A rapid micro method for counting cells “in situ” using a fluorogenic alkaline phosphatase enzyme assay
- 1 January 1989
- journal article
- research article
- Published by Springer Nature in In Vitro Cellular & Developmental Biology
- Vol. 25 (1) , 105-108
- https://doi.org/10.1007/bf02624419
Abstract
A new method has been developed to count cells “in situ”, based on a fluorogenic enzyme assay that measures the activity of alkaline phosphatase. Increasing cell number was shown to correlate closely with alkaline phosphatase activity and this relationship did not change with time in culture. The alkaline phosphatase assay (ALP assay) was able to estimate relative cell numbers over a range from about 104 to 5×105 for many cell types, including Hep-2, a derivative of HeLa, several human colorectal cell lines SW1222, SW837, LS174T and HT29, a normal human diploid cell strain MRC5 and a rodent line NIH-3T3. The ALP assay is rapid and efficient, making it a useful method for studying growth assays.This publication has 13 references indexed in Scilit:
- Genetics and biochemistry of collagen binding-triggered glandular differentiation in a human colon carcinoma cell line.Proceedings of the National Academy of Sciences, 1988
- EVALUATION OF A TETRAZOLIUM-BASED SEMIAUTOMATED COLORIMETRIC ASSAY - ASSESSMENT OF CHEMOSENSITIVITY TESTING1987
- Differential expression of alkaline phosphatase and ATPase activities in human colon carcinoma cell line HT‐29.18 during differentiationBiology of the Cell, 1987
- Ultrasensitive Enzyme ImmunoassayScandinavian Journal of Immunology, 1978
- Human colonic adenocarcinoma cellsIn Vitro Cellular & Developmental Biology - Plant, 1976
- CLASSIFICATION OF HUMAN COLORECTAL ADENOCARCINOMA CELL LINES1976
- Characteristics of a Human Diploid Cell Designated MRC-5Nature, 1970
- Detection of mycoplasma in cell culturesThe Journal of Pathology and Bacteriology, 1967