Composite
Part:BBa_K3219000
Designed by: LEE Hong Kiu Group: iGEM19_HK_SSC (2019-09-24)
dCas9-GFP
- ↑ . Different from traditional CRISPR Cas9 enzymes, dCas9 lacks endonuclease activity. It does not cleave DNA. Instead, with the help of a guide RNA, it specifically binds to the target, usually 20 -30 bp, and blocks transcript elongation by RNA polymerase.
In this part, a GFP is added to the C-terminus of the dCas9, connected using an SGAAAAGGS linker. The GFP is added so that the expression of both proteins could be checked easier.
This sequence can be used by cloning it into a desired vector with a promoter and ribosome binding site.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1837
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 4116
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 644
- 10
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Categories
Parameters
None |