I am planning to test the activity of a proteinase using an old casein-agar plate assay. According to a protocol I followed, it requires sterilizing the media with casein in it. The first time I did, the media turned black. No aggregate formation, just clear black media(which might have burnt). Can I autoclave the casein+agar?

Also, I am planning to use casein enzymatic hydrolysate instead of casein. Will that make a difference in the activity assay?

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