the cloned gene is about 1kb, there are 8 codons i want to change by PCR method. but these codons were scattered in the sequence. i read several articles on overlapping or megaprimers PCR, could some people give me some ideas or experiences how to carry out this? or it's difficult to realize?
how to design PCR site-directed multiple mutagenesis
Started by lufang, Mar 24 2009 03:47 AM
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