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GP5 antibody (APC)

GP5 Reactivity: Mouse, Rat ICFC Host: Armenian Hamster Monoclonal 1C2 APC
Catalog No. ABIN2658230
  • 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 APC
    Application
    • 9
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Intracellular Flow Cytometry (ICFC)
    Purification
    The antibody was purified by affinity chromatography and conjugated with APC under optimal conditions. The solution is free of unconjugated APC 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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