[Histonet] PAS STAIN
sgoebel <@t> xbiotech.com
sgoebel <@t> xbiotech.com
Wed Oct 6 15:31:25 CDT 2010
I know there were a ton of posts about this, but I deleted them o accident...Did you test your Schiff's? Put a drop of 10% formalin i n it...if it turns pink, it's good...if not, throw it out =)
Sarah Goebel
Histotechnician
XBiotech US
8201 East Riverside Dr. Bldg 4 Suite 100
A (512)386-5107
-------- Original Message --------
Subject: Re: [Histonet] PAS STAIN
From: Geoff McAuliffe <[1]mcauliff <@t> um Date: Wed, October 06, 2010 1:28 pm
To: Diana McCaig <[2]dmccaig <@t> ckha.on. <[3]histonet <@t> lists.uts I make my Schiff's from scratch and store it in the refrigerator.
I use a minimum amount of charcoal and I heat it in the oven at over
100 C the night before to be sure it is nice and dry.
I make periodic acid fresh that day.
I make bisulfite rinses fresh that day.
Aqueous formalin for 48 hours at room temp. is OK for rat and mouse
liver glycogen, I don't know about other species. Slices of liver
should be thin.
When in doubt formalin+alcohol+acetic acid is an excellent fixative.
Geoff
Diana McCaig wrote:
> Hi
> We have been doing a PAS stain on the same control block and same
> reagent supplier for a long time.
> Yesterday when we ran the slides, they failed to stain
>
> We opened new bottles of Periodic Acid and Schiff's Reagent and
recut< >
> Still, we are unable to get any staining.
>
> Suggestions to help would be appreciated
>
> Diana
> _______________________________________________
> Histonet mailing list
> [4]Histonet <@t> lists.ut > [5] >
>
>
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Geoff McAuliffe, Ph.D.
Neuroscience and Cell Biology
Robert Wood Johnson Medical School
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voice: (732)-235-4583
[6]mcauliff <@t> umdnj.edu
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