pEn-C1.1
(Plasmid
#61479)
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PurposeEncodes CRISPR sgRNA for Gateway or conventional cloning of 1-3 sgRNAs into pDe-CAS9 or pCAS9-TPC
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 61479 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepGEM-T-easy
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Backbone manufacturerPromega Corp.
- Backbone size w/o insert (bp) 3000
- Total vector size (bp) 3700
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Vector typePlant Expression, CRISPR
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameAtU6-26:sgRNA
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SpeciesA. thaliana (mustard weed), Synthetic
- Promoter U6-26
Cloning Information
- Cloning method TOPO Cloning
- 5′ sequencing primer M13 fw
- 3′ sequencing primer M13 rev (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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
Based on pEn-Chimera; MluI and Bsu36I RS added to each side of the U6-26:sgRNA sequence for cloning of up to 3 sgRNAs into Cas9 expression vector.
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:
pEn-C1.1 was a gift from Holger Puchta (Addgene plasmid # 61479 ; http://n2t.net/addgene:61479 ; RRID:Addgene_61479) -
For your References section:
The CRISPR/Cas system can be used as nuclease for in planta gene targeting and as paired nickases for directed mutagenesis in Arabidopsis resulting in heritable progeny. Schiml S, Fauser F, Puchta H. Plant J. 2014 Oct 18. doi: 10.1111/tpj.12704. 10.1111/tpj.12704 PubMed 25327456