pH-Sensitive K2P Channel Antibody Explorer Kit

pH-Sensitive K2P Channel Antib

ody Explorer Kit
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  • $1427
  • Alomone
  • ZK-0039397
  • 以色列
  • 2025年11月20日
  • 见官方网站
  • 见 说 明 书
  • 见官方网站
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  • 企业认证

    • 详细信息
    • 技术资料
    • 供应商

      上海再康生物科技有限公司

    • 库存

      大量

    • 靶点

      见官方网站

    • 级别

    • 目录编号

      AK-465

    • 克隆性

      多克隆

    • 抗原来源

      见 说 明 书

    • 保质期

      6个月

    • 抗体英文名

      pH-Sensitive K2P Channel Antibody Explorer Kit

    • 抗体名

      pH-Sensitive K2P Channel Antibody Explorer Kit

    • 标记物

      见官方网站

    • 宿主

      见 说 明 书

    • 适应物种

      见官方网站

    • 免疫原

      见官方网站

    • 亚型

      见官方网站

    • 形态

      液体或冻干粉

    • 应用范围

      见官方网站

    • 浓度

      见官方网站

    • 保存条件

      -20°C

    • 规格

      18 Vials

    pH-Sensitive K2P Channel Antibody Explorer Kit

    A Screening Package of pH-Sensitive K2P Channel Antibodies Economically Priced
    Cat #: AK-465
    18 Vials

    Alomone Labs is pleased to offer the pH-Sensitive K2P Channel Antibody Explorer Kit (#AK-465). The Explorer Kit contains pH-sensitive K2P channel antibodies, ideal for screening purposes.

    • Compounds
    • Scientific Background
    pH-Sensitive K2P Channel Antibody Explorer KitScientific Background 

    Two-pore domain potassium (K2P) channels have four transmembrane domains, two pore-forming loops between transmembrane domains 1 and 2 as well as 3 and 4, and a large extracellular linker region between transmembrane domain 1 and the first pore-forming loop, which forms the K+ selectivity filter.
    The TASK subfamily of this group is highly sensitive to variations in extracellular pH. TASK-1, TASK-2 and TASK-3 homo- and heteromers are inhibited by extracellular acidification but are left unaffected by intracellular pH changes. Acid-induced inhibition of TASK channel activity enhances nerve excitability and thus indirectly indicates the presence of acid. The high proton sensitivity of the TASK channels suggests a role in surveillance of tissue acidification by ischemia, inflammation or back-diffusion of luminal acid.

    TREK-1 and TREK-2 do not respond to changes in extracellular pH but are inhibited by intracellular alkalization and are activated by intracellular acidification such that they become constitutively active.

    TRESK K2P member is blocked by extra- and intracellular acidification and is activated by extra and intracellular alkalization.

    Additional pH-sensitive K2P channels include TWIK-1 and TWIK-2 which are inhibited by intracellular acidification, TRAAK channels that are activated by intracellular alkalization but not acidification and lastly, TALK-1 and TALK-2 are blocked by extracellular acidification but are gated open by extracellular alkalization1.


    References 
    1. Holzer, P. (2009) Handb. Exp. Pharmacol. 194, 283.

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