COLD-PCR: Applications and advantages

Zhuang Zuo, Kausar J. Jabbar

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Scopus citations

Abstract

Co-amplification at lower denaturation temperature-based polymerase chain reaction (COLD-PCR) is a single-step amplification method that results in the enhancement of both known and unknown minority alleles during PCR, irrespective of mutation type and position. This method is based on exploitation of the critical temperature, Tc, at which mutation-containing DNA is preferentially melted over wild type. COLD-PCR can be a good strategy for mutation detection in specimens with high nonneoplastic cell content, small specimens in which neoplastic cells are difficult to micro-dissect and therefore enrich, and whenever a mutation is suspected to be present but is undetectable using conventional PCR and sequencing methods. We describe in this chapter our COLD-PCR-based pyrosequencing method for KRAS mutation detection in various clinical samples using DNA extracted from either fresh or fixed paraffinembedded tissue specimens.

Original languageEnglish (US)
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages17-25
Number of pages9
DOIs
StatePublished - Feb 1 2016

Publication series

NameMethods in Molecular Biology
Volume1392
ISSN (Print)1064-3745

Keywords

  • Co-amplification at lower denaturation temperature PCR (COLD-PCR)
  • KRAS
  • Mutation detection
  • Polymerase chain reaction (PCR)

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

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