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GP5 anticorps (PE)

GP5 Reactivité: Souris, Rat FACS Hôte: Hamster arménien Monoclonal 1C2 PE
N° du produit ABIN2662644
  • Antigène Voir toutes GP5 Anticorps
    GP5 (Glycoprotein V (Platelet) (GP5))
    Reactivité
    • 10
    • 8
    • 7
    Souris, Rat
    Hôte
    • 8
    • 5
    • 2
    • 1
    Hamster arménien
    Clonalité
    • 9
    • 7
    Monoclonal
    Conjugué
    • 13
    • 2
    • 1
    Cet anticorp GP5 est conjugé à/à la PE
    Application
    • 9
    • 5
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Flow Cytometry (FACS)
    Purification
    The antibody was purified by affinity chromatography and conjugated with PE under optimal conditions. The solution is free of unconjugated PE and unconjugated antibody.
    Clone
    1C2
    Isotype
    IgG
    Top Product
    Discover our top product GP5 Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Buffer
    Phosphate-buffered solution, pH 7.2, containing 0.09 % sodium azide.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Conseil sur la manipulation
    Protect from prolonged exposure to light. Do not freeze.
    Stock
    4 °C
    Stockage commentaire
    The antibody solution should be stored undiluted between 2°C and 8°C.
  • Antigène
    GP5 (Glycoprotein V (Platelet) (GP5))
    Autre désignation
    CD42d (GP5 Produits)
    Synonymes
    anticorps lib, anticorps GPV, anticorps PLGPV, anticorps CD42d, anticorps glycoprotein V platelet L homeolog, anticorps glycoprotein V platelet, anticorps glycoprotein 5 (platelet), anticorps glycoprotein V (platelet), anticorps gp5.L, anticorps GP5, anticorps Gp5
    Sujet
    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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