re: Use of FDA

Michael Fox (MFox@vines.ColoState.EDU)
Wed, 16 Aug 95 11:12:30 MDT

We have used FDA to discriminate between viable and non-viable cells (based
upon membrane integrity). We were using CHO cells but it should work with
virtually any cells that have esterases. You only have to use a very small
amount of FDA since fluorescein is so bright. We add 0.02 ml to 100 ng/ml of
FDA in PBS to 1 ml of a cell suspension in PBS and incubate for 10 min at
room temperature. You can also co-stain with PI which gives the opposite
test of viability - PI is excluded from live cells and FDA (actually the free
fluorescein) is contained in live cells.

Mike Fox
Colorado State University
Ft. Collins, CO


Home Page Table of Contents Sponsors E-Mail Archive Web Sites

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 http://www.cyto.purdue.edu , EMAIL cdrom3@flowcyt.cyto.purdue.edu