Does anyone know why skin sections do not seem to take up haematoxylin as well
as other tissues. The chromatin detail is not as good as with other tissues.
**
This email and any files transmitted with it are confidential and
I am interested in the reasons behind the lack of chromatin detail in skin
sections. Although this is not always a problem it is a concern. Could the
problem be the processing? or are there other factors related to skin?
**
Hello Histonetters!
Is anyone using a Microm HM325 microtome?
Please contact me if you want to share some tricks and useful hints, concerning
sectioning to me :)
I don't have a question in particular, just want to see if anyone is doing sth
like cooling the blade or so.
Bye,
V. Neubert
Greetings
I recall that years ago Biomeda had a product called Stable DAB. It was
a ready-to-use product that was stored in the freezer. Does anyone know
if it is still being produced and whom I should contact?
William (Bill) O'Donnell, HT (ASCP) QIHC
Lead Histologist
Good Samaritan Hospital
10
There was a discussion about the Stable DAB on the histonet a few weeks ago. I
would suggest you search the archieves of the histonet. The company that has
this product was listed at that time.
Frances L. Swain HT(ASCP) A. A. S.
Special Procedures Technician
Department of Orthopaedic
Greetings!
The research scientist of Biomeda has founded ImmunoBioScience Corp., therefore
offering a direct replacement of Biomeda products. Please visit
www.ImmunoBioScience.com
Thank you.
Best regards,
Anita
-Original Message-
From: O'Donnell, Bill
Hi there,
I am having problems with my brain sections (15 um - flash-frozen)
curling up once I remove the antiroll plate on my cryostat... does
anyone know how i can prevent this?
Also - does anybody have a quick guide on what to improve while
cutting, based on the damage seen on the
I am having problems with my brain sections (15 um - flash-frozen)
curling up once I remove the antiroll plate on my cryostat...
I cut many of the same on a regular basis, and I find that letting them
sit for a a few moments (~10 seconds) helps keep them from curling, at
least long enough
er, sit for a few moments under the anti-curling plate, that is...
Peter Carroll wrote:
I am having problems with my brain sections (15 um - flash-frozen)
curling up once I remove the antiroll plate on my cryostat...
I cut many of the same on a regular basis, and I find that letting
them
Hello All,
Just a quick Hello to let you all know that I am looking for talented
histotech's for *Corpus Christi, TX and Las Vegas, NV*. These are full time,
Permanent Positions. Contact me @ aly...@alliedsearchpartners.com for the
details if you are interested. The positions offer full benefits,
I make 8um-thick sections of various tissues and sometimes they do curl. I
do not use an anti-roll plate. So what I do while making the section is to
cut just enough of the section so that it is attached by a very small
amount to the top of the block, (so that most of the block has gone down
CAP is OK with their guidelines ( BUT is CLIA on line with the
Processing (Low Complexity?) vs Grossing (High Complexity?). If CLIA is not on
board with processing (dumb naming) being low complexity and grossing being
higher complexity your lab may be in violation of CLIA Guidelines.
At the temperture just after what I call the crumple stage, when the tissue
and medium are stiff enough to form under the blade in a complete section, the
section will lie flat with out shattering. If your brush is clean you can cut
multiple in a row like ribbons. This is in the - 16 to -18C
Good morning. We are a Pathology Lab in Pinellas Park, Florida. We're
looking to add to our team!
Candidates should be an HTL or HT (ASCP) or equivalent, have a valid
driver's license and proof of insurability. Primary responsibilities include
on site frozen sections including mobile
Dear Colleagues
I should detect /stain Succinate dehydrogenase in mouse muscle non-fixed frozen
sections. Could someone please share detailed protocol and sources of the
reagents. Does it exist any kit for detection? I performed some on-line
search but did not find a sufficient information.
Hi dear histonetters,
I have a question about chromatin and its stainability. Heterochromatin is
said to be the inactive part (perhaps hypermethylated) and the only part of
the chromatin, that can be stained. Euchromatin on the other side is the
active part and can't be stained.
The question is:
My first question is in what region of skin is the staining poor? The
fibroblasts of the dermis should stain really well with HE = as
should the cells of the stratum germinativum. From there out nucle ar
staining gets worse and worse. I attribute it to two things, and
Sarah,
Skin surface tends to dry out as well as the epithelial cells lose their
nuclei as they migrate to the surface.
The surface can also dry out after the application of antiseptics etc
prior to biopsy.
AND there is often the issue of the biopsy being allowed to dry prior to
fixation.
This
I have found the following method easy to use. The DAB Concentrate is aliquoted
in small volumes and frozen. It is quite stable for at least a year. The
following method is also used by our Haematology department for their
myeloperoxidase staining:
Peroxidase
Peroxidase catalyses the transfer
Abcam monoclonal rat-anti BrdU
http://www.abcam.com/BrdU-antibody-BU1-75-ICR1-ab6326.html
Just compare to other Abcam anti-BrdU, it has most citations at least.
2009-03-18
TF
发件人: Amy Lee
发送时间: 2009-03-18 07:14:56
收件人: tifei
抄送:
主题: Re: [Histonet] BrdU immunostain on rat brain
We stain for SDH in fresh frozen mouse skeletal muscle using a kit from
Sigma.
Galina Deyneko galinadeyn...@yahoo.com
Sent by: histonet-boun...@lists.utsouthwestern.edu
03/17/2009 12:45 PM
Please respond to
galinadeyn...@yahoo.com
To
histonet@lists.utsouthwestern.edu
cc
Subject
Hi all,
Currently I am working with brains from 7 day old rat pups, that undergo an
hypoxic-ischemic injury (Levine/Vannucci technique). These brains are
unfixed, frozen in isopentane and cut at 20um on a croystat. These brains
are not cutting very well compared to an adult brain (potenially
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