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Ceruloplasmin 抗体 (AA 20-258)

CP 适用: 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN4950633
发货至: 中国
  • 抗原 See all Ceruloplasmin (CP) 抗体
    Ceruloplasmin (CP) (Ceruloplasmin (Ferroxidase) (CP))
    抗原表位
    • 7
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 20-258
    适用
    • 52
    • 10
    • 9
    小鼠, 大鼠
    宿主
    • 46
    • 7
    • 5
    • 4
    • 1
    克隆类型
    • 55
    • 6
    多克隆
    标记
    • 38
    • 10
    • 6
    • 3
    • 2
    • 2
    • 2
    This Ceruloplasmin antibody is un-conjugated
    应用范围
    • 39
    • 28
    • 25
    • 14
    • 13
    • 11
    • 9
    • 8
    • 6
    • 6
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    Antigen affinity
    免疫原
    Amino acids 20-258 of mouse Ceruloplasmin were used as the immunogen for the CP antibody.
    亚型
    IgG
    Top Product
    Discover our top product CP Primary Antibody
  • 应用备注
    Optimal dilution of the CP antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL,IHC (Paraffin): 0.5-1 μg/mL
    限制
    仅限研究用
  • 缓冲液
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    储存条件
    -20 °C
    储存方法
    After reconstitution, the CP antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原
    Ceruloplasmin (CP) (Ceruloplasmin (Ferroxidase) (CP))
    别名
    Ceruloplasmin / CP (CP 产品)
    别名
    CP-2 antibody, fi23f10 antibody, wu:fi23f10 antibody, D3Ertd555e antibody, CERP antibody, CP antibody, ceruloplasmin antibody, CP antibody, cp antibody, Cp antibody, LOC100533122 antibody
    背景
    Ceruloplasmin (or Caeruloplasmin) is a ferroxidase enzyme that in humans is encoded by the CP gene. It is mapped to 3q23-q25. The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene.
    UniProt
    Q61147
    途径
    Transition Metal Ion Homeostasis
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