Fluorescence activated cell sorting (FACS) at UCSF

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.
→ Fluorescence activated cell sorting (FACS)
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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: Rosa Navarro (415) 516-7437 sarah.elmes@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 Flow Cytometry Core

Research Resource Program, Parnassus
Contact: General Contact 415-939-8195 flowassist@ucsf.edu

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

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