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EPH Receptor A2 抗体 (AA 24-534)

This 兔 单克隆 antibody specifically detects EPH Receptor A2 in ELISA 和 FACS. It exhibits reactivity toward 人.
产品编号 ABIN7092966
发货至: 中国
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Quick Overview for EPH Receptor A2 抗体 (AA 24-534) (ABIN7092966)

抗原

See all EPH Receptor A2 (EPHA2) 抗体
EPH Receptor A2 (EPHA2)

适用

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宿主

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克隆类型

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单克隆

标记

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This EPH Receptor A2 antibody is un-conjugated

应用范围

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ELISA, Flow Cytometry (FACS)

克隆位点

DM167
  • 抗原表位

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    AA 24-534

    纯化方法

    Powder

    免疫原

    Recombinant human EPHA2(Ala24-Asn534) (ABIN6964101) produced by using human HEK293 cells

    亚型

    IgG
  • 应用备注

    ELISA 1/5000-10000,Flow Cyt 1/100

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Reconstitute with deionized water

    缓冲液

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.,0.1 % Procline 300

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C,-80 °C

    储存方法

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    有效期

    12 months
  • 抗原

    EPH Receptor A2 (EPHA2)

    别名

    EPHA2

    背景

    Synonyms:ARCC2, CTPA, CTPP1, CTRCT6, ECK
    Description:This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene encodes a protein that binds ephrin-A ligands. Mutations in this gene are the cause of certain genetically-related cataract disorders.

    分子量

    108.3KDa

    途径

    RTK signaling
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