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.
Original language | English |
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Pages (from-to) | 459-464 |
Number of pages | 6 |
Journal | Cytometry |
Volume | 14 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1993 |