Difference between revisions of "Part:BBa K4630201:Design"
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+ | Zhao, D., Yuan, S., Xiong, B. et al. Development of a fast and easy method for Escherichia coli genome editing with CRISPR/Cas9. Microb Cell Fact 15, 205 (2016). |
Revision as of 15:02, 10 October 2023
The optimized pCas
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1344
Illegal EcoRI site found at 7542
Illegal EcoRI site found at 11785
Illegal SpeI site found at 5392
Illegal PstI site found at 11075 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1344
Illegal EcoRI site found at 7542
Illegal EcoRI site found at 11785
Illegal NheI site found at 1103
Illegal SpeI site found at 5392
Illegal PstI site found at 11075
Illegal NotI site found at 5711 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1344
Illegal EcoRI site found at 7542
Illegal EcoRI site found at 11785
Illegal BglII site found at 4205
Illegal BamHI site found at 3382
Illegal BamHI site found at 7476
Illegal BamHI site found at 11664 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1344
Illegal EcoRI site found at 7542
Illegal EcoRI site found at 11785
Illegal SpeI site found at 5392
Illegal PstI site found at 11075 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1344
Illegal EcoRI site found at 7542
Illegal EcoRI site found at 11785
Illegal SpeI site found at 5392
Illegal PstI site found at 11075
Illegal NgoMIV site found at 10624
Illegal AgeI site found at 7311
Illegal AgeI site found at 8973
Illegal AgeI site found at 11499 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 4231
Illegal BsaI.rc site found at 4219
Illegal SapI site found at 7293
Illegal SapI site found at 10564
Illegal SapI site found at 10774
Illegal SapI site found at 11481
Design Notes
The plasmid is temperature sensitive.
Source
Zhao, D., Yuan, S., Xiong, B. et al. Development of a fast and easy method for Escherichia coli genome editing with CRISPR/Cas9. Microb Cell Fact 15, 205 (2016).
References
Zhao, D., Yuan, S., Xiong, B. et al. Development of a fast and easy method for Escherichia coli genome editing with CRISPR/Cas9. Microb Cell Fact 15, 205 (2016).