Difference between revisions of "Part:BBa K3128001:Design"

(Design Notes)
Line 8: Line 8:
 
===Design Notes===
 
===Design Notes===
 
To do a BACTH assay the reporter gene need to :
 
To do a BACTH assay the reporter gene need to :
 +
 
Have a CAP inducible promoter : PLac
 
Have a CAP inducible promoter : PLac
 +
 
A strong RBS to optimize protein expression
 
A strong RBS to optimize protein expression
 +
 
A easly measurable protein : NanoLuciferase
 
A easly measurable protein : NanoLuciferase
  
Line 15: Line 18:
  
 
https://2019.igem.org/wiki/images/thumb/7/70/T--Grenoble-Alpes--Plasmid_PLacNanoLuc.png/595px-T--Grenoble-Alpes--Plasmid_PLacNanoLuc.png
 
https://2019.igem.org/wiki/images/thumb/7/70/T--Grenoble-Alpes--Plasmid_PLacNanoLuc.png/595px-T--Grenoble-Alpes--Plasmid_PLacNanoLuc.png
 
 
  
 
===Source===
 
===Source===

Revision as of 19:30, 15 September 2019


NanoLuciferase reporter for BACTH assay


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

To do a BACTH assay the reporter gene need to :

Have a CAP inducible promoter : PLac

A strong RBS to optimize protein expression

A easly measurable protein : NanoLuciferase


595px-T--Grenoble-Alpes--Plasmid_PLacNanoLuc.png

Source

iGEM plate : Bba_J04450 and Bba_K1680009

References