Correct ...... you cannot use acid decal if you want to do molecular testing.  
We switched to EDTA for small biopsy specimens that needed decalcifying prior 
to processing.  It is also important that the specimen be adequately fixed 
before decalcification.  I am no longer at Hartford Hospital, but I will try to 
find out where they purchase their EDTA now.  Note that you cannot use EDTA for 
large specimens (e.g., femoral head) because it takes way too long.  You can 
also carefully separate all the soft tissue fragments from bone, and process 
them separately without decalcification.
Richard Cartun

    On Thursday, May 29, 2025 at 04:10:03 AM EDT, MANAHIL EL BIREIR via 
Histonet <[email protected]> wrote:  
 
 I hope this email finds you well.

I am reaching  out regarding the optimisation of our bone marrow trephine 
specimen decalcification process. Currently, we are utilizing a ready-to-use 
acid rapid decalcification method. However, our Molecular Department has 
observed that the acid affects the quality of molecular results.

To enhance our process and ensure optimal molecular sequencing outcomes, we 
would greatly appreciate it if you could share your bone marrow trephine 
decalcification protocol with us. Additionally, which decalcification reagent 
you use to mitigate potential adverse effects on molecular analysis.

Kind regards,

Manahil


Sent from my iPhone
_______________________________________________
Histonet mailing list
[email protected]
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
  
_______________________________________________
Histonet mailing list
[email protected]
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

Reply via email to