Difference between revisions of "Part:BBa K1893007:Design"

 
Line 7: Line 7:
  
 
===Design Notes===
 
===Design Notes===
−
Lots of stuff
+
This part does not include an LVA tag on the CinR gene. This means that the protein is not rapidly degraded. When active, the CinR protein binds to the pCin promoter, activating transcription of downstream genes. This part contains everything necessary for O3C14-HSL-induced expression of genes inserted downstream of the pCin promoter, which is, in this case, GFPmut3b. GFPmut3b was included in this part so that we could characterize the activation range of the CinR system.
  
  
Line 13: Line 13:
 
===Source===
 
===Source===
  
−
More Stuff
+
The CinR gene was synthesised and assembled with the other parts using Biobrick assembly.
  
 
===References===
 
===References===

Revision as of 19:45, 22 October 2016


Cin receiver with GFP (CinR+pCin+GFP)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 611
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1698


Design Notes

This part does not include an LVA tag on the CinR gene. This means that the protein is not rapidly degraded. When active, the CinR protein binds to the pCin promoter, activating transcription of downstream genes. This part contains everything necessary for O3C14-HSL-induced expression of genes inserted downstream of the pCin promoter, which is, in this case, GFPmut3b. GFPmut3b was included in this part so that we could characterize the activation range of the CinR system.


Source

The CinR gene was synthesised and assembled with the other parts using Biobrick assembly.

References