I would suggest subclone in a plasmid vector and then test the inserts
by a reverse Northern technique (see for example Liu C and Raghotama, KG
(1996) BioTechniques 20, 576-580.). I have no personnal experience of
this but this is how I would proceeed.
Hope this helps
Akihiro Yamaguchi wrote:
>> I have isolated bands from differential display gels. I understand that each
> band might contain more than one PCR product. I would appreciate advice on
> what is the best way for screening.
>> Best wishes,
> David Yu
>dtyyu at ucla.edu