Difference between revisions of "Part:BBa K1886006:Design"
(→Source) |
(→Source) |
||
Line 14: | Line 14: | ||
===Source=== | ===Source=== | ||
− | From E coli genome, obtained from iGEM team HZAU's lab | + | From E coli genome, obtained from iGEM team HZAU's lab. |
This plasmid is bought from Addgene Company. | This plasmid is bought from Addgene Company. | ||
Revision as of 22:50, 17 October 2016
broken Ptet-cph8
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2332
Illegal XhoI site found at 439 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
There was a SpeI site in the sequence encoding protein cph8, so we designed a silent mutation.
Source
From E coli genome, obtained from iGEM team HZAU's lab. This plasmid is bought from Addgene Company.
References
Levskaya, A. et al (2005). Engineering Escherichia coli to see light. Nature, 438(7067), 442.
Olson E J, Hartsough L A, Landry B P, et al. Characterizing bacterial gene circuit dynamics with optically programmed gene expression signals[J]. Nature methods, 2014, 11(4): 449-455. MLA