Difference between revisions of "Part:BBa K4725001:Design"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K4725000 short</partinfo> | ||
+ | |||
+ | <partinfo>BBa_K4725000 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | ===Design Notes=== | ||
+ | The promoter can be fused with fluorescent protein for reporter assay. This promoter is leaky in E. coli. It is suggested not to use it in E. coli unless there is a specific reason. | ||
+ | |||
+ | |||
+ | ===Source=== | ||
+ | |||
+ | The sequence of this promoter is extracted from ‘Negative Interplay between Biofilm Formation and Competence in the Environmental Strains of Bacillus subtilis’ https://journals.asm.org/doi/10.1128/msystems.00539-20 | ||
+ | |||
+ | |||
+ | ===References=== |
Latest revision as of 15:53, 12 October 2023
-- No description --
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The promoter can be fused with fluorescent protein for reporter assay. This promoter is leaky in E. coli. It is suggested not to use it in E. coli unless there is a specific reason.
Source
The sequence of this promoter is extracted from ‘Negative Interplay between Biofilm Formation and Competence in the Environmental Strains of Bacillus subtilis’ https://journals.asm.org/doi/10.1128/msystems.00539-20