| Literature DB >> 18770687 |
M Fortuna1, M J Sousa, M Côrte-Real, C Leão, A Salvador, F Sansonetty.
Abstract
Staining protocols generally designed for the flow cytometric analysis of the cell cycle in mammalian cells are frequently not satisfactory for quantification of the various cell-cycle phases in yeasts. High CVs limit the accuracy of DNA content measurement and estimates of populations in cell-cycle compartments. This unit describes a staining procedure for yeasts using the sensitive nucleic acid stain SYBR Green I, which binds to double-stranded DNA with high selectivity and which has a much higher fluorescence quantum yield upon binding than most other commonly used fluorophores. The properties of this dye combined with optimized sample processing provide high-resolution DNA analysis, with half-peak CVs around 3 to 4% and clear-cut identification of the S phase.Entities:
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Year: 2001 PMID: 18770687 DOI: 10.1002/0471142956.cy1113s13
Source DB: PubMed Journal: Curr Protoc Cytom ISSN: 1934-9297