Anti-KCNA5 antibody

Anti-KCNA5 antibody

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  • 询价
  • gelatins
  • JC220896
  • 2025年07月12日
  • ELISA, WB
  • Rabbit
  • 人/动物/植物
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    • 详细信息
    • 技术资料
    • 供应商

      上海机纯实业有限公司

    • 库存

      大量

    • 克隆性

      多克隆

    • 保质期

      12个月

    • 抗体英文名

      Anti-KCNA5 antibody

    • 宿主

      Rabbit

    • 适应物种

      人/动物/植物

    • 应用范围

      ELISA, WB

    • 浓度

      0.4 mg/ml

    • 保存条件

      -20°C

    • 规格

      25 μl/100 μl/200 μl

    Anti-KCNA5 antibody

    Cat. No.     JC220896
    Package    25 μl/100 μl/200 μl
    Storage    -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol

    Product overview
    Description                   Anti-KCNA5 rabbit polyclonal antibody
    Applications        ELISA, WB 
    Immunogen               Fusion protein of human KCNA5
    Reactivity                 Human, Mouse, Rat
    Content                     0.4 mg/ml
    Host species               Rabbit
    Ig class                  Immunogen-specific rabbit IgG
    Purification                 Antigen affinity purification

    Target information
    Symbol                 KCNA5
    Full name                 potassium voltage-gated channel, shaker-related subfamily, member 5
    Synonyms    HK2, HCK1, PCN1, ATFB7, HPCN1, KV1.5
    Swissprot    P22460

    Target Background
    Potassium channels represent the most complex class of voltage-gated ino channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, the function of which could restore the resting membrane potential of beta cells after depolarization and thereby contribute to the regulation of insulin secretion. This gene is intronless, and the gene is clustered with genes KCNA1 and KCNA6 on chromosome 12. Defects in this gene are a cause of familial atrial fibrillation type 7 (ATFB7).

    Applications
    Western blotting
    Predicted band size:67 kDa
    Positive control:Mouse spleen tissue 
    Recommended dilution: 500-2000

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    资料下载:

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