Difference between revisions of "Part:BBa K3505024"
(→Verification of Cloning) |
|||
Line 3: | Line 3: | ||
<partinfo>BBa_K3505024 short</partinfo> | <partinfo>BBa_K3505024 short</partinfo> | ||
+ | ===Usage And Biology=== | ||
+ | B-arrestin has the ability to normally bind to the GPCR receptor and facilitate its endocytosis, desensitization or GPCR-independent signaling effects. The second composite of our TANGO system is a fusion of the b-arrestin-2 with the TEV protease.TEV protease recognizes and cleaves the cleavage site. This low proximity allows the TEV protease that is tagged to the βarrestin-2 carrier to cleave its substrate (TCS) . | ||
Latest revision as of 00:36, 28 October 2020
B-arrestin:TEV Protease GB compatible with B2-B5
Usage And Biology
B-arrestin has the ability to normally bind to the GPCR receptor and facilitate its endocytosis, desensitization or GPCR-independent signaling effects. The second composite of our TANGO system is a fusion of the b-arrestin-2 with the TEV protease.TEV protease recognizes and cleaves the cleavage site. This low proximity allows the TEV protease that is tagged to the βarrestin-2 carrier to cleave its substrate (TCS) .
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 presents in pUPD2 and has overhangs compatible for Golden Braid cloning. The CDS has position B2-B5.
Verification of Cloning
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 1611
Illegal PstI site found at 303
Illegal PstI site found at 390 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 1611
Illegal PstI site found at 303
Illegal PstI site found at 390 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 203
Illegal XhoI site found at 600
Illegal XhoI site found at 994 - 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 1611
Illegal PstI site found at 303
Illegal PstI site found at 390 - 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 1611
Illegal PstI site found at 303
Illegal PstI site found at 390
Illegal AgeI site found at 586 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 1545
Illegal SapI.rc site found at 1893