Composite
Part:BBa_K5047043:Design
Designed by: Clément Alain Serge Corneil Vanmerris Group: iGEM24_UNILausanne (2024-10-01)
Sequence encodes pCYC1 promoter and mCherry for expression in S. cerevisiae.
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 640
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 640
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 39
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 640
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 640
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
None.
Source
The pCYC1 promoter originates from the pDA120 plasmid and the mCherry reporter originates from the pDA95 plasmid, both plasmids were provided by Prof. Serge Pelet (DMF, University of Lausanne).