Difference between revisions of "Part:BBa K2243015"
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Reporter of the first latch in bio-flip-flop | Reporter of the first latch in bio-flip-flop | ||
− | + | ||
− | === | + | ===Usage=== |
+ | This part is the elementary reporter unit of our Bio-Flip-Flop. It generate another state when the promoter orientation changed along with the recombination of the attB and attP sites. | ||
+ | |||
+ | ===Biology=== | ||
+ | J23119 is the consensus sequence of a combinatorial constitutive promoter library family. In nature, Mycobacteriophage Bxb1 integrates its DNA at the attB site of the Mycobacterium smegmatis genome using the viral attP site. We obtained the promoter, attL and attR sites by oligo synthesis. | ||
+ | |||
+ | |||
+ | |||
+ | ===Design note=== | ||
+ | We construct this structure by Gibson Assembly. | ||
+ | |||
+ | ===Characterize=== | ||
+ | The characterization have not done yet. | ||
+ | |||
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Revision as of 13:42, 31 October 2017
Bxb1 attB_pTAC_Bxb1 attP
Reporter of the first latch in bio-flip-flop
Usage
This part is the elementary reporter unit of our Bio-Flip-Flop. It generate another state when the promoter orientation changed along with the recombination of the attB and attP sites.
Biology
J23119 is the consensus sequence of a combinatorial constitutive promoter library family. In nature, Mycobacteriophage Bxb1 integrates its DNA at the attB site of the Mycobacterium smegmatis genome using the viral attP site. We obtained the promoter, attL and attR sites by oligo synthesis.
Design note
We construct this structure by Gibson Assembly.
Characterize
The characterization have not done yet.
Sequence and Features
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 29
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 49
Illegal BsaI.rc site found at 162