Solid support quantitation of c-myc PCR products using a cleavable reporter

We described here a simple and specific methodology to quantify competitive PCR products for the determination of c-myc gene copies number. The c-myc oncogene is coamplified with a synthetic standard gene, followed by a separate hybridization of the two PCR products in conditions previously determin...

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Veröffentlicht in:Nucleic acids research 1994-02, Vol.22 (3), p.547-548
Hauptverfasser: Rhoer-Moja, Sandrine, Bazin, Hervé, Sauvaigo, Sylvie, Chypre, Camille, Vindimian, Monique
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container_end_page 548
container_issue 3
container_start_page 547
container_title Nucleic acids research
container_volume 22
creator Rhoer-Moja, Sandrine
Bazin, Hervé
Sauvaigo, Sylvie
Chypre, Camille
Vindimian, Monique
description We described here a simple and specific methodology to quantify competitive PCR products for the determination of c-myc gene copies number. The c-myc oncogene is coamplified with a synthetic standard gene, followed by a separate hybridization of the two PCR products in conditions previously determined. The PCR efficiency, cycle number, sensitivity and hybridization parameters have been described, as well as the evaluation of the level of c-myc gene amplification through a reference curve established from serial normal DNA concentrations run along with the tumoral samples.
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source MEDLINE; Oxford University Press Journals Digital Archive Legacy; PubMed Central
subjects Base Sequence
Biological and medical sciences
Diverse techniques
DNA Primers - chemistry
Fundamental and applied biological sciences. Psychology
Gene Amplification
Genes, myc
Humans
Molecular and cellular biology
Molecular Sequence Data
Polymerase Chain Reaction - methods
title Solid support quantitation of c-myc PCR products using a cleavable reporter
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