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10.1038/cr.2010.178 74 MorrisD.GuerraC.DonohueC.OhH.KhurasanyM.VenketaramanV
MosenzonORazISciricaBMHirshbergBStahreCIStegPGet al
[ 4 ] Instead, several hypotheses have been proposed based on preclinical investigations
After dilution by TE buffer, the immunoprecipitated and input DNA were treated with RNase A (0.2 mg/mL) at 37 C for 2 h, followed by proteinase K (0.2 mg/mL) treatment at 55 C for 2 h, and then subjected to phenol:chloroform:isoamyl alcohol extraction and ethanol precipitation
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