- THIS ARTICLE
- Full Text
- Full Text (PDF)
-
All Versions of this Article:
genetics.108.094508v1
180/3/1763 most recent - Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Email this article to a friend
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Bateman, J. R.
- Articles by Wu, C.-t.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Bateman, J. R.
- Articles by Wu, C.-t.
Originally published as Genetics Published Articles Ahead of Print on September 14, 2008.
Genetics, Vol. 180, 1763-1766, November 2008, Copyright © 2008
doi:10.1534/genetics.108.094508
A Simple Polymerase Chain Reaction-Based Method for the Construction of Recombinase-Mediated Cassette Exchange Donor Vectors
Jack R. Bateman1 and C.-ting Wu
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115
1 Corresponding author: Department of Biology, Bowdoin College, 6500 College Station, Brunswick, ME 04011.
E-mail: jbateman{at}bowdoin.edu
Here we describe a simple method for generating donor vectors suitable for targeted transgenesis via recombinase-mediated cassette exchange (RMCE) using the
C31 integrase. This PCR-based strategy employs small attB "tails" on the primers used to amplify a sequence of interest, permitting the rapid creation of transgenes for in vivo analysis.
This article has been cited by other articles:
![]() |
J. Huang, W. Zhou, W. Dong, A. M. Watson, and Y. Hong From the Cover: Directed, efficient, and versatile modifications of the Drosophila genome by genomic engineering PNAS, May 19, 2009; 106(20): 8284 - 8289. [Abstract] [Full Text] [PDF] |
||||
