We have been trying to section 120hpf fish and are having trouble with maintaining the integrity of the tissue. Also, we use hematoxylin and eosin stains.
We have made great experience on zebrafish larvae with 2% PFA fixation and cryoprotection in 30% Sucrose in 1x PBS. We then infiltrate with OCT, snap freeze in liquid nitrogen and take sections at -20°C. We take sections ranging from 20µm - 4µm. Our protocol can be found here: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333633/
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