A high efficiency flow cytometer.
Author(s) -
M J Skogen-Hagenson,
G.C. Salzman,
P. F. Mullaney,
W H Brockman
Publication year - 1977
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/25.7.330729
Subject(s) - propidium iodide , fluorescence , chemistry , optics , flow cytometry , flow (mathematics) , biophysics , materials science , biology , microbiology and biotechnology , physics , biochemistry , mechanics , apoptosis , programmed cell death
A flow chamber has been developed which collects about 60% of the total cell fluorescence for analysis compared to about 2.5% for conventional flow systems. The chamber, an ellipsoid of revolution, is gold-plated for increased reflectivity. Fluorochrome-stained cells enter the flow cell directly above the primary focus of the ellipsoid at the rate of 1000 cell/sec. A focused argon-ion laser beam enters the flow cell parallel to the semiminor axis and intersects the cell stream at the primary focus. Fluorescent light emanating from this point is reflected toward the secondary focus, where it exits the chamber for analysis. The high efficiency flow cytometer has been used to obtain nucleotide fluorescence distributions from samples of Micrococcus glutamicus bacteria stained with propidium iodide and of spermatozoa stained by the acriflavine-Feulgen procedure.
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