Reduction of mispriming in amplification reactions with restricted PCR.
Author(s) -
László G. Puskás,
Sándor Bottka
Publication year - 1995
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.5.3.309
Subject(s) - biology , primer (cosmetics) , oligonucleotide , primer dimer , polymerase chain reaction , computational biology , base pair , inverse polymerase chain reaction , microbiology and biotechnology , genetics , applications of pcr , in silico pcr , dna , digital polymerase chain reaction , multiplex polymerase chain reaction , gene , chemistry , organic chemistry
A simple method is described for reducing nonspecific background, which is caused by mispriming during PCR. Besides the standard pair of primers, 3'-dideoxy-terminated competitor oligonucleotides were added to the amplification. Sequences to those of the primers which had identical base. In this way enhanced specificity was achieved. The competitor oligonucleotides may act by masking possible sites of nonspecific primer-template interaction, thus excluding undesired chain extensions. This technique is generally applicable when highly degenerate primers are used and therefore expands the potential of "restricted" PCR.
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