Composite

Part:BBa_K4779003

Designed by: Ziqi Mi   Group: iGEM23_Nanjing-BioXstem   (2023-09-26)
Revision as of 13:30, 26 September 2023 by Registry (Talk | contribs)

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CMPS Pro:A yeast copper-induced reporter pathway with Positive feedback loop with prm1pro promoter

It is a copper ion reaction reporting pathway in Saccharomyces cerevisiae. We utilized the pprm1 Pro for optimizing GFP expression, and employed the prm1 promoter to express Ste5ΔN-CTM for positive feedback regulation in the yeast copper-induced reporting pathway.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 3138
    Illegal XbaI site found at 279
    Illegal XbaI site found at 517
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal SpeI site found at 4393
    Illegal SpeI site found at 4939
    Illegal PstI site found at 49
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 3138
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal SpeI site found at 4393
    Illegal SpeI site found at 4939
    Illegal PstI site found at 49
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 3138
    Illegal BglII site found at 55
    Illegal BglII site found at 3586
    Illegal BglII site found at 4894
    Illegal BamHI site found at 510
    Illegal XhoI site found at 8
    Illegal XhoI site found at 4831
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 3138
    Illegal XbaI site found at 279
    Illegal XbaI site found at 517
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal SpeI site found at 4393
    Illegal SpeI site found at 4939
    Illegal PstI site found at 49
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 3138
    Illegal XbaI site found at 279
    Illegal XbaI site found at 517
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal SpeI site found at 4393
    Illegal SpeI site found at 4939
    Illegal PstI site found at 49
    Illegal NgoMIV site found at 36
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 2694
    Illegal SapI site found at 529


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