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Oligophrenin 1 Protein (OPHN1) (Myc-DYKDDDDK Tag)

OPHN1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2727904
  • Antigène Voir toutes Oligophrenin 1 (OPHN1) Protéines
    Oligophrenin 1 (OPHN1)
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 2
    • 1
    Humain
    Source
    • 2
    • 2
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette Oligophrenin 1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Oligophrenin-1 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 OPHN1 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
    Oligophrenin 1 (OPHN1)
    Autre désignation
    Oligophrenin-1 (OPHN1 Produits)
    Synonymes
    ARHGAP41 Protein, MRX60 Protein, OPN1 Protein, C130037N19Rik Protein, Opn1 Protein, MGC68856 Protein, zgc:92603 Protein, OPHN1 Protein, mrx60 Protein, opn1 Protein, oligophrenin 1 Protein, oligophrenin 1 L homeolog Protein, OPHN1 Protein, Ophn1 Protein, ophn1.L Protein, ophn1 Protein, Tsp_13482 Protein
    Sujet
    This gene encodes a Rho-GTPase-activating protein that promotes GTP hydrolysis of Rho subfamily members. Rho proteins are important mediators of intracellular signal transduction, which affects cell migration and cell morphogenesis. Mutations in this gene are responsible for OPHN1-related X-linked mental retardation with cerebellar hypoplasia and distinctive facial dysmorhphism.
    Poids moléculaire
    91.5 kDa
    NCBI Accession
    NP_002538
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