Part:BBa_K4139028
Rec. CP-MAF
This construct begins with a lysine rich region, with this region being included to enhance conjugation with fluorophore reporter molecules. After this, we have utilized the framework three region of a mouse IGG antibody as a scaffold for our chimeric protein against PbEL04. We have inserted our chimeric protein into the CDR3 region of the framework 3 region of the mouse antibody and have repeated this framework 3 - chimeric protein motif once with the only difference being that the chimeric protein utilized was complementary to PRO1 in the second interaction. After this, we included a 6x His-tag to aid in purification. We first made this coding region as a basic part (BBa_K4139019) which we have made as a composite part with a ribosome binding site, promoter, and terminator.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 980
Illegal PstI site found at 1238 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 27
Illegal NheI site found at 50
Illegal PstI site found at 980
Illegal PstI site found at 1238 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1312
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 980
Illegal PstI site found at 1238 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 980
Illegal PstI site found at 1238
Illegal AgeI site found at 529 - 1000COMPATIBLE WITH RFC[1000]
//function/reporter
direction | Forward |
protein | CP-MAF |
tag | His-Tag |