RE: [Histonet] Space requirements for AP lab

2012-12-13 Thread Lynette Pavelich
We are Joint Commission. I've never run across this issue (and God forbid 
bringing it up in front of one!) in 40+ years and 3 lab renovations. CAP people 
out there??

Lynette


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Morken, Timothy 
[timothy.mor...@ucsfmedctr.org]
Sent: Wednesday, December 12, 2012 4:43 PM
To: jmasla...@stpetes.org; Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Space requirements for AP lab

Administrators rule of thumb: If there is free space in Histology, they are 
taking up too much space!

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
jmasla...@stpetes.org
Sent: Monday, December 10, 2012 9:41 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Space requirements for AP lab

Greetings All, Are there any JACHO or CAP space requirements for an AP 
laboratory? Looking for recommended square footage per tech, equipment, and/or 
work area.
Thanks


Joe Maslanka BS, CT,HT (ASCP)
Anatomical Pathology Technical Supervisor St Peter's Hospital,MT 59601
(P)(406) 447-2406
(F)(406)444-2126

Give thanks for ALL things.
Kindness is the language the blind can see  the deaf can hear- Mark Twain 
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RE: [Histonet] Her2 Dual ISH and breast processing

2012-12-13 Thread Hoekert, W.E.J.
I was wondering,is there any literature on this subject? i.e. the minimal 
required fixation time of breast tissue in order to get reliable immuno 
staining (Oestro, Prog and Her2neu and ISH). We immunologists are alway trying 
to convince our pathologists about the importance of good fixation, but the 
pathologist are always in a hurry to get the diagnosis out. Many mamma biopsies 
do not get to be fixed long enough (some are even put in the processor after a 
few hours of fixation). It would be helpfull if I can show them some literature 
to back me up.
 
Willem



Van: histonet-boun...@lists.utsouthwestern.edu namens Rene J Buesa
Verzonden: ma 10-12-2012 18:23
Aan: vtol...@cox.net; histonet@lists.utsouthwestern.edu
Onderwerp: Re: [Histonet] Her2 Dual ISH and breast processing



Val:
Acknowledging that you have a fixation problem is the fundamental step to 
solving your staining problems.
You state that the slices have now a consistent thickness of between 2-3 mm and 
that is great BUT what about the fixation time?
Thin slices is a first step but until you have the slices properly fixed, you 
will keep having some problems.
Even when one should never assume, I assume that you are using NBF at room 
temperature. With that fixative and under those temperature conditions, your 
2-3 mm thick breast slices will require 4 hours to be fully penetrated; will 
require 24 hours to be 100% covalent bound and will require 96 hours to be 
completely cross-linked.
The 48 hours of maximum exposition to NBF recommended by ASCO-CAP will 
guarantee a 100% cross-linking of 1 mm thick slices, but your 2-3 mm slices 
will require 96 hours to be completely cross-linked.
Until you reach an optimum fixation you will keep having sporadic problems of 
your protocols (depending on greater or lower fat contents of the samples).
René J.

From: vtol...@cox.net vtol...@cox.net
To: histonet@lists.utsouthwestern.edu
Sent: Monday, December 10, 2012 11:48 AM
Subject: [Histonet] Her2 Dual ISH and breast processing

Hello all--

My lab is having some problems with inconstant results with our Her2 Dual ISH 
on the Ventana Ultra.  Right now, we know we have a problem with our large 
breast tissue being under-fixed.  There have been many gripes to the PAs and 
residents about the thickness of the tissue sections and they have listened.  
We are now getting breast sections that are consistently cut between 2-3mm in 
thickness.  However, we are still having issues with inconsistency in our dual 
ISH staining.  Many times, the staining is absent.

We are currently processing our breast tissue on a Tissue-Tek VIP6 processor.  
Are there any labs out there that are using this processor and also running 
Her2 Dual ISH on the Ventana with nice, consistent results?  If so, would any 
of you be willing to share your processing protocol?

Thanks in advance for your help! 



Val



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RE: [Histonet] Space requirements for AP lab

2012-12-13 Thread Bartlett, Jeanine (CDC/OID/NCEZID)
Years ago I worked in a small, community hospital. The histology lab was TINY!  
very well organized and tidy...but TINY!  Every inspection we got cited for 
being too small.  Can't remember which agency but we were a teaching 
hospital.

Jeanine H. Bartlett
Centers for Disease Control and Prevention
Infectious Diseases Pathology Branch
404-639-3590
jeanine.bartl...@cdc.hhs.gov

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lynette Pavelich
Sent: Thursday, December 13, 2012 7:05 AM
To: Morken, Timothy; jmasla...@stpetes.org; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Space requirements for AP lab

We are Joint Commission. I've never run across this issue (and God forbid 
bringing it up in front of one!) in 40+ years and 3 lab renovations. CAP people 
out there??

Lynette


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Morken, Timothy 
[timothy.mor...@ucsfmedctr.org]
Sent: Wednesday, December 12, 2012 4:43 PM
To: jmasla...@stpetes.org; Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Space requirements for AP lab

Administrators rule of thumb: If there is free space in Histology, they are 
taking up too much space!

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
jmasla...@stpetes.org
Sent: Monday, December 10, 2012 9:41 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Space requirements for AP lab

Greetings All, Are there any JACHO or CAP space requirements for an AP 
laboratory? Looking for recommended square footage per tech, equipment, and/or 
work area.
Thanks


Joe Maslanka BS, CT,HT (ASCP)
Anatomical Pathology Technical Supervisor St Peter's Hospital,MT 59601
(P)(406) 447-2406
(F)(406)444-2126

Give thanks for ALL things.
Kindness is the language the blind can see  the deaf can hear- Mark Twain 
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[Histonet] VIP6 Questions

2012-12-13 Thread Tim Wheelock

Good morning Everyone:

For those of you who have a Sakura VIP6, do you actually use the bulk 
reservoirs to let the machine automatically rotate the absolute alcohols 
and xylene?

If not, why not?
Also do you let the machine automatically rotate the paraffin 
reservoirs, or do you do this manually, and if so, why?


Also, do you find the touch screen graphics easy to use?
Have any problems developed with the display itself?

Thanks,

Tim Wheelock
Harvard Brain Bank
McLean Hospital
Belmont, MA




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[Histonet] VIP6 issue

2012-12-13 Thread Nancy Schmitt
Good Morning-
We have recently purchased  VIP6 processors.  Has anyone else experienced a 
problem with the lids coming off during pump in and pump out?  Causes the 
cassettes to float all over and be completely out of order:(  We now place an 
extra rack or lid on top to weigh down and insure this does not happen.  I 
talked with the rep. and they said they had never heard of this.  I know this 
is not  a huge deal, but with new instrumentation I don't think we be cobbling 
things already.
Thank you for any input-
Nancy Schmitt
Dubuque, IA



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[Histonet] Path Lab Assistant Job

2012-12-13 Thread rmweber113


Northeast Philadelphia physician in office path laboratory is looking for a 
laboratory assistant.  Must have strong computer skills.  Duties include data 
entry, phones, inventory control, filing of slides, and miscellaneous tasks. 

15 to 20 hours per week. 

Please fax resume to 215 947-2015 attention Laboratory Manager. 


  
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[Histonet] Synoptic Reporting

2012-12-13 Thread Anita Buchiane

What are people doing for synoptic reporting?   Are the CAP templates the only 
option?

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Re: [Histonet] VIP6 issue

2012-12-13 Thread Brendal Finlay

I've always used a lid on the basket when using the VIP.  If we did
not do so, the blocks will float around, but we have not experienced
cassette lids coming off. Is the lid or rack something in addition to
a lid being on the basket already?


Brendal Finlay, HT (ASCP)
Medical Center Clinic
brendal.fin...@medicalcenterclinic.com
850.474.8758
http://medicalcenterclinic.com


-Original message-
From: Nancy Schmitt nancy_schm...@pa-ucl.com
Date: Thu, 13 Dec 2012 09:17:24 -0600
To: Histonet
(histonet@lists.utsouthwestern.edu)histonet@lists.utsouthwestern.edu
Subject: [Histonet] VIP6 issue

Good Morning-
We have recently purchased VIP6 processors. Has anyone else
experienced a problem with the lids coming off during pump in and pump
out? Causes the cassettes to float all over and be completely out of
order:( We now place an extra rack or lidon top to weigh down and
insure this does not happen. I talked with the rep. and they said they
had never heard of this. I know this is not a huge deal, but with new
instrumentation I don't think we be cobbling things already.
Thank you for any input-
Nancy Schmitt
Dubuque, IA



NOTICE: This email may contain legally privileged information. The
information
is for the use of only the intended recipient(s) even if addressed
incorrectly. If you are not the intended recipient, please notify the
sender
that you have received it in error and then delete it along with any
attachments. Thank you.



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Re: [Histonet] Her2 Dual ISH and breast processing

2012-12-13 Thread Rene J Buesa
My mistake: the web site is: http://www.histosearch.com/rene.html


From: Rene J Buesa rjbu...@yahoo.com
To: Hoekert, W.E.J. w.e.j.hoek...@olvg.nl; vtol...@cox.net 
vtol...@cox.net; histonet@lists.utsouthwestern.edu 
histonet@lists.utsouthwestern.edu 
Sent: Thursday, December 13, 2012 10:47 AM
Subject: Re: [Histonet] Her2 Dual ISH and breast processing

Please go to http://www.histosearch.co/rene.html
There are 2 articles on the subject: one about the general fixation issue and 
another about the minimum amount of NBF required to obtain complete fixation.
René J.

From: Hoekert, W.E.J. w.e.j.hoek...@olvg.nl
To: Rene J Buesa rjbu...@yahoo.com; vtol...@cox.net; 
histonet@lists.utsouthwestern.edu 
Sent: Thursday, December 13, 2012 7:35 AM
Subject: RE: [Histonet] Her2 Dual ISH and breast processing

I was wondering,is there any literature on this subject? i.e. the minimal 
required fixation time of breast tissue in order to get reliable immuno 
staining (Oestro, Prog and Her2neu and ISH). We immunologists are alway trying 
to convince our pathologists about the importance of good fixation, but the 
pathologist are always in a hurry to get the diagnosis out. Many mamma biopsies 
do not get to be fixed long enough (some are even put in the processor after a 
few hours of fixation). It would be helpfull if I can show them some literature 
to back me up.

Willem



Van: histonet-boun...@lists.utsouthwestern.edu namens Rene J Buesa
Verzonden: ma 10-12-2012 18:23
Aan: vtol...@cox.net; histonet@lists.utsouthwestern.edu
Onderwerp: Re: [Histonet] Her2 Dual ISH and breast processing



Val:
Acknowledging that you have a fixation problem is the fundamental step to 
solving your staining problems.
You state that the slices have now a consistent thickness of between 2-3 mm and 
that is great BUT what about the fixation time?
Thin slices is a first step but until you have the slices properly fixed, you 
will keep having some problems.
Even when one should never assume, I assume that you are using NBF at room 
temperature. With that fixative and under those temperature conditions, your 
2-3 mm thick breast slices will require 4 hours to be fully penetrated; will 
require 24 hours to be 100% covalent bound and will require 96 hours to be 
completely cross-linked.
The 48 hours of maximum exposition to NBF recommended by ASCO-CAP will 
guarantee a 100% cross-linking of 1 mm thick slices, but your 2-3 mm slices 
will require 96 hours to be completely cross-linked.
Until you reach an optimum fixation you will keep having sporadic problems of 
your protocols (depending on greater or lower fat contents of the samples).
René J.

From: vtol...@cox.net vtol...@cox.net
To: histonet@lists.utsouthwestern.edu
Sent: Monday, December 10, 2012 11:48 AM
Subject: [Histonet] Her2 Dual ISH and breast processing

Hello all--

My lab is having some problems with inconstant results with our Her2 Dual ISH 
on the Ventana Ultra.  Right now, we know we have a problem with our large 
breast tissue being under-fixed.  There have been many gripes to the PAs and 
residents about the thickness of the tissue sections and they have listened.  
We are now getting breast sections that are consistently cut between 2-3mm in 
thickness.  However, we are still having issues with inconsistency in our dual 
ISH staining.  Many times, the staining is absent.

We are currently processing our breast tissue on a Tissue-Tek VIP6 processor.  
Are there any labs out there that are using this processor and also running 
Her2 Dual ISH on the Ventana with nice, consistent results?  If so, would any 
of you be willing to share your processing protocol?

Thanks in advance for your help! 



Val



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Re: [Histonet] Her2 Dual ISH and breast processing

2012-12-13 Thread Rene J Buesa
Please go to http://www.histosearch.co/rene.html
There are 2 articles on the subject: one about the general fixation issue and 
another about the minimum amount of NBF required to obtain complete fixation.
René J.

From: Hoekert, W.E.J. w.e.j.hoek...@olvg.nl
To: Rene J Buesa rjbu...@yahoo.com; vtol...@cox.net; 
histonet@lists.utsouthwestern.edu 
Sent: Thursday, December 13, 2012 7:35 AM
Subject: RE: [Histonet] Her2 Dual ISH and breast processing

I was wondering,is there any literature on this subject? i.e. the minimal 
required fixation time of breast tissue in order to get reliable immuno 
staining (Oestro, Prog and Her2neu and ISH). We immunologists are alway trying 
to convince our pathologists about the importance of good fixation, but the 
pathologist are always in a hurry to get the diagnosis out. Many mamma biopsies 
do not get to be fixed long enough (some are even put in the processor after a 
few hours of fixation). It would be helpfull if I can show them some literature 
to back me up.

Willem



Van: histonet-boun...@lists.utsouthwestern.edu namens Rene J Buesa
Verzonden: ma 10-12-2012 18:23
Aan: vtol...@cox.net; histonet@lists.utsouthwestern.edu
Onderwerp: Re: [Histonet] Her2 Dual ISH and breast processing



Val:
Acknowledging that you have a fixation problem is the fundamental step to 
solving your staining problems.
You state that the slices have now a consistent thickness of between 2-3 mm and 
that is great BUT what about the fixation time?
Thin slices is a first step but until you have the slices properly fixed, you 
will keep having some problems.
Even when one should never assume, I assume that you are using NBF at room 
temperature. With that fixative and under those temperature conditions, your 
2-3 mm thick breast slices will require 4 hours to be fully penetrated; will 
require 24 hours to be 100% covalent bound and will require 96 hours to be 
completely cross-linked.
The 48 hours of maximum exposition to NBF recommended by ASCO-CAP will 
guarantee a 100% cross-linking of 1 mm thick slices, but your 2-3 mm slices 
will require 96 hours to be completely cross-linked.
Until you reach an optimum fixation you will keep having sporadic problems of 
your protocols (depending on greater or lower fat contents of the samples).
René J.

From: vtol...@cox.net vtol...@cox.net
To: histonet@lists.utsouthwestern.edu
Sent: Monday, December 10, 2012 11:48 AM
Subject: [Histonet] Her2 Dual ISH and breast processing

Hello all--

My lab is having some problems with inconstant results with our Her2 Dual ISH 
on the Ventana Ultra.  Right now, we know we have a problem with our large 
breast tissue being under-fixed.  There have been many gripes to the PAs and 
residents about the thickness of the tissue sections and they have listened.  
We are now getting breast sections that are consistently cut between 2-3mm in 
thickness.  However, we are still having issues with inconsistency in our dual 
ISH staining.  Many times, the staining is absent.

We are currently processing our breast tissue on a Tissue-Tek VIP6 processor.  
Are there any labs out there that are using this processor and also running 
Her2 Dual ISH on the Ventana with nice, consistent results?  If so, would any 
of you be willing to share your processing protocol?

Thanks in advance for your help! 



Val



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[Histonet] VIP6 issue

2012-12-13 Thread Nancy Schmitt
Sorry for the confusion - the cassettes lids are not coming off.  The lid for 
the rack which came with the new processor get off kilter during  processing 
allowing the cassettes to float up out of the rack.
Nancy



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is for the use of only the intended recipient(s) even if addressed
incorrectly. If you are not the intended recipient, please notify the sender
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RE: [Histonet] Space requirements for AP lab

2012-12-13 Thread Morken, Timothy
It's not a theoretical question. 

When I came here I found our EM lab / Muscle histochem Lab / IF lab are crammed 
into one small space. It had 30years of accumulated stuff that no one wanted to 
throw out. There were microscope tables in the middle of walkways, the 
histochem staining area is the primary path into the lab - and the walkway 
itself is inadequately sized - imagine crowding through when staining is going 
on!  

JC inspectors cited the lab for inadequate working space. That put focus on a 
lab that had been largely ignored and we spent a long while decluttering, 
surplussing unused equipment and getting a new, larger,  fume hood. (Thank you 
JC!!)

That said, I think it is a very subjective judgment by an inspector and I am 
not aware of any specific space requirements that any agency applies beyond 
adequate. In this case it was one inspector out of dozens that had been 
through the lab previously.


Tim Morken
Supervisor, Electron Microscopy/Neuromuscular Special Studies
Department of Pathology
UC San Francisco Medical Center


-Original Message-
From: Lynette Pavelich [mailto:lpave...@hurleymc.com] 
Sent: Thursday, December 13, 2012 4:05 AM
To: Morken, Timothy; jmasla...@stpetes.org; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Space requirements for AP lab

We are Joint Commission. I've never run across this issue (and God forbid 
bringing it up in front of one!) in 40+ years and 3 lab renovations. CAP people 
out there??

Lynette


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Morken, Timothy 
[timothy.mor...@ucsfmedctr.org]
Sent: Wednesday, December 12, 2012 4:43 PM
To: jmasla...@stpetes.org; Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Space requirements for AP lab

Administrators rule of thumb: If there is free space in Histology, they are 
taking up too much space!

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
jmasla...@stpetes.org
Sent: Monday, December 10, 2012 9:41 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Space requirements for AP lab

Greetings All, Are there any JACHO or CAP space requirements for an AP 
laboratory? Looking for recommended square footage per tech, equipment, and/or 
work area.
Thanks


Joe Maslanka BS, CT,HT (ASCP)
Anatomical Pathology Technical Supervisor St Peter's Hospital,MT 59601
(P)(406) 447-2406
(F)(406)444-2126

Give thanks for ALL things.
Kindness is the language the blind can see  the deaf can hear- Mark Twain 
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[Histonet] Ubiquitin and alpha synuclein

2012-12-13 Thread Harvey, Jennifer Lynn

What is histoland using to stain Lewy bodies these days? I am not happy with 
the ubiquitin or the alpha synuclein that we have. I would like to know what 
manufactures others are using.

Thanks


Jennifer Harvey, HT(ASCP) QIHC
Vanderbilt University Medical Center
Neuropathology Lab Supervisor
C-2309 Medical Center North
Nashville, TN  37232-2561
Phone: 615-343-0083
Fax: 615-343-7089

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[Histonet] RE: VIP6 issue

2012-12-13 Thread Morken, Timothy
 I talked with the rep. and they said they had never heard of this.

Right. 

Yes, it happens. Often. Too much air caught in the cassettes. Worse with the 
fine-mesh cassettes. Bounce the racks in the formalin tray a few times before 
loading on the processor to try to get as much air out as possible. That will 
improve processing as well. And weight down the tops if it continues.


Tim Morken
Department of Pathology
UC San Francisco Medical Center




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Nancy Schmitt
Sent: Thursday, December 13, 2012 6:17 AM
To: Histonet (histonet@lists.utsouthwestern.edu)
Subject: [Histonet] VIP6 issue

Good Morning-
We have recently purchased  VIP6 processors.  Has anyone else experienced a 
problem with the lids coming off during pump in and pump out?  Causes the 
cassettes to float all over and be completely out of order:(  We now place an 
extra rack or lid on top to weigh down and insure this does not happen.  I 
talked with the rep. and they said they had never heard of this.  I know this 
is not  a huge deal, but with new instrumentation I don't think we be cobbling 
things already.
Thank you for any input-
Nancy Schmitt
Dubuque, IA



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[Histonet] RE: Ubiquitin and alpha synuclein

2012-12-13 Thread Morken, Timothy
Jennifer, Thermo/Lab Vision has some excellent Synuclein antibodies. 

Tim Morken

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Harvey, 
Jennifer Lynn
Sent: Thursday, December 13, 2012 9:03 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Ubiquitin and alpha synuclein


What is histoland using to stain Lewy bodies these days? I am not happy with 
the ubiquitin or the alpha synuclein that we have. I would like to know what 
manufactures others are using.

Thanks


Jennifer Harvey, HT(ASCP) QIHC
Vanderbilt University Medical Center
Neuropathology Lab Supervisor
C-2309 Medical Center North
Nashville, TN  37232-2561
Phone: 615-343-0083
Fax: 615-343-7089

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[Histonet] RE: Ubiquitin and alpha synuclein

2012-12-13 Thread Sebree Linda A
Jennifer,

We use p62/SQSTM1 from MBL (Medical  Biological Laboratories, Co., LTD), code 
M162-3, as our Ubiquitin and alpha Synuclein from Invitrogen, #18-0215.

Linda A. Sebree

University of Wisconsin Hospital  Clinics
IHC/ISH Laboratory
600 Highland Ave.
Madison, WI 53792

(608)265-6596
FAX: (608)262-7174
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Harvey, 
Jennifer Lynn
Sent: Thursday, December 13, 2012 11:03 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Ubiquitin and alpha synuclein


What is histoland using to stain Lewy bodies these days? I am not happy with 
the ubiquitin or the alpha synuclein that we have. I would like to know what 
manufactures others are using.

Thanks


Jennifer Harvey, HT(ASCP) QIHC
Vanderbilt University Medical Center
Neuropathology Lab Supervisor
C-2309 Medical Center North
Nashville, TN  37232-2561
Phone: 615-343-0083
Fax: 615-343-7089

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[Histonet] VIP6 questions

2012-12-13 Thread Nancy Schmitt
We do not use the bulk reservoirs at this time - our storeroom is 6 feet away.  
 
We do automatically rotate paraffin and love it!
Yes - we find the touch screen easy to use.
No problems have developed, but it is still very new. 
Would you share your opinions on these questions?

Nancy Schmitt
United Clinical Laboratories
Dubuque, IA
--

Message: 10
Date: Thu, 13 Dec 2012 09:05:19 -0500
From: Tim Wheelock twheel...@mclean.harvard.edu
Subject: [Histonet] VIP6 Questions
To: Histonet@lists.utsouthwestern.edu
Message-ID: 50c9e09f.2060...@mclean.harvard.edu
Content-Type: text/plain; charset=ISO-8859-1; format=flowed

Good morning Everyone:

For those of you who have a Sakura VIP6, do you actually use the bulk 
reservoirs to let the machine automatically rotate the absolute alcohols and 
xylene?
If not, why not?
Also do you let the machine automatically rotate the paraffin reservoirs, or do 
you do this manually, and if so, why?

Also, do you find the touch screen graphics easy to use?
Have any problems developed with the display itself?

Thanks,

Tim Wheelock
Harvard Brain Bank
McLean Hospital
Belmont, MA


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[Histonet] Maximum bone sample size for methyl methacrylate embedding

2012-12-13 Thread Orla M Gallagher
Dear Histonetters,

Would anyone advise on the maximum size sample of undecalcified bone which
could be properly processed into methyl methacrylate for sectioning and
staining for Goldner's trichrome? Would anyone have a protocol for
processing large bone samples (possibly 2 x1cm) into MMA as most of the
protocols I've seen are based on Bordier trephine 5mm iliac crest biopsies.

Thank you,
Orla

-- 
**
Ms. Orla Gallagher
Bone Analysis Laboratory
Mellanby Centre for Bone Research
D Floor Medical School
University of Sheffield
Beech Hill Road
Sheffield
S10 2RX

Website: http://mellanbycentre.dept.shef.ac.uk

Tel: 00353114-2713337 (office)
  00353114-2713174 (lab)
E-Mail:o.m.gallag...@sheffield.ac.uk


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*BE GREEN:* Keep it on the screen.


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[Histonet] RE: VIP6 issue

2012-12-13 Thread Connolly, Brett M
One of the products I learned about at the 2012 NSH convention was ActivFlo 
tissue cassettes. Designed by JB McCormick (I think) they are biopsy cassettes 
that have side vents to help disperse the trapped air bubbles.

Here is a link from Leica, they sell several different ActiveFlo cassettes... 

http://www.leicabiosystems.com/products/consumables/cassettes-base-molds/biopsy-cassettes/
 

Brett


Brett M. Connolly, Ph.D.
Principal Scientist, Imaging Dept.
Merck  Co., Inc.
PO Box 4, WP-44K
West Point, PA 19486
brett_conno...@merck.com
T- 215-652-2501
F- 215-993-6803



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lynette Pavelich
Sent: Thursday, December 13, 2012 12:45 PM
To: Morken, Timothy; Nancy Schmitt; Histonet (histonet@lists.utsouthwestern.edu)
Subject: [Histonet] RE: VIP6 issue

Tim brings up a good point.
I would monitor the processing in the fine mesh type cassettes as well. For 
years, and I do mean years, we struggled with our tiny specimens. Why did some 
specimens in mesh cassettes do just fine, some notit was an absolute 
nightmare! Monitored how the specimen was handled starting right at the sight 
of surgery on through changing processing schedules/times/heat?/no 
heat/xylene/xylene substitute/staining schedules. We wet the mesh cassettes 
prior to loading, then trying to swish the air pocket out of the cassette 
before processing. (did not experience the lids coming off)

We found that the only thing that has produced consistently good results was 
when we went back to the lens paper. What we think was going on, was that the 
little biopsies would intermittently get caught up in a air bubble during 
processing (agitation, pumping in/out), thus missing being in that current 
solution(s). It truly was a nightmare.. 

We now purchase cheap lens paper, and cut it into 4 squares..paper cutter 
does a large amount quickly and we're good to go. Yes, it is a little more 
hassle unwrapping them in the morning, but if it gives a better quality 
specimen then it doesn't matter!! 

Just my two cents worth;)
Lynette

Lynette Pavelich, HT(ASCP)
Histology Supervisor
Hurley Medical Center
One Hurley Plaza
Flint, MI 48503

ph: 810.262.9948
mobile: 810.444.7966


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Morken, Timothy 
[timothy.mor...@ucsfmedctr.org]
Sent: Thursday, December 13, 2012 12:03 PM
To: Nancy Schmitt; Histonet (histonet@lists.utsouthwestern.edu)
Subject: [Histonet] RE: VIP6 issue

 I talked with the rep. and they said they had never heard of this.

Right.

Yes, it happens. Often. Too much air caught in the cassettes. Worse with the 
fine-mesh cassettes. Bounce the racks in the formalin tray a few times before 
loading on the processor to try to get as much air out as possible. That will 
improve processing as well. And weight down the tops if it continues.


Tim Morken
Department of Pathology
UC San Francisco Medical Center




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Nancy Schmitt
Sent: Thursday, December 13, 2012 6:17 AM
To: Histonet (histonet@lists.utsouthwestern.edu)
Subject: [Histonet] VIP6 issue

Good Morning-
We have recently purchased  VIP6 processors.  Has anyone else experienced a 
problem with the lids coming off during pump in and pump out?  Causes the 
cassettes to float all over and be completely out of order:(  We now place an 
extra rack or lid on top to weigh down and insure this does not happen.  I 
talked with the rep. and they said they had never heard of this.  I know this 
is not  a huge deal, but with new instrumentation I don't think we be cobbling 
things already.
Thank you for any input-
Nancy Schmitt
Dubuque, IA



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for affiliates is available at 

[Histonet] Re: Histonet Digest, Vol 109, Issue 14

2012-12-13 Thread Madeleine Huey
Val,
Go to CAP website (http://www.cap.org/apps/cap.portal) and you will
find the answer to your question, or give them a call @ 800-323-4040.
HER2 have a very specific guide line for clinical test.  My
understanding the fixation should be minimun 6 hrs  maximum 48 hrs.
Your problem could be resolved if you have a good rapid tissue
processor (ie. Leica - Peloris, etc).  We have the same problem with
VIP5 before I purchased the Peloris.  I haven't have one single
re-process since then.
There is a trick to my problem.  Give me an email if you want to know.
Madeleine Huey, HTL  QIHC (ASCP)
madelein...@elcaminohospital.com

On Thu, Dec 13, 2012 at 9:04 AM,
histonet-requ...@lists.utsouthwestern.edu wrote:
 Her2 Dual ISH and breast processing

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[Histonet] Re: VIP6 issue14

2012-12-13 Thread Debbie Dreesen

Nancy,
Like you, we had that problem and had to put something on top to prevent the 
cassettes from floating around. 
 
Debbie Dreesen
 
Message: 11
Date: Thu, 13 Dec 2012 14:17:24 +
From: Nancy Schmitt nancy_schm...@pa-ucl.com
Subject: [Histonet] VIP6 issue
To: Histonet (histonet@lists.utsouthwestern.edu)
    histonet@lists.utsouthwestern.edu
Message-ID:
    906b4da90ed1db4db6c7e94d7cee6c36220c1...@peitha.wad.pa-ucl.com
Content-Type: text/plain; charset=us-ascii

Good Morning-
We have recently purchased  VIP6 processors.  Has anyone else experienced a 
problem with the lids coming off during pump in and pump out?  Causes the 
cassettes to float all over and be completely out of order:(  We now place an 
extra rack or lid on top to weigh down and insure this does not happen.  I 
talked with the rep. and they said they had never heard of this.  I know this 
is not  a huge deal, but with new instrumentation I don't think we be cobbling 
things already.
Thank you for any input-
Nancy Schmitt
Dubuque, IA



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is for the use of only the intended recipient(s) even if addressed
incorrectly. If you are not the intended recipient, please notify the sender
that you have received it in error and then delete it along with any
attachments. Thank you.





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