[Histonet] Grocott's Methenamine Silver Stain
Kathleen Roberts
kgrobert <@t> rci.rutgers.edu
Wed May 5 14:18:52 CDT 2004
I made up everything fresh just before I did the stain... :oP I'll
try the 10% chromic acid.
Thanks,
Kathleen
Wayne Holland wrote:
> Make sure your solutions are fresh, especially the silver. ALso try
> 10% chromic for 10 minutes.
>
>
>> From: Kathleen Roberts <kgrobert <@t> rci.rutgers.edu>
>> To: "'histonet <@t> lists.utsouthwestern.edu'"
>> <histonet <@t> lists.utsouthwestern.edu>
>> Subject: [Histonet] Grocott's Methenamine Silver Stain
>> Date: Wed, 05 May 2004 13:54:18 -0400
>>
>> Hey, all-
>>
>> I've been trying to stain some FFPE slides of decalcified rat sinuses
>> for fungi using the AFIP protocol for Grocott's stain, and despite
>> using fresh reagents, the positive control and unknowns do not stain
>> at all, except for some random deposition of silver that does not
>> even begin to look like fungi. The positive control is loaded with
>> Candida, and can be seen with H&E easily.
>>
>> So far, we don't see any fungi in the rat sinuses and lungs (they
>> were sneezing, and the bedding came back positive for Aspergillus)
>> with H&E staining, which is why we decided to try the Grocott's-one
>> way or another we should be able to visualize it in the tissues.
>>
>> Any ideas why the Candida-loaded positive control would not stain
>> with Grocott's? Right now I am thinking that perhaps they didn't sit
>> long enough in the 4% chromic acid, even though the protocol says to
>> soak the slides for an hour to oxidize them. Either that or a longer
>> soak in the methenamine-silver solution at 60 degrees C (also for one
>> hour).
>>
>> Thanks in advance for your help-
>> Kathleen Roberts
>> Principal Lab Technician
>> Neurotoxicology Labs
>> Dept of Pharmacology & Toxicology
>> Ernest Mario School of Pharmacy
>> Rutgers University
>> 41 B Gordon Rd
>> Piscataway, NJ 08854
>>
>>
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>
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