Difference between revisions of "Part:BBa K3183003:Design"
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===Source=== | ===Source=== | ||
− | Derived from the <i>C. difficile</i> strain CD196 Genome; synthesized in IDT gBlocks. | + | 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. |
Latest revision as of 21:52, 21 October 2019
Putative Promoter Regulated by AgrA2 in C. difficile
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE 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.