Difference between revisions of "Part:BBa K3726024:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | This part was designed to optimize the expression of the enzyme garK encoded by the part BBa_K3726025 | |
− | + | but has not been tested alone but within the composite part BBa_K3726028. | |
===Source=== | ===Source=== | ||
+ | Coding sequence of this RBS has been found within the genome of <i>E.Coli BL21</i>. | ||
− | |||
===References=== | ===References=== | ||
+ | H. Jeong, H. Kim and S. Lee, "Complete Genome Sequence of Escherichia coli Strain BL21", Genome Announcements, vol. 3, no. 2, 2015. |
Latest revision as of 18:05, 10 October 2021
RBS_garK
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
This part was designed to optimize the expression of the enzyme garK encoded by the part BBa_K3726025 but has not been tested alone but within the composite part BBa_K3726028.
Source
Coding sequence of this RBS has been found within the genome of E.Coli BL21.
References
H. Jeong, H. Kim and S. Lee, "Complete Genome Sequence of Escherichia coli Strain BL21", Genome Announcements, vol. 3, no. 2, 2015.