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PurposeSth1 dCas9 TetR and KanR L5 Int attP for M. tuberculosis
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 115163 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonecustom design
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Vector typeUnspecified
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 1
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Gene/Insert nameSth1 sgRNA scaffold
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SpeciesStreptcoccus thermophilus
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Insert Size (bp)101
Gene/Insert 2
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Gene/Insert nameSth1 dCas9
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Alt namenuclease-dead dcas9 allele
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SpeciesStreptcoccus thermophilus
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Insert Size (bp)3366
Gene/Insert 3
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Gene/Insert nameTetR (deleted TetON) MtbCO
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Alt nameTet repressor protein
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Insert Size (bp)624
Gene/Insert 4
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Gene/Insert nameL5 attP
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Insert Size (bp)43
Gene/Insert 5
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Gene/Insert nameL5 Int
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Insert Size (bp)1116
Gene/Insert 6
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Gene/Insert nameKanR
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Alt nameKanamycin resistance protein
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Insert Size (bp)816
Resource Information
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Supplemental Documents
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Articles Citing this Plasmid
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.
Depositor Comments
The group constructed this plasmid in a BSL1 laboratory for the purpose of expressing them in BSL2 organism (such as M. smegmatis) or BSL3 (such as M. tuberculosis). Otherwise, if it's only in E. coli, then it is BSL1.
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:
PLJR965 was a gift from Sarah Fortune (Addgene plasmid # 115163 ; http://n2t.net/addgene:115163 ; RRID:Addgene_115163) -
For your References section:
Programmable transcriptional repression in mycobacteria using an orthogonal CRISPR interference platform. Rock JM, Hopkins FF, Chavez A, Diallo M, Chase MR, Gerrick ER, Pritchard JR, Church GM, Rubin EJ, Sassetti CM, Schnappinger D, Fortune SM. Nat Microbiol. 2017 Feb 6;2:16274. doi: 10.1038/nmicrobiol.2016.274. 10.1038/nmicrobiol.2016.274 PubMed 28165460