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Why siRNA peak AUC vary for sense and antisense strands after denaturation. Isn't it ideally it should be in 1:1 ratio and hence AUC to be same?
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Currently, I tried with siRNA using mobile phase A: 100mM TEAA+ Acetonitrile (20:80) and mobile phase B: 100mM TEAA+ Acetonitrile (95:5). But the RT keeps changing and baseline is not straight.
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