Fluorescence activated cell sorting (FACS) at UCSF

Definition
A flow cytometry assay that provides a method for sorting a heterogeneous mixture of biological cells into two or more containers, one cell at a time, based upon the specific light scattering and fluorescent characteristics of each cell.
Synonyms
FACS
Categories
→ → → Fluorescence activated cell sorting (FACS)
Filter by location:
All Mission Bay Mt. Zion Parnassus SFGH
Mission Bay

Gladstone Flow Cytometry Core

Gladstone Institute for Virology and Immunology, Mission Bay
Contact: Marielle Cavrois 415-734-4824 mcavrois@gladstone.ucsf.edu

  • Intellicyt High Throughput Flow Cytometer
Mission Bay, Mt. Zion

Laboratory for Cell Analysis (Diller Comprehensive Cancer Center Cytometry Core)

Helen Diller Family Comprehensive Cancer Center, Mission Bay, Mt. Zion
Contact: Ben Braun 415-514-4176 braunb@peds.ucsf.edu

  • MB GH-S252 BD FACS Aria 2
  • MB HD-335 BD FACS Aria 3
  • MB HD-335 BD SONY Sorter
  • Cell Sorting
  • Flow cytometry
Parnassus

Parnassus Flow Cytometry Core

Research Resource Program, Parnassus
Contact: Michael Lee 415-430-7676 michael.lee@ucsf.edu

  • FACS Aria, FACS Aria 2, FACS Aria 3, FACS Aria Fusion sorters
  • Flow Cytometer Sorters
  • MoFlo XDP sorter
  • SH800 sorter
  • Cell Sorting
  • FACS (Aria II with 365 nm laser)
  • FACS (Aria II with 561 nm laser)
SFGH

Core Immunology Laboratory/CFAR Immunology Core

Division of Experimental Medicine, SOM-SFGH, SFGH
Contact: Jeffrey Milush 415-206-3881 jeffrey.milush@ucsf.edu

  • BD Bioscience FACS Aria 2 (17 color)
  • FACS sorting of BSL2 level specimens
  • Immunophenotyping for live cell sorting