Literature DB >> 27587774

Analyzing Cell Death by Nuclear Staining with Hoechst 33342.

Lisa C Crowley1, Brooke J Marfell1, Nigel J Waterhouse2.   

Abstract

The nuclei of healthy cells are generally spherical, and the DNA is evenly distributed. During apoptosis the DNA becomes condensed, but this process does not occur during necrosis. Nuclear condensation can therefore be used to distinguish apoptotic cells from healthy cells or necrotic cells. Dyes that bind to DNA, such as Hoechst 33342 or 4',6-diamidino-2-phenylindole (DAPI), can be used to observe nuclear condensation. These dyes fluoresce at 461 nm when excited by ultraviolet light and can therefore be visualized using conventional fluorescent microscopes equipped with light sources that emit light at ∼350 nm and filter sets that permit the transmission of light at ∼460 nm. This protocol describes staining and visualization of cells stained with Hoechst 33342, but it can be adapted for staining with DAPI or other dyes.
© 2016 Cold Spring Harbor Laboratory Press.

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Year:  2016        PMID: 27587774     DOI: 10.1101/pdb.prot087205

Source DB:  PubMed          Journal:  Cold Spring Harb Protoc        ISSN: 1559-6095


  52 in total

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