Re: [Histonet] Fixation

2013-03-14 Thread Massimo
Hi,

you can find a pratical suggestion at your problem by watching the Step 9: 
Expedite Large
Specimen Fixation

on the guide:
101 Steps to Better
Histology - a Practical Guide to Good Histology Practice
You can download it from:
http://www.leicabiosystems.com/pathologyleaders/101-steps-to-better-histology-a-practical-guide-to-good-histology-practice/

I don't know if such procedure is suitable for the study of your specimen but 
take it just like a suggestion.

My Best.
Massimo Tosi
A humble
Chemical Engineer who loves Histology



 Da: Giulia Zunino giuli.zun...@gmail.com
A: histonet@lists.utsouthwestern.edu 
Inviato: Mercoledì 13 Marzo 2013 11:31
Oggetto: [Histonet] Fixation
 
I would like to have some informations about fetal brain fixation..
In general, it is in use the fomalin, but during the cut it is possible to
see that in the deep layer the formalin doesn't arrive...
So, Could you give some suggestion to improve this technique?!

Thanks in advance

Best





Giulia Zunino, PhD Student

Laboratory of Molecular Neuropathology
Centre for Integrative Biology (CIBIO), University of Trento
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[Histonet] SOS EGFRV3

2013-03-14 Thread Zimmerman, Billie
Does anyone perform this particular clone of EGFR?? Thanks in advance for your 
help.


Billie Zimmerman MT(ASCP)QIHC

706-721-5617/3630


Augusta State University and Georgia Health Sciences University have 
consolidated to become Georgia Regents University. Effective January 9, 2013, 
my email address has changed to bzimm...@gru.edu. Please update your address 
book to reflect this change.
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[Histonet] Technical Laboratory Coordinator of Pathology Surgical Services- Atlanta, GA

2013-03-14 Thread Brannon Owens
Full time/permanent opening for a Lab Coordinator of Pathology Surgical
Services.
Ideal candidate is HT/HTL/CT certified with at least 4 years of supervisory
experience.
Send an email to bran...@alliedsearchpartners.com for a full job
description.


To view a complete list of Allied Search Partners current openings go to:
http://www.alliedsearchpartners.com/careers.php
-- 
Brannon Owens
Recruitment Manager
Allied Search Partners



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[Histonet] Re: Histonet Digest, Vol 112, Issue 13

2013-03-14 Thread Marilyn . A . Weiss
Have a question to ask the group. One of the Pathologists is complaining 
about anucleate squames on her breast biopsies. Blames the tech for 
fingers being in the water bath, which may or may not happen. If she 
recuts the case it is great and she does not do anything different. what 
could cause  this phenomenon? molds?  It is driving us crazy. HELP

NOTICE TO RECIPIENT:  If you are not the intended recipient of this 
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From:   histonet-requ...@lists.utsouthwestern.edu
To: histonet@lists.utsouthwestern.edu
Date:   03/12/2013 10:03 AM
Subject:Histonet Digest, Vol 112, Issue 13
Sent by:histonet-boun...@lists.utsouthwestern.edu



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Today's Topics:

   1. Re: Fw: news (Kim Donadio)
   2. Detecting monoclonas in mouse lung (Leyva-Grado, Victor)
   3. Reagent containers for VIP 3000 (Vickroy, Jim)


--

Message: 1
Date: Mon, 11 Mar 2013 13:47:55 -0400
From: Kim Donadio one_angel_sec...@yahoo.com
Subject: Re: [Histonet] Fw: news
To: Kim Donadio one_angel_sec...@yahoo.com
Cc: histonet histonet@lists.utsouthwestern.edu,confirm 
unsub
 2m2s2bpqnls4gcuu00bqawlkaga4rn0q
 confirm-unsub-2m2s2bpqnls4gcuu00bqawlkaga4r...@yahoogroups.com,
 Pathrm35 pathr...@comcast.net, 
PensacolaToyBreedAdoption unsubscribe
 pensacolatoybreedadoption-unsubscr...@yahoogroups.com
Message-ID: faa7e81b-723f-4446-b4a3-e945ca593...@yahoo.com
Content-Type: text/plain;charset=us-ascii

Disregard something is up with my account. 

Sent from my iPhone

On Mar 11, 2013, at 11:38 AM, Kim Donadio one_angel_sec...@yahoo.com 
wrote:

  http://www.britvoice.co.uk/wwvc/woszquloax/hkjmnqu=bvdzq
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Message: 2
Date: Mon, 11 Mar 2013 19:37:29 +
From: Leyva-Grado, Victor victor.leyva-gr...@mssm.edu
Subject: [Histonet] Detecting monoclonas in mouse lung
To: 'histonet@lists.utsouthwestern.edu'
 histonet@lists.utsouthwestern.edu
Message-ID:
 
a7d5472945c4e4448fb56d16f814743d071...@exch-2kx-mbxeb2.exchmail.mssm.edu
 
Content-Type: text/plain; charset=us-ascii

Dear all,

I have a couple of monoclonal antibodies raised against a respiratory 
virus. I used as treatment for disease and they worked. In trying to 
elucidate some mechanisms, I'm planning to biotinylate the antibody and at 
specific time points collect the lungs and do IHC to determine the 
distribution of the monoclonal. Do you think this will be feasible? I'm 
also planning to use some section for double labeling IF to determine the 
site of interaction antigen-antibody. Do you guys have any reference for 
this?

Thanks a lot,

Victor

Victor H Leyva-Grado DVM, PhD
Postdoctoral Fellow
Microbiology Department
Global Health and Emerging Pathogens Institute
Icahn School of Medicine at Mount Sinai
One Gustave L Levy Place
Box 1124 Annenberg 16-15
New York, NY 10029
Phone 1-212-241-7094
Fax 1-212-534-1684



--

Message: 3
Date: Tue, 12 Mar 2013 08:11:09 -0500
From: Vickroy, Jim vickroy@mhsil.com
Subject: [Histonet] Reagent containers for VIP 3000
To: histonet@lists.utsouthwestern.edu
 histonet@lists.utsouthwestern.edu
Message-ID:
 bb0b9f1a8373f14fa2974e8cb24bf9cf255c2...@mmc-mail.ad.mhsil.com
Content-Type: text/plain; charset=us-ascii

We have two old VIP 3000's and are trying to keep them running. 
Unfortunately finding some parts are getting g very hard.   Can anyone 
steer me to who might have some old reagent containers for the VIP 3000? 
We have one container that started leaking yesterday and I suspect this is 
going to be an ongoing problem because of the age of the instrument. 
Thanks for your assistance.

Jim

James Vickroy BS, HT(ASCP)

Surgical  and Autopsy Pathology Technical Supervisor
Memorial Medical Center
217-788-4046



This message (including any attachments) contains 

[Histonet] Thawing brain tissue

2013-03-14 Thread Maria Navas-Moreno
Hello Histonet community,

I recently froze a primate brain using isopentane immerse in a bath of 100%
ethanol and chunks of dry ice. Two out of the 3 blocks froze fine but the
third one shows a very bad convex surface, although to be fair,
the defective block was embedded in gelatin while the other ones weren't.
We have had this issue before, even without the embedding, and my PI thinks
it could be due in part to a bad blocking procedure in which the surface is
not completely flat. Before we were able to deal with the convex defect.
This time it is so bad that we think it should be better to thaw and
re-freeze. When dealing with thawing is usually for other purposes (i.e.,
live cells retrieval) and I think it is suggested to thaw very fast, to
avoid water crystal issues. But in the case of morphology and IHC, will it
be beneficial to thaw quickly? I am trying to learn from others experience
so I can try so salvage this sample so any information is appreciated. I
know this is far from being a standard procedure but since the block got so
deformed I don't think there is any other option, I am just trying to find
the optimum conditions for a non-ideal situation.

Thanks

Maria Navas
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[Histonet] Thawing brain tissue

2013-03-14 Thread Maria De Los Angeles Navas
Hello Histonet community,

I recently froze a primate brain using isopentane immerse in a bath of 100% 
ethanol and chunks of dry ice. Two out of the 3 blocks froze fine but the third 
one shows a very bad convex surface, although to be fair, the defective block 
was embedded in gelatin while the other ones weren't.  We have had this issue 
before, even without the embedding, and my PI thinks it could be due in part to 
a bad blocking procedure in which the surface is not completely flat. Before we 
were able to deal with the convex defect. This time it is so bad that we 
think it should be better to thaw and re-freeze. When dealing with thawing is 
usually for other purposes (i.e., live cells retrieval) and I think it is 
suggested to thaw very fast, to avoid water crystal issues. But in the case of 
morphology and IHC, will it be beneficial to thaw quickly? I am trying to learn 
from others experience so I can try so salvage this sample so any information 
is appreciated. I know this is far from being a standard procedure but since 
the block got so deformed I don't think there is any other option, I am just 
trying to find the optimum conditions for a non-ideal situation.

Thanks,

Maria
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RE: [Histonet] RE: AFB and negative control

2013-03-14 Thread joelle weaver
This practice is listed as a QC measure for issues of cross contamination in 
the ASCP publication Quality Management in Anatomic Pathology, Nakhleh, R. 
M.D. I have never had any issues that were persistant enough to warrant this 
measure myself, but it is one of the suggestions made under the section for use 
of control tissue/slides. 




Joelle Weaver MAOM, HTL (ASCP) QIHC
  From: tnma...@mdanderson.org
 To: histonet@lists.utsouthwestern.edu
 Date: Thu, 14 Mar 2013 17:52:39 +
 Subject: [Histonet] RE: AFB and negative control
 
 While I don't use a negative control for the AFB, I will use distilled water 
 throughout the procedure.  Most of the time the water in the waterbath is 
 distilled as well, to rule out contamination there as well.  Make sure the 
 waterbath has been disinfected.
 
 Toysha N. Mayer, MBA, HT (ASCP)
 Instructor, Education Coordinator
 Program in Histotechnology
 School of Health Professions
 MD Anderson Cancer Center
 (713) 563-3481
 tnma...@mdanderson.org
 
 
 
 
 Date: Thu, 14 Mar 2013 12:42:30 +
 From: Ian R Bernard ibern...@uab.edu
 Subject: [Histonet] AFB and Negative Control
 To: Lee  Peggy Wenk lpw...@sbcglobal.net, Tighe, Sean T
   sti...@ufl.edu,   histonet@lists.utsouthwestern.edu
   histonet@lists.utsouthwestern.edu
 Message-ID:
   d4f4c602b10b9f45b4e9271af6380e16181a1...@uabexmb1.ad.uab.edu
 Content-Type: text/plain; charset=utf-8
 
 The only special stain that I know that requires the use of a negative 
 control is for the AFB. I understand to rule out false positives as the AFB 
 bacteria might exist in tap water. Nevertheless, a good QA practice which we 
 will implement now.  
 
 Other than Carson, does anyone know of a regulatory or accreditation agency 
 is requiring this as well?  Any suggestion on a good control tissue type? 
 Carson recommends uterus.  Also if there is a pick up on the negative slide 
 (link to the tap water) will use of distilled water and a repeat procedure 
 fix this?
 
 Any thoughts from fellow histonetters?
 
 Thanks
 Ian Bernard
 
 
 
 
 
 
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Re: [Histonet] RE: AFB and negative control

2013-03-14 Thread Cristi Rigazio
Isn't a gram stain the only special that requires a positive and negative 
control?  

Sent from my iPhone

On Mar 14, 2013, at 1:51 PM, joelle weaver joellewea...@hotmail.com wrote:

 This practice is listed as a QC measure for issues of cross contamination in 
 the ASCP publication Quality Management in Anatomic Pathology, Nakhleh, R. 
 M.D. I have never had any issues that were persistant enough to warrant this 
 measure myself, but it is one of the suggestions made under the section for 
 use of control tissue/slides. 
 
 
 
 
 Joelle Weaver MAOM, HTL (ASCP) QIHC
 From: tnma...@mdanderson.org
 To: histonet@lists.utsouthwestern.edu
 Date: Thu, 14 Mar 2013 17:52:39 +
 Subject: [Histonet] RE: AFB and negative control
 
 While I don't use a negative control for the AFB, I will use distilled water 
 throughout the procedure.  Most of the time the water in the waterbath is 
 distilled as well, to rule out contamination there as well.  Make sure the 
 waterbath has been disinfected.
 
 Toysha N. Mayer, MBA, HT (ASCP)
 Instructor, Education Coordinator
 Program in Histotechnology
 School of Health Professions
 MD Anderson Cancer Center
 (713) 563-3481
 tnma...@mdanderson.org
 
 
 
 
 Date: Thu, 14 Mar 2013 12:42:30 +
 From: Ian R Bernard ibern...@uab.edu
 Subject: [Histonet] AFB and Negative Control
 To: Lee  Peggy Wenk lpw...@sbcglobal.net, Tighe, Sean T
sti...@ufl.edu,histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
 Message-ID:
d4f4c602b10b9f45b4e9271af6380e16181a1...@uabexmb1.ad.uab.edu
 Content-Type: text/plain; charset=utf-8
 
 The only special stain that I know that requires the use of a negative 
 control is for the AFB. I understand to rule out false positives as the AFB 
 bacteria might exist in tap water. Nevertheless, a good QA practice which we 
 will implement now.  
 
 Other than Carson, does anyone know of a regulatory or accreditation agency 
 is requiring this as well?  Any suggestion on a good control tissue type? 
 Carson recommends uterus.  Also if there is a pick up on the negative slide 
 (link to the tap water) will use of distilled water and a repeat procedure 
 fix this?
 
 Any thoughts from fellow histonetters?
 
 Thanks
 Ian Bernard
 
 
 
 
 
 
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