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WIPF1 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

WIPF1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2735594
  • Antigène Voir toutes WIPF1 Protéines
    WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 2
    Origine
    • 4
    • 1
    Humain
    Source
    • 1
    • 1
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette WIPF1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human WIPF1 (transcript variant 2) 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 WIPF1 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
    WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))
    Autre désignation
    Wipf1 (WIPF1 Produits)
    Synonymes
    WASPIP Protein, PRPL-2 Protein, WIP Protein, AI115543 Protein, D2Ertd120e Protein, Waspip Protein, Wip Protein, WAS/WASL interacting protein family member 1 Protein, WAS/WASL interacting protein family, member 1 Protein, WIPF1 Protein, Wipf1 Protein
    Sujet
    This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene.
    Poids moléculaire
    51.1 kDa
    NCBI Accession
    NP_001070737
    Pathways
    Signalisation RTK
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