Reporter

Part:BBa_K934025

Designed by: Toshiki Hashimoto   Group: iGEM12_Tokyo_Tech   (2012-09-17)
Revision as of 01:06, 26 September 2012 by Toshiki (Talk | contribs)

Plux/tet-GFP

We constructed this part by ligating Plux/tet hybrid promoter (BBa_K934024) to the upstream of promoterless GFP generator (BBa_I13504).

Pluxtet assay.png

In the presence of both inducers, the culture showed about 500-fold higher fluorescence intensity than that in the absence of both inducers.


For more information, see [http://2012.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2012 wiki]. 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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 751


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