[Histonet] RE: IHC free floating sections
Montina Van Meter
Montina.VanMeter <@t> pbrc.edu
Fri Jul 31 11:05:36 CDT 2009
Mike,
I free float all of my rat brain sections (40-60um) and transfer them
with a paintbrush. It takes a delicate touch to do this without causing
damage to the tissue. I do know people who use pipettes to change the
solutions. Either way works, it's a matter of personal preference.
There are plastic vessels with mesh screens that can be purchased
commercially, that allow you to transfer tissue without touching them.
The only problem with that method is it requires additional amounts of
antibody. For example: I dispense 500ul of antibody+diluent into the
well when using the paintbrush transfer method (this is done under
constant agitation on a shaker table). The plastic tissue vessel method
requires 2 ml. of antibody+diluent (to cover tissue with enough fluid to
account for the size of the vessel within the well itself). The link
below offers commercially made tissue transfer vessels (look under
circular staining nets and dishes).
http://www.brainresearchlab.com/productinform.html
Good luck,
Tina
Montina J. Van Meter, HT (ASCP)
Lab Manager
Autonomic Neuroscience
Pennington Biomedical Research Center
6400 Perkins Rd.
Baton Rouge, LA 70791
225-763-2564
-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Mitchell
Jean A
Sent: Friday, July 31, 2009 8:30 AM
To: Michael Patrick; histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] RE: IHC free floating sections
Michael: I use 1.5mm nichrome transfer loops for IHC staining of 50um
free floating sections and I move them into clean culture wells for each
solution. I purchase mine from Ted Pella. It does takes some practice
but the loops work quite well with minimal damage to the tissue.
Jean Mitchell, BS, HT (ASCP)
University of Wisconsin Hospital & Clinics
Neuromuscular Laboratory
600 Highland Avenue
Madison, WI 53792-5132
-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Michael
Patrick
Sent: Friday, July 31, 2009 2:14 AM
To: histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] IHC free floating sections
I would like to stain free floating sections (fixed rat brain; 50um). Is
it necessary to transfer sections to "clean" culture wells with a paint
brush every time I wash or incubate with antibodies? I find this causes
significant damage to my tissue (especially since I do a lot of washes
etc.). Could I simply use a pipette to draw out the old solution and
then replace with the appropriate solution? What do most people do in
these situations?
Much thanks
Mike
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