MCIM 326 Study Guide - Final Guide: Buoyancy, Ribonuclease H, Reca

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Some things to think about regarding the pbr322 sequence: How many genes are there and what is their size (amino acids and nucleotides). It would be a good idea to highlight the amino acid composition for each gene. (remember that the sense strand is not the same for all the genes. ) What is the stop codon for the tet gene? (maybe look u same for the other genes. ) Assume: we want to clone a dna fragment into the bamhi site in tet but we also want to remove the tet promoter. What are the last three amino acids (at cooh end) of the bla gene. We will pcr out the tet gene (including the termination signal, but not the rbs), placing a bamhi restriction site at the cooh end of the gene and a hindiii site at the nh2 end of the gene. We will include bases 5"-atat as additions to the primer sequence, just ahead of the restriction sequence.

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