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CLCN1 抗体

CLCN1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6570089
发货至: 中国
  • 抗原 See all CLCN1 抗体
    CLCN1 (Chloride Channel 1, Skeletal Muscle (CLCN1))
    适用
    • 20
    • 8
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 24
    克隆类型
    • 24
    多克隆
    标记
    • 14
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CLCN1 antibody is un-conjugated
    应用范围
    • 13
    • 9
    • 3
    • 2
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human CLCN1
    亚型
    IgG
    Top Product
    Discover our top product CLCN1 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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
    CLCN1 (Chloride Channel 1, Skeletal Muscle (CLCN1))
    别名
    CLCN1 (CLCN1 产品)
    别名
    CLCN1 antibody, si:dkey-14o18.5 antibody, Clc-1 antibody, Clc1 antibody, SMCC1 antibody, adr antibody, mto antibody, myotonia antibody, nmf355 antibody, SMCC antibody, CLC1 antibody, chloride voltage-gated channel 1 antibody, chloride channel, voltage-sensitive 1a antibody, chloride channel protein 1 antibody, chloride channel, voltage-sensitive 1 antibody, CLCN1 antibody, clcn1a antibody, LOC100550479 antibody, LOC703944 antibody, Clcn1 antibody
    背景

    Synonyms: Chloride channel protein 1,Chloride channel protein,Chloride channel protein skeletal muscle,CIC 1,CIC1,ClC-1,CLC1,Clcn1,CLCN1,MGC138361,MGC142055,skeletal muscle

    Background: The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. The protein encoded by this gene regulates the electric excitability of the skeletal muscle membrane. Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). Alternative splicing results in multiple transcript variants.

    分子量

    Observed_MW: 115kDa

    Calculated_MW: 108kDa

    基因ID
    1180
    UniProt
    P35523
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