Re: CFDA SE compensation control

From: Jeffrey Rice <rice@aecom.yu.edu>
Date: Wed May 26 2004 - 08:06:30 EST
At 04:21 PM 5/25/2004, Wolfraim, Lawrence (NIH/NCI) wrote:
>What type of cells and how many did you transfer?

None yet!  The transfer is today of B220+ splenocytes from an immunized 
mouse into a SCID.  I am hoping for 2e7 cells.

>The extend of dilution of CFSE (i.e., proliferation) depends entirely upon
>what cells you are transferring (T cells?, other) and into what host

Yup, that's the big question.  I don't know how many divisions they will 
undergo.  Anyway, this is just a pilot since I can't sort at the moment... 
just about the entire flow world is off in France!  Depending how this 
goes, I'll repeat it later on sorted (rather than dynel-selected) populations.

But I think the easiest course is to do leave FL2 empty for the time being 
and use PerCP and APC with the CFSE cells.  I am a little concerned that if 
I use freshly labeled cells they will be unmanageably bright...

Thanks,
Jeff


--
Jeffrey Rice <rice@aecom.yu.edu>
Diamond Lab
Microbiology and Immunology/Sue Golding Graduate Division
Albert Einstein College of Medicine, Bronx, NY 10461
[voice] 718-430-4112  [fax] 718-430-8711
Received on Wed May 26 13:38:00 2004

This archive was generated by hypermail 2.1.8 : Fri May 28 2004 - 03:12:04 EST