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GP6 antibody (Biotin)

GP6 Reactivity: Human FACS Host: Human, Rabbit Chimeric DMC427 Biotin
Catalog No. ABIN7608232
  • Target See all GP6 Antibodies
    GP6 (Glycoprotein VI (Platelet) (GP6))
    Reactivity
    • 49
    • 17
    • 16
    Human
    Host
    • 49
    • 1
    Human, Rabbit
    Clonality
    • 48
    • 1
    • 1
    Chimeric
    Conjugate
    • 13
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GP6 antibody is conjugated to Biotin
    Application
    • 38
    • 16
    • 13
    • 12
    • 6
    • 5
    • 4
    • 3
    • 2
    Flow Cytometry (FACS)
    Purpose
    Biotinylated Anti-GP6 antibody(DMC427), IgG1 Chimeric mAb
    Purification
    Purified from cell culture supernatant by affinity chromatography
    Clone
    DMC427
    Isotype
    IgG1
    Top Product
    Discover our top product GP6 Primary Antibody
  • Application Notes
    Flow Cyt 1:100
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.
    Storage
    -20 °C,-80 °C
    Storage Comment
    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
    Expiry Date
    12 months
  • Target
    GP6 (Glycoprotein VI (Platelet) (GP6))
    Alternative Name
    GP6 (GP6 Products)
    Background
    This gene encodes a platelet membrane glycoprotein of the immunoglobulin superfamily. The encoded protein is a receptor for collagen and plays a critical role in collagen-induced platelet aggregation and thrombus formation. The encoded protein forms a complex with the Fc receptor gamma-chain that initiates the platelet activation signaling cascade upon collagen binding. Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
    UniProt
    Q9HCN6
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