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.
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Authors | N U Matsenko, V S Rijikova, S P Kovalenko |
Journal | Bulletin of experimental biology and medicine
(Bull Exp Biol Med)
Vol. 145
Issue 2
Pg. 240-4
(Feb 2008)
ISSN: 0007-4888 [Print] United States |
PMID | 19023979
(Publication Type: Evaluation Study, Journal Article)
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Chemical References |
- Benzothiazoles
- Diamines
- Fluorescent Dyes
- Organic Chemicals
- Quinolines
- SYBR Green I
- ERBB2 protein, human
- Receptor, ErbB-2
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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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