1um bead party

From: Sarah Leavell <leavell.8@osu.edu>
Date: Tue Oct 23 2007 - 18:06:14 EDT
Hi all -

I have recently started optimizing a phagocytosis assay using those 
cute, little 1um yellow-green fluorescent beads.   I am having a 
carry over issue.  I have run multiple clean-out protocols (lots of 
warming of reagents, whole tank switchout, cleanse solution) and 
still I get this blip of junk on my scatter plot.

It is below my calibration bead threshold - so I can still pass my 
calibration, but it is annoying me that I cannot seem to get them all 
out!  Any experience out there???

Thanks in advance!!
Sarah
-- 
Sarah E. Leavell
Research Associate
The Ohio State University
College of Veterinary Medicine
Department of Veterinary Biosciences
1925 Coffey Road
Columbus, OH 43210
614-247-8025 (lab)
leavell.8@osu.edu
Received on Wed Oct 24 12:58:00 2007

This archive was generated by hypermail 2.1.8 : Wed Jan 31 2007 - 03:12:00 EST