Coding
Part:BBa_K2957096:Design
Designed by: Ye Cheng Zheng Group: iGEM19_MIT (2019-10-19)
Flag-C5a
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 3055
Illegal SpeI site found at 2167 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 3055
Illegal SpeI site found at 2167 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 3055
Illegal BglII site found at 1016
Illegal XhoI site found at 1132 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 3055
Illegal SpeI site found at 2167 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 3055
Illegal SpeI site found at 2167 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 2668
Design Notes
We used Modular Cloning Golden Gate Type II Assembly, so we had to consider how parts came together. We also used the natural secretion tag given in the part so we could use it to test chemokine secretion success by HEKs. We also had to consider which terminal the fluorescence/protein tag was added so as not to render the chemokine dysfunctional. See more on the MIT iGEM 2019 wiki: https://2019.igem.org/Team:MIT.
Source
This part was ordered from IDT/Twist Biosciences as a gBlock and then assembled into a plasmid. The sequence was taken from this site: https://www.uniprot.org/uniprot/P01031 and then codon-optimized using IDT's codon optimization tool. The Flag tag was a part in the Weiss lab database.