RE: Thomas Histology (metanil yellow)
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From: | "Hewlett Bryan (CMH)" <HEWLETT@EXCHANGE1.CMH.ON.CA> |
To: | Histonet <histonet@pathology.swmed.edu>, "'J. A. Kiernan'" <jkiernan@julian.uwo.ca> |
Reply-To: | |
Date: | Thu, 07 Oct 1999 07:27:39 -0400 |
Content-Type: | text/plain |
I agree with John, I have used saturated tartrazine in 70% cellosolve as a
counterstain to PAS for over 35 years. The solution is much more stable than
Metanil yellow. Martius yellow is an excellent alternative, as is an
alcoholic solution of Picric acid. I know, I know!!! All you safety minded
people stay OFF my back!
Bryan
> ----------
> From: J. A. Kiernan[SMTP:jkiernan@julian.uwo.ca]
> Sent: October 7, 1999 12:33 AM
> To: Histonet
> Subject: Re: Thomas Histology (metanil yellow)
>
> On Thu, 7 Oct 1999, Ken Turner wrote:
>
> > I have a copy of Thompson, which, on page 480 gives a metanil yellow
> > counterstain after PAS. The solution is: 0.25% metanil yellow in 0.25%
> > acetic acid prepared with distilled water. Mix, filter and store in a
> clean
> > brown bottle.
> > After conventional periodic acid and Schiff sequence, and water washing,
> > stain 1 minute in metanil yellow, rinse in distilled water, 95% ethyl
> > alcohol, absolute ethyl alcohol and xylene. Thompson suggests mounting
> with
> > Permount.
>
> For what it's worth, I agree 100%. Metanil yellow provides
> a splendid yellow counterstain for cytoplasm and collagen.
> Unfortunately the dye solution is not very stable. Its colour
> changes to brown over the course of a few months, and the
> staining properties also deteriorate. I don't know why, but
> it's so. For another yellow anionic dye you might try
> tertrazine. Look it up in Bryan Llewellyn's StainsFile: a
> splendid collection of histo-wisdom.
>
> John A. Kiernan,
> Department of Anatomy & Cell Biology,
> The University of Western Ontario,
> LONDON, Canada N6A 5C1
>
>
>
>
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