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3′ End cDNA amplification using classic RACE

  • Stony Brook University

Research output: Contribution to journalArticlepeer-review

210 Scopus citations

Abstract

Having knowledge of the entire 3′ sequence of a cDNA is often important because the non-coding terminal region can contain signals that regulate the stability or subcellular localization of the mRNA. Also, some messages use alternative genomic sites for cleavage and polyadenylation that can alter the above properties, or change the encoded protein. Full-length cDNAs can be obtained from complex mixtures of cellular mRNA using rapid amplification of cDNA ends (RACE) PCR as long as part of the mRNA sequence is known; adding non-specific tags to the ends of the cDNA allows the regions between the known parts of the sequence and the ends to be amplified. In 3′ RACE, the poly(A) tail functions as a non-specific tag at the 3′ end of the mRNA. cDNA ends can be obtained in 1-3 days using this protocol.

Original languageEnglish
Pages (from-to)2742-2745
Number of pages4
JournalNature Protocols
Volume1
Issue number6
DOIs
StatePublished - Jan 2007

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