I am confused and exausted about PCRs... PCR, RT-PCR and mutagenesis PCR...
Any more?
For the Tm of primers, they have different ways to caculate? Even for the annealing, elongation temperarture. Despearted asking for help
Now, my current headache. To desigh a site-directed mutagenesis primer for a high GC% region. I did design as the protocl suggested; 1) Tm>78C, GC at the both ends, and proper size.
Then, my nightmare came. Because of the high Tm, and GC rich, (or something else), I got nothing after DpnI digestion. Then, raise the annealing temperature to 65. And 68C is the elongation temperature suggested by the kit. Still nothing.... What the hell!!
Well, can some one give a general diagnose and small "lecture"!
Thanks a lot














