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Addgene

GEV 1
(Plasmid #12615)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 12615 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    pET21a
  • Backbone manufacturer
    Novagen
  • Backbone size w/o insert (bp) 5443
  • Vector type
    Bacterial Expression

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    Low Copy

Gene/Insert

  • Gene/Insert name
    GB1 domain of protein G as N terminal tag, with Bcl2 as insert
  • Alt name
    GB1 domain of protein G
  • Alt name
    Bcl-2
  • Alt name
    Bcl2 (aa 82-204)
  • Species
    M. musculus (mouse)
  • Insert Size (bp)
    369
  • Entrez Gene
    Bcl2 (a.k.a. Bcl-2, C430015F12Rik, D630044D05Rik, D830018M01Rik)
  • Tags / Fusion Proteins
    • G protein (N terminal on backbone)
    • His (C terminal on backbone)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site Nhe I (not destroyed)
  • 3′ cloning site Xho I (not destroyed)
  • 5′ sequencing primer T7 terminal
  • (Common Sequencing Primers)

Terms and Licenses

  • Academic/Nonprofit Terms
  • Industry Terms
    • Not Available to Industry
Trademarks:
  • Zeocin® is an InvivoGen trademark.

Depositor Comments

In GEV1, a noncleavable linker (Pro-Gly-Gly-Pro-Ala-Ser) is encoded between the GBl domain and the N-terminus of the protein of interest. Genes can be inserted into this vector using Nhe I and Xho I cloning sites, and, if no stop codons are introduced at the 5' end of an insert, the vector encodes a C-terminal poly His-tag.

Also see: "A rapid method to attain isotope labeled small soluble peptides for NMR studies", Journal of Biomolecular NMR, Vol 26, No 3, July 2003.

How to cite this plasmid ( Back to top)

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.

  • For your Materials & Methods section:

    GEV 1 was a gift from John Louis (Addgene plasmid # 12615 ; http://n2t.net/addgene:12615 ; RRID:Addgene_12615)
  • For your References section:

    Design of an expression system for detecting folded protein domains and mapping macromolecular interactions by NMR. Huth JR, Bewley CA, Jackson BM, Hinnebusch AG, Clore GM, Gronenborn AM. Protein Sci. 1997 Nov . 6(11):2359-64. 10.1002/pro.5560061109 PubMed 9385638