Berkeley LBL/JoyceNotebook

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Contruction of pET3a Derivatives Containing bchD and bchI

1. Amplify Rhodobacter's gene and introduce restriction sites by PCR (Using Phusion Polymerase), which allow cloning PCR fragments into pET3a

bchD bchI
length of gene fragment 1695 b.p. 1005 b.p.
Restriction sites introduced when amplified by PCR NdeI, BamHI NdeI, BglI