Subcloning Site Directed Mutants

jayni76 at my-deja.com jayni76 at my-deja.com
Wed Jan 31 04:20:53 EST 2001

I create a lot of point mutants using site directed mutagenesis.  The
plasmids are usually around 7kb and I use promega Pfu enzyme.  I have been
subcloning the mutants after PCR to eliminate other mutations but have been
informed that people generally no longer bother as the enzymes are efficient.
 If I no longer did the subcloning this would save me a lot of time and
money!!  Any advice please as I am confused.


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