Difference between revisions of "Part:BBa K1723001"
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− | <b>PAM rich URS J23117 is an improvement of the J23117 (BBa_J23117) weak promoter</b> [1]. This promoter is the promoter J23117 flanked with a PAM (PAM = NGG sequence) rich Upstream Regulatory Sequence (URS) to enable the use of protein dCas9-ω (BBa_K1723000) as a gene transcription regulator when in complex with one sgRNA targeting the promoter such as: the activator sgRNA | + | <b>PAM rich URS J23117 is an improvement of the J23117 (BBa_J23117) weak promoter</b> [1]. This promoter is the promoter J23117 flanked with a PAM (PAM = NGG sequence) rich Upstream Regulatory Sequence (URS) to enable the use of protein dCas9-ω (BBa_K1723000) as a gene transcription regulator when in complex with one sgRNA targeting the promoter such as: the activator sgRNA Z4 (BBa_K1723003), the inhibitor sgRNA Z0 (BBa_K1723002), or the other inhibitor sgRNA Z35 (BBa_K1723004). dCas9 can only bind if the DNA target sequence is preceded by a PAM sequence. |
− | Discover | + | <b>This part was experimentally validated, see </b> https://parts.igem.org/Part:BBa_K1723001:Experience |
+ | |||
+ | Discover more parts that can work with this one: | ||
http://2015.igem.org/Team:EPF_Lausanne/Part_Collection | http://2015.igem.org/Team:EPF_Lausanne/Part_Collection |
Latest revision as of 00:47, 19 September 2015
PAM rich URS j23117 promoter
PAM rich URS J23117 is an improvement of the J23117 (BBa_J23117) weak promoter [1]. This promoter is the promoter J23117 flanked with a PAM (PAM = NGG sequence) rich Upstream Regulatory Sequence (URS) to enable the use of protein dCas9-ω (BBa_K1723000) as a gene transcription regulator when in complex with one sgRNA targeting the promoter such as: the activator sgRNA Z4 (BBa_K1723003), the inhibitor sgRNA Z0 (BBa_K1723002), or the other inhibitor sgRNA Z35 (BBa_K1723004). dCas9 can only bind if the DNA target sequence is preceded by a PAM sequence.
This part was experimentally validated, see https://parts.igem.org/Part:BBa_K1723001:Experience
Discover more parts that can work with this one:
http://2015.igem.org/Team:EPF_Lausanne/Part_Collection
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 56
Illegal NheI site found at 79 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 43
- 1000COMPATIBLE WITH RFC[1000]
References
[1] Bikard, D., Jiang, W., Samai, P., Hochschild, A., Zhang, F., & Marraffini, L. A. (2013). Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system. Nucleic acids research, 41(15), 7429-7437.