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  4. IFT80 Antibody, HRP conjugated

IFT80 Antibody, HRP conjugated

  • 中文名稱：
    IFT80兔多克隆抗體, HRP偶聯
  • 貨號：
    CSB-PA885802LB01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) IFT80 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    IFT80
  • 別名：
    ATD2 antibody; Ift80 antibody; IFT80_HUMAN antibody; Intraflagellar transport 80 homolog (Chlamydomonas) antibody; Intraflagellar transport protein 80 homolog antibody; KIAA1374 antibody; WD repeat domain 56 antibody; WD repeat-containing protein 56 antibody; WDR56 antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Intraflagellar transport protein 80 homolog protein (1-268AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    HRP
  • 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：
    Component of the intraflagellar transport (IFT) complex B, which is essential for the development and maintenance of motile and sensory cilia.
  • 基因功能參考文獻：
    1. Mutations in IFT80 can be responsible for a lethal form of short-rib polydactyly and provide the molecular basis for the Jeune-Verma-Naumoff dysplasia spectrum. PMID: 19648123
    2. Mutations in IFT80 is associated with Jeune asphyxiating thoracic dystrophy PMID: 17468754
    3. Identification and characterization of a human IFT80 long isoform (namely IFT80-L), the carboxyl terminus of which shares the protein sequence of IFT80, is reported. PMID: 18601909
  • 相關疾病：
    Short-rib thoracic dysplasia 2 with or without polydactyly (SRTD2)
  • 亞細胞定位：
    Cytoplasm. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, cilium axoneme.
  • 組織特異性：
    Isoform IFT80-L is widely expressed.
  • 數據庫鏈接：

    HGNC: 29262

    OMIM: 611177

    KEGG: hsa:57560

    STRING: 9606.ENSP00000312778

    UniGene: Hs.478095



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