Hi all,
We have collected a specific lung cell via FACS from mice, stained the
cells with PKH, and then returned the cells to congenic mice via 1.
tracheal injection or 2. tail vein injection. We can see the PKH
positive cells in the recipient lungs on microscopy, but we are having a
real
--- On Wed, 10/14/09, Rene J Buesa rjbu...@yahoo.com wrote:
From: Rene J Buesa rjbu...@yahoo.com
Subject: Pathos Tissue Processor vs Tissue Xpress
To: Kiranjit Grewal kira...@sbcglobal.net
Date: Wednesday, October 14, 2009, 9:28 AM
Under separate cover I am sending you an article where
You might be able to shrink it a little by putting the gasket in the
refrigerator for a while.
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]on Behalf Of Diana
McCaig
Sent: Wednesday, October 14, 2009 6:34 AM
To:
Hi Donna:
Thank you for your comment. As you write if the Pathos Classic is still
available what I wrote is still valid. Unfortunately when somebody writes an
article the conclusions remain valid as long as the subjects don't change, but
the approach remains.
As you can see I have forwarded
I wouldn't get rid of the isotype control altogether; it's fulfilling it's
purpose in trying to tell you something. Have you tried a no-primary
control in parallel with your isotype control to see what the secondary is
binding to - the tissue or bound goat IgG? What type of tissue is it? Maybe
Does anyone have any experience using the Dako HerCep kit?
And do you have any problems with cytoplasmic staining?
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I wish to unsubscribe and return in 6 weeks.
Thank you,
Susan E. Bryant
Knoxville Dermatopathology
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Hi Histonetters!
I have a new position that I want to let everyone know about. I am
assisting a client located in Atlanta GA that is in need of a
histotechnologist.
This is a full time permanent position on the night shift
(12:30a-8:30a). My client offers excellent benefits and compensation
and
Good for you!
You should probably FOLLOW THE LINK IN EVERY EMAIL JUST LIKE WE SAY EVERY
TIME SOMEONE WRITES IN TO UNSUBSCRIBE.
Emily
...the thrill of being close to that hidden knowledge. That's the way I feel
when I read Nabokov. Encrypted within his words, encoded indecipherably,
ambiguously,
Depending on the tissue fixation processing, you can see some cytoplasmic
staining. How does the cell pellet control look? We seldom see cytoplasmic
staining on that. Are you tracking that your retrieval buffer is 95-100
after you add the slides starting your retrieval times when the buffer
temp
LOL! Oh my I can't stop laughing...must be a serious, stressful day...
--On Wednesday, October 14, 2009 12:56 PM -0400 Peter Carroll
carro...@umdnj.edu wrote:
FOLLOW THE LINK IN EVERY EMAIL JUST LIKE WE SAY EVERY TIME SOMEONE
WRITES IN TO UNSUBSCRIBE
Histonet Fun-Fact:
Hits for the
Remember when we did do it that way and we had a count of how many ways
you can spell it - unscribe, unsuscribe, etc!
Ah the good ole days...
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Merced M
Hi,
Does anyone have a method for doing a combination of Bielschowsky
Luxol Fast Blue? If anyone has the method any comments on it I would
appreciate it.
Thanks
Sharon Allen
HSC, Winnipeg, MB, CA
sal...@hsc.mb.ca
This email and/or any documents in this transmission is intended for the
Hi Adam,
I always do the isotype control parallel with a no-primary control in parallel
with my real Ab.
May I suggest you to use Protein block serum free and pure Ab diluent without
adding 2% donkey serum?
Try this and let me know your results.
If histonetters think I am wrong, fill free
Hey All
A fulltime Histotech position is open at Dayton Children's Hospital in Dayton
Ohio. We are a small hospital. We have one part time, one full time (that
could be you) and myself. We process about 5000 cases a year, we average about
15-40 blocks a day. Monday's are kinda heavy with
Our lab is inquiring about how other labs are validating their IHC
stains. We currently are processing specimens both in a microwave and
conventional processors. Are labs validating every type of program on
the conventional and microwave processors? (i.e. small biopsies vs.
larger tissue
Hi Adam,
We have had the exact same experience you have sometimes when we're using Goat
isotype and Rabbit isotype negative controls. Sometimes you can fiddle with the
protocol and minimize some of the background, and sometimes you can't. Rabbit
and goat antibodies/Igs are notoriously sticky.
Anyone in histo-land who has worked up PHH3 (anti-phospo-Histone H3,
mitosis marker). I would like to perform this immuno on paraffin sections
that are formalin fixed, using the Ventana Benchmark XT platform. My
primary workups will be one brain tumors.
Thanks for any help that you may be
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