Difference between revisions of "Part:BBa K2558201:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | Sequence is modified at A1403T in order to be RFC10 compatible. | |
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===References=== | ===References=== | ||
+ | Gilbert LA et al. Genome-Scale CRISPR-Mediated Control of Gene Repression and Activation. Cell. 2014 Oct 23;159(3):647-61. |
Latest revision as of 08:12, 2 October 2018
dCas9 generator with Anderson weak promotor
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 1163 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 3442
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Sequence is modified at A1403T in order to be RFC10 compatible.
Source
The sequence came from the registry and a commonly used CRISPRi system from Chen Lab.
References
Gilbert LA et al. Genome-Scale CRISPR-Mediated Control of Gene Repression and Activation. Cell. 2014 Oct 23;159(3):647-61.