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Purpose(Empty Backbone) E.coli expression vector for His8-SUMO tagged recombinant protein
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 51300 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET SUMO
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Backbone manufacturerInvitrogen
- Backbone size (bp) 5643
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Modifications to backbone1) MultiCloning Site (MCS) of pET28b vector inserted in the pET SUMO cloning site 2) Addition of 2 codon for His residues to the 6 already present in the original vector 3) Removal of the original EcoRI site located inside SUMO ORF 4) Removal of the original HindIII site
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Vector typeBacterial Expression
- Promoter T7
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Tag
/ Fusion Protein
- His8 + SUMO (N terminal on backbone)
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)DH5alpha
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Copy numberUnknown
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer T7
- 3′ sequencing primer T7 reverse (Common Sequencing Primers)
Resource Information
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Articles 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
This vector is a modified version of the commercial (sell as linearized) pET SUMO vector of Invitrogen. This vector has been optimized for restriction enzyme cloning, thanks to the inserted MultiCloning Site of pET28b.
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:
pCIOX was a gift from Andrea Mattevi (Addgene plasmid # 51300 ; http://n2t.net/addgene:51300 ; RRID:Addgene_51300)