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WIPF1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

WIPF1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2735595
  • Target See all WIPF1 Proteins
    WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 1
    Origin
    • 4
    • 1
    Human
    Source
    • 1
    • 1
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This WIPF1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human WIPF1 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product WIPF1 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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.
  • Target
    WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))
    Alternative Name
    Wipf1 (WIPF1 Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    51.1 kDa
    NCBI Accession
    NP_003378
    Pathways
    RTK Signaling
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