Flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.

An optimal technology for cell cycle analysis would allow the concomitant measurement of apoptosis, G0, G1, S, G2 and M phases in combination with cell surface phenotyping. We have developed an easy method in flow cytometry allowing this discrimination in an only two-color fluorescent plot. It is ba...

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Autores principales: Christine Vignon, Christelle Debeissat, Marie-Thérèse Georget, Didier Bouscary, Emmanuel Gyan, Philippe Rosset, Olivier Herault
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/15449e40bade46b0b85c696e0fc59e71
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spelling oai:doaj.org-article:15449e40bade46b0b85c696e0fc59e712021-11-18T09:02:05ZFlow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.1932-620310.1371/journal.pone.0068425https://doaj.org/article/15449e40bade46b0b85c696e0fc59e712013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23935867/?tool=EBIhttps://doaj.org/toc/1932-6203An optimal technology for cell cycle analysis would allow the concomitant measurement of apoptosis, G0, G1, S, G2 and M phases in combination with cell surface phenotyping. We have developed an easy method in flow cytometry allowing this discrimination in an only two-color fluorescent plot. It is based on the concomitant use of 7-amino-actinomycin D and the antibodies anti-Ki67 and anti-phospho(Ser10)-histone H3, both conjugated to Alexa Fluor®488 to discriminate G0 and M phases, respectively. The method is particularly valuable in a clinical setting as verified in our laboratory by analyzing human leukemic cells from marrow samples or after exposure to cell cycle modifiers.Christine VignonChristelle DebeissatMarie-Thérèse GeorgetDidier BouscaryEmmanuel GyanPhilippe RossetOlivier HeraultPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 7, p e68425 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Christine Vignon
Christelle Debeissat
Marie-Thérèse Georget
Didier Bouscary
Emmanuel Gyan
Philippe Rosset
Olivier Herault
Flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.
description An optimal technology for cell cycle analysis would allow the concomitant measurement of apoptosis, G0, G1, S, G2 and M phases in combination with cell surface phenotyping. We have developed an easy method in flow cytometry allowing this discrimination in an only two-color fluorescent plot. It is based on the concomitant use of 7-amino-actinomycin D and the antibodies anti-Ki67 and anti-phospho(Ser10)-histone H3, both conjugated to Alexa Fluor®488 to discriminate G0 and M phases, respectively. The method is particularly valuable in a clinical setting as verified in our laboratory by analyzing human leukemic cells from marrow samples or after exposure to cell cycle modifiers.
format article
author Christine Vignon
Christelle Debeissat
Marie-Thérèse Georget
Didier Bouscary
Emmanuel Gyan
Philippe Rosset
Olivier Herault
author_facet Christine Vignon
Christelle Debeissat
Marie-Thérèse Georget
Didier Bouscary
Emmanuel Gyan
Philippe Rosset
Olivier Herault
author_sort Christine Vignon
title Flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.
title_short Flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.
title_full Flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.
title_fullStr Flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.
title_full_unstemmed Flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.
title_sort flow cytometric quantification of all phases of the cell cycle and apoptosis in a two-color fluorescence plot.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/15449e40bade46b0b85c696e0fc59e71
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