RE: [Histonet] Help With Hemo Fading

2009-07-03 Thread Kemlo Rogerson
I agree.. Also you're not storing them in sunlight are you? Silly question 
I know.



Kemlo Rogerson  
e-mail kemloroger...@nhs.net if not at work.
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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
Sent: 02 July 2009 20:28
To: histonet@lists.utsouthwestern.edu; sr...@aol.com
Subject: Re: [Histonet] Help With Hemo Fading

The fading most probably is caused by acid in the permanent slide, probably 
because the sections were passed through the alcohols very quickly after the 
acid differentiation, or they stayed little time in tap water after 
differentiation or no bluing agent was used.
It is unlikely that the mounting medium is acidic, although that could also be 
the cause also. An acid environment over the cover slipped section is the most 
probable culprit for the henatoxylin fading.
Check the staining protocol.
René J.

--- On Thu, 7/2/09, sr...@aol.com sr...@aol.com wrote:


From: sr...@aol.com sr...@aol.com
Subject: [Histonet] Help With Hemo Fading
To: histonet@lists.utsouthwestern.edu
Date: Thursday, July 2, 2009, 2:42 PM



Hello everyone,

?

We are having problems with short-term hematoxylin fading and loss of detail. 
The pathologist is freaking out! I've seen hemo fade over a long period of time 
but not in a matter of a few months. Slides from one year ago are really bad.

?

I've been out of the business for a number of years and in the interim much has 
changed including reagents. These are GI tract biopsies processed by microwave. 

?

Any thoughts at all?

?

Thanks! Marg
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Re: [Histonet] Help With Hemo Fading

2009-07-03 Thread louise renton
Even long term exposure to indoor lighting (fluorescent type) will fade
sectiions. We work in a building where ther lights are permanently on. If we
want to keep our sections fresh and helathy, they get covered up as soon as
.

best regards

On Fri, Jul 3, 2009 at 9:09 AM, Kemlo Rogerson 
kemlo.roger...@waht.swest.nhs.uk wrote:

 I agree.. Also you're not storing them in sunlight are you? Silly
 question I know.



 Kemlo Rogerson
 e-mail kemloroger...@nhs.net if not at work.
 DD   01934 647057 or extension 3311 Mob 07749 754194;
 Embrace uncertainty. Hard problems rarely have easy solutions. --Jonah
 Lehrer
 This e-mail is confidential and privileged. If you are not the intended
 recipient please accept my apologies; please do not disclose, copy or
 distribute information in this e-mail or take any action in reliance on its
 contents: to do so is strictly prohibited and may be unlawful. Please inform
 me that this message has gone astray before deleting it. Thank you for your
 co-operation



 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu [mailto:
 histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
 Sent: 02 July 2009 20:28
 To: histonet@lists.utsouthwestern.edu; sr...@aol.com
 Subject: Re: [Histonet] Help With Hemo Fading

 The fading most probably is caused by acid in the permanent slide, probably
 because the sections were passed through the alcohols very quickly after the
 acid differentiation, or they stayed little time in tap water after
 differentiation or no bluing agent was used.
 It is unlikely that the mounting medium is acidic, although that could also
 be the cause also. An acid environment over the cover slipped section is the
 most probable culprit for the henatoxylin fading.
 Check the staining protocol.
 René J.

 --- On Thu, 7/2/09, sr...@aol.com sr...@aol.com wrote:


 From: sr...@aol.com sr...@aol.com
 Subject: [Histonet] Help With Hemo Fading
 To: histonet@lists.utsouthwestern.edu
 Date: Thursday, July 2, 2009, 2:42 PM



 Hello everyone,

 ?

 We are having problems with short-term hematoxylin fading and loss of
 detail. The pathologist is freaking out! I've seen hemo fade over a long
 period of time but not in a matter of a few months. Slides from one year ago
 are really bad.

 ?

 I've been out of the business for a number of years and in the interim much
 has changed including reagents. These are GI tract biopsies processed by
 microwave.

 ?

 Any thoughts at all?

 ?

 Thanks! Marg
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 Histonet@lists.utsouthwestern.edu
 http://lists.utsouthwestern.edu/mailman/listinfo/histonet




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-- 
Louise Renton
Bone Research Unit
University of the Witwatersrand
Johannesburg
South Africa
There are nights when the wolves are silent and only the moon howls.
George Carlin
No trees were killed in the sending of this message.
However, many electrons were terribly inconvenienced.
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[Histonet] New Ventana IHC stainer

2009-07-03 Thread Gomez, Milton
Dear Histonetters:
Do you folks recommend getting a maintenance contract on a new ventana 
instrument? May you share your protocol for setting up the instrument?
Thanks in advance,
MG

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[Histonet] IHC stainer

2009-07-03 Thread Gomez, Milton
Dear Histonetters:
 
What is the best, most reliable workhorse immunostainer out there nowadays? and 
why.
 
Thanks in advance,
MG

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The information transmitted by this e-mail and any included
attachments are from ARUP Laboratories and are intended only for the
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international, federal, or state securities laws, or protected health
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Unauthorized forwarding, printing, copying, distributing, or use of
such information is strictly prohibited and may be unlawful. If you
are not the intended recipient, please promptly delete this e-mail
and notify the sender of the delivery error or you may call ARUP
Laboratories Compliance Hot Line in Salt Lake City, Utah USA at (+1
(800) 522-2787 ext. 2100

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[Histonet] Fading of H E sections

2009-07-03 Thread kamal prasad
Mostly it could be the acidic mounting media. Please check the pH of mounting 
media.
 
Kamal


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