[Histonet] (kinda) silly questions about IHC
Joanne Mauger
MAUGER <@t> email.chop.edu
Fri Oct 29 10:31:30 CDT 2004
To Anna,
My experience is that it is best to dry frozen sxn slides. I used to keep them in a dessicator for weeks before staining sometimes, and then use acetone to further remove water from tissue.
Jo
>>> "Anna Elisse Beaudin" <aep10 <@t> cornell.edu> 10/29/04 09:52AM >>>
Hello,
I have a question about IHC. I am trying to do multiple labeling on
sagittal brain sections that were fixed by perfusion. I cut these
sections on a cryostat, and I am having a lot of trouble deciding
whether to do IHC on mounted sections vs. free-floating. When I try to
mount fixed sections directly while sectioning, I get air bubbles
caught between the section and the slide.. the sections just don't seem
to want to lie smoothly on the slide. Alternatively, when I stain
free-floating sections, these long sagittal sections curl up and as
such I get extremely uneven (and ugly) staining. My actual (silly)
question is whether it is possible to collect sections into solution
(free-floating), mount them, let them dry overnight, and then do IHC on
them. I'm torn because I need to let the section dry a little on the
slide so that they stick, but at the same time I think it might be bad
for them to dry out? As you can see, I am very confused, and would
really appreciate anyone's advice. Thanks in advance for your help!
Best,
Anna Beaudin
Division of Nutritional Sciences
Cornell University
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