Re: [Histonet] need tips for cross-sectioning of cortical bone

2010-05-11 Thread Jack Ratliff
Why not embed in resin (MMA) and take thicker sections and then grind/ 
polish them down? If you went this route, you could then use  
flourescent labels and quantify mineral apposition rate and bone  
formation rate. Let me know if you are interested. I can help you get  
started and direct you to low cost equipment options.


Jack

On Apr 22, 2010, at 9:58 AM, Connolly, Brett M brett_conno...@merck.com 
 wrote:



A colleague is having trouble getting wrinkle-free sections of
decalcified, paraffin embedded femur.

Any tips??

Thanks,

Brett M. Connolly, Ph.D.
Molecular Imaging Team Leader
Merck  Co., Inc.
PO Box 4, WP-44K
West Point, PA 19486
tel. 215-652-2501 fax. 215-993-6803
brett_conno...@merck.com



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FW: [Histonet] Are Histotechs considered exempt employees?

2010-05-11 Thread Thomas Jasper
 

-Original Message-
From: Thomas Jasper 
Sent: Tuesday, May 11, 2010 3:45 AM
To: 'Anthony Sandoval'
Cc: 'histonet-boun...@lists.utsouthwestern.edu'
Subject: RE: [Histonet] Are Histotechs considered exempt employees?

Anthony,

Don't know where you live in Cali or where you work.  But if you are an
HTL and have any decent skill/experience, I would think you are being
totally ripped off.  The cost of living in most parts of Cali alone
makes me wonder about this salary.  And when you ask about being
exempt...I'm assuming you are exempt?  If this is the case again a total
rip off.  I think you need to look for work elsewhere and check into
wages.  New students that are registry eligible start out much higher
than that to my knowledge.

Tom Jasper

Thomas Jasper HT (ASCP) BAS
Histology Supervisor
CORPS
Bend, Oregon 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Anthony
Sandoval
Sent: Monday, May 10, 2010 9:01 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Are Histotechs considered exempt employees?

Hello fellow Histotechs, I have recently become certified as an HTL and
was wondering if anyone out there is an 'exempt' employee? I live in
California and feel that I am being taken advantage of.  I make 16.15$
per hour and frequently work 50 hour weeks. Am I off base? should I just
be grateful that I have a job, as my employer so frequently reminds me?
Thank you Histonet! 
you have been an invaluable resource in my career and assisting me in
passing the HTL! 


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[Histonet] RE: Idea for a new recycler

2010-05-11 Thread Beth Austin
If formalin, xylene, hemo-de, Formula 83 and alcohol were all collected as
one waste stream, no recycler could separate this waste into recycled
formalin, recycled solvent (xylene/hemo-de/F83), and recycled alcohol all in
one run due in part to the small range of boiling points and in part to the
azeotropes formed between the various chemicals. In this particular
scenario, the alcohol and the formalin would distill over together along
with any water in the formalin, and there would be a considerable amount
solvent in the alcohol making it contaminated and not of any use in the lab.

If you have any questions, please contact us off site and we'll be happy to
assist you. 

Best Regards, 
Elizabeth Sell
CBG Biotech
1-800-941-9484


-Original Message-
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[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
histonet-requ...@lists.utsouthwestern.edu
Sent: None
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 78, Issue 7

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Today's Topics:

   1. clo test (Tench, Bill)
   2. IDEA FOR A NEW RECYCLER (Madary, Joseph)
   3. RE: RE: Barcode and Tracking Information (Rae Staskiewicz)
   4. CD 133 (Ingles Claire )
   5. Disposable blade holder - amateur microscopist lookingfor a
  cheap one! (Gordon Brown)
   6. Disposable blade holder - amateur microscopist lookingfor a
  cheap one! (Gordon Brown)
   7. NSH Region II Meeting-discount hotel rate deadline is coming
  up! (Goodwin, Diana)
   8. dehydration of hydrated slide (Eva Permaul)
   9. RE: dehydration of hydrated slide (Sebree Linda A)
  10. RE: dehydration of hydrated slide (Mauger, Joanne)
  11. B5 fixative (histot...@imagesbyhopper.com)
  12. myocyte damage (Bartlett, Jeanine (CDC/OID/NCZVED))
  13. RE: Responses to IHC CAP Validation question
  (tonia.richm...@gracepathology.com)
  14. Starting up new lab (Shaw, Sharon)
  15. Formalin fixation time for breast specimens (Richard Cartun)
  16. RE: Responses to IHC CAP Validation question
  (bsulli...@shorememorial.org)
  17. Re: myocyte damage (Merced M Leiker)


--

Message: 1
Date: Wed, 5 May 2010 13:57:20 -0700
From: Tench, Bill bill.te...@pph.org
Subject: [Histonet] clo test
To: histonet@lists.utsouthwestern.edu
Message-ID: 2820431bf953bb4da3e9e1a5882265fd02863...@mail1.pph.local
Content-Type: text/plain; charset=us-ascii

The Clo test is a clinical lab test.  You need to go to that part of the
CPT coding book (sorry I don't have it available).  88300 is an anatomic
code (gross only, ie, it requires examination of a piece of tissue or
foreign body) and is entirely inappropriate for this test.

Bill Tench
Associate Dir. Laboratory Services
Chief, Cytology Services
Palomar Medical Center
555 E. Valley Parkway
Escondido, California  92025
bill.te...@pph.org
Voice: 760- 739-3037
Fax: 760-739-2604
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
histonet-requ...@lists.utsouthwestern.edu
Sent: Wednesday, May 05, 2010 1:36 PM
To: histonet@lists.utsouthwestern.edu
Subject: [BULK] Histonet Digest, Vol 78, Issue 6




Hi everyone,
 
I am looking to see what CPT code everyone is using for reading Clo
Tests in the pathology department. I have heard of using 87081 but I am
not sure if this is accurate as this is for culture and the CLO is
biochemical reaction not a culture.  Currently I have been using 88300
gross only.
Any help would be appreciated.
 
Thank you,
Amy Farnan

***

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Message: 2
Date: Wed, 5 May 2010 17:22:22 -0400
From: Madary, Joseph mada...@medimmune.com
Subject: [Histonet] IDEA FOR A 

RE: [Histonet] Are Histotechs considered exempt employees?

2010-05-11 Thread Heckford, Karen - SMMC-SF
$16.15 per hour. They are getting a great deal.   I believe you should
be making at least double that. What I believe is happening is that a
lot of offices are now starting to open their own labs and they are
trying to get us cheap.  We all need to stick to our guns and not let
them get us cheaper than we are worth.  Yes, I realize that San
Francisco is more but the starting wage for a HT's should be $25.00 to
$30.00 an hour to start for a newly certified tech. No matter of
location in California.  You can always negotiate higher if you have
more experience and more certifications.

Just my two cents worth,

Karen Heckford HT ASCP CE
Lead Histology Technician
St. Mary's Medical Center
450 Stanyan St.
San Francisco, Ca. 94117
415-668-1000 ext. 6167

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Anthony
Sandoval
Sent: Monday, May 10, 2010 9:01 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Are Histotechs considered exempt employees?

Hello fellow Histotechs, I have recently become certified as an HTL and
was 
wondering if anyone out there is an 'exempt' employee? I live in
California 
and feel that I am being taken advantage of.  I make 16.15$ per hour and

frequently work 50 hour weeks. Am I off base? should I just be grateful
that 
I have a job, as my employer so frequently reminds me? Thank you
Histonet! 
you have been an invaluable resource in my career and assisting me in 
passing the HTL! 


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[Histonet] RE: Histonet Digest, Vol 78, Issue 12

2010-05-11 Thread Nancy Schmitt
Hi Jason

We cut 200+ a day - we have histo tech in at 400, 430, 500 and 2 at 6am.  One 
is student in training, and one is on the brink of retirement, so there will be 
only 1 coming in at 6.  I am the coordinator the dept. so after cutting is 
finished, and if we are at full staff, I then switch to desk work.

Nancy Schmitt HT, MLT (ASCP)
Histology Coordinator
Dubuque, IA


Message: 3
Date: Mon, 10 May 2010 08:43:30 -0400
From: Jason Keller jke...@capefearvalley.com
Subject: [Histonet] Number of Techs
To: histonet@lists.utsouthwestern.edu
Message-ID:
7d41e97c787df44996e0055c81703663f17...@ntexchange3.capefear.local
Content-Type: text/plain; charset=us-ascii

Hello,

 

I am looking to compile information on the average number of techs that
different hospitals have in their histology labs.  I would appreciate
any feedback that I could get as far as how many techs are used to run
hospital histology labs with a block count range of 200 to 400 blocks
per day. 

 

Thanks for any input you can provide,

 

Jason


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[Histonet] Cytotech Position

2010-05-11 Thread Sheila Haas
Hi everyone! If anyone knows a cytotechnologist interested in a position, we 
have one here in Lakeland, Florida. It is a full-time position, M-F and 
candidate must have FL state license or be eligible to obtain one. 
Please contact me for further information. Thank you in advance.
 
Sheila Haas
Laboratory Supervisor
MicroPath Laboratories, Inc.


   
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RE: [Histonet] Specimen Delivery

2010-05-11 Thread Horn, Hazel V
We have a central drop off area.  Occasionally we will have shared
specimens with microbiology and shared fluid specimens with the clinical
lab.   This helps ensure all tests ordered are performed.   We pick up
our specimens from the central area.

Hazel Horn
Hazel Horn, HT/HTL (ASCP)
Supervisor of Histology
Arkansas Children's Hospital
1 Children's WaySlot 820
Little Rock, AR   72202
 
phone   501.364.4240
fax501.364.3155
 
visit us on the web at:www.archildrens.org
 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
mwh...@mcleodhealth.org
Sent: Monday, May 10, 2010 1:35 PM
To: histonet@lists.utsouthwestern.edu
Cc: tbai...@mcleodhealth.org
Subject: [Histonet] Specimen Delivery 


For those of you who do tissue/cytology  processing in a hospital or
similar facility: Are tissue or fluid specimens brought directly to the
Anatomic Pathology/Cytology area, or are specimens dropped off in a
clinical accessioning area ?  We are debating the pros/cons of having
our
specimens dropped at a centralized location  since our Lab is becoming
more
spread out and nurses are confused about where to bring stuff.


Melanie S. White, MT(ASCP)
Laboratory Supervisor, Systems/Anatomic Pathology
McLeod Regional Medical Center
(843) 777-2072


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RE: [Histonet] Are Histotechs considered exempt employees?

2010-05-11 Thread Kim . Donadio
Starting out at $16 an hour is not acceptable. I've hired recently 
graduated students at a better pay than that. And this is Florida where 
the cost of living is a lot cheaper than Cali. 

Hope this helps. :-) 

Kim Donadio 
Pathology Supervisor
Baptist Hospital
1000 W Moreno St.
Pensacola FL 32501
Phone (850) 469-7718
Fax (850) 434-4996



Heckford, Karen - SMMC-SF karen.heckf...@chw.edu 
Sent by: histonet-boun...@lists.utsouthwestern.edu
05/11/2010 07:15 AM

To
Anthony Sandoval sandoval.1...@hotmail.com
cc
histonet@lists.utsouthwestern.edu
Subject
RE: [Histonet] Are Histotechs considered exempt employees?






$16.15 per hour. They are getting a great deal.   I believe you should
be making at least double that. What I believe is happening is that a
lot of offices are now starting to open their own labs and they are
trying to get us cheap.  We all need to stick to our guns and not let
them get us cheaper than we are worth.  Yes, I realize that San
Francisco is more but the starting wage for a HT's should be $25.00 to
$30.00 an hour to start for a newly certified tech. No matter of
location in California.  You can always negotiate higher if you have
more experience and more certifications.

Just my two cents worth,

Karen Heckford HT ASCP CE
Lead Histology Technician
St. Mary's Medical Center
450 Stanyan St.
San Francisco, Ca. 94117
415-668-1000 ext. 6167

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Anthony
Sandoval
Sent: Monday, May 10, 2010 9:01 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Are Histotechs considered exempt employees?

Hello fellow Histotechs, I have recently become certified as an HTL and
was 
wondering if anyone out there is an 'exempt' employee? I live in
California 
and feel that I am being taken advantage of.  I make 16.15$ per hour and

frequently work 50 hour weeks. Am I off base? should I just be grateful
that 
I have a job, as my employer so frequently reminds me? Thank you
Histonet! 
you have been an invaluable resource in my career and assisting me in 
passing the HTL! 


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RE: [Histonet] per deim work

2010-05-11 Thread Gill, Caula A.
Have you tried Aerotech scientific(sp). I know they are in several states you 
should look them up in your area. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of richard shook
Sent: Monday, May 10, 2010 2:23 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] per deim work

Hello Histoland 

I have question pertaining to temporary histology tech work/per Diem 
positions.I find myself currently out of work and am looking for my next 
adventure in  the great world of histology and one of the ideas i had was to 
check out the possibility's of doing temp work.The only thing is I'm not sure 
if there is a temp agency for histo techs,or is there someone in histo land 
that currently working as a temp . I would greatly appreciate any help in my 
endeavors into this new world. Any information as to how much the pay rate or 
what to charge for daily work travel lodging or any other expenses that would 
be incurred in this type of work.

Thanks for any help
Richard Shook HT(ASCP)


  

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Re: [Histonet] Are Histotechs considered exempt employees?

2010-05-11 Thread Andrea Grantham

Anthony,
You live in CA, work 50 hour weeks and you are a HTL with an  
unprecedented and valuable resource at your disposal, Histonet and you  
know how to use it. For this you get paid $16.15/hour by what appears  
to be an employer who isn't grateful to have you. I'd start looking  
for another job.

Just my humble opinion.

Andi

Andrea Grantham, HT (ASCP)
Senior Research Specialist
University of Arizona
Cell Biology and Anatomy
Histology Service Laboratory
P.O.Box 245044
Tucson, AZ 85724

algra...@email.arizona.edu
Tel: 520.626.4415 Fax: 520.626.2097

happy slicing and dicing and may all your stains work perfectly -  
Paula Sicurello

P Please consider the environment before printing this email.




On May 10, 2010, at 9:00 PM, Anthony Sandoval wrote:

Hello fellow Histotechs, I have recently become certified as an HTL  
and was wondering if anyone out there is an 'exempt' employee? I  
live in California and feel that I am being taken advantage of.  I  
make 16.15$ per hour and frequently work 50 hour weeks. Am I off  
base? should I just be grateful that I have a job, as my employer so  
frequently reminds me? Thank you Histonet! you have been an  
invaluable resource in my career and assisting me in passing the HTL!


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RE: [Histonet] Are Histotechs considered exempt employees?

2010-05-11 Thread Heckford, Karen - SMMC-SF
I am so with you on this one.   HT's need to start demanding and
higher wages everywhere.  We are a rare breed with special talents.
Without a good tech you do not get good slides!!  We are not a dime a
dozen.  AUGH!  

I know just a hour north of where I am the wages can be $10-$15.00 less.
Not much difference in living expenses either.


Karen Heckford HT ASCP CE
Lead Histology Technician
St. Mary's Medical Center
450 Stanyan St.
San Francisco, Ca. 94117
415-668-1000 ext. 6167

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Andrea
Grantham
Sent: Tuesday, May 11, 2010 7:35 AM
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Are Histotechs considered exempt employees?

Anthony,
You live in CA, work 50 hour weeks and you are a HTL with an  
unprecedented and valuable resource at your disposal, Histonet and you  
know how to use it. For this you get paid $16.15/hour by what appears  
to be an employer who isn't grateful to have you. I'd start looking  
for another job.
Just my humble opinion.

Andi

Andrea Grantham, HT (ASCP)
Senior Research Specialist
University of Arizona
Cell Biology and Anatomy
Histology Service Laboratory
P.O.Box 245044
Tucson, AZ 85724

algra...@email.arizona.edu
Tel: 520.626.4415 Fax: 520.626.2097

happy slicing and dicing and may all your stains work perfectly -  
Paula Sicurello
P Please consider the environment before printing this email.




On May 10, 2010, at 9:00 PM, Anthony Sandoval wrote:

 Hello fellow Histotechs, I have recently become certified as an HTL  
 and was wondering if anyone out there is an 'exempt' employee? I  
 live in California and feel that I am being taken advantage of.  I  
 make 16.15$ per hour and frequently work 50 hour weeks. Am I off  
 base? should I just be grateful that I have a job, as my employer so  
 frequently reminds me? Thank you Histonet! you have been an  
 invaluable resource in my career and assisting me in passing the HTL!

 ___
 Histonet mailing list
 Histonet@lists.utsouthwestern.edu
 http://lists.utsouthwestern.edu/mailman/listinfo/histonet


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RE: [Histonet] need tips for cross-sectioning of cortical bone

2010-05-11 Thread gayle callis
You did not say whether these are cross sections or mid sagittal?  Cross
sections are always tougher.  Key is to make sure the cortical bone is well
processed and infiltrated with a hard paraffin e.g. Tissue Prep 2 (Fisher
Scientific ala Thermo Scientific).  Try this old bonehead trick is cut tiny
V-shaped notches with razor blade or used microtome blade on the sides of
block, parallel to the blade.  You may have to do this top and bottom too.
Take care to NOT make these notches huge.  This permits the paraffin of each
section in ribbon to expand, relax onto the water bath along with the bone
section. 

Another trick is try laying section on RT 5 to 10% alcohol, pick up on
slide, then go to warm water bath, lower section slowly to flattening.  The
key here is to NOT let upper part of paraffin of a section totally release
from slide while going into warm water (at an angle) in other words, the
section flattens while paraffin portion is still attached to slide during
flattening. 

Also, change the blade frequently.  Sharpest possible edge helps, and
hopefully high profile which is more stable than low profile for decalcified
bone microtomy.  

Good luck

Gayle M. Callis
HTL/HT/MT(ASCP)



   

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jack Ratliff
Sent: Tuesday, May 11, 2010 5:03 AM
To: Connolly, Brett M
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] need tips for cross-sectioning of cortical bone

Why not embed in resin (MMA) and take thicker sections and then grind/ 
polish them down? If you went this route, you could then use  
flourescent labels and quantify mineral apposition rate and bone  
formation rate. Let me know if you are interested. I can help you get  
started and direct you to low cost equipment options.

Jack

On Apr 22, 2010, at 9:58 AM, Connolly, Brett M brett_conno...@merck.com 
  wrote:

 A colleague is having trouble getting wrinkle-free sections of
 decalcified, paraffin embedded femur.

 Any tips??

 Thanks,

 Brett M. Connolly, Ph.D.
 Molecular Imaging Team Leader
 Merck  Co., Inc.
 PO Box 4, WP-44K
 West Point, PA 19486
 tel. 215-652-2501 fax. 215-993-6803
 brett_conno...@merck.com



 Notice:  This e-mail message, together with any attachments,  
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 Whitehouse Station, New Jersey, USA 08889), and/or its affiliates  
 Direct contact information for affiliates is available at
http://www.merck.com/contact/contacts.html 
 ) that may be confidential, proprietary copyrighted and/or legally  
 privileged. It is intended solely for the use of the individual or  
 entity named on this message. If you are not the intended recipient,  
 and have received this message in error, please notify us  
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[Histonet] Article for Er/PR vaidation

2010-05-11 Thread Liz Chlipala
Hello everyone

 

I have been trying to locate this article on line and I'm either
challenged or its not there.  

 

Its from the Arch Pathol Lab Med (in press)  it says in press so I don't
know what that that means but its not available off the Journals web
site

 

Fitzgibbons, P. L. , D. A. Murphy , M. E. H. Hammond , et al.
Recommendations for validating estrogen and progesterone receptor
immunohistochemistry assays. Arch Pathol Lab Med (in press). 

 

Does anyone have a copy of this that they are willing to forward to me,
the new ER/PR guidelines that just came out reference this article for
validation, even through at the end of the article there is a statement
---  there is no universal acceptable procedure for validating tests
any help would be appreciated.

 

Thanks in advance

 

Liz

 

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC

Manager

Premier Laboratory, LLC

PO Box 18592

Boulder, Colorado 80308

office (303) 682-3949 

fax (303) 682-9060

www.premierlab.com

 

 

Ship to Address:

1567 Skyway Drive, Unit E

Longmont, Colorado 80504

 

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[Histonet] processing/cutting cell blocks

2010-05-11 Thread Carol Bryant
We typically use a media called histogel for our cytology cell blocks with very 
good results.  Our pathologists also send us clots from other locations that 
they are collecting like a bone marrow aspirate clot.  The FNAs are expressed 
into a lid and allowed to clot.  We are processing these on an overnight run 
used for all our other cases.  The histotechs are having a great deal of 
trouble cutting these as they are very dried out and break apart on the water 
bath.  Is there any techniques you can recommend to get better results when 
cutting  specimens collected this way?  I would think we need to process them 
on a shorter program to begin with.

Thank you in advance for any suggestions.

Carol Bryant, CT (ASCP)
Cytology/Histology Manager
Pathology Services
Lexington Clinic
Phone (859) 258-4082
Fax (859) 258-4081
cb...@lexclin.com



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[Histonet] Thanks for bone cutting suggestions - and anti-Rat CD3

2010-05-11 Thread Connolly, Brett M
Thanks to all for your suggestions for cutting cross sections of
cortical bone. I have passed them along.

Now, what is the latest on CD3 IHC in FFPE rat tissues. I saw Ray
Koelling's suggestion in the archives using an Ab from BD Biosciences.
Is it cat # 550295?

What others if any do you suggest? HEIR ? protocol tips?

Thanks,
Brett

Brett M. Connolly, Ph.D.
Molecular Imaging Team Leader
Merck  Co., Inc.
PO Box 4, WP-44K
West Point, PA 19486
tel. 215-652-2501 fax. 215-993-6803
brett_conno...@merck.com

 
Notice:  This e-mail message, together with any attachments, contains
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[Histonet] Forwarding Request for Control Mehtod

2010-05-11 Thread WILLIAM DESALVO

 I wonder if you could help me find someone who would kindly donate a
 paraffin tissue block containing candida or other fungi to be used as a
 control block. We have had difficulty in obtaining such tissue and have
 tried all the hospitals in northern Ireland for a tissue block suitable
 enough to act as a control. Many of the pathology departments are in the
 same position as ourselves in that the control tissue being used is
 getting in short supply. 
 
 I tried to make one using a culture from microbiology with fresh lambs
 lung from a local abattoir but unfortunately the tissue seems to stain
 with PAS as well and the candida where obscured although visible
 probably due to post mortem changes in the tissue.
 
 Alternatively have any of your members successfully produced fungal
 control material by other means. 
 
 Thanking you in advance
 
 Ian Clarke
 Biomedical Scientist
 Cellular Pathology Department
 Craigavon Area Hospital 
 Sothern Health and Social Services Trust.
 66 Lurgan Road
 Craigavon
 BT63 5QQ
 Northern Ireland


William DeSalvo, B.S., HTL(ASCP)



  
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RE: [Histonet] Thanks for bone cutting suggestions - and anti-Rat CD3

2010-05-11 Thread Liz Chlipala
Dako has a rabbit polyclonal that works in rat.  The other thing with
the bone, is place the slide with a section on a flat hotplate (60 C)
until it turns clear - not too long or the articular cartilage will
flip.

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Manager
Premier Laboratory, LLC
PO Box 18592
Boulder, Colorado 80308
office (303) 682-3949 
fax (303) 682-9060
www.premierlab.com
 
 
Ship to Address:
1567 Skyway Drive, Unit E
Longmont, Colorado 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Connolly, Brett M
Sent: Tuesday, May 11, 2010 11:38 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Thanks for bone cutting suggestions - and anti-Rat
CD3

Thanks to all for your suggestions for cutting cross sections of
cortical bone. I have passed them along.

Now, what is the latest on CD3 IHC in FFPE rat tissues. I saw Ray
Koelling's suggestion in the archives using an Ab from BD Biosciences.
Is it cat # 550295?

What others if any do you suggest? HEIR ? protocol tips?

Thanks,
Brett

Brett M. Connolly, Ph.D.
Molecular Imaging Team Leader
Merck  Co., Inc.
PO Box 4, WP-44K
West Point, PA 19486
tel. 215-652-2501 fax. 215-993-6803
brett_conno...@merck.com

 
Notice:  This e-mail message, together with any attachments, contains
information of Merck  Co., Inc. (One Merck Drive, Whitehouse Station,
New Jersey, USA 08889), and/or its affiliates Direct contact information
for affiliates is available at 
http://www.merck.com/contact/contacts.html) that may be confidential,
proprietary copyrighted and/or legally privileged. It is intended solely
for the use of the individual or entity named on this message. If you
are
not the intended recipient, and have received this message in error,
please notify us immediately by reply e-mail and then delete it from 
your system.
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[Histonet] CYP.07680 - cytology cross contamination

2010-05-11 Thread Brandi Higgins
Hello all,

For CAP policy CYP.07680 for procedures to prevent cross-contamination of
specimens during processing and staining - what are your labs doing?

 I work in a small lab so the histotechs process the cytology specimens and
the pathologists read the slides (we have no PA's or cytoprep techs or
cytotechs to screen slides).  We also process only non-GYN, so we don't have
to worry about GYN/non-GYN cross contamination.

The notes under this policy say procedures must prevent cross-contamination
between highly cellular specimens and suggest the screening method of
toluidine blue stain to determing if specimens are highly cellular.

Does anyone use the toluidine blue for this purpose?  If so could you tell
me the procedure for toluidine blue you use?  And how do you determing which
specimens you stain with toluidine blue and what qualifies as highly
cellular.  If so do you retain these toluidine blue slides for any period of
time?

CAP policy also suggests inserting a clean blank slide in each stain run and
examine for contamination.  Is anyone doing this?

We have been inspected before with no problems with this CAP question, but I
just want to make sure we are doing everything we can to prevent
cross-contamination.

Thanks in advance for your input!
Brandi Higgins, HT (ASCP)
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[Histonet] L-DNAse II vs neutrophil (leukocyte) elastase inhibitor

2010-05-11 Thread Fabrice gankam
Hi guys
Would like to know if any of you have used the L DNAse II or the serpin B1
antibody in the rat.
very few references mentioning this antibody. Sigma has one prestige
antibody for serpin B1 but do no know if it will work on rats.
I was wondering if the DNAse II is the equivalent of the L DNAse II (product
of the degradation of serpin)
thanks for your help
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[Histonet] ICC

2010-05-11 Thread sgoebel

   Hello all,

   I am starting ICC and flourescence for  the first time.  I have done
   tons  of  IHC  in  the  past  with DAB and AEC=   staining, but I am
   slightly confused with the way the flourescence  works.  Do you have
   to  buy  a  secondary  that  is  already tagged, or is=   there some
   system  where  it  attaches to the secondary like DAB does? =   Does
   anyone have any advice or some site where I can go to get some info on
   this.   Also,  what  do you use for positive and negative controls fo   r  
ICC?

   Thanks fellow histo hotties!!

   [DEL: Sarah= Goebel, B.A., HT (ASCP) :DEL]

   Histotechni= cian

   XBiotech USA Inc.

   8201 East Riverside Dr. Bldg 4 Suite 100

   Austin, Texas  78744
   (512)386-5107
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[Histonet] Genemed antibodies

2010-05-11 Thread Toine van der Aa
Hi,

Does anybody have experience with Genemed Biotechnologies antibodies and/or 
probes of Histosonda?


Kind regards,

A.Van der Aa


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RE: [Histonet] CYP.07680 - cytology cross contamination

2010-05-11 Thread Jeter, Brent
Hi Brandi,

The clean, blank slide is some times inserted between cases in the staining 
rack to determine if floaters are present.  It's sort of a retroactive test - 
if you see cells on the blank slide, then you already have cross-contamination 
and you need to re-prep and restain the cases separately.  Some people feel 
that you've caught the floaters on your clean slide and the problem is solved, 
but there's no guarantee others won't be present on your specimen slides, too.

Toluidine blue is an example of a stain you could use to determine cellularity; 
another option often used is a modified Wright Giemsa stain such as Diff-Quik.  
You're not looking to make a final diagnosis, but to make a quick preparation 
and use a simple stain just to see if there are a lot of cells present.  This 
is a more proactive test.  The idea is that highly cellular specimens have an 
increased likelihood of shedding cells into the stains and contaminating other 
cases; it also can be used to identify obviously malignant cases, which should 
definitely be stained separately.

If you're using a rapid stain to look for high cellularity, you need to 
centrifuge and concentrate the specimen(s) first, just as you would in regular 
prep.  The Diff-Quik stain is a Romanovsky stain and is used on air-dried 
slides, so there's no need for fixation.

Hope that helps - 


Brent Jeter
Anatomic Pathology Supervisor
The George Washington University Hospital
202-715-5076 (phone)
202-715-4691 (fax)
brent.je...@gwu-hospital.com

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Brandi Higgins 
[brandihigg...@gmail.com]
Sent: Tuesday, May 11, 2010 2:55 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] CYP.07680 - cytology cross contamination

Hello all,

For CAP policy CYP.07680 for procedures to prevent cross-contamination of
specimens during processing and staining - what are your labs doing?

 I work in a small lab so the histotechs process the cytology specimens and
the pathologists read the slides (we have no PA's or cytoprep techs or
cytotechs to screen slides).  We also process only non-GYN, so we don't have
to worry about GYN/non-GYN cross contamination.

The notes under this policy say procedures must prevent cross-contamination
between highly cellular specimens and suggest the screening method of
toluidine blue stain to determing if specimens are highly cellular.

Does anyone use the toluidine blue for this purpose?  If so could you tell
me the procedure for toluidine blue you use?  And how do you determing which
specimens you stain with toluidine blue and what qualifies as highly
cellular.  If so do you retain these toluidine blue slides for any period of
time?

CAP policy also suggests inserting a clean blank slide in each stain run and
examine for contamination.  Is anyone doing this?

We have been inspected before with no problems with this CAP question, but I
just want to make sure we are doing everything we can to prevent
cross-contamination.

Thanks in advance for your input!
Brandi Higgins, HT (ASCP)
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[Histonet] Labomed LX400 compound microscope

2010-05-11 Thread Steve Wong
Hello,

 

Does anyone have any experience with that Labomed Lx 400 compound
microscope?  It is new and it is cheap (scope with Moticam 2000 camera -
~$2,000), but I cannot find any reviews on it.

 

I'm looking for a simple microscope to take digital pictures of cross
sections of rat spinal cords for some volumetric measurements.

 

Steve

 

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RE: [Histonet] Forwarding Request for Control Mehtod

2010-05-11 Thread Tony Henwood
Ian,

What I have done in the past is to raid the Staff Fridge (or your son's
bedroom!).
There is usually old food left there that has gone moldy - bread or even
strawberries.
Wearing gloves  in a fume hood slice the bread or fruit into slices
(ensuring visible growth of fungi is present), fix for two or more days
in NBF, process as usual.

Voila - fungi controls

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 4001, Westmead NSW 2145, AUSTRALIA 




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of WILLIAM
DESALVO
Sent: Wednesday, 12 May 2010 4:01 AM
To: histonet
Subject: [Histonet] Forwarding Request for Control Mehtod



 I wonder if you could help me find someone who would kindly donate a 
 paraffin tissue block containing candida or other fungi to be used as 
 a control block. We have had difficulty in obtaining such tissue and 
 have tried all the hospitals in northern Ireland for a tissue block 
 suitable enough to act as a control. Many of the pathology departments

 are in the same position as ourselves in that the control tissue being

 used is getting in short supply.
 
 I tried to make one using a culture from microbiology with fresh lambs

 lung from a local abattoir but unfortunately the tissue seems to stain

 with PAS as well and the candida where obscured although visible 
 probably due to post mortem changes in the tissue.
 
 Alternatively have any of your members successfully produced fungal 
 control material by other means.
 
 Thanking you in advance
 
 Ian Clarke
 Biomedical Scientist
 Cellular Pathology Department
 Craigavon Area Hospital
 Sothern Health and Social Services Trust.
 66 Lurgan Road
 Craigavon
 BT63 5QQ
 Northern Ireland


William DeSalvo, B.S., HTL(ASCP)



  
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[Histonet] RE: L-DNAse II vs neutrophil (leukocyte) elastase inhibitor

2010-05-11 Thread Fabrice GANKAM
 

Hi guys

Would like to know if any of you have used the L DNAse II or the serpin B1
antibody in the rat.

very few references mentioning this antibody. Sigma has one prestige
antibody for serpin B1 but do no know if it will work on rats.

I was wondering if the DNAse II is the equivalent of the L DNAse II (product
of the degradation of serpin)

thanks for your help

 

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