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SH3PXD2B Protein (Myc-DYKDDDDK Tag)

SH3PXD2B Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2731965
  • Antigène Voir toutes SH3PXD2B Protéines
    SH3PXD2B (SH3 and PX Domains 2B (SH3PXD2B))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    Humain
    Source
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette SH3PXD2B protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human SH3 and PX domains 2B (SH3PXD2B) 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 SH3PXD2B 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
    SH3PXD2B (SH3 and PX Domains 2B (SH3PXD2B))
    Abstract
    SH3PXD2B Produits
    Synonymes
    FAD49 Protein, FTHS Protein, HOFI Protein, KIAA1295 Protein, TKS4 Protein, TSK4 Protein, G431001E03Rik Protein, fad49 Protein, SH3 and PX domains 2B Protein, SH3PXD2B Protein, Sh3pxd2b Protein
    Sujet
    This gene encodes an adapter protein that is characterized by a PX domain and four Src homology 3 domains. The encoded protein is required for podosome formation and is involved in cell adhesion and migration of numerous cell types. Mutations in this gene are the cause of Frank-ter Haar syndrome (FTHS), and also Borrone Dermato-Cardio-Skeletal (BDCS) syndrome. Alternative splicing of this gene results in multiple transcript variants.
    Poids moléculaire
    101.4 kDa
    NCBI Accession
    NP_001017995
    Pathways
    Positive Regulation of fat Cell Differentiation
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