Fluorescent Oligonucleotide Probes for the Quantification of RNA by Real-Time qPCR.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2020
Historique:
entrez: 2 2 2020
pubmed: 2 2 2020
medline: 28 1 2021
Statut: ppublish

Résumé

Quantitative real-time PCR (qPCR) is a widely adopted technique used for scientific, clinical, diagnostic, or quality control purposes. One of the main applications of qPCR is gene expression analysis, although mutation detection, genotyping, DNA detection, and quantification (from pathogens or genetically modified organisms) are also investigated using this technique.Although nonspecific detection based on DNA-binding dyes (including SYBR Green I) offers versatility in qPCR assays, detection of the PCR product using fluorescent probes confers higher specificity and sensitivity to assays, justifying the use of fluorescent probes as a detection method.This chapter seeks to propose a procedure for the design of qPCR assays using fluorescent hydrolysis probe technology. Particular attention will be paid to explaining the steps necessary to ensure the specificity of the oligonucleotides used as primers or fluorescent probes.

Identifiants

pubmed: 32006320
doi: 10.1007/978-1-0716-0278-2_18
doi:

Substances chimiques

Fluorescent Dyes 0
Oligonucleotide Probes 0
RNA 63231-63-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

263-280

Auteurs

Florent Busi (F)

Unité de Biologie Fonctionnelle et Adaptative, Université de Paris, CNRS UMR 8251, Paris, France. florent.busi@univ-paris-diderot.fr.

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Classifications MeSH