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PMID: 7573945 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Review

Revolutions in rapid amplification of cDNA ends: new strategies for polymerase chain reaction cloning of full-length cDNA ends.

Analytical biochemistry ·Vol. 227 ·No. 2 ·1995-05-20 ·Pages 255-73

Schaefer BC

Abstract

Rapid amplification of cDNA ends (RACE) is a polymerase chain reaction (PCR)-based technique which was developed to facilitate the cloning of full-length cDNA 5'- and 3'-ends after a partial cDNA sequence has been obtained by other methods. While RACE can yield complete sequences of cDNA ends in only a few days, the RACE procedure frequently results in the exclusive amplification of truncated cDNA ends, undermining efforts to generate full-length clones. Many investigators have suggested modifications to the RACE protocol to improve the effectiveness of the technique. Based on first-hand experience with RACE, a critical review of numerous published variations of the key steps in the RACE method is presented. Also included is a detailed, effective protocol based on RNA ligase-mediated RACE/reverse ligation-mediated PCR, as well as a demonstration of its utility.

MeSH Terms
Base Sequence Cloning, Molecular DNA, Complementary/genetics Molecular Sequence Data Polymerase Chain Reaction/methods
Chemicals
DNA, Complementary
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schaefer B C
Division of Tumor Virology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1995-05-20
Pages
255-73
Language
English
Region
United States
NLM ID
0370535
Subset
IM
Grants
NCI NIH HHS · CA43143 · United States
NCI NIH HHS · CA47554 · United States
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