| Literature DB >> 23592493 |
Elizabeth B Speltz1, Lynne Regan.
Abstract
Cloning is an essential prerequisite to test protein design and engineering ideas. However, it is often time consuming, unreliable, and therefore frustrating. Here, we present a streamlined cloning strategy that incorporates a powerful white and green screening protocol to identify colonies with inserts. We use circular polymerase extension cloning, which is both ligation and sequence independent. Furthermore, our entire procedure requires only three quick steps and one enzyme making it easy to use, inexpensive, and tractable. We anticipate that this method will be particularly useful for protein engineers who frequently subclone or make focused deletion, insertion, or substitution libraries.Mesh:
Substances:
Year: 2013 PMID: 23592493 PMCID: PMC3690724 DOI: 10.1002/pro.2268
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725