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cytometria prietoková
SYS d005434 LBL 00000nz--a2200000o--4500 005 20250606214044.3 008 920224|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a E01.370.225.500.363.342 065 $a E01.370.225.500.386.350 065 $a E05.196.712.516.600.240.350 065 $a E05.200.500.363.342 065 $a E05.200.500.386.350 065 $a E05.242.363.342 065 $a E05.242.386.350 066 $a 01 $c 03 150 $a cytometria prietoková $x CL $x EC $x ES $x HI $x IS $x MT $x SN $x ST $x TD $x VE $2 slo 450 $w v $a Cytofluorometry, Flow $2 eng 450 $w v $a Cytometry, Flow $2 eng 450 $w v $a Flow Microfluorimetry $2 eng 450 $w v $a Fluorescence-Activated Cell Sorting $2 eng 450 $w v $a Microfluorometry, Flow $2 eng 665 $a 82; FLOW MICROFLUORIMETRY was see FLUOROIMMUNOASSAY 1989-90 $2 eng 680 9-
$i Technique using an instrument system for making, processing, and displaying one or more measurements on individual cells obtained from a cell suspension. Cells are usually stained with one or more fluorescent dyes specific to cell components of interest, e.g., DNA, and fluorescence of each cell is measured as it rapidly transverses the excitation beam (laser or mercury arc lamp). Fluorescence provides a quantitative measure of various biochemical and biophysical properties of the cell, as well as a basis for cell sorting. Other measurable optical parameters include light absorption and light scattering, the latter being applicable to the measurement of cell size, shape, density, granularity, and stain uptake. $2 eng 680 $a flow cell sorting & FLUORESCENCE-ACTIVATED CELL SORTING: coord with CELL SEPARATION $2 eng 750 -2
$a Flow Cytometry $2 eng 980 $x M
Number of the records: 1