Difference between revisions of "Part:BBa K4511007"
Line 4: | Line 4: | ||
This part is a measurement device for degradation-tuning RNAs, which contains medium strength J23106 promoter, medium RBS B0032, and a reporter protein coding sequence GFP. The effectiveness of dtRNA is evaluated by measuring GFP fluorescence and bacterial growth curve. It could be used as an inter-lab study device to compare experimental conditions among different labs. This plasmid could also be directly transformed into other species or strains of E.coli to study the effectiveness of dtRNA on another chassis. | This part is a measurement device for degradation-tuning RNAs, which contains medium strength J23106 promoter, medium RBS B0032, and a reporter protein coding sequence GFP. The effectiveness of dtRNA is evaluated by measuring GFP fluorescence and bacterial growth curve. It could be used as an inter-lab study device to compare experimental conditions among different labs. This plasmid could also be directly transformed into other species or strains of E.coli to study the effectiveness of dtRNA on another chassis. | ||
+ | |||
+ | |||
+ | ==Improvement by 2022 team HUS_United== | ||
+ | |||
+ | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 14:29, 12 October 2022
Reporter device with J23106 , B0032, and GFP for dtRNA1 strength measurement
This part is a measurement device for degradation-tuning RNAs, which contains medium strength J23106 promoter, medium RBS B0032, and a reporter protein coding sequence GFP. The effectiveness of dtRNA is evaluated by measuring GFP fluorescence and bacterial growth curve. It could be used as an inter-lab study device to compare experimental conditions among different labs. This plasmid could also be directly transformed into other species or strains of E.coli to study the effectiveness of dtRNA on another chassis.
Improvement by 2022 team HUS_United
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 753