Difference between revisions of "Part:BBa K2876000:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This promoter has been optimized for E. coli | + | This promoter has been optimized for E. coli, and has been modified from a traditional pLacZ promoter to allow upstream lambda-cl bonding. |
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===Source=== | ===Source=== |
Latest revision as of 06:50, 17 October 2018
placOL2-62 E. coli promoter
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1
Illegal PstI site found at 25 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1
Illegal PstI site found at 25 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1
Illegal PstI site found at 25 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1
Illegal PstI site found at 25 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
This promoter has been optimized for E. coli, and has been modified from a traditional pLacZ promoter to allow upstream lambda-cl bonding.
Source
Dove, S. L., Joung, J. K., & Hochschild, A. (1997). Activation of prokaryotic transcription through arbitrary protein- protein contacts. Nature. http://doi.org/10.1038/386627a0
References
Dove, S. L., Joung, J. K., & Hochschild, A. (1997). Activation of prokaryotic transcription through arbitrary protein- protein contacts. Nature. http://doi.org/10.1038/386627a0