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In cell culture, can treated surface survive autoclaving?

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If I treat a surface for cell adhesion with fibronectin, collagen, etc., can I autoclave it and expect it to function in allowing the attachment of mammalian cells?  Since denatured collagen is used to promote adhesion, it seems like it might be feasible, but I don't know.  If this is a less than optimal idea, does anyone know of any alternatives?  If anyone has any insight, I'd appreciate it.  I'll thank you in advance.

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