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CCDC115 Protein (Myc-DYKDDDDK Tag)

CCDC115 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2713282
  • Antigène Voir toutes CCDC115 Protéines
    CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette CCDC115 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human CCDC115 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 CCDC115 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
    CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))
    Autre désignation
    Ccdc115 (CCDC115 Produits)
    Synonymes
    ccp1 Protein, 2310061I09Rik Protein, Ccp1 Protein, RGD1304653 Protein, ccdc115 Protein, coiled-coil domain containing 115 Protein, CCDC115 Protein, Ccdc115 Protein, ccdc115 Protein
    Sujet
    The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans.
    Poids moléculaire
    19.6 kDa
    NCBI Accession
    NP_115733
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