TA cloning -Promega
Paul N Hengen
pnh at fcsparc6.ncifcrf.gov
Tue Mar 14 13:13:45 EST 1995
On 14 Mar 1995, Edward Wang (ez022056 at rocky.ucdavis.edu) wrote:
| I have been using the TA cloning Kit (p-Gem T system) by Promega.
| Talking to others, I found out that the T overhangs on the PCR products
| falls off after a certain amount of time, therefore decreasing the
| cloning efficiency in a TA system. The best way was to PCR, and then
| immediately clone into vector. Has anyone else heard anyting like this?
This thread has been going on for some time now, and I reviewed most of the
major points in last month's TIBS M&R column:
@article{Hengen1995Febtibs,
author = "P. N. Hengen",
title = "Methods and reagents - Cloning {PCR} products using {T}-vectors",
journal = "Trends in Biochemical Sciences",
volume = "20",
number = "2",
pages = "85-86",
month = "feb",
year = "1995"}
*******************************************************************************
* Paul N. Hengen, Ph.D. /--------------------------/*
* National Cancer Institute |Internet: pnh at ncifcrf.gov |*
* Laboratory of Mathematical Biology | Phone: (301) 846-5581 |*
* Frederick Cancer Research and Development Center| FAX: (301) 846-5598 |*
* Frederick, Maryland 21702-1201 USA /--------------------------/*
* - - - - - Methods FAQ list -> http://www-lmmb.ncifcrf.gov/~pnh - - - - - - *
* - - - Anonymous FTP from ftp.ncifcrf.gov as file pub/methods/FAQlist - - - *
*******************************************************************************
More information about the Methods
mailing list