problems with RNAs denatured with Glyoxal(in Northerns)
Saverio Brogna Genetics
sb at mole.bio.cam.ac.uk
Sun Feb 25 14:37:44 EST 1996
could you explaine why when I run Northerns with RNAs denetured in Glyoxal
I see two bands from my transcript, and anly one when I used the more
commun formaldeyde gels. I dont think that is due to a better resolution
of the first method, but I rather think that is an artifact.
Do you have any suggestions.
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