Difference between revisions of "Part:BBa K2549030"
Line 2: | Line 2: | ||
<partinfo>BBa_K2549030 short</partinfo> | <partinfo>BBa_K2549030 short</partinfo> | ||
− | This part is one of the response elements of our amplifier, also executing the combiner function. 8*ZF42.10 binding sites ([[Part: | + | This part is one of the response elements of our amplifier, also executing the combiner function. 8*ZF42.10 binding sites ([[Part:BBa_K2549012]]) is assembled using two 4*ZF42.10 binding sites ([[Part:BBa_K2446005]]) with a biobrick scar between them. CMV ([[Part:BBa_K2549050]]) is a promotor which has a high-level constitutive expression. This part can switch off the expression of gene downstream after induced by our zinc finger-based transcription repressor. |
<!-- --> | <!-- --> |
Revision as of 04:49, 13 October 2018
8*ZF42.10-CMV
This part is one of the response elements of our amplifier, also executing the combiner function. 8*ZF42.10 binding sites (Part:BBa_K2549012) is assembled using two 4*ZF42.10 binding sites (Part:BBa_K2446005) with a biobrick scar between them. CMV (Part:BBa_K2549050) is a promotor which has a high-level constitutive expression. This part can switch off the expression of gene downstream after induced by our zinc finger-based transcription repressor.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Biology
It works as we designed
interaction between ZF42.10-KRAB and 8*ZF42.10-CMV promotor
@@@@
Synthetic promotor operators regulated by artificial zinc finger-based transcription factors
Khalil AS et al have reported several synthetic promotor operators which can interact with artificial zinc finger-based transcription factors with high specificity and high orthogonality[1].
References
- ↑ A synthetic biology framework for programming eukaryotic transcription functions. Khalil AS, Lu TK, Bashor CJ, ..., Joung JK, Collins JJ. Cell, 2012 Aug;150(3):647-58 PMID: 22863014; DOI: 10.1016/j.cell.2012.05.045