Why does my RT-PCR suck? Because the RT-extension primer has a nasty hairpin Tm one degree below the protocol's RNA-to-DNA temp. Why didn't I know this? I assumed the previous worker checked the primer design before placing the order. Why didn't using the alternate primers help? Because they were designed by a second person who hadn't checked their
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biotech drove her back to teaching btw
biotech drove most of us to other careers in fact- lots of nurses, teachers,CNAs...
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