Difference between revisions of "Part:BBa K3338019"

 
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<partinfo>BBa_K3338019 short</partinfo>
 
<partinfo>BBa_K3338019 short</partinfo>
  
This part consists of an interleukin-6 promoter that is mutagenized to make it compatible with the RFC10 assembly standard that controls the expression of the reporter hGLuc. It can be used to determine the basal promoter activity and the activity following changes in the surrounding of the cell like LPS supplementation. As a control CMV-hGLuc (<html><a href="https://parts.igem.org/Part:BBa_K3338017"> BBa_K3338017</a></html>) can be used.
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This part consists of an interleukin-6 promoter that is mutagenized to make it compatible with the RFC10 assembly standard that controls the expression of the reporter hGLuc. It can be used to determine the basal promoter activity and the activity following changes in the surrounding of the cell like LPS supplementation. As a control CMV-hGLuc (<html><a href="https://parts.igem.org/Part:BBa_K3338017">BBa_K3338017</a></html>) can be used.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 21:23, 23 October 2020


IL-6 Pmut-hGLuc

This part consists of an interleukin-6 promoter that is mutagenized to make it compatible with the RFC10 assembly standard that controls the expression of the reporter hGLuc. It can be used to determine the basal promoter activity and the activity following changes in the surrounding of the cell like LPS supplementation. As a control CMV-hGLuc (BBa_K3338017) can be used.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1347
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 220
    Illegal BamHI site found at 395
    Illegal XhoI site found at 1581
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 340
    Illegal BsaI.rc site found at 387
    Illegal BsaI.rc site found at 696