Difference between revisions of "Part:BBa K3365001"
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<partinfo>BBa_K3365001 short</partinfo> | <partinfo>BBa_K3365001 short</partinfo> | ||
− | This part is used to detect whether dCas9 protein is on-target.The sequence is made up of PDCD1, which is the binding site of dCas9, and J23117 | + | This part is used to detect whether dCas9 protein is on-target.The sequence is made up of PDCD1, which is the binding site of dCas9, and J23117 [https://parts.igem.org/Part:BBa_J23117] weak promoter spaced by 35 base pairs. The dCas9 in part [https://parts.igem.org/Part:BBa_K3365001] could bind to the PDCD1, wihch as the target of dCas9, under guidence of specific designed sgRNA, while submit Omega could bind to J23117 and activating the expression of downsream fluorescent protein. According to reference, we knew that 35 base pairs is the best spacer for activating, so we chose 35 base pairs in plasmid pUC57 at random. |
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Revision as of 02:27, 25 October 2020
Target binding site for dCas9 and subnit Omega
This part is used to detect whether dCas9 protein is on-target.The sequence is made up of PDCD1, which is the binding site of dCas9, and J23117 [1] weak promoter spaced by 35 base pairs. The dCas9 in part [2] could bind to the PDCD1, wihch as the target of dCas9, under guidence of specific designed sgRNA, while submit Omega could bind to J23117 and activating the expression of downsream fluorescent protein. According to reference, we knew that 35 base pairs is the best spacer for activating, so we chose 35 base pairs in plasmid pUC57 at random.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 66
Illegal NheI site found at 89 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]