Difference between revisions of "Part:BBa K3081057"
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This composite part is the principal design of the inducible CRISPR-based DNA replication interference system, with the 20 bp sgRNA targeting to the bottom strand of initiation site on p15A origin. In this part, we add a degradation signal peptide "ssrA" to the dCas9 to alleviate its effect. | This composite part is the principal design of the inducible CRISPR-based DNA replication interference system, with the 20 bp sgRNA targeting to the bottom strand of initiation site on p15A origin. In this part, we add a degradation signal peptide "ssrA" to the dCas9 to alleviate its effect. | ||
| + | https://2019.igem.org/wiki/images/3/3b/T--Peking--p15A_control_schematic.png | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
Revision as of 12:27, 21 October 2019
CRISPR-based replication interference system for p15A plasmid copy number control, ini(+) site
This composite part is the principal design of the inducible CRISPR-based DNA replication interference system, with the 20 bp sgRNA targeting to the bottom strand of initiation site on p15A origin. In this part, we add a degradation signal peptide "ssrA" to the dCas9 to alleviate its effect.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1205
Illegal NheI site found at 2321
Illegal NheI site found at 5495
Illegal NheI site found at 5518 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1144
Illegal BamHI site found at 4600 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 979
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 961