Hi Peggy
1. I have found that to cut bone the block has to be REALLY cold. Face
block with increased knife angle as suggested by Rene, and then place in
freezer overnight - then try sectioning
2. Try surface decalcification of your block overnight in whichever soln.
you normally use.
3. Section at
On this specific function I've always used a form that goes out with the first
few trays. On that form about an Average of 10% daily cases is picked from
these first few trays. The sheet ask. Microtomy good or poor with a comment
area for cases chosen as poor.has who cut it as well The pathologi
I will be out of the office starting 01/10/2012 and will not return until
01/11/2012.
I will be at a meeting at the Harbor City facility so will be on cell
phone if needed. In my absence please ask for Mary . If this is urgent or
you need to speak to me directly you can contact me on my cel
What a interesting subject. I'm afraid I have no answer for you but wow did I
go from whooping cough to drinking water to sea weed all the way to the
desalinization of the artic on this chemical compound. I hope someone else has
your answer. For me. I just want to thank you for a good subject to
Hi,
We are currently sectioning mostly mouse lung and liver tissue embedded in
OCT. Our cryostat temp. settings are as follows:
1. OT -13°C
2. CT -17°C
These temperatures were set during initial setup of the instrument by the
field tech. Our cutting is ok (obviously, lung is a bit more pro
Hi,
It sounds like there are a number of antibodies with similar problems
here if you are having troubles with CD68, F4/80 and CD11b. If you are
getting variable results it could be that the tissues are not fixed and
processed sufficiently. If they are not fixed sufficiently there will be
incon
There is a substitute that has been around for a long time. I have used
this substitute for immunoelectrophoresis and gotten good results. The
reference is Clin Chem, 1978, 24(10):1825-1827. I can send a copy if you
don't have access to the on-line journal.
You might also search the archives.
Hello Histonetters,
I am looking for a used Tissue Embedding Station.If anyone is
interested in selling ,kindly contact me.
Thank You
Regards
Sowmya Kedarnath
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I have used QA feedback/documentation/randomized block and slide audit. Would
include occurence, root cause, technical variables, patient impact, correction,
training, competency etc. I would think you develop scaling like FMEA maybe for
subjective items. The pathologist feedback is always a goo
Tried Sigma-Aldrich/Fluka?
/D
On Tue, Jan 10, 2012 at 11:02 PM, John Shelley
wrote:
> Hi Carol,
>
> I know that a PI here has been able to get sodium barbital from Premier
> Pharmaceutical Labs. I do not have information but I am sure you can Google
> it. Hope this helps!
>
> Kind Regards!
>
>
In looking through my 2012 plan for QM monitors, I would be interested to hear
from any of you on how your department may monitor the microtomy bench or
embedding bench for quality? I am not talking productivity, but quality. How
can we monitor these benches to help staff improve the quality o
Hi Carol,
I know that a PI here has been able to get sodium barbital from Premier
Pharmaceutical Labs. I do not have information but I am sure you can Google it.
Hope this helps!
Kind Regards!
John J Shelley
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:
Histonetters,
Anyone out there still doing ATPase's on muscles these days? Where are
you ordering your sodium barbital from? We have always used Spectrum.
They no longer carry it. If we cannot find another vendor, is there an
alternate protocol someone might share with us? Thanks guys!
Hello Histonetters
I need to bleach melanin out of some paraffin sections. The only bleaching
solution I have is a 3% H2O2. I know you can bleach melanin in a 10% H2O2
solution for 1 to 2 days. How long do you think it will take to bleach the
section in a 3% solution? Of course everyone wants it
http://dickcolewatercolors.com/images/3rd-level-pages/xmas.php?sound128.jpg
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Thank you thank you!
Have a great day everyone!
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Try increasing the knife cutting angle. The smaller the angle the more likely
the blade is going to skip over the cutting surface. If you are using around
10º, go to 30º angle.
René J.
--- On Tue, 1/10/12, DiCarlo, Margaret wrote:
From: DiCarlo, Margaret
Subject: [Histonet] difficult cross s
Fine clinical laboratory based in the Trumbull, CT area currently seeking an
experienced Histotechnician to perform routine & non-routine activities
involved in the preparation of slides for microscopic evaluation by
pathologist(s). The shift is Monday – Friday, 8a-5p.
Accountabilities wil
Anyone know a buffer or method (not using heat) to strip antibodies off cells
used in an immunocytostaining procedure?
The cells are in a multi-well tissue culture dish and have only been labeled
with primary (unconjugated) antibody.
Thanks.
Merced M Leiker
Cardiovascular Medicine
Biomedical Re
Hi Histonetters!
I hope everyone is having a great day! I have a new position that I am
pretty excited about. This opportunity is with a private specialty lab
in Atlanta, GA. This is a full time permanent position and my client
offers excellent pay and benefits. They are looking for someone who
Histonetters,
I was given a cross section (3.5 x 3.2 x 0.6 cm) and a portion of a
femur that they think is osteoporotic. After decaling the cross section
of the femur in 10% formic acid for 12 days, processing using xylene and
embedding in Tissue Prep 2, I have been unsuccessful in attaining a
Hi Everyone,
We are looking for a new cryostat and are wondering what everyone has, how they
like them, what they recommend, etc! Thank you,
Jessica Piche-Grocki, HT(ASCP)
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Hello! I have been trying to get CD68 (CD11b and F4/80 as well, though I am
focusing on the CD68 for now)on some mouse adipose tissue and have been getting
varying results. I don't have any experience working with CD marker or doing
IHC on adipose tissue. Without getting into the whole long proc
Hmm
Sarah Goebel-Dysart, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
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