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ROR2 抗体 (pSer449)

The 兔 多克隆 anti-ROR2 antibody (ABIN8124274) specifically detects ROR2 in WB. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN8124274
发货至: 中国
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Quick Overview for ROR2 抗体 (pSer449) (ABIN8124274)

抗原

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

适用

  • 104
  • 41
  • 27
  • 2
  • 1
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 78
  • 27
  • 1
兔

克隆类型

  • 64
  • 42
多克隆

标记

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  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This ROR2 antibody is un-conjugated

应用范围

  • 61
  • 42
  • 36
  • 32
  • 11
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  • 9
  • 8
  • 6
Western Blotting (WB)
  • 抗原表位

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    • 2
    • 1
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    pSer449

    原理

    ROR2 (Phospho Ser449) Antibody

    特异性

    This antibody detects endogenous levels of ROR2 (Phospho-Ser449) at Human, Mouse,Rat

    纯化方法

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

    免疫原

    Synthesized peptide derived from human ROR2 (Phospho-Ser449)

    亚型

    IgG
  • 应用备注

    WB 1:500-2000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

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

    储存液

    Sodium azide

    注意事项

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

    储存条件

    -20 °C

    储存方法

    Store at -20°C/1 year

    有效期

    12 months
  • 抗原

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

    别名

    ROR2

    背景

    Synonyms: Tyrosine-protein kinase transmembrane receptor ROR2 (EC 2.7.10.1) (Neurotrophic tyrosine kinase, receptor-related 2)

    Background: 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],

    Gene Name: ROR2 NTRKR2

    Protein Name: ROR2 (Phospho-Ser449)

    基因ID

    4920

    UniProt

    Q01974

    途径

    RTK signaling, WNT signaling
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