Agarose gel electrophoresis/Common issues

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Current revision (20:19, 3 January 2006) (view source)
m (Common Agarose Gel Issues moved to Agarose gel electrophoresis/Common issues)
 

Current revision

There are a number of issues which plague gels far a variety of reasons. This page will contain some of the more common problems and show examples of gel images that have those problems.

So if you get a gel with something bizarre, keep the image and post it here so that others can learn from your trouble.

Possible unexpected bands:

Contents

Supercoiled

Nicked

Primer-dimers

The bright fuzzy bands at the bottom of the gel are typical of those caused by primer dimers. Primer-dimers can be minimized by using hot start PCR or by using a higher annealing temperature. Preventative measures include designing primers that do not form homo- or hetero-dimers.

Empty site in BB vector (~300bp band)

Can anyone explain this smearing? Is it nonspecific primer binding? Nuclease activity? The gel is the product of PCR to amplify clpX from a Sauer lab plasmid. The lanes are from left to right: 2 log ladder, 0.5 ng template, 5 ng, and 13 ng. The 13 ng seem to give the desired product at around 1275 bp. Should I go even higher in template mass? I'd appreciate any suggestions on optimizing primer-template ratio.

Sean 11:32, 3 Aug 2005 (EDT)

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