D. vulgaris sp2 CRISPR/pACYCDuet-1
(Plasmid
#81186)
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PurposeExpresses CRISPR array containing 3 copies of Desulfovibrio vulgaris spacer 2 and flanking repeats 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 | 81186 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepACYCDuet-1
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Backbone manufacturerNovagen
- Backbone size w/o insert (bp) 4008
- Total vector size (bp) 3896
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Vector typeBacterial Expression, CRISPR
Growth in Bacteria
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Bacterial Resistance(s)Chloramphenicol, 25 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 nameSynthetic CRISPR array (3 copies of D. vulgaris spacer #2 flanked by repeats)
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gRNA/shRNA sequenceTTGATGAGTGGCGCACTCGCCAGCCTGAGCATGGC
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SpeciesDesulfovibrio vulgaris str. Hildenborough
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Insert Size (bp)873
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GenBank ID
- Promoter T7
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Tag
/ Fusion Protein
- None
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoNI (not destroyed)
- 3′ cloning site KpnI (not destroyed)
- 5′ sequencing primer Custom
- 3′ sequencing primer T7 terminator (Common Sequencing Primers)
Resource Information
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Article 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
Spacer sequence: GCCATGCTCAGGCTGGCGAGTGCGCCACTCATCAA
Repeat sequence: GTCGCCCCCCACGCGGGGGCGTGGATTGAAAC
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:
D. vulgaris sp2 CRISPR/pACYCDuet-1 was a gift from Jennifer Doudna (Addgene plasmid # 81186 ; http://n2t.net/addgene:81186 ; RRID:Addgene_81186) -
For your References section:
DNA Targeting by a Minimal CRISPR RNA-Guided Cascade. Hochstrasser ML, Taylor DW, Kornfeld JE, Nogales E, Doudna JA. Mol Cell. 2016 Sep 1;63(5):840-51. doi: 10.1016/j.molcel.2016.07.027. 10.1016/j.molcel.2016.07.027 PubMed 27588603