Report

Rapid generation of random mutant libraries

Volume 1, Issue 5   September/October 2010
Pages 337 - 340
http://dx.doi.org/10.4161/bbug.1.5.12942
Mary Abou-Nader and Michael J. Benedik

View affiliations

A simple and efficient method utilizing in vivo recombination to create recombinant libraries incorporating the products of PCR amplification is described. This will be especially useful for generating large pools of randomly mutagenized clones after error-prone PCR mutagenesis. Here we investigate various parameters to optimize this approach and we demonstrate that as little as1 pmole of PCR fragment can generate a library with greater than 104 clones in a single transformation without ligation.


Comments

Please Log In to comment on this article.
If you do not have an account Create One Here.

blog comments powered by Disqus

Advertisements