(* in /pub/flowcyt/mfi at flowcyt.bio.umass.edu)
In message Fri, 24 Mar 1995 18:06:20 +0000 (GMT),
"P.Openshaw Medicine" <p.openshaw@ic.ac.uk> writes:
> We have been staining weak antigens and never get much above 2 logs of
> specific shift. On Lysis II and Cellquest, I've zoomed one axis of
> dotplots to make the weak and the strong look more comprable. I want to
> do this on data from the Elite, that we also analize on WinMDI. I havn't
> found a way to zoom, and Coulter Tech support think it can't be done.
/*- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
Eric Martz, Professor of Immunology emartz@microbio.umass.edu
Dept Microbiology Voice: 413-545-2325 FAX: 413-545-1578
Morrill IVN 203, Box 35720, Univ Massachusetts, Amherst MA 01003-5720
- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -*/
![]() |
![]() |
![]() |
![]() |
![]() |
CD-ROM Vol 3 was produced by Monica M. Shively and other staff at the
Purdue University Cytometry Laboratories and distributed free of charge
as an educational service to the cytometry community.
If you have any comments please direct them to
Dr. J. Paul Robinson, Professor & Director,
PUCL, Purdue University, West Lafayette, IN 47907.
Phone: (765)-494-0757;
FAX(765) 494-0517;
Web