pART7
(Plasmid
#247985)
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Purpose(Empty Backbone) Cloning vector to transiently express an inserted gene in plant cells under the control of the 35S CaMV promoter.
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Depositing Labs
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Publication
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 247985 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 | |
Backbone
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Vector backbonepART7
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Backbone manufacturerAndrew Gleave
- Backbone size (bp) 5042
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Vector typePlant Expression
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 nameNone
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
pART7 is a synthetic cloning vector harbouring a CaMV 35S promoter and a multi cloning site for inserting genes intended to be transiently expressed in plants. Two NotI restriction sites allow to excise the cloned gene for subcloning into a binary vector. pART7 is a derivative of pGEM-9zf- (GenBank X65312). See the Supplemental Document under Resource Information for more details, including annotated maps.
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:
pART7 was a gift from Andrew Gleave & Christoph Plieth (Addgene plasmid # 247985 ; http://n2t.net/addgene:247985 ; RRID:Addgene_247985) -
For your References section:
A versatile binary vector system with a T-DNA organisational structure conducive to efficient integration of cloned DNA into the plant genome. Gleave AP. Plant Mol Biol. 1992 Dec;20(6):1203-7. PubMed 1463857