Rapid Amplification of cDNA Ends (RACE)

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Liu Peigang
Yang Qian*

Abstract

Rapid amplification of cDNA ends is a polymerase chain reaction-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. Many investigators have suggested modifications to the RACE protocols to improve the effect of the technique.


Keywords: RACE, PCR


Corresponding author: E-mail: [email protected]

Article Details

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Review Ariticle

References

[1] M.A. Frohman and M.K. Dush, Rapid production of full-length cDNA from raretranscripts. J. Proc. Nalt. Aad. Sci., USA, 85, 1998, 8998-9002.
[2] E.Y. Loh and J.F. Elliotl, Polymerase chain reaction with single-sided specificity. Science, 243, 1989, 217-220.
[3] O. Ohora and R.L. Dorit, One-sided polymerase chain reaction: the amplification of cDNA, PNAS, 86, 1989, 5673-5677.
[4] A.B. Troutt, Ligation-anchored PCR. PNAS, 89, 1992, 9823-9825.
[5] M.E. Dumas, Molecular Biology (White, b.a.), 151, 1993, 265-285.
[6] M. Gorovasky, NAR, 21, 1993, 4954-4960.
[7] M. Fromont-Racine, NAR, 21, 1993, 1683-1684.
[8] I.N. Manyama, cRACE: a simple method for identification of 5’ end of mRNA. NAR, 23, 1995, 3796-3797.
[9] J.D.A. Fritz, novel 3’ extension technique using random primers in RNA-PCR. NAR, 19, 1991, 3747.
[10] F. Struck and J. Collins, Simple and rapid 5’ and 3’ extension technique in RT-PCP, NAR, 22, 1994, 1923-1924.