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ROR2 抗体 (AA 34-403)

The 兔 单克隆 anti-ROR2 antibody is suitable to detect ROR2 in samples from 人. It has been validated for ELISA 和 FACS.
产品编号 ABIN7092973
发货至: 中国
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Room 801-803
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Quick Overview for ROR2 抗体 (AA 34-403) (ABIN7092973)

抗原

See all ROR2 抗体
ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

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 ROR2 antibody is un-conjugated

应用范围

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ELISA, Flow Cytometry (FACS)

克隆位点

DM174
  • 抗原表位

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    AA 34-403

    纯化方法

    Powder

    免疫原

    Recombinant human ROR2(Glu34-Gly403) (ABIN6964076) 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

    ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

    别名

    ROR2

    背景

    Synonyms:ROR2,NTRKR2
    Description:The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.

    分子量

    104.8KDa

    途径

    RTK signaling, WNT signaling
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