Difference between revisions of "Part:BBa K3505033"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | This parts consists of AndersonJ23115 promoter <bbpart>BBa_K3505012</bbpart> , TetR <bbpart>BBa_K3505005</bbpart> and Double Terminator <bbpart>BBa_K3505017</bbpart>. By this way ,as AndersonJ23115 is a strong constitutive promoter, TetR is constitutively expressed. TetR | + | This parts consists of AndersonJ23115 promoter <bbpart>BBa_K3505012</bbpart> , TetR <bbpart>BBa_K3505005</bbpart> and Double Terminator <bbpart>BBa_K3505017</bbpart>. By this way ,as AndersonJ23115 is a strong constitutive promoter, TetR is constitutively expressed. TetR binds to tetracycline response element and inhibits the expression of a desirable transcription unit |
===Design Notes=== | ===Design Notes=== |
Revision as of 17:12, 27 October 2020
pAndersonJ23115:RBS:tetR-terminator
Usage and Biology
This parts consists of AndersonJ23115 promoter BBa_K3505012 , TetR BBa_K3505005 and Double Terminator BBa_K3505017. By this way ,as AndersonJ23115 is a strong constitutive promoter, TetR is constitutively expressed. TetR binds to tetracycline response element and inhibits the expression of a desirable transcription unit
Design Notes
The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in alpha1R vector BBa_K3505008 and has overhangs compatible for Golden Braid cloning.
Verification of Cloning
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 76
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 11
Illegal NheI site found at 34 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 76
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 76
- 1000COMPATIBLE WITH RFC[1000]