purify PCR products using Wizard Prep (Promega)

Winoto lab lab_winoto at maillink.berkeley.edu.
Wed Jun 29 14:16:07 EST 1994

In article <2urvht$c1b at triton.unm.edu>
dkim at unm.edu writes:

> Finally, people often get acceptable yields using straight physical methods
> for DNA from gel purification, such as freeze and squeeze, etc. You might want
> to check out a very quick and dirty method in BioTechniques (sometime this
> year) in which the gel slice is simply pushed through a 0.45 micron syringe
> filter.
> Daniel Kim


I've tried the squeeze method you mentioned and was never able to get
it to work that well.  Have you tried it?  What kind of results did you


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