Generator
Part:BBa_K1179040:Design
Designed by: Lauren St. Hilaire Group: iGEM13_MIT (2013-09-15)
TRE_Cas9-VP16
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 3695
Illegal XbaI site found at 30
Illegal PstI site found at 2084
Illegal PstI site found at 2318
Illegal PstI site found at 3530
Illegal PstI site found at 3834 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 3695
Illegal PstI site found at 2084
Illegal PstI site found at 2318
Illegal PstI site found at 3530
Illegal PstI site found at 3834 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 3695
Illegal BglII site found at 1060
Illegal BamHI site found at 1878
Illegal XhoI site found at 3416 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 3695
Illegal XbaI site found at 30
Illegal PstI site found at 2084
Illegal PstI site found at 2318
Illegal PstI site found at 3530
Illegal PstI site found at 3834 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 3695
Illegal XbaI site found at 30
Illegal PstI site found at 2084
Illegal PstI site found at 2318
Illegal PstI site found at 3530
Illegal PstI site found at 3834
Illegal NgoMIV site found at 2612 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
For people interested in using this part, the Cas9-VP16 has only been used as a transactivator on a minimal CMV promoter.
Source
Constructed by performing a Gateway reaction of the TRE-tight promoter and the Cas9-VP16 entry vector. The Cas9 protein originates from the type II prokaryotic CRISPR system in the bacterium Streptococcus pyogenes.