Hi All! I'm working with primate mammary tissue that was given to us from a pathology group off campus. They say the tissue was fixed in NBF for at least two days, and sent to us in 70% EtOH, where it has sat for a couple months. We are treating these samples as we would with human tissue. After grossing, processing (14hr schedule), and sectioning (4-5um, high-profile blade)), I find the tissue is difficult/ near impossible to section. Even after leaving the blocks on ice for 30+min, the tissue continuously mushes against the blade. If I do get it to cut, multiple knife marks develop quickly and I find I am going through blades like crazy. I am staying superficial incase the fix didn't penetrate deep into the tissue. So far I've only processed a few samples from a larger group to resolve these issues before processing the remainder.
Does anyone have any tips for processing or sectioning? Besides grossing the tissue into smaller pieces, would it help to re-fix them overnight or an additional day? How would you tell if the issue is from fixation or insufficient clearing/infiltration of paraffin? Any information would be appreciated! Andrea Calhoun B.S., CEMT Research Assistant 2, Schedin Lab Dept. of Cell, Developmental, & Cancer Biology Oregon Health & Sciences University [email protected] , RJH-5350 _______________________________________________ Histonet mailing list [email protected] http://lists.utsouthwestern.edu/mailman/listinfo/histonet
