Reporter
Part:BBa_K1088007:Design
Designed by: Andreas Kjær Group: iGEM13_SDU-Denmark (2013-08-20)
E. coli dxs-GFP fusion (lac promoter without lac inhibitor: IPTG uninducible)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2756
Illegal SapI.rc site found at 946
Design Notes
We used USER cloning to assemble this part and therefore there are no scar sites. However we did insert a scarsite between the RBS and the start codon aswell as between the promoter and RBS, for optimal expression of our protein.
Source
The subparts of this composite part is derived from E. coli K-12 MG1655. The GFP derives from Aequorea victoria.