It depends on your decalcification method. If EDTA is used, you might have better antigenic preservation as with say acid-decalcification.m Loss of antigenicity is a major problem associated with decalcification.
thanks for your comment. We process the marrow biopsy according to the 'hammersmith protocol'.The issue was other IHC markes were staining well ( eg 79a) I was wondering if there was something about the MIB1 that is prone to poor staining on bone marrowbiopsy
Heavy metal fixatives (B5) plus acid decalcification kills reactivity completely. Zinc-formalin and formic acid decal solution reduces reactivity. Some remains but I don't know how reliable the result is. EDTA decalcification sounds like a reasonable approach.