rick00100 at aol.com
Mon Feb 16 14:48:32 EST 1998
I've been trying to gel purify my PCR products using the Qiagen kit. After
purification I usually elute the DNA with 50ul water. To do ligation, I'd like
to concentrate the DNA to about 6-8 ul. When I EtOH ppt, I usually got bad
yield. I heard that you can just speed-vac the DNA dissolved in water to
concentrate it. Is that true? What about DNA dissolved in buffers?
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