REVOLUTIONS IN RAPID AMPLIFICATION OF CDNA ENDS - NEW STRATEGIES FOR POLYMERASE CHAIN-REACTION CLONING OF FULL-LENGTH CDNA ENDS

Authors
Citation
Bc. Schaefer, REVOLUTIONS IN RAPID AMPLIFICATION OF CDNA ENDS - NEW STRATEGIES FOR POLYMERASE CHAIN-REACTION CLONING OF FULL-LENGTH CDNA ENDS, Analytical biochemistry, 227(2), 1995, pp. 255-273
Citations number
79
Categorie Soggetti
Biology
Journal title
ISSN journal
00032697
Volume
227
Issue
2
Year of publication
1995
Pages
255 - 273
Database
ISI
SICI code
0003-2697(1995)227:2<255:RIRAOC>2.0.ZU;2-T
Abstract
Rapid amplification of cDNA ends (RACE) is a polymerase chain reaction (PCR)-based technique which was developed to facilitate the cloning o f full-length cDNA 5'- and 3'-ends after a partial cDNA sequence has b een obtained by other methods, While RACE can yield complete sequences of cDNA ends in only a few days, the RACE procedure frequently result s in the exclusive amplification of truncated cDNA ends, undermining e fforts to generate full-length clones, Many investigators have suggest ed modifications to the RACE protocol to improve the effectiveness of the technique, Based on first-hand experience with RACE, a critical re view of numerous published variations of the hey steps in the RACE met hod is presented. Also included is a detailed, effective protocol base d on RNA ligase-mediated RACE/reverse ligation-mediated PCR, as well a s a demonstration of its utility, (C) 1995 Academic Press, Inc.