I'm new to the the world of methylation and am trying to amplify CpG islands after bisulfite conversion. But when i run the PCR products on a gel i get smears and they aren't even in the correct range. I designed my primers using meth primer and when the first PCR didn't work i tried lowering the extension temperature to 63 C ( first i used 72 C).
Any suggestions would be greatly appreciated.
Edited by vaidhi, 12 February 2012 - 09:41 PM.