Difference between revisions of "Part:BBa K3505006:Design"
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===Design Notes=== | ===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 present in pUPD2 as Level 0 and has overhangs compatible for Golden Braid cloning. | |
+ | The CDS has position B3-B5. | ||
+ | <p style="text-align: center;"> | ||
+ | [[Image:T--Thessaly--GB-AATG-GCTT.jpeg|900px|thumb|none|]] | ||
===Source=== | ===Source=== | ||
− | Tyr1 from Rhizobium etli in the supplementary of [3] | + | *Tyr1 from Rhizobium etli in the supplementary of [3] |
− | AIDA from E.coli in the supplementary of [2] | + | *AIDA from E.coli in the supplementary of [2] |
===References=== | ===References=== | ||
+ | *[1] | ||
+ | *[2] | ||
+ | *[3] |
Revision as of 09:33, 13 October 2020
Tyr1-AIDAc Tyrosinase fused to membrane protein AIDAc. GB compatible B3-B5
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal PstI site found at 1487
Illegal PstI site found at 2073
Illegal NotI site found at 1211 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal BglII site found at 471
Illegal BamHI site found at 454
Illegal BamHI site found at 2337 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073
Illegal AgeI site found at 533 - 1000COMPATIBLE WITH RFC[1000]
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 present in pUPD2 as Level 0 and has overhangs compatible for Golden Braid cloning. The CDS has position B3-B5.
Source
- Tyr1 from Rhizobium etli in the supplementary of [3]
- AIDA from E.coli in the supplementary of [2]
References
- [1]
- [2]
- [3]