Hi there,
I am very new to basic sciences research and am planning an experiment to
quantify and compare adipose tissue macrophage infiltration in sheep model
using immunohistochemistry. I am specifically interested in CD11c as a marker
of M1 activation of Macrophages. I have been advised that
From the research point of view, I've heard of people not fixing tissue
before they section it. Since I work with embryonic tissue (which is mostly
water!), we always fix our tissue. It definitely is better to not fix tissue
when you want to stain with antibodies because anything you do to the
I was cutting some bone/joint tissue and noticed that the cartilaginous
portion was concave/indented, instead of flush with the rest of the
block surface. Even as I continued to cut that portion always seemed a
little sunken into the block face and all the sections crumbled. I
didn't seal the
Hi,
I am looking for a lab or a supplier for SV-40 control blocks or
slides. If anyone can help us out it would be appreciated.
Thanks
Sharon Allen
Senior Technologist
Neuropathology Lab MS435U
Health Sciences Centre
825 Sherbrook St.
Winnipeg, Manitoba R3A 1R9
Ph# 787-4615
This email and/or
CD68 - clone KP1 has not worked on sheep (also not dogs, cows, horses, and
chickens) in my experience. I have found it to stain primates well (and
rare cells in pigs and cats).
Jan Shivers
Senior Scientist
Histology/IHC/EM Section Head
Pathology Teaching Program
University of Minnesota
Why not try resin embedding techniques? Less shrinkage than paraffin, more
specimen/block stability in cutting, no damaging effects of decalcification and
a many times you have a better and more clear morphological representation. I
could help you to achieve this if interested, so feel free to
Why not save yourself some time and simply purchase the staining kit from
Polysciences or Dorn and Hart Micredge.
Jack
On Jun 23, 2011, at 3:48 PM, Jesus Hernandez jesus.w@gmail.com wrote:
Dear all,
Does anyone have a protocol on how to prepare Sirius Red stain with known
To those who were not able to open to the site, I tried to copy and
paste and hopefully you can read it. This is a very interesting story
about Joplin's St John's Regional Medical Center and code Gray.
If you still have problems. please visit this link.
That sounds like insufficient infiltration with paraffin.
Melt your block again and let it sit in paraffin for a few hours or even
over night.
Most time this helps to get better sections.
Gudrun
-Ursprüngliche Nachricht-
Von: histonet-boun...@lists.utsouthwestern.edu
Hi Histonetters!
I am looking for a temp histology assignment for a couple of weeks in July. I
am
HT (ascp) and have 17 years experience. Please respond to this email if you are
looking for some help, thank you, Jill
Jill Cox, HT ASCP
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If sometimes you are experiencing compression problems it could be because your
paraffin has some xylene contamination, or your blocks are not cold enough when
cutting, or you are using a paraffin of lower melting point as needed for the
tissue you regularly process.
Paraplast X-tra always
Hello,
Does anyone out there have any experience with HistoGel? It's Richard
Allan/Thermo Fisher. They claim that you can embed scant tissues in the gel
and then process, embed, and cut as usual. Just wondering how it works in the
real world
Michael J. Dessoye, M.S. | Histology
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We use histogel a lot in our lab. It's a research lab and we use it for a few
purposes - pelleting cultured cells then creating multi-culture TMAs for
testing antibodies and also pelleting cells from ascites and pleural effusions.
Has also been used to process really small samples that could
Hi,
I've encountered this problem before in my previous lab. To reduce the
Histogel from shrinking that badly, avoid putting the tissue at the very edge
of the Histogel, space them out nicely in the middle, providing sufficient
amount of extra Histogel between each tissue and surrounding them.
Looking to change my bluing step in the HE process to obtain a bluer (less
purple) hue to the nuclear detail. What is everyone using in their bluing
step??
Thanks for all of your ideas!!
This e-mail and any files transmitted with it are confidential and
There are several bluing solutions in the market, or you could use lithium
carbonate at different concentrations until you find one of your liking.
René J.
--- On Fri, 6/24/11, Webb, Dorothy L dorothy.l.w...@healthpartners.com wrote:
From: Webb, Dorothy L dorothy.l.w...@healthpartners.com
Hi Dorothy,
Try Richard Allan Bluing Reagent.
Here's what they say about their product: It is a buffered product
that ensures the proper alkalinity (pH=8.0). Unlike ammonia and lithium
carbonate, RA's Bluing Reagent does not allow for the pH shift which can
affect the crispness of nuclear
Trying to clean up some things hanging out there in our lab and wondering what
everyone does with a blade that has been used minimally and tech done for the
day with the microtome. Where do you store that blade for use tomorrow or do
you toss and not worry about the cost involved? I do not
Dorothy,
I put ours in a 15 mL centrifuge tube with a cap sit it on the base of the
microtome for the next use, that way, no one gets cut the blade is able to be
used to the fullest of it's potential. :-)
Best regards,
~Sean McBride
Scientific Specialist
Bone Tissue Engineering Center
I use the cardboards that come in a box of slides. A small piece of tape on
the open side and mark it used. I just always make sure I have the blade
edge facing the folded part. I know some who will tape this folded
board it to the side of their microtome and use it as a trimming blade
holder.
We use plastic 5 slide mailers
Sent from my iPhone
On Jun 24, 2011, at 1:53 PM, Webb, Dorothy L
dorothy.l.w...@healthpartners.com wrote:
Trying to clean up some things hanging out there in our lab and wondering
what everyone does with a blade that has been used minimally and tech done
for
Hi Histonet,
We are currently looking for a full-time Histotechnician (preferably HT
certified) with experience in IHC. Please read the description below and if
you're interested please submit your resume via e-mail to: *
eric.velazq...@agendia.com*.
*ESSENTIAL DUTIES AND RESPONSIBILITIES*
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