Hello to everyone, I've used RNA plus micro kit (Qiagen) to extract RNA from an insect tissue. I kept the flow through from RNAeasy spin column. The protocol itself suggest to precipitate proteins with acetone, but as far as I know, it's not the best way to enhance purity. As a downstream process, I would like to test this proteic extract for antibacterial / antifungine / citotoxic activities, so the proteins must stay folded, or, otherwise, could you suggest me a refolding protocol?

Thank you

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