F-actin

DR M AL-RUBEAI (ALRUBEAM@novell1.bham.ac.uk)
Wed, 13 Dec 1995 11:34:17 BST

I have been treating hybridoma cells grown in suspension with
cytochalasin D to disrupt the F-actin cytoskeleton prior to staining
with FITC-phalloidin. Cells treated with cytochalasin seem to have a
higher mean fluorescence than untreated cells, this I believe is due
to cytochalasin induced clumping of the F-actin into dense aggregates
that fluoresce more brightly than the difuse F-actin network of
untreated cells. Has anyone noticed a similar result? If so, is it
possible to use this as a quantitative measure of disruption of the
F-actin by cytochalasin?
Thank you
Jon Welsh
University of Birmingham
School of Chemical Engineering


Home Page Table of Contents Sponsors Web Sites
CD ROM Vol 2 was produced by 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:(317) 494-0757; FAX (317) 494-0517; Web http://www.cyto.purdue.edu EMAIL robinson@flowcyt.cyto.purdue.edu