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GP5 antibody (PerCP-Cy5.5)

GP5 Reactivity: Mouse, Rat FACS Host: Armenian Hamster Monoclonal 1C2 PerCP-Cy5.5
Catalog No. ABIN2660118
  • Target See all GP5 Antibodies
    GP5 (Glycoprotein V (Platelet) (GP5))
    Reactivity
    • 8
    • 6
    • 3
    Mouse, Rat
    Host
    • 8
    • 2
    • 1
    • 1
    Armenian Hamster
    Clonality
    • 9
    • 3
    Monoclonal
    Conjugate
    • 11
    • 1
    This GP5 antibody is conjugated to PerCP-Cy5.5
    Application
    • 9
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Flow Cytometry (FACS)
    Purification
    The antibody was purified by affinity chromatography and conjugated with PerCP/Cy5.5 under optimal conditions. The solution is free of unconjugated PerCP/Cy5.5 and unconjugated antibody.
    Clone
    1C2
    Isotype
    IgG
    Top Product
    Discover our top product GP5 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    0.2 mg/mL
    Buffer
    Phosphate-buffered solution, pH 7.2, 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.
    Handling Advice
    Protect from prolonged exposure to light. Do not freeze.
    Storage
    4 °C
    Storage Comment
    The antibody solution should be stored undiluted between 2°C and 8°C.
  • Target
    GP5 (Glycoprotein V (Platelet) (GP5))
    Alternative Name
    CD42d (GP5 Products)
    Synonyms
    lib antibody, GPV antibody, PLGPV antibody, CD42d antibody, glycoprotein V platelet L homeolog antibody, glycoprotein V platelet antibody, glycoprotein 5 (platelet) antibody, glycoprotein V (platelet) antibody, gp5.L antibody, GP5 antibody, Gp5 antibody
    Background
    CD42d is an 83 kD surface glycoprotein that non-covalently associates with GPIb and GPIX to form a receptor complex for von Willebrand factor on megakaryocytes and resting platelets. Binding sites for von Willebrand factor and thrombin have been localized to the GPIba chain of the GPI-b-V-IX complex. Platelet activation with thrombin cleaves the GPI-b-V-IX complex to release a 69 kD soluble fragment. Presence of the GPI-b-V-IX complex is important in Bernard-Soulier syndrome, a rare bleeding disorder.
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