Dear all,

I have done polyacrylamide hydrogels for cell cultures.

For preparing the glass, I add 0.1M NaOH, heat at 100°C and then add APES/APTES (3-aminopropyltriethoxysilane). I was wondering if this prepared glass could undergo autoclaving without destroying the coating.

The idea is to go under sterile conditions after autoclaving, filtering glultaraldehyde and the rest of the protocol.

Thanks for your help!

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