RE: Counterstain
<< Previous Message | Next Message >>
From: | Cynthia Favara <cfavara@atlas.niaid.nih.gov> (by way of histonet) |
To: | histonet <histonet@magicnet.net> |
Reply-To: | |
Content-Type: | text/plain; charset="us-ascii" |
Beth,
Kirkegard and Perry make a product called contrast red. We tried it
here and it was considered suboptimal for nuclear detail. Also tried methyl
green.
Cynthia Favara
Rocky Mountain Laboratories
903 S 4th Street
Hamilton, MT 59840
ph: 406-363-9317
FAX: 406-363-9286
e-mail: cfavara@nih.gov
> ----------
> From: broche@wlgore.com[SMTP:broche@wlgore.com]
> Sent: Tuesday, November 24, 1998 3:09 PM
> To: Histonet@pathology.swmed.edu
> Subject: Counterstain
>
> Histonetters:
>
> We are "staining" frozen sections of B-gal. cells to end up with a
> turquoise-blue reaction product. The color is soluble in alcohols and
> clearants. We use crystal mount to permanently mount. We are looking for
> a counterstain that will not obscure the turquoise-blue color and will not
> leach out into the aqueous mounting media. So far our hematoxylin
> (Mayers)
> is too dark, and neutral and nuclear fast red bleed out into the mountant.
> Anyone have any suggestions? I sort of remember discussions of this
> nature
> in the past but , of course, didn't archive them at the time.
>
> Thanks for the help,
>
> Beth Roche
> Gore Hybrid Technologies
> Flagstaff, AZ
> broche@wlgore.com
>
>
>
<< Previous Message | Next Message >>