[Histonet] Searching for Horizontal Slide Racks

2015-07-01 Thread Erin Sarricks
Hi Histonet-

Does anyone have any slide racks that hold the slides horizontally that
they no longer need?  Like this but for maybe 50-60 slides?
http://grale.com.au/products/view/297
I am willing to purchase and pay for shipping if anyone has any they are
getting rid of.  Thank you!

Erin
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Re: [Histonet] Trichrome troubleshooting

2015-07-01 Thread Bernice Frederick
Actually, I have microwaved the  Bouins (and still do) for small numbers of 
slides and the results are the same. I ran a liver bx both ways as well as 
larger tissue to compare. I use the 10 slide plastic coplin jar and generally 
have 5 or less slides when I do this. One microwaves the Bouins for 30 seconds 
on power level 7 in a lab grade microwave. A higher level will cause the 
Bouin's to spill. Slides are then added and left for 5 minutes.  Excess rinsed 
out and then proceed as per your SOP.  As for the blue- I rinse out excess and 
do 1 dip in 1% GAA. Rinse and dehydrate (10 dips each solution)
Bernice

Bernice Frederick HTL (ASCP)
Senior Research Tech
Pathology Core Facility
Robert. H. Lurie Cancer Center
Northwestern University
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723
b-freder...@northwestern.edu

-Original Message-
From: Elizabeth Chlipala [mailto:l...@premierlab.com] 
Sent: Tuesday, June 30, 2015 3:30 PM
To: Suzanne Martin; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Trichrome troubleshooting

Suzanne

How many times have you used the kit and reagents, I did look up how the kit 
works but the trichrome stain can be tricky.  First of all you need to make 
sure that the mordant (bouins solution) is at 60C prior to placing your slides 
in them.  We normally heat up our bouins for at least an hour prior to placing 
the slides in the solution.  We leave in bouins for an hour and a half rather 
than an hour.   I see that this is a microwave protocol I cannot comment on 
that but I don't think that the hematoxylin is the issue, if you leave longer 
in 1% acetic acid that may pull some of the blue stain out or I would try 
dehydrating with lower alcohol percentage that can pull some of the blue stain 
out.   I would also try leaving it a bit longer in the bouins after you 
microwave it - that might help.

Trichrome staining works best with fresh reagents so if you have used these 
reagents too much that could cause problems.  I'm also not a big fan of the one 
step trichromes, they are quicker but sometimes not as good as the two steps, 
just my opinion.

FYI - to evaluate your staining look for a smaller vessel, the smooth muscle 
should be nice a red, if its greyish or blue you have not done the stain 
properly.  Good Luck

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC Premier Laboratory, LLC PO Box 18592 
Boulder, CO 80308
(303) 682-3949 office
(303) 682-9060 fax
(303) 881-0763 cell
l...@premierlab.com
www.premierlab.com

March 10, 2014 is Histotechnology Professionals Day

Ship to Address:

Premier Laboratory, LLC
1567 Skyway Drive, Unit E
Longmont, CO 80504


-Original Message-
From: Suzanne Martin [mailto:smar...@lcpath.com]
Sent: Tuesday, June 30, 2015 12:37 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Trichrome troubleshooting


Hi all,

We are having trouble troubleshooting our trichrome. It is too blue. We are 
using Leica's kit with the Weigerts iron with Gills. Most of the small bowel 
controls have seen improvement but patient tissue is not... strange. 

We have tried lessening the time in Gills, adding time for the last acid step, 
even lessening time and adding time in the Weigerts. 


Thoughts?

Thank you.

Suzanne HT




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[Histonet] Unsubscribe

2015-07-01 Thread Alminde, Lea S


Lea S. Alminde
Anatomic Pathology Supervisor
Jeanes Hospital
215-728-2034

  email lea.almi...@tuhs.temple.edu







  

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and may contain information that is confidential or privileged. This 
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Re: [Histonet] Trichrome troubleshooting

2015-07-01 Thread Terri Braud
Please clarify if you are referring to the Aniline blue, or the Hematoxylin 
blue.  I, also, have never heard of using Gills in association with any 
Trichrome stain, but as a long time user and educator of using a one-step 
(Gomori's) trichrome stain (which is the Leica blue collagen stain), if you 
rinse with any water between the stain step and the acetic acid step, you will 
end up with a stain that is overpoweringly blue.
Here are the steps copied from the Leica blue collagen kit instructions.  
Notice NO WATER RINSE between the stain and Acetic Acid Solution.  It is a 
common mistake.
10. Gently mix the Gomori's Trichrome Blue Solution by swirling and allow to 
stand for 6 minutes.
11. Place sections in 1% Acetic Acid solution for 1 minute.
I hope this helps. Sincerely, Terri

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Holy Redeemer Hospital Laboratory
1648 Huntingdon Pike
Meadowbrook, PA 19046
Ph: 215-938-3676
Fax: 215-938-3874

2. Trichrome troubleshooting (Suzanne Martin)
From: Suzanne Martin smar...@lcpath.com
Hi all,

We are having trouble troubleshooting our trichrome. It is too blue. We are 
using Leica's kit with the Weigerts iron with Gills. Most of the small bowel 
controls have seen improvement but patient tissue is not... strange. 

We have tried lessening the time in Gills, adding time for the last acid step, 
even lessening time and adding time in the Weigerts. 
Thoughts?
Thank you.
Suzanne HT



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[Histonet] RELIA Histology Careers Bulletin 7-02-2015 Have a Safe and Happy 4th of July Holiday!!

2015-07-01 Thread Pam Barker
Hi Histonetters!!!

I hope you Have a safe and Happy July 4th Weekend.

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Have a Safe and Happy 4th of July!!

Thanks-Pam

Right Place, Right Time, Right Move with RELIA!

Thank You!
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Pam Barker
President/Senior Recruiting Specialist-Histology
RELIA Solutions
Specialists in Allied Healthcare Recruiting
5703 Red Bug Lake Road #330
Winter Springs, FL 32708-4969
Phone: (407)657-2027
Cell: (407)353-5070
FAX: (407)678-2788
E-mail: rel...@earthlink.net 
www.facebook.com/PamBarkerRELIA
www.linkedin.com/in/reliasolutions
www.twitter.com/pamatrelia 

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Re: [Histonet] Suggestions for staining ground substances in the Heart

2015-07-01 Thread John Kiernan
Movat's pentachrome is unnecessarily complicated when you want to look only at 
one component of a tissue. 

Most ground substance (extracellular material between cells, collagen fibres 
etc) is weakly stainable with PAS, alcian blue pH2.5 or both. It's usual to 
stain with alcian blue first (Mowry's method). If you do the PAS first, the 
PAS-positive materials will also stain with alcian blue and be darker. For the 
reasons, see:

Johannes, M.-L. and Klessen, C. (1984). Alcian blue/PAS or PAS/alcian blue? 
Remarks on a classical technique used in carbohydrate histochemistry. 
Histochemistry 80:129-132.

Yamabayashi, S. (1987). Periodic acid-Schiff-alcian blue: a method for the 
differential staining of glycoproteins. Histochemical Journal 19:565-571.

Reid, P.E. and Owen, D.A. (1988). Some comments on the mechanism of the 
periodic acid-Schiff-Alcian blue method. Histochemical Journal 20:651-654.

If you can predict the PAS-AB effect without further reading, you already have 
a good understanding of how the traditional methods of carbohydrate 
histochemistry work!

John Kiernan
London, Canada
= = =
On 30/06/15, Wolfe, Christina  christina.wo...@bms.com wrote:
 Hi all,
 We are interested in staining ground substances in the heart. Are there other 
 stains that will work beside the Pentachrome? We have tried the Movat's 
 pentachrome (commercial kit) and are able to demonstrate ground substance in 
 the bone with the alcian blue part of this stain. In our hands the goblet 
 cells of the gut and the ground substance in the heart are devoid of 
 staining. We have tried sections cut at 4 and 6 microns. Any 
 thoughts/suggestions?
 
 Kristie
 
 Christina Wolfe, BSHA, MLT (ASCP), HT, QIHC
 Drug Safety Evaluation/Bristol-Myers Squibb
 Pathology Dept.
 812-307-2093
 
 
 
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Re: [Histonet] Unsubscribe

2015-07-01 Thread Weems, Joyce K.
Hello Lea,

You must go to the website listed at the bottom of the email  and unsubscribe.

Here it is...
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

Best wishes,

Joyce Weems
Pathology Manager
678-843-7376 Phone
678-843-7831 Fax
joyce.we...@emoryhealthcare.org



www.saintjosephsatlanta.org
5665 Peachtree Dunwoody Road
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-Original Message-
From: Alminde, Lea S [mailto:lea.almi...@tuhs.temple.edu]
Sent: Wednesday, July 01, 2015 5:51 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Unsubscribe



Lea S. Alminde
Anatomic Pathology Supervisor
Jeanes Hospital
215-728-2034

  email lea.almi...@tuhs.temple.edu







  

This electronic message is intended to be for the use of the named recipient, 
and may contain information that is confidential or privileged. This 
communication may contain protected health information (PHI) that is legally 
protected from inappropriate disclosure by the Privacy Standards of the Health 
Insurance Portability and Accountability Act (HIPAA) and relevant Pennsylvania 
Laws. You can direct questions concerning PHI or HIPAA to the Corporate 
Compliance and Privacy Officer at (215) 707-5605. If you are not the intended 
recipient, please note that any dissemination, distribution or copying of this 
communication is strictly prohibited. If you have received this message in 
error, you should notify the sender immediately by telephone or by return 
e-mail and delete and destroy all copies of this message.
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