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©2005 Baishideng Publishing Group Inc.
World J Gastroenterol. Mar 7, 2005; 11(9): 1297-1302
Published online Mar 7, 2005. doi: 10.3748/wjg.v11.i9.1297
Published online Mar 7, 2005. doi: 10.3748/wjg.v11.i9.1297
Figure 4 Processing of long dsRNAs into siRNAs with recombinant E.
coli RNase III. A: 1, 3 and 5 μg dsRNAs (Lanes 2-4) were digested with 1 µg RNase III at 37 °C for 1 h in 10 µg reaction mixture containing 50 mmol/l Tris–HCl, 50 mmol/L NaCl, 10 mmol/L MnCl2 and 1 mmol/L DTT (pH 7.5). The siRNA-like products were indicated by an arrow on the right. Lane 1: undigested dsRNAs; B: The siRNAs were recovered from the gel (Lane 2).
- Citation: Qian ZK, Xuan BQ, Min TS, Xu JF, Li L, Huang WD. Cost-effective method of siRNA preparation and its application to inhibit hepatitis B virus replication in HepG2 cells. World J Gastroenterol 2005; 11(9): 1297-1302
- URL: https://www.wjgnet.com/1007-9327/full/v11/i9/1297.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i9.1297