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ROR2 抗体 (N-Term)

There is 1 publication for this product available. The 兔 多克隆 anti-ROR2 antibody is suitable to detect ROR2 in samples from 人. It has been validated for EIA.
产品编号 ABIN359930
发货至: 中国
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Quick Overview for ROR2 抗体 (N-Term) (ABIN359930)

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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多克隆

标记

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This ROR2 antibody is un-conjugated

应用范围

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Enzyme Immunoassay (EIA)
  • 抗原表位

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    N-Term

    特异性

    This antibody reacts to ROR2.

    纯化方法

    Protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS

    免疫原

    This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the N-terminal region of human ROR2.

    亚型

    Ig Fraction
  • 应用备注

    ELISA: 1/1,000. Western Blot.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.25 mg/mL

    缓冲液

    PBS with 0.09 % (W/V) 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.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
  • Arabzadeh, Hossein, Salehi-Dulabi, Zarnani: "WNT5A-ROR2 is induced by inflammatory mediators and is involved in the migration of human ovarian cancer cell line SKOV-3." in: Cellular & molecular biology letters, Vol. 21, pp. 9, (2017) (PubMed).

  • 抗原

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

    别名

    ROR2

    背景

    ROR2 is a tyrosine-protein kinase receptor which may be involved in the early formation of the chondrocytes. It seems to be required for cartilage and growth plate development. This Type I membrane protein is expressed at high levels during early embryonic development. The expression levels drop strongly around day 16 and there are only very low levels in adult tissues. Defects in ROR2 are a cause of brachydactyly type B1 (BDB1). BDB1 is an autosomal dominant skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In BDB1 the middle phalanges are short but in addition the terminal phalanges are rudimentary or absent. Both fingers and toes are affected. The thumbs and big toes are usually deformed. Defects in ROR2 are a cause of recessive Robinow syndrome (RRS). RRS is an autosomal disorder characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly and a dysmorphic facial appearance. The protein contains 1 frizzled (FZ) domain, 1 immunoglobulin-like C2-type domain, and 1 kringle domain.Synonyms: NTRKR2, Tyrosine-protein kinase transmembrane receptor ROR2

    基因ID

    4920, 9606

    UniProt

    Q01974

    途径

    RTK signaling, WNT signaling
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