Reporter
Part:BBa_K2150018:Design
Designed by: Jianyi Huang Group: iGEM16_UCAS (2016-10-12)
pT7+pTet+RBS+GFP+DT
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 752
Design Notes
By adding a T7 promoter, we hope to achieve positive feedback in the presence of T7RNAP. We used GFP to test whether this can work before experimenting with our target gene.
Source
pT7 PCR amplified from BBa_K525998,pTet from BBa_R0040,RBS from BBa_B0034,GFP from BBa_E0040,DT from BBa_B0015