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C12orf57 Antibody

  • 中文名稱：
    C12orf57兔多克隆抗體
  • 貨號：
    CSB-PA859105LA01HU
  • 規格：
    ￥440
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) C12orf57 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    C12orf57
  • 別名：
    C10_HUMAN antibody; C12orf57 antibody; Protein C10 antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Protein C10 protein (2-126AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    Non-conjugated

    本頁面中的產品，C12orf57 Antibody (CSB-PA859105LA01HU)，的標記方式是Non-conjugated。對于C12orf57 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-PA859105LB01HU C12orf57 Antibody, HRP conjugated ELISA
    FITC CSB-PA859105LC01HU C12orf57 Antibody, FITC conjugated
    Biotin CSB-PA859105LD01HU C12orf57 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
  • 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：
    In brain, may be required for corpus callosum development.
  • 基因功能參考文獻：
    1. Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizures. PMID: 24798461
    2. The findings strongly support the candidacy of C12orf57 as a gene that is mutated in a distinct syndromic form of colobomatous microphthalmia in humans. PMID: 23453665
  • 相關疾病：
    Temtamy syndrome (TEMTYS)
  • 亞細胞定位：
    Cytoplasm.
  • 蛋白家族：
    UPF0456 family
  • 組織特異性：
    Ubiquitously expressed, with higher expression in lung and fetal brain.
  • 數據庫鏈接：

    HGNC: 29521

    OMIM: 218340

    KEGG: hsa:113246

    STRING: 9606.ENSP00000229281

    UniGene: Hs.405913