Difference between revisions of "Part:BBa K2371000:Design"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K2371000 short</partinfo> | ||
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+ | <partinfo>BBa_K2371000 SequenceAndFeatures</partinfo> | ||
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+ | ===Design Notes=== | ||
+ | |||
+ | ===Source=== | ||
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+ | Sequence of T7 polymerase is obtained from Eco.li BL21(DE3), whose genome is genetically modified to contain the coding sequence for T7 polymerase. | ||
+ | |||
+ | ===References=== | ||
+ | 1.Yihao,Z.et al.,2017.Paired Design of dCas9 as a Systematic Platform for the Detection of Featured Nucleic Acid Sequences in Pathogenic Strains. ACS Synth. Biol., 2017, 6 (2), pp 211–216. | ||
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+ | 2.Tiyun,H.et al.,2016.Engineered photoactivatable genetic switches based on the bacterium phage T7 RNA polymerase.ACS Synthetic Biology,http://pubs.acs.org on October 31, 2016. |
Latest revision as of 13:18, 31 October 2017
N-t7-dCas9
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1973
Illegal BamHI site found at 1708 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 2800
Illegal NgoMIV site found at 3904
Illegal NgoMIV site found at 3977
Illegal NgoMIV site found at 4462
Illegal NgoMIV site found at 5371 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Source
Sequence of T7 polymerase is obtained from Eco.li BL21(DE3), whose genome is genetically modified to contain the coding sequence for T7 polymerase.
References
1.Yihao,Z.et al.,2017.Paired Design of dCas9 as a Systematic Platform for the Detection of Featured Nucleic Acid Sequences in Pathogenic Strains. ACS Synth. Biol., 2017, 6 (2), pp 211–216.
2.Tiyun,H.et al.,2016.Engineered photoactivatable genetic switches based on the bacterium phage T7 RNA polymerase.ACS Synthetic Biology,http://pubs.acs.org on October 31, 2016.