ROR2 Polyclonal Antibody

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2616117

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商品描述
  • 靶点-Target

    ROR2

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Observed)

    110kD

  • 推荐稀释比

    WB 1:500-1:2000;ELISA 1:5000;Not yet tested in other applications.

  • 组成

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • 纯化工艺

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • 储存

    -15°C to -25°C/1 year(Do not lower than -25°C)

  • 浓度

    1 mg/ml

  • 克隆性

    Polyclonal

  • 免疫原

    Synthesized peptide derived from ROR2 . at AA range: 450-530

  • 特异性

    ROR2 Polyclonal Antibody detects endogenous levels of ROR2 protein.

  • 基因名称

    ROR2

  • 蛋白名称

    Tyrosine-protein kinase transmembrane receptor ROR2

  • 别名

    ROR2;NTRKR2;Tyrosine-protein kinase transmembrane receptor ROR2;Neurotrophic tyrosine kinase;receptor-related 2

  • Organism-1

    Human

  • 基因ID-1

    4920

  • SwissProt-1

    Q01974

  • Organism-2

    Mouse

  • SwissProt-2

    Q9Z138

  • 背景

    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. [provided by RefSeq, Jul 2008],

  • 细胞定位

    Cell membrane ; Single-pass type I membrane protein .