pGEX-N-TEV-Twin-Strep
(Plasmid
#222014)
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Purpose(Empty Backbone) Express C-terminal Tobacco Etch Virus (TEV) protease cleavable Twin-Strep-tagged protein (ENLYFQGS-WSHPQFEK-(GGGS)2-GGSA-WSHPQFEK) in E.coli
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 222014 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepGEX-6P-1
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Backbone manufacturerCytiva
- Backbone size (bp) 3679
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Modifications to backboneThe TEV cleavable site (ENLYFQG) and Twin-strep tag were inserted instead of GST protein.
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Vector typeBacterial Expression
- Promoter lac promoter
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Tags
/ Fusion Proteins
- TEV cleavable site (ENLYFQG) (C terminal on backbone)
- Twin-strep-tag (C terminal on backbone)
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 numberUnknown
Cloning Information
- Cloning method Gibson Cloning
- 5′ sequencing primer CATTAGGCACCCCAGGCTTTACACTTTATG
- 3′ sequencing primer GCTTACAGACAAGCTGTGACCGTC (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
The plasmid can be linearized using the restriction enzyme (XhoI).
DNA (CDS) can be inserted through in-fusion cloning.
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:
pGEX-N-TEV-Twin-Strep was a gift from Chiaki Murakami (Addgene plasmid # 222014 ; http://n2t.net/addgene:222014 ; RRID:Addgene_222014)