Hi everybody,
I want to perform a preliminary study to detect RNase activity on agarose gel and the protein I want to test has very high degree of purity (>99%): can you please suggest me a protocol to perform this experiment? Do I have to preliminarily treat the protein before incubating with RNA?
Thanks for the answers
PS. the protein buffer is 20mM TRIS, 100mM NaCl pH 8,5