Hi,
I am looking to buy a slide scanner for highthrouput project. Could you
give me your opinion if you are using one of the next 3: Mirax Scan
Zeiss, Nanozoomer Hamamatsu and XT Aperio?
Best regards
Jeanne
Jeanne Estabel, PhD
MGP Histology Operations Manager
Wellcome Trust/Sanger
Hi All,
Has anyone had experience doing IHC on FFPE tissues with HRP-labeled primary
antibodies? I was wondering what the best way to detect them would be. I
assume that going strait to DAB would not work, since no amplification is
there. I was thinking of using a biotinyl tyramide step to
I have been very happy with the Olympus C-7000. It will focus at 3 1/4 inches
(8 cm) in its macro mode.
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Reuel Cornelia
Sent: Wednesday, May 20, 2009 4:53 PM
Friends,
Can someone recommend to me how to store bones (juvenile rat femur) that I have
fixed and decalcified, but am not yet ready to cut (they're for vibratome, so
not embedded).
Thanks!
Redward.
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Dear Histonetters,
I am new in fixation and processing bones. I need your full protocol with
details how to fix and process mice bone to visualize the tumor metastases?
Thanks in advance,
Naira
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Histonet mailing list
If there is enough of the antigen in the tissue or sample you can detect
without amplification. HRP/DAB is an enzymatic reaction so it is also is
amplification. I would try it the straight up way before diving into more
complex protocols.
Alternatively another option would be that you could
I got some great ideas. Thanks everyone!
Kim
Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA
From: anh2...@med.cornell.edu anh2...@med.cornell.edu
To: Kim Merriam kmerriam2...@yahoo.com; Histonet
histonet@lists.utsouthwestern.edu; ih...@googlegroups.com
Sent:
Can somebody help me with my bone tissue to remain intact during antigen
retrieval for IHC staining. I have used subbed slides but It did not help me.
Is there more better adhesive. Does Haupts Gelatin works better? I know this
is a hundred year old question and hopefully this problem have
Thanks Kemlo...
I thought of that, but was worried about over-fixation,- what do you think?
Redward.
--
In 10% neutral buffered formalin?
Kemlo Rogerson
e-mail kemloroger...@nhs.net if not at work.
DD 01934 647057 or extension 3311
IMEB also has a Bone Band Saw.
http://www.imebinc.com/Item/BBS-82203.htm
Jack
Date: Thu, 21 May 2009 09:05:50 -0700
From: cb...@memorialcare.org
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Bone saw
Good Morning,
I was wondering if anyone can help me find a really
Has anyone had a problem with their formalin getting cloudy in their
tissue processor? We have a VIP tissue processor and just recently
started having problems with cloudy formalin. Any suggestions would be
appreciated. I checked the archives and couldn't find any articles on
this particular
Haupts Gelatin works really well at a 1:1 ratio (Concentrate:50% EtOH). The
only limitation is background staining from say a hematoxylin counterstain
after the IHC. You can purchase the concentrate from Fisher (Haupts Fixative
#785-71).
Jack
Date: Thu, 21 May 2009 10:12:23 -0500
I do not routinely perform decalcified bone preparations as I predominantly
utilize undemineralized resin (MMA) applications, so maybe someone else can
better respond to this question. However, I would say that you could store your
bone in 70% EtOH until you are ready to process, but the
I agree with Kim, if I was worried about a weak signal using abs directly
conjugated to hrp I would just ignore the fact that they have the hrp and
use a detection such as labeled polymer matched to the species of the
primary ab just like I would without the direct hrp conjugation, there
should
Fellow Histonetters,
Does anyone have knowledge of guidelines or regulations on whether a
fume hood must remain on 24/7? In a cost cutting measure a facility
is considering turning off the fume hoods from 7pm to 5am. I have
expressed my concern with the idea because of the huge health and
Is your formalin picking up water from the air in the room? Check the humidity
level in your room.
Lynn Burton
Lab Assoc. I
Animal Disease Lab
Galesburg, Il 61401
From: histonet-boun...@lists.utsouthwestern.edu on behalf of Christine I.
Braaten
Sent: Thu
Hi,
At the University of Washington we have been told to lower the sash all the
way when the hood is not in use to save energy and money. I believe there
have been several Universities that have done some cost analysis of this and
have show large savings in money (one study stated $1500 per year
Hello all!
I have an antibody that has a 2 month expiration date.
It is recommended that we aliquot, and freeze (-80) the antibody- per the
vendor.
How do you interpret:
The CAP reg pertaining to expired antibody use: ANP .22432 ???
Are all immunohistochemical reagents used within
Are there any restrictions on the transportation of dry ice (and human tissue)
in private vehicles? Our PAs cover a surgical center off-site and we need to
transport frozen tissue back to the hospital for biobanking purposes. They
drive back and forth in their own vehicles. Thanks.
Richard
In a similar situation we have gotten documentation (e-mail) from the
vendor stating the recommendation to freeze aliquots and to what degree
that extends the shelf life. We haven't been queried on these
particular antibodies by an inspector but our supervisor feels that this
satisfies the CAP
If anyone out in histonet land is doing above, could you please contact me by
email directly?
Thanks
Luis
/PRE
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body
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This email message, including any attachments, is for the sole use of the
intended recipient(s) and may
Richard:
There may be local regulations that could vary. Here you can buy dry
ice in the grocery store (if you bring an appropriate container). The
safety warnings associated with dry ice indicate (as you would expect) -
transport in unsealed insulated container (Styrofoam chest), transport
in
We have used 5% Tite-bond glue( from the Hardware store) on slides with
great success. Just take a Kimwipe and wipe it evenly over the slide and it
holds the tissue very well.
Annette Featherstone,
Supervisor of Pathology and Anatomical Sciences
The University of Buffalo
If you use NBF it will get cloudy when it mixes (in some step) with alcohol.
The NBF has salts that are not soluble in alcohol and will produce cloudiness.
You are getting your NBF mixed with alcohol.
René J.
--- On Thu, 5/21/09, Burton, Lynn lynn.bur...@illinois.gov wrote:
From: Burton, Lynn
This can result from not drying the retort or tissue tank after the clean cycle
which will leave alcohol in the bottom. Dry the tank beofre starting the next
run. Ocassionally I have even seen some xylene end up in a mixture in the
tissue tank if it is not dried well. Both of these will
I will be out of the office starting 05/21/2009 and will not return until
05/26/2009.
Please forward all urgent messages to Eric Halpern at ext. 5852 or
eric.halp...@comphealth.com
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Histonet@lists.utsouthwestern.edu
Christine Bark asks about saws for cutting surgical pathology bone
specimens like femoral heads.
I posted something to Histonet about this fairly recently - here it is again.
Stephen Peters, a pathologist in Hackensack NJ, describes for us a
bone saw he's invented.
Kim,
The direct IPX is the easiest method apart from a direct
immunofluorescence. Very few steps:
1.Block endogenous enzyme
2.Block non-specific Ab binding
3.Put the HRP-conjugated Ab on (a an appropriate dilution, usually
more concentrated than if you were using an ABC or Polymer
Interestingly,
This data sheet does not seem to list the clone of the CMV monoclonal
antibody, or am I misreading it?
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Possible carry over of xylene from the flush program?
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag
Michael,
I have used both the Dako (Clones CCH2 + DDG9) and the Novocastra
products (Clones 2 and 6) and they both stain the same.
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital
Are you certain that it is formalin and not paraformaldehyde? The latter
will get cloudy. Also, is there any way that your clearing solvent might be
making its way in to the formalin solution?
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Histonet@lists.utsouthwestern.edu
Hi All,
Has anyone had experience doing IHC on FFPE tissues with Collagen Type IV
subunit antibodies?
These are Collagen Type IV alpha 1, alpha 3 and alpha 5 chains. They are
used for the diagnosis of Alport syndrome and all antibodies are from KAMIYA
BIOMEDICAL COMPANY, Seatle. At present,
Hello to all in histoland. My lab is looking to start processing whole
prostate specimens and doing the wholemount
process. Can anyone give me a starting point on how to proceed. I would need
information on processing times,
embedding and cutting equipment, staining information and the glass
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