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Erythrocyte Ankyrin 抗体 (AA 1300-1844)

The 小鼠 单克隆 anti-Erythrocyte Ankyrin antibody is suitable to detect Erythrocyte Ankyrin in samples from 人. It has been validated for WB.
产品编号 ABIN7870500
发货至: 中国
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Quick Overview for Erythrocyte Ankyrin 抗体 (AA 1300-1844) (ABIN7870500)

抗原

See all Erythrocyte Ankyrin (ANK1) 抗体
Erythrocyte Ankyrin (ANK1) (Ankyrin 1, Erythrocytic (ANK1))

适用

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宿主

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小鼠

克隆类型

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单克隆

标记

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This Erythrocyte Ankyrin antibody is un-conjugated

应用范围

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Western Blotting (WB)

克隆位点

9I6C3
  • 抗原表位

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    AA 1300-1844

    原理

    Ankyrin-1 Antibody / ANK1 / Erythrocyte

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids N1300-Q1844) was used as the immunogen for the Ankyrin-1 antibody.

    亚型

    IgG1
  • 应用备注

    Optimal dilution of the Ankyrin-1 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the Ankyrin-1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    Erythrocyte Ankyrin (ANK1) (Ankyrin 1, Erythrocytic (ANK1))

    别名

    Ankyrin-1

    背景

    Ankyrin 1, erythrocytic, also known as ANK1, is a protein that in humans is encoded by the ANK1 gene. Ankyrins are a family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Multiple isoforms of ankyrin with different affinities for various target proteins are expressed in a tissue-specific, developmentally regulated manner. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats, a central region with a highly conserved spectrin binding domain, and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. Ankyrin 1, the prototype of this family, was first discovered in the erythrocytes, but since has also been found in brain and muscles. Mutations in erythrocytic ankyrin 1 have been associated in approximately half of all patients with hereditary spherocytosis. Complex patterns of alternative splicing in the regulatory domain, giving rise to different isoforms of ankyrin 1 have been described. Truncated muscle-specific isoforms of ankyrin 1 resulting from usage of an alternate promoter have also been identified.

    UniProt

    P16157

    途径

    Synaptic Membrane
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