RE: Mouse testes processing
We use ROUTINELY Bouin for Testes, epidydimes and eyes (even if we would try
Davidson for eyes) and formalin for all other tissues.
> -----Original Message-----
> From: Johnson, Teri [SMTP:TJJ@Stowers-Institute.org]
> Sent: marted́ 30 luglio 2002 17:21
> To: Histonet (E-mail)
> Subject: Mouse testes processing
> Hello all!
> I'm having difficulty with routine processing of mouse testes. I haven't
> been able to preserve the intertubular connective tissue. I've tried
> bouins fixative and it's well preserved. It mostly disappears with 4%
> paraformaldehyde and 10% neutral buffered formalin. The simple answer is
> to use bouins, but what I'd really like to do is figure out how to
> preserve it with routine fixation/processing.
> My processor is set up as follows:
> 70% alcohol
> Prosoft x5 stations
> ProPar x3 stations
> paraffin x4 stations
> I will post a picture to the histonet.org site and will send another email
> with the path when it's posted.
> Also, for those of you using Davidson's fixative on mouse tissues, have
> there been many problems with subsequent immunostaining?
> Thanks for your help,
> Teri Johnson
> Managing Director Histology Core Facility
> Stowers Institute for Medical Research
> 1000 E. 50th St.
> Kansas City, Missouri 64110
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