RE: [Histonet] COX/SDH Combo staining

2013-07-09 Thread Florence Leomiti
Easier way to do this stain...since you do these two stains separately incubate 
the slide in a the COX solution for 1 hour rinse in distilled water and 
incubate in SDH solution for 1 hr. rinse 5min in physiological saline, 10min in 
10% formalin saline, rinse in 15% ethanol then mount with Crystal mount media. 
Let dry then cover slip as usual 

Florence Leomiti    HT (ASCP)
Neuromuscular Lab Tech.
Phone 503-494-6781
Fax 503-418-4249
Pager 16822







-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tony Henwood 
(SCHN)
Sent: Tuesday, July 09, 2013 4:18 PM
To: 'Helene Degan'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] COX/SDH Combo staining

Here is our technique:
Cytochrome Oxidase - SDH

Use

1.  Defects of cytochrome oxidase activity
2.  Demonstration of mitochondria

Underlying Principle

Combining the COX with the SDH can demonstrate COX negative fibres. These may 
be SDH positive and may be ragged red fibres. 3 of the 13 subunits of COX are 
encoded by mitochondrial DNA whereas SDH is encoded by nuclear DNA. Therefore 
SDH is not affected by mitochondrial DNA mutations. Ragged red fibres in 
mitochondrial myopathies are generally COX neg (except in MELAS). Intra fibre 
mosaicism (mixture of bluish COX deficient and brownish COX positive 
mitochondria within the same fibre are also well demonstrated by this combined 
technique).


Fixation and Sectioning

Air dried unfixed 8µM cryostat sections


Reagents

1.  PBS Buffer:

Dissolve one Dulbecco PBS Tablet in 100ml distilled water

2.  COX A Solution:
Warning: DAB is carcinogenic – Avoid contact with skin
Sucrose 0.75g
3,3' Diaminobenzidine.4HCl (DAB)0.05g
Adjust to pH 7.6
PBS Buffer  up to 50ml

Aliquot in 2ml amounts (labelled CA), store at -20oC 

3.  COX B Solution:

  Catalase (Sigma C9322)0.001g
  Cytochrome C (Sigma C2037)0.05g
  Adjust to pH 7.6
  PBS Bufferup to 50ml

Aliquot in 2ml amounts (labelled CB), store at -20oC 

4.  Incubating medium

Defrost one CA and one CB vial, mix and place in a 2-slide plastic 
slide mailer. Place mailer in a coplin jar for support.

5.  SDH Reagents 
1   Stock 0.2M Sodium Dihydrogen Phosphate (NaH2PO4)  
Sodium Dihydrogen Phosphate 23.996 g
Distilled water 1000 ml
Store at room temperature

2   Stock 0.2M Disodium Hydrogen Phosphate (Na2HPO4)  
Disodium Hydrogen Phosphate 28.392 g
Distilled water 1000 ml
Store at room temperature

3   0.6M succinate solution (adjusted to pH 7.6)
Warning: Irritant – see MSDS
Sodium succinate12.96 g
Distilled water 64.00 ml
1M HCl  0.40 ml
pH to 7.6 with 0.2M Disodium Hydrogen Phosphate
Distilled water up to 80 ml
Aliquot 800μl into eppendorf vials (labelled S) and store at 
-20°C 


3.  Yellow SDH Incubation Medium

Stock 0.2M Sodium Hydrogen Phosphate52ml
Stock 0.2M Disodium Hydrogen Phosphate  348ml
Nitro Blue Tetrazolium (NBT)0.6 g
Adjust to pH 7.6 with stock phosphate solutions
Aliquot 4ml into tubes labelled “SY” and store at -20°C (enough 
for 100 tubes)


4.  Incubating medium (prepare fresh)

1.  Defrost a vial of succinate solution (S) and a Yellow 
Incubation Solution (SY)
2.  Add solution “S” to “SY”, prior to use, mix and place 
in a small plastic slide mailer.



Method

1.  Prepare incubation solution
2.  Immediately place frozen sectioned slides in incubation solution and 
incubate for two hours at room temperature.
3.  Check staining and replace for longer if required
4.  Rinse slides in distilled water and prepare SDH incubation medium.
5.  Add slides to SDH medium and incubate at 37oC for 1-2 hour.
6.  Rinse slides in distilled water.
7.  Rinse in water, dehydrate, clear and mount.

Results

Cytochrome Oxidase positive mitochondriaBrown.
Cytochrome Oxidase negative mitochondriaBlue
References

1.  Seligman etal (1968) J Cell Biol 38:1-14.
2.  Loughlin M. (1993). Muscle biopsy. A laboratory investigation. 
Butterworth-Heinemann p.38-39.
3.  Sheehan D, Hrapchak B. (1987). Histotechnology, 2nd Ed

RE: [Histonet] COX staining in frosen muscles

2009-09-28 Thread Florence Leomiti
No Problem Delores

Send me your fax number and I will send over our protocol.

Florence LeomitiHT (ASCP)
OHSU Neuromuscular Lab Tech.
Phone 503-494-6781
Fax 503-494-6787
Pager 16822

-Original Message-
From: Diaz, Dolores [mailto:dolores.d...@ttuhsc.edu] 
Sent: Monday, September 28, 2009 12:41 PM
To: Florence Leomiti
Subject: RE: [Histonet] COX staining in frosen muscles

Hello, Florence

I work in a research facility and we are beginning to stain frozen rat muscle. 
I will attempt to stain for COX and would also love to have a copy of your 
protocol if it isn't asking too much.

Thank you,
Dolores Diaz HT (ASCP)
TTUHSC

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Florence Leomiti
Sent: Monday, September 28, 2009 12:51 PM
To: Galina Deyneko; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] COX staining in frosen muscles

Hi Galina

I work in the neuromuscular lab and perform this stain on a weekly basis I have 
a protocol I can share with you. Just contact me and I can send it on.


Florence LeomitiHT (ASCP)
OHSU Neuromuscular Lab Tech.
Phone 503-494-6781
Fax 503-494-6787
Pager 16822


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Galina Deyneko
Sent: Monday, September 28, 2009 11:42 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] COX staining in frosen muscles



Dear Colleagues.
Please help. I have been asking to perform staining for  COX (which is 
cytochrome oxidase I believe) activity on mouse fresh frozen leg muscles. I am 
not very  familiar with enzyme histochemistry. I found one method 
(Seligman,1968) in J.Bancroft , 5 edition book, and the other in J. Kiernan 
Histochemical Methods book, but the methods are described for the fixed 
brain. I  am absolutely not sure that I have found the required methods. 
Could you share with me your experience, detailed protocol or the sources where 
i can find the reliable protocol siutable for muscle histochemistry.Thank you 
in advance.
Galina Deyneko
Novartis Cambridge, MA


  
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