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PurposeExpression of sgRNA from a imyc promoter (Pimyc)
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 84380 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepTE-10M-0X
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Backbone manufacturerAddgene 20318
- Backbone size w/o insert (bp) 6608
- Total vector size (bp) 6638
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Modifications to backboneThe sequence Pmyc1tetO (2) followed by 2 BbsI sites and the sgRNA sequences were synthesized and cloned in pTE-10M-0X at a ClaI site to produce pRH2521
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Vector typeBacterial Expression, CRISPR
Growth in Bacteria
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Bacterial Resistance(s)Hygromycin, 200 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 namesgRNA cloning site
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Insert Size (bp)30
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site ClaI (not destroyed)
- 3′ cloning site ClaI (not destroyed)
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A (Common Sequencing Primers)
Resource Information
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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.
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:
pRH2521 was a gift from Robert Husson (Addgene plasmid # 84380 ; http://n2t.net/addgene:84380 ; RRID:Addgene_84380) -
For your References section:
Investigating essential gene function in Mycobacterium tuberculosis using an efficient CRISPR interference system. Singh AK, Carette X, Potluri LP, Sharp JD, Xu R, Prisic S, Husson RN. Nucleic Acids Res. 2016 Jul 12. pii: gkw625. 10.1093/nar/gkw625 PubMed 27407107