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KCNJ6 抗体

KCNJ6 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7264952
发货至: 中国
  • 抗原 See all KCNJ6 抗体
    KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))
    适用
    • 43
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    • 2
    • 2
    • 1
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    人, 小鼠
    宿主
    • 42
    • 1
    • 1
    • 1
    • 1
    克隆类型
    • 45
    • 1
    多克隆
    标记
    • 20
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    • 1
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    This KCNJ6 antibody is un-conjugated
    应用范围
    • 39
    • 20
    • 19
    • 12
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human KCNJ6 (NP_002231.1).
    亚型
    IgG
    Top Product
    Discover our top product KCNJ6 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    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
    KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))
    别名
    KCNJ6 (KCNJ6 产品)
    别名
    kcnj6 antibody, BIR1 antibody, GIRK-2 antibody, GIRK2 antibody, KATP-2 antibody, KATP2 antibody, KCNJ7 antibody, KIR3.2 antibody, hiGIRK2 antibody, Kir3.2 antibody, weaver antibody, wv antibody, potassium voltage-gated channel subfamily J member 6 antibody, potassium channel, inwardly rectifying subfamily J, member 5 antibody, potassium inwardly-rectifying channel, subfamily J, member 6 antibody, KCNJ6 antibody, kcnj5 antibody, Kcnj6 antibody
    背景
    This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability.
    分子量

    Observed_MW: 48 kDa

    Calculated_MW: 48 kDa

    基因ID
    3763
    UniProt
    P48051
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