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SWEHSC > Facility Cores > Cellular Imaging > About > Equipment & Services >

Cytometry Core Facility

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See also: Fluorescence Techniques on the WWW
This page: Cytometry, Advantages & Disadvantages, Instrument Capabilities, Menu

 

 


 

Cytometry Core Facility


  •  Location:
Arizona Cancer Center, room 4920
  •  Contact: Barb Carolus, 621-2047 or the facility at 626-2450
  •  Administration: Imaging Facility, Div. of Biotechnology, Arizona Research Laboratories.
  • 
Fees for Services: see the facility's list of Cytometry service fees
  • 
WWW: http://cytometry.arl.arizona.edu/index.php

Reminder: SWEHSC Investigators (including their staff and students) should contact the Cellular Imaging Core directly for assistance.

Advantages and Disadvantages:

Advantages: An ideal technique for performing quantitative fluorescence measurements on a population of cells. Data can be aquired quickly, many parameters can be measured simultaneously and the cells of interest can be seperated into sub-populations. Other types of studies available include kinetics and FRET.

Disadvantages: Data is of a population of cells, users will not know which individual cell produced a particular measurement. While some sub-populations of cells can be recovered, usually the sample is analyzed and discarded. This technique measures cells, therefore intact tissues usually require pre-treatment with a enzyme to release the individual cells for analysis.

Instrument Capabilities:


The new (Sept 2004) BD Biosciences FACSAria cell sorter has three lasers (407/488/633 nm) and can detect eleven colors. It is very fast, being able to count over 30,000 events/second and sort 20,000 cells/second. It can sort four different populations of cells onto tubes of many sizes, plates, slides and culture dishes. The instrument can sort out a single cell if needed.

The following list of includes some of the measurable parameters of cells and particles using flow cytometry (list courtesy of the FACS facility) :

  • Cell size/shape
  • Cytoplasmic granularity
  • Cell surface antigens
  • Membrane integrity (viability)
  • DNA content, and base ratio
  • DNA degradation (apoptosis)
  • Chromatin structure
  • DNA synthesis
  • Membrane permeability
  • Membrane potential (dye/drug uptake)
  • Membrane-bound/Cytoplasmic Calcium


Douglas W. Cromey, M.S.
Manager, SWEHSC Cellular Imaging Core

Office: AHSC 4212
Voice: 520-626-2824
FAX: 520-626-2097
Email: Cromey@Arizona.edu



Funded by NIEHS grant # ES06694

© 1996-2007, The University of Arizona
Last update:  May 9, 2007
Page Content:  Doug Cromey
Web Master:  Mike Kopplin