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Biotin Plus-conjugated ATP1A2-

Specific 多克隆抗体 Biotin-55179
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  • ¥3200
  • Proteintech已认证
  • Biotin-55179
  • 2025年10月09日
  • IHC
  • Rabbit
  • human, mouse
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 亚型

      IgG

    • 保存条件

      Store at -20°C. Avoid exposure to light. Stable for one year after shipment.

    • 克隆性

      Polyclonal

    • 标记物

      Biotin Plus

    • 适应物种

      human, mouse

    • 宿主

      Rabbit

    • 应用范围

      IHC

    • 靶点

      ATP1A2-Specific

    • 抗体英文名

      Biotin Plus-conjugated ATP1A2-Specific Polyclonal antibody

    • 抗体名

      Biotin Plus-conjugated ATP1A2-Specific Polyclonal antibody

    • 规格

      100ul

    经过测试的应用

    Positive IHC detected inmouse heart tissue
    Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

    推荐稀释比

    应用推荐稀释比
    Immunohistochemistry (IHC)IHC : 1:50-1:500
    It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
    Sample-dependent, Check data in validation data gallery.

    产品信息

    Biotin-55179 targets ATP1A2-Specific in IHC applications and shows reactivity with human, mouse samples.

    经测试应用 IHC
    经测试反应性 human, mouse
    免疫原

    fusion protein

    宿主/亚型 Rabbit / IgG
    抗体类别 Polyclonal
    产品类型 Antibody
    全称 ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide
    别名 ATP1A2, Sodium pump subunit alpha-2, Na(+)/K(+) ATPase alpha-2 subunit, EC:7.2.2.13, ATP1A 2
    计算分子量 112 kDa
    观测分子量 100 kDa
    GenBank蛋白编号NM_000702
    基因名称 ATP1A2
    Gene ID (NCBI) 477
    偶联类型 Biotin Plus
    形式Liquid
    纯化方式Antigen Affinity Purified
    UNIPROT IDP50993
    储存缓冲液 PBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
    储存条件Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

    背景介绍

    ATP1A2, also named as KIAA0778, belongs to the cation transport ATPase (P-type) family and Type IIC subfamily. It is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. Defects in ATP1A2 are the cause of familial hemiplegic migraine type 2 (FHM2). Defects in ATP1A2 are a cause of alternating hemiplegia of childhood (AHC). This antibody is specific to ATP1A2.

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