Re: [Histonet] Maximow Method

[Rene J Buesa via Histonet]

Tyrone:A.A.Maximow's Azur-eosin, etc staining produces wonderful results but 
this, and many very old procedures, essentially rest on the use of mercury 
salts which produce special chemical compounds with tissue components.Any, and 
I mean any, deviation from the original procedure will not produce the same 
results as those expected from the original recipes.You can try and you will 
get a staining but without the crisp and delightful colorations obtained with 
the original recipe containing mercury. The same goes for the Harris 
hematroxylin that now is manufactured and sold without mercury oxide and is 
still  named Harris, when really it is not. The results are similar, but not 
exactly as those obtained with the original recipe.So, in my humble opinion, 
you can substitute whatever you want from an original recipe, but please do not 
be surprised if the results do not "live" to your expectations or the original 
description.René  

On Monday, November 21, 2016 2:40 PM, Tyrone Genade via Histonet 
 wrote:
 

 Hello,

I was reading a book from the 60s on the anatomy of aging in man and
animals and the author mentioned using a hematoxylin-eosin Y-Azure-II stain
to show the lymphocytes. Some searching came up with the Maximow Method.
The online protocol I found (for bone marrow):
https://emsdiasum.com/microscopy/technical/datasheet/26252.aspx mentions
the use of Zenker’s or Formalin.

In another old book, Putt's Manual of Histochemical Staining Methods, the
authors says 10% fomalin, Helly's or Zenker's fluid for fixation. I am
definitely not going to start using Zenker's (I get enough grief from the
H officer about picric acid). I normally use Davidson's fixative to fix
and decalsify my fish (formaldehyde, acetic acid + ethanol). Anyone know if
this staining method is compatible with Davidson's fixative?

Would this eosin-Y solution be suitable:
http://www.sigmaaldrich.com/catalog/product/sigma/ht110316?lang=en®ion=US
 for preparing the Eosin-Y Azure-II working solution?

Thanks
-- 
Tyrone Genade
Orange City, Iowa
tel: (+1) 712 230 4101
http://tgenade.freeshell.org

Romans 6:23: The gift of God is eternal life through Christ Jesus our Lord.
To find out how to receive this FREE gift visit http://www.alpha.org.
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[Histonet] Maximow Method

[Tyrone Genade via Histonet]

Hello,

I was reading a book from the 60s on the anatomy of aging in man and
animals and the author mentioned using a hematoxylin-eosin Y-Azure-II stain
to show the lymphocytes. Some searching came up with the Maximow Method.
The online protocol I found (for bone marrow):
https://emsdiasum.com/microscopy/technical/datasheet/26252.aspx mentions
the use of Zenker’s or Formalin.

In another old book, Putt's Manual of Histochemical Staining Methods, the
authors says 10% fomalin, Helly's or Zenker's fluid for fixation. I am
definitely not going to start using Zenker's (I get enough grief from the
H officer about picric acid). I normally use Davidson's fixative to fix
and decalsify my fish (formaldehyde, acetic acid + ethanol). Anyone know if
this staining method is compatible with Davidson's fixative?

Would this eosin-Y solution be suitable:
http://www.sigmaaldrich.com/catalog/product/sigma/ht110316?lang=en=US
 for preparing the Eosin-Y Azure-II working solution?

Thanks
-- 
Tyrone Genade
Orange City, Iowa
tel: (+1) 712 230 4101
http://tgenade.freeshell.org

Romans 6:23: The gift of God is eternal life through Christ Jesus our Lord.
To find out how to receive this FREE gift visit http://www.alpha.org.
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet