| Literature DB >> 11721938 |
M A McClain1, C T Culbertson, S C Jacobson, J M Ramsey.
Abstract
Flow cytometry of the bacterium Escherichia coli was demonstrated on a microfabricated fluidic device (microchip). The channels were coated with poly(dimethylacrylamide) to prevent cell adhesion, and the cells were transported electrophoretically by applying potentials to the fluid reservoirs. The cells were electrophoretically focused at the channel cross and detected by coincident light scattering and fluorescence. The E. coli were labeled with a membrane-permeable nucleic acid stain (Syto15), a membrane-impermeable nucleic acid stain (propidium iodide), or a fluorescein-labeled antibody and counted at rates from 30 to 85 Hz. The observed labeling efficiencies for the dyes and antibody were greater than 94%.Entities:
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Year: 2001 PMID: 11721938 DOI: 10.1021/ac010504v
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986