Susan,
If you are talking about frozen sections of fixed tissue, they do not adhere 
well to slides (even charged slides) no matter how thick or thin. I'm not sure 
why you are treating the sections with alcohol chloroform either. That is 
pretty harsh treatment and totally unnecessary for Nissl staining. 

Why not stain the sections free-floating and then mount them from xylene?

Ronnie Houston
Anatomic Pathology Manager
Nationwide Children's Hospital
Columbus OH 43205
(614) 722 5450

-----Original Message-----
From: [email protected] 
[mailto:[email protected]] On Behalf Of Truscott, Tom
Sent: Friday, July 29, 2011 10:22 AM
To: Michael, Susan; [email protected]
Subject: [Histonet] RE: Cresyl violet stain on 50 um mouse brain sections

Hi Susan, I would suggest cutting lots thinner sections. The plus slides seem 
to have trouble holding on to very thick sections. Another possibility is too 
much glacial acetic acid in your working solution of cresyl-too much acid can 
loosen the bonds on the plus slides. Tom T

-----Original Message-----
From: [email protected] 
[mailto:[email protected]] On Behalf Of Michael, Susan
Sent: Friday, July 29, 2011 6:12 AM
To: [email protected]
Subject: [Histonet] Cresyl violet stain on 50 um mouse brain sections

I am having trouble keeping my sections on the slides when I stain with cresyl 
violet.  These are fixed frozen sections, 50 um, dried overnight on plus 
slides, overnight in 1 to 1 alcohol/chloroform, then rehydrated through 100, 95 
ETOHs then to water.  Into the cresyl violet solution, then 100% to 95% ETOH.  
Is it the water?  Is it the slides?  Any suggestions?

Susan
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