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10H
Bio-Lit
Process of cloning
1. Chemically "cut" the gene you want to study from the DNA strand
3. Put the plasmid into an E. coli cell (or another type of bacteria).
As each E. coli cell divides, each new cell contains a copy of the
plasmid containing the gene.
6. Filter the mixture of broken E. coli cells and collect only the
plasmids containing the gene.
7. Put the plasmids into human cells. The type of cell varies
depending on the research.
8. Over time, the plasmid will be incorporated into the host cell DNA
and the new gene will change the proteins produced.
9. Observe physical changes between the cells with the plasmid and
those without.