Re: CD45 Negative PBL

From: Dennis_Young@CIS.ucsd.edu
Date: Fri Mar 07 1997 - 12:46:00 EST


1- Are these really cells - have you SORTED them and looked under the 
microscope? There are CD45 DIM events (debris?) that could be sticking to 
your cells. 
2- What sort of frequency are these events?
3- Are they positive for other markers?

I don't use this clone, so I couldn't say if it's clone specific.

Dennis
*************************************************************************
* Dennis J. Young                            Voice : (619) 822-0407     *
* Flow Cytometry Core Facility               FAX   : (619) 822-0412     *
* University of California, San Diego  USA   e-mail: djyoung@ucsd.edu   *
*                       http://www-core.ucsd.edu/flow-core.html         *
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______________________________ Reply Separator _________________________________
Subject: CD45 Negative PBL
Author:  markrehse@CellPro.com at @UCSD
Date:    3/6/97 9:42 AM


Dear Flow Community,
We use CD45 FITC (Immunotech clone J33)  in our two color 
immunophenotyping panels to identify the WBC component in apheresis 
and buffy coat and eliminate RBC's, debris and dim staining platelets 
from subsequent enumeration of T and B cells, stem cells, NK cells, 
monocytes and granulocytes using PE-conjugated antibodies. This
method is superior to traditional light scatter gating, however, there is a 
population of CD45- cells which are equivalent in size and granularity to
T and B cells which we have not yet been able to identify in our panels. 
Does anyone have experience with this population? Is it a problem with 
this clone?
Thanks in advance.
MarkRehse@CellPro.com


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