Se I (B, C and D) was also included as positive control. The protein solutions were shown on the top and the nucleic acids were indicated on the right. 1 μg of nucleic acids were respectively incubated with 1.5 μg of the purified GBSV1-NSN protein in 20 μl of reaction buffer at 37°C for six hours.<p><b>Copyright information:</b></p><p>Taken from "Characterization of a novel non-specific nuclease from thermophilic bacteriophage GBSV1"</p><p>http://www.biomedcentral.com/1472-6750/8/43</p><p>BMC Biotechnology 2008;8():43-43.</p><p>Published online 28 Apr 2008</p><p>PMCID:PMC2390534.</p><p></p
