Hi everyone!

We are working with corneal endothelium on Descemet membrane. It can be considered as a cell monolayer on thin protein membrane, so you can treat it like a fresh tissue slide. We want to perform IHC. In a paper where they studied the same tissue they have air dried fresh Descemet membrane on a slide, then "fixed in acetone and stored at -20C".

https://iovs.arvojournals.org/article.aspx?articleid=2600835

The question is how to store this tissue slides after acetone fixation at -20C - dry (wait until acetone evaporate and put a slide in some plastic bag and leave at -20C) or in acetone (leave slide in a bottle with acetone and store it at -20)?

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