[Histonet] RE: ORO tissue falling off
Caroline Miller
mills <@t> 3scan.com
Wed Apr 15 19:44:00 CDT 2015
+1 to Linda, but I have found no difference on overnight vs multiple days.
Fatty liver is hard to do on all counts! It is tough enough sometimes to get a decent section on the slide.
Thanks for the other suggestions, certainly something I would try in the future
Yours
Caroline
Caroline Miller (mills)
Director of Histology
3Scan, Inc
415-2187297
> On Apr 15, 2015, at 5:07 PM, Linda Prasad (SCHN) <linda.prasad <@t> health.nsw.gov.au> wrote:
>
> Usually with the fatty tissues, I pick them up on superfrost slides and let it air dry for 2-3 days at room temperature and then perform the ORO stains. So far they seem to stay on.
>
> Linda Prasad | Senior Scientist | Histopathology
> t: (02) 9845 3306 | f: (02) 9845 3318 | e: linda.prasad <@t> health.nsw.gov.au | w: www.schn.health.nsw.gov.au
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> -----Original Message-----
> From: histonet-bounces <@t> lists.utsouthwestern.edu [mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Jo-Ann Bader, Ms.
> Sent: Thursday, 16 April 2015 1:40 AM
> To: histonet <@t> lists.utsouthwestern.edu
> Subject: [Histonet] ORO tissue falling off
>
> We are having difficulty with a particulate set of very, very fatty mouse livers. The normal livers from this set stay on the slides the fatty livers fall off. We have used different types of charged slides and we have even tried to drench the charged slides in Stay-On, dry them and then put the frozen tissues on (despirate times call for despirate measures). No luck Does anyone have any other ideas. Help Help
>
> Jo-Ann Bader
> Histology Coordinator
> Goodman Cancer Research Center
> 1600 Pine Ave. W,
> Room 312
> Montreal Quebec, H3A 1A3
> Email: jo-ann.bader <@t> mcgill.ca<mailto:jo-ann.bader <@t> mcgill.ca>
> Office Tel: 514-398-5647
> Lab: Tel: 514-398-8270
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