Facs Sorting

FACS sorting, or fluorescence-activated cell sorting, is a flow cytometry technique that separates individual cells according to measurable characteristics, making it valuable for isolating defined populations in bioengineering. Cells pass single file through a laser, and fluorescently labeled markers generate signals that identify target cells; the instrument then encloses them in droplets and uses electrostatic deflection to direct selected droplets into collection vessels. Researchers apply FACS sorting to enrich stem cells, immune cells, engineered cell lines, and other populations for downstream culture, molecular analysis, tissue engineering, and regenerative research. This precise separation supports reproducible studies of cell function and population heterogeneity.

Facs Sorting - Related Videos

Education

JoVE Science Education - Advanced Biology

Flow Cytometry and Fluorescence-Activated Cell Sorting (FACS): Isolation of Splenic B Lymphocytes

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2023

Source: Perchet Thibaut1,2,3, Meunier Sylvain1,2,3, Sophie Novault4, Rachel Golub1,2,3 1 Unit for Lymphopoiesis, Department of Immunology, Pasteur Institute, Paris, France 2 INSERM U1223, Paris, France 3 Université Paris Diderot, Sorbonne Paris Cité, Cellule Pasteur, Paris, France 4 Flow Cytometry Platfrom, Cytometry and Biomarkers UtechS, Center for Translational Science, Pasteur Institute, Paris, France The overall function of the immune system is to defend the body against infectious...

Research

JoVE Journal - Immunology and Infection
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Purification of Specific Cell Population by Fluorescence Activated Cell Sorting (FACS)

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Cited by 137 •

2010

For many scientific studies requiring a biological and chemical analysis of cell populations the cells must be in a high state of purity. Fluorescence activated cell sorting (FACS) is a superior method in which to obtain pure cell populations.

Isolation of Normal and Cancer-associated Fibroblasts from Fresh Tissues by Fluorescence Activated Cell Sorting (FACS)

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Cited by 79 •

2013

Cancer Associated Fibroblasts (CAFs) facilitate tumor initiation, growth and progression through signaling that promotes proliferation, angiogenesis, and inflammation. Here we describe a method to isolate pure populations of normal fibroblasts and CAFs from fresh mouse and human tissues by cell sorting, using PDGFRα as a surface marker.

Fluorescence Activated Cell Sorting (FACS) and Gene Expression Analysis of Fos-expressing Neurons from Fresh and Frozen Rat Brain Tissue

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Cited by 34 •

2016

Here we present a Fluorescence Activated Cell Sorting (FACS) protocol to study molecular alterations in Fos-expressing neuronal ensembles from both fresh and frozen brain tissue. The use of frozen tissue allows FACS isolation of many brain areas over multiple sessions to maximize the use of valuable animal subjects.

Murine Dermal Fibroblast Isolation by FACS

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Cited by 28 •

2016

Fibroblast behavior underlies a spectrum of clinical entities, but they remain poorly characterized, largely due to their inherent heterogeneity. Traditional fibroblast research relies upon in vitro manipulation, masking in vivo fibroblast behavior. We describe a FACS-based protocol for the isolation of mouse skin fibroblasts that does not require cell culture.

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