alex.berkow at gmail.com
Fri Jul 21 07:24:50 EST 2006
Hi, I'm new to this whole listserve thing, but I'm interested to see how it
works. Here is one question I have been stumped by recently:
Why, in the first round of DNA extractions, do you use phenol (tris-HCl
saturated) and in the second round you use phenol chloroform? I'm
interested in an answer that explains the chemistry.
One other thing: Why, when you wash a DNA pellet with 70% ethanol, does the
30% water in the solution not cause the DNA to go back into solution?
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