Processing of human temporal bones is a long, expensive process and the res
ulting celloidin sections are difficult to use for immunohistochemistry. We
tested the ability of immunohistochemical assays to work in human temporal
bones that were decalcified using a microwave oven. Tissue was trimmed to
an approximate cube (1.5-2 cm/side) containing only the cochlea and immerse
d in fresh EDTA with paraformaldehyde every 6 h. This sized block required
190-400 h to decalcify. The decalcified tissue was embedded in paraffin and
sectioned. Sections were immunoassayed with anti-cytochrome c oxidase, ant
i-neurofilament or anti-peripherin. All three antibodies labeled the approp
riate structures. This procedure may stimulate advancement in the understan
ding of human inner ear pathology. (C) 2000 Elsevier Science B.V. All right
s reserved.