Fig. 2.
In vitro translated PCV 1 RdRp is active as an RT. (A) a schematic of in vitro translation of PCV1 RdRp and determination the RT activity of protein through RT-PCR. (B) RT-PCR analysis using PCV1 dsRNA as RNA template and PCV1-RdRp primers; M, DNA marker, 1, in vitro translated PCV1 RdRp as enzyme, 2, negative control (no enzyme), 3, negative control (no primer), 4, MMuLV used as enzyme. (C) RT-PCR analysis using PCV1 dsRNA as RNA template and PCV1-RdRp primers, RT reactions at 42°C; M, DNA marker, 1, negative control (no enzyme), 2, in vitro translated PCV1 RdRp used as RT enzyme, 3, MMuLV used as enzyme.

In vitro translated PCV 1 RdRp is active as an RT. (A) a schematic of in vitro translation of PCV1 RdRp and determination the RT activity of protein through RT-PCR. (B) RT-PCR analysis using PCV1 dsRNA as RNA template and PCV1-RdRp primers; M, DNA marker, 1, in vitro translated PCV1 RdRp as enzyme, 2, negative control (no enzyme), 3, negative control (no primer), 4, MMuLV used as enzyme. (C) RT-PCR analysis using PCV1 dsRNA as RNA template and PCV1-RdRp primers, RT reactions at 42°C; M, DNA marker, 1, negative control (no enzyme), 2, in vitro translated PCV1 RdRp used as RT enzyme, 3, MMuLV used as enzyme.

Close
This Feature Is Available To Subscribers Only

Sign In or Create an Account

Close

This PDF is available to Subscribers Only

View Article Abstract & Purchase Options

For full access to this pdf, sign in to an existing account, or purchase an annual subscription.

Close