FACS

(redirected from fluorescence-activated cell sorting)
Also found in: Medical.
Related to fluorescence-activated cell sorting: cytometry, FACS

FACS

fluorescence-activated cell sorter: a machine that sorts cells according to whether or not they have been tagged with antibodies carrying a fluorescent dye.
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To detect changes in the DNA methylation and gene expression, I have developed state-of-the-art techniques such as fluorescence-activated cell sorting and micromanipulation to isolate all types of male SL cells to high purity.
The anti-apoptotic effects of Grail were determined by fluorescence-activated cell sorting in KB/vector and KB/Grail cells.
Food and Drug Administration; EpCAM, epithelial cell adhesion molecule; PCa, prostate cancer; EMT, epithelial-to-mesenchymal transition; PSA-EPISPOT, prostate-specific antigen-enzyme-linked immunospotassay; IV, intravenous; RBC, red blood cell; FACS, fluorescence-activated cell sorting; laPCa, locally advanced prostate cancer; DAPI, 4',6-diamidino-2-phenylindole.
Cas9-D10A nickase-mediated myostatin knockout and fluorescence-activated cell sorting
Positive clones were enriched using fluorescence-activated cell sorting and a FITC-labelled antiCD20 monoclonal antibody (R&D Systems, Minneapolis, MN).
Hart et al., "High-throughput fluorescence-activated cell sorting for lipid hyperaccumulating Chlamydomonas reinhardtii mutants," Plant Biotechnology Journal, vol.
MSCs were characterized by standard markers using fluorescence-activated cell sorting (FACS): MHC molecules (HLA-ABC+) and adhesion molecules (CD44+, CD54 (low), CD90+, CD106+, CD29+, CD49b (low), and CD105); however, they were negative for hematopoietic markers (CD34-, CD45-, and HLA-DR-) and the marker CD117 (Dominici et al.
(a) Fluorescence-Activated Cell Sorting (FACS) showed the FAP expression of CAFs.
Fluorescence-activated cell sorting (FACS) and Magnetic-activated cell sorting (MACS) are the most common methods for cancer stem cell isolation.
Fluorescence-activated cell sorting analysis using DNA propidium iodide staining was conducted for a sample of 45 WO transition strains and 9 white phase strains picked out in a random manner.
Besides several well-established methods, such as micromanipulation, laser-capture microdissection and fluorescence-activated cell sorting, there is an increasing number of novel techniques to isolate single cells with even greater accuracy and specificity [6,7].
After incubation at 4[degrees]C for 30 min in the dark, stained cells were washed with fluorescence-activated cell sorting buffer (1 x phosphate-buffered saline, 0.2% fetal bovine serum, 0.09% NAN3).

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