Purpose(Empty Backbone) Empty backbone for cloning sgRNA sequence to be used in nanoblades system (Optimized for increased genome editing efficiency via Chen B et al., 2013)
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||134913||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
- Backbone size (bp) 5194
Modifications to backboneIncludes stabilizing sgRNA mutations in backbone to increase genome editing efficiency
Vector typeCRISPR, Synthetic Biology
- Promoter U6
Growth in Bacteria
- Cloning method Unknown
- 5′ sequencing primer Unknown (Common Sequencing Primers)
Includes stabilizing sgRNA mutations in backbone to increase genome editing efficiency designed using the method outlined in “Dynamic imaging of genomic loci in living human cells by an optimized CRISPR/Cas system” (PMID 24360272).
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
For your Materials & Methods section:SUPERBLADE5 was a gift from Philippe Mangeot & Théophile Ohlmann & Emiliano Ricci (Addgene plasmid # 134913 ; http://n2t.net/addgene:134913 ; RRID:Addgene_134913)
For your References section:Genome editing in primary cells and in vivo using viral-derived Nanoblades loaded with Cas9-sgRNA ribonucleoproteins. Mangeot PE, Risson V, Fusil F, Marnef A, Laurent E, Blin J, Mournetas V, Massourides E, Sohier TJM, Corbin A, Aube F, Teixeira M, Pinset C, Schaeffer L, Legube G, Cosset FL, Verhoeyen E, Ohlmann T, Ricci EP. Nat Commun. 2019 Jan 3;10(1):45. doi: 10.1038/s41467-018-07845-z. 10.1038/s41467-018-07845-z PubMed 30604748