期刊
JOURNAL OF IMMUNOLOGICAL METHODS
卷 254, 期 1-2, 页码 85-98出版社
ELSEVIER
DOI: 10.1016/S0022-1759(01)00404-5
关键词
CyQUANT; fluorescence assay; fluorometric dye; cell growth; cell proliferation; serum-stimulation; cell number quantitation
We describe here the development and characterization of the CyQUANT((R)) cell proliferation assay, a highly sensitive, fluorescence-based microplate assay for determining numbers of cultured cells. The assay employs CyQUANT GR dye, which produces a large fluorescence enhancement upon binding to cellular nucleic acids that can be measured using standard fluorescein excitation and emission wavelengths. The fluorescence emission of the dye-nucleic acid complexes correlated linearly with cell number over a large range using a wide variety of cell types. Under the recommended assay conditions, standard curves were linear(r(2) > 0.995), detecting as few as 10-50 cells and as many as 25,000-50,000 cells with a single dye concentration, depending on cell type. Increasing the dye concentration extended the linear range of the assay to 100,000-250,000 cells. Results of cell proliferation and growth inhibition studies with the assay were similar to those obtained in published studies using other standard assays. CyQUANT assay measurements of serum-stimulated cell proliferation correlated well with measurements made using [H-3]-thymidine. Also. the assay was used to analyze cellular DNA or RNA content. with the addition of a nuclease digestion step to the protocol, The assay procedure is simple and convenient, with no wash steps, and is readily amenable to automation. (C) 2001 Elsevier Science B.V. All rights reserved.
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