Difference between revisions of "Part:BBa K3187043"
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This part is a generator for the P22 bacteriophage scaffold protein fused to a super folder GFP. This part was used together with <a | This part is a generator for the P22 bacteriophage scaffold protein fused to a super folder GFP. This part was used together with <a | ||
− | href=" https://parts.igem.org/Part:BBa_K3187044" target="_blank">BBa_K3187044</a> for the dual expression of the P22 scaffold protein and the P22 coat protein fused to a LPETGG-tag for | + | href=" https://parts.igem.org/Part:BBa_K3187044" target="_blank">BBa_K3187044</a> for the dual expression of the P22 scaffold protein and the P22 coat protein fused to a LPETGG-tag for sortase-mediated ligation of GGGG-tagged proteins to the surface of P22 Virus-like particles. The potential of fine tuning the expression levels of both parts was tested via <a |
+ | href=" https://parts.igem.org/Part:BBa_K3187011" target="_blank">BBa_K3187011</a>. | ||
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− | <span class='h3bb'>Sequence and Features</span> | + | <h2><span class='h3bb'>Sequence and Features</span></h2> |
<partinfo>BBa_K3187043 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3187043 SequenceAndFeatures</partinfo> | ||
Latest revision as of 08:53, 20 October 2019
Superfolder GFP + P22 Bacteriophage Scaffolding Protein Generator (tetR/tetA promotor)
This part is a generator for the P22 bacteriophage scaffold protein fused to a super folder GFP. This part was used together with BBa_K3187044 for the dual expression of the P22 scaffold protein and the P22 coat protein fused to a LPETGG-tag for sortase-mediated ligation of GGGG-tagged proteins to the surface of P22 Virus-like particles. The potential of fine tuning the expression levels of both parts was tested via BBa_K3187011.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 76
Illegal PstI site found at 1334 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 76
Illegal NheI site found at 1339
Illegal PstI site found at 1334 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 76
Illegal BamHI site found at 796 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 76
Illegal PstI site found at 1334 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 76
Illegal PstI site found at 1334
Illegal NgoMIV site found at 1185 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 94