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WIPF1 antibody (AA 150-200)

WIPF1 Reactivity: Human WB, IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7450906
  • Target See all WIPF1 Antibodies
    WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))
    Binding Specificity
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 150-200
    Reactivity
    • 18
    • 7
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 17
    • 1
    Rabbit
    Clonality
    • 18
    Polyclonal
    Conjugate
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This WIPF1 antibody is un-conjugated
    Application
    • 11
    • 8
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Purpose
    Rabbit anti-WIPF1 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    Between AA 150 and 200
    Isotype
    IgG
    Top Product
    Discover our top product WIPF1 Primary Antibody
  • Application Notes

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
    Expiry Date
    12 months
  • Target
    WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))
    Alternative Name
    WIPF1 (WIPF1 Products)
    Synonyms
    WASPIP antibody, PRPL-2 antibody, WIP antibody, AI115543 antibody, D2Ertd120e antibody, Waspip antibody, Wip antibody, WAS/WASL interacting protein family member 1 antibody, WAS/WASL interacting protein family, member 1 antibody, WIPF1 antibody, Wipf1 antibody
    Background
    Background: WAS/WASL-interacting protein family member 1 (WIPF1) plays an important role in the organization of the actin cytoskeleton. WIPF1 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 diseae [taken from NCBI Entrez Gene (Gene ID: 7456)].
    Gene ID
    7456
    UniProt
    O43516
    Pathways
    RTK Signaling
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