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  4. ODAPH Antibody

ODAPH Antibody

  • 中文名稱：
    ODAPH兔多克隆抗體
  • 貨號：
    CSB-PA613780LA01HU
  • 規(guī)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(chǎn)品詳情

  • 產(chǎn)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(yīng)種屬：
    Human
  • 免疫原：
    Recombinant Human Odontogenesis associated phosphoprotein protein (24-130AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標(biāo)記方式：
    Non-conjugated

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

    可提供標(biāo)記
    標(biāo)記方式 貨號 產(chǎn)品名稱 應(yīng)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(chǎn)品提供形式：
    Liquid
  • 應(yīng)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(chǎn)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(guān)疾?。?/div>
    Amelogenesis imperfecta, hypomaturation type, 2A4 (AI2A4)
  • 亞細(xì)胞定位：
    Secreted.
  • 組織特異性：
    Highly expressed in placenta.
  • 數(shù)據(jù)庫鏈接：

    HGNC: 26300

    OMIM: 614829

    KEGG: hsa:152816

    STRING: 9606.ENSP00000406925

    UniGene: Hs.24510