faint PCR product

Adam . via methods%40net.bio.net (by anonwums1 from gmail.com)
Thu Apr 22 11:33:41 EST 2010

Many years ago, I used to do some methylation validation on genomic DNA
using bisulfite treatment followed by restriction digest. The only way we
could get it to work was nested PCR. I think that re-amplifying your PCR
product is probably your best bet.


On Thu, Apr 22, 2010 at 9:53 AM, WS <novalidaddress from nurfuerspam.de> wrote:

> Hi Lebo,
> a) have you tried to re-amplify an aliquot of your PCR product?
> Transfer say 1µl of your reaction into a new one.
> b) do you get stronger bands with that locus when cloned into a
> plasmid? -> then check fpor PCR inhibitors in your sample.
> Wo
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