pRWJB006
(Plasmid
#160113)
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Purpose(Empty Backbone) Destination vector expressing plant-codon-optimized Cas9 under 35S promoter (BamHI and NotI), with sgRNAs be shuffled in; seed coat specific red fluorescence for screening trangene free
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 160113 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepZ001
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Backbone manufacturerLampropoulos et al
- Backbone size (bp) 4114
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Modifications to backboneCassettes of pro::pcoCas9 and At2S3::mcherry are engineered into the backbone; and the cassette of ccdB-Chloramphenicol is replaced with proLacZ::LacZ expressing unit; BamHI and NotI are used to change the promoter for driving Cas9
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Vector typeBacterial Expression, Plant Expression, CRISPR
- Promoter 35S
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Selectable markersred fluorescence
Growth in Bacteria
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Bacterial Resistance(s)Spectinomycin, 50 μg/mL
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Growth Temperature30°C
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Growth Strain(s)DH5alpha
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Copy numberLow Copy
Cloning Information
- Cloning method Restriction Enzyme
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.
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:
pRWJB006 was a gift from Detlef Weigel (Addgene plasmid # 160113 ; http://n2t.net/addgene:160113 ; RRID:Addgene_160113) -
For your References section:
An efficient CRISPR vector toolbox for engineering large deletions in Arabidopsis thaliana. Wu R, Lucke M, Jang YT, Zhu W, Symeonidi E, Wang C, Fitz J, Xi W, Schwab R, Weigel D. Plant Methods. 2018 Aug 2;14:65. doi: 10.1186/s13007-018-0330-7. eCollection 2018. 10.1186/s13007-018-0330-7 PubMed 30083222