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COG7 Protein (Myc-DYKDDDDK Tag)

COG7 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2712951
  • Antigène Voir toutes COG7 Protéines
    COG7 (Component of Oligomeric Golgi Complex 7 (COG7))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette COG7 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human COG7 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product COG7 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    COG7 (Component of Oligomeric Golgi Complex 7 (COG7))
    Autre désignation
    Cog7 (COG7 Produits)
    Synonymes
    CG31040 Protein, CG7880 Protein, Dmel\\CG31040 Protein, MGC80865 Protein, COG7 Protein, MGC107838 Protein, zgc:152912 Protein, zgc:153470 Protein, CDG2E Protein, 5630400E24Rik Protein, Gm167 Protein, CG31040 gene product from transcript CG31040-RA Protein, component of oligomeric golgi complex 7 Protein, component of oligomeric golgi complex 7 L homeolog Protein, Cog7 Protein, COG7 Protein, cog7.L Protein, cog7 Protein
    Sujet
    The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010].
    Poids moléculaire
    86.2 kDa
    NCBI Accession
    NP_705831
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