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rnase assay


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helo

i used kamekura and onishi method for rnase activity.briefly its steps r:

buffer pH 7

enzyme .1ml

rna 1mg

incubation for 2 hr

stop solution

centrifuge

then in end dilution of supernatent.

in many other protocol more or less all steps are same but i cant get the logic related to dilutions.

is it the necessary step or what??? as if i have the O.D 2.06 of test y i dilute it????

and if i dilute at which dilution i used???

ooooh so confusing:^

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