Hi, I need to separate 300 - 1100 bp DNA fragments in the gel
electroferesis. Would it be suitable to use agarose-acrylamide mixture or
is there some other material (modified agarose?)that could be used for
this size of DNA fragments? How to make and run agarose-acrylamide
gel? Can I blot DNA into the filter from this kind of gel?
Kimmo