z-logo
open-access-imgOpen Access
Semi-Multiplex PCR Technique for Screening of Abundant Transcripts During Systematic Sequencing of cDNA Libraries
Author(s) -
Beniamina Pacchioni,
Sara Trevisan,
S. Gomirato,
Stefano Toppo,
Giorgio Valle,
Gerolamo Lanfranchi
Publication year - 1996
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/96214st01
Subject(s) - complementary dna , biology , cdna library , multiplex , multiplex polymerase chain reaction , dna sequencing , microbiology and biotechnology , genomic library , computational biology , genetics , polymerase chain reaction , identification (biology) , agarose , gene , base sequence , botany
The systematic sequencing of cDNA libraries is an efficient approach for the identification of new genes, but the presence of abundant mRNAs is often a major problem. This paper describes a very simple method of "semi-multiplex PCR" that allows specific identification of such abundant transcripts before DNA sequencing without using nonrepresentative subtracted libraries. The PCR utilizes a series of forward primers specific for abundant transcripts with a pair of universal primers used for template generation. cDNA clones corresponding to abundant mRNAs are then revealed by double bands in agarose gel.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom