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CLCN7 抗体

CLCN7 适用: 人, 大鼠, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7252435
发货至: 中国
  • 抗原 See all CLCN7 抗体
    CLCN7 (Chloride Channel, Voltage-Sensitive 7 (CLCN7))
    适用
    人, 大鼠, 小鼠
    宿主
    • 33
    • 2
    克隆类型
    • 34
    • 1
    多克隆
    标记
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CLCN7 antibody is un-conjugated
    应用范围
    • 25
    • 20
    • 16
    • 15
    • 7
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human CLCN7
    亚型
    IgG
    Top Product
    Discover our top product CLCN7 Primary Antibody
  • 应用备注
    IHC 1:50-1:100, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.56 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    CLCN7 (Chloride Channel, Voltage-Sensitive 7 (CLCN7))
    别名
    CLCN7 (CLCN7 产品)
    别名
    CLC-7 antibody, CLC7 antibody, OPTA2 antibody, OPTB4 antibody, PPP1R63 antibody, AA409691 antibody, AW538136 antibody, ClC-7 antibody, D17Wsu51e antibody, MGC80627 antibody, im:7155923 antibody, zgc:153490 antibody, CLCN7 antibody, chloride voltage-gated channel 7 antibody, chloride channel, voltage-sensitive 7 antibody, chloride channel, voltage-sensitive 7 L homeolog antibody, chloride channel 7 antibody, chloride channel protein 7 antibody, CLCN7 antibody, Clcn7 antibody, clcn7.L antibody, clcn7 antibody, CpipJ_CPIJ008618 antibody
    背景
    The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood.
    UniProt
    P51798
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