pDT-SuperFi-Cas9
(Plasmid
#183630)
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PurposeExpression and purification of N-terminal His-MBP tagged SuperFi Cas9 in E. coli
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 183630 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMJ806
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Backbone manufacturerAddgene
- Backbone size w/o insert (bp) 6470
- Total vector size (bp) 10577
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Vector typeBacterial Expression, CRISPR
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameSuperFi-Cas9
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SpeciesSynthetic
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Insert Size (bp)4107
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MutationY1010D, Y1013D, Y1016D, V1018D, R1019D, Q1027D, K1031D
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GenBank IDAAK33936.1 13622193
- Promoter T7
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Tag
/ Fusion Protein
- 6xHis-MBP (N terminal on backbone)
Cloning Information
- Cloning method Ligation Independent Cloning
- 5′ sequencing primer T7 promoter
- 3′ sequencing primer T7 terminator (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made byThe original Cas9 gene was received from Addgene (pMJ806).
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
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.
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For your Materials & Methods section:
pDT-SuperFi-Cas9 was a gift from David Taylor (Addgene plasmid # 183630 ; http://n2t.net/addgene:183630 ; RRID:Addgene_183630) -
For your References section:
Structural basis for mismatch surveillance by CRISPR-Cas9. Bravo JPK, Liu MS, Hibshman GN, Dangerfield TL, Jung K, McCool RS, Johnson KA, Taylor DW. Nature. 2022 Mar 2. pii: 10.1038/s41586-022-04470-1. doi: 10.1038/s41586-022-04470-1. 10.1038/s41586-022-04470-1 PubMed 35236982