Re: Re: [Histonet] Re: IHC on frozens

TF tifei <@t> foxmail.com
Tue Jul 7 06:17:36 CDT 2009


it is because when mentioning "frozen section", we r talking about different procedures.

some fix brain, sucrose sink, then perform OCT embedding and cryostat section;you can use enzyme digestion or HIER for antigen retrieval

some other use fresh brain, snap freezing, and cryostat section; this approach does not require HIER.


2009-07-07 



TF 



发件人: Colleen Forster 
发送时间: 2009-07-07  02:41:59 
收件人: Johnson, Teri 
抄送: histonet <@t> lists.utsouthwestern.edu 
主题: Re: [Histonet] Re: IHC on frozens 
 
I disagree. I do heat retrieval on frozen sections that have been fixed 
in a formalin fix. If you use the correct protocol you can get very nice 
IHC on these.
Colleen Forster HT(ASCP)QIHC
Anatomic Pathology Research Laboratory
U of MN
Johnson, Teri wrote:
> In response to this thread:
>
>   
>> <snip><
>>     
> Kimberly:
> Your question has a two parts answer:
> 1- it cannot be done because the sections will peel off, but most importantly
> 2- it is not necessary since HIER was developed to "undo" the cross linkage produced by the NBF fixation, and the tissues used for?FS are not fixed. ren? J.?
>
> --- On Thu, 7/2/09, Kimberly Tuttle <ktuttle <@t> umm.edu> wrote:
>
>
> From: Kimberly Tuttle <ktuttle <@t> umm.edu>
> Subject: [Histonet] IHC on frozens
> To: "histonet" <histonet <@t> lists.utsouthwestern.edu>
> Date: Thursday, July 2, 2009, 12:55 PM
>
>
> Can you do heat retrieval on frozens?
>
> Kimberly C. Tuttle? HT (ASCP)
> Pathology Biorepository and Research Core
> University of Maryland
> Room NBW58, UMMC
> 22 S. Greene St
> Baltimore, MD 21201
> (410) 328-5524
> (410) 328-5508 fax
> Please consider the environment before printing this e-mail.
>   
>> <snip><
>>     
>
> I disagree that you cannot do HIER on frozen sections. We do them all the time. All our samples are fixed in formalin, and then cryoprotected in sucrose prior to freezing them, so providing an antigen retrieval step usually produces good IHC results in frozen sections. We section and dry the slides, then use citrate buffer pH 6.0 in the microwave at 60 degrees C for 10 minutes, cool 10 minutes, then rinse and continue with IHC protocol. Use Plus slides and keep the solution under boiling temperature and you should be fine. For things like brain or bone, you might want to use lower temperatures for longer period of time instead of high temps for less time.
>
> It can even work in fresh-frozen samples which are sectioned and then fixed prior to immunostaining. Some great information on this is included in this article: Yamashita and Okada, Application of Heat-induced Antigen Retrieval to Aldehyde-fixed Fresh Frozen Sections, JHC Vol 53(11): 1421-1432, 2005. A big thanks to Gayle Callis for the heads up on this paper!
>
> Teri Johnson, HT(ASCP)QIHC
> Managing Director Histology Facility
> Stowers Institute for Medical Research
> 1000 E. 50th St.
> Kansas City, MO 64110
>
>
> _______________________________________________
> Histonet mailing list
> Histonet <@t> lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>   
_______________________________________________
Histonet mailing list
Histonet <@t> lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


More information about the Histonet mailing list