Abstract
The design and implementation of a real-time signal processing system for slit-scan flow cytometry is described. The system is used to measure the separate scatter and fluorescence peak heights of 2 adherent cells. Preliminary measurements of changes in the membrane potential induced by interactions between natural killer (NK) cells and their target cells are presented.
MeSH terms
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Barbiturates
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Cell Adhesion*
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Cytotoxicity, Immunologic
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Electronics / instrumentation
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Flow Cytometry / instrumentation*
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Fluorescence
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Humans
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Isoxazoles
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Killer Cells, Natural / cytology*
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Leukemia, Erythroblastic, Acute
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Membrane Potentials
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Scattering, Radiation
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Tumor Cells, Cultured
Substances
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Barbiturates
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Isoxazoles
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bis(1,3-dibutylbarbiturate)trimethine oxonol