Difference between revisions of "Part:BBa K5133000"
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<partinfo>BBa_K5133000 short</partinfo> | <partinfo>BBa_K5133000 short</partinfo> | ||
− | Group: <b>GEC-China (iGEM 2024, team number: 5133)</b> | + | Group: <b>GEC-China (iGEM 2024, team number: #5133)</b> |
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+ | This basic part is derived from plasmid pJL1 (Addgene: #69496)<sup>[1]</sup>, including a conserved DNA sequence of T7 promoter as <b>5'-taatacgactcactatagggaga-3'</b><sup>[2]</sup>. The plasmid pJL1 is commonly used for the sfGFP expression for cell-free protein synthesis (CFPS). Hence, this part is used for the construction of three composite parts: BBa_K5133004 (sfGFP generator for CFPS), BBa_K5133006 (Microcin H47 generator for CFPS), and BBa_K5133008 (Microcin M generator for CFPS), respectively. | ||
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Revision as of 02:35, 27 July 2024
T7 promoter (from plasmid pJL1)
Group: GEC-China (iGEM 2024, team number: #5133)
This basic part is derived from plasmid pJL1 (Addgene: #69496)[1], including a conserved DNA sequence of T7 promoter as 5'-taatacgactcactatagggaga-3'[2]. The plasmid pJL1 is commonly used for the sfGFP expression for cell-free protein synthesis (CFPS). Hence, this part is used for the construction of three composite parts: BBa_K5133004 (sfGFP generator for CFPS), BBa_K5133006 (Microcin H47 generator for CFPS), and BBa_K5133008 (Microcin M generator for CFPS), respectively.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 51
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 51
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 51
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 32