Viability/nuclear stain

From: Patricex Petit (pxpetit@cochin.inserm.fr)
Date: Fri Mar 12 1999 - 04:38:37 EST


You wrote
Has anyone used anything other than PI to do viability staining on the
FLOW?  7-AAD? 
 I have a researcher using PI and AO and they co-stain ALL the cells,
virtually 100%, in what they believe to be live samples  of Chondrocytes. 
Any hints?  Does the collagenase used to break up the matrix of the
cartilage cause permeabilization?  I'm kind of at a loss to explain to him
what is happening.  Any better dye for this application?
 Thanks in advance!
 Susan DeMaggio, MS BSMT(ASCP)QCym
 Resource Manager
 Optical Biology Shared Resource
 University of California, Irvine
 Irvine, CA  92697-2275
 phone   949-824-4110
 fax     949-824-3571

 Dear Susan,

I routinely use the 7AAD instead of PI... It works weel exept that the
scale of fluorescence is a bit less large. The emisson max is at 647 nm and
the MW 1270. Pi has a MW of 668. The diffrence can explain some discripency
in using the two dyes. But at the main value.... 7 AAD is very usefull.
Patrice

Dr. Petit Patrice X.
Institut Cochin de Génétique Moléculaire
INSERM U129 - CHU Cochin Port-Royal
24, rue du Faubourg Saint-Jacques
F-75014 Paris, France.

Tel: 33 01 44 41 24 11
Fax: 33 01 44 41 24 21
E-mail: pxpetit@icgm.cochin.inserm.fr



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