Difference between revisions of "Part:BBa K3171175:Design"

 
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===Design Notes===
 
===Design Notes===
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Enhanced by
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Enhanced by in order to enhance function and inducibility. We optimized tetracycline-inducibility in E. coli by creating randomizations in the sequence to obtain arbitrary promoters. The screening was done based on quantifications of the fluorescence intensity measured. The best version of the promoter was determined based on fold change in the fluorescence intensity and low basal level. This promoter is used in the composite part with mCherry fusion protein.
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===Source===
 
===Source===

Revision as of 20:28, 19 October 2019


pTet-mCherry optimized in E. coli


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]


Design Notes

Enhanced by in order to enhance function and inducibility. We optimized tetracycline-inducibility in E. coli by creating randomizations in the sequence to obtain arbitrary promoters. The screening was done based on quantifications of the fluorescence intensity measured. The best version of the promoter was determined based on fold change in the fluorescence intensity and low basal level. This promoter is used in the composite part with mCherry fusion protein.

Source

iGEM registry pTET: BBa_R0040 mCherry: BBa_J06504

References