Difference between revisions of "Part:BBa K4855003:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | Assembled following the rules of the BioBrick RFC10 assembly procedure from parts J23101 and BBa_K4855002. | + | Assembled following the rules of the BioBrick RFC10 assembly procedure from parts J23101 and BBa_K4855002. Dual promoters: J23101 for screening and T7 for mutagenesis. |
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===Source=== | ===Source=== |
Latest revision as of 23:23, 11 October 2023
J23101 - T7 - medium RBS - blaNDM2&5 CDS
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Assembled following the rules of the BioBrick RFC10 assembly procedure from parts J23101 and BBa_K4855002. Dual promoters: J23101 for screening and T7 for mutagenesis.
Source
This part was designed to be cloned in low copy number vectors and used with the dual gene-specific mutator system from Addgene (doi: 10.1093/nar/gkad266)