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Comparison of SYBR Green I and TaqMan real-time PCR formats for the analysis of her2 gene dose in human breast tumors.

Abstract
We compared two technologies of real-time PCR (with the use of fluorescent SYBR Green I dye and specific TaqMan probe) for quantification of the dose of her2 gene in breast tumors. The maximum increase in the gene dose in TaqMan and SYBR Green I analyses was 10- and 5-fold, respectively. In was found that TaqMan and SYBR Green I technologies allow detection of the matrix in amounts corresponding to 1-100 and 2.5-40.0 ng genomic DNA, respectively. Tenfold increase in the gene dose leads to incorrect evaluation of multiplication ratio in the SYBR Green I analysis. These results suggest that TaqMan technology is more preferable for correct evaluation of her2 gene dose.
AuthorsN U Matsenko, V S Rijikova, S P Kovalenko
JournalBulletin of experimental biology and medicine (Bull Exp Biol Med) Vol. 145 Issue 2 Pg. 240-4 (Feb 2008) ISSN: 0007-4888 [Print] United States
PMID19023979 (Publication Type: Evaluation Study, Journal Article)
Chemical References
  • Benzothiazoles
  • Diamines
  • Fluorescent Dyes
  • Organic Chemicals
  • Quinolines
  • SYBR Green I
  • ERBB2 protein, human
  • Receptor, ErbB-2
Topics
  • Benzothiazoles
  • Breast Neoplasms (genetics)
  • Diamines
  • Female
  • Fluorescent Dyes (metabolism)
  • Gene Dosage
  • Humans
  • Organic Chemicals (metabolism)
  • Polymerase Chain Reaction (instrumentation, methods)
  • Quinolines
  • Receptor, ErbB-2 (genetics)

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