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smmoh4 smmoh4
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11 years ago
what are the steps for lambda DNA library creation  in puc19 vectors?How will you design the experiment ? On what basis we select 1 or 2 enzymes to digest both lambda phage DNA and puc19 plasmid DNA
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wrote...
11 years ago
When you are creating a library, you are basically cloning all the required DNA in fragments.

If you select puc19 as a vector, you must ensure in your selection of restriction enzymes that both the DNA and the vector have the same restriction sites i.e. cut sites. Furthermore, you must make sure that the restriction sites are far apart enough to create fragments of the proper size for the vector.
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