cloning of small DNA fragments (66 bp)

rogier stuger at
Fri Aug 6 08:06:22 EST 1999

I'd say just anneal some oligos.
if you wanna do PCR, pull the products thru a gel, cut out
your band, and do an in-gel ligation
or just destroy your template with restriction enzymes that
cut outside the PCRed seq
Good luck,

* Sent from RemarQ The Internet's Discussion Network *
The fastest and easiest way to search and participate in Usenet - Free!

More information about the Methods mailing list