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Biology, 17.02.2020 23:04 anna4060

In class we described the use of recombinant DNA to produce human insulin protein in bacterial cells. This procedure relied on cloning a human gene into a plasmid at a location directly adjacent to a bacterial promoter sequence. Why not use the promoter from the human insulin gene for this application?

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In class we described the use of recombinant DNA to produce human insulin protein in bacterial cells...
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