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Chimeric CRISPR-CasX enzymes and guide RNAs for improved genome editing activity.

Tsuchida CA, Zhang S, Doost MS, Zhao Y, Wang J, O'Brien E, Fang H, Li CP, Li D, Hai ZY, Chuck J, Brotzmann J, Vartoumian A, Burstein D, Chen XW, Nogales E, Doudna JA, Liu JG
Mol Cell. 2022 Mar 17;82(6):1199-1209.e6. doi: 10.1016/j.molcel.2022.02.002. Epub 2022 Feb 25. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
180509pCAT079Plasmid expressing mammalian codon optimized wt DpbCasX, sgRNAv2 scaffold, and restriction sites to clone in new spacers
180510pCAT105Plasmid expressing mammalian codon optimized engineered DpbCasX-R3, sgRNAv2 scaffold, and restriction sites to clone in new spacers
180511pCAT077Plasmid expressing mammalian codon optimized wt PlmCasX, sgRNAv2 scaffold, and restriction sites to clone in new spacers
180512pCAT100Plasmid expressing mammalian codon optimized engineered chimeric PlmCasX-R1, sgRNAv2 scaffold, and restriction sites to clone in new spacers
180513pCAT526Plasmid expressing mammalian codon optimized wt PlmCasX, mNeonGreen, sgRNAv1 scaffold, and restriction sites to clone in new spacers
180514pCAT527Plasmid expressing mammalian codon optimized engineered chimeric PlmCasX-R1, mNeonGreen, sgRNAv2 scaffold, and restriction sites to clone in new spacers
180605pJJGL001Plasmid expressing E. coli codon optimized His-MBP-TEV-DpbCasX
180606pJJGL002Plasmid expressing E. coli codon optimized His-MBP-TEV-PlmCasX
180607pJJGL003Plasmid expressing E. coli codon optimized His-MBP-TEV-DpbCasX+Region3 insertion
180608pJJGL004Plasmid expressing E. coli codon optimized His-MBP-TEV-PlmCasX+Region1 insertion

Antibodies from Article