19 October 2019 3 6K Report

I grow cells on Silicon substrates as part of my research. However, i usually throw out the substrates afterwards. I was wondering if there is a way to clean them in order to re-use them, but without changing the micro and nano-scale topographies.

I tried alcohol or trypsin (which we use to remove cells) but it did not work (i can see that there is GFP signal after cleaning, and possibly lots of ECM proteins). I was wondering if there is a protocol you use.

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