Plasmid_Backbone
Part:BBa_K1621009:Design
Designed by: Ramona Emig, Julika Neumann, Lara Stuehn Group: iGEM15_Freiburg (2015-08-30)
pOP - protein expression vector compatible with RFC[25]
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found at 4984
Illegal suffix found at 10 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 4984
Illegal SpeI site found at 11
Illegal PstI site found at 25
Illegal NotI site found at 18
Illegal NotI site found at 4990 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 4984
Illegal BglII site found at 4837 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found at 4984
Illegal suffix found at 11 - 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI site found at 1054
Design Notes
The original sequence of pET22b+ was modified to make it compatible to iGEM standard cloning procedures. This includes the removal of recognition sites of several restriction enzymes as well as the insertion of RFC[25] as a multiple cloning site. Further details can be found on the main page.
Source
The sequence is a modified version of the common expression vector pET22b+. Five fragments that were needed for the assembly of the whole part were synthesized by Integrated DNA Technologies.