Difference between revisions of "Part:BBa K3726026:Design"
Line 12: Line 12:
  
 
===Source===
 
===Source===
−
Coding sequence of this RBS has been found within the genome of E.Coli BL21.
+
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.
 
H. Jeong, H. Kim and S. Lee, "Complete Genome Sequence of Escherichia coli Strain BL21", Genome Announcements, vol. 3, no. 2, 2015.

Revision as of 16:43, 10 October 2021


RBS_garR


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

This part corresponds was designed to optimize the expression of the enzyme garR encoded by the part BBa_K3726027 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.