Difference between revisions of "Part:BBa K1401007"

 
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<partinfo>BBa_K1401007 short</partinfo>
 
<partinfo>BBa_K1401007 short</partinfo>
  
This tandem promoter was created using the MoClo assembly method. This is a Level 0 MoClo part with flanking sites A on the 5' side and site B on the 3' side of the part. The fusion site letters refer to 4bp fusion sites: A = GGAG; B = TACT; C = AATG; D = AGGT; E = GCTT; F = CGCT; G = TGCC; H = ACTA. This transcriptional unit has Kanamycin resistance. The promoter is induced by atc and arabinose.
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This tandem promoter was created using the MoClo assembly method. This is a Level 0 MoClo part with flanking sites A on the 5' side and site B on the 3' side of the part. The fusion site letters refer to 4bp fusion sites: A = GGAG; B = TACT; C = AATG; D = AGGT; E = GCTT; F = CGCT; G = TGCC; H = ACTA.  
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This tandem promoter has chloramphenicol resistance as it is located in pSB1C3. The promoter is induced by anhydrotetracycline and arabinose.
  
The characterization data will be updated before the jamboree.  
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[[File:K1401007_flow.png]]
  
 
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Revision as of 00:01, 14 October 2014

Tandem promoter pTet-pBad

This tandem promoter was created using the MoClo assembly method. This is a Level 0 MoClo part with flanking sites A on the 5' side and site B on the 3' side of the part. The fusion site letters refer to 4bp fusion sites: A = GGAG; B = TACT; C = AATG; D = AGGT; E = GCTT; F = CGCT; G = TGCC; H = ACTA.

This tandem promoter has chloramphenicol resistance as it is located in pSB1C3. The promoter is induced by anhydrotetracycline and arabinose.

K1401007 flow.png

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 324
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 159
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 141