Magnetic bead capture of cDNAs from double-stranded plasmid cDNA libraries
Author(s) -
Allan R. Shepard
Publication year - 1997
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/25.15.3183
Subject(s) - plasmid , biology , complementary dna , cdna library , oligonucleotide , oligomer restriction , microbiology and biotechnology , streptavidin , genomic library , biotinylation , library , escherichia coli , dna , genetics , gene , base sequence , biotin , 16s ribosomal rna
We have developed a cDNA library screening method which allows the simultaneous screening of >10 ( 12 ) double-stranded plasmid cDNA molecules with minimal a priori sequence knowledge. A biotinylated, gene-specific oligonucleotide probe along with abutting 'blocking' oligos is hybridized to the plasmid cDNA library and the target plasmid retrieved with paramagnetic streptavidin beads and transformed into Escherichia coli. Multiple rounds of enrichment with a target plasmid represented at 0.002-0.0001% resulted in over one-third positive clones. Our method will be useful for isolating even the rarest cDNAs starting from ESTs, isolated exons or homologous sequence information.
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