Difference between revisions of "Part:BBa K3924053"
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Latest revision as of 03:50, 22 October 2021
ParaBAD-dCas9-linker-PmCDA1-terminator
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 311
Illegal EcoRI site found at 1656 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 311
Illegal EcoRI site found at 1656
Illegal NheI site found at 300
Illegal NheI site found at 1415 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 311
Illegal EcoRI site found at 1656
Illegal BglII site found at 5091
Illegal BamHI site found at 239
Illegal BamHI site found at 3694
Illegal XhoI site found at 4700 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 311
Illegal EcoRI site found at 1656 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 311
Illegal EcoRI site found at 1656
Illegal AgeI site found at 74 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 5843
Illegal SapI site found at 56
Profile
Name:ParaBAD-dCas9-linker-PmCDA1-terminator
Base Pairs: 5965bp
Origin: Escherichia coli
Properties: A mutanted Cas9 protein fused to a deaminase which can change C into U.A linker, terminator and a Arabinose induced induced promoter have been added
Usage and Biology
dCas9 can bind sgRNA and help CDA to target a specific site of target gene.The expression of dCas9 cen be induced by arabinose induced
Design and Construction
For this part, we can purchase directly. But to save time, we got it from Xing Lab, Tsinghua University.
Functional Verification
It has been reported functional ,but we failed to repeat it in our lab due to some reasons explained in Wiki.
Reference
[1]Banno S, Nishida K, Arazoe T, Mitsunobu H, Kondo A. Deaminase-mediated multiplex genome editing in Escherichia coli. Nat Microbiol. 2018;3(4):423-429. doi:10.1038/s41564-017-0102-6