Difference between revisions of "Part:BBa K2365047"

 
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<partinfo>BBa_K2365047 parameters</partinfo>
 
<partinfo>BBa_K2365047 parameters</partinfo>
 
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[[File: TDH1 TDH1-cyc1 NAU-04.jpeg|300px|center]]
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[[File: TDH1 TDH1-cyc1 NAU-04.jpeg|500px|center]]
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We used reserved restriction enzyme cutting site to inserted GPF (S6GT) between promoter and termiator as the index of promoter test. After 30 hours incubation, we measured the fluorescence intensity of the transformed yeast at 440 nm to 530 nm
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[[File: U-disk test.jpg|500px|center]]
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[[File:酵母荧光.jpg|700px|center]]

Latest revision as of 09:17, 1 November 2017


TDH1 promoter-CYC1 terminator

Between the TDH1 and cyc1,having the restriction enzyme cutting site.And you can insert the gene if you want

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 431
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


TDH1 TDH1-cyc1 NAU-04.jpeg

We used reserved restriction enzyme cutting site to inserted GPF (S6GT) between promoter and termiator as the index of promoter test. After 30 hours incubation, we measured the fluorescence intensity of the transformed yeast at 440 nm to 530 nm

U-disk test.jpg
酵母荧光.jpg