+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) 
> <[email protected]> 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: [email protected] | 
> w: www.schn.health.nsw.gov.au
> 
> Cnr Hawkesbury Road and Hainsworth Street, Westmead, NSW Australia
> Locked Bag 4001, Westmead 2145, NSW Australia
> 
> ♲  Please consider the environment before printing this email.
> 
> -----Original Message-----
> From: [email protected] 
> [mailto:[email protected]] On Behalf Of Jo-Ann Bader, 
> Ms.
> Sent: Thursday, 16 April 2015 1:40 AM
> To: [email protected]
> 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: [email protected]<mailto:[email protected]>
> Office Tel:  514-398-5647
> Lab:  Tel:  514-398-8270
> 
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