Analysis of variant gene family expression by quantitative PCR

Methods Mol Biol. 2013:923:179-88. doi: 10.1007/978-1-62703-026-7_12.

Abstract

Real-time polymerase chain reaction (PCR), or quantitative PCR (qPCR), is a rapid, sensitive, and specific method used for a broad variety of applications including quantitative gene expression analysis, DNA copy number measurement, characterization of gene and chromosomal deletions, and genotyping. Real-time reverse transcription (RT)-PCR has largely supplanted Northern blot and RNase protection assays, as two examples, as a means of quantifying transcript levels. The method utilizes small amounts of RNA and allows efficient screening of a large number of samples. Here, we describe the materials and methods required to perform real-time RT-PCR, including RNA purification, cDNA synthesis, and real-time PCR analysis of cDNA samples.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Computational Biology / methods
  • Erythrocytes / parasitology
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation*
  • Genes, Protozoan
  • Humans
  • Multigene Family*
  • Plasmodium / genetics*
  • RNA, Protozoan / isolation & purification
  • Real-Time Polymerase Chain Reaction / methods*

Substances

  • RNA, Protozoan