Hi
I want to separate and purify an 40 nt DNA oligo from a non-denatured
PAGE gel. When I did a test run using only 2 ug of the DNA oligo, it
runs like a smear rather than a sharp band. I wonder whether I have
over-loaded the gel. If so, I can always use a 1.5 mm gel.
I wonder how the DNA synthesis company use PAGE to purify oligos and
how much one can load into a mini gel. Because if I overload a mini
gel by using just 2 ug of DNA, how can those companies purify "tons"
of oligos with preparative PAGE gel?
Best
sz
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