1.Digest remaining DNA with DNAse I 1.7 µl 10x RDD buffer 2.1 µl Superasin RNAse inhibitor 3.2.5 µl DNAse I 2.Leave 30’ @ 37˚ C 3.Add 15 µl 10 M ammonium.
Digest remaining DNA with DNAse I 7 µl 10x RDD buffer 1 µl Superasin RNAse inhibitor
