Myself and my colleagues are thinking about maximising our small supply of lab rats, and so (with some helpful external information) we have been thinking about fixing femurs and tibiae in 10% neutral buffered formalin for 2 days, then preserving the bones in 70% ethanol and microCT scanning them all one by one, and then once every bone has been scanned, transferring the bones to EDTA for decalcification and normal FFPE processing for histology.

Does this sound viable? Would this work? Does anyone have experience with something similar? Is it ok to NOT immediately transfer the bones from the fixative to the decalcifying solution?

Kind regards and thanks for your time,

Flynn

Similar questions and discussions