dave at nucleus.immunol.washington.edu
Mon Jan 31 12:18:10 EST 1994
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Date: Mon, 31 Jan 1994 08:55:38 +0100 (CET)
From: Dr Stephen Young <s.p.young at bham.ac.uk>
Sender: steve at rheuma.bham.ac.uk
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To: KWEBER%IMVS4.decnet at uv1.im.med.umich.edu
Cc: cytometry at flowcyt.cyto.purdue.edu
Subject: RE: BIG FILES
We are also measuring calcium fluxes but have kept away from attempting
simultaneous surface labelling becuase of the possible effects of the
antibody on the subsequent calcium flux. How do you get over this? and which
surface proteins are you labelling?
For the last several years we've been measuring calcium flux along with two
surface markers on cells from mouse thymus, spleen, or peripheral blood.
Antibodies against CD4 and CD8 are routine, and we've done some with three
surface markers (FITC, PE, and PE-Cy5 conjugates all excite with 488nm light).
Calcium flux has been induced with agents including anti-CD3, phorbol esters,
or peptides. Surface-labeled cells when probed with ionomycin display an indo-1
violet/blue ratio that is 12-16 times greater than the resting state.
Data files become large, necessarily so since some phenotypes (which you can
identify directly with multiple surface markers) are present at low frequency.
We can read and analyze these multi-megabyte files quite easily with ReproMan.
Dept. of Immunology
Univ. of Washington
dcoder at u.washington.edu
More information about the Cytometry