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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 31809 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCAMBIA 1300
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Backbone manufacturerCambia Labs
- Backbone size w/o insert (bp) 8935
- Total vector size (bp) 11443
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Modifications to backboneCLCrV VIGS A component empty vector was inserted between the SacI and SalI sites in the pCAMBIA 1300 backbone.
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Vector typeAgrobacterium Binary
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Selectable markersHygromycin
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)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameJRTCLCrVA.008
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Alt nameJRT.008
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Alt nameCLCrVA:Empty Vector
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SpeciesBegomovirus
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Insert Size (bp)2508
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GenBank IDEU541444.1
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SacI (not destroyed)
- 3′ cloning site SalI (destroyed during cloning)
- 5′ sequencing primer AACAGCTATGACCATG
- 3′ sequencing primer GTAAAACGACGGCCAGT (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
Addgene NGS results have detected an IS4 family transposase upstream of the kanamycin resistance cassette. This element had no effect on virus-induced gene silencing of genes in cotton in the depositing lab. However, the concentration of kanamycin for selection may need to be reduced from 50 to 25 mg/l.
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:
pJRT.Agro.CLCrVA.008 was a gift from Niki Robertson (Addgene plasmid # 31809 ; http://n2t.net/addgene:31809 ; RRID:Addgene_31809) -
For your References section:
Method: low-cost delivery of the cotton leaf crumple virus-induced gene silencing system. Tuttle JR, Haigler CH, Robertson D. Plant Methods. 2012 Aug 1;8(1):27. doi: 10.1186/1746-4811-8-27. 10.1186/1746-4811-8-27 PubMed 22853641