Plasmid
Part:BBa_K1391112:Design
Designed by: Shinjini Saha Group: iGEM14_MIT (2014-10-17)
pEXPR_Tret:Cofilin (Inactivated - pseudophosphorylated)
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 954
Illegal XbaI site found at 915
Illegal SpeI site found at 249
Illegal PstI site found at 949
Illegal PstI site found at 2797 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 954
Illegal NheI site found at 895
Illegal SpeI site found at 249
Illegal PstI site found at 949
Illegal PstI site found at 2797
Illegal NotI site found at 926 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 954
Illegal BglII site found at 12
Illegal XhoI site found at 921 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 954
Illegal XbaI site found at 915
Illegal SpeI site found at 249
Illegal PstI site found at 949
Illegal PstI site found at 2797 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 954
Illegal XbaI site found at 915
Illegal SpeI site found at 249
Illegal PstI site found at 949
Illegal PstI site found at 2797
Illegal NgoMIV site found at 1907
Illegal NgoMIV site found at 3248
Illegal NgoMIV site found at 3531 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 882
Illegal BsaI.rc site found at 1233
Illegal BsaI.rc site found at 5056
Illegal SapI site found at 1073
Illegal SapI site found at 3976
Illegal SapI.rc site found at 3097
Illegal SapI.rc site found at 3307
Design Notes
This part was created using a single pot LR reaction. The promoter is flanked by B4 and P1 sites and the gene is flanked by P1 and B2 sites. Either of these can be extracted using a BP reaction. This part adheres to RFC 65 for recombination based cloning of mammalian parts.
Source
Human