Hi
If you are using the peroxidase method the hydrogen peroxide step will remove
the eosin and some of the haematoxylin.
No need to do a decolorisation step before staining.
As Gudren said the only problem may be not having coated slides.
Good luck.
Sadly retired histologist
Tony
Sent from my
Oh no!!! We cut all slides on +
BUT you can do this. It’s what we do when we have H&E on plain slides.
Whether you have a dry unstain from another lab that sent u a slide, or your
H&E that you just took the coverslip off…
Place it in. Coplin jar with 1-3 DROPS of formalin, cover, place In 60f
Hi Nancy,
You should have no problem doing so. If you want proof, just run a couple
of your IHC control sections through the H&E stainer as you would for a
patient specimen (so right through to coverslipping) and then start the
process of removing coverslip, hydration, destain in acid alcohol and t
We do restaining for IHC also, but without destaining at all. Hematoxylin
doesn't matter because nuclei are stained after IHC with hematoxylin anyway.
And Eosin gets lost through all the washing in buffer.
The problem is, that HE section are usually mounted on non-adhesive slides,
and they float aw
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> -Original Message-
> From: Cooper, Brian
> Sent: Wednesday, February 8, 2023 12:46 PM
> To: Nancy Schmitt ; Histonet
>
> Subje
: Wednesday, February 8, 2023 12:46 PM
To: Nancy Schmitt ; Histonet
Subject: Re: [Histonet] destain for IHC
We used to do this all the time in my old reference lab.
Thanks,
Brian D. Cooper, HT (ASCP)CMQIHCCM| Histology Supervisor
Department of Pathology and Laboratory Medicine
Children's Hos
We used to do this all the time in my old reference lab.
Thanks,
Brian D. Cooper, HT (ASCP)CMQIHCCM| Histology Supervisor
Department of Pathology and Laboratory Medicine
Children's Hospital Los Angeles
4650 Sunset Blvd MS#43- Los Angeles, CA 90027
Ph: 323.361.3357
bcoo...@chla.usc.edu