Part:BBa_K3425060:Design
T7 polymerase regulated Juniper GFP substrate for Qβ replicase
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 550
Illegal XbaI site found at 83 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 550
Illegal NheI site found at 859 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 550
Illegal BglII site found at 86
Illegal BamHI site found at 759
Illegal XhoI site found at 90
Illegal XhoI site found at 890 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 550
Illegal XbaI site found at 83 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 550
Illegal XbaI site found at 83 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
none
Source
QB recognition sites
Yao, Y., Zhang, W., Zhang, M., Jin, S., Guo, Y., Zu, Y., Ren, K., Wang, K., Chen, G., Lou, C., and Wu, Q. (2019) A Direct RNA-to-RNA Replication System for Enhanced Gene Expression in Bacteria. ACS Synth. Biol. 8, 1067–1078
Registry of Standard Biological Parts
References
QB recognition sites
Refereces
[1]
Yao, Y., Zhang, W., Zhang, M., Jin, S., Guo, Y., Zu, Y., Ren, K., Wang, K., Chen, G., Lou, C., and Wu, Q. (2019) A Direct RNA-to-RNA Replication System for Enhanced Gene Expression in Bacteria. ACS Synth. Biol. 8, 1067–1078
Note, that the authors declared the following competing financial interest(s): Y. Y., W. Z., and Q. W. have filed a patent on RNA replication system and its usage.