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KCNJ2 抗体

KCNJ2 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7245515
发货至: 中国
  • 抗原 See all KCNJ2 抗体
    KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))
    适用
    • 44
    • 35
    • 26
    • 1
    人, 小鼠, 大鼠
    宿主
    • 48
    • 13
    • 2
    • 1
    克隆类型
    • 52
    • 12
    多克隆
    标记
    • 22
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    • 3
    • 1
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    • 1
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    • 1
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    • 1
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    This KCNJ2 antibody is un-conjugated
    应用范围
    • 55
    • 22
    • 21
    • 19
    • 15
    • 14
    • 13
    • 13
    • 10
    • 6
    • 4
    • 2
    • 2
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    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of human KCNJ2
    亚型
    IgG
    Top Product
    Discover our top product KCNJ2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.72 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
    KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))
    别名
    KCNJ2 (KCNJ2 产品)
    别名
    KCNJ2 antibody, ATFB9 antibody, HHBIRK1 antibody, HHIRK1 antibody, IRK1 antibody, KIR2.1 antibody, LQT7 antibody, SQT3 antibody, Kir2.1 antibody, Kcnf1 antibody, IRK-1 antibody, potassium voltage-gated channel subfamily J member 2 antibody, potassium inwardly-rectifying channel, subfamily J, member 2 antibody, KCNJ2 antibody, Kcnj2 antibody
    背景
    Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 48 kDa

    UniProt
    P63252
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