Reporter
Part:BBa_K649001
Designed by: Tomoyuki Ohno Group: iGEM11_Tokyo_Tech (2011-09-26)
Revision as of 05:30, 3 October 2011 by Takuya 1613 (Talk | contribs)
GFP regulated by 3OC12-HSL and LasR
Fluorescence intensity of BBa_K649001 was increased by 3OC12-HSL induction.
Generally, in the presence of 3OC12-HSL, lasR activates lasI promoter and the transcription level of downstream gene increases, but in the absence of 3OC12-HSL, lasR can't activate lasI promoter. 2011 iGEM Tokyo-Tech characterized BBa_K649000 by means of using BBa_K649001 composed of BBa_K649000 and BBa_J54103.
We improved previous lasI promoter(BBa_J64010).our assay of BBa_J64010
For more information, see our work in Tokyo_Tech 2011 wiki
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 118
Illegal BamHI site found at 106 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 805
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Categories
Parameters
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