When you checked your 12 genes of interest on cancer cell lines (whose RNA was extracted using olidodT primers) did you come across any problems? Is that the reason you want to use oligodT? If you have stumbled upon any problems, then why can't you sgo ahead with random hexamer primers? I am curious to know if there is any specific reason.
Kart
Neanderthal
Member Since 15 Nov 2011Offline Last Active Apr 03 2013 08:32 PM





Find content
Male


