Measuring Cell Death by Propidium Iodide Uptake and Flow Cytometry.
Identifieur interne : 003792 ( Ncbi/Merge ); précédent : 003791; suivant : 003793Measuring Cell Death by Propidium Iodide Uptake and Flow Cytometry.
Auteurs : Lisa C. Crowley [Australie] ; Adrian P. Scott [Australie] ; Brooke J. Marfell [Australie] ; Jeanne A. Boughaba [France] ; Grace Chojnowski [Australie] ; Nigel J. Waterhouse [Australie]Source :
- Cold Spring Harbor protocols [ 1559-6095 ] ; 2016.
Descripteurs français
- KwdFr :
- MESH :
- métabolisme : Colorants fluorescents, Intercalants, Propidium.
- Animaux, Coloration et marquage, Cytométrie en flux, Humains, Mort cellulaire.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Fluorescent Dyes, Intercalating Agents, Propidium.
- methods : Flow Cytometry, Staining and Labeling.
- Animals, Cell Death, Humans.
Abstract
Propidium iodide (PI) is a small fluorescent molecule that binds to DNA but cannot passively traverse into cells that possess an intact plasma membrane. PI uptake versus exclusion can be used to discriminate dead cells, in which plasma membranes become permeable regardless of the mechanism of death, from live cells with intact membranes. PI is excited by wavelengths between 400 and 600 nm and emits light between 600 and 700 nm, and is therefore compatible with lasers and photodetectors commonly available in flow cytometers. This protocol for PI staining can be used to quantitate cell death in most modern research facilities and universities.
DOI: 10.1101/pdb.prot087163
PubMed: 27371595
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pubmed:27371595Le document en format XML
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<term>Humans</term>
<term>Intercalating Agents (metabolism)</term>
<term>Propidium (metabolism)</term>
<term>Staining and Labeling (methods)</term>
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<term>Intercalants (métabolisme)</term>
<term>Mort cellulaire</term>
<term>Propidium (métabolisme)</term>
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<term>Propidium</term>
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<front><div type="abstract" xml:lang="en">Propidium iodide (PI) is a small fluorescent molecule that binds to DNA but cannot passively traverse into cells that possess an intact plasma membrane. PI uptake versus exclusion can be used to discriminate dead cells, in which plasma membranes become permeable regardless of the mechanism of death, from live cells with intact membranes. PI is excited by wavelengths between 400 and 600 nm and emits light between 600 and 700 nm, and is therefore compatible with lasers and photodetectors commonly available in flow cytometers. This protocol for PI staining can be used to quantitate cell death in most modern research facilities and universities.</div>
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