Difference between revisions of "Part:BBa K3866033"
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<partinfo>BBa_K3866033 short</partinfo> | <partinfo>BBa_K3866033 short</partinfo> | ||
+ | Bglx <bbpart>BBa_K523002</bbpart> under control of a constitutive promoter <bbpart>BBa_K3505012</bbpart>. | ||
+ | ===Usage and Biology=== | ||
+ | <p>Τhis part consists of AndersonJ23115 promoter <bbpart>BBa_K3505012</bbpart>, bglx <bbpart>BBa_K523002</bbpart> and Double Terminator <bbpart>BBa_K3505017</bbpart>. By this way, as AndersonJ23115 is a strong constitutive promoter, bglx is constitutively expressed. The product protein is expected to be in the periplasm. | ||
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− | === | + | ===Design Notes=== |
+ | Τhe 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 <bbpart>BBa_K3505008</bbpart>and has overhangs compatible for GoldenBraid cloning. | ||
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<partinfo>BBa_K3866033 parameters</partinfo> | <partinfo>BBa_K3866033 parameters</partinfo> | ||
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+ | ===Source=== | ||
+ | Synthesized by IDT. |
Revision as of 14:37, 27 September 2021
pAndersonJ23115:RBS-bglX-terminator
Bglx BBa_K523002 under control of a constitutive promoter BBa_K3505012.
Usage and Biology
Τhis part consists of AndersonJ23115 promoter BBa_K3505012, bglx BBa_K523002 and Double Terminator BBa_K3505017. By this way, as AndersonJ23115 is a strong constitutive promoter, bglx is constitutively expressed. The product protein is expected to be in the periplasm.
Design Notes
Τhe 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_K3505008and has overhangs compatible for GoldenBraid cloning.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 11
Illegal NheI site found at 34 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 62
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1721
Illegal AgeI site found at 1943
Illegal AgeI site found at 2132 - 1000COMPATIBLE WITH RFC[1000]