[Histonet] Mohs HE QC

2010-12-01 Thread Breal, Kari
What is the easiest way to be compliant with the CLIA guideline of a daily HE 
positive and negative control slide in a Mohs lab?  Would a slide with a known 
positive and a known negative precut and stored in the freezer, then one run 
with the first case be acceptable?  Anyone performing Mohs, please let me know 
how you are handling this.

Thanks,
Kari




 
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[Histonet] used equipment

2010-12-01 Thread Matthew Frindall
Hello All,
I'm an amateur microscopist, mostly interested in botanical specimens. I
recently acquired an American Optical A820 microtome. It appears to be in
good working condition but is missing the blade. I am considering purchasing
a used blade or a used disposable blade holder from Ebay or a lab surplus
website. I realise the condition of this material may not be optimal and
unfortunately the sellers generally do not know the history of these items.
My question is - should I be worried about safety? If there is a chance this
material came from pathology labs, do I need worry about any potential
prions/viruses etc?
Thanks in advance,
Matthew
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[Histonet] RE: Mohs HE QC

2010-12-01 Thread John Shelley
Hi Kari,

I worked doing Mohs for over 10 years and the way that we handled the issue of 
a quality control slide is that typically you can find some positive and 
negative areas within the first patient sample. We would take the very first 
sample and section for the control slide and run it down to ensure that the 
stainer was set-up correctly and that the solutions were still viable.

If you have any other questions please feel free to contact me. Thanks!!!

Kind Regards!
 
John J Shelley
Senior Research Associate, Histology Core Facility
Sanford-Burnham Medical Research Institute at Lake Nona
6400 Sanger Road    
Orlando, FL 32827    
Tel: (407) 745-2000 Ext.2517
Fax: (407) 745-2001
email:  jshel...@sanfordburnham.org



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Breal, Kari
Sent: Wednesday, December 01, 2010 8:11 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Mohs HE QC 

What is the easiest way to be compliant with the CLIA guideline of a daily HE 
positive and negative control slide in a Mohs lab?  Would a slide with a known 
positive and a known negative precut and stored in the freezer, then one run 
with the first case be acceptable?  Anyone performing Mohs, please let me know 
how you are handling this.

Thanks,
Kari




 
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[Histonet] sentinel nodes

2010-12-01 Thread King, Laurie
Good morning all,

I've been having a strange artifact on sentinel nodes, in only one lab of the 
two where I perform frozen sectioning services. This artifact does not show up 
any any other tissue type either.

The node is usually almost totally covered with a bubbling, like the tissue is 
not laying flat. There can be intermittent unaffected areas. These aren't round 
bubbles, more rectangular and almost orderly in their pattern. I can do nodes 
in the other lab and they are fine. A colleague here was wondering if the 
tissue came in saline or some other liquid, which it hasn't. 

Any ideas?

Laurie King HT (ASCP

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RE: [Histonet] sentinel nodes

2010-12-01 Thread sgoebel
Crystals maybe?  How cold is the cryostat?

Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of King,
Laurie
Sent: Wednesday, December 01, 2010 8:01 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] sentinel nodes

Good morning all,

I've been having a strange artifact on sentinel nodes, in only one lab
of the two where I perform frozen sectioning services. This artifact
does not show up any any other tissue type either.

The node is usually almost totally covered with a bubbling, like the
tissue is not laying flat. There can be intermittent unaffected areas.
These aren't round bubbles, more rectangular and almost orderly in their
pattern. I can do nodes in the other lab and they are fine. A colleague
here was wondering if the tissue came in saline or some other liquid,
which it hasn't. 

Any ideas?

Laurie King HT (ASCP

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[Histonet] The Milestone PATHOS

2010-12-01 Thread Annette Featherstone
Has anyone used or is currently using The Milestone PATHOS for tissue
processing? What are your results, pros and cons? Would this be good for
breast biopsies?
Thanks
 
Annette Featherstone
 
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Re: [Histonet] c-erbB2

2010-12-01 Thread Mark Turner
Yes.  What's up with that?


Mark



 Cindy Bulmer cjbul...@sbcglobal.net wrote: 
 Hello Histoland,
  
 Has anyone seen any B-9 ducts staining positive with the c-erbB2 Oncoprotein
 (Rabbit, conc.) # A0485 from Dako?
  
 Thank you,
 Cindy
 
 Cynthia Bulmer HT(ASCP)QIHC
 IHC Supervisor, CTPL
 Waco, TX
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[Histonet] Special Stain Automation

2010-12-01 Thread Barbara Richmond
We are in the market for a new stainer to do special stains.  We
currently are using the Nexus and have been unhappy with it,
particularly with the silver stains for which we do a lot of.  I'm
wondering what techs out there recommend for us to check into.



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[Histonet] H. PYLORI STAIN

2010-12-01 Thread Rathborne, Toni
Hi,
I was wondering if anyone has used the Poly Scientific Rapid Staining Method 
for H. Pylori in Gastric Biopsies staining kit.  Is it easy to use? Is the 
stain crisp and easy to read? Any feedback would be appreciated.

Toni


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[Histonet] RE: Special Stain Automation

2010-12-01 Thread Nails, Felton
The problem with the Nexus is that you can not do silver and AFB on the same 
run.
We use the Dako artisan with very consistent results and it is very easy to 
use. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Barbara Richmond
Sent: Wednesday, December 01, 2010 9:56 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Special Stain Automation

We are in the market for a new stainer to do special stains.  We currently are 
using the Nexus and have been unhappy with it, particularly with the silver 
stains for which we do a lot of.  I'm wondering what techs out there recommend 
for us to check into.



-
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positive impact in the lives and health of persons and communities by providing 
quality services guided by Christian values. Avera is sponsored by the 
Benedictine and Presentation Sisters.
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 The information in this e-mail may be confidential and/or
 privileged.  If you are not the intended recipient or an
 authorized representative of the intended recipient, you
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 copying of this e-mail and its attachments, if any, or
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[Histonet] RE: Special Stain Automation

2010-12-01 Thread Weems, Joyce
I recommend the Artisan from DAKO. J

Joyce Weems 
Pathology Manager 
Saint Joseph's Hospital 
5665 Peachtree Dunwoody Rd NE 
Atlanta, GA 30342 
678-843-7376 - Phone 
678-843-7831 - Fax 

 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Barbara Richmond
Sent: Wednesday, December 01, 2010 10:56
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Special Stain Automation

We are in the market for a new stainer to do special stains.  We currently are 
using the Nexus and have been unhappy with it, particularly with the silver 
stains for which we do a lot of.  I'm wondering what techs out there recommend 
for us to check into.



-
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positive impact in the lives and health of persons and communities by providing 
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Benedictine and Presentation Sisters.
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RE: [Histonet] Special Stain Automation

2010-12-01 Thread Feher, Stephen
Barbara,

We are using the Dako Artisan Link for our special stains and love it.
We are getting set to interface the Link to our LIS (SoftPath).  This
will give us the capability to use the barcodes printed on our slides to
bring up the pathologist order directly on the Artisan.  We also do a
fair number of GMS stains on Non-gyn Thin Prep slides for respiratory
specimens looking for Pneumocystis.  

I would recommend getting a demo from the Dako rep. 


Steve

Stephen A. Feher, MS, SCT (ASCP)

Pathology Supervisor

Catholic Medical Center

100 McGregor Street

Manchester, NH 03102

603-663-6707

sfe...@cmc-nh.org



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Barbara
Richmond
Sent: Wednesday, December 01, 2010 10:56 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Special Stain Automation

We are in the market for a new stainer to do special stains.  We
currently are using the Nexus and have been unhappy with it,
particularly with the silver stains for which we do a lot of.  I'm
wondering what techs out there recommend for us to check into.



-
Avera is a health ministry rooted in the Gospel. Our mission is to make
a positive impact in the lives and health of persons and communities by
providing quality services guided by Christian values. Avera is
sponsored by the Benedictine and Presentation Sisters.
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[Histonet] Question from one of our researchers

2010-12-01 Thread Johnson, Teri
Can someone give me ideas to pass along to one of our researchers? Of course 
adhesion molecule antibodies are the first thought, but not for heterogeneous 
cell populations. So I was wondering maybe an antibody cocktail? Are there any 
lectins that might show this? Thanks!

I am wondering what kind of cell membrane marker is recommended to stain 
tissue section for imaging (going to process the image with 3D Imaris software).
Cells are mouse tissue section in paraffin and very heterogeneous. To see 
cell-cell boundary clearly.

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Re: [Histonet] Question from one of our researchers

2010-12-01 Thread Adam .
While not a cell membrane marker, you can often use differential
interference contrast (DIC) microscopy. The microscope I use has a special
setting that lets you add DIC without any additional staining. In the mouse
bone marrow paraffin sections, it lets you see most edges of most cells.

Adam

On Wed, Dec 1, 2010 at 11:19 AM, Johnson, Teri t...@stowers.org wrote:

 Can someone give me ideas to pass along to one of our researchers? Of
 course adhesion molecule antibodies are the first thought, but not for
 heterogeneous cell populations. So I was wondering maybe an antibody
 cocktail? Are there any lectins that might show this? Thanks!

 I am wondering what kind of cell membrane marker is recommended to stain
 tissue section for imaging (going to process the image with 3D Imaris
 software).
 Cells are mouse tissue section in paraffin and very heterogeneous. To see
 cell-cell boundary clearly.

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[Histonet] Small biopsy specimens

2010-12-01 Thread Sharon . Davis-Devine
We have been using eosin to stain our small biopsies prior to tissue processing 
so that they are easier to see when embedding.  Recently one of our PA's 
started using Hematoxylin instead of the eosin, because that is what they used 
where she trained. Upon further investigation the manufacturers of both of our 
tissue processors discourage the use of eosin because it is very hard on the 
working parts of the machines and requires more PM's to prevent damage.  So we 
are considering switching to using Heme instead.  Do any of you out there use 
Heme on your biopsy specimens?  Do your embedders find it easier to see these 
tiny tissues when embedding?  Any pros or cons greatly appreciated.  Thanks.

Sharon Davis-Devine, CT (ASCP)
Cytology-Histology  Supervisor
Carle Foundation Hospital
Laboratory and Pathology Services
611 West Park Street
Urbana, Illinois 61801
217-383-3572
sharon.davis-dev...@carle.com

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RE: [Histonet] Small biopsy specimens

2010-12-01 Thread Sebree Linda A
We've always only used hematoxylin where ever I've worked.  I haven't
embedded in eons so can't tell you how visible those specks of tissue
are. 


Linda A. Sebree
University of Wisconsin Hospital  Clinics
IHC/ISH Laboratory
DB1-223 VAH
600 Highland Ave.
Madison, WI 53792
(608)265-6596


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Sharon.Davis-Devine
Sent: Wednesday, December 01, 2010 12:02 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Small biopsy specimens

We have been using eosin to stain our small biopsies prior to tissue
processing so that they are easier to see when embedding.  Recently one
of our PA's started using Hematoxylin instead of the eosin, because that
is what they used where she trained. Upon further investigation the
manufacturers of both of our tissue processors discourage the use of
eosin because it is very hard on the working parts of the machines and
requires more PM's to prevent damage.  So we are considering switching
to using Heme instead.  Do any of you out there use Heme on your biopsy
specimens?  Do your embedders find it easier to see these tiny tissues
when embedding?  Any pros or cons greatly appreciated.  Thanks.

Sharon Davis-Devine, CT (ASCP)
Cytology-Histology  Supervisor
Carle Foundation Hospital
Laboratory and Pathology Services
611 West Park Street
Urbana, Illinois 61801
217-383-3572
sharon.davis-dev...@carle.com

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[Histonet] RE: Special Stain Automation

2010-12-01 Thread Angela Bitting
Just wondering how many people hate the Artisan's plastic well things that you 
have to clip on the slides??

 Nails, Felton flna...@texaschildrens.org 12/1/2010 11:06 AM 
The problem with the Nexus is that you can not do silver and AFB on the same 
run.
We use the Dako artisan with very consistent results and it is very easy to 
use. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Barbara Richmond
Sent: Wednesday, December 01, 2010 9:56 AM
To: histonet@lists.utsouthwestern.edu 
Subject: [Histonet] Special Stain Automation

We are in the market for a new stainer to do special stains.  We currently are 
using the Nexus and have been unhappy with it, particularly with the silver 
stains for which we do a lot of.  I'm wondering what techs out there recommend 
for us to check into.



-
Avera is a health ministry rooted in the Gospel. Our mission is to make a 
positive impact in the lives and health of persons and communities by providing 
quality services guided by Christian values. Avera is sponsored by the 
Benedictine and Presentation Sisters.
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[Histonet] Special stain Automation

2010-12-01 Thread Barbara Richmond
Does anyone have experience with the Gemini ES from Thermo Shandon?



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[Histonet] positive slides

2010-12-01 Thread zodiac29
Hello,

Can anyone recommend a brand of positive slides that are good for IHC. We are 
having problems with tissue falling off of the slides.  

Thank You
Jenny

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RE: [Histonet] RE: Special Stain Automation

2010-12-01 Thread Houston, Ronald
Don't have a problem with them at all

Ronnie Houston
Anatomic Pathology Manager
Nationwide Children's Hospital
Columbus OH 43205
(614) 722 5450

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Angela Bitting
Sent: Wednesday, December 01, 2010 1:30 PM
To: 'Barbara Richmond'; histonet@lists.utsouthwestern.edu; Felton Nails
Subject: [Histonet] RE: Special Stain Automation

Just wondering how many people hate the Artisan's plastic well things that you 
have to clip on the slides??

 Nails, Felton flna...@texaschildrens.org 12/1/2010 11:06 AM 
The problem with the Nexus is that you can not do silver and AFB on the same 
run.
We use the Dako artisan with very consistent results and it is very easy to 
use. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Barbara Richmond
Sent: Wednesday, December 01, 2010 9:56 AM
To: histonet@lists.utsouthwestern.edu 
Subject: [Histonet] Special Stain Automation

We are in the market for a new stainer to do special stains.  We currently are 
using the Nexus and have been unhappy with it, particularly with the silver 
stains for which we do a lot of.  I'm wondering what techs out there recommend 
for us to check into.




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positive impact in the lives and health of persons and communities by providing 
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Re: [Histonet] positive slides

2010-12-01 Thread Vanessa J. Phelan
We use VWR Superfrost Slides Cat # 48311-703 and they are great, no lifting 
sections.


On 12/1/10 1:57 PM, zodia...@comcast.net zodia...@comcast.net wrote:

Hello,

Can anyone recommend a brand of positive slides that are good for IHC. We are 
having problems with tissue falling off of the slides.

Thank You
Jenny

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[Histonet] Shurwave Microwave

2010-12-01 Thread JOSEPH FRAZEE

Histonetters , does anyone have a protocol for large polyps 0.5 cm and larger 
using the TBS Shurwave Microwave Processor. Thanks Histojoe 
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[Histonet] HT Position

2010-12-01 Thread Hale, Meredith
Great opportunity for a Histotechnician in a brand new laboratory!
Bellmeade Dermatology in Nashville, TN is looking for a certified HT or
HTL to run their newly constructed laboratory. Bellmeade Dermatology has
been in the dermatology business for 18 years with 3 physicians and 2
Nurse Practitioners' . Candidate must be ASCP certified and CLIA
certified to perform gross dissection, prior supervisory experience
preferred. The candidate will be responsible for the following: Creation
and maintenance of policies and procedures to CLIA standards, leading
lab through CLIA inspection, maintenance and quality control for
equipment, and routine histology duties. This is a part time  position
that offers a competitive salary and  the flexible hours allows you to
put your own personal stamp on the laboratory .  Interested applicants
should contact Meredith Hale phone 214-596-2219 or through email
mh...@carisls.com

 

 

 

Meredith Hale HT (ASCP) CM

Operations Liaison Director and Education Coordinator 

 

Caris Life Sciences

6655 North MacArthur Blvd, Irving Texas 75039

direct: 214-596-2219

cell: 469-648-8253

fax: 972-929-9966

mh...@carisls.com mailto:mh...@carisls.com  

 

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[Histonet] Part time postition for histology lab assistant

2010-12-01 Thread Cathy . Crumpton

   We  have  a part time with benefits histology lab assistant positio= n
   open  in Hillsboro, OR.  Go to [1]www.Tuality.org for more information
   if  interested.   W=  e  are  looking  for  someone  to gross with the
   pathologists  and  handle  the  acc=  essioning  and  closing  of  our
   department.  The hours are M-F 12-5 pm.



   Cathy Crumpton HT(ASCP), Histology Lead
   Tu= ality Community Hospital
   Hillsboro, OR 97123
   (503)681-1292

   = /FONT
References

   1. 3Dhttp://www.Tuality.org/
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[Histonet] High temp/paraffin oven

2010-12-01 Thread histopathy
Hello to all,

Any idea why my middle paraffin oven would be out of range, but the othet two 
on opposite sides are not?

Histopathy
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[Histonet] Technovit 7200 VLC

2010-12-01 Thread Patel.Payal

Hello Histonetters!

Hope everyone had a nice Thanksgiving. I am using Technovit 7200 VLC kit to 
embed undecalcified 5-8mm, (varies per sample), thick sections of vertebral 
samples. If anyone has experience with infiltration times and length of time 
under yellow and blue light and would not mind sharing that knowledge, I would 
greatly appreciate it!

Thank you,
Payal


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[Histonet] Hellerstrom Hellman anyone?

2010-12-01 Thread Amos Brooks
Hi,
I just did a Hellerstrom  Hellman alcoholic silver stain for 
pancreatic D-
cells. I followed the method described by Bancroft  Stevens. When the slides 
were placed into the reducing solution they instantly precipitated into a 
toasty mess, the solution turned milky brown and the slides (even around the 
sections) picked up a lot of silver precipitate. If anyone has done this of 
could offer suggestions about it, I'd really like to trouble shoot the stain a 
bit.
A bit of background about the stain that I thought I should add. 
According to 
the published method I used a 10% silver solution in ETOH with 100ul of 1M 
nitric acid. The pH of the solution was 5.0. The reducing solution was 
alcoholic formalin with 5% pyrogallic acid.
I thought the silver solution seemed really concentrated (It hardly 
even 
disolved). Incubating such a solution overnight at 37 deg C (as indicated in 
the method) seemed a bit much. Has anyone heard of modifications of this 
stain? There is no sense reinventing the wheel, but I certainly don't want to 
repeat it knowing that it will innevitably do the same thing again unless 
there is something glaringly obvious that I did wrong.

Thanks,
Amos

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Re: [Histonet] Question from one of our researchers

2010-12-01 Thread Collette, Nicole M.
Hi, Teri,

How about this? It also gives a brief blurb in the description about
commonly used alternatives, if this isn't your thing. I've never tried it,
so I can't vouch for it myself, but Invitrogen does make some pretty darn
good stuff...

http://probes.invitrogen.com/media/pis/mp10045.pdf

Sincerely,
Nicole Collette
Lawrence Livermore National Lab



On 12/1/10 9:19 AM, Johnson, Teri t...@stowers.org wrote:

 Can someone give me ideas to pass along to one of our researchers? Of course
 adhesion molecule antibodies are the first thought, but not for heterogeneous
 cell populations. So I was wondering maybe an antibody cocktail? Are there any
 lectins that might show this? Thanks!
 
 I am wondering what kind of cell membrane marker is recommended to stain
 tissue section for imaging (going to process the image with 3D Imaris
 software).
 Cells are mouse tissue section in paraffin and very heterogeneous. To see
 cell-cell boundary clearly.
 
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RE: [Histonet] High temp/paraffin oven

2010-12-01 Thread Ingles Claire
 
Not as much room/air flow for vents to dissipate extra heat?
Claire

 


From: histonet-boun...@lists.utsouthwestern.edu on behalf of 
histopa...@hotmail.com
Sent: Wed 12/1/2010 4:19 PM
To: Histonet
Subject: [Histonet] High temp/paraffin oven



Hello to all,

Any idea why my middle paraffin oven would be out of range, but the othet two 
on opposite sides are not?

Histopathy
Sent on the Sprint® Now Network from my BlackBerry® 


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RE: [Histonet] Hellerstrom Hellman anyone?

2010-12-01 Thread Ingles Claire
Did you acid clean your glassware before hand?
Claire



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Amos Brooks
Sent: Wed 12/1/2010 12:07 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Hellerstrom  Hellman anyone?



Hi,
I just did a Hellerstrom  Hellman alcoholic silver stain for 
pancreatic D-
cells. I followed the method described by Bancroft  Stevens. When the slides
were placed into the reducing solution they instantly precipitated into a
toasty mess, the solution turned milky brown and the slides (even around the
sections) picked up a lot of silver precipitate. If anyone has done this of
could offer suggestions about it, I'd really like to trouble shoot the stain a
bit.
A bit of background about the stain that I thought I should add. 
According to
the published method I used a 10% silver solution in ETOH with 100ul of 1M
nitric acid. The pH of the solution was 5.0. The reducing solution was
alcoholic formalin with 5% pyrogallic acid.
I thought the silver solution seemed really concentrated (It hardly even
disolved). Incubating such a solution overnight at 37 deg C (as indicated in
the method) seemed a bit much. Has anyone heard of modifications of this
stain? There is no sense reinventing the wheel, but I certainly don't want to
repeat it knowing that it will innevitably do the same thing again unless
there is something glaringly obvious that I did wrong.

Thanks,
Amos

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