Difference between revisions of "Part:BBa K2450501:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | The TorA leader sequence must be at the N terminal end. | |
+ | The part has been designed so that the sfGFP stays attached to the membrane when the TEV protease cleaves the quencher, and the dark quencher is at the C terminus. This allows the quencher to be removed during PCR to produce a protein without the quencher. This part without the fluorophore can be used to compare the increase in fluorescence against, when the quencher is cleaved off. | ||
Latest revision as of 20:04, 21 October 2017
SpyCatcher sfGFP quencher
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 4
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 397
Illegal SapI.rc site found at 1291
Design Notes
The TorA leader sequence must be at the N terminal end.
The part has been designed so that the sfGFP stays attached to the membrane when the TEV protease cleaves the quencher, and the dark quencher is at the C terminus. This allows the quencher to be removed during PCR to produce a protein without the quencher. This part without the fluorophore can be used to compare the increase in fluorescence against, when the quencher is cleaved off.
Source
tba