Any suggestions on appropriate staining and fixation are welcome.
Good technical references for procedures would be welcome.
Do we need to syncronize the cells and drug treat to amplify G2
recovery?
Our setup: FACStar+, UV/488 Enterprise and HeNe lasers
We have experience in Heoscht, and PI DNA stains.
Please post all answers to the list, I'd rather not do the
summary thing.
Thanks in advance.
Denis Snider
Associate Professor
Dept. of Pathology
McMaster University
![]() |
![]() |
![]() |
![]() |
![]() |
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