sullivan at gwis2.circ.gwu.edu
Tue Feb 24 20:56:44 EST 1998
I've been running my radioactive RT-PCR products (100-300 bp)on vertical
5% polyacrylamide minigels. These are nondenaturing gels (no urea). For a
given primer pair, I often get the expected band *plus* a higher MW band
which, from what I read, could be some sort of heteroduplex (these higher
MW bands don't show up on agarose gels). A 100 bp DNA ladder, however,
runs just fine.
Can I eliminate the higher MW band by heating the samples before
loading? Or will I need to use a heated sample *AND* a denaturing gel?
Or am I on the wrong track completely?
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