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The ‘PREXCEL-Q Method’ for qPCR

The purpose of this manuscript is to describe a reliable approach to quantitative real-time polymerase chain reaction (qPCR) assay development and project management, which is currently embodied in the Excel 2003-based software program named “PREXCEL-Q” (P-Q) (formerly known as “FocusField2-6Gallup-...

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Detalles Bibliográficos
Autores principales: Gallup, Jack M., Ackermann, Mark R.
Formato: Texto
Lenguaje:English
Publicado: Master Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2744046/
https://www.ncbi.nlm.nih.gov/pubmed/19759920
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author Gallup, Jack M.
Ackermann, Mark R.
author_facet Gallup, Jack M.
Ackermann, Mark R.
author_sort Gallup, Jack M.
collection PubMed
description The purpose of this manuscript is to describe a reliable approach to quantitative real-time polymerase chain reaction (qPCR) assay development and project management, which is currently embodied in the Excel 2003-based software program named “PREXCEL-Q” (P-Q) (formerly known as “FocusField2-6Gallup-qPCRSet-upTool-001,” “FF2-6-001 qPCR set-up tool” or “Iowa State University Research Foundation [ISURF] project #03407”). Since its inception from 1997-2007, the program has been well-received and requested around the world and was recently unveiled by its inventor at the 2008 Cambridge Healthtech Institute’s Fourth Annual qPCR Conference in San Diego, CA. P-Q was subsequently mentioned in a review article by Stephen A. Bustin, an acknowledged leader in the qPCR field. Due to its success and growing popularity, and the fact that P-Q introduces a unique/defined approach to qPCR, a concise description of what the program is and what it does has become important. Sample-related inhibitory problems of the qPCR assay, sample concentration limitations, nuclease-treatment, reverse transcription (RT) and master mix formulations are all addressed by the program, enabling investigators to quickly, consistently and confidently design uninhibited, dynamically-sound, LOG-linear-amplification-capable, high-efficiency-of-amplification reactions for any type of qPCR. The current version of the program can handle an infinite number of samples.
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spelling pubmed-27440462009-09-15 The ‘PREXCEL-Q Method’ for qPCR Gallup, Jack M. Ackermann, Mark R. Int J Biomed Sci Article The purpose of this manuscript is to describe a reliable approach to quantitative real-time polymerase chain reaction (qPCR) assay development and project management, which is currently embodied in the Excel 2003-based software program named “PREXCEL-Q” (P-Q) (formerly known as “FocusField2-6Gallup-qPCRSet-upTool-001,” “FF2-6-001 qPCR set-up tool” or “Iowa State University Research Foundation [ISURF] project #03407”). Since its inception from 1997-2007, the program has been well-received and requested around the world and was recently unveiled by its inventor at the 2008 Cambridge Healthtech Institute’s Fourth Annual qPCR Conference in San Diego, CA. P-Q was subsequently mentioned in a review article by Stephen A. Bustin, an acknowledged leader in the qPCR field. Due to its success and growing popularity, and the fact that P-Q introduces a unique/defined approach to qPCR, a concise description of what the program is and what it does has become important. Sample-related inhibitory problems of the qPCR assay, sample concentration limitations, nuclease-treatment, reverse transcription (RT) and master mix formulations are all addressed by the program, enabling investigators to quickly, consistently and confidently design uninhibited, dynamically-sound, LOG-linear-amplification-capable, high-efficiency-of-amplification reactions for any type of qPCR. The current version of the program can handle an infinite number of samples. Master Publishing Group 2008-12 /pmc/articles/PMC2744046/ /pubmed/19759920 Text en © Jack M. Gallup et al. Licensee Master Publishing Group http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Gallup, Jack M.
Ackermann, Mark R.
The ‘PREXCEL-Q Method’ for qPCR
title The ‘PREXCEL-Q Method’ for qPCR
title_full The ‘PREXCEL-Q Method’ for qPCR
title_fullStr The ‘PREXCEL-Q Method’ for qPCR
title_full_unstemmed The ‘PREXCEL-Q Method’ for qPCR
title_short The ‘PREXCEL-Q Method’ for qPCR
title_sort ‘prexcel-q method’ for qpcr
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2744046/
https://www.ncbi.nlm.nih.gov/pubmed/19759920
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