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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2013
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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) |
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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 |
work_keys_str_mv |
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