Difference between revisions of "Part:BBa K3183003:Design"

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===Source===
 
===Source===
  
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Derived from the <i>C. difficile</i> strain CD196 Genome; synthesized in IDT gBlocks.
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Derived from the <i>C. difficile</i> strain CD196 Genome by selecting the upstream region of agr operon; synthesized in IDT gBlocks.
  
 
===References===
 
===References===
 
Martin, Melissa J., et al. “The Agr Locus Regulates Virulence and Colonization Genes in Clostridium Difficile 027.” Journal of Bacteriology, vol. 195, no. 16, Aug. 2013, pp. 3672–81. PubMed, doi:10.1128/JB.00473-13.
 
Martin, Melissa J., et al. “The Agr Locus Regulates Virulence and Colonization Genes in Clostridium Difficile 027.” Journal of Bacteriology, vol. 195, no. 16, Aug. 2013, pp. 3672–81. PubMed, doi:10.1128/JB.00473-13.

Latest revision as of 21:52, 21 October 2019


Putative Promoter Regulated by AgrA2 in C. difficile


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

RF10, 12, 21, 23, 25, and 1000 Compatible

Source

Derived from the C. difficile strain CD196 Genome by selecting the upstream region of agr operon; synthesized in IDT gBlocks.

References

Martin, Melissa J., et al. “The Agr Locus Regulates Virulence and Colonization Genes in Clostridium Difficile 027.” Journal of Bacteriology, vol. 195, no. 16, Aug. 2013, pp. 3672–81. PubMed, doi:10.1128/JB.00473-13.