No.
14 407 001 Per
Pero
as w
use
a sa
21 705 001 DN
For
dete
rest
22 221 001 Ma
Rec
coh
info
Fsp
22 230 001 Ma
Rec
coh
not
22 248 001 Ma
Rec
coh
not
27 754 001 Dra
Dra
blun
the
isos
35 242 001 Am
Am
med
35 269 001 Am
Am
med
35 277 001 Asp
Rec
with
met
inhi
35 307 001 Dde
Dde
5-c
hyd
Hpy
35 315 001 Nco
Rec
coh
of 6
Bsp
35 323 001 Nco
Rec
coh
of 6
Bsp
37 016 001 For
Mos
deh
cyst
37 059 001 Lys
Use
of p
hea
to is
37 091 001 PM
Inhi
prot
mos
solu
38 039 001 Fib
Pro
adh
and
dish
by Catalo
cience.com
roxidase (POD)
oxidase (POD) can
well as its carbohy
ed directly for conju
alt-free lyophilizate
A Molecular We
ermination of doub
ae I
cognizes the seque
hesive termini. Sup
ormation is availab
B I, Bfa I, Xsp I.
ae III
cognizes the seque
hesive termini. Sup
known to be inhib
ae III
cognizes the seque
hesive termini. Sup
known to be inhib
a I
nt ends. Dra I is no
site indicated () o
schizomer of Aha I
mpicillin
picillin is ideal for
dia, it selects for p
mpicillin
picillin is ideal for
dia, it selects for p
p700 I (Xmn I)
cognizes the seque
h blunt termini. Inh
thyladenine at the
ibit. Isoschizomers
e I
e I recognizes the
cohesive termini. It
droxymethylcytosin
yF3 I.
o I
cognizes the seque
6-methyladenine d
p19 I.
o I
cognizes the seque
6-methyladenine d
p19 I.
rmate Dehydroge
st widely used in c
hydrogenase is a d
teine residue whic
sozyme
e Lysozyme from h
protoplasts, bacter
aling), food and dri
solation of nucleic
MSF
ibits serine proteas
tease papain [reve
st cysteine or aspa
uble, water-stable
ronectin
motes attachment
hesion region (cell
d promotes their bi
hes. Lyophilizate.
og Numb
Product N

n be coupled to oth
ydrate moiety. The
ugation without pr
e.
ight Marker V
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
ence CTAG and g
plied with the spe
le concerning met
ence GTNAC and
plied with the spe
bited by methylatio
ence GTNAC and
plied with the spe
bited by methylatio
sequence TTTAA
ot inhibited by the
on the recognition
III.
gene-cloning stra
lasmid-bearing, dr
gene-cloning stra
lasmid-bearing, dr
ence G*AANNN
hibited by 6-methy
other A() or pres
s: MroX I, Pdm I, Xm
sequence *CTNA
t is inhibited by the
e at the site indica
ence *CCATGG a
bited by 5-methylc
oes not influence
ence *CCATGG a
bited by 5-methylc
oes not influence
enase
cofactor recycling
imer of two identic
ch is essential for a
en egg white for c
iolysis, pharmacolo
inks (flavor enhanc
c acids.
ses (chymotrypsin
ersible by DTT trea
artic proteases. Pef
alternative.
t and subsequent s
binding domain) i
inding and spread
ber
Name
her proteins via its
reconstituted solu
rior dialysis. EIA gr
mplifies accurate m
A fragments genera
ize range: 8 to 587
generates fragmen
cial 2x incubation
thylation sensitivity
d generates fragme
cial 2x incubation
on. Isoschizomers:
d generates fragme
cial 2x incubation
on. Isoschizomers:
AA and generates
presence of 6-me
sequence. Dra I is
tegies. When pres
rug-resistant bacte
tegies. When pres
rug-resistant bacte
NTTC and genera
yladenine at the (*)
sence of 5-methylc
mn I.
AG and generates f
e presence of 5-m
ated (*). Isoschizom
and generates frag
cytosine as indicat
the cleavage (). Is
and generates frag
cytosine as indicat
the cleavage (). Is
systems for NADH
cal subunits. The e
activity or structura
cell wall degradatio
ogy (anti-inflamma
cer), and sample p
, trypsin, thrombin
atment]). Does not
fabloc
SC is a no
spreading of cells.
interacts with mam
ing on plastic. Use
s amino groups,
tion can be
rade, supplied as
molecular weight
ated by
7 bp.
nts with 5-
buffer. No
y. Isoschizomers:
ents with 5-
buffer. Mae III is
none known.
ents with 5-
buffer. Mae III is
none known.
fragments with
ethyladenine at
s an
ent in growth
erial colonies.
ent in growth
erial colonies.
ates fragments
). 6-
cytosine does not
fragments with
methyl- or 5-
mers: BstDE I,
gments with 5-
ted (*). Presence
soschizomers:
gments with 5-
ted (*). Presence
soschizomers:
H. Formate
enzyme has a
al integrity.
on, preparation
atory, tissue
preparation prior
, cysteine
inhibit metallo-,
ontoxic, water-
The cell
mmalian cells
e to coat culture

50 g in 200 l
Pack Size

100 mg
(1 A
260
unit) for up
250 U (1 - 5 U/l)
50 U (1 - 5 U/l)
250 U (1 - 5 U/l)
5,000 U (10 U/l)
5 g
50 g
500 U (10 U/l)
1,000 U (10 U/l)
200 U (10 U/l)
1,000 U (10 U/l)
250 U
10 g
10 g
5 mg
p to 50 gel lanes
)
)

Price in

301,80
152,00
369,50
90,90
369,50
143,30
43,40
260,20
73,90
171,70
104,60
393,40
294,90
245,90
97,70
546,70

Pr

Cat.

10 83
10 84
10 84
10 86
10 87
10 87
10 87
10 87
10 88
10 88
10 88
10 88
10 88
10 88
10 88
10 89
roducts b

No.
38 292 001 T4
Pho
RNA
CM
labe
43 547 001 Dra
Dra
frag
(*).
43 555 001 Hyg
Hyg
synt
phe
hyg
62 495 001 Ma
Rec
coh
by t
Hpy
74 477 001 Pla
Plas
plas
74 515 001 Bes
Bes
leuc
loca
carb
74 523 001 E-6
Stro
cath
of p
betw
75 406 001 N-A
Use
(ap
gluc
81 767 001 T7
Tran
pro
Use
synt
81 775 001 T7
Tran
pro
Use
synt
84 308 001 CPR
Colo
The
be e
85 819 001 pUC
Plas
orie
man
coli
85 843 001 Nhe
Nhe
5-c
reco
85 851 001 Nhe
Nhe
5-c
reco
85 860 001 Nhe
Nhe
5-c
reco
99 186 001 Kpn
Rec
coh
both

by Catalo
Polynucleotide K
osphorylate 5'-hydr
A and DNA, 3' end
MP, forming 5'[
32
P]p
eling of RNA with
a III
a III recognizes the
gments with 3-coh
Isoschizomer: Ade
gromycin B
gromycin B is an a
thesis in prokaryot
enotype of eukaryo
gromycin-resistanc
ae II
cognizes the seque
hesive termini. Sup
the presence of 5-
yCH4 IV.
asminogen
sminogen from hu
sminogen activato
statin
statin is an inhibito
cine aminopeptida
ated on the surface
boxypeptidases.
64
ong, irreversible in
hepsin B and L, br
proteins and enzym
ween the SH comp
Acetyl--D-Gluco
e N-Acetyl--D-G
prox. 50 tests) for
cosaminidase in u
RNA Polymerase
nscribe RNA from
moter. Perform syn
e RNA in RNA/DNA
thesis, and synthe
RNA Polymerase
nscribe RNA from
moter. Perform syn
e RNA in RNA/DNA
thesis, and synthe
RG
orimetric determin
e reaction product
evaluated photome
C 18 DNA
smid for loning do
entation with respe
ny unique sites for
i by transformation
e I
e I recognizes the
cohesive termini. N
ognition sequence
e I
e I recognizes the
cohesive termini. N
ognition sequence
e I
e I recognizes the
cohesive termini. N
ognition sequence
n I
cognizes the seque
hesive termini. Kpn
h C-residues or by
og Numb
Product N

Kinase, 3'-phosph
roxyl ends of oligo
ds of RNA, and add
pCp. This substrate
T4 RNA ligase.
sequence C*A*CN
e I.
minoglycosidic an
tes and eukaryotes
otic cells that are s
ce gene (hyg or hp
ence A*CGT and
plied with the spe
methylcytosine as
man serum is used
rs; substrate of t-P
or of aminopeptida
ase, tripeptide amin
e of mammalian ce
hibitor of papain a
romelain, and ficin
mes. Inhibition of th
ponents.
osaminidase (NA
Glucosaminidase (N
the determination
rine in life science
e
cloned DNA temp
nthesis with labele
A blots, ISH, RNas
sis of capped RNA
e
cloned DNA temp
nthesis with labele
A blots, ISH, RNas
sis of capped RNA
nation of -Gal act
has a dark red col
etrically at 574 or 5
uble-digested rest
ect to the lac prom
r cloning of foreign
n.
sequence GCTAG
Nhe I is inhibited b
sequence GCTAG
sequence GCTAG
ence GGTACC an
n I is not inhibited b
y 6-methyladenine
ber
Name
hatase free
onucleotides and li
d a 5'[
32
P]-termina
e is commonly use
NNNGTG and ge
s methlation sensit
tibiotic that inhibit
s. Selects and mai
stably transfected w
ph ).
generates fragme
cial 2x incubation
indicated (*). Isos
d to determine the
PA.
ases, such as amin
nopeptidase, and a
ells. Does not inhi
and cysteine protea
during isolation a
hiol proteases is n
AG)
NAG) in a colorime
of N-Acetyl--D
e research applicat
plate downstream
ed NTPs, generatin
se protection, micro
A in vitro .
plate downstream
ed NTPs, generatin
se protection, micro
A in vitro .
tivity in cell extract
lor and is soluble i
578 nm.
triction fragments
moter. Polylinker (M
n DNA. Easily intro
G*C and generates
y 5'-methylcytosin
soschizomers: Asu
G*C and generates
y 5'-methylcytosin
soschizomers: Asu
G*C and generates
y 5'-methylcytosin
soschizomers: Asu
nd generates fragm
by 5-methylcytosin
. Isoschizomers:As
nkers, 5' ends of
al label to 3'-
ed for 3'-end
nerates
tive as indicated
ts protein
ntains the
with the E. coli
nts with 5-
buffer. Inhibited
chizomers:
e activity of
opeptidase B,
aminopeptidases
bit
ases, such as
nd purification
on-competitive
etric assay
-
tions.
from a T7
ng labeled RNA.
oarray target
from a T7
ng labeled RNA.
oarray target
ts and ELISA.
n water. It can
in either
MCS) provides
oduced into E.
s fragments with
e within the
uNH I.
s fragments with
e within the
uNH I.
s fragments with
e within the
uNH I.
ments with 3-
ne at either or
sp718 II, Acc65 I.

1 g
ap

Pack Size

1,000 U
500 U (1 - 5 U/l)
50 U (1 - 5 U/l)
20 U
10 mg
10 mg
pproximately 50 tes
1,000 U
5,000 U
250 mg
50 g (200 l)
200 U (10 U/l)
1,000 U (10 U/l)
1,500 U (40 U/l)
5,000 U (10 U/l)
www.roche
)
ered)
sts

e-applied-science

Price in

947,10
274,00
304,10
347,90
234,20
183,30
270,20
605,60
111,90
433,40
87,30
468,30
72,80
291,00
345,60
121,70

249

e.com

Pr
250

www.r

Cat.

10 89
10 89
10 89
10 90
10 90
10 90
10 90
10 90
10 90
10 97
10 97
10 97
10 97
10 98
10 98
roducts b
roche-applied-sc

No.
99 194 001 Xho
Xho
with
met
Pae
99 208 001 Apa
Apa
with
indi
120
99 224 001 Bgl
Rec
coh
but
Bgl
01 393 001 Gly
Mo
prec
rep
pico
04 988 001 m7
Use
Poly
09 700 001 Mlu
Rec
coh
seq
met
09 718 001 Mlu
Rec
coh
seq
met
09 831 001 Nsi
Nsi
3-c
5-m
Zsp
09 840 001 Nsi
Nsi
3-c
5-m
Zsp
72 975 001 Ssp
Ssp
blun
as i
72 983 001 T4
Sing
stim
DNA
and
72 991 001 T4
Sing
stim
DNA
and
76 776 001 Nic
Lab
of t
the
DNA
81 249 001 Nitr
Nitr
nitr
pre
81 532 001 Apr
Prot
cult
chy
qua

by Catalo
cience.com
o I
h 5-cohesive term
thyladenine and 5-
a I
h 3-cohesive term
icated (*) in the re
0 I and Psp OMI.
l II
cognizes the seque
is sensitive to 5-m
II has no known is
ycogen
lecular biology gra
cipitation of nucle
lace tRNAs or son
ogram amounts of
G(5')ppp(5')G
e the nucleotide, m
ymerase promoter
u I
cognizes the seque
uence as indicated
thyladenine (). Iso
u I
cognizes the seque
uence as indicated
thyladenine (). Iso
i I
I recognizes the s
cohesive termini. N
methylcytosine is no
p2 I.
i I
I recognizes the s
cohesive termini. N
methylcytosine is no
p2 I.
p I
p I recognizes the s
nt ends. The enzym
ndicated (*). Isosc
Gene 32 Protein
gle-strand-specific
mulate in vitro DNA
A or RNA. It is also
d to help RE digest
Gene 32 Protein
gle-strand-specific
mulate in vitro DNA
A or RNA. It is also
d to help RE digest
ck Translation Kit
bel DNA with radio
he helix, incorpora
nicked site. Use la
A/RNA transfer hy
rate Reductase
rate Reductase is u
ate in culture med
paration is a cruci
rotinin
tect proteins durin
ture studies. Used
ymotrypsin on imm
og Numb
Product N

sequence *CT*CG
-methylcytosine as
I, Str I, Tli I.
sequence GGG*CC
cognition sequenc
ence AGAT*CT a
not inhibited by ov
methyl and 5-hydro
soschizomers.
ade Glycogen is us
ic acids (DNA or R
icated DNAs; 20
f DNA or RNA from
m7G(5')ppp(5')G, t
systems to initiate
ence A*CGCGT a
bited by 5-methylc
d (*). It is not influ
oschizomers: none
ence A*CGCGT a
bited by 5-methylc
d (*). It is not influ
oschizomers: none
sequence ATGC*A
Nsi I is inhibited by
ot inhibiting. Isosc
sequence ATGC*A
Nsi I is inhibited by
ot inhibiting. Isosc
sequence AAT*A
me is inhibited by t
chizomers: none kn
c DNA-binding pro
A synthesis, and st
o used in site-spec
ts go to completion
c DNA-binding pro
A synthesis, and st
o used in site-spec
ts go to completion
t
oactive or modified
ating labeled nucle
abeled probes in c
ybridization, and IS
used for nitrate de
dia, and determinat
al step. Deproteina
for purification of
krein activity.
ber
Name
G*AG and generat
ted by the presenc
C*C and generate
by 5'-methylcytosin
ce. Apa I is a neosc
and generates frag
verlapping dam m
oxy-methylcytosine
sed as a carrier for
RNA). As an inert m
g (1 l solution) p
m a volume of 1 ml
ogether with the S
e in vitro RNA synt
and generates frag
cytosine within the
enced by the pres
e known.
and generates frag
cytosine within the
enced by the pres
e known.
T and generates
y 6-methyladenine,
chizomers: EcoT22
T and generates
y 6-methyladenine,
chizomers: EcoT22
ATT and generates
the presence of 6-
nown.
otein used to optim
tabilize single-stran
cific mutagenesis e
n.
otein used to optim
tabilize single-stran
cific mutagenesis e
n.
d dNTPs. Enzymes
eotides as polymer
colony/plaque hybr
SH.
etermination: Assay
tion of NO
3
in seru
ation is required fo
ation, increasing c
urokinase, trypsin
protein-folding st
es fragments
ce of 6-
schizomers:
es fragments
ne at the sites
chizomer to Bsp
gments with 5-
ethylation (),
e, as shown (*).
r the
material it may
precipitates
l.
SP6 and T7 RNA
thesis.
gments with 5-
e recognition
ence of 6-
gments with 5-
e recognition
ence of 6-
fragments with
as indicated (*).
I, Mph1103 I,
fragments with
as indicated (*).
I, Mph1103 I,
fragments with
-methyladenine
mize PCR,
nded regions of
experiments,
mize PCR,
nded regions of
experiments,
nick one strand
rase proofreads
ridization,
y of nitrite and
um. Sample
or good results.
cell lifetime in
, and
tudies, and

1 kit for up to

Pack Size

5,000 U (10 U/l)
5,000 U (10 U/l)
2,000 U (40 U/l)
20 mg (1 ml)
5 U (at 260 nm)
500 U (10 U/l)
2,500 U (10 U/l)
200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (10 U/l)
100 g
500 g
o 50 standard labe
20 U
50 mg

eling reactions

Price in

102,30
97,90
181,90
99,50
170,90
69,40
239,90
97,80
269,40
269,40
189,20
755,80
408,50
186,40
275,40

Pr

Cat.

10 98
10 98
10 99
11 00
11 00
11 00
11 00
11 00
11 00
11 00
11 00
11 00
11 00
11 00
11 01
roducts b

No.
82 962 001 N-A
Stan
rese
gluc
Hita
88 537 001 7-D
7-D
term
com
stre
99 644 001 SP6
For
SP6
non
hyb
04 638 001 Chy
Chy
inhi
04 646 001 Ant
Ant
to a
than
fold
04 760 001 Ran
Uni
mod
man
Sou
04 786 001 T4
Lab
hyb
mus
Gen
04 794 001 T4
Lab
hyb
mus
Gen
04 816 001 Fok
Rec
5'-c
dist
Neo
04 875 001 His
Lys
kina
exit
form
08 404 001 Kle
Use
tech
in re
olig
08 412 001 Kle
Use
tech
in re
olig
08 943 001 Spe
Rec
coh
and
I, A
08 951 001 Spe
Rec
coh
and
I, A
11 375 001 Nut
Ser
with
P3x
and
by Catalo
Acetyl--D-Gluco
ndard for the dete
earch samples with
cosaminidase. It ca
achi 705, 704, and
Deaza-2'-deoxy-g
Deaza-2'-deoxy-gu
mination sequencin
mpression problem
etches of DNA.
6/T7 Transcriptio
in vitro transcript
6 or T7 promoter. S
nradioactively labe
bridizations, genom
ymostatin
ymostatin is a mixt
ibitor of -, -,
tipain dihydrochl
tipain dihydrochlor
a small extent. Note
n leupeptin. The in
d higher than that o
ndom Primed DN
formly label plasm
dified dNTP. High
ny hybridization te
uthern and norther
DNA Polymerase
bel 3'-termini of DN
bridization probe. D
st have 5-protrud
ne 32 Protein in sit
DNA Polymerase
bel 3'-termini of DN
bridization probe. D
st have 5-protrud
ne 32 Protein in sit
k I
cognizes the seque
cohesive termini. A
tances from the se
oschizomers: BseG
stone H1
ine-rich preparatio
ases. The linker his
t sites of the DNA,
mation of higher o
enow Enzyme
e this labeling-grad
hniques, such as 3
ecessed DNA end
gonucleotides durin
enow Enzyme
e this labeling-grad
hniques, such as 3
ecessed DNA end
gonucleotides durin
e I
cognizes the seque
hesive termini. Spe
d 5-methylcytosine
hl I.
e I
cognizes the seque
hesive termini. Spe
d 5-methylcytosine
hl I.
tridoma-SP
um-free media sup
h an intact cholest
x63Ag8.653, and ly
d other cell types (n
og Numb
Product N

osaminidase Sta
rmination of NAG
h the aid of the Te
an be used in auto
Epos 5060.
guanosine-5'-trip
anosine-5'-triphos
ng methods, in pla
ms in gel electropho
on Kit
ion of DNA seque
Synthesize labeled
led ribonucleotide
mic sequencing, an
ture of chymostatin
-, and -chymo
loride
ride inhibits papain
e: Antipain is more
nhibitory potency o
of elastatinal.
NA Labeling Kit
mid or phage DNA
specific activity lab
echniques, includin
rn blots, and in situ
e
NA, producing high
DNA labeled with r
ing ends. Blunt-en
te-directed mutage
e
NA, producing high
DNA labeled with r
ing ends. Blunt-en
te-directed mutage
ence GG*ATG(N)9/
A Class II S enzyme
equence. Inhibited
G I, BstF5 I, BtsC I.
on from calf thymu
stone H1 binds the
locking the DNA
rder structure.
de enzyme from E.
3-end labeling, ran
s to create blunt-e
ng site-directed m
de enzyme from E.
3-end labeling, ran
s to create blunt-e
ng site-directed m
ence *A*CTAGT a
I is inhibited by th
e ( mA?m CTAGT)
ence *A*CTAGT a
e ( mA?m CTAGT)
pplement for muri
terol biosynthesis p
mphoblastoid cell
neural explants).
ber
Name
andard (NAG Stan
activity in urine lif
est-Combination N
omated analyzers,
phosphate
sphate is used in d
ace of dGTP to ove
oresis when seque
nces cloned down
RNA using radioa
s. Use in DNA/RN
nd S1 nuclease stu
ns a, b and c and i
otrypsin.
n and trypsin. Plas
e specific for papa
of antipain is appro
with any [-
32
P]-
beled DNA probes
ng gene library scr
u hybridizations.
hly labeled DNA fo
recombinant T4 DN
nd DNA will not wo
enesis.
hly labeled DNA fo
recombinant T4 DN
nd DNA will not wo
enesis.
/13 and generates
e which cleaves ds
by 6-methyladenin
us used as a subst
e nucleosome and
into place and allo
. coli in many mole
ndom primed DNA
ended DNA, and e
utagenesis.
. coli in many mole
ndom primed DNA
ended DNA, and e
utagenesis.
and generates frag
he presence of N6-
as shown (*) . Isos
and generates frag
he presence of N6-
as shown (*) . Isos
ne myelomas and
pathway (derived f
lines), primary lym
ndard)
fe science
-Acetyl--D-
such as the
dideoxy-chain
ercome
encing GC-rich
stream of the
active or
A
dies.
s a specific
min is inhibited
ain and trypsin
oximately 100-
-dNTP or
s are used in
eening,
or use as
NA Polymerase
ork. Use with T4
or use as
NA Polymerase
ork. Use with T4
s fragments with
sDNA at precise
ne as shown (*).
rate for protein
the entry and
owing the
ecular biology
A labeling, filling
longation of
ecular biology
A labeling, filling
longation of
gments with 5'-
-methyladenine
schizomers: Bcu
gments with 5'-
-methyladenine
schizomers: Bcu
hybridomas
from SP2/0,
mphoid cultures,

20
1 kit for up t
1 kit for
1
Pack Size

5 x 3 ml
0 l (2 mol, 10 m
10 mg
10 mg
up to 50 labeling r
100 U
500 U
100 U (1 - 5 U/l)
5 mg
100 U
500 U
200 U (10 U/l)
1,000 U (10 U/l)
100 ml (100x) steri
www.roche
mM)
tion reactions
reactions
)

le
e-applied-science

Price in

189,30
95,70
587,00
185,70
185,70
452,70
204,10
771,90
128,50
707,10
109,20
438,70
90,90
351,40
762,70

251

e.com

Pr
252

www.r

Cat.

11 01
11 01
11 01
11 01
11 01
11 02
11 02
11 02
11 03
11 03
11 03
11 03
11 03
11 03
roducts b
roche-applied-sc

No.
11 456 001 Inte
Allo
natu
lym
thym
14 706 001 Not
Not
GC
by 5
not
14 714 001 Not
Not
GC
by 5
not
17 101 001 Leu
Prot
prot
alph
the
17 128 001 Leu
Prot
prot
alph
the
26 534 001 Sph
Rec
coh
met
hyd
26 542 001 Sph
Rec
coh
met
hyd
26 950 001 Sph
Rec
coh
met
hyd
31 163 001 T3
Tran
pro
Use
synt
31 171 001 T3
Tran
pro
Use
synt
33 484 001 End
ECG
stim
has
grow
34 626 001 Leu
Prot
prot
alph
the
34 731 001 Prim
Ran
ens
stru
34 758 001 His
Hist
in th
glob
nuc

by Catalo
cience.com
erleukin-2, huma
phocytes and natu
mocyte, splenocyte
t I
t I is a rare-cutter e
GG*C*CGC, gen
5-methylcytosine a
inhibiting (). Isos
t I
GG*C*CGC, gen
5-methylcytosine a
inhibiting (). Isos
upeptin
tect proteins durin
tease inhibitor. Le
ha-amino group. It
reaction by dialys
upeptin
tect proteins durin
tease inhibitor. Le
ha-amino group. It
reaction by dialys
h I
cognizes the seque
droxymethylcytosin
h I
cognizes the seque
droxymethylcytosin
h I
cognizes the seque
droxymethylcytosin
RNA Polymerase
nscribe RNA from
moter. Perform syn
e labeled RNA in R
thesis of capped R
RNA Polymerase
nscribe RNA from
moter. Perform syn
e labeled RNA in R
thesis of capped R
dothelial Cell Gro
GF and basic fibrob
mulate the growth
s also been reporte
wth of hybridomas
upeptin
tect proteins durin
tease inhibitor. Le
ha-amino group. It
reaction by dialys
mer "random"
ndom hexamer prim
suring reverse tran
ucture. It is a prime
stone H3
tone H3 from calf t
he structure of chr
bular domain and
cleosome "beads o
og Numb
Product N

an (hIL-2)
human/murine IL-2
s and proliferation
e, or PBL derived T
enzyme and recog
erating fragments
as shown (*). 5-me
schizomers: CciN I.
enzyme and recog
erating fragments
as shown (*). 5-me
schizomers: CciN I.
ng isolation from ti
upeptin is a tripep
t is highly soluble
is.
upeptin is a tripep
t is highly soluble
is.
ence GC*ATG?C.
bited by 6-methyla
C() or simultaneou
e at both Cs. Isosc
ence GC*ATG?C.
bited by 6-methyla
C() or simultaneou
e at both Cs. Isosc
ence GC*ATG?C.
bited by 6-methyla
C() or simultaneou
e at both Cs. Isosc
e
cloned DNA temp
nthesis with labele
RNA/DNA blots, IS
RNA in vitro with m
e
cloned DNA temp
nthesis with labele
RNA/DNA blots, IS
RNA in vitro with m
owth Factor, bovi
blast growth facto
of endothelial cells
ed to eliminate the
s and other cell typ
upeptin is a tripep
t is highly soluble
is.
mers bind through
scription of all RN
er for cDNA synthe
thymus is one of t
romatin in eukaryo
a long N-terminal
on a string" structu
ber
Name
2 dependent T-cel
of mitogen-activa
tablishes human/m
T-cell lines.
gnizes the sequenc
with 5-cohesive t
ethylcytosine in the
.
gnizes the sequenc
with 5-cohesive t
.
ssues or membran
ptide derivative with
in water and can b
ssues or membran
in water and can b
Generates fragme
adenine(*). No inh
us presence of 5-
chizomers: Bbu I, P
Generates fragme
adenine(*). No inh
us presence of 5-
chizomers: Bbu I, P
Generates fragme
adenine(*). No inh
us presence of 5-
chizomers: Bbu I, P
plate downstream
ed NTPs, generatin
H, RNase protectio
m7GpppG or m7Gp
plate downstream
ed NTPs, generatin
H, RNase protectio
m7GpppG or m7Gp
ine (bECGF)
r are the only mito
s. ECGF, bovine (c
need for feeder c
pes.
ssues or membran
in water and can b
hout the entire leng
A sequences due
esis.
he five histone pro
otic cells. Featuring
tail, H3 is involved
ure.
ll lines and
ted T-
murine
ce
termini. Inhibited
e 5'-C position is
ce
termini. Inhibited
e 5'-C position is
nes using this
h an acetylated
be removed from
nes using this
h an acetylated
be removed from
nts with 3-
ibition by 5-
Pae I
nts with 3-
ibition by 5-
Pae I
nts with 3-
ibition by 5-
Pae I
from a T3
ng labeled RNA.
on, and
pppA.
from a T3
ng labeled RNA.
on, and
pppA.
ogens that
ulture grade)
ells in the clonal
nes using this
h an acetylated
be removed from
gth of RNA,
to their random
oteins involved
g a main
d in the

1
2 mg (Random
units, 1 mo

Pack Size

0,000 U (5 g, 1 m
200 U (10 U/l)
1,000 U (10 U/l)
5 mg
25 mg
2,500 U (10 U/l)
2,500 U (40 U/l)
200 U (10 U/l)
1,000 U
5,000 U
75 mg
50 mg
m pd(N)
6
Potassiu
primers)
1 mg
ml)

um Salt, 50 A
260

ctions 5 ng

Price in

250,20
90,90
351,40
82,90
292,80
931,20
931,20
121,70
111,90
433,40
493,60
418,40
258,50
200,10

Pr

Cat.

11 03
11 04
11 04
11 04
11 04
11 04
11 04
11 04
11 04
11 04
11 04
11 04
11 04
11 04
11 04
roducts b

No.
37 668 001 Not
Not
GC
by 5
not
40 197 001 Eco
Rec
blun
(*).
Hyd
40 219 001 Nde
Nde
with
reco
Isos
40 227 001 Nde
Nde
with
reco
Isos
40 243 001 Nde
Rec
coh
No
I, Bs
40 596 001 Inte
Rec
pur
inve
47 612 001 Sal
Sal
5-c
met
Isos
47 639 001 Sm
Rec
Not
othe
Neo
47 655 001 Sac
Rec
coh
met
().
47 663 001 Xba
Rec
term
gen
hyd
47 671 001 Rsa
Rec
end
how
inhi
47 680 001 Stu
Stu
blun
indi
47 698 001 Nco
Rec
coh
of 6
Bsp
47 817 001 End
End
is a
ana
47 825 001 End
End
is a
seq
poly
by Catalo
t I
GG*C*CGC, gen
5-methylcytosine a
inhibiting (). Isos
oR V
cognizes the seque
nt ends. Inhibited
droxymethylcytosin
e I
e I recognizes the
h 5-cohesive term
ognition sequence
schizomers: FauND
e I
e I recognizes the
h 5-cohesive term
ognition sequence
schizomers: FauND
e II (Mbo I)
cognizes the seque
inhibition by 5-me
stMB I, Dpn II, Kzo
erferon-, huma
combinant Interfero
ified by standard c
estigate IFN- act
I
I recognizes the se
cohesive termini. S
thyladenine within
schizomers: none k
ma I
cognizes sequence
t inhibited by 5-me
er positions or 4-m
oschizomers: Cfr9
c I (Sst I)
cognizes the seque
thylcytosine at the
Isoschizomers: Ps
a I
cognizes sequence
mini. Requires at l
ne which methylate
droxymethylcytosin
a I
cognizes the seque
wever, the presenc
u I
I recognizes the s
nt ends. Stu I is inh
o I
cognizes the seque
6-methyladenine d
p19 I.
doproteinase Glu
doproteinase Glu-C
highly purified an
alysis and for seque
doproteinase Lys
doproteinase Lys-C
highly purified, sp
uence analysis. Su
yacrylamide gels, o
og Numb
Product N

enzyme and recog
erating fragments
as shown (*). 5-me
schizomers: CciN I.
ence G*ATATC a
by the presence of
by the presence of
ne. Isoschizomer: E
sequence CAT*A
mini. Nde I is inhibit
e as indicated (*), b
D I.
sequence CAT*A
mini. Nde I is inhibit
e as indicated (*), b
D I.
ence G*ATC, gen
bited by overlappi
ethylcytosine. Isosc
o9 I, Mbo I, Sau3A
an (hIFN-)
on-, human (hIF
chromatographic t
tivities in human c
equence GT*CG*
the recognition se
known.
e*CC*CGGG. Gen
ethylcytosine at mi
methylcytosine in e
I, TspM I, Xma I, X
ence GAG*CTC a
bited by 5-methylc
other C does not
p124B I, Sst I.
e T*CTAGA. Gene
east two nucleotid
es 6N of adenine i
ence GT*AC and
bited by the prese
ce of 6-methyladen
d (*). Isoschizomer
sequence AGG*C
hibited by the pres
zomers: Aat I, Eco1
ence *CCATGG a
bited by 5-methylc
oes not influence
u-C Sequencing G
C Sequencing Grad
nd specific serine p
ence analysis.
s-C Sequencing G
C Sequencing Grad
pecific serine prote
uitable to digest pr
or on blotting mem
ber
Name
gnizes the sequenc
with 5-cohesive t
.
and generates frag
f 6-methyladenine
f 5-methylcytosine
Eco 32I.
ATG and generate
ted by 6-methylad
but not by 5-methy
ATG and generate
ted by 6-methylad
but not by 5-methy
erating fragments
ng dam-methylatio
chizomers: BfuC I,
I.
FN-), is produce
techniques. It can b
cell systems.
*AC and generates
5-methylcytosine
equence as indica
nerates fragments
ddle C(). 5-methy
XmaC I.
and generates frag
cytosine at the cen
inhibit, nor does 6
erates fragments w
des around target s
nhibits; 5-methylcy
schizomers: none.
d generates fragme
ence of 5-methylcy
nine or 4-methylcyt
rs: Afa I.
C*CT and generates
sence of 5-methylc
47 I, Pce I, SseB I.
and generates frag
cytosine as indicat
the cleavage (). Is
Grade
de from Staphyloco
protease used for p
Grade
de from Lysobacte
ease for protein str
roteins in solution,
mbranes.
ce
termini. Inhibited
e 5'-C position is
gments with
e, as indicated
e () or 5-
es fragments
enine within the
ylcytosine ().
es fragments
enine within the
ylcytosine ().
with 5-
on as shown (*).
Bsp143 I, BssM
d in E. coli and
be used to
s fragments with
and N6-
ted (*).
with blunt ends.
ylcytosine at
bits(*).
gments with 3-
ntral C (*). 5-
6-methyladenine
with 5-cohesive
sequence; dam
ytosine and 5-
ents with blunt
ytosine (),
tosine is
s fragments with
cytosine as
gments with 5-
ted (*). Presence
soschizomers:
occus aureus V8
protein structure
r enzymogenes
ructure and
in

10
Pack Size

1,000 U (40 U/l)
10,000 U (40 U/l)
200 U (10 U/l)
1,000 U (10 U/l)
1,000 U (5 U/l)
00,000 U (5 g, 1 m
2,500 U (40 U/l)
5,000 U (40 U/l)
5,000 U (40 U/l)
20,000 U (40 U/l)
5,000 U (40 U/l)
2,500 U (40 U/l)
1,000 U (40 U/l)
3 x 50 g
3 x 5 g
www.roche

)

ml)

)

e-applied-science

Price in

351,40
282,00
86,40
344,50
314,90
240,20
203,60
365,00
340,00
400,20
291,00
314,90
393,40
397,10
326,30

253

e.com

Pr
254

www.r

Cat.

11 04
11 05
11 05
11 05
11 05
11 05
11 05
11 05
11 06
11 06
11 06
11 07
11 07
11 07
11 07
roducts b
roche-applied-sc

No.
47 841 001 Try
Dig
prot
ana
prot
51 407 001 Fib
Pro
adh
and
coa
51 440 001 dAT
Use
amp
clea
51 458 001 dCT
Use
amp
mM
51 466 001 dGT
Use
amp
100
51 482 001 dTT
Use
amp
mM
54 589 001 End
End
spe
ana
55 682 001 Sta
Mos
dep
effe
, dia
62 573 001 Mv
Mvn
blun
seq
BstF
62 590 001 DN
For
dete
rest
62 603 001 Rev
For
pre
M-M
Full
74 032 001 Col
Use
hep
suc
adip
74 059 001 Col
Use
hep
suc
adip
74 440 001 Pen
Prev
inhi
Stre
inhi
74 547 001 Ins
Con
free
fact
fact

by Catalo
cience.com
psin Sequencing
est proteins in sol
tein-structure eluc
alysis, and transloc
teins in polyacryla
ronectin (pure)
motes attachment
hesion region (cell
d promotes their bi
ating of culture dis
TP
e dATP, lithium salt
ar, colorless solutio
TP
e dCTP, lithium salt
M clear, colorless so
TP
e dGTP, lithium salt
0 mM clear, colorle
TP
e dTTP, lithium salt
M clear, colorless so
doproteinase Asp
doproteinase Asp-N
ecific metalloprotea
alysis.
aurosporine
st potent PKC inhi
pendent protein kin
ectively than with e
acylglycerol, or pho
vn I (FnuD II)
n I recognizes the
nt ends. Mvn I is in
uence, as indicate
FN I, BstU I.
A Molecular We
ermination of doub
verse Transcripta
transcription of R
paration and synth
MuLV lacks endon
-length copies of
llagenase H
e to dissociate tissu
patocytes from rat
ch as for large vess
pocytes from epidi
llagenase H
patocytes from rat
pocytes from epidi
nicillin-Streptom
vent and eliminate
ibits bacterial grow
eptomycin, aminog
ibiting protein synt
ulin-Transferrin-
ntains the most ess
e culture media in
tor supplement to
tors are added.
og Numb
Product N

g Grade
ution, in gels, or o
cidation, tryptic ma
cation studies. It is
mide gels.
t and subsequent s
binding domain) i
inding to and spre
hes. Highly purifie
t, for DNA sequen
ns or primer-extens
on of the lithium sa
t, for DNA sequen
ns or primer-extens
olution of the lithiu
t, for DNA sequen
ns or primer-extens
ess solution of the
t, for DNA sequenc
ns or primer-extens
olution of lithium s
p-N Sequencing
N Sequencing Gra
ase used for protei
bitor known. Also
nases. Protein tyro
erbstatin and genis
ospholipids.
sequence *CGCG
nhibited by 5-meth
ed (*).Isoschizomer
ight Marker VI
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
ase M-MuLV
NA fragments up t
hesis of 1st-strand
nuclease activity an
large mRNA are o
ues to establish pr
liver and for the p
sel endothelial cell
idymal fat pads of
ues to establish pr
liver and for the p
idymal fat pads of
ycin
e bacterial contam
wth by inhibiting p
glycoside antibiotic
thesis.
-Sodium Selenite
sential growth-pro
an optimized ratio
which other cell ty
ber
Name
n blotting membra
apping, fingerprint
suitable for the di
spreading of cells.
interacts with mam
ading on plastic. U
d lyophilizate.
cing, labeling, and
sion reactions. dAT
alt (pH 7).
cing, labeling, and
sion reactions. Sup
um salt (pH 7).
cing, labeling, and
sion reactions. It is
lithium salt (pH 7)
cing, labeling, and
sion reactions. Sup
salt (pH 7).
Grade
ade is a highly puri
in structure and se
inhibits cAMP- an
osine kinases are b
stein. Does not com
G and generates fr
hylcytosine within
rs: Acc II, Bsh1236
mplifies accurate m
A fragments genera
to 10 kb. Use in cD
cDNA for RT-PCR
nd has lower RNas
btained.
rimary cell cultures
reparation of othe
s, and for the isola
rats.
reparation of othe
rats.
inants in cell cultu
eptidoglycan synth
c, inhibits bacteria
e Supplement
omoting componen
o. It is used as a ba
ype-specific nutrie
anes. Use for
ing, sequence
gestion of
The cell
mmalian cells
Used for the
d all types of
TP is a 100 mM
d all types of
pplied as a 100
d all types of
s supplied as a
).
all types of
pplied as a 100
ified and
equence
nd cGMP-
blocked more
mpete with Ca
2+

ragments with
the recognition
I, BspFN I,
molecular weight
ated by
2.1 kbp.
DNA library
R. Unlike AMV,
se H activity.
s. Isolate
r types of cells,
ation of
s. Isolate
r types of cells,
ation of
ure. Penicillin G
hesis.
al growth by
nts of serum-
asal growth-
ents and growth

250 l (25
standard
250 l (25 m
a
250 l (25
standard
250 l (25 m
a
50 g in 200 l
for 20 ml
50

Pack Size

4 x 100 g
1 mg
mol, 100 mM) for
d PCR assays of 20
assays of 20 l eac
mol, 100 mM) for
d PCR assays of 20
assays of 20 l eac
3 x 2 g
500 g
200 U (10 U/l)
(1 A
260
unit) for up
500 U
100 mg
500 mg
((500x), lyophiliza
0 mg (for 5 l mediu
r up to 6,250
0 l each
standard PCR
ch
r up to 6,250
0 l each
standard PCR
ch
p to 50 gel lanes
te, sterile)
um)

Price in

278,10
174,60
68,80
68,80
68,80
68,80
403,90
426,00
109,10
152,00
231,50
59,00
250,90
67,10
168,80

Pr

Cat.

11 08
11 08
11 08
11 08
11 08
11 08
11 08
11 08
11 08
11 08
11 08
11 08
11 08
11 08
roducts b

No.
80 725 001 Neu
From
(2
glyc
hyd
80 938 001 Fib
Pro
adh
and
coa
82 035 001 SuR
One
and
bee
acti
82 132 001 Phy
Phy
phy
pro
86 090 001 Cal
Stro
and
prot
wei
87 789 001 Col
Use
hep
suc
adip
88 726 001 End
Use
glyc
glyc
N-G
88 793 001 Col
Diss
mam
sus
viab
88 807 001 Col
Diss
mam
sus
and
88 815 001 Col
Diss
mam
sus
and
88 831 001 Col
Diss
mam
sus
and
88 858 001 Col
Diss
bloo
esta
inte
88 866 001 Col
Diss
bloo
esta
inte
88 882 001 Col
Diss
bloo
esta
inte

by Catalo
uraminidase (Sia
m Vibrio cholerae ;
2,3-, 2,6-, 2,8-
coproteins, and gly
drolytic cleavage of
ronectin (pure)
motes attachment
hesion region (cell
d promotes their bi
ating of culture dis
RE/Cut Buffer Se
e set containing 1
d H for DNA restric
en determined in e
vity in double-dige
ytohemagglutinin
ytohemagglutinin P
ytohemagglutinin.
liferation in lymph
lpain Inhibitor I
ong inhibitor of Ca
d II. Inhibits calpain
tein kinase C. Mos
ght and lack of ch
llagenase H
patocytes from rat
pocytes from epidi
doglycosidase H
e recombinant End
coproteins. Endogl
copeptides and pro
Glycosidase A to cl
llagenase A
sociate tissue (lun
mmary gland, bloo
pensions to establ
llagenase B
sociate tissue (lun
mmary gland, bloo
pensions to establ
d viability are impo
llagenase B
sociate tissue (lun
mmary gland, bloo
pensions to establ
llagenase B
sociate tissue (lun
mmary gland, bloo
pensions to establ
llagenase D
sociate tissue (lun
ablish primary cell
egrity of cell-surfac
llagenase D
sociate tissue (lun
ablish primary cell
llagenase D
sociate tissue (lun
ablish primary cell
og Numb
Product N

alidase)
; hydrolyzes termin
-linked to oligo-, p
ycolipids). For glyc
f sialic acid from b
t and subsequent s
binding domain) i
inding to and spre
hes. Highly purifie
et for Restriction
ml 10x solutions e
ction digests. Activ
each buffer to selec
ests.
n-M (PHA-M)
PHA-M is the muc
It is a potent mitog
ocyte cultures.
a
2+
-dependent neu
n, which activates
st likely membrane
harged residues.
ues to establish pr
liver and for the p
idymal fat pads of
doglycosidase H fo
lycosidase H hydro
oteins. It cleaves o
leave glycopeptide
g, heart, muscle, b
ality are important
g, heart, muscle, b
rtant.
g, heart, muscle, b
rtant.
g, heart, muscle, b
rtant.
g, heart, muscle, b
etc.), and prepare
culture systems. U
ce proteins are imp
g, heart, muscle, b
etc.), and prepare
culture systems. U
ce proteins are imp
g, heart, muscle, b
etc.), and prepare
culture systems. U
ce proteins are imp
ber
Name
nal N- or 0-acylneu
poly-, mucopolysac
coconjugate structu
biological material.
spreading of cells.
interacts with mam
ading on plastic. U
d lyophilizate.
Enzymes
each of SuRE/Cut B
vity of all restriction
ct 100% activity or
oprotein form of
gen used to stimul
utral cysteine prote
myosin light chain
e permeable due to
reparation of othe
rats.
r the deglycosylati
olyzes N-linked oli
only high mannose
es.
ulture systems. Use
t.
ulture systems. Use
ulture systems. Use
ulture systems. Use
bone, liver, mamma
single-cell suspen
Use when function
portant.
bone, liver, mamma
single-cell suspen
Use when function
portant.
bone, liver, mamma
single-cell suspen
Use when function
portant.
uraminic acids
ccharides,
ural studies and
The cell
mmalian cells
Used for the
Buffer A, B, L, M,
n enzymes has
to calculate
ate cell
eases calpain I
n kinase and
o low molecular
s. Isolate
r types of cells,
ation of
ion of
gosaccarides of
structures. Use
cartilage,
single-cell
e when yield,
cartilage,
single-cell
e when yield
cartilage,
single-cell
e when yield
cartilage,
single-cell
e when yield
ary, kidney,
sions to
nality and
ary, kidney,
sions to
nality and
ary, kidney,
sions to
nality and

Pack Size

1 U
5 mg
1 set
20 mg
25 mg
2.5 g
1 U (200 l)
2.5 g
100 mg
500 mg
2.5 g
100 mg
500 mg
2.5 g

Price in

104,00
694,00
23,40
150,20
224,80
1.009,90
406,10
1.009,90
59,00
251,90
1.009,90
59,00
251,90
1.009,90

255

e.com

Pr
256

www.r

Cat.

11 08
11 08
11 08
11 08
11 09
11 09
11 09
11 09
11 09
11 09
11 09
11 09
11 09
11 09
11 09
roducts b
roche-applied-sc

No.
88 939 001 Tum
Has
acti
acti
Rec
88 947 001 BM
BM
the
use
thaw
89 153 001 Stre
Use
imm
Stre
89 161 001 Stre
Use
imm
and
pho
92 758 001 Cla
Rec
coh
met
I, Bs
93 037 001 Chr
Use
in p
use
93 070 910 Bio
For
tran
(Tra
colo
93 088 910 Dig
Sub
tran
labe
and
93 266 910 Stre
Use
imm
and
pho
93 274 910 Ant
Det
colo
imm
non
nort
93 657 910 DIG
Non
dUT
sub
dot
96 176 001 Blo
Bloc
filte
Bloc
97 059 001 Bcl
Rec
coh
pos
met
97 075 001 Alk
Use
pho
enz
con
97 113 001 Col
Col
vari
Col
dete
by Catalo
cience.com
mor Necrosis Fac
s cytolytic, cytostat
vating/growth stim
vity on cell types i
combinant (yeast),
M Condimed H1
Condimed H1 is a
growth of B-cell h
ed to replace feede
wing cells stored i
eptavidin-POD
e Streptavidin-POD
munohistocytochem
eptavidin is covale
eptavidin-AP
e Streptavidin-AP t
munohistocytochem
d western blotting.
osphatase. Supplie
a I
cognizes the seque
thylcytosine as sho
spD I, BspX I, Bsu1
romozym t-PA
e Chromozym t-PA
purified preparation
ed to evaluate the c
otin-16-dUTP
nonradioactive DN
nslation. Substrate
anscriptor). Detect
or or chemilumines
goxigenin-11-dUT
bstrate for Taq, E. c
nsalation, random
eled DNA needs to
d reprobing, use D
eptavidin-AP
e Streptavidin-AP t
munohistocytochem
d western blotting.
osphatase. Supplie
ti-Digoxigenin-A
tect digoxigenin-la
ony/plaque hybridi
munohistocytochem
nradioactive DNA s
thern blotting.
G DNA Labeling a
nradioactive rando
TP, followed by col
bstrates NBT and B
blots, and colony
ocking Reagent
cking Reagent is u
er hybridization and
cking reagent doe
I
cognizes the seque
sition of adenine. In
thylcytosine. Isosch
kaline Phosphata
e this calf intestina
osphates from DNA
zyme (20 U/l), con
ncentration (1 U/l
llagenase/Dispas
lagenase/Dispase
ety of different tiss

lagenase/Dispase
ermined empirical
og Numb
Product N

ctor-, human (h
tic activity on trans
mulating activity on
in vitro , and can ca
10 g/ml PBS, 1 m
a supplement to no
hybridomas after fu
er cells, and optimi
n liquid nitrogen.
D to detect biotinyl
mistry, in situ hybr
ntly coupled to ho
mistry,
Streptavidin is cov
ed as clear, colorles
ence *AT*CG*AT
inhibited by overla
own (*). Isoschizom
15 I, BsuTU I.
A as a substrate for
ns and in cell cultu
content of one-cha
NA labeling by ran
for TdT, DNA poly
t using streptavidin
scent substrate (C
TP, alkali-stable
coli polymerase, R
primed labeling, a
o survive alkaline t
IG-11-dUTP, alkali
mistry, ISH,
Streptavidin is cov
ed as a clear, color
AP, Fab fragments
abeled compounds
ization, ELISA, gel
sequncing blots, a
and Detection Kit
om primed labeling
lor detection using
BCIP. Use labeled p
and plaque screen
used to decrease t
d the detection of
es not contain BSA
ence TG*AT*CA, g
bited by the dam g
nhibited by 5-hydr
hizomers: Fba I, Ks
ase
al alkaline phospha
A or RNA. This pre
nvenient for large-
) is also available.
se
is used for the p

sues and organs. T
for preparation o
ly.
ber
Name
hTNF-)
sformed cell lines,
n many normal cel
ause tumor necros
mg/ml BSA.
ormal culture med
usion and during c
izes growth of hyb
ated compounds i
ridization, and wes
rseradish peroxida
ted compounds us
valently coupled to
ss solution.
and generates fra
apping dam-methy
r the determination
ure supernatants. I
ain and two-chain
ndom priming, PCR
ymerase I, Taq, and
n-alkaline phospha
CSPD, CDP-Star ).
RT, and TdT. Replac
nd PCR. Use when
treatment. For mem
i-labile.
ted nucleic acids in
valently coupled to
less solution.
s
s using cDNA array
shift assays,
ridization, RNase p
nd Southern, west
t
g of DNA probes u
g anti-DIG-AP conj
probes in Southern
ning.
he background in
nucleic acid hybri
A.
generating fragme
gene and methylat
roxymethyl-cytosin
sp22 I.
atase to remove 5'-
ep has a high conc
scale experiments
preparation of cells
The suitability of
of a particular cell
ls, antiviral
sis in vivo .
ium to support
cloning. It is
ridomas after
n ELISA,
stern blotting.
ase.
sing ELISA,
o alkaline
gments with 5'-
ylation and 5-
9 I, BseC I, BshV
n of t-PA, both
It can also be
t-PA.
R, or nick
d RT
atase and a
ces dTTP in nick
n the DIG-
mbrane stripping
n ELISA,
o alkaline
ys,
protection,
tern, and
using DIG-11-
jugate and the
n, northern, and
nonradioactive
ds. This Roche
ents with 5-
tes the 6N-
e, but not by 5-
-terminal
centration of
s. A lower
s from a wide
type must be

10
50
25
1 kit for up to 2
of 50 blots, 10
Pack Size

g (1,000,000 U, 1
100 ml (10x)
500 U
1,000 U (1 ml)
2,500 U (40 U/l)
20 mg
0 l (50 nmol) (1 m
5 l (25 nmol) (1 m
150 U (200 l)
150 U (200 l)
5 labeling reaction
ng to 3 g per ass
cm
2

50 g
2,500 U (40 U/l)
1,000 U (20 U/l)
500 mg
ml)

mM)
mM)
ns and detection
say, blots of 100

Price in

908,20
411,80
239,40
336,20
299,10
333,70
286,00
225,80
139,90
191,90
801,40
88,60
175,10
103,40
454,20

Pr

Cat.

11 10
11 10
11 10
11 11
11 11
11 11
11 11
11 11
11 11
11 11
11 11
11 11
11 12
11 12
11 12
roducts b

No.
02 982 001 Mro
Rec
coh
inhi
Aor
03 024 001 Nar
Rec
coh
met
pos
04 616 001 Bas
Mit
vasc
cho
and
12 422 001 ABT
Idea
mar
sub
sod
12 481 001 Stre
Use
imm
cov
12 589 001 Blo
This
bind
12 597 001 ABT
For
pero
as a
pho
17 777 001 Bst
Rec
with
met
enz
17 785 001 Bst
Rec
with
met
enz
17 807 001 Ksp
Belo
frag
gen
of 5
17 831 001 cDN
Syn
libra
gen
for
19 915 001 RNa
Effic
pre
deo
a bo
20 166 001 Eryt
Eryt
diffe
resp
and
20 417 001 Bas
Mit
vasc
cho
and
23 149 001 Bas
Mit
vasc
cho
and
by Catalo
o I (Acc III)
cognizes the seque
hesive ends. Inhibit
ibition by overlapp
r13H I, BseA I, Bsp
r I
cognizes the seque
hesive ends. Inhibit
thylcytosine at the
sitions. Isoschizome
sic Fibroblast Gro
ogen for mesoderm
cular and corneal
ondrocytes, and os
d limb and lens reg
TS Tablets
al substrate for enz
rker enzyme. Each
bstrate solution. Th
ium perborate, cit
eptavidin--Gal
e Streptavidin--G
munohistocytochem
valently coupled to
ocking Reagent
s Blocking Reagen
ding sites in ELISA
TS Buffer
preparing the enz
oxidase as the ma
a powder: sodium
osphate.
tX I
cognizes the seque
h 3-overhanging e
thylcytosine within
zyme has no known
tX I
cognizes the seque
h 3-overhanging e
thylcytosine within
zyme has no known
p I (Sac II)
ongs to a class of
gments of genomic
nerates fragments
5'-methylcytosine.
NA Synthesis Sys
nthesize ready-to-u
aries, for substract
nes, and to in vitro
hybridization on m
ase, DNase-free
ciently removes co
parations. Heterog
oxyribonuclease. U
oiling step. Solutio
thropoietin, hum
thropoietin is a gly
erentiation of eryth
ponsive to EPO hav
d adult spleen.
sic Fibroblast Gro
ogen for mesoderm
cular and corneal
ondrocytes, and os
d limb and lens reg
sic Fibroblast Gro
ogen for mesoderm
cular and corneal
ondrocytes, and os
d limb and lens reg
og Numb
Product N

ence T*CCGGA,
ted by 5-methylcyt
ping dam-methylat
13 I, BspE I, Kpn2
ence GG*CGCC a
ted by 5-methylcyt
3'-position and by
ers: Mly113 I.
owth Factor (156
m- and neuroectod
endothelial, muscl
teoblasts). Induces
generation in vivo .
zyme immunoassa
tablet contains 50
e buffer solution f
ric acid, and disod
l
Gal to detect biotin
mistry, and western
-galactosidase
nt preparation is us
A procedures. Supp
zyme immunoassay
rker enzyme for hi
perborate, citric ac
ence *CC*A(N)5N
ends. BstX I is inhi
n the recognition s
n isoschizomers.
ence *CC*A(N)5N
ends. BstX I is inhi
n the recognition s
n isoschizomers.
rare-cutter enzym
c DNA. Recognizes
with 3'-cohesive e
Isoschizomers: Sac
stem
use ds cDNA to co
tive hybridization t
transcribe whole
microarrays.
ontaminating RNA
geneous mixture of
se directly in any D
on: 500 g/ml.
man (hEPO)
ycoprotein which s
hroid precursor ce
ve been identified
owth Factor, hum
m- and neuroectod
endothelial, muscl
teoblasts). Induces
owth Factor, hum
m- and neuroectod
endothelial, muscl
teoblasts). Induces
ber
Name
generating fragme
tosine(*). In contra
tion(). Isoschizom
I.
and generates frag
tosine as shown (*
y 5'-hydroxymethy
6 Aa), bovine (bb
derm-derived cells
le, and glial cells, m
s vessel growth, w
ays with horseradis
0 mg ABTS substra
for ABTS substrate
dium hydrogen pho
nylated compound
n blotting. Streptav
from E. coli .
sed for the blockin
plied as a yellowis
y buffer when usin
igh reaction sensit
cid, disodium hydr
NTGG and generat
bited by 6-methyla
equence as indica
NTGG and generat
bited by 6-methyla
equence as indica
es which generate
s the sequence CC
ends. Not sensitive
c II, Sst II.
onstruct non-direct
to enrich differenti
cDNA to generate
from plasmid or g
f ribonucleases, pr
DNA isolation tech
stimulates prolifera
ells to mature eryth
in adult bone mar
man (hbFGF)
derm-derived cells
s vessel growth, w
man (hbFGF)
derm-derived cells
s vessel growth, w
ents with 5'-
ast to BseA I, no
ers: Acc III,
gments with 5-
). Inhibited by 4-
lcytosine in all
bFGF)
s (fibroblasts,
myoblasts,
wound healing,
sh peroxidase as
ate, for a 50 ml
e consists of
osphate.
s in ELISA,
vidin is
ng of nonspecific
h powder.
ng horseradish
tivity. Supplied
rogen
tes fragments
adenine and 5-
ated (*). The
tes fragments
adenine and 5-
ated (*). The
e large
CGCGG and
to the presence
tional cDNA
ally expressed
e labeled cRNA
genomic DNA
repared free of
hnique, without
ation and
hrocytes. Cells
rrow, fetal liver,
s (fibroblasts,
myoblasts,
wound healing,
s (fibroblasts,
myoblasts,
wound healing,

20 tablets (ea
27 g for
1 kit
2
Pack Size

100 U (1 - 5 U/l)
1,000 U (10 U/l)
10 g
solution)
500 U
one liter blocking
16.7 g (for 1 l)
250 U (10 U/l)
1,250 U (10 U/l)
1,000 U (10 U/l)
500 g (1 ml)
250 U (2.5 g, 1 m
25 g
10 g
www.roche

0 ml substrate
solution

tions
l)
e-applied-science

Price in

353,50
251,10
302,00
65,90
279,20
49,60
48,30
64,80
261,50
94,40
651,70
154,00
363,80
769,90
342,00

257

e.com

Pr
258

www.r

Cat.

11 13
11 13
11 13
11 14
11 14
11 14
11 14
11 14
11 14
11 14
11 16
11 16
11 16
11 16
11 16
roducts b
roche-applied-sc

No.
31 397 001 EclX
Rec
coh
sho
Bse
34 515 001 Pro
Affi
from
ente
cult
38 600 001 Inte
Rec
cell
mur
stan
40 922 001 CTP
CTP
suc
is te
40 949 001 UTP
This
tran
mM
40 957 001 GTP
Suit
pre
salt
40 965 001 ATP
Suit
pre
salt
46 165 001 Taq
Taq
pro
PCR
labe
46 173 001 Taq
Taq
pro
PCR
labe
47 528 001 Inte
Allo
natu
lym
thym
62 306 001 ATP
ATP
Hyd
thio
Sup
64 368 001 N-A
Add
life
Ace
67 103 001 Eco
Eco
with
as i
Aor
68 851 001 Bss
Rec
ove
gen
indi
68 860 001 Bbr
Rec
blun
reco
I, Pm

by Catalo
cience.com
X I (Xma III)
cognizes the seque
own (*). 5-methylcy
eX3 I, BstZ I, Eag I,
otein A Agarose
nity chromatograp
m many species. Te
erotoxins. Use to p
ture supernatant.
erleukin-6, huma
combinant IL-6, hu
s, and can be used
rine and human hy
ndard chromatogra
P
P, a 100 mM soluti
ch as in vitro RNA
ested for the absen
P
s special quality pr
nscription since it i
M solution of the lit
P
paration is tested f
t solution, 100 mM
P
paration is tested f
t solution, 100 mM
q DNA Polymeras
q DNA Polymerase
duced using rigoro
R, and other prime
eling.
q DNA Polymeras
q DNA Polymerase
duced using rigoro
R, and other prime
eling.
erleukin-2, huma
phocytes and natu
mocyte, splenocyte
P--S
P--S is a substra
drolyzed very slowl
ophosphorylated, p
pplied as a lithium
Acetyl--D-Gluco
ditional control sol
science research s
etyl--D-glucosam
o47 III
o 47 III recognizes t
h blunt ends. Eco4
ndicated (*). 6-me
r51H I.
sH II
cognizes the seque
rhanging ends. Be
nerate large fragme
rP I (PmaC I)
cognizes the seque
nt ends. The enzym
ognition site as ind
maC I, Pml I, and P
og Numb
Product N

ence *CGG*C*CG
bited by 5-methylc
ytosine in position
Eco52 I.
phy using Protein A
ested for the abse
purify mouse mono
an (hIL-6)
uman is a growth f
d to replace feede
ybridomas. It is pro
aphic techniques.
on of the lithium s
transcription. This
nce of RNases.
reparation of UTP
is tested for the ab
thium salt (pH 7).
ons such as in vitro
for the absence of
, pH 7.
ons such as in vitro
for the absence of
, pH 7.
se, 5 U/l
(5 U/l) is ideal fo
ous purity and qua
er-extension reactio
se, 5 U/l
(5 U/l) is ideal fo
ous purity and qua
an (hIL-2)
human/murine IL-2
s and proliferation
e, or PBL derived T
ate and inhibitor of
ly by phosphatases
proteins are resista
salt, 100 mM solu
osaminidase Con
ution for the deter
samples with the a
minidase on autom
the sequence AG
47 III is inhibited by
etyladenine is not i
ence G*CG*CGC
elongs to a class o
ents of DNA. Inhib
zomers: BseP I, Pau
ence CA*CGTG a
me is inhibited by 5
dicated (*). BbrP I
PspC I.
ber
Name
G and generates fra
cytosine in position
4 also inhibits. Iso
A agarose is ideal
nce of staphylococ
oclonal antibodies
actor for murine a
r cells in the prepa
oduced in E. coli a
salt, is suitable for
s special quality pre
is suitable for in vi
bsence of RNases.
o RNA transcriptio
f RNases. Supplied
o RNA transcriptio
f RNases. Supplied
or routine PCR. Th
ality standards for
ons, such as seque
or routine PCR. Th
ality standards for
ons, such as seque
2 dependent T-cel
of mitogen-activa
tablishes human/m
T-cell lines.
f ATP-dependent e
s and most ATPase
ant to protein phos
tion, pH 7.
ntrol (NAG Contr
rmination of NAG a
aid of the Test-Com
mated analyzers.
*CGCT and gene
y the presence of 5
nhibiting.Isoschizo
and generates frag
f rare-cutter enzym
bited by 5'-methylc
u I.
nd generates frag
5-methylcytosine w
is an isoschizomer
agments with 5-
n 1 and 5 as
oschizomers:
for purifying IgG
ccal
from ascites or
nd human B-
aration of
and purified by
applications
eparation of CTP
itro RNA
UTP is a 100
on. The
d as a lithium
on. The
d as a lithium
e enzyme is
use in PCR, RT-
encing and
e enzyme is
use in PCR, RT-
encing and
ll lines and
ted T-
murine
enzyme systems.
es. Once
sphatases.
rol)
activity in urine
mbination N-
erates fragments
5-methylcytosine
omers: Afe I,
gments with 5-
mes, which
cytosine as
ments with
within the
r of Acv I, Eco72

5 ml
20
400
400
400
400
100 U for up
volume eac
500 U for up
volume eac
50

Pack Size

1,000 U (10 U/l)
00,000 U (2 g, 1 m
l (40 mol, 100 m
l (40 mol, 100 m
l (40 mol, 100 m
l (40 mol, 100 m
p to 200 reactions
ch containing 0.5 U
Polymerase
to 1,000 reactions
ch containing 0.5 U
Polymerase
0,000 U (25 g, 5 m
20 mol (200 l)
3 x 1 ml
100 U (5 U/l)
200 U (10 U/l)
500 U (10 U/l)

ume)
ml)
mM)
mM)
mM)
mM)
of 20 l final
U Taq DNA
s of 20 l final
U Taq DNA
ml)

Price in

490,00
531,50
257,20
108,40
108,40
108,40
108,40
89,00
356,00
1.046,40
469,10
98,20
189,80
114,90
91,40

Pr

Cat.

11 17
11 17
11 17
11 17
11 17
11 17
11 17
11 17
11 17
11 17
11 19
11 20
11 20
11 20
11 20
roducts b

No.
70 376 001 Ant
Ant
bloo
on a
cryo
75 025 910 DIG
Com
(SP
effic
and
75 033 910 DIG
Non
dUT
dete
chro
75 041 910 DIG
Con
acid
labe
and
75 050 001 Asp
Rec
frag
5-m
not
75 068 001 Bgl
Rec
coh
but
Bgl
75 084 001 Eco
Eco
with
or b
isos
75 114 001 Taq
Taq
coh
indi
79 179 001 Col
Col
for t
lyop
79 896 001 Res
Hig
acid
seq
of r
98 939 001 Bfr
Rec
coh
met
I, M
02 332 001 Am
Am
acti
term
poly
02 367 001 Am
Am
acti
term
poly
02 375 001 DO
Hig
for t
cha
and
02 693 001 Ant
Ant
in b
sing
cryo
by Catalo
ti-Bromodeoxyur
ti-Bromodeoxyurid
od, tissues, and tu
a single-cell level
osections, and par
G RNA Labeling K
mplete kit for RNA
6/T7). DIG-labeled
ciency. Used in no
d RNase protection
G DNA Labeling K
nradioactive rando
TP. Used for in situ
ection. Detect labe
omogenic or chem
G Nucleic Acid De
ntains all reagents
d hybrids. Used in
eled nucleic acids
d the color substrat
p718 I
cognizes GGTAC
gments with 5 coh
influence activity(
l II
cognizes the seque
is sensitive to 5-m
II has no known is
oR I
o RI recognizes the
h 5-cohesive term
both A residues, an
schizomer to Rsr I.
q I
q l recognizes the s
hesive termini. Taq
llagen
lagen is used as a
the coating of cult
philizate is cell cult
striction Protease
hly purified, specia
d sequence IleGl
uence may also be
ecombinant fusion
I (Afl II)
cognizes the seque
hesive ends. The en
thylcytosine at the
MspC I, and Vha464
myloglucosidase
yloglucosidase is u
vity: approx. 6 U/m
minal glucoses tha
ysaccharide of mu
myloglucosidase
yloglucosidase is u
vity: approx. 6 U/m
minal glucoses tha
ysaccharide of mu
TAP Liposomal T
hly efficient transf
transient or stable
arged molecules, s
d proteins into mam
ti-Bromodeoxyur
ti-Bromodeoxyurid
blood, tissues, and
gle-cell level using
osections, and par
og Numb
Product N

ridine
ine is used for mo
mors, as well as fo
using flow cytome
raffin sections.
Kit (SP6/T7)
A labeling using DIG
d run-off transcript
orthern/Southern b
n experiments.
Kit
om primed labeling
u and filter hybridiz
eled hybrids using
miluminescence AP
etection Kit
to detect membra
Southern, norther
are detected using
tes NBT and BCIP
C*C; same sequenc
hesive ends, not 3
ndicated (*). Meth
(). Neoschizomer:
ence AGAT*CT a
not inhibited by ov
methyl and 5-hydro
soschizomers.
e sequence G*A*A
nd by 5-methylcyto
sequence TCG*A
I is inhibited by ov
zomers: Tth HB8 I.
substrate for cultu
ture dishes and the
ture grade.
e Factor Xa
al quality serine pr
uGlyArg with
e used as a restric
n proteins.
ence *CTTAAG an
nzyme is inhibited
site indicated (*).
4 I.
used for the determ
mg lyo. at +25C w
at are 1,4- or 1
ltiple glucose unit
used for the determ
mg lyo. at +25C w
at are 1,4- or 1
ltiple glucose unit
Transfection Rea
fection of DNA inc
e gene expression,
uch as RNA, oligo
mmalian cells.
ridine-Fluorescei
ine-Fluorescein is
tumors, and to de
g flow cytometry, im
raffin sections.
ber
Name
onitoring proliferati
or determining Brd
etry, immunohistoc
G-11-UTP by in vit
ts are synthesized
blots, ISH, plaque o
g of DNA probes w
zations and single
anti-DIG-AP conju
P substrates.
ane-blotted, DIG-la
n, and dot blots, a
g anti-DIG-AP ant
.
ce as Kpn I but gen
ends as from Kpn
ylation of A and ce
Kpn I.
and generates frag
verlapping dam m
oxy-methylcytosine
ATT*C and genera
bited by 6-methylad
osine as indicated
A and generates fra
verlapping dam-m
uring a variety of c
e preparation of co
rotease, recognizin
h a high degree of
ction cleavage site
nd generates fragm
by the presence o
Isoschizomers: Af
mination of starch
with glycogen as su
s; supplied as lyop
mination of starch
with glycogen as su
s; supplied as lyop
agent
cluding YACs into e
and for transfer o
s, nucleotides, RN
in
used to monitor p
etermine BrdU inco
mmunohistocytoch
ng cells in
dU incorporation
ytochemistry,
tro transcription
with high
or colony lifts,
with DIG-11-
-copy gene
ugate and
abeled nucleic
nd ISH. DIG-
ibody conjugate
nerates
I. Inhibited by
entral C does
gments with 5-
ethylation (),
e, as shown (*).
tes fragments
denine at either
(*). Eco RI is an
agments with 5'-
ethylation, as
cells. It is used
ollagen gels. The
ng the amino
specificity. This
for processing
ments with 5-
of 5-
l II, BspT I, Bst98
. Specific
ubstrate. Cleaves
go- or
philizate.
. Specific
ubstrate. Cleaves
go- or
philizate.
eukaryotic cells
f negatively
P complexes,
proliferating cells
orporation on a
hemistry,

1 kit for up
1 kit for up to 4
1 kit for up
5
Pack Size

50 g (500 l)
0 labeling reaction
DNA per assay
p to 40 blots of 10
5,000 U (40 U/l)
10,000 U (40 U/l)
10,000 U (10 U/l)
10,000 U (10 U/l)
30 mg
3 x 250 g
500 U (10 U/l)
500 U
3,500 U
x 400 l (5 x 400
50 g (500 l)
www.roche
g reactions
ns, 10 ng to 3 g
cm x 10 cm

)
)
)
g)
e-applied-science

Price in

432,90
590,90
626,60
413,20
284,20
534,30
52,30
309,10
138,60
1.064,70
64,80
98,30
364,10
327,80
542,90

259

e.com

Pr
260

www.r

Cat.

11 20
11 20
11 20
11 20
11 20
11 20
11 20
11 20
11 20
11 20
11 20
11 20
11 21
11 21
roducts b
roche-applied-sc

No.
04 521 001 ABT
Idea
mar
sub
sod
04 530 001 ABT
Idea
mar
disp
per
06 893 001 Pro
Eac
a w
and
reso
07 644 001 Spe
Rec
coh
and
I, A
07 733 910 Ant
Det
Imm
Pero
07 741 910 Ant
Det
in g
imm
can
07 750 910 Ant
Use
com
rese
imm
09 183 001 Afl
Afl
frag
met
III h
09 256 910 Dig
Sub
vitro
of 3
the
09 264 001 DN
For
dete
rest
09 272 001 Nyl
Mat
(DIG
RNA
Stro
hyb
09 299 001 Nyl
Mat
(DIG
RNA
Stro
hyb
10 238 001 DIG
Ana
of s
nitr
tiss
13 857 001 Col
Use
high
and
epid

by Catalo
cience.com
TS Tablets
al substrate for enz
rker enzyme. Each
bstrate solution. Th
ium perborate, cit
TS Buffer
al enzyme immuno
rker enzyme. The r
play "over" after se
borate, citric acid,
otease Inhibitors
ch inhibitor in the s
wide variety of prote
d sensitively verifie
orufin-labeled).
e I
cognizes the seque
hesive termini. Spe
d 5-methylcytosine
hl I.
ti-Digoxigenin-P
tect digoxigenin-la
munohistocytochem
oxidase substrates
ti-Digoxigenin-Fl
tect digoxigenin-la
glycoconjugate res
munohistocytochem
nnot be used for m
ti-Digoxigenin-R
e Anti-Digoxigenin
mpounds using dig
earch, fluorescent
munohistocytochem
III
III recognizes the s
gments with 5-coh
thylcytosine at the
has no known isosc
goxigenin-11-UTP
o transcription RN
35 to 65. Detect lab
DIG Nucleic Acid
A Molecular We
ermination of doub
lon Membranes,
trix for hybridizatio
G) and biotin, or ra
A, or oligonucleoti
ongest signals and
brids.
lon Membranes,
A, or oligonucleoti
ongest signals and
brids.
G Glycan Differen
alyze and characte
selected lectins. In
ocellulose membra
ue sections.
llagenase P
h collagenase activ
d rat. The preparati
didymal fat pads o
og Numb
Product N

zyme immunoassa
tablet contains 5
e buffer solution f
ric acid, and disod
oassay substrate u
reaction's high sen
everal minutes. Su
disodium hydroge
Set
set can be used se
eases. Effectivenes
d using the Univer
ence *A*CTAGT a
e ( mA?m CTAGT)
OD, Fab fragmen
abeled compounds
s include DAB and
luorescein, Fab f
abeled compounds
search, fluorescent
mistry, and in situ
embrane applicati
Rhodamine, Fab fr
-Rhodamine to de
goxigenin-labeled s
mistry, and in situ
sequence A*C(A
hesive ends. Afl III
site indicated (*) o
chizomers.
P
and T7 RNA Polym
NA labeling reactio
beled RNA using A
Detection (color o
ight Marker VII
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
positively charge
on with nonradioac
adioactive labeling
de probes, for So
d lowest backgroun
positively charge
on with nonradioac
adioactive labeling
de probes, for So
d lowest backgroun
ntiation Kit
erize carbohydrate
addition to differe
anes, lectins can id
ues to establish pr
vity, you can isolat
ion is also used to
of rats.
ber
Name
ays with horseradis
mg ABTS substrat
for ABTS substrate
dium hydrogen pho
sing horseradish p
nsitivity can cause
pplied in solution:
en phosphate.
eparately or as coc
ss of protease inhi
rsal Protease Subs
and generates frag
he presence of N6-
as shown (*) . Isos
nts
s using dot blots, E
ridization, and wes
d BM Blue.
fragments
s using digoxigenin
t in situ hybridizati
hybridization. The
ions.
ragments
etect digoxigenin-l
sugars in glycocon
on (FISH),
hybridization.
,G)(T,C)GT and ge
is inhibited by the
on the recognition
merases. Replaces
on using a percent
Anti-DIG-AP and c
or chemiluminesce
mplifies accurate m
A fragments genera
ize range: 0.081 to
ed
ctive labeling using
g using
32
P,
35
S,
3
H
uthern, northern a
nd obtained with D
ed
g using
32
P,
35
S,
3
H
uthern, northern a
nd obtained with D
structures by the
entiating glycoprot
dentify carbohydra
te pancreatic islets
isolate adipocytes
sh peroxidase as
te, for a 5 ml
e consists of
osphate.
peroxidase as a
autoreaders to
sodium
cktails to inhibit
bition is quickly
strate (casein,
gments with 5'-
-methyladenine
schizomers: Bcu
ELISA,
stern blotting.
n-labeled sugars
on (FISH),
antibody
abeled
njugate
nerates
e presence of 5-
n sequence. Afl
s UTP in the in
Dig-UTP ratio
choose one of
ent) Kits.
molecular weight
ated by
8.57 kbp.
g digoxigenin
H with DNA,
nd dot blotting.
DIG-labeled
g digoxigenin
H with DNA,
nd dot blotting.
DIG-labeled
specific binding
eins bound to
ate structures on
s. Because of its
s from mouse
s from

20 tablets (e
1 set (10 in
25
50 g in 200 l
10
20
1 kit for the de

Pack Size

solution)
125 ml
ndividual protease
1,000 U (40 U/l)
150 U
200 g
200 g
100 U (5 U/l)
l (250 nmol, 10 m
(1 A
260
unit) for up
0 sheets (20 x 30 c
0 sheets (10 x 15 c
etection on 25 blot
cm
100 mg
ml substrate
e inhibitors)

mM)
p to 50 gel lanes
cm)
cm)
ts, each 10 x 10

Price in

53,70
29,40
346,30
351,40
210,20
210,20
210,20
261,50
260,60
152,00
423,20
235,20
620,40
80,80

Pr

Cat.

11 21
11 21
11 21
11 21
11 21
11 21
11 21
11 24
11 24
11 24
11 24
11 24
11 27
11 27
11 27
roducts b

No.
13 865 001 Col
Use
high
and
epid
13 873 001 Col
Use
high
and
epid
14 667 001 Ant
Ant
usin
wes
ligh
18 590 910 DN
DNA
in S
labe
18 603 910 DN
DNA
in S
labe
18 611 910 DN
DNA
stan
acid
19 847 001 Pol
Use
biop
It is
the
42 008 001 L-C
Det
enz
the
43 217 001 Lam
Coa
pro
hum
neu
43 233 001 Pro
Affi
for t
for t
mito
43 497 001 Sfu
Rec
coh
inse
Bsp
49 738 001 Phy
Con
high
Hig
lym
71 156 001 Tum
TNF
tum
cyto
syn
71 164 001 Inte
Sup
inhi
inhi
pha
73 922 001 Qui
Rea
unin
reac
dsD

by Catalo
llagenase P
h collagenase activ
didymal fat pads o
llagenase P
h collagenase activ
didymal fat pads o
ti-Digoxigenin, Fa
ti-Digoxigenin, FAB
ng ELISA, immuno
stern blotting. Pref
ht-chain specific an
A Molecular We
A Molecular Weig
Southern blot analy
eling and detection
A Molecular We
A Molecular Weig
Southern blot analy
eling and detection
A Molecular We
A Molecular Weig
ndard in Southern
d labeling and dete
y[d(I-C)]
e as a template for
physical investigat
s also used as a pr
determination of s
Carnitine
termine L-carnitine
zymatic UV test. Lin
test solution. For u
minin
at cell culture dishe
mote attachment a
man carcinoma, sa
uroblastoma and e
otein G Agarose
nity chromatograp
the purification of
the absence of sta
ogenic.
u I (Asu II)
cognizes the seque
ensitive to 5-methy
pT104 I, BstB I, Csp
ytohemagglutinin
nsists of only L-typ
h-efficiency induct
hly purified and te
phocytes.
mor Necrosis Fac
F- causes select
mor-bearing mice. I
ostatic activity on c
ergistically with in
erleukin-2, mous
pports growth of m
ibits binding of rec
ibits binding to hu
armacological/phys
ick Spin Columns
ady-to-use disposa
ncorporated nucle
ctions. Use in low-
DNA: <10 base pai
og Numb
Product N

ues to establish pr
ion is also used to
of rats.
ues to establish pr
ion is also used to
of rats.
ab fragments
B Fragments detec
histocytochemistry
ferentially used for
nti-sheep conjugat
ight Marker II, D
ht Marker II, DIG-l
ysis when using th
n. Size range: 0.12
ight Marker III, D
ht Marker III, DIG-
ysis when using th
n.Size range: 0.12 t
ight Marker VI, D
ht Marker VI, DIG-
blot analysis when
ection. Size range:
r RNA polymerases
tions.
imer template with
small amounts of d
e levels in seminal
nearity in the rang
use in life science
es with this highly
and growth of a va
arcoma, and retino
mbryonic carcinom
phy using Protein G
IgG from many sp
aphylococcal enter
ence TTCG*AA a
bited by 6-methyla
ylcytosine (). Isosc
p45 I, Nsp V.
n-L (PHA-L)
pe subunits (isolec
tion and functiona
ested for high-effic
ctor-, mouse (m
tive necrosis of mu
In vitro , human TN
certain transforme
terferon-.
se (mIL-2)
murine CTLL cells, n
combinant hIL-2 to
man responder ce
siological IL-2 acti
s for radiolabele
able columns quick
eotides from DNA l
-speed, swinging-b
irs. Sample size: up
ber
Name
isolate adipocytes
isolate adipocytes
ct digoxigenin-labe
y, in situ hybridiza
r secondary detect
te.
DIG-labeled
labeled, is used as
he DIG System for
to 23.1 kbp.
DIG-labeled
-labeled, is used as
he DIG System for
to 21.2 kbp.
DIG-labeled
-labeled, is used a
n using the DIG Sy
0.15 to 2.1 kbp.
s and as a DNA m
h Kornberg DNA p
dITP, dGTP, and dC
plasma, serum, or
e of 5.6 - 112 M
research applicati
y pure attachment
ariety of cell types,
blastoma cells, an
ma cells.
G agarose is the m
pecies. Recombina
and generates frag
adenine as indicat
chizomers: Bpu14
tin L4, leuko-agglu
al analysis of T-lym
ciency stimulation
mTNF-)
urine tumors when
NF- has direct cy
d cells. In this con
not human T-cells
o murine responde
ells. Study
vity in murine mod
d DNA purificatio
kly and efficiently
labeling and polym
bucket centrifuges
p to 50 l.
s. Because of its
s from mouse
s from
s. Because of its
s from mouse
s from
eled compounds
tion, and
ion using a
s a size standard
nucleic acid
s a size standard
nucleic acid
s a size
ystem for nucleic
odel for
polymerase for
CTP.
r urine using this
L-carnitine in
ons.
factor to
including
d murine
method of choice
nt form is tested
nown to be
gments with 5-
ed (*), but is
I, Bsp119 I,
utinin). Ideal for
mphocytes.
of human
injected into
ytolytic or
text, it acts
. Strongly
er cells; weakly
dels.
on
remove
merization
s. Exclusion limit

50
50
50
approximately
approxim
5 ml
5
1

Pack Size

500 mg
2.5 g
1 mg
00 l (5 g, 10 g/m
00 l (5 g, 10 g/m
00 l (5 g, 10 g/m
50 A
260
units
1 mg (2 ml)
2,000 U (10 U/l)
5 mg
g (2,000,000 U, 1
0,000 U (5 g, 1 m
20 columns
www.roche
ml)
ml)
ml)
combination for
minations)
ume)

ml)
ml)
e-applied-science

Price in

326,40
1.296,50
159,40
205,30
205,30
203,90
523,30
462,60
240,30
877,20
103,40
349,30
401,00
294,80
188,00

261

e.com

Pr
262

www.r

Cat.

11 27
11 27
11 27
11 27
11 27
11 27
11 27
11 27
11 27
11 27
11 27
11 27
11 27
11 27
roducts b
roche-applied-sc

No.
73 949 001 Qui
Rea
unin
reac
dsD
73 965 001 Qui
Rea
unin
reac
dsD
73 973 001 Qui
Rea
unin
reac
dsD
73 990 001 Qui
Rea
unla
reac
RNA
74 015 001 Qui
Rea
unla
reac
RNA
74 031 001 Bam
Rec
coh
met
resi
74 040 001 Hin
Rec
coh
hyd
inhi
74 082 001 Hin
Rec
coh
met
hyd
76 905 001 Inte
Rec
pur
the
77 049 001 Deo
Use
prim
vials
solu
77 057 001 Rib
Suit
DNA
ATP
solu
77 065 910 DIG
Eas
11-d
or in
0.65
77 073 910 DIG
Mix
(SP
and
(eac
77 081 001 Hex
This
prim
in m
and

by Catalo
cience.com
ick Spin Columns
ady-to-use disposa
ncorporated nucle
ctions. Use in low-
DNA: <10 base pai
ick Spin Columns
ady-to-use disposa
ncorporated nucle
ctions. Use in low-
DNA: <72 base pai
ick Spin Columns
ady-to-use disposa
ncorporated nucle
ctions. Use in low-
DNA: <72 base pai
ick Spin Columns
ady-to-use disposa
abeled or radioact
ctions. Use in low-
A: <12 bases. Sam
ick Spin Columns
ady-to-use disposa
abeled or radioact
ctions. Use in low-
A:<72 bases. Sam
mH I
cognizes the seque
hesive termini. Bam
due as indicated (
nd III
cognizes the seque
droxymethylcytosin
ibit (). Isoschizom
nf I
cognizes the seque
hesive termini. Sen
thylcytosine at 3po
droxymethylcytosin
erferon-, mous
combinant, Interfer
ified by standard c
study of IFN- (i
oxynucleoside Tr
e for sequencing/c
mer extension, and
s: dATP, dCTP, dG
ution of the lithium
bonucleoside Trip
table for in vitro tr
A sequencing. Thi
P, CTP, GTP, and TT
G DNA Labeling M
y-to-use nonradio
dUTP. For Souther
5 mM dTTP, 0.35 m
G RNA Labeling M
xture for RNA labe
6/T7/T3). Used in
d RNase protection
ch), 6.5 mM UTP, 3
xanucleotide Mix
s 10x Hexanucleot
med DNA labeling.
many hybridization
d northern blots, an
og Numb
Product N

s for radiolabele
able columns quick
eotides from DNA l
-speed, swinging-b
s for radiolabele
able columns quick
eotides from DNA l
-speed, swinging-b
s for radiolabele
able columns quick
eotides from DNA l
-speed, swinging-b
s for radiolabele
able columns quick
tively labeled RNA
-speed swinging-b
mple size: up to 50
s for radiolabele
able columns quick
tively labeled RNA
-speed swinging-b
ple size: up to 100
ence GGAT*CC
ence *AAG*CTT
bited by 6-methyla
mers: none known.
ence G*ANTC an
sitive to 6-methyla
osition () does no
e does. Isoschizom
se (mIFN-)
ron-, mouse (ml
chromatographic t
nterferon-) actio
riphosphate Set
cycle sequencing, l
d all types of ampli
TP, dTTP; each co
m salt (pH 7).
phosphate Set
ranscription reactio
s special quality se
TP, each containin
m salt (pH 7).
Mix
oactive rapid rando
rn, northern, and d
n; 10x solution wit
mM DIG-11-dUTP.
Mix
ling using DIG-11-
northern/Southern
n experiments; 10x
3.5 mM DIG-11-UT
x
ide Mix has all pos
. High specific acti
techniques for sc
nd in situ hybridiza
ber
Name
d DNA purificatio
kly and efficiently
labeling and polym
bucket centrifuges
p to 50 l.
d DNA purificatio
kly and efficiently
labeling and polym
bucket centrifuges
p to 100 l.
d DNA purificatio
kly and efficiently
labeling and polym
bucket centrifuges
p to 100 l.
d RNA purificatio
kly, efficiently sepa
from nucleotides
bucket centrifuges
l.
d RNA purificatio
kly, efficiently sepa
from nucleotides
bucket centrifuges
l.
and generates fra
ed by overlapping
methylcytosine at t
BstI.
and generates fra
adenine or 5-meth
methyladenine at A
nd generates fragm
adenine (*). Presen
ot prevent cleavage
mers: none known.
FN-) is produce
techniques. It is a v
ons in mouse mod
abeling, reverse tr
fication reactions.
ntains 100 mM cle
ons and RNA poly
et consists of 4 se
ng a 100 mM clear
om primed labeling
dot blots, colony an
th 1 mM dATP, dCT
-UTP by in vitro tra
n blots, ISH, plaque
x solution of 10 mM
TP.
ssible sequences f
ivity labeled DNA
creening gene libra
ation.
on
remove
merization
s. Exclusion limit
on
remove
merization
s. Exclusion limit
on
remove
merization
s. Exclusion limit
on
arate small
and labeling
. Exclusion limit
on
arate small
and labeling
. Exclusion limit
agments with 5'-
dam
the internal C
gments with 5-
ylcytosine (*). 5-
A does not
ments with 5-
nce of 5-
e, but 5-
.
ed in E. coli and
valuable tool for
el systems.
ranscription,
Set contains 4
ear, colorless
merase-directed
parate vials of
, colorless
g mix with Dig-
nd plaque lifts,
TP, dGTP (each),
anscription
e or colony lifts,
M ATP, CTP, GTP
for random
probes are used
aries, Southern

10
4 x
4 x 200 l
50 l for
40
100

Pack Size

50 columns
20 columns
50 columns
20 columns
20 columns
50,000 U (40 U/l)
50,000 U (40 U/l)
20,000 U (40 U/l)
00,000 U (20 g, 1
x 10 mol (4 x 100
(4 x 20 mol, 100
up to 25 standard
l for up to 20 reac
l for up to 50 reac
)
)
)
ml)
l)
mM, each)
reactions
ctions
ctions

Price in

420,50
188,00
420,50
280,60
280,60
807,70
359,00
814,10
797,70
126,10
222,30
164,50
168,70
60,40

Pr

Cat.

11 28
11 28
11 28
11 28
11 29
11 29
11 29
11 33
11 33
11 33
11 33
11 33
11 33
11 33
11 33
roducts b

No.
84 932 001 DN
DN
deg
DNA
this
88 024 001 Sfi
Ana
GG
Inhi
Cs i
88 059 001 Sfi
Ana
GG
Inhi
Cs i
88 075 001 Mv
Rec
coh
resi
met
92 307 001 Bsm
Rec
3'-c
seq
Isos
96 736 001 Bro
Non
imm
or o
emb
99 964 001 Bro
Non
imm
alka
add
32 465 001 Twe
Use
mem
for
and
32 473 001 Non
Solu
com
stab
nitr
32 481 001 Trit
Com
dur
elec
inje
33 054 001 Dig
hyd
For
via
with
gro
33 062 910 Ant
Use
digo
in s
33 089 001 Ant
Use
digo
in s
33 151 001 Mo
Eas
mou
of a
type
34 115 001 Ent
Ente
use
acti
by Catalo
ase I
ase I (double-stran
grades DNA. Durin
A which causes ce
s extracellular DNA
I
alyze and clone lar
C*CNNNNNGG
ibited by 5-methyl
is not inhibiting ()
I
alyze and clone lar
C*CNNNNNGG
ibited by 5-methyl
is not inhibiting ()
va I (BstN I)
cognizes sequence
hesive termini. Sen
dues, and 4-methy
thyladenine. Isosch
m I
cognizes the seque
cohesive termini.In
uence as indicated
schizomers: BsaM
omo-2'-deoxy-ur
nradioactively dete
munofluorescence.
organ cultures, or b
bedded tissue mus
omo-2'-deoxy-ur
nradioactively dete
munohistocytochem
aline phosphatase
ded, then bound to
een 20
e Tween 20 to solu
mbrane-protein co
a subsequent prot
d immunoblotting.
nidet P40 Substit
ubilize membrane
mplexes. Also inclu
bilize enzymes suc
ogen in injection v
ton X-100
mmonly used non-
ing isolation of me
ctrophoresis. Aque
ection vials. CMC: a
goxigenin-3-O-m
droxysuccinimide
DIG labeling of pr
amino groups (un
h NH
2
-groups of p
up, digoxigenin, is
ti-Digoxigenin
e Anti-Digoxigenin
oxigenin-labeled c
itu hybridization, a
ti-Digoxigenin
e Anti-Digoxigenin
oxigenin-labeled c
itu hybridization, a
ouse IgG ELISA
y, fast (2-4 hours)
use IgG in hybrido
all mouse IgG-subc
e. No crossreactivi
terokinase
erokinase is a high
ed for the cleavage
vates trypsinogen
og Numb
Product N

nd specific endonu
ng tissue dissociati
ell clumping. Addin
A. Lyophilized.
rge DNA fragment
CC. Generates fr
cytosine at central
). Isoschizomers: n
rge DNA fragment
CC. Generates fr
cytosine at central
). Isoschizomers: n
e *C*C(A,T) GG, g
sitive to simultane
ylcytosine at exten
hizomers: BstN I, B
ence G*AATGCN
hibited by 6-methy
d (*). 5-methylcyto
I, Mva1269 I, Pct I
idine Labeling an
ect BrdU incorpora
. Detect DNA synth
by in vivo labeling
st be prepared bef
idine Labeling an
ect BrdU incorpora
mistry. In the BrdU
(AP)-labeled antib
o the anti-BrdU ant
bilize membrane p
omplexes. Due to it
tein detection by U
CMC: approx. 0.06
tute
proteins during is
uded in buffers for
ch as Taq. Aqueous
vials. CMC: 0.25 m
-ionic detergent so
embrane-protein c
eous solution, 10%
approx. 0.2 mM at
methylcarbonyl-
e ester
roteins and 5'-amin
der gentle conditio
proteins or oligonu
s bound by Anti-Di
antibody (clone 1
compounds using E
and western blotti
antibody from she
compounds using E
and western blotti
, and sensitive (10
oma supernatants,
classes are detecte
ty with FBS.
hly purified prepar
e of fusion proteins
to trypsin.
ber
Name
uclease) from bovi
on, some cells are
ng DNase I to the
ts. Recognizes the
agments with 3-c
l C (*). 5-methylcyt
none.
ts. Recognizes the
agments with 3-c
l C (*). 5-methylcyt
none.
generating fragmen
eous 5-methylation
nal C. Inhibited by
BseBI, BstOI, Bst2U
N and generates
yladenine within th
osine does not inhi
.
nd Detection Kit
ated into cellular D
hesis by in vitro la
, in which frozen/p
fore fixation.
nd Detection Kit
ated into cellular D
U Labeling and Det
body to mouse imm
tibody.
proteins during iso
ts low UV absorba
UV light absorption
6 mM.
olation of membra
microplate assays
s solution, 10% (w
M.
olubilizes membran
complexes. Used f
% (w/v), filled under
+25C.
-aminocaproic a
no-substituted olig
ons). One reactive
ucleotides. The oth
igoxigenin and det
.71.256) for the de
ELISA, immunohis
ng.
eep for the detecti
ELISA, immunohis
ng.
ng/ml) ELISA for
ascites, mouse se
ed independent of
ration from calf inte
s at definite cleava
ine pancreas
e lysed, releasing
buffer degrades
sequence
cohesive termini.
tosine at other
sequence
cohesive termini.
tosine at other
nts with 5-
n at both C
6-
UI.
fragments with
he recognition
ibit ().
I
DNA by
abeling of cells
paraffin-
II
DNA by
tection Kit II, an
munoglobulin is
olation of
ance, it is ideal
n. Used in ELISA
ane-protein
s and used to
w/v), filled under
ne proteins
or native gel
r nitrogen in
acid-N-
gonucleotides
group interacts
er functional
tected.
etection of
tocytochemistry,
on of
tocytochemistry,
determining
ra, etc. Presence
f light-chain
estine and is
age site;

1 k
1 k
1 k
Pack Size

100 mg
1,250 U (10 U/l)
5,000 U (40 U/l)
5,000 U (10 U/l)
200 U (10 U/l)
5 x 10 ml
5 x 10 ml
5 x 10 ml
5 mg
100 g
200 g
3 x 30 g
www.roche

ests
ests
ests
e-applied-science

Price in

157,20
240,90
792,40
203,60
114,90
621,80
621,80
116,70
102,40
83,50
190,90
255,50
152,50
654,80
287,80

263

e.com

Pr
264

www.r

Cat.

11 33
11 34
11 35
11 35
11 35
11 36
11 36
11 36
11 36
11 36
11 36
11 36
11 36
11 36
11 36
roducts b
roche-applied-sc

No.
36 045 001 DN
For
dete
rest
47 101 001 O-G
Rele
thre
acid
glyc
51 311 001 Ent
Ente
use
acti
59 053 001 Pep
Prot
inve
clas
pha
59 061 001 PM
Inhi
prot
mos
solu
62 399 001 Me
Very
larg
epis
chro
63 514 910 DIG
Hig
Sou
che
met
63 727 001 CAT
Non
euk
repo
the
63 735 001 Hyb
Sup
cell
cell
thaw
63 743 001 Nut
Def
grow
Opt
seru
63 905 910 Dig
Sub
reve
reco
DNA
65 169 001 N-G
N-G
reco
glyc
fuco
65 177 001 N-G
N-G
reco
glyc
fuco
65 185 001 N-G
N-G
reco
glyc
fuco
65 193 001 N-G
N-G
reco
glyc
fuco
by Catalo
cience.com
A Molecular We
ermination of doub
Glycosidase
eases Gal-(1,3)-G
eonine are hydroly
d) prevent hydrolys
coproteins before p
terokinase
erokinase is a high
ed for the cleavage
vates trypsinogen
pstatin
tect proteins and e
estigation of enzym
armacological, HIV
MSF
ibits serine proteas
tease papain [reve
st cysteine or aspa
uble, water-stable
eganuclease I-Sc
y rare-cutter endo
ge DNA fragments
somal DNA, cloned
omosomal DNA is
G Luminescent D
hly sensitive, spec
uthern/northern blo
emiluminescent su
thods, with shorter
T ELISA
nradioactively and
karyotic cells transf
orter gene. Assay
sensitivity of the r
bridoma Fusion a
pplement to the no
hybridomas after
s and is also used
wing of cells store
tridoma-CS
fined supplement r
wth of SP2/0-, P3x
timizes growth of f
um-free cell cultur
goxigenin-11-ddU
bstrate for E. coli D
erse transcriptase.
ombinant TdT. DIG
A/RNA transfers, I
Glycosidase F
Glycosidase F PNG
ombinant from E.c
copeptides and gly
ose residues prese
Glycosidase F
Glycosidase F PNG
ombinant from E.c
copeptides and gly
ose residues prese
Glycosidase F
Glycosidase F PNG
ombinant from E.c
copeptides and gly
ose residues prese
Glycosidase F
Glycosidase F PNG
ombinant from E.c
copeptides and gly
ose residues prese
og Numb
Product N

ight Marker VIII
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
GaINAc from O-gly
yzed. Substituents a
sis and must be re
protein sequencin
hly purified prepar
e of fusion proteins
to trypsin.
enzymes during iso
me mechanisms, b
finity chromatogra
V, and cancer resea
ses (chymotrypsin
ersible by DTT trea
artic proteases. Pef
alternative.
ce I
onuclease. Use in a
, and for mapping
d mammalian DNA
olated from pulsed
Detection Kit
cific detection of D
ots and plaque/co
bstrate CSPD. Sign
r exposure times.
quantitatively mea
fected with a plasm
time approximatel
radioactive CAT as
and Cloning Supp
ormal culture medi
fusion and during
to optimize the gr
d in liquid nitroge
replaces FBS in hy
x63Ag8.653-, and N
freshly fused hybri
re without feeder c
UTP
DNA polymerase, T
Ideal for 3'-end la
G-labeled oligos ca
ISH, and colony/pl
Gase F of Flavobact
coli ; hydrolyzes all
ycoproteins unless
ent in insect and p
Gase F of Flavobact
ycoproteins unless
ent in insect and p
Gase F of Flavobact
ycoproteins unless
ent in insect and p
Gase F of Flavobact
ycoproteins unless
ent in insect and p
ber
Name
mplifies accurate m
A fragments genera
ize range: 19 to 11
ycans. Bindings to
at the disaccharide
emoved. For deglyc
g.
ration from calf inte
s at definite cleava
olation and purific
iological function,
phy, and structura
arch.
, trypsin, thrombin
atment]). Does not
fabloc
SC is a no
adapter cloning an
bacterial or yeast
A fragments, or ma
d-field gels.
IG-labeled nucleic
lony lifts with anti-
nal is as sensitive a
asure CAT express
mid bearing a CAT
y 4 hours. Sensitiv
ssay.
plement
um to support the
g cloning. HFCS rep
rowth of hybridom
n.
ybridoma cell cultu
NS-1-derived hybr
domas during sele
cells.
T4 /T7 DNA polym
abeling of oligonuc
an be used as a pr
aque screening.
terium meningosep
types of N-glycan
s they carry -1
plant glycoproteins
terium meningosep
types of N-glycan
s they carry -1
plant glycoproteins
terium meningosep
types of N-glycan
s they carry -1
plant glycoproteins
terium meningosep
types of N-glycan
s they carry -1
plant glycoproteins
molecular weight
ated by
14 bp.
serine and
e (e.g., sialic
cosylation of
estine and is
age site;
ation. Facilitates
and protease
al,
, cysteine
inhibit metallo-,
ontoxic, water-
nd subcloning of
chromosomes,
ammalian
c acids in
-DIG-AP and the
as radioactive
sion in
T-encoding
vity equivalent to
growth of B-
places feeder
as after the
ures. Supports
ridomas.
ection/cloning in
erase, Taq, and
cleotides with
obe for
pticum ,
chains from
-3 linked core
. In solution.
pticum ,
chains from
-3 linked core
. In solution.
pticum ,
chains from
-3 linked core
Lyophilizate.
pticum ,
chains from
-3 linked core
Lyophilizate.

50 g in 200 l
1 kit for u
1 k
25
Pack Size

(1 A
260
unit) for up
25 mU
3 x 250 g
10 mg
25 g
1,000 U
up to 50 blots of 1
10 ml (50x)
10 ml (50x)
5 l (25 nmol; 1 mM
100 U (0.1 ml)
250 U (0.25 ml)
100 U
250 U
p to 50 gel lanes
0 x 10 cm
ests
M)

Price in

173,70
328,90
1.115,30
163,10
184,40
414,90
541,40
431,80
219,10
180,30
274,20
243,20
456,00
243,20
456,00

Pr

Cat.

11 37
11 37
11 37
11 37
11 37
11 37
11 37
11 38
11 38
11 38
11 38
11 38
11 38
11 41
11 41
roducts b

No.
70 529 001 End
End
pur
map
solu
71 517 001 Sw
Swa
with
gen
Isos
71 843 001 Tum
Has
acti
acti
Rec
73 099 910 RNA
RNA
size
nuc
73 242 910 Fluo
Sub
tran
and
or E
76 454 001 Epi
Rec
pro
and
form
76 497 001 Ins
Insu
stim
insu
prim
83 175 001 Fre
Enz
sam
rese
role
83 213 001 NBT
For
colo
nort
Sup
83 221 001 BCI
For
Sou
is in
diss
88 908 910 Bio
Non
can
Det
usin
88 983 001 Aga
Aga
ana
of h
88 991 001 Aga
Aga
ana
of h
11 446 001 Iso
Isop
lac
ana
12 272 001 Tra
Tran
grow
Rec
stan

by Catalo
doproteinase Arg
doproteinase Arg-C
ified, specific cyste
ution, gels, or on m
a I
a I recognizes the
h blunt ends. The e
nomes. No informa
schizomers: Smi I.
mor Necrosis Fac
s cytolytic, cytostat
vating/growth stim
vity on cell types i
combinant (E. coli )
A Molecular Wei
A Molecular Weigh
e standard in north
cleic acid labeling
orescein-12-dUT
bstrate for termina
nscriptase. Replace
d PCR. Use labeled
ELISA with Anti-Flu
dermal Growth F
combinant, human
liferation and diffe
d mesodermal orig
mulations.
ulin, human
ulin has many activ
mulates growth and
ulin activity on sen
mary cells and cell
ee Fatty Acids, Ha
zymatic colorimetri
mples from serum a
earch tool to incre
e of free fatty acids
T
use in the sensitiv
ony/plaque hybridi
thern, and western
pplied as 100 mg/m
IP
alkaline phosphat
uthern and western
nsoluble in water. T
solved (50 mg/ml)
otin-16-UTP
nradioactively labe
n replace UTP as a
tect labeled RNA w
ng a Streptavidin-A
arose MP
arose MP is a high
high molecular wei
arose MP
arose MP is a high
high molecular wei
propyl--D-thiog
propyl--D-thioga
operon. It binds a
alog of galactose th
ansforming Growt
nsforming Growth
wth factor affectin
combinant, human
ndard chromatogra
og Numb
Product N

g-C Sequencing G
C Sequencing Grad
eine protease to cl
ng, and sequence
membrane blots.
sequence ATTTA
enzyme is very use
ation is available co
ctor-, human (h
tic activity on trans
mulating activity on
in vitro , and can ca
), 10 g/ml PBS, 1
ight Marker III, D
ht Marker III, digox
hern blot analysis w
and detection. Size
TP
l transferase, DNA
es dTTP in random
d probes for ISH wi
uorescein-AP.
Factor, human (h
Epidermal Growth
erentiation of a wid
in, and is a constit
vities on somatic c
d proliferation of c
nsitive cells. Compo
lines.
alf Micro Test
c assay to determi
and plasma. The te
ase scientific know
s in blood.
ve detection of alka
ization, immunohis
n blots, and to dete
ml solution in 70%
tase detection usin
n blotting. The reac
The blue color can
in dimethylformam
el RNA during in vi
substrate for SP6,
with a fluorescent s
AP conjugate.
h strength, multipu
ative electrophores
ight DNA via pulse
h strength, multipu
ative electrophores
ight DNA via pulse
galactoside
alactoside (IPTG) i
and inactivates the
hat cannot be clea
th Factor-1, hu
Factor-1, human
ng many functions
TGF- 1 is produc
aphic techniques.
ber
Name
Grade
de from C. histolyt
leave proteins/pep
analysis, and to di
AAAT and generate
eful for digesting G
oncerning methyla
hTNF-)
sformed cell lines,
n many normal cel
ause tumor necros
mg/ml BSA.
DIG-labeled
xigenin (DIG)-labe
when the DIG Syst
e range: 0.3 to 1.5
A polymerase I, Taq
m primed labeling,
ith direct fluoresce
EGF)
h Factor (EGF) stim
de variety of cells o
tuent of many seru
cells. Recombinant
cells and is used to
onent of serum-fre
ine free fatty acids
est combination is
wledge about the p
aline phosphatase
stocytochemistry, I
ect proteins and g
DMF.
ng immunohistocyt
ction product has
mide.
itro transcription. B
, T3, and T7 RNA p
streptavidin conjug
rpose agarose dev
rpose agarose dev
s a very effective i
lac repressor. It i
aved by -galacto
uman (hTGF-1)
n (hTGF-1), is a m
in a variety of diffe
ced in CHO cells a
ticum is a highly
ptides for
igest protein in
es fragments
GC-rich bacterial
ation sensitivity.
ls, antiviral
sis in vivo .
eled is used as a
tem is used for
kb.
q, and reverse
nick translation,
ence detection
mulates the
of ectodermal
um-free media
t human insulin
o investigate
ee media for
s in research
intended as a
physiological
e using BCIP. For
ISH, Southern,
lycoconjugates.
tochemistry and
a blue color and
ted. BCIP is
Biotin-16-UTP
polymerase.
gate or by ELISA
veloped for
s and separation
phoresis (PFGE).
veloped for
s and separation
phoresis (PFGE).
nducer of the
s a chemical
osidase.
)
multifunctional
erent cells.
and purified by

10
25
app
25

Pack Size

3 x 5 g
200 U (10 U/l)
g (1,000,000 U, 1
2 g (200 l)
5 l (25 nmol) (1 m
100 g
100 mg
3 ml (300 mg)
3 ml (150 mg)
l (250 nmol) (10 m
100 g
500 g
5 g
1 g (1 ml)
www.roche
ml)
mM)
tests
mM)
e-applied-science

Price in

305,00
103,40
908,20
322,50
257,90
426,10
140,40
604,20
108,40
86,20
253,90
219,10
768,50
308,00
702,80

265

e.com

Pr
266

www.r

Cat.

11 41
11 41
11 41
11 41
11 41
11 41
11 41
11 41
11 41
11 41
11 41
11 41
11 41
11 42
11 42
roducts b
roche-applied-sc

No.
17 240 001 Nyl
Mat
(DIG
RNA
Stro
hyb
17 959 001 SuR
10x
sele
Tris
mM
17 967 001 SuR
10x
dete
dige
mer
17 975 001 SuR
10x
dete
dige
(at
17 983 001 SuR
10x
dete
dige
dith
17 991 001 SuR
10x
dete
dige
dith
18 009 001 DN
For
dete
rest
18 025 001 Try
Use
stru
and
to c
18 033 001 Try
Use
stru
and
to c
18 165 001 Bio
The
suc
18 432 001 Taq
Taq
pro
PCR
labe
18 467 001 Chy
Use
chy
for
18 475 001 Try
Dig
prot
ana
prot
20 399 001 End
End
is a
ana
20 429 001 End
End
is a
seq
poly

by Catalo
cience.com
lon Membranes,
A, or oligonucleoti
ongest signals and
brids.
RE/Cut Buffer A
x optimized incubat
ect 100% activity o
s-acetate, 660 mM
M dithiothreitol, pH
RE/Cut Buffer B
x optimized incubat
ermined to select
ests. 100 mM Tris-
rcaptoethanol, pH
RE/Cut Buffer L
x optimized incubat
ermined to select
ests. 100 mM Tris-
+37C).
RE/Cut Buffer M
x optimized incubat
ermined to select
ests. 100 mM Tris-
hioerythritol, pH 7.5
RE/Cut Buffer H
x optimized incubat
ermined to select
ests. 500 mM Tris-
hioerythritol, pH 7.5
A Molecular We
ermination of doub
psin Sequencing
e to generate glyco
ucture elucidation,
d translocation stud
cross-linking.
psin Sequencing
e to generate glyco
ucture elucidation,
d translocation stud
cross-linking.
otin Protein Label
e kit is suitable for
ch as immunohisto
q DNA Polymeras
q DNA Polymerase
duced using rigoro
R, and other prime
eling.
ymotrypsin Sequ
e Chymotrypsin Se
ymotrypsin alone o
peptide mapping,
psin Sequencing
est proteins in sol
tein-structure eluc
alysis, and transloc
teins in polyacryla
doproteinase Glu
doproteinase Glu-C
highly purified an
alysis and for seque
doproteinase Lys
doproteinase Lys-C
highly purified, sp
uence analysis. Su
yacrylamide gels, o
og Numb
Product N

positively charge
on with nonradioac
adioactive labeling
de probes, for So
d lowest backgroun
tion buffer for RE d
or to calculate activ
potassium-acetat
7.9 (at +37C).
tion buffer for rest
100% activity or to
-HCl, 1 M NaCl, 50
8.0 (at +37C).
100% activity or to
-HCl, 100 mM MgC
100% activity or to
-HCl, 500 mM NaC
5 (at +37C).
100% activity or to
-HCl, 1 M NaCl, 10
5 (at +37C).
ight Marker IV
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
g Grade, modified
opeptides from pur
tryptic mapping, f
dies. Enzyme resis
g Grade, modified
opeptides from pur
tryptic mapping, f
dies. Enzyme resis
ling Kit
the labeling of pro
chemistry, immuno
se, 5 U/l
(5 U/l) is ideal fo
ous purity and qua
uencing Grade
quencing Grade fo
r in combination w
fingerprinting, and
g Grade
ution, in gels, or o
cidation, tryptic ma
cation studies. It is
mide gels.
u-C Sequencing G
C Sequencing Grad
nd specific serine p
ence analysis.
s-C Sequencing G
C Sequencing Grad
pecific serine prote
uitable to digest pr
or on blotting mem
ber
Name
ed
g using
32
P,
35
S,
3
H
uthern, northern a
nd obtained with D
digests. Activity de
vity in double-dige
te, 100 mM magne
tricition digests. Ac
o calculate activity
0 mM MgCl
2
, 10 m
Cl
2
, 10 mM dithioe
Cl, 100 mM MgCl
2
,
00 mM MgCl
2
, 10 m
mplifies accurate m
A fragments genera
d
rified glycoprotein
fingerprinting, sequ
stance to autolysis
d
rified glycoprotein
fingerprinting, sequ
stance to autolysis
oteins with biotin f
oblotting, and ELIS
or routine PCR. Th
ality standards for
ons, such as seque
or the hydrolysis o
with other protease
d sequence analys
n blotting membra
apping, fingerprint
suitable for the di
Grade
de from Staphyloco
protease used for p
Grade
de from Lysobacte
ease for protein str
roteins in solution,
mbranes.
g digoxigenin
H with DNA,
nd dot blotting.
DIG-labeled
etermined to
ests. 330 mM
esium acetate, 5
ctivity
in double-
mM 2-
ctivity
in double-
erythritol, pH 7.5
ctivity
in double-
, 10 mM
ctivity
in double-
mM
molecular weight
ated by
19.3 kbp.
s in protein-
uence analysis,
is increased due
s in protein-
uence analysis,
is increased due
for applications,
SA.
e enzyme is
use in PCR, RT-
encing and
f proteins by
es. It is suitable
sis.
anes. Use for
ing, sequence
gestion of
occus aureus V8
protein structure
r enzymogenes
ructure and
in

50 g in 200 l
1 kit for
1,000 U (4 x 25
20 l final vo

Pack Size

1 roll (0.3 x 3 m)
5 x 1 ml
5 x 1 ml
5 x 1 ml
5 x 1 ml
5 x 1 ml
(1 A
260
unit) for up
4 x 25 g
4 x 100 g
50 U) for up to 2,0
lume each contain
DNA Polymerase
4 x 25 g
4 x 25 g
50 g
5 g
p to 50 gel lanes
reactions
00 reactions of
ning 0.5 U Taq

Price in

552,10
25,80
25,80
25,80
25,80
25,80
161,70
112,30
379,80
282,90
640,50
101,60
76,20
157,90
128,30

Pr

Cat.

11 42
11 42
11 42
11 42
11 42
11 42
11 42
11 42
11 42
11 42
11 42
11 43
11 44
11 44
11 44
roducts b

No.
20 470 001 dUT
For
reac
DNA
con
20 488 001 End
End
spe
ana
26 320 001 Ant
Det
imm
The
anti
26 338 910 Ant
Det
imm
wes
imm
26 346 910 Ant
Det
imm
wes
imm
26 362 001 Hex
For
biol
sac
assa
27 598 910 Bio
Sub
reve
usin
colo
27 857 910 Fluo
Sub
vitro
hyb
Fluo
28 861 001 Per
Use
solu
For
she
29 868 001 Pef
Spe
com
valu
bloc
29 876 001 Pef
Spe
com
valu
bloc
35 094 001 Taq
Taq
pro
PCR
labe
41 337 001 Mu
Mu
5-c
reco
42 066 001 BM
Rea
app
sen
reac
42 074 001 BM
Colo
nort
situ
bott
by Catalo
TP
sequencing, label
ctions. DNA conta
A glycosylase. This
ntamination; 100 m
doproteinase Asp
doproteinase Asp-N
ecific metalloprotea
alysis.
ti-Fluorescein
tect fluorescein-lab
munohistocytochem
e antibody is not st
ibody in sandwich
ti-Fluorescein-AP
munohistocytochem
stern blots. Use the
munohistochemistr
ti-Fluorescein-PO
munohistocytochem
stern blots. Conjug
munohistochemistr
xokinase (HK)
the determination
logical research sa
charides which co
ay of many glycos
otin-16-ddUTP
bstrate for DNA po
erse transcriptase
ng TdT. Biotin-labe
ony/plaque screen
orescein-12-UTP
o transcription for
bridization and dire
orescein-AP, or An
roxidase (POD), a
e Peroxidase (POD
uble substances w
coupling of Ig, Ig
eep, and goat with
fabloc
SC
ecific, potent, irreve
mpared to PMSF or
ues. Completely ina
cker of thrombin in
fabloc
SC
mpared to PMSF or
ues. Completely ina
cker of thrombin in
q DNA Polymeras
q DNA Polymerase
duced using rigoro
R, and other prime
eling.
un I (Mfe I)
n I recognizes the
cohesive termini. M
ognition sequence
M Blue POD Subst
ady-to-use colorim
plications, such as
sitive than DAB an
ctions using alkali
M Purple
orimetric AP subst
thern, and Southe
u hybridization. Us
tle with no mixing
og Numb
Product N

ing, primer extens
aining dUTP is susc
s allows dUTP to b
mM lithium salt solu
p-N Sequencing
N Sequencing Gra
ase used for protei
beled compounds
tabilized with prote
-ELISAs and label
P, Fab fragments
beled compounds
e conjugate in ELIS
ry with an anti-mo
OD, Fab fragmen
beled compounds
gate only usable in
ry using anti-mous
n of D-glucose, D-f
amples. It may also
onvert to glucose o
ides.
olymerase I, TdT, Ta
(Transcriptor). Lab
eled oligo is used f
ns, and in situ hybr
P
and T7 RNA Polym
r RNA labeling. De
ect fluorescence or
nti-Fluorescein-PO
activated
), activated,withou
with reactive and ac
Fab, and Ig F(ab')
2
POD. Use in ELISA
ersible inhibitor of
r DFP with higher
activates proteinas
n serum and plasm
r DFP with higher
activates proteinas
n serum and plasm
se, 5 U/l
(5 U/l) is ideal fo
ous purity and qua
sequence CA*AT
Mun I is inhibited b
e as indicated. Isos
trate, precipitatin
metric peroxidase s
western , northern
nd produces less b
ne phosphatase de
trate for immunoh
rn blotting, colony
e stabilized substr
or reconstitution.
ber
Name
sion,and all types o
ceptible to hydroly
be used to prevent
ution.
Grade
ade is a highly puri
in structure and se
using ELISA,
ridization, and wes
ein and is suitable
ing procedures.
s
in ELISA,
ridization, Southern
SA, immunoblottin
use Ig fluorescein,
nts
in ELISA,
ridization, Southern
ELISA, immunobl
fructose, and D-so
o be used to assay
or fructose, making
aq, T4 DNA polym
bel the 3'-end of o
for DNA/RNA tran
ridization..
merase. Can repla
etect labeled RNA
r detection by ELIS
OD.
ut pre-activation to
ccessible primary a
2
fragments from r
A, IHC, and immun
serine proteases.
stability at physiol
se K. Unlike PMSF
ma.
serine proteases.
se K. Unlike PMSF
ma.
or routine PCR. Th
ality standards for
ons, such as seque
TTG and generates
by 6-methyladenin
schizomers: Mfe I.
ng
ubstrate solution f
n, and Southern bl
background stainin
etection.
istocytochemistry,
y and plaque hybrid
rate solution direct
of amplification
ysis using uracil-
carryover
ified and
equence
stern blotting.
as a coating
n, dot, and
ng, and
, Fab2 fragment.
n, dot, and
otting, and
Fab2 fragment.
orbitol in food or
other
g it useful in the
erase, and
ligonucleotides
sfers,
ce UTP in in
by in situ
SA using Anti-
o label water-
amino groups.
rabbit, mouse,
noblotting.
Nontoxic
ogical pH
, excellent
Nontoxic
ogical pH
, excellent
e enzyme is
use in PCR, RT-
encing and
s fragments with
e in the
for a variety of
otting. It is more
ng than
western,
dization, and in
tly from the

250 l (25
standard
25
25
app
5,000 U (20 x 25
20 l final vo
Pack Size

mol, 100 mM) for
d PCR assays of 20
2 g
100 g
150 U (200 l)
150 U
1,500 U (1 ml)
5 l (25 nmol) (1 m
l (250 nmol) (10 m
prox. 40 mg lyophil
100 mg
1 g
50 U) for up to 10,
lume each contain
DNA Polymerase
200 U (10 U/l)
100 ml
100 ml
www.roche
r up to 6,250
0 l each
mM)
mM)
izate
000 reactions of
ning 0.5 U Taq
e-applied-science

Price in

94,30
161,80
320,90
223,90
189,60
85,40
263,40
354,70
362,90
101,60
505,30
2.703,80
172,80
107,10
86,70

267

e.com

Pr
268

www.r

Cat.

11 44
11 44
11 44
11 44
11 45
11 45
11 46
11 46
11 46
11 46
11 46
11 46
11 48
11 48
11 48
roducts b
roche-applied-sc

No.
44 611 001 Bro
The
inco
form
44 646 001 Ura
Clea
incr
labe
carr
49 451 910 DN
DNA
stan
acid
49 460 001 DN
For
dete
rest
57 756 001 Inte
Rec
pur
mon
for
59 643 001 Pro
Mix
sing
tiss
of g
64 752 001 Alk
Act
prim
with
rab
64 825 001 Tru
Tru9
coh
ava
65 007 001 Cel
Non
in 9
Ana
anti
65 015 001 Cel
Non
in 9
Ana
anti
67 140 001 DN
The
prev
DNA
den
68 120 910 Rev
Rap
cult
retr
scre
80 022 001 Tth
Perf
tem
clon
amp
83 188 001 Firs
Syn
seq
gen
qua
84 281 001 BM
BM
ELIS
phe
non

by Catalo
cience.com
omo-2'-deoxy-ur
e kit is used for the
orporated into cell
mat.
acil-DNA Glycosy
aves DNA where a
rease efficiency of
eled oligonucleotid
ryover contaminati
A Molecular We
A Molecular Weig
ndard in Southern
d labeling and dete
A Molecular We
ermination of doub
erleukin-1, hum
combinant Interleu
ified by standard c
nocytes or macrop
a variety of sensiti
onase
x of nonspecific en
gle amino acids. D
ue dissociation alo
glycopeptides from
kaline Phosphata
ivated Alkaline Ph
mary amino groups
hout pre-activation
bit, mouse, sheep,
u9 I
9 I recognizes the
hesive termini. No i
ilable. Isoschizome
ll Proliferation Ki
nradioactive spect
96-well plates. Mea
ibodies. Requires s
ll Proliferation Ki
nradioactive spect
96-well plates. Mea
ibodies. No solubil
A, MB-grade
e ready-to-use solu
vents nonspecific
A hybridizations. A
naturing are not re
verse Transcripta
pid, sensitive ELISA
tures and other bio
roviruses in infecte
eening for RT inhib
DNA Polymeras
form reverse trans
mperatures, allowin
ning, and analysis
plification of RNA
st Strand cDNA S
nthesize 1st strand
uence-specific pri
nerate cDNA librar
antify mRNA to mo
M Blue POD Subst
Blue POD Substra
SA applications. Th
enylendiamine (oPD
ntoxic.
og Numb
Product N

idine Labeling an
e nonradioactive q
ular DNA using a
ylase
a deoxyuridylate re
site-directed muta
de probes, and, wit
ion.
ight Marker VIII,
ht Marker VII, DIG
blot analysis when
ection. Size range:
ight Marker IX
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
man (hIL-1)
ukin-1, human (h
chromatographic t
phages and other c
ve cells.
ndo- and exoprotea
Degrade protein du
ong with collagena
m glycoproteins.
ase (AP), activate
osphatase labels w
s (peptides/protein
n to label Ig, Ig Fab
and goat.
sequence TTAA
information conce
ers: Mse I, Tru1 I.
it I (MTT)
rophotometric qua
asure proliferation
ostatic compounds
solubilization.
it II (XTT)
rophotometric qua
asure proliferation
ostatic compounds
lization step.
ution is directly add
hybridization in all
Addition of NaCl, s
quired.
ase Assay, colori
A for quantitative d
ological samples. D
ed mammalian cell
bitors.
se
scription and DNA
ng its use in RT-PC
of gene expressio
at least 1 kb lengt
Synthesis Kit for
cDNA as the start
imers, poly(dT)
15
p
ries, first step in dif
onitor expression.
trate, soluble
ate, soluble, is an i
he reagent shows
D) or ABTS substr
ber
Name
nd Detection Kit
uantitative determ
96-well microplate
esidue has incorpo
agenesis, to produ
th dUTP, to elimina
DIG-labeled
G-labeled, is used a
n using the DIG Sy
19 - 1114 bp.
mplifies accurate m
A fragments genera
ize range: 72 to 13
hIL-1) is produc
techniques. Secret
cell types, it is a pl
ases that digest pr
ring DNA and RNA
ase and trypsin. Us
ed
water-soluble subs
ns) with alkaline p
b, and Ig F(ab')
2
fr
and generates fra
rning methylation
in response to gro
s. Assess growth-i
in response to gro
s. Assess growth-i
ded to the hybridiz
l types of membra
sonication or shear
imetric
determination of R
Determine propaga
s in culture. Also u
amplification at e
CR for detection, qu
n at the RNA level
th.
RT-PCR (AMV)
ting reaction for R
primers, or random
fferential display o
ideal ready-to-use
higher sensitivity t
rates and can be c
III
ination of BrdU
e cell ELISA
orated. Used to
uce highly
ate PCR product
as a size
ystem for nucleic
molecular weight
ated by
353 bp.
ed in E. coli and
ed by activated
eiotropic factor
rotein down to
A isolation. For
se in production
stances carrying
hosphatase. Use
agments from
gments with 5-
sensitivity is
feration/viability
owth factors.
nhibitory
feration/viability
owth factors.
nhibitory
zation mix. It
ne or in situ
ring, and
T activity in cell
ation of
used for in vitro
levated
uantification,
l. For RT-PCR
T PCR. Use with
m primers to
of mRNA, or
solution for
than o-
lassified as

1 k
500
50 g in 200 l
10
10 m
1 k
1 k
1 k
500 U (2 x 250
final volume
1 kit for up to

Pack Size

100 U
0 l (10 g/ml) (5
(1 A
260
unit) for up
00,000 U (2 g, 1 m
5 g
mg (approx. 40 mg
1,000 U (10 U/l)
500 mg (50 ml)
U) for up to 200 re
each containing 2
Polymerase
30 reactions, inclu
reactions
100 ml
ests
g)
p to 50 gel lanes
ml)
lyo.)

ests
ests
ests
eactions of 50 l
2.5 U Tth DNA
uding 5 control

Price in

621,80
148,40
256,00
190,70
452,70
396,10
542,40
251,10
338,80
435,60
197,80
594,10
322,00
244,00
66,50

Pr

Cat.

11 48
11 49
11 49
11 49
11 49
11 49
11 50
11 50
11 52
11 52
11 52
11 52
11 52
11 52
11 53
roducts b

No.
87 671 001 SP6
Tran
pro
Use
prot
93 027 001 IsoS
Hig
and
com
add
96 549 001 Fas
Use
with
org
usin
97 995 001 Sex
Sex
with
(*).
98 037 001 DN
For
dete
rest
98 045 910 Act
Act
qua
hyb
hum
00 694 001 BM
Idea
<10
than
mem
00 708 001 BM
Idea
<10
than
mem
20 709 001 BM
Idea
sen
than
sen
24 488 001 Pep
Prot
inve
clas
pha
26 430 001 Mlu
Rec
blun
indi
26 529 910 RNA
RNA
size
nuc
26 537 910 RNA
RNA
size
nuc
29 048 001 Leu
Prot
prot
alph
the
34 378 910 Tet
Use
tran
Lab
hyb

by Catalo
6 RNA Polymeras
nscribe RNA from
moter. Perform syn
e labeled RNA in D
tection, and synthe
Strip Mouse Mon
hly specific, fast a
d light-chain types
mparable results to
ditional equipment
st Red Tablets
ed as a substrate in
h alkaline phospha
anic solvent, which
ng organic solvent
xA I
xAI recognizes the
h 5'-cohesive term
Isoschizomers: Ma
A Molecular We
ermination of doub
tin RNA Probe, D
in RNA Probe, DIG
antity of various RN
bridization and nort
man cell lines and
M Chemiluminesc
al substrate (POD)
0 pg antigen in we
n other nonradioac
mbranes.
M Chemiluminesc
al substrate (POD)
0 pg antigen in we
n other nonradioac
mbranes.
M Chemiluminesc
al chemiluminesce
sitivity is required.
n colorimetric met
sitive as radioactiv
pstatin
tect proteins and e
estigation of enzym
armacological, HIV
uN I (Bal I)
cognizes the seque
nt ends. MluN I is
A Molecular Wei
A Molecular Weigh
e standard in north
cleic acid labeling
A Molecular Wei
A Molecular Weigh
e standard in north
cleic acid labeling
upeptin
tect proteins durin
tease inhibitor. Le
ha-amino group. It
reaction by dialys
ramethyl-Rhoda
ed in nonradioactiv
nslation, random-p
beled probes show
bridization for direc
og Numb
Product N

se
cloned DNA temp
nthesis with labele
DNA/RNA blots, in
esis of capped RN
noclonal Antibod
nd easy kit for rap
of mouse monocl
o the standard ELIS
and reagents.
n immunohistocyto
atase. The Fast Red
h may cause probl
t-containing moun
sequence AC*C(
mini. SexA I is dcm
ab I.
ight Marker X
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
DIG-labeled
G-labeled is ideal f
NA species. Applic
thern blot analysis
tissue samples.
cence Western B
) for protein and n
estern blots. Shows
ctive or radioactive
cence Western B
) for protein and n
estern blots. Shows
ctive or radioactive
cence Western B
ence system for we
. Obtain 1 to 3 orde
thods. Chemilumin
vity with shorter ex
enzymes during iso
me mechanisms, b
finity chromatogra
V, and cancer resea
ence TGGC*CA a
inhibited by overla
zomers: Mls I, Bal I
ight Marker I, DI
ht Marker I, digoxi
and detection. Size
ight Marker II, D
ht Marker II, digox
and detection. Size
upeptin is a tripep
t is highly soluble
is.
mine-5-dUTP
ve labeling of DNA
primed labeling, PC
w red fluorescence
ct fluorescence det
ber
Name
plates downstream
ed NTPs to generat
situ hybridization,
NA in vitro .
dy Isotyping Kit
pid identification of
onal antibodies. Y
SA assay without t
ochemistry and we
d reaction product
lems for in situ hy
ting media.
(T,A)GGT and gene
methylation sensit
mplifies accurate m
A fragments genera
ize range: 100 bp t
for evaluating the q
cations include in s
s to evaluate RNA
lotting Substrate
ucleic acid detecti
s at least 10-fold h
e detection system
lotting Substrate
ucleic acid detecti
s at least 10-fold h
e detection system
lotting Kit (Mous
estern and dot blot
ers of magnitude h
nescence image is
xposure.
olation and purific
iological function,
phy, and structura
arch.
nd generates frag
apping dcm-methy
, Msc I, Msp20 I.
G-labeled
igenin (DIG)-labele
when the DIG Syst
e range: 0.3 to 6.9
IG-labeled
xigenin (DIG)-label
when the DIG Syst
e range: 1.5 to 6.9
ssues or membran
in water and can b
A. Replaces dTTP in
CR, 3-tailing, and c
and are suitable fo
tection.
m from an SP6
te labeled RNA.
, RNase
f class, subclass,
ields
the need for
estern blotting
t is soluble in
bridization when
erates fragments
tive as indicated
molecular weight
ated by
to 12.2 kbp.
quality and
situ
from various
e (POD)
on. Sensitivity:
igher sensitivity
ms on PVDF
e (POD)
on. Sensitivity:
igher sensitivity
ms on PVDF
se/Rabbit)
ts where high
higher sensitivity
at least as
ation. Facilitates
and protease
al,
ments with
ylation as
ed is used as a
tem is used for
kb.
led is used as a
tem is used for
kb.
nes using this
h an acetylated
be removed from
n nick
cDNA synthesis.
or in situ

1
100 g in 400
1 set
1 set
1 kit
25

Pack Size

5,000 U
20 tablets
200 U (10 U/l)
l (2 A
260
units) fo
lanes
2 g
(4,000 cm
2
memb
(1,000 cm
2
memb
(2,000 cm
2
memb
50 mg
200 U (10 U/l)
4 g (200 l)
2 g (200 l)
100 mg
5 l (25 nmol) (1 m
www.roche
sts
or up to 50 gel
brane)
brane)
brane)
mM)
e-applied-science

Price in

433,40
314,70
85,40
152,30
125,60
399,40
344,40
165,60
417,20
457,00
106,80
355,50
392,50
630,90
241,80

269

e.com

Pr
270

www.r

Cat.

11 53
11 54
11 55
11 55
11 55
11 57
11 57
11 57
11 57
11 58
11 58
11 58
11 58
11 58
11 58
roducts b
roche-applied-sc

No.
39 426 001 -G
Qua
with
prot
enc
44 675 001 Cel
Fast
req
ELIS
cyto
58 161 001 Bln
Bln
5-c
met
58 170 001 Bln
Bln
5-c
met
58 706 910 Dig
Sub
tran
labe
and
70 013 910 Dig
Sub
tran
labe
and
73 152 910 Dig
Sub
Rep
Use
Sou
73 179 910 Dig
Sub
Rep
Use
Sou
78 553 001 PCR
Con
con
sen
sup
81 074 001 COT
Use
repe
(CIS
hyb
81 295 001 PCR
Con
dCT
Wat
cDN
82 950 001 BM
Sub
syst
ELIS
form
83 786 001 DTT
For
extr
prot
mon
83 794 001 Apr
Prot
cult
chy
qua
83 816 001 Ant
Det
tagg
imm
10-f
by Catalo
cience.com
Gal ELISA
antitatively measur
h a plasmid bearin
teins produced by
coding DNA constr
ll Death Detectio
t (5-6 hrs), sensitiv
uires coating of th
SA. For specific de
oplasmic fraction o
n I (Avr II)
I recognizes the s
cohesive termini. T
thylation. Bln I is a
n I (Avr II)
I recognizes the s
cohesive termini. T
thylation. Bln I is a
goxigenin-11-dUT
nsalation, random
eled DNA needs to
d reprobing, use D
goxigenin-11-dUT
nsalation, random
eled DNA needs to
d reprobing, use D
goxigenin-11-dUT
places dTTP in nick
e this alkaline-labil
uthern blots planne
goxigenin-11-dUT
places dTTP in nick
e this alkaline-labil
uthern blots planne
R Core Kit
ntains everything fo
nditions for basic P
sitivity/specificity u
pplied Mg-free buf
T Human DNA
e COT Human DNA
etitive DNA in in s
SS) hybridizations,
bridizations.
R Nucleotide Mix
nvenient, easy-to-u
TP, dGTP, and dTTP
ter. Optimized for
NA synthesis, and
M Chemiluminesc
bstrate solution for
tems for highly sen
SA and use with a
mat) or tube-forma
T
luminometric dete
racts. Superb prote
teins/enzymes (co
nothiols in the red
rotinin
tect proteins durin
ture studies. Used
ymotrypsin on imm
ti-HA (12CA5)
tect native influenz
ged protein contai
munoprecipitation,
fold lower conc., u
og Numb
Product N

re -Gal expressio
ng a -Gal-encod
y in-frame cloning
ruct.
on ELISA
ve, nonradioactive
e microplates with
etermination of mo
of cell lysates.
sequence CCTAG
The enzyme is not k
an isoschizomer of
sequence CCTAG
The enzyme is not k
an isoschizomer of
TP, alkali-stable
coli polymerase, R
primed labeling, a
IG-11-dUTP, alkali
TP, alkali-stable
coli polymerase, R
primed labeling, a
IG-11-dUTP, alkali
TP, alkali-labile
coli DNA polymera
k transalation, rand
le formulation whe
ed.
TP, alkali-labile
coli DNA polymera
k transalation, rand
le formulation whe
ed.
or PCR except tem
PCRs using Taq. Op
using non-standar
ffer.
A to suppress cros
situ hybridizations,
hybridization to m
x
use, clear colorless
P, each at 10 mM
direct use in all typ
primer-extension.
cence ELISA Subs
r peroxidase-based
nsitive, enhanced c
microplate chemi
at luminometers.
ermination of Lucif
ompared to -mer
uced state and qu
for purification of
krein activity.
za hemagglutinin p
ining the HA epito
and western and
use Anti-HA High A
ber
Name
on in eukaryotic ce
ing reporter gene.
into an appropriat
2-step colorimetri
h anti-histone antib
ono- and oligonucl
GG and generates f
known to be affect
Avr II, AspA2 I, an
GG and generates f
known to be affect
Avr II, AspA2 I, an
RT, and TdT. Replac
nd PCR. Use when
treatment. For mem
i-labile.
RT, and TdT. Replac
nd PCR. Use when
treatment. For mem
i-labile.
ase, RT, and termi
dom primed labeli
en stripping and re
ase, RT, and termi
dom primed labeli
en stripping and re
mplate and primers
ptimize assays for
rd Mg-concentrati
ss-hybridization to
, chromosome in si
microarrays, and filt
s solution of sodiu
concentration in P
pes of amplificatio
strate (POD)
d (POD, HRP) seco
chemiluminescenc
luminescence read
ferase gene activit
sulfhydryl groups o
rcaptoethanol). Ma
ation, increasing c
urokinase, trypsin
protein-folding st
protein and recom
pe in immunocyto
dot blots. For high
Affinity.
ells transfected
Quantify fusion
e -Gal
ic ELISA
body prior to the
eosomes in the
fragments with
ted by
nd Xma I.
fragments with
ted by
nd Xma I.
ces dTTP in nick
n the DIG-
mbrane stripping
ces dTTP in nick
n the DIG-
mbrane stripping
nal transferase.
ng, and PCR.
eprobing of
nal transferase.
ng, and PCR.
eprobing of
s. Determine
greater
ons using the
human
itu suppression
ter
m salts of dATP,
PCR Grade
on reactions,
ondary detection
ce. Optimized for
der (96-well
ty in cell
of
aintains
es disulfides.
cell lifetime in
, and
tudies, and
binant epitope-
chemistry,
her sensitivity at

1 k
1
125
5 x 125
25
125
1 kit for up to 1
volume eac
200 l 10 mM, e
l
250 ml for u
Pack Size

200 U (10 U/l)
1,000 U (10 U/l)
5 l (125 nmol) (1 m
l (5 x 125 nmol) (5
5 l (25 nmol) (1 m
5 l (125 nmol) (1 m
00 reactions of 50
ch containing 2.5 U
Polymerase
500 g (500 l)
each, for up to 500
final reaction volu
25 g
100 mg
200 g (lyo.)
ests
sts

mM)
5 x 1 mM)
mM)
mM)
l final reaction
U Taq DNA
0 reactions of 20
me
r 1.000 tubes

Price in

456,00
428,10
131,80
528,70
826,40
3.325,20
225,80
826,40
292,60
161,10
60,00
201,80
417,60
488,00
466,50

Pr

Cat.

11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 58
roducts b

No.
85 002 001 BCI
Use
imm
reac
can
85 029 001 NBT
For
Solu
hyb
wes
85 045 001 Cel
Non
qua
dur
apo
85 371 001 Ace
Ace
usin
gro
Pur
85 398 001 Chr
Use
prot
85 541 001 PCR
For
of D
buff
con
85 550 910 PCR
For
PCR
in P
pro
85 584 001 Hig
Con
solu
trip
kit f
85 592 001 Hig
Lab
prim
libra
50 t
85 606 910 DIG
Pre
Obt
incu
dot
85 614 910 DIG
Com
che
labe
Sou
85 622 910 Fluo
Con
prim
at h
lifts
85 649 910 Bio
Com
pro
afte
situ
85 681 001 E-6
Stro
cath
of p
betw
85 738 910 DIG
Esti
hyb
tem
by Catalo
IP
e BCIP for alkaline
munohistocytochem
ction product has
T
use in the sensitiv
uble in water, aque
bridization, immuno
stern blots, and to
llular DNA Fragm
nradioactive, fast (
antification of BrdU
ing necrosis or ce
optotic cells.
etyl-Coenzyme A
etyl-Coenzyme A is
ng radioisotopes. C
ups from acetylcoe
ity: 85% acetyl-Co
romozym TH
e Chromozym TH a
R Core Kit
PLUS

running PCR usin
DNA contamination
fer without Mg2+,
ntaminating DNA.
R DIG Labeling M
direct labeling of
R. The PCR DIG lab
PCR. The nucleotid
duct combined wit
gh Prime DNA La
nvenient, rapid ran
utions offer a choic
hosphates (
32
P,
35
S
for many different
gh Prime
bel DNA with radio
mers. Labeled prob
ary screening, and
to remove unincor
G-High Prime
mixed solution for
tain high yields of
ubation. Use labele
blots, and colony/
G-High Prime DN
mplete, convenient
emilumiluminescen
eled probe in 1 ho
uthern/northern blo
orescein-High Pr
nvenient enzyme a
med labeling of DN
high yield for use in
s, ISH, and library s
otin-High Prime
mplete reaction mi
bes. Biotin-labeled
er overnight incuba
u , and colony and
64
ong, irreversible in
hepsin B and L, br
proteins and enzym
ween the SH comp
G-labeled Contro
mate the yield of D
bridization probe in
mplate DNA and ap
og Numb
Product N

phosphatase dete
mistry and Souther
a blue color and is
ted. Supplied as a
ve detection of alka
eous buffer, and D
ohistocytochemistr
detect proteins/gl
mentation ELISA
(4.5 - 5.5 hours), se
U-labeled DNA fra
ll-mediated cytoto
A
s used to assay CA
CAT enzyme activit
enzyme A to chlor
A (enzymatic/abso
y thrombin in aque
g non-standard bu
n from prior ampli
, and Uracil-DNA G
Mix
amplification prod
beling mix can rep
e concentration en
th DIG detection.
beling Kit
ndom-primed DNA
ce in the selection
S,
3
H, digoxigenin
hybridization tech
oactive dCTP using
bes are used in So
porated nucleotide
random primed D
labeled probes wit
ed probes in librar
/plaque hybridizati
NA Labeling and D
t kit for random-pr
nt detection of labe
ur to overnight inc
ots, colony/plaque
rime
and nucleotide mix
NA with fluorescein
n Southern, northe
screening.
x for efficient rand
d probes are gener
ation. Use in South
plaque lifts.
hibitor of papain a
romelain, and ficin
mes. Inhibition of th
ponents.
ol DNA
DIG-labeled nucle
n Southern blots. T
pprox. 250 ng synth
ber
Name
ection using
rn and western blo
s insoluble in wate
powder.
aline phosphatase
DMF. For colony/pl
ry, ISH, Southern, n
ycoconjugates. Cry
ensitive (1 x 10
3
ce
gments either rele
xicity, or within the
AT enzyme activity
ramphenicol.
orbance), 2% Li.
the determination o
esous solutions.
uffer conditions w
fications. Includes
Glycosylase for de
ducts using digoxig
place the unlabeled
nsures maximum y
A labeling kit. Supp
of modified deoxy
, fluorescein, bioti
hniques.
g random oligonuc
uthern northern, a
ions. Use Quick Sp
es.
DNA labeling using
thin one hour or o
ry screening, South
ions.
Detection Starter
rimed DNA labelin
eled hybrids. Obta
cubation. Use in
e hybridization.
x for highly efficien
n-dUTP. Generate
ern, and dot blots,
dom primed labelin
rated at high yield
hern, dot, and nort
and cysteine protea
during isolation a
hiol proteases is n
ic acids or use as
The solution contai
hesized DIG-labele
otting. The
er. The blue color
e using BCIP.
aque
northern,
ystalline form.
ells/well)
eased from cells
e cytoplasm of
in cell extracts
ansfer of acetyl
of serine
ith samples free
MgCl
2
solution,
egrading
genin-dUTP in
d nucleotide mix
yield of PCR
plied nucleotide
yribonucleoside
n, etc). Use this
leotides as
and dot blots,
pin Columns, G-
g DIG-11-dUTP.
vernight
hern, northern,
r Kit II
g with DIG and
in high yield of
t random
labeled probes
colony/plaque
ng of DNA
within 1 hour or
hern blotting, in
ases, such as
nd purification
on-competitive
a control
ns 1 g
ed DNA.

1 k
1 kit for up to 5
volume, ea
500 l (2 x 250
reactions of 1
co
1 kit for up
labeled nucleo
200 l fo
160 l for up t
tem
1 kit for up to 1
of 24 blots, 10
100 l for up t
tem
100 l for up t
tem
50 l (5 g/
Pack Size

1 g
5 g
200 mg
100 mg
50 reactions of 50
ch containing 2.5
Polymerase
00 l final reaction
oncentration 200
to 50 labeling reac
per assay
or up to 50 labelin
o 40 labeling assay
mplate DNA per as
2 labeling reaction
ng to 3 g per ass
cm
2

o 25 labeling assay
mplate DNA per as
o 25 labeling assay
mplate DNA per as
25 mg
/ml DIG-labeled pl
www.roche
ests
l final reaction
U Taq DNA
25 PCR assays,
n volume, final
M
ctions with a
01 to 2 g DNA
g assays
ys, 0.01 to 3 g
ssay
ns and detection
say, blots of 100
ys, 0.01 to 3 g
ssay
ys, 0.01 to 3 g
ssay
asmid DNA)
e-applied-science

Price in

434,20
551,90
465,10
1.466,90
1.199,50
214,40
414,40
505,10
382,80
560,20
493,20
430,70
351,60
542,80
118,30

271

e.com

Pr
272

www.r

Cat.

11 58
11 58
11 58
11 58
11 58
11 58
11 58
11 59
11 60
11 62
11 63
11 63
11 63
11 63
roducts b
roche-applied-sc

No.
85 746 910 DIG
Esti
pro
of D
tem
85 762 001 DIG
The
hyb
bloc
85 860 001 Ant
Ant
in b
sing
and
85 878 001 hGH
Fast
cult
con
com
85 886 001 Neu
From
acid
etc)
2
85 916 001 Pef
Spe
com
valu
bloc
85 924 001 Res
Hig
acid
seq
of r
96 594 001 Taq
Taq
pro
PCR
labe
03 558 001 DIG
Rea
usin
Hyb
non
26 353 001 D(-
Use
extr
toge
biol
33 716 001 Ant
Det
dot
frag
sen
35 379 001 Rap
Cov
plas
reci
just
36 090 910 PCR
Gen
low
Pro
rem
36 103 001 PCR
2x c
up t
Con
pipe

by Catalo
cience.com
G-labeled Contro
mate the yield of D
be in Southern and
DIG-labeled neo-R
mplate DNA (fragm
G Wash and Bloc
e DIG Wash and Bl
bridization and DIG
cking solution and
ti-Bromodeoxyur
ti-Bromodeoxyurid
blood, tissues, and
d paraffin sections.
H ELISA
t, sensitive ELISA f
ture supernatants
ntaining a reporter
mparison even if ki
uraminidase (Sia
m Clostridium perf
ds (2,3-, 2,6-,
). In contrast to oth
2,8 sialic acids are
fabloc
SC
mpared to PMSF or
ues. Completely ina
cker of thrombin in
striction Protease
hly purified, specia
d sequence IleGl
uence may also be
ecombinant fusion
q DNA Polymeras
q DNA Polymerase
duced using rigoro
R, and other prime
eling.
G Easy Hyb
ady-to-use blockin
ng nonradioactive,
b buffer cannot be
ntoxic solution and
-)-Luciferin
e for the luminome
racts. It is a natura
ether with firefly lu
luminescence.
ti-Digoxigenin-P
tect digoxigenin-la
blots. Obtain high
gments conjugated
sitivity. Not evalua
pid DNA Ligation
valently joins sticky
smid or phage vec
ircularizing linear D
t 5 minutes at room
R DIG Probe Syn
nerate highly sensi
w-copy gene detect
bes labeled with a
moval of digoxigeni
R Master
concentrated, read
to 2 kb. Use in pla
ntains everything e
etting steps.
og Numb
Product N

ol RNA
DIG-labeled RNA o
d northern blots. T
RNA (760 bp length
ments of 798 and 32
k Buffer Set
lock Buffer Set is u
G detection. The se
d maleic acid, wash
ridine-Peroxidase
ine-Peroxidase is
tumors, and to de
g ELISA, immunohi
.
for quantitatively m
of eukaryotic cells
gene encoding fo
ts are from differe
alidase)
fringens ; hydroyze
2,8-linked to oli
her neuraminidase
cleaved with simila
r DFP with higher
activates proteinas
n serum and plasm
e Factor Xa
al quality serine pr
uGlyArg with
e used as a restric
n proteins.
se, 5 U/l
(5 U/l) is ideal fo
ous purity and qua
g buffer for all me
digoxigenin-label
used for in situ hy
d does not contain
etric determination
al substrate of lucif
uciferase for the de
OD (poly), Fab fr
abeled compounds
her signal-to-noise
d to unpolymerized
ated in immunohist
n Kit
y- or blunt-end DN
ctors, adding linker
DNA. Contains all
m temperature.
nthesis Kit
itive hybridization
tion of rare mRNA
alkaline-labile digo
in label after detec
dy-to-use mix for r
ce of Taq or the PC
except template DN
ber
Name
or use as a contro
The solution contai
h) and 0.5 g pSPT
281 bp).
used at various ste
et contains 10x pre
hing, and detection
e, Fab fragments
used to monitor p
etermine BrdU inco
istocytochemistry,
measuring hGH ex
s transfected with a
r hGH. Allows dire
ent lots.
s terminal N- or 0-
go-, poly-, mucop
es, cleaves 2,3 fa
ar velocity as 2,6
serine proteases.
se K. Unlike PMSF
ma.
rotease, recognizin
h a high degree of
ction cleavage site
or routine PCR. Th
ality standards for
ons, such as seque
embrane hybridizat
ed nucleic acid pr
ybridization. The b
formamide.
n of Luc gene activ
ferase from firefly a
etermination of AT
ragments
s in ELISA, Souther
e values compared
d HRP (ELISA). Use
tochemistry.
NA fragments for c
rs to plasmids or o
reagents needed f
probes using PCR
A in Southern and n
oxigenin (DIG)-dUT
ction are stable for
outine genomic an
CR Core Kit for rou
NA and primers. R
l hybridization
ins approx. 5 g
T18-neo
eps of DIG
parations of
n buffers.
s
roliferating cells
orporation on a
cryosections,
pression level in
a plasmid
ect data
-acylneuraminic
olysaccharides,
aster than 2,6;
6.
Nontoxic
ogical pH
, excellent
ng the amino
specificity. This
for processing
e enzyme is
use in PCR, RT-
encing and
tion applications
robes. DIG Easy
buffer is a
vity in cell
and is used
TP using
rn, western, and
to Anti-Dig-Fab
e for high
cloning into
other DNAs, and
for ligation in
. Suitable for
northern blots.
TP for easy
r over one year.
nd cDNA targets
utine PCRs.
Requires only 2

50 l (10
1
1 k
2,500 U (10 x 2
50 l final vo
1 kit for up
1 kit for up to 2
volume (one
labeled pro
1 kit for up to
reaction volume

Pack Size

00 g/ml DIG-labe
15 U
5 U
500 mg
3 x 100 g
lume each contain
DNA Polymerase
500 ml
50 mg
50 U
p to 40 DNA ligatio
25 reactions of 50
e reaction can prod
obe to analyze 650
membrane)
o 200 PCR reaction
e each containing
Polymerase
led RNA)
ots
ests
000 reactions of
ning 0.5 U Taq
on reactions
l final reaction
duce enough
cm
2
of blot
s of 50 l final
2.5 U Taq DNA-

Price in

118,30
264,40
448,50
543,60
190,90
271,40
765,50
1.480,10
279,30
716,80
320,30
286,10
457,50
271,10

Pr

Cat.

11 63
11 63
11 63
11 63
11 64
11 64
11 64
11 64
11 64
11 64
11 64
11 64
11 64
11 64
roducts b

No.
36 111 910 PCR
Con
100
ELIS
seq
36 120 910 PCR
Con
pro
con
Mic
36 138 001 PCR
Con
vary
incr
opti
36 154 910 PCR
Add
hyb
whe
ELIS
41 778 001 Stre
Poly
biot
part
suc
41 786 001 Stre
Poly
biot
part
suc
42 995 001 N-G
N-G
glyc
core
solu
43 053 001 End
Use
glyc
glyc
N-G
44 793 001 Cyt
Fast
mea
cell
cyto
44 807 001 Cel
Non
in 9
Ana
anti
44 947 001 Pw
Hig
fold
extr
cha
44 955 001 Pw
Hig
fold
extr
cha
45 692 001 Stre
Stre
bind
imm
Not
47 229 001 Cel
Prec
qua
inco
diffe

by Catalo
R ELISA, DIG-De
nvenient, nonradio
0 times more sensit
SA format makes d
uence in large sam
R ELISA, DIG-Lab
nvenient nonradioa
ducts for detection
nventional ethidium
croplate format is i
R Optimization K
nvenient, reliable re
y buffer pH, and m
rease yield and spe
imize conditions in
R Fluorescein La
d mix directly to PC
bridization probes.
en limited amounts
SA, membrane hyb
eptavidin Magne
ydisperse paramag
tin-labeled molecu
ticles/ml. Magneti
ccessfully used in m
eptavidin Magne
ydisperse paramag
tin-labeled molecu
ticles/ml. Magneti
ccessfully used in m
Glycosidase A
Glycosidase A from
can chains from gl
e fucose residues
ution.
doglycosidase H
e recombinant End
coproteins. Endogl
copeptides and pro
Glycosidase A to cl
totoxicity Detecti
t and simple 6-we
asuring LDH activi
-mediated cytotox
otoxic potential of
ll Proliferation Re
nradioactive spect
96-well plates. Mea
ibodies. Ready-to-
o DNA Polymera
h thermal stability
d lower than Taq D
remely accurate D
aracterization of ra
o DNA Polymera
h thermal stability
d lower than Taq D
remely accurate D
aracterization of ra
eptaWell, High B
eptaWell, streptavid
ding capacity are u
munoassays. Not st
t suitable in cell cu
ll Proliferation EL
cise, fast (1.5-3 hrs
antitate cell prolife
orporation during
erent in vitro cell s
og Numb
Product N

etection
active method for
tive than ethidium
determining prese
mple numbers easy
beling
active method add
n using PCR ELISA
m bromide staining
deal for automatio
Kit
eady-to-use soluti
magnesium, DMSO
ecificity. Use with
n multiplex PCR.
abeling Mix
CRs to produce flu
Particularly useful
s of target DNA is
bridization, or ISH.
etic Particles
gnetic particles for
ules. Supplied in su
c separation of bio
many applications.
etic Particles
gnetic particles for
ules. Supplied in su
c separation of bio
many applications.
m sweet almond m
lycopeptides, even
present in insect a
doglycosidase H fo
lycosidase H hydro
oteins. It cleaves o
leave glycopeptide
ion Kit (LDH)
ll plate method to
ity released from d
xicity, determine m
compounds.
eagent WST-1
rophotometric qua
asure proliferation
ostatic compounds
-use solution.
ase
polymerase with a
DNA Polymerase). I
NA synthesis, such
re mutations.
ase
polymerase with a
DNA Polymerase). I
NA synthesis, such
re mutations.
Bind (transparent
din-coated microp
used in colorimetr
terile as sterilizatio
ulture.
LISA, BrdU (color
s), and simple non
ration based on th
DNA synthesis in
systems.
ber
Name
labeling and detec
bromide staining
nce or absence of
y.
ds a DIG label to yo
A; 100 times more
g of products using
on.
ons to optimize PC
, glycerol concent
FastStart High Fide
uorescein-labeled D
for synthesizing D
available. Use lab
r fast separation of
uspension, contain
otin-labeled molec
.
r fast separation of
uspension, contain
otin-labeled molec
.
eal; hydrolyzes all
those carrying
and plant glycopro
r the deglycosylati
olyzes N-linked oli
only high mannose
es.
quantify cytotoxic
damaged cells. Det
ediator-induced cy
in response to gro
s. Assess growth-i
an extremely low e
Ideal for applicatio
h as high fidelity P
an extremely low e
Ideal for applicatio
h as high fidelity P
t, 12 x 8-well stri
plates (12 x 8-well
ic and fluorescent
on impairs streptav
rimetric)
nradioactive colorim
he measurement of
replicating cells. U
ct PCR products;
on agarose gels.
specific target
our PCR
sensitive than
g agarose gels.
CR setup. Easily
rations to
elity System to
DNA
DNA probes
eled probes in
f a variety of
ning 10 mg
cules is
f a variety of
ning 10 mg
cules is
types of N-
1,3-bound
oteins. In
ion of
gosaccarides of
structures. Use
ity/cytolysis by
tect and quantify
ytolysis, and
feration/viability
owth factors.
nhibitory
error rate (18-
ons that require
PCR and
error rate (18-
ons that require
PCR and
ps)
strips) with high
nucleic acid
vidin coating.
metric assay to
f BrdU
Used in many

1 kit for 1
microplates
detec
1 kit
1 kit for up to 1
optimization
100 l for up t
1 k
25 m
100 U for up
volume eac
500 U (2 x 250
l final volume
5 plates (
1 k

Pack Size

192 detection react
ction of 50 PCR pro
100 one-step or up
n assays of 100 l f
volume
to 10 PCR reaction
100 l
2 ml
10 ml
5 mU (0.1 ml)
2.5 U (500 l)
p to 40 reactions o
ch containing 2.5 U
Polymerase
U) for up to 200 r
e each containing 2
Polymerase
www.roche
tions (two
-quantitative
oducts
tions
p to 50 two-step
final reaction
ns, reactions of
ests
tests
of 100 l final
U Pwo DNA
reactions of 100
2.5 U Pwo DNA
and frame)
ests
e-applied-science

Price in

527,20
576,00
256,40
338,80
189,80
719,10
431,00
749,00
615,70
568,60
136,60
547,10
229,20
705,90

273

e.com

Pr
274

www.r

Cat.

11 64
11 64
11 65
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
roducts b
roche-applied-sc

No.
47 679 001 Taq
Low
con
con
exte
47 687 001 Taq
Low
con
con
exte
55 884 001 CSP
Che
extr
labe
shif
63 925 910 My
Pho
con
cult
dete
64 778 001 Stre
Stre
for
ster
suit
66 606 001 Ant
Det
tagg
imm
10-f
66 649 001 Hyb
Use
stan
pro
seq
66 657 001 Lum
Lum
is id
che
tech
66 681 001 Buf
Stab
resi
for t
tem
66 690 001 Buf
Stab
resi
for t
tem
66 703 001 Buf
Stab
resi
for t
tem
66 789 001 Buf
Stab
resi
for t
tem
66 851 001 Ant
Det
tagg
stre
fold
66 878 001 Ant
Loc
sha
usin
Ant

by Catalo
cience.com
q DNA Polymeras
wer concentration
nvenient pipetting o
ncentration (5 U/l
ension reactions (s
q DNA Polymeras
wer concentration
nvenient pipetting o
ncentration (5 U/l
ension reactions (s
PD
emiluminescent su
remely fast and se
eled nucleic acids
ft assays, and sequ
ycoplasma PCR E
otometric ELISA fo
ntaminating Mycop
tures or other sam
ection for fast (6 h
eptaWell (transp
colorimetric and fl
rile as sterilization
table for cell cultur
ti-HA (12CA5)
ged protein contai
munoprecipitation,
fold lower conc., u
bridization Bags
e these bags in non
ndard radioactive p
cedures. All hybrid
uentially to the sa
mi-Film Chemilum
mi-Film Chemilumi
deal for the detecti
emiluminescent su
hniques.
ffers in a Box, Pre
ble 20x solution of
stant to enzymatic
the absence of nu
mperature.
ffers in a Box, Pre
ble 10x solution of
stant to enzymatic
the absence of nu
mperature.
ffers in a Box, Pre
ble 10x solution of
stant to enzymatic
the absence of nu
mperature.
ffers in a Box, Pre
ble 10x solution of
stant to enzymatic
the absence of nu
mperature.
ti-HA-Biotin
ged protein in wes
eptavidin fluoresce
d lower conc. using
ti-HA-Fluorescei
calize recombinant
rper images with c
ng unlabeled Anti-
ti-HA-Fluorescein,
og Numb
Product N

se, 1 U/l
of recombinant Ta
of small amounts o
) Taq. Use in PCR,
sequencing, labelin
se, 1 U/l
of recombinant Ta
of small amounts o
) Taq. Use in PCR,
sequencing, labelin
ubstrate for alkaline
nsitive visible light
on film or lumines
uencing.
ELISA
r the detection of
plasma, Acholeplas
ple materials. Rea
hrs) and semi-auto
parent, 12 x 8-we
din-coated microp
luorescent protein
procedures impair
re.
za hemagglutinin p
ining the HA epito
and western and
use Anti-HA High A
nradioactive hybrid
probe hybridization
dization solutions a
me bag.
minescent Detec
nescent Detection
ion of signals from
bstrates (e.g., CSP
emixed SSC Buff
f SSC, filtered throu
c and nonenzymati
clease or protease
emixed TAE Buffe
f TAE, filtered throu
c and nonenzymati
clease or protease
emixed TBE Buffe
f TBE, filtered throu
c and nonenzymati
clease or protease
emixed PBS Buff
f PBS, filtered throu
c and nonenzymati
clease or protease
za hemagglutinin p
stern blots and imm
ent or POD systems
g Anti-HA-Biotin, H
n
t HA-tagged protei
cleaner backgroun
-HA. For higher se
High Affinity.
ber
Name
aq allows more acc
of enzyme. Identic
, RT-PCR, and othe
ng).
aq allows more acc
of enzyme. Identic
, RT-PCR, and othe
ng).
e phosphatase, en
t detection of nonr
scence imagers. Fo
PCR-amplified DN
sma, and Ureaplas
dy-to-use mix and
omatic sample proc
ell strips)
plates (12 x 8-well
immunoassays. Th
r the streptavidin c
protein and recom
pe in immunocyto
dot blots. For high
Affinity.
dization and detec
ns, and western bl
and blocking buffe
ction Film
n Film 8 x 10 inche
m alkaline phospha
PD) in membrane
fer, 20x
ugh 0.2 m pore s
ic degradation. Eac
e activity, and store
er, 10x
ugh 0.2 m pore s
ic degradation. Eac
er, 10x
ugh 0.2 m pore s
ic degradation. Eac
fer, 10x
ugh 0.2 m pore s
ic degradation. Eac
protein and recom
munofluorescence
s. Obtain higher se
High Affinity.
ins by immunofluo
nd compared to ind
nsitivity at 10-fold
curate and
al to our higher
er primer-
curate and
al to our higher
er primer-
abling
radioactively
or blotting, gel
NA of
sma in cell
d ELISA
cessing.
strips) are used
he plates are not
coating. Not
binant epitope-
chemistry,
her sensitivity at
ction procedures,
otting
er can be added
s, 20.3 x 25.4 cm
atase
hybridization
ize membrane,
ch lot is tested
es easily at room
ize membrane,
ch lot is tested
es easily at room
ize membrane,
ch lot is tested
es easily at room
ize membrane,
ch lot is tested
es easily at room
binant HA-
e with
ensitivityat 10-
orescence. Yields
direct methods
lower conc., use

250 U for up
volume eac
1,000 U (4 x 25
20 l final vo
1 kit
5 plates (
100 films (
100

Pack Size

p to 500 reactions
ch containing 0.5 U
Polymerase
50 U) for up to 2,0
lume each contain
DNA Polymerase
1 ml
5 mg (5 mg/ml)
50 bags
(8 x 10 inches, 20.3
4 l
4 l
4 l
4 l
g (0.2 mg/ml; 50
100 g (500 l)
of 20 l final
U Taq DNA
00 reactions of
ning 0.5 U Taq
tions
and frame)
3 x 25.4 cm)
00l)

Price in

202,60
640,50
237,90
810,20
317,00
1.322,90
107,50
298,10
127,20
127,20
116,60
114,30
350,80
352,10

Pr

Cat.

11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 66
11 68
roducts b

No.
66 916 001 Lum
Lum
is id
che
tech
66 975 001 HA
The
gen
con
anti
67 009 001 Stri
Stri
ther
cDN
Cap
67 149 001 Ant
Ant
nati
that
imm
67 157 001 TriP
Pre
DNA
synt
den
67 165 001 TriP
Pre
DNA
synt
den
67 203 001 Ant
Ant
nati
that
imm
67 246 001 c-m
The
C-te
can
chro
67 289 001 Sod
Pur
app
67 327 001 DN
Rap
or b
dige
pur
67 475 001 Ant
Sing
blot
HA-
nee
69 893 001 Luc
Che
luci
lum
film
69 915 001 Cel
Prec
assa
inco
diffe
69 940 910 DN
DNA
stan
acid
80 293 001 X-G
Use
pro
met
dete
by Catalo
mi-Film Chemilum
mi-Film Chemilumi
deal for detecting t
emiluminescent su
hniques.
Peptide
e synthetic HA Pep
ntly elute tagged fu
ntrol to verify immu
i-HA and HA-tagg
ip PCR Tubes an
p PCR Tubes and
rmal cyclers; desig
NA synthesis, and
ps are DNase- and
ti-c-myc
ti-c-myc (clone 9E
ive human c-myc p
t contain the c-my
munocytochemistry
Pure Isolation Re
pare total RNA, ge
A-free RNA in nor
thesis, RT-PCR. Us
natured protein in S
Pure Isolation Re
pare total RNA, ge
A-free RNA in nor
thesis, RT-PCR. Us
natured protein in S
ti-c-myc
ti-c-myc (clone 9E
ive human c-myc p
t contain the c-my
munocytochemistry
myc peptide
e synthetic peptide
erminus of human
n be used in compe
omatography of pr
dium Dodecyl Su
e quality preparati
plications as a dena
A Isolation Kit fo
pidly isolate DNA f
buffy coat samples
ests, and Southern
ification steps, and
ti-HA-Peroxidase
gle-step detection
tting. For higher se
-Peroxidase High A
ed for a secondary
ciferase Reporter
emiluminescent as
ferase activity in tr
minometers, microp
m. More sensitive th
ll Proliferation EL
cise, fast (1.5-3 hrs
ay to quantitate ce
orporation during
erent in vitro cell s
A Molecular We
A Molecular Weig
ndard in Southern
d labeling and dete
Gal
e X-Gal for immuno
duct has a blue co
ected.
og Numb
Product N

minescent Detec
nescent Detection
the signals from al
bstrates (e.g ., CSP
ptide YPYDVPDYA
usion proteins from
unospecificity, and
ged fusion proteins
d Caps
Caps, either 8 or 1
gned for rapid, opt
sequencing and c
d RNase-free.
10) is used for the
protein and recom
yc epitope in weste
y, and immunoprec
eagent
enomic DNA, and p
rtherns, in vitro tra
se RNA-free DNA
SDS-PAGE and we
eagent
enomic DNA, and p
rtherns, in vitro tra
se RNA-free DNA
SDS-PAGE and we
10) is used for the
protein and recom
yc epitope in weste
y, and immunoprec
e EQKLISEEDL, com
c-myc protein, is
etition experiments
roteins that contai
ulfate (SDS)
ion, suitable in mo
aturing agent for p
or Mammalian Bl
from 1 -10 ml mam
s. Use in PCR or lon
n blots. Eliminate o
d chaotropic reage
e
of HA-tagged rec
ensitivity at 10-fold
Affinity. Use of Ant
detection step.
r Gene Assay, hig
ssay for quantitativ
ransfected cells. U
plate or tube forma
han isotopic CAT a
LISA, BrdU (chem
s), and simple non
ell proliferation bas
DNA synthesis in
systems.
ight Marker VII,
ht Marker VII, DIG
blot analysis when
ection. Size range:
ohistocytochemist
olor and is soluble
uble in water. The
ber
Name
ction Film
n Film 7.1 x 9.4 inch
lkaline phosphatas
PD) in membrane
is recognized by A
m immunocomplex
in competition ex
s.
2 tubes per strip,
imal heat transfer
cycle sequencing. P
e immunochemical
mbinant epitope ta
ern and dot blots,
cipitation.
protein from a sing
anslation, RNase p
in PCR and clonin
estern blots.
protein from a sing
anslation, RNase p
in PCR and clonin
estern blots.
e immunochemical
mbinant epitope ta
ern and dot blots,
cipitation.
mprising 10-amino
recognized by Ant
s, including affinity
n this epitope.
ost routine electrop
proteins.
lood
mmalian whole bloo
ng PCR, sequencin
organic extractions
ents.
combinant proteins
d lower concentrat
ti-HA-Peroxidase e
gh sensitivity
ve determination of
Use in manual or au
at, and scintillation
assay.
miluminescent)
nradioactive chemi
sed on the measur
replicating cells. U
DIG-labeled
G-labeled, is used a
n using the DIG Sy
0.081 to 8.57 kbp
in dimethylformam
e blue color can be
hes, 18 x 24 cm
se
hybridization
Anti-HA. Use to
xes, as positive
periments using
are used in
in PCR, RT-PCR,
PCR Tubes and
detection of
agged proteins
gle sample. Use
rotection, cDNA
ng. Use
gle sample. Use
rotection, cDNA
ng. Use
detection of
agged proteins
o acids from the
ti-c-myc and
y
phoretic
od, lymphocyte,
ng, restriction
s, column
s by western
tion, use Anti-
eliminates the
f firefly
utomated
counters or
luminescent
rement of BrdU
Used in many
as a size
ystem for nucleic
.
he reaction
mide and
e visually

100 films (
125
2
1 kit for up to
50
1 k
1 k
50
Pack Size

(7.1 x 9.4 inches, 1
5 mg
200 g (lyophilizate
50 ml
200 ml
5 mg (1 ml)
5 mg
1 kg
25 purifications of
g (0.1 mg/ml; 500
00 l (5 g, 10 g/m
100 mg
www.roche
8 x 24 cm)
trip)
e)
f 10 ml samples
0 l)
says
ests
ml)
e-applied-science

Price in

305,40
549,80
187,60
417,90
160,20
530,90
1.322,90
495,00
359,50
242,60
408,60
297,90
712,70
231,40
91,90

275

e.com

Pr
276

www.r

Cat.

11 68
11 68
11 68
11 68
11 68
11 68
11 68
11 68
11 68
11 68
11 68
11 68
11 68
11 69
11 69
roducts b
roche-applied-sc

No.
81 451 001 NBT
Stoc
colo
and
nitr
81 460 001 INT
Colo
pho
blot
81 982 001 Atto
Atto
pho
sen
sub
84 302 001 ABT
ABT
imm
solu
dilu
84 795 910 In S
Prec
apo
qua
and
84 809 910 In S
Prec
cell
cells
drug
84 817 910 In S
Prec
cell
cells
drug
85 597 910 Bio
Lab
poly
nort
and
85 619 910 Fluo
RNA
T7,
enz
(So
85 627 001 CD
Che
ultr
acid
and
85 660 001 Aga
Aga
pre
ana
pha
85 678 001 Aga
Aga
pre
ana
pha
85 929 001 Gua
Suit
stro
91 112 001 Hum
Pre
(bu
con
Exp
93 417 001 EPO
The
scie
con
pro
by Catalo
cience.com
T/BCIP Stock So
ck solution for sen
orimetric AP subst
d western blots, an
ocellulose and nyl
T/BCIP Stock Sol
orimetric substrate
osphatase (AP) in b
t, and for applicati
oPhos
oPhos is a highly s
osphatase-conjuga
sitive by a factor o
bstrate 4-methylum
TS Solution
TS Solution is an id
munoassays with h
ution is supplied as
ution.
Situ Cell Death D
cise, fast, and simp
optosis at the single
antitative detection
d formalin-fixed tiss
Situ Cell Death D
l death at the single
ls in frozen or form
g-induced apoptos
Situ Cell Death D
l death at the single
ls in frozen or form
g-induced apoptos
otin RNA Labeling
bel RNA with Biotin
ymerases (SP6, T3
thern, and dot blot
d in situ and micro
orescein RNA La
A labeling with Flu
or T3 RNA polyme
zyme-conjugated a
utherns, northerns
P-Star
emiluminescent su
a-sensitive visible
ds on film or lumin
d dot blots, and ge
arose LE
arose LE (low elect
parative gel electro
alysis of PCR, exam
age DNA, and sepa
arose LE
arose LE (low elect
parative gel electro
alysis of PCR, exam
age DNA, and sepa
anidine thiocyan
table as denaturing
onger denaturant t
man Genomic DN
paration of high m
ffy coat). Suitable
nstruction, and the
pand System.
O ELISA
e EPO ELISA is a fa
ence research stud
ncentrations in plas
cedures.
og Numb
Product N

olution
nsitive detection of
trate is used in imm
d to detect protein
on membranes.
lution
e solution for the s
blotting protocols,
ons in immunohist
sensitive substrate
ated secondary det
of 100 than the mo
mbelliferyl-phospha
deal chromogenic
horseradish peroxid
s one component
Detection Kit, Flu
ple nonradioactive k
e-cell level using flu
by flow cytometry.
sue sections.
Detection Kit, AP
e-cell level using lig
malin-fixed tissue an
sis.
Detection Kit, PO
e-cell level using lig
malin-fixed tissue an
sis.
g Mix
n-16-UTP by in vitr
, and T7). Labeled
ts, plaque and colo
oarray hybridization
abeling Mix
uorescein-12-UTP
erases. Detect labe
anti-fluorescein, an
s, plaque lifts, ISH)
light detection of
nescence imager sy
l shift assays.
troendosmosis) is
ophoresis of nucle
mination of RE dige
aration of RNA.
troendosmosis) is
ophoresis of nucle
mination of RE dige
aration of RNA.
ate
g agent for protein
than guanidine hyd
NA
molecular weight D
for Southern hybri
reliable amplificat
ast, highly sensitive
dies as a method fo
sma and serum. N
ber
Name
f alkaline phosphat
munohistocytochem
ns and glycoconjug
sensitive detection
including Souther
tocytochemistry.
for ELISA using a
tection systems. It
ost commonly used
ate (MUP).
substrate for enzy
dase as a marker e
reagent, ready-to-
uorescein
uorescence micros
. Detect apoptotic
P
kit to detect and qu
ght microscopy. De
nd determine cell s
OD
kit to detect and qu
ght microscopy. De
nd determine cell s
ro transcription us
RNA can be used
ony lifts, RNase pr
ns.
by in vitro transcr
eled RNA directly o
nd use in hybridiza
).
e phosphatase, en
nonradioactively la
ystems. For Southe
ideal for routine a
eic acids. Applicati
estsfrom plasmid, c
ideal for routine a
eic acids. Applicati
estsfrom plasmid, c
ns. Guanidine thioc
drochloride.
DNA isolated from
idization analysis,
tion of large DNA
e and easy assay fo
or the determinatio
ot for use in diagn
tase. The
mistry, Southern
gates. Use with
of alkaline
rn blot, western
lkaline
is more
d fluorescence
yme
enzyme. ABTS
-use at working
detection of
scopy or
cells in frozen
uantify apoptotic
etect apoptotic
ensitivity to
uantify apoptotic
etect apoptotic
ensitivity to
ing RNA
d in Southern,
otection assays,
iption using SP6,
or with an
ation techniques
abling fast,
abeled nucleic
ern, northern,
nalytical and
ons include
cosmid, and -
nalytical and
ons include
cosmid, and -
cyanate is a
human blood
genomic library
targets by the
or use in life
on of EPO
nostic

1 set for u
3 x 100 ml (f
1
1
1
40 l for up
40
1
Pack Size

8 ml
3 ml
up to 1,800 wells 1
for 1,500 to 3,000 E
l for up to 20 reac
1 ml
100 g
500 g
500 g
100 g
00 l each
ELISA assays)
sts
sts
sts
on reactions
ctions
sts

Price in

110,00
130,20
542,40
177,20
591,40
651,70
651,70
184,80
168,70
286,10
244,70
828,80
307,60
181,50
711,40

Pr

Cat.

11 69
11 69
11 69
11 69
11 69
11 69
11 69
11 69
11 69
11 69
11 71
11 71
11 71
11 71
11 71
roducts b

No.
96 505 001 Aga
The
frag
frag
prim
97 471 001 NBT
Rea
colo
and
nitr
97 498 001 cOm
Rely
and
New
Sup
99 075 001 Nyl
Unc
pha
che
biot
99 083 001 Nyl
Unc
pha
che
biot
99 105 001 PCR
For
reac
mM
the
99 113 001 Mg
Mg
Mg
for
any
99 121 001 PCR
For
cha
a 25
mM
99 695 001 ATP
Opt
a co
kine
ATP
99 709 001 ATP
Hig
mic
dete
ATP
17 472 001 Hyb
Use
ELIS
18 096 001 DA
DAB
of a
and
19 386 001 Imm
For
Prot
solu
19 394 001 Imm
For
Prot
solu
19 408 001 Pro
Affi
from
ente
cult

by Catalo
arose Gel DNA Ex
e Agarose DNA Ext
gments from stand
gments are suitabl
med labeling, and s
T/BCIP Ready-to
ady-to-use tablets
ony/plaque lifts, im
d western blots, an
ocellulose and nyl
mplete
y on proven perfor
d metalloproteases
w for EDTA inhibiti
pplied in glass vials
lon Membranes f
charged microporo
age/cosmid librarie
emiluminescent/ ch
tinylated or radioac
lon Membranes f
charged microporo
age/cosmid librarie
emiluminescent/ ch
tinylated or radioac
R Buffer Without
amplification of sp
ction. The buffer is
M Tris-HCl and 500
MgCl
2
Stock Solu
gCl
2
Stock Soluti
Cl
2
Stock Solution
Cl
2
, when optimiz
a particular templa
y PCR type: hot sta
R Buffer Set
optimizing the ma
ain reaction using T
5 mM magnesium
M Tris-HCl, 500 mM
P Bioluminescen
timized for tube an
onstant light signa
etic studies and AT
P Bioluminescence
P Bioluminescen
hly sensitive/quan
croplate-format lum
ection of microbia
P Bioluminescence
bridization Buffer
e in combination w
SAs for application
B Substrate
B Substrate is a co
applications, such
d western and dot
munoprecipitatio
the immunoprecip
tein-G-Agarose. T
ubilization, stabiliza
munoprecipitatio
the immunoprecip
tein A Agarose. Th
ubilization, stabiliza
otein A Agarose
nity chromatograp
m many species. Te
erotoxins. Use to p
ture supernatant.
og Numb
Product N

xtraction Kit
traction Kit efficien
dard or low melting
e for ligation, trans
sequencing.
o-Use Tablets
for sensitive detec
mmunohistocytoche
d to detect protein
on membranes.
rmance: cOmplete
ion: IMAC with cO
s.
for Colony and P
ous nylon membra
es with DIG probes
hromogenic substr
ctive probes. Pore
for Colony and P
ous nylon membra
es with DIG probes
hromogenic substr
ctive probes. Pore
t MgCl
2
, 10x con
pecific DNA fragm
s a tenfold concen
0 mM KCl, and sho
ution.
on
n (25 mM) for supp
ing the magnesium
ate or target. Use w
rt, high fidelity, lon
agnesium chloride
Taq DNA Polymera
solution and a PC
M KCl; pH 8.3).
nce Assay Kit CLS
nd microplate-form
al, sustained for sev
TP determinations
e Assay Kit HS II.
nce Assay Kit HS
ntitative determinat
minometers. Conta
l contamination. Fo
e Assay Kit CLS II.
r
with the PCR ELISA
n in nucleic-acid h
olor substrate for p
as immunohistocy
blotting.
on Kit (Protein G)
pitation of proteins
he kit contains all
ation, and the imm
on Kit (Protein A)
pitation of proteins
he kit contains all r
ation, and the imm
phy using Protein A
ested for the abse
purify mouse mono
ber
Name
ntly isolates small
g point agarose. R
sformation, RE dig
ction of alkaline ph
emistry, ISH, South
ns/glycoconjugate
Tablets inhibit ser
types as cOmplete
Omplete His-Tag Pu
Plaque Hybridizat
ane for nonradioac
s and detection wi
rates. Use in hybrid
size: 1.2 m.
Plaque Hybridizat
ane for nonradioac
s and detection wi
rates. Use in hybrid
size: 1.2 m.
c.
ments using the po
trated solution con
ould be used in com
plementing PCR bu
m concentration of
with other PCR bu
ng PCR.
concentration in t
ase. This PCR Buff
CR buffer (10x conc
S II
mat luminometers.
veral minutes and
. For higher sensit
II
tion of ATP, for use
ains a cell lysis reag
or a constant light
A and the series of
hybridization reacti
peroxidase and is u
ytochemistry, in situ
)
s from cellular extr
reagents necessa
munopurification of
)
s from cellular extr
reagents necessar
munopurification of
A agarose is ideal
nce of staphylococ
oclonal antibodies
and large DNA
Recovered DNA
ests, random
hosphatase. For
hern, northern,
s. Use with
rine, cysteine,
ULTRA Tablets.
urification Resin.
ion
tive screening of
th
dizations with
ion
tive screening of
th
dizations with
lymerase chain
ntaining 100
mbination with
uffers without
f a standard PCR
ffers to optimize
the polymerase
fer Set contains
centrate; 100
The kit exhibits
is used for
ivity, use the
e in tube and
gent for
t signal, use the
DIG-detection
ons.
used in a variety
u hybridization,
racts using
ry for cell lysis,
f proteins.
racts using
y for cell lysis,
f proteins.
for purifying IgG
ccal
from ascites or

1 kit
20 tablets in a
for a volum
50 disc
50 discs
2 x 2 ml
1 kit for 1,600 a
1 kit for 1,000 a
1 kit
1 kit
2 ml

Pack Size

t for max. 100 reac
20 tablets
me of 50 ml extract
cs (each 82 mm dia
s (each 132 mm d
3 x 1 ml
3 x 1 ml
(2 x 1 ml of each
assays (microplate)
(tube).
assays (microplate)
(tube).
100 ml
1 pack
www.roche
ctions
blet is sufficient
ion solution
ameter)
iameter)
solution)
), for 800 assays
), for 500 assays
tions
tions
ume)
e-applied-science

Price in

182,80
146,40
257,20
282,20
525,30
40,30
40,30
49,70
566,70
566,70
80,70
184,50
332,30
279,40
265,80

277

e.com

Pr
278

www.r

Cat.

11 71
11 72
11 72
11 72
11 72
11 72
11 73
11 73
11 73
11 73
11 73
11 73
11 74
11 74
roducts b
roche-applied-sc

No.
19 416 001 Pro
Affi
for t
for t
mito
21 615 001 DN
Ma
Allo
Tem
clea
aga
21 666 001 Stre
Use
soli
hap
dete
21 674 001 Stre
Use
soli
hap
dete
21 925 001 DN
For
dete
rest
21 933 001 DN
For
dete
rest
add
32 641 001 Exp
Exp
resu
to T
targ
32 650 001 Exp
Exp
resu
to T
targ
32 668 001 Hig
Pur
Use
seq
frag
32 676 001 Hig
Pur
Use
seq
frag
34 334 001 Uni
Use
acti
Prot
fluo
34 776 001 Stre
Stre
and
ster
for
41 985 001 mR
Isol
cell
nort
Isol
42 027 001 Glu
Fast
dete
scie
is c

by Catalo
cience.com
otein G Agarose
nity chromatograp
the purification of
the absence of sta
ogenic.
A Molecular We
arker)
ows accurate sizing
mplate PCR System
aved with rare-cutt
arose gels. Size ran
eptavidin, recom
e Streptavidin, reco
d phases (e.g., mic
ptens and antibodi
ection systems.
eptavidin, recom
e Streptavidin, reco
d phases (e.g., mic
ptens and antibodi
ection systems.
A Molecular We
ermination of doub
A Molecular We
ermination of doub
ditional band of 264
pand High Fidelity
pand High Fidelity S
ults with twofold h
Taq. Choose this sy
gets up to 5 kb, in
pand High Fidelity
ults with twofold h
Taq. Choose this sy
gets up to 5 kb, in
gh Pure PCR Prod
ify and concentrat
e purified DNA dire
uencing, cloning,
gments that are >1
gh Pure PCR Prod
ify and concentrat
e purified DNA dire
uencing, cloning,
gments that are >1
iversal Protease
e as a general subs
vities, such as con
tease Substrate ca
orimetrically in a ho
eptaWell (transp
d fluorescent prote
rilization procedure
cell culture purpos
RNA Isolation Kit
ate highly purified
s, or tissue (withou
thern blotting, cDN
ate at least 70 g
ucosidase Assay
t, sensitive, specifi
ermination of neut
ence research app
ompatible with mi
og Numb
Product N

phy using Protein G
IgG from many sp
aphylococcal enter
ight Marker XV (
g of DNA fragmen
m or restriction dige
ting restriction end
nge: 2.3 to 48.5 kbp
mbinant
ombinant from Stre
croplates, beads et
es in universal imm
mbinant
ombinant from Stre
croplates, beads et
es in universal imm
ight Marker XIII
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
ight Marker XIV
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
42 bp.
y PCR System
System is an enzym
higher yield and thr
ystem for the most
PCR/RT-PCR.
y PCR System
System is an enzym
ystem for the most
PCR/RT-PCR.
duct Purification
te amplified DNA (
ectly in downstrea
ligation, and PCR.
100 bp in length.
duct Purification
te amplified DNA (
ectly in downstrea
ligation, and PCR.
100 bp in length.
Substrate
strate for protease
ntamination in enzy
an be measured sp
omogeneous assay
parent 96-well)
din-coated microp
ein immunoassays.
e would impair the
ses.
d mature mRNA fro
ut isolation of tota
NA synthesis, RT-P
of poly (A)
+
RNA.
ic colorimetric assa
tral -glucosidase
lications. Cannot b
croplate and cuvet
ber
Name
G agarose is the m
pecies. Recombina
(Expand DNA Mo
nts generated by th
est of high molecu
donucleases and s
p.
eptomyces avidinii
tc.), as well with b
munological strept
eptomyces avidinii
tc.), as well with b
munological strept
(50 bp ladder)
mplifies accurate m
A fragments genera
ize range: 50 to 75
(100 bp ladder)
mplifies accurate m
A fragments genera
ize range: 100 to 1
me blend deliverin
reefold greater fid
t sensitive PCR res
me blend deliverin
reefold greater fid
t sensitive PCR res
Kit
(or DNA from othe
m applications, su
Efficiently recover
Kit
(or DNA from othe
m applications, su
Efficiently recover
es and to detect tra
yme preparations.
pectrophotometrica
y.
plates can be used
The plates are no
e streptavidin coat
om RNA preparatio
l RNA). Use isolate
PCR, in vitro transl
ay for the quantita
e in human semen
be used in other sp
tte formats.
method of choice
nt form is tested
nown to be
olecular Weight
he Expand Long
ular weight DNA
separated on
for coating of
iotin-labeled
tavidin/biotin
for coating of
iotin-labeled
tavidin/biotin
molecular weight
ated by
50 bp.
molecular weight
ated by
500 bp and an
g superior
elity compared
sults for genomic
g superior
elity compared
sults for genomic
er reactions).
ch as labeling,
rs DNA
er reactions).
ch as labeling,
rs DNA
ace protease
The Universal
ally and
for colorimetric
t sterile as any
ing. Not suitable
ons, cultured
ed mRNA in
ation, etc.
ative
n samples in life
pecimens. Assay

2 ml
50 g (1 A
2
50 g in 200 l
100 U for up to
each con
500 U (2 x 250
final volume ea
1 kit f
1 kit fo
1
1 kit (for isolat
1 kit fo

Pack Size

50 g (1 A
260
unit)
1 mg
5 mg
260
unit) for up to 5
(1 A
260
unit) for up
40 reactions of 50
ntaining 2.6 U enzy
U) for up to 200 re
ch containing 2.6
40 mg
15 plates (96 wells
tion of at least 70
RNA)
or 30 tests and 10
ume)
)
50 gel lanes
p to 50 gel lanes
0 l final volume
yme blend
eactions of 50 l
U enzyme blend
cations
cations
s)
g of poly (A)
+

blanks

Price in

438,00
121,90
155,40
569,20
132,80
139,80
123,10
492,10
109,00
458,50
565,00
745,00
348,90
363,50

Pr

Cat.

11 74
11 74
11 74
11 74
11 74
11 75
11 75
11 75
11 75
11 75
11 75
11 75
11 75
11 75
11 75
roducts b

No.
45 808 910 Nic
Opt
hyb
to d
chro
45 816 910 DIG
Con
labe
for
the
45 824 910 Bio
Enz
Biot
for
Hig
45 832 910 DIG
Com
dUT
pro
and
46 081 001 Nitr
Sem
wat
and
the
54 599 001 Non
Solu
com
stab
0.25
54 777 001 Hig
Qui
cult
tran
54 785 001 Hig
Qui
cult
tran
55 633 001 CSP
Rea
ena
non
For
56 281 001 Nitr
Det
Nitr
nico
of t
58 241 001 -G
Qua
with
tech
extr
58 888 001 HN
Com
non
use
and
59 051 001 CD
Che
ultr
acid
and
59 078 001 Exp
Exp
resu
to T
targ
59 779 001 BM
Che
con
ELIS
sou
by Catalo
ck Translation Mi
timized enzyme mi
bridization. Designe
detect multicopy or
omsomes or interp
G-Nick Translatio
nvenient enzyme n
eled using DIG-11
filter hybridization
DIG-High Prime k
otin-Nick Transla
zyme nucleotide m
tin-16-dUTP for us
filter hybridization
h Prime.
G-High Prime DN
mplete, convenient
TP and color detec
bes in 1 hour to ov
d colony/plaque hy
rite/Nitrate, Colo
mi-micro method fo
ter, plant material,
d biological sample
presence of nitrat
nidet P40 Substit
ubilize membrane
mplexes. Also inclu
bilize enzymes suc
5 mM.
gh Pure Plasmid I
ckly prepare up to
tures. Use directly
nsfection, and to g
gh Pure Plasmid I
ckly prepare up to
tures. Use directly
nsfection, and to g
PD ready-to-use
ady-to-use chemilu
abling extremely fa
nradioactively labe
blotting, gel shift
ric Oxide, Colorim
termination of nitri
rate present in the
otinamide adenine
he enzyme nitrate
Gal Reporter Gen
antify -Gal expre
h the -Gal-enco
hnology to detect a
racts.
PP Fluorescent D
mbined with Fast R
nradioactively labe
ed for nonradioacti
d colony and plaqu
P-Star
emiluminescent su
a-sensitive visible
ds on film or lumin
d dot blots, and ge
pand High Fidelity
ults with twofold h
Taq. Choose this sy
gets up to 5 kb, in
M Chemiluminesc
emiluminescent su
nvenient and highly
SA and SEAP repo
rces, such as intes
og Numb
Product N

ix
ix generates sensit
ed for direct fluoro
r very large hybrid
phase nuclei.
on Mix
nucleotide mix to g
-dUTP for in situ h
. For highly sensiti
kits.
tion Mix
ixture for generati
se in in situ hybrid
. For highly sensiti
NA Labeling and D
t kit for random pr
ction of labeled hyb
vernight incubatio
ybridizations.
orimetric Test
or determining nit
foodstuffs, drugs,
es. Nitrate reduced
te reductase.
tute
proteins during is
uded in buffers for
ch as Taq. Supplied
Isolation Kit
o 15 g highly puri
for PCR, sequenci
enerate labeled hy
Isolation Kit
o 15 g highly puri
for PCR, sequenci
enerate labeled hy
e
uminescent substr
ast and sensitive vi
led nucleic acids o
assays, and seque
metric Assay
c oxide via nitrite i
sample is reduced
e dinucleotide phos
reductase.
ne Assay, chemilu
ession in eukaryoti
ding lacZ reporter
approximately 20 f
Detection Set
Red, HNPP is used
led probe in in situ
ve blots: Southern
ue hybridizations.
light detection of
nescence imager sy
l shift assays.
y PCR System
System is an enzym
ystem for the most
PCR/RT-PCR.
cence ELISA Subs
ubstrate system ba
y sensitive method
orter gene assays. M
stine, placenta, mi
ber
Name
tive probes for fluo
ophore-labeling of
ization targets on
generate highly sen
hybridization. The
ive filter hybridizat
ng sensitive probe
dization. The mix ca
ive filter hybridizat
Detection Starter
rimed DNA labelin
brids. Obtain high
n. Use in Southern
rite and/or nitrate
cosmetics, and en
d to nitrite by redu
olation of membra
microplate assays
d as a Gel under n
fied plasmid DNA
ng, cloning, in vitr
ybridization probes
fied plasmid DNA
ng, cloning, in vitr
ybridization probes
rate for alkaline ph
sible light detectio
on film or luminesc
encing.
in biological fluids
d to nitrite by redu
sphate (NADPH) i
uminescent
ic cells transfected
r gene. Use chemi
fg -galactosidas
for fluorescent de
u hybridization. HN
n, northern, DNA se
e phosphatase, en
nonradioactively la
ystems. For Southe
me blend deliverin
reefold greater fid
t sensitive PCR res
strate (AP)
sed on CSPD prov
d to detect alkaline
Measures AP from
lk, and bacteria.
orescence in situ
in situ probes,
metaphase
nsitive probes
mix can be used
ion probes, use
es labeled with
an also be used
ion, use Biotin-
r Kit I
g using DIG-11-
yields of labeled
n/northern blots,
to investigate
nvironmental
ced NADPH in
ane-protein
s and used to
itrogen. CMC:
from bacterial
o transcription,
s.
from bacterial
o transcription,
s.
hosphatase,
on of
cence imagers.
in a microplate.
uced
n the presence
d with a plasmid
luminescence
e in cell
etection of a
NPP alone is
equencing blots,
abling fast,
abeled nucleic
ern, northern,
g superior
elity compared
sults for genomic
vides a
e phosphatase in
m various

200 l for
160 l for
160 l for
1 kit for up to 1
of 24 blots, 10 n
1 test combina
1 kit f
1 kit fo
1 test
1 kit for 500 as
2,500 U (10 x 2
50 l final volum
Pack Size

r up to 50 labeling
r up to 40 labeling
r up to 40 labeling
2 labeling reaction
ng to 3 g DNA pe
100 cm
2

ation for approxim
100 ml
2 x 50 ml
combination for 9
ssays (microplate),
(tube format)
1 set
2 x 1 ml
me each containin
blend
150 ml
www.roche
reactions
reactions
reactions
ns and detection
er assay, blots of
ately 64 assays
cations
cations
6 wells
, for 250 assays
000 reactions of
ng 2.6 U enzyme
e-applied-science

Price in

350,60
508,80
508,80
484,80
262,10
122,30
102,60
448,30
227,20
458,30
458,70
441,40
514,80
1.969,60
387,30

279

e.com

Pr
280

www.r

Cat.

11 76
11 76
11 77
11 77
11 77
11 77
11 77
11 77
11 78
11 78
11 78
11 79
11 79
11 81
roducts b
roche-applied-sc

No.
67 291 910 TUN
TUN
reac
to la
leve
67 305 001 TUN
This
tran
TUN
dea
72 457 001 TUN
TUN
assa
anti
visu
72 465 001 TUN
TUN
assa
is la
sub
74 425 001 Cel
Fast
ELIS
dete
frac
75 367 001 Ura
Prim
hea
reac
deo
75 375 001 Ura
Prim
hea
reac
deo
79 842 001 SEA
Sim
med
eas
sam
85 826 001 Exp
A R
amp
RAC
Exp
hum
85 834 001 Exp
A R
amp
RAC
Exp
hum
87 896 001 mR
Isol
hom
Use
and
96 828 001 Hig
Pur
cult
trea
SNP
96 895 001 DIG
Bloc
labe
100
mad
10 740 001 In S
Sec
sing
vivo
pro
by Catalo
cience.com
NEL Label Mix
NEL Mix contains f
ction to detect apo
abel DNA strand b
el.
NEL Enzyme
s enzyme solution
nsferase for the TU
NEL reaction mix la
ath at single-cell le
NEL AP
NEL AP is an antib
ays into colorimetr
ibody is bound to
ualized using Fast
NEL POD
NEL POD is an ant
ays into colorimetr
abeled with peroxid
bstrate such as DA
ll Death Detectio
SA supplied with p
ermination of mon
ction of cell lysates
acil-DNA Glycosy
marily used to prev
at-labile, is easily in
ction by heating to
oxyuridylate (dUTP)
acil-DNA Glycosy
marily used to prev
at-labile, is easily in
ction by heating to
oxyuridylate (dUTP)
AP Reporter Gen
mple, fast, sensitive
dium of transfecte
ily sampled and as
mpling of medium o
pand Reverse Tra
RNase H
-
reverse
plification of long R
CE. A two-step RT-
pand Long Templat
man dystrophin RN
pand Reverse Tra
RNase H
-
reverse
plification of long R
CE. A two-step RT-
pand Long Templat
man dystrophin RN
RNA Capture Kit
ate highly purified
mogenization, and
e immobilized mRN
d cDNA-AFLP.
gh Pure PCR Tem
ify nucleic acids fr
tured cells, and tis
atment with lysozym
P detection, blottin
G Easy Hyb Granu
cking buffer for m
eled nucleic acid p
0 ml of a 1x workin
de solutions and lo
Situ Cell Prolifer
cond generation no
o systems. Detect
liferating cells in h
og Numb
Product N

fluorescein-dUTP a
optosis in situ . Use
breaks to quantity
contains recombin
UNEL reaction to d
abels DNA strand
evel.
body that converts
ric assays for light
FITC-dUTP, labeled
Red or NBT/BCIP.
tibody that convert
ric assays suitable
dase and is visuali
AB Substrate.
on ELISA
PLUS

ve, nonradioactive
plates, pre-coated
no- and oligonucle
s.
ylase, heat-labile
vent PCR product c
nactivated at the b
o +95C. DNA is cl
) residue has inco
ylase, heat-labile
vent PCR product c
nactivated at the b
o +95C. DNA is cl
) residue has inco
e Assay, chemilu
assay measures s
d cells. SEAP is se
ssayed. Eliminating
or other analysis.
anscriptase
transcriptase for t
RNA targets, gene
-PCR using Expan
te was used to am
NA.
anscriptase
transcriptase for t
RNA targets, gene
-PCR using Expan
te was used to am
NA.
d poly (A)
+
RNA fro
immobilize in stre
NA directly for qua
mplate Preparatio
rom different samp
sue. Bacteria and
me or lyticase. Use
ng, etc.
ules
embrane hybridiza
probes (not for ISH
g solution; 6 x 100
ong-term storage.
ration Kit, FLUOS
onradioactive kit for
immunohistocytoc
and quantify cells
heterogeneous pop
ber
Name
and -dNTPs for th
e this mix with the
apoptotic cell deat
nant terminal deox
etect apoptosis in
breaks to quantity
fluorescence-base
microscopy. Anti-
d with alkaline pho
ts fluorescence-ba
for light microsco
ized using a precip
1-step photometr
with streptavidin.
osomes in the cyto
e
carryover contamin
beginning of the am
leaved at any site w
rporated.
e
carryover contamin
beginning of the am
leaved at any site w
rporated.
uminescent
secreted placental
ecreted into the su
g cell lysis allows r
two-step RT-PCR,
eration of cDNA lib
d Reverse Transcr
mplify up to 13.5 kb
two-step RT-PCR,
eration of cDNA lib
d Reverse Transcr
mplify up to 13.5 kb
om cells and tissu
ptavidin-coated 0.
alitative and quanti
on Kit
ple materials, such
yeast require a sp
e purified nucleic a
ation using nonrad
H). Dissolve granul
0 ml portions allow
S
r detecting DNA sy
chemistry. Ideal for
in S phase, and de
pulations.
e TUNEL
TUNEL Enzyme
th at single-cell
xynucleotidyl
situ . The
y apoptotic cell
ed TUNEL
-fluorescein
osphatase, and
ased TUNEL
opy. The antibody
pitating
ic sandwich
For specific
oplasmic
nation. UNG,
mplification
where a
nation. UNG,
mplification
where a
AP in culture
pernatant and is
repeated
especially
braries, and 5'/3'
riptase and
cDNA from
especially
braries, and 5'/3'
riptase and
cDNA from
e after lysis and
2 ml PCR tubes.
itative RT-PCR
as whole blood,
ecific prelysis
acids in PCR,
dioactive DIG-
es in water for
w for freshly
ynthesis at the
many in vitro /in
etect

3 x 5
2 x
3.5
3.5
1
1 kit for 500 a
250
1 kit
1 kit fo
gr
1 k
Pack Size

550 l for up to 30
50 l for up to 20 t
100 U
500 U
assays, microplate
0 assays, tube form
1,000 U (20 l)
5,000 U (100 l)
for up to 192 reac
ranules for 6 x 100
tests
tests
ests
ests
sts
formate, or for
mate
ctions
cations
ml
ests

Price in

141,80
181,00
115,60
122,20
541,70
143,80
534,50
458,70
99,80
377,70
459,70
279,90
321,10
671,50

Pr

Cat.

11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
11 81
roducts b

No.
11 002 001 Exp
Am
buff
and
larg
14 036 001 Luc
Che
luci
lum
film
14 150 001 Ant
Use
reco
dot
nee
14 273 001 Tris
Tris
com
pre
14 320 001 For
Colo
hyb
elec
to s
14 362 001 PCR
Con
dCT
Wat
cDN
14 389 001 Red
Use
lyse
cell
use
14 397 001 min
Rea
quic
from
14 419 001 min
Rea
quic
of e
seq
14 427 001 min
Rea
quic
from
limi
14 460 001 Ant
Mo
imm
type
14 524 001 rGF
Use
PAG
exp
eas
14 770 001 DN
Eas
Sou
Elim
reag
15 016 001 Ant
Eas
mam
of H
wes
15 024 001 Ant
Eas
mam
prot
prot
by Catalo
pand 20 kb
PLUS
PC
plify genomic DNA
fer and enzyme ble
d DNA produce fra
ge-fragment amplif
ciferase Reporter
emiluminescent as
ferase activity in tr
minometers, microp
m. More sensitive th
ti-c-myc-Peroxid
e for single-step de
ombinant epitope-
blots and western
ed for a secondary
s base
s Base is extensive
mponent of buffer s
paration is free of
rmamide
orless liquid suitab
bridization. Formam
ctrophoresis by de
stabilize single stra
R Nucleotide Mix
nvenient, easy-to-u
TP, dGTP, and dTTP
ter. Optimized for
NA synthesis, and
d Blood Cell Lysi
ed for isolate DNA
es red blood cells i
s free of red blood
e with other specie
ni Quick Spin Olig
ady-to-use, microc
ck and efficient re
m end-labeled olig
ni Quick Spin DN
ady-to-use, microc
ck, efficient purific
excess dye-labeled
uencing. Exclusion
ni Quick Spin RN
ady-to-use, microc
ck and efficient re
m RNA labeled by
t: = 20 bases
ti-GFP
noclonal antibody
munoprecipitation
e and mutant form
FP
e as a positive cont
GE and western blo
periments involving
ily detected using
A Isolation Kit fo
ily and quickly iso
uthern blots, restric
minates organic ext
gents.
ti-HA Affinity Ma
y method for imm
mmalian, bacterial
HA-tagged protein
stern blotting or sil
ti-Protein C Affin
y method for imm
mmalian, bacterial
tein C-tagged prot
teins by western b
og Numb
Product N

CR System
A fragments up to
end to amplify pro
agments of 23 kb in
fication.
r Gene Assay, hig
ssay for quantitativ
ransfected cells. U
plate or tube forma
han isotopic CAT a
dase
etection of native h
-tagged proteins th
n blots. Use of Anti
detection step.
ly used in biochem
solutions, especial
proteases, DNase
ble for denaturing
mide is used as an
eionizing RNA. In c
ands of denatured
x
use, clear colorless
P, each at 10 mM
direct use in all typ
primer-extension.
s Buffer
and RNA, this rea
n human whole bl
d cells, for use in d
s.
go Columns
centrifuge-compati
moval of unincorp
gonucleotides. Excl
NA Columns
centrifuge-compati
cation of DNA from
d dideoxynucleotid
n limit: = 20 bp
A Columns
centrifuge-compati
moval of unincorp
polymerase or end
to detect GFP or G
and western blotti
ms of GFP.
trol when detectin
ot analysis. It can a
g fluorescence mic
blue or UV light.
or Cells and Tissu
lates DNA from m
ction digests, PCR/
tractions, anion ex
atrix
unoprecipitation o
, and yeast extract
s from crude extra
lver staining.
nity Matrix
unoprecipitation o
, and yeast extract
teins from crude e
blotting or silver sta
ber
Name
35 kb. Includes an
oducts over 20 kb.
n length. Use in PC
gh sensitivity
ve determination of
Use in manual or au
at, and scintillation
assay.
human c-myc prot
hat contain the c-m
i-c-myc-Peroxidas
mistry and molecul
lly for nucleic acid
s and RNases.
gels and nucleic a
RNA stabilizer in g
capillary electropho
DNA.
s solution of sodiu
concentration in P
pes of amplificatio
ady-to-use buffer p
lood, yielding intac
downstream applic
ible chromatograp
porated radiolabele
lusion limit: = 8 bp
ible chromatograp
m labeling reaction
e terminators prio
ible chromatograp
porated radiolabele
d-labeling techniq
GFP fusion protein
ing. Anti-GFP reco
g GFP Fusion Prot
also be used as a
croscopy. rGFP fluo
ues
ost cells and tissu
/long PCR, and seq
xchange columns,
of HA-tagged prote
ts and column affi
acts. Analyze tagge
of protein C-tagged
ts and affinity purif
extracts. For analyz
aining.
n optimized
Control primers
CR, RT-PCR, and
f firefly
utomated
counters or
tein and
myc epitope in
se eliminates the
ar biology as a
solutions. This
acid
gel
oresis, it is used
m salts of dATP,
PCR Grade
on reactions,
preferentially
ct white blood
ations. Not for
hy columns for
ed nucleotides
p
hy columns for
s, and removal
r to fluorescent
hy columns for
ed nucleotides
ues. Exclusion
s using
gnizes both wild
teins by SDS-
standard for
orescence is
es. Use for
quencing.
and chaotropic
eins from
nity purification
ed proteins by
d proteins from
fication of
zing tagged

200 U for up to
each co
1 kit
2,000 l (10 x
5,000 reaction
100 ml (for 50
sam
1 kit (10 isola
or 5
1 ml
1 ml
Pack Size

40 reactions of 50
ntaining 5 U enzym
500 g (500 l)
5 kg
500 ml
x 200 l) 10 mM, e
0 to 500 reactions,
mple size 1 to 500
50 columns
50 columns
50 columns
200 g
50 g (1 mg/ml)
ations of 400 mg e
5 x 10
7
cultured ce
www.roche
0 l final volume
me blend
ssays
each, for up to
action volume
depending on
l)
each for tissue
ells)
ume)
ume)
e-applied-science

Price in

204,30
1.099,80
407,40
588,20
91,10
445,60
51,00
206,40
206,40
222,90
342,90
197,40
234,80
852,30
473,20

281

e.com

Pr
282

www.r

Cat.

11 81
11 82
11 82
11 82
11 82
11 82
11 83
11 83
11 83
11 83
11 83
11 83
11 85
11 85
11 85
roducts b
roche-applied-sc

No.
16 586 001 Aga
Aga
bp)
sizin
frag
28 665 001 Hig
Rap
cell
pur
RNa
28 673 001 -G
Opt
sect
pro
28 681 001 Ann
Ann
cyto
on o
diffe
28 789 001 p53
Det
hom
betw
type
29 696 001 Per
Com
acc
anti
imm
35 238 001 Ant
PAR
reco
sub
imm
35 246 001 Apo
For
gel
a qu
apo
35 289 910 PCR
Dire
PCR
dige
Ura
36 145 001 cOm
Rely
and
New
Sup
36 153 001 cOm
Rely
and
New
Sup
36 170 001 cOm
Rely
EDT
type
54 666 910 T e
Qua
tube
prim
and
55 476 001 Tita
Sen
tube
amp
enz
55 638 001 DN
For
dete
rest
by Catalo
cience.com
arose MS
arose MS is ideal f
. It can be used in
ng, and STR analys
gments that differ
gh Pure RNA Isola
pidly isolate small a
s. Blood, yeast, an
ified and intact RN
ase protection, and
Gal Staining Set
timized staining se
tions demonstratin
duct can be seen
nexin-V-FLUOS
nexin-V-FLUOS de
ometry or fluoresce
outer leaflets of ce
erentiates apoptot
3 pan ELISA
termine p53 (huma
mogenates (tumor
ween elevated p53
e and mutant form
roxidase Labeling
mplete kit for label
cessible primary am
ibodies with POD,
munoblotting. All re
ti-Poly (ADP-Rib
RP is a zinc-depen
ognizes DNA stran
bstrate for apoptos
munochemistry, im
optotic DNA-Lad
rapid isolation of
electrophoresis fo
uick and documen
optosis and necros
R DIG Labeling M
ect labeling of amp
R. Prevent PCR car
est contaminating
acil-DNA Glycosyla
mplete
y on proven perfor
d metalloproteases
w for EDTA inhibiti
pplied in glass vials
mplete, Mini
y on proven perfor
d metalloproteases
w for EDTA inhibiti
pplied in a glass via
mplete, Mini, EDT
y on proven perfor
TA-free Tablets inh
es as cOmplete UL
loTAGGG Telom
alitative detection o
e ready-to-use mix
mer to immobilize T
d a DIG probe for d
an One Tube RT-
nsitive, quick and r
e system reverse t
plifies cDNA with a
zyme blend from th
A Molecular We
ermination of doub
og Numb
Product N

for separation of sm
separation of PCR
sis. Agarose MS d
by only 4 base pai
ation Kit
amounts of high q
d bacteria require
NA in RT-PCR, nort
d much more.
et for the histochem
ng -galactosidas
by the naked eye o
etects apoptotic ce
ence microscopy b
ell membranes. Pro
tic from necrotic ce
an, mouse, rat) in s
tissue/cell lines). U
3 levels and tumor
ms of p53 protein.
g Kit
ling water-soluble
mino groups with P
and downstream
equired reagents a
bose) Polymerase
ndent, eukaryotic D
nd breaks produce
is-specific proteas
munoprecipitation
dder Kit
DNA, which can b
or the determinatio
ntable form of data
sis.
Mix
PLUS

plification products
rryover by incorpor
PCR products from
ase.
rmance: cOmplete
ion: IMAC with cO
s.
rmance: cOmplete
ion: IMAC with cO
al.
TA-free
rmance combined
hibit serine and cy
LTRA Tablets. Supp
merase PCR ELISA
of telomerase activ
x for elongation and
TRAP products in a
detection.
PCR System
reproducible analy
transcribes RNA in
a thermal cycling r
he Expand High Fid
ight Marker XVI
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
ber
Name
mall DNA fragmen
R products, genoty
iscriminates betwe
rs.
uality total RNA fr
a pre-lysis treatm
thern blotting, prim
mical staining of ce
se activity. The -
or using light micr
ells in suspension c
by binding to phos
opidium iodide lab
ells.
serum/plasma, or f
Used to investigate
development by q
biomolecules with
POD. Ideal for coup
use in ELISA, IHC,
are supplied.
e
DNA-binding prote
ed by genotoxic ag
ses from the ICE-fa
n, and western blot
be analyzed and ch
on of apoptotic cel
a to differentiate be
s using digoxigeni
rating dUTP instea
m previous amplifi
Tablets inhibit ser
types as cOmplete
Omplete His-Tag Pu
Tablets inhibit ser
types as cOmplete
Omplete His-Tag Pu
with high conveni
steine proteases in
plied in a glass via
A
vity in cell extracts.
d amplification. Us
a streptavidin-coate
sis of RNA with hi
nto cDNA (AMV) u
reaction using an o
delity PCR System.
(250 bp ladder)
mplifies accurate m
A fragments genera
nts (50 to 1500
yping, allele
een DNA
rom cultured
ent. Use the
mer extension,
ells and tissue
-gal reaction
roscopy.
cells using flow
sphatidylserine
eling
from tissue
e relationships
quantifying wild
h reactive and
pling of
and
ein that
gents. It is a
amily. For
tting.
haracterized by
l death. Provides
etween
n (DIG)-dUTP in
ad of dTTP and
cations using
rine, cysteine,
ULTRA Tablets.
urification Resin.
rine, cysteine,
ULTRA Tablets.
urification Resin.
ence. cOmplete
n the same cell
al.
One-step/one-
es a biotinylated
ed microplate,
gh fidelity. One-
up to 6 kb and
optimized
.
molecular weight
ated by
3.0 kbp.

1 kit
1 set for up
500
1
1 kit for
100
1
2 x 250 l for u
50
3 x 20 tablet
sufficient fo
25 tablets in a
for a volum
25 tablets in a
for a volum
1 kit
50 g in 200 l
Pack Size

100 g
0 l for up to 250 t
0 l for up to 50 b
or a volume of 50 m
solution
me of 10 ml extract
me of 10 ml extract
100 reactions
(1 A
260
unit) for up
tions
5 cm dishes
ests
sts
reactions
lots
sts
ons, reactions of
lume
each tablet is
ml extraction
blet is sufficient
ion solution
blet is sufficient
ion solution
tions
p to 50 gel lanes

Price in

595,00
238,70
200,00
663,60
785,50
494,10
372,40
329,40
414,40
692,90
136,00
136,00
1.026,60
576,50
115,70

Pr

Cat.

11 85
11 85
11 85
11 85
11 86
11 86
11 87
11 87
11 87
11 88
11 90
11 90
11 92
11 92
11 92
roducts b

No.
55 646 001 DN
For
dete
rest
58 777 001 Ann
Kit w
and
sing
cell
58 874 001 Hig
Qui
who
incl
PCR
58 882 001 Hig
Qui
fluid
ana
67 423 001 Ant
Det
con
imm
Sinc
labe
67 431 001 Ant
Det
con
imm
Sinc
labe
73 580 001 cOm
Rely
EDT
type
73 601 001 Pef
Spe
com
atta
con
73 628 001 Pef
Spe
com
atta
con
88 412 001 PCR
Rea
eac
reac
dUT
09 282 001 Lig
The
ach
32 p
09 312 001 Lig
Sim
Cap
stan
8-w
20 685 001 Cel
Fast
ELIS
dete
frac
21 673 001 We
10x
exp
mem
21 681 001 We
10x
exp
mem

by Catalo
A Molecular We
ermination of doub
nexin-V-FLUOS S
with FLUOS-conju
d quantification of
gle-cell level. Seco
ular characterizati
gh Pure Viral Nuc
ckly purify viral nu
ole blood. When us
uding viral nucleic
R, directly after elu
gh Pure Viral RNA
ckly purify viral RN
ds, or cell culture s
alysis directly after
ti-HA High Affinit
ntain the HA epitop
munoprecipitation,
ce it is a rat monoc
eling.
ti-HA High Affinit
ntain the HA epitop
munoprecipitation,
ce it is a rat monoc
eling.
mplete, EDTA-fre
y on proven perfor
TA-free Tablets inh
es as cOmplete UL
fabloc
SC PLUS
ecific, potent irreve
mpared to PMSF or
achment of Pefablo
ncentration for long
fabloc
SC PLUS
ecific, potent irreve
mpared to PMSF or
achment of Pefablo
ncentration for long
R Nucleotide Mix
ady-to-use premixe
ch at 10 mM, and d
ctions. Prevent car
TP instead of dTTP
htCycler
Sampl
e LightCycler
Sam
hievable with the L
positions to hold L
htCycler
Centri
mplify cooling, filling
pillaries. Adapter e
ndard centrifuges.
well multichannel p
ll Death Detectio
SA supplied with p
ermination of mon
ction of cell lysates
estern Blocking R
x solution used as a
periments. The reag
mbrane, membran
estern Blocking R
x solution used as a
periments. The reag
mbrane, membran
og Numb
Product N

ight Marker XVII
n agarose gels. Sim
ble-stranded DNA
CR, and RT-PCR. Si
Staining Kit
ugated annexin-V a
apoptosis and diff
ondary labeling (ph
on.
cleic Acid Kit
ucleic acids (DNA,
sing whole blood,
c acids. Use purifie
ution in water.
A Kit
NA from mammalia
supernatants. Isola
elution in PCR gra
ty
za hemagglutinin a
pe in ELISA, immun
and western and
clonal, use with m
ty
za hemagglutinin a
pe in ELISA, immun
and western and
clonal, use with m
ee
rmance combined
hibit serine and cy
LTRA Tablets. Supp
S
r DFP. Pefabloc
S
oc
SC to proteins
ger incubation tim
S
r DFP. Pefabloc
S
oc
SC to proteins
ger incubation tim
x
PLUS

ed solution of sodi
dUTP at 30 mM. Op
rryover contaminat
P by pretreatment w
le Carousel
mple Carousel is u
ightCycler
1.5 Ins
LightCycler
Capill
ifuge Adapters
g, and centrifugati
easily fits holes in r
Cooling block hol
pipettes.
on ELISA
PLUS
, 10x
ve, nonradioactive
plates pre-coated w
no- and oligonucle
s. Contains 10x buf
Reagent, Solution
a general blocking
gent is used in ste
e washing steps, a
Reagent, Solution
a general blocking
gent is used in ste
e washing steps, a
ber
Name
I (500 bp ladder)
mplifies accurate m
A fragments genera
ize range: 0.5 to 5.
and propidium iod
ferentiaton from ne
hycoerythrin, TRITC
RNA) from serum
total nucleic acids
ed nucleic acids in
an serum, plasma,
ated viral RNA is u
ade water.
and recombinant p
nocytochemistry,
dot blots.
urine monoclonals
and recombinant p
nocytochemistry,
dot blots.
urine monoclonals
with high conveni
steine proteases in
plied in glass vials
serine proteases. N
SC and the PLUS a
s. They can be use
es at alkaline pH.
serine proteases. N
SC and the PLUS a
s. They can be use
es at alkaline pH.
ium salts of dATP,
ptimized for most
tion using PCR pro
with Uracil-DNA G
used to increase th
strument and olde
laries (20 l).
ion of all types of L
rotors for Eppendo
ds 32 adapters in
1-step photometr
with streptavidin. F
osomes in the cyto
ffers.
n
g agent during wes
ps such as blockin
and diluting detect
n
g agent during wes
ps such as blockin
and diluting detect
)
molecular weight
ated by
0 kbp.
ide for detection
ecrosis at the
C) is possible for
m, plasma, or
s are isolated
PCR and RT-
other body
sed for RT-PCR
proteins that
s for double
proteins that
s for double
ence. cOmplete
n the same cell
.
Nontoxic
additive prevent
d at higher
Nontoxic
additive prevent
d at higher
dGTP, dCTP,
amplification
oducts with
Glycosylase.
he throughput
er versions. It has
LightCycler

orf tubes in
4 rows; use with
ic sandwich
For specific
oplasmic
stern blotting
ng the
tion antibodies.
stern blotting
ng the
tion antibodies.

50 g in 200 l
1
1 kit fo
1 kit fo
20 tablets in a
for a volum
set I (100 mg P
set II (1 g Pefab
2 x 100 l f
reactions o
1 set (32 ada
1 kit
100
6 x 10

Pack Size

(1 A
260
unit) for up
50 g
500 g
me of 50 ml extract
Pefabloc
SC; 5 m
solution)
bloc
SC; 2 x 25 m
solution)
for up to 10 mM, e
of 20 l final react
1 sample carouse
apters in a dedicat
cooling block)
t for up to 10 x 96
ml (10 blots, 100 c
00 ml (60 blots, 100
www.roche
p to 50 gel lanes
sts
cations
cations
blet is sufficient
ion solution
l PSC-Protector
ml PSC-Protector
ach, for 500
ion volume
l
ted aluminum
tests
cm
2
)
0 cm
2
)
e-applied-science

Price in

115,70
280,80
335,70
363,50
347,10
2.945,40
257,20
153,60
724,60
120,80
inquire
inquire
951,50
91,40
321,90

283

e.com

Pr
284

www.r

Cat.

11 92
11 92
11 93
11 93
11 93
11 93
11 93
11 93
11 93
11 93
11 96
11 96
11 96
11 96
roducts b
roche-applied-sc

No.
22 416 001 Ant
Spe
of e
imm
22 505 001 Deo
Use
prim
vials
solu
34 317 001 RNA
Eas
For
bon
long
34 333 001 mR
Isol
with
yiel
blot
34 511 001 dAT
Use
reag
reac
of t
34 520 001 dCT
Suit
as r
seq
solu
34 538 001 dGT
Suit
as r
seq
solu
34 546 001 dTT
Suit
as r
seq
solu
34 554 001 dUT
Use
req
con
Sup
39 823 001 Tita
Ana
up t
inhi
relia
65 085 001 Ant
Sing
blot
inde
epit
65 409 910 PCR
Con
pro
No.
para
66 006 001 TUN
Use
deo
app
brea
69 013 001 dAT
Use
reag
reac
of t

by Catalo
cience.com
ti-His
6

ecific and sensitive
expression vector u
munocytochemistry
oxynucleoside Tr
e for sequencing/c
mer extension, and
s: dATP, dCTP, dG
A/DNA Stabilizat
y-to-use reagent f
simultaneous cell
ne marrow samples
g-term storage.
RNA Isolation Kit
ate high-quality m
h RNA/DNA Stabil
d of 50 to 200 ng m
tting, cDNA library
TP
e dATP, PCR Grade
gents are required
ctions, and sequen
he sodium salt (pH
TP
uencing/cycle seq
ution of the sodium
TP
uencing/cycle seq
ution of the sodium
TP
uencing/cycle seq
ution of the sodium
TP
e dUTP, PCR Grade
uired: RT, PCR, RT
ntamination betwee
pplied as 100 mM s
an One Tube RT-
alyze RNA from ma
to 6 kb. Includes re
ibitor, and PCR-gra
able analysis of RN
ti-His
6
-Peroxidas
gle-step detection
tting and ELISA. R
ependent of epitop
tope with high sen
R ELISA, DIG-De
nvenient, nonradio
ducts; 5-pack is th
11636111910), pr
allel testing of a la
NEL Dilution Buff
e with In Situ Cell
oxynucleotidyl tran
plications. The resu
aks to quantity apo
TP
e dATP, PCR Grade
gents are required
ctions, and sequen
he sodium salt (pH
og Numb
Product N

e detection for hist
used. For immunob
y, immunofluoresc
riphosphate Set
cycle sequencing, l
d all types of ampli
TP, dTTP; each co
m salt (pH 7).
tion Reagent for
for collection of sa
lysis and stabiliza
s. Also ideal for nu
for Blood/Bone
mRNA from blood o
lization Reagent fo
mRNA/ml blood ca
y preparation, and
e sodium salt for a
ncing. Supplied as
H 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
en PCRs to elimina
solution of the sod
PCR Kit
any sources (anim
eagents, control p
ade water to perfo
NA with high fideli
se
of His
6
-tagged re
eacts with native a
pe-sequence locat
nsitivity.
etection, 5-pack
active method for
he high capacity ve
oviding more reag
arge number of sam
fer
Death Detection K
sferase for the TU
ulting reaction mix
optotic cell death
e sodium salt for a
ncing. Supplied as
H 8.3).
ber
Name
idine-tagged prote
blotting, immunop
cence, and ELISA.
abeling, reverse tr
fication reactions.
ntains 100 mM cle
Blood/Bone Ma
amples for nucleic
tion of nucleic aci
ucleic acid stabiliza
Marrow
or bone marrow lys
or Blood/Bone Mar
an be used in RT-P
more.
pplications where
ption, PCR, RT-PCR
100 mM clear col
uality reagents are
DNA labeling reac
It is a 100 mM cle
uality reagents are
DNA labeling reac
It is a 100 mM cle
uality reagents are
DNA labeling reac
This is a 100 mM
where high-quality
quencing. Avoid c
dium salt.
al, plant, human, v
rimers, nucleotide
orm RT-PCR. For q
ty.
ecombinant protein
and denatured tag
tion. Recognizes th
labeling and detec
ersion of the stand
gents, but lacking c
mples.
Kits to dilute termin
NEL reaction in sp
x is used to label D
at the single-cell l
pplications where
ption, PCR, RT-PCR
100 mM clear col
eins regardless
recipitation,
ranscription,
Set contains 4
ear, colorless
rrow
acid isolation.
ds in blood and
ation during
sates preserved
rrow. Resulting
PCR, northern
high-quality
R, DNA labeling
orless solution
required, such
ctions, and
ear colorless
required, such
ctions, and
ear colorless
required, such
ctions, and
clear colorless
y reagents are
arryover
se positives.
viral, bacterial)
s, RNase
uick, sensitive,
ns by western
ged proteins
he C-terminal
6

cting PCR
dard kit (see Cat.
controls. For
nal
pecial
NA strand
evel.
high-quality
R, DNA labeling
orless solution

40 x 100 l
500 ml (for
1 kit (for up to
m
250 l (25
standard
250 l (25 m
6,250 stand
250 l (25
standard
250 l (25
standard
250 l (25
standard
50 reactions
1 kit for 4
microplates), th
number of
standar
1,250 l (125
31,250 stand

Pack Size

100 g
l (40 x 10 mol, 40
r up to 50 ml samp
30 (100) isolations
ml) sample volume
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) 100
dard PCR assays o
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) for
d PCR assays of 20
mol, 100 mM) for
d PCR assays of 20
, including 10 cont
50 U
480 detection reac
he number of tests
required sample d
rd and/or control r
2 x 10 ml
mol, 100 mM) 100
dard PCR assays o
x 100 mM)
ple material)
s from 5 ml (1.5
s)
r up to 6,250
0 l each
mM, for up to
f 20 l each
r up to 6,250
0 l each
r up to 6,250
0 l each
r up to 6,250
0 l each
trol reactions
tions (five
depends on the
dilutions and
eactions
0 mM, for up to
of 20 l each

Price in

334,90
885,00
96,10
587,60
89,10
89,10
89,10
89,10
89,10
530,90
388,40
911,30
216,30
328,70

Pr

Cat.

11 96
11 96
11 96
11 96
11 96
11 97
11 98
11 98
11 98
12 01
12 01
12 01
12 01
12 01
roducts b

No.
69 021 001 dCT
Suit
as r
seq
solu
69 030 001 dGT
Suit
as r
seq
solu
69 048 001 dTT
Suit
as r
seq
solu
69 056 001 dUT
Use
req
con
Sup
69 064 001 Deo
PCR
RT-
sod
colo
76 826 001 MIA
One
mel
stre
88 506 001 Ant
Use
reco
imm
use
88 549 001 Ann
Kit w
and
sing
cell
89 685 001 Stre
Stre
are
Plat
coa
11 875 001 Hig
Use
Nuc
Vira
be p
12 952 001 Cas
Use
ana
step
rese
13 789 001 T e
Sen
acti
PCR
mea
13 819 001 Ant
For
blot
Sinc
con
15 102 001 Lig
Eas
Ligh
dete
Mg

by Catalo
TP
uencing/cycle seq
ution of the sodium
TP
uencing/cycle seq
ution of the sodium
TP
uencing/cycle seq
ution of the sodium
TP
e dUTP, PCR Grade
uired: RT, PCR, RT
ntamination betwee
pplied as 100 mM s
oxynucleoside Tr
R-Grade set for ap
-PCR, DNA labeling
ium salts of dATP,
orless solutions in
A ELISA
e-step, 2 hour ELIS
lanoma inhibitory a
eptavidin-coated m
ti-HA-Fluorescei
e Anti-HA-Fluoresc
ombinant HA-tagg
munofluorescence.
ed with murine mo
nexin-V-FLUOS S
with FLUOS-conju
d quantification of
gle-cell level. Seco
ular characterizati
eptaWell, High B
used in colorimetr
tes are not sterile a
ating. Not suitable
gh Pure Viral Nuc
e this Buffer Set in
cleic Acid Kit, the H
al Nucleic Acid Lar
processed.
spase 3 Activity A
e this assay to dete
alyze caspase 1, 2,
p, and to perform i
earch of apoptosis
loTAGGG Telom
nsitive, nonradioacti
ivity in cell extracts
R ELISA, but also h
asure amount of re
ti-HA-Peroxidase
single-step detect
t analysis and ELIS
ce Anti-HA High A
njunction with mur
htCycler
DNA M
y-to-use mix for se
htCycler
Carouse
ection format. For
Cl
2
is supplied for
og Numb
Product N

ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
ons where high-qu
on, PCR, RT-PCR, D
quencing analysis.
m salt (pH 8.3).
en PCRs to elimina
solution of the sod
riphosphate Set
plications requirin
g, sequencing. Co
, dCTP, dGTP, dTTP
water (pH 8.3).
SA for the quantita
activity (MIA) prot
microplates.
n, High Affinity
cein, High Affinity
ged proteins using
. Since the antibod
noclonals for doub
Staining Kit
ugated annexin-V a
apoptosis and diff
ondary labeling (ph
on.
Bind (transparent
din-coated microp
ric and fluorescent
as sterilization pro
for cell culture.
cleic Acid Buffer
combination with
High Pure Viral Nu
rge Volume Kit wh
Assay
ect and quantify ca
3, or 7 activity by o
inhibitor studies fo
s.
merase PCR ELISA
tive photometric EIA
s. One-tube mix sim
has an optimized st
eaction product.
e, High Affinity
tion of HA-tagged
SA.
Affinity is a rat mon
ine monoclonals fo
Master HybProbe
ensitive, robust PC
el-Based Systems,
quantitative PCR,
r specific applicatio
ber
Name
uality reagents are
DNA labeling reac
It is a 100 mM cle
uality reagents are
DNA labeling reac
It is a 100 mM cle
uality reagents are
DNA labeling reac
This is a 100 mM
where high-quality
quencing. Avoid c
dium salt.
ng high-quality rea
ntains individual v
P at 100 mM conc
ative in vitro determ
tein in serum and p
for direct detectio
flow cytometry an
dy is a rat monoclo
ble labeling.
and propidium iod
ferentiaton from ne
hycoerythrin, TRITC
t, 96-well)
plates with high bin
t nucleic acid imm
cedures impair str
Set
the High Pure 16
ucleic Acid Kit, or t
hen larger sample v
aspase 3 activity in
omitting the captu
or caspase 3 in life
A
PLUS
A to detect/quantif
milar to TeloTAGGG
tandard and contro
recombinant prot
noclonal, it is poss
or double labeling
e
CR in LightCycler
using the HybProb

and SNP and muta
ons.
required, such
ctions, and
ear colorless
required, such
ctions, and
ear colorless
required, such
ctions, and
clear colorless
y reagents are
arryover
se positives.
gents: RT, PCR,
ials of the
entration. Clear,
mination of
plasma within
n of
nd
onal, it can be
ide for detection
ecrosis at the
C) is possible for
nding capacity
munoassays.
reptavidin
System Viral
the High Pure
volumes must
n cell lysates,
ure-antibody
science
fy telomerase
G Telomerase
l template to
teins by western
ible to use it in
.
Capillaries on
be probes
ation detection.

1,250 l (125
standard
1,250 l (125
standard
1,250 l (125
standard
1,250 l (125
standard
4 x 250 l (4 x
6,250 rea
1
1 k
1
1 set
1
1 kit
1 kit for up to 9

Pack Size

mol, 100 mM) fo
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
mol, 100 mM) fo
d PCR assays of 20
x 25 mol, 4 x 100
25 g
15 plates (96 wells
for up to 100 isola
25 U (25 g)
96 reactions of 20
volume
www.roche
or up to 31,250
0 l each
or up to 31,250
0 l each
or up to 31,250
0 l each
or up to 31,250
0 l each
mM) for up to
al volume
sts
ests
s)
ations
sts
tions
l final reaction
e-applied-science

Price in

328,70
328,70
328,70
328,70
235,50
972,30
326,80
855,20
657,00
146,30
940,20
1.085,40
408,60
inquire

285

e.com

Pr
286

www.r

Cat.

12 01
12 01
12 01
12 01
12 01
12 01
12 03
12 03
12 03
12 03
12 03
12 03
12 03
12 04
roducts b
roche-applied-sc

No.
15 137 001 Lig
Eas
Ligh
dete
risk
15 145 001 Lig
Eas
Ligh
dete
risk
15 161 001 Lig
Use
com
olig
suff
olig
15 196 001 Lum
Che
PVD
sen
allo
15 200 001 Lum
Che
PVD
esp
for
15 218 001 Lum
Che
PVD
high
hou
32 902 001 Fas
The
sup
Idea
prio
32 929 001 Fas
The
sup
Idea
prio
32 937 001 Fas
The
sup
Idea
prio
32 945 001 Fas
The
sup
Idea
prio
32 953 001 Fas
The
sup
Idea
prio
33 674 001 Hig
Qui
live
nort
con
39 672 910 DIG
Pro
che
Des
reag
41 677 001 CD
Rea
Ena
labe
For

by Catalo
cience.com
htCycler
RNA A
y-to-use mix for o
htCycler
Carouse
ection. Provides re
k of contamination.
htCycler
RNA A
y-to-use mix for o
htCycler
Carouse
ection. Provides re
k of contamination.
htCycler
Red 64
mbination with 3'-L
gonucleotides whe
ficient amount of e
gonucleotides.
mi-Light
PLUS
West
emiluminescent PO
DF or nitrocellulose
sitivity western blo
owing multiple expo
mi-Light Western
emiluminescent PO
pecially when quan
multiple exposures
mi-Light
PLUS
West
emiluminescent PO
h sensitivity weste
urs, allowing for mu
stStart Taq DNA P
ermostable, chemic
perb results due to
al tool for hot start
or to initial denatur
stStart Taq DNA P
ermostable, chemic
perb results due to
stStart Taq DNA P
ermostable, chemic
perb results due to
stStart Taq DNA P
ermostable, chemic
perb results due to
stStart Taq DNA P
ermostable, chemic
perb results due to
gh Pure RNA Tiss
ckly purify total int
r, spleen, lung, and
thern blotting, RNa
nstruction, and in v
G Northern Starte
duce DIG-labeled
emiluminescent de
signed for the novi
gents proven to pr
P-Star , ready-to
ady-to-use chemilu
ables fast, ultra-sen
eled nucleic acids
Southern, dot, and
og Numb
Product N

Amplification Kit
ne-step RT-PCR in
el-Based Instrumen
eproducibility, high
. MgCl
2
is supplied
Amplification Kit
ne-step RT-PCR in
el-Based Instrumen
eproducibility, high
. MgCl
2
is supplied
40-N-hydroxysuc
the 5'-amino end o
LightCycler
Fluor
n using HybProbe
ester to label a min
tern Blotting Sub
OD substrate detec
e membranes usin
otting, requiring qu
osures.
n Blotting Substra
OD substrate detec
e membranes. For
ntification is require
s.
tern Blotting Kit
OD substrate detec
e membranes usin
rn blotting requirin
ultiple exposures.
Polymerase, 5 U/
cally modified reco
its unique enzyme
t PCR, since it stay
ration step.
Polymerase, 5 U/
cally modified reco
its unique enzyme
ration step.
Polymerase, 5 U/
cally modified reco
its unique enzyme
ration step.
Polymerase, 5 U/
cally modified reco
its unique enzyme
ration step.
Polymerase, 5 U/
cally modified reco
its unique enzyme
ration step.
sue Kit
tact RNA from ma
d heart. Use isolate
ase protection, pri
vitro translation.
er Kit
RNA probes to us
tection reagents fo
ice DIG system use
rovide successful,
o-use
uminescent substr
nsitive visible light
on film/luminesce
d northern blots, g
ber
Name
SYBR Green I
n LightCycler
Cap
nts and SYBR Gre
h performance, and
d for optimization.
HybProbe
n LightCycler
Cap
nts and HybProbe
h performance, and
d for optimization.
ccinimide ester
of oligonucleotides
rescein CPG -label
probes for detecti
nimum of 5 50 n
bstrate
cts 1-5 pg antigen
ng secondary antib
uantification. Signa
ate
cts 10-50 pg antige
high-sensitivity w
ed. Signal lasts >3
(Mouse/Rabbit)
cts 1-5 pg antigen
ng mouse/rabbit an
ng quantification. S
/l
ombinant Taq poly
e design and optim
ys inactive during P
/l
ombinant Taq poly
e design and optim
/l
ombinant Taq poly
e design and optim
/l
ombinant Taq poly
e design and optim
/l
ombinant Taq poly
e design and optim
ammalian tissues, s
ed RNA directly in
mer extension, cD
se with the supplie
or northern blottin
er. This Starter Kit
reproducible resul
rate for alkaline ph
t detection of nonr
ence imagers.
gel shift assays.
pillaries using
en I dye for
d minimizes the
pillaries using
probes for
d minimizes the
s. Use in
ed
ion. One vial has
mol
blotted onto
bodies. For high
al lasts >9 hrs,
en blotted onto
estern blotting,
3 hours, allowing
blotted onto
ntibodies. For
Signal lasts >9
merase. Delivers
mized buffer.
PCR setup and
merase. Delivers
mized buffer.
PCR setup and
merase. Delivers
mized buffer.
PCR setup and
merase. Delivers
mized buffer.
PCR setup and
merase. Delivers
mized buffer.
PCR setup and
such as mouse
n RT-PCR,
NA library
d
g techniques.
contains the
lts.
hosphatase.
adioactively

1 kit for up to 9
1 kit for up to 9
1 vial (for 5
100 m
400 m
1 kit
100 U for up to
each conta
500 U (2 x 250
final volume e
2,500 U (10 x 2
50 l final volu
Ta
5,000 U (20 x 2
50 l final volu
Ta
1 kit
1 kit for up to 1
of 10 blots, blot
DNA, yielding

Pack Size

96 reactions of 20
volume
96 reactions of 20
volume
5 x 50 nmol oligon
ml (1,000 cm
2
mem
ml (4,000 cm
2
mem
(1,000 cm
2
memb
50 reactions of 50
aining 2 U FastStar
Polymerase
U) for up to 250 re
ach containing 2 U
DNA Polymerase
1,000 U (4 x 250 U
250 U) for up to 12
me each containin
aq DNA Polymeras
me each containin
aq DNA Polymeras
0 labeling reaction
ts of 10 x 10 cm
2
r
approx. 20 g labe
2 x 50 ml
l final reaction
l final reaction
nucleotides)
mbrane)
mbrane)
brane)
0 l final volume
rt Taq DNA
eactions of 50 l
U FastStart Taq
U)
250 reactions of
ng 2 U FastStart
se
500 reactions of
ng 2 U FastStart
se
tions
ns and detection
reactions of 1g
eled RNA, each

Price in

inquire
inquire
inquire
497,50
230,80
812,50
119,40
486,10
837,20
1.991,10
3.349,20
238,70
508,20
410,90

Pr

Cat.

12 14
12 14
12 14
12 14
12 15
12 15
12 15
12 15
12 15
12 15
12 18
12 18
12 18
12 19
roducts b

No.
40 306 001 GC
Blen
diffi
RIC
high
40 314 001 Hig
Cho
Exp
opti
high
40 322 001 M3
Det
earl
imm
both
40 349 001 M3
Det
earl
imm
both
56 792 910 In S
Prec
qua
tissu
cyto
58 167 001 Ant
Det
wes
mon
mon
58 817 001 Lig
Eas
Ligh
form
is s
58 825 001 Lig
Eas
Ligh
dete
Mg
58 833 001 Lig
Con
Inst
and
dua
58 850 001 Lig
Rea
Ligh
pre
and
89 666 001 Ma
Coo
elut
Bloc
Car
89 674 001 Ma
Coo
(0.2
vials
pos
89 704 001 Ma
Coo
Ligh
the
sixt
reag
90 664 001 Ma
Coo
con
usin
pos

by Catalo
-RICH PCR Syste
nd of Taq DNA Po
icult templates up
CH Resolution Solu
h yield and accura
gh Fidelity PCR M
oose this convenie
pand High Fidelity P
imized reaction bu
her fidelity than Ta
30 CytoDEATH
tect a cytokeratin 1
ly marker of apopt
munocytochemistry
h cryostat and par
30 CytoDEATH
tect a cytokeratin 1
ly marker of apopt
munocytochemistry
h cryostat and par
Situ Cell Death D
antitating apoptotic
ues using a red flu
ometry.
ti-HA-Biotin, Hig
tect HA-tagged rec
stern and dot blott
noclonal, it is poss
noclonals for doub
htCycler
DNA M
y-to-use mix for se
htCycler
Carouse
mat. Use for quant
upplied for specifi
htCycler
DNA M
y-to-use mix for se
htCycler
Carouse
ection format. For
Cl
2
is supplied for
htCycler
Contro
nfirms PCR system
truments. Quality c
d specific primers a
al-color experimen
htCycler
Color
ady-to-use solution
htCycler
Carouse
requisite for multip
d Cy5.5-labeled Hy
agNA Pure LC Co
tion pipetting by M
ck as required with
rousel, LC Centrifu
agNA Pure LC Co
2 ml, 96-well plate)
s. It fits directly on
st-elution pipetting
agNA Pure LC Co
htCycler
Capillar
post-elution prog
een 1.5 ml reaction
gents.
agNA Pure LC Co
ntaining LightCycle
ng MagNA Pure LC
sitions for 1.5 ml re
og Numb
Product N

em
olymerase and a pr
to 5 kb. Enhanced
tion deliver superb
acy.
Master
nt, 2x-concentrate
PCR System with P
uffer. Delivers two
aq DNA Polymeras
18 epitope produce
tosis in cells and ti
y, flow cytometry, a
raffin-embedded s
18 epitope produce
tosis in cells and ti
y, flow cytometry, a
raffin-embedded s
Detection Kit, TM
ple nonradioactive
c DNA fragmentatio
orescent label for f
h Affinity (3F10)
combinant protein
ting, and ELISA. Sin
sible to use it in co
ble labeling.
Master SYBR Gre
ensitive, robust PC
el-Based Systems,
titative PCR, and SN
c applications.
Master HybProbe
ensitive, robust PC
el-Based Systems,
quantitative PCR,
r specific applicatio
ol Kit DNA
m performance of L
check of both hum
and HybProbe pro
ts and color comp
Compensation S
ns generate color c
el-Based Instrumen
plex experiments w
ybProbe probes in
ooling Block, Rea
ding thirty-two 1.5
MagNA Pure LC Ins
h the MagNA Pure
ge Adapters, or 96
ooling Block, 96-w
ding either one Lig
), or 0.2 ml 8-strip
nto block cyclers, a
g of master mixes b
ooling Block, LC S
ding the LightCycl
ies for robotic pipe
ram of MagNA Pu
n tube positions fo
ooling Block, LC C
ding 32 LightCycle
er
Capillaries for
C Instruments. Thi
eaction tubes for m
ber
Name
roofreading polyme
d processivity and
b performance in P
ed, ready-to-use m
PCR-Grade dNTPs
times the yield and
se alone.
ed after caspase c
ssues. Use the M3
and immunohistoc
ections.
ed after caspase c
ssues. Use the M3
and immunohistoc
ections.
MR red
technique for dete
fluorescence micro
s with high sensiti
nce Anti-HA-High
onjunction with mu
een I
CR in LightCycler
using the SYBR G

NP and mutation d
e
CR in LightCycler
using the HybProb

and SNP and muta
ons.
LightCycler
Carou
man DNA used in a
bes, and as a func
pensation.
Set
compensation files
nts. Generated file
with both LightCyc
a single capillary.
action Tubes
5 ml reaction tubes
struments. Combin
e Cooling Blocks fo
6-well PCR Plate.
well PCR Plate
ghtCycler
480 Mu
vials, or 0.2 ml sin
and can be used fo
by MagNA Pure LC
Sample Carousel
er
Sample Carou
etting of up to 32 c
ure LC Instruments
or master mixes an
Centrifuge Adapt
er
Centrifuge Ada
automated post-e
s Cooling Block al
master mixes and o
erase amplify
the unique GC-
PCR, providing
mix, combining
, MgCl
2
, and an
d three times
cleavage, an
30 antibody in
chemistry with
cleavage, an
30 antibody in
chemistry with
cting and
level in cells and
oscopy or flow
vity using
Affinity is a rat
urine
Capillaries on
Green I detection
detection. MgCl
2

Capillaries on
be probes
ation detection.
usel-Based
a specific assay
ctional check of
s on
es are a
cler
Red 640-
s for use in post-
ne this Cooling
or either the LC
ultiwell Plate
gle reaction
or automated
C Instruments.
l
usel with
capillaries using
s. It also has
nd other
ters
apters
lution pipetting
so has fifteen
other reagents.

100 U for up to
each co
1 kit for up to 5
1
1 kit for up to 4
1 kit for up to 4
1 kit for up
1 set (4
1 cooling bloc

Pack Size

50 reactions of 50
ntaining 2 U enzym
00 reactions of 20
volume
50 tests
250 tests
50 g
80 reactions of 20
volume
80 reactions of 20
volume
to 50 reactions wit
reaction volume
1 cooling block
1 cooling block
1 cooling block
ck (with 32 LightCy
adapters)
www.roche
0 l final volume
me blend
l final reaction
sts
l final reaction
l final reaction
th 20 l final
on runs)
ycler centrifuge
e-applied-science

Price in

206,60
575,10
224,20
620,30
591,40
524,30
inquire
inquire
inquire
inquire
inquire
inquire
inquire
inquire

287

e.com

Pr
288

www.r

Cat.

12 20
12 23
12 23
12 23
roducts b
roche-applied-sc

No.
09 136 001 T e
Use
DNA
orga
leng
36 869 001 Hom
Spe
dete
thro
39 264 001 Lig
Eas
Ligh
dete
RT-
39 272 001 Lig
Eas
Ligh
dete
PCR
by Catalo
cience.com
loTAGGG Telom
e in life science res
NA in cell cultures a
anisms, including h
gth of these sample
mogeneous Casp
ecific, one-step fluo
ermination of casp
oughput screening
htCycler
FastSt
y-to-use hot start
htCycler
Carouse
ection. For qPCR, S
-PCR. MgCl
2
is sup
htCycler
FastSt
y-to-use hot start
htCycler
Carouse
ection. For qPCR, S
R. MgCl
2
is supplie
og Numb
Product N

mere Length Assa
search applications
and other biological
humans and mice.
les.
pases Assay, fluo
orimetric assay for
pases activity in mi
g.
tart DNA Master
mix for sensitive P
el-Based Systems w
SNP, and mutation
pplied for specific
tart DNA Master
mix for sensitive P
el-Based Systems w
SNP and mutation
ed for specific app
ber
Name
ay
for sensitive detec
l research samples
Use to determine t
orimetric
r the quantitative in
icroplates. Ideally s
SYBR Green I
PCR in LightCycler
when using SYBR

n detection. Use al
applications.
HybProbe
PCR in LightCycler
when using HybPr

detection. Use in
plications.
ction of telomeric
s from a variety of
the telomere
n vitro
suited for high-
Capillaries on
Green I for
so for two-step
Capillaries on
robe probes for
two-step RT-

1 kit
1 kit for 1,000
tes
1 kit for up to 4
1 kit for up to 4
Pack Size

tests on 96-well p
sts on 384-well pla
80 reactions of 20
volume
80 reactions of 20
volume
tions
plates, for 4,000
ates
l final reaction
l final reaction

Price in

771,60
2.762,20
inquire
inquire

Published by
Roche Diagnostics GmbH
Sandhofer Strae 116
D-68305 Mannheim
2013 Roche Diagnostics. All rights reserved.

Catalogo de Genomica ROCHE 2014

Transféré par

Informations du document

Description originale:

Copyright

Formats disponibles

Partager ce document

Partager ou intégrer le document

Options de partage

Avez-vous trouvé ce document utile ?

Ce contenu est-il inapproprié ?

Droits d'auteur :

Formats disponibles

Catalogo de Genomica ROCHE 2014

Transféré par

Droits d'auteur :

Formats disponibles

Genomics and Cell Research

Instruments and Reagents

96 Real-Time PCR Instrument

480 Real-Time PCR System is the

Block, 96-well PCR

and melting curve

480 Multiwell Pla

480 it can only

scanner. This optio

8-Tube Strip Ada

1.5 and old

Software for Lig

ompatible with all L

eLibrary and hydro

when using HybPro

when using SYBR G

1.5 and old

scanner. This optio

and melting curve

480 Multiwell Pla

8-Tube Strip Ada

480 it can only

when using HybPro

when using SYBR G

eLibrary and hydro

ompatible with all L

Software for Lig

Block, 96-well PCR

when using SYBR

when using HybPr

ls for BAL, sputum

Systems and blo

sign assays using

rary Set, Human

Systems and oth

ar) using the Light

l and are compat

ction, gene quantif

480 it can only

ety of different tiss

is used for the p

ety of different tiss

is used for the p

using the HybProb

using the SYBR G

using the HybProb

when using SYBR

when using HybPr

Vous aimerez peut-être aussi