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Your Good Partner in Biology Research

ODAPH Antibody

  • 中文名稱:
    ODAPH兔多克隆抗體
  • 貨號:
    CSB-PA613780LA01HU
  • 規格:
    ¥440
  • 圖片:
    • Immunohistochemistry of paraffin-embedded human placenta tissue using CSB-PA613780LA01HU at dilution of 1:100
    • Immunohistochemistry of paraffin-embedded human bladder cancer using CSB-PA613780LA01HU at dilution of 1:100
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) ODAPH Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    ODAPH
  • 別名:
    ODAPH antibody; C4orf26 antibody; Odontogenesis associated phosphoprotein antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Odontogenesis associated phosphoprotein protein (24-130AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated

    本頁面中的產品,ODAPH Antibody (CSB-PA613780LA01HU),的標記方式是Non-conjugated。對于ODAPH Antibody,我們還提供其他標記。見下表:

    可提供標記
    標記方式 貨號 產品名稱 應用
    HRP CSB-PA613780LB01HU ODAPH Antibody, HRP conjugated ELISA
    FITC CSB-PA613780LC01HU ODAPH Antibody, FITC conjugated
    Biotin CSB-PA613780LD01HU ODAPH Antibody, Biotin conjugated ELISA
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA, IHC
  • 推薦稀釋比:
    Application Recommended Dilution
    IHC 1:20-1:200
  • Protocols:
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能:
    May promote nucleation of hydroxyapatite.
  • 基因功能參考文獻:
    1. Autozygosity mapping and clonal sequencing of an Omani family identified mutations in the uncharacterized gene, C4orf26, as a cause of recessive hypomineralized amelogenesis imperfecta PMID: 22901946
  • 相關疾?。?/div>
    Amelogenesis imperfecta, hypomaturation type, 2A4 (AI2A4)
  • 亞細胞定位:
    Secreted.
  • 組織特異性:
    Highly expressed in placenta.
  • 數據庫鏈接:

    HGNC: 26300

    OMIM: 614829

    KEGG: hsa:152816

    STRING: 9606.ENSP00000406925

    UniGene: Hs.24510



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