Deleted
Sample Discontinued
Experience: None
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Part:BBa_J100211

Designed by: Julia Preziosi   Group: Campbell M Lab   (2015-06-09)


tCloneTet+Red; Fusion Protein Reporter

This part was made from adding the TetA gene from part J119140 in front of the RFP gene in the tCloneRed part J119361. The Tet and RFP genes were combined, by deleting the "stop" sequence in the Tet gene and adding a linker sequence of proteins GGGS x4 to create a fusion protein. The resultant protein is a single protein with both the Tetracycline resistance protein and the Red fluorescent protein, combined with a linker chain. This part still contains tClone, and will not transcribe the reporter gene (Tet+Red) without the insertion of a riboswitch etc. between the BsaI sites.

Sequence and Features


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]


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