RE: PKH26 for RBC survival study

From: Andrew Beernink (ABeernink@novasite.com)
Date: Fri Mar 16 2001 - 20:28:21 EST


I tried both to track human lymphocyte engraftment in SCID mice.  CFSE was
more stable over several divisions, and less toxic, than PKH26.  It's also
cheaper!  I seem to remember it being a bit leaky, though I don't remember
how it compared to PKH in that respect.

Suerte.

Andrew Beernink
Novasite Pharmaceuticals, Inc.
3520 Dunhill St.
San Diego, CA  92121
(858) 638-8584



-----Original Message-----
From: Mark Kukuruga [mailto:kukuru@med.umich.edu]
Sent: Friday, March 16, 2001 4:14 AM
To: cyto-inbox
Subject: Re: PKH26 for RBC survival study



Jeff,
First . . .have you tried this at 488nm?  PKH26 is fairly bright stain . . .
we
usually see about a 3 decade shift from background.  So, I wouldnn't worry
too much
about maximizing excitation.  Remember, it's not so much signal intensity,
but rather
signal-to-noise ratio that improves resolution.
Second . . .  you could narrow the band range on your filter.  When I need a
better
separation against a ~575nm signal, I'll use a 574/14 filter . . . helps
when I use
CFSE vs. PE by eliminating much of the green crossover from the extremely
bright CFSE.
Third . . . have you tried CFSE?  Very bright, and I have a sense that it
may be less
toxic than the PKH dyes.
MAK.


--
Mark A. KuKuruga, Managing Director
University of Michigan Flow Core
7416 CCGC 0946
(734) 647-3216, fax (734) 936-7376
kukuru@umich.edu


>>> Jeff Louie <jlouie@hsc.usc.edu> 03/15/01 02:42PM >>>

I have a researcher who would like to utilize PKH26 as a tracking dye
for rabbit rbc's survival studies. I have gotten reasonable separation
of positives and negatives using a "PE" filter setup (555DLP beam
splitter and 580/30 band pass) with 488 excitation on a MoFlo. The
researcher is worried about cell toxicity of the PKH26 and wants to use
as little as possible in his staining procedure. In an attempt to
maximize fluorescence intensity, I've tried to "tune" the dye head laser
(INNOVA 70) on the MoFlo to maximum excitation for PKH26 (551 nm) but
seem to overwhelm the detection PMT with its 580/30 band pass. Any
suggestions or advice on filter setup or use of PKH26 in this scenario
is much appreciated.



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