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GP5 抗体 (PE)

GP5 适用: 小鼠, 大鼠 FACS 宿主: Armenian Hamster Monoclonal 1C2 PE
产品编号 ABIN2662644
发货至: 中国
  • 抗原 See all GP5 抗体
    GP5 (Glycoprotein V (Platelet) (GP5))
    适用
    • 9
    • 9
    • 6
    小鼠, 大鼠
    宿主
    • 9
    • 2
    • 2
    • 1
    • 1
    Armenian Hamster
    克隆类型
    • 10
    • 5
    单克隆
    标记
    • 13
    • 2
    This GP5 antibody is conjugated to PE
    应用范围
    • 11
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Flow Cytometry (FACS)
    纯化方法
    The antibody was purified by affinity chromatography and conjugated with PE under optimal conditions. The solution is free of unconjugated PE and unconjugated antibody.
    克隆位点
    1C2
    亚型
    IgG
    Top Product
    Discover our top product GP5 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 缓冲液
    Phosphate-buffered solution, pH 7.2, containing 0.09 % sodium azide.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    注意事项
    Protect from prolonged exposure to light. Do not freeze.
    储存条件
    4 °C
    储存方法
    The antibody solution should be stored undiluted between 2°C and 8°C.
  • 抗原
    GP5 (Glycoprotein V (Platelet) (GP5))
    别名
    CD42d (GP5 产品)
    别名
    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
    背景
    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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