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  4. IFT172 Antibody, FITC conjugated

IFT172 Antibody, FITC conjugated

  • 中文名稱：
    IFT172兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA887019LC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) IFT172 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    IFT172
  • 別名：
    IF172_HUMAN antibody; ift172 antibody; Intraflagellar transport 172 homolog (Chlamydomonas) antibody; Intraflagellar transport protein 172 homolog antibody; Osm 1 antibody; Selective LIM binding factor homolog antibody; SLB antibody; Wim antibody; Wimple homolog antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Intraflagellar transport protein 172 homolog protein (1368-1502AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    FITC
  • 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
  • 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：
    Required for the maintenance and formation of cilia. Plays an indirect role in hedgehog (Hh) signaling, cilia being required for all activity of the hedgehog pathway.
  • 基因功能參考文獻：
    1. This is the second report of IFT172 mutations in BBS patients validating IFT172 as the twentieth BBS gene (BBS20). PMID: 26763875
    2. Findings identified mutations in IFT172 that lead to a recessive form of non-syndromic retinitis pigmentosa and Bardet-Biedl syndrome and suggest that the primary IFT172 mutations alone are not sufficient to explain the wide range of phenotypes. PMID: 25168386
    3. We have identified defects in IFT172 as a cause of complex asphyxiating thoracic dystrophy and Mainzer-Saldino syndrome. PMID: 24140113
  • 相關疾病：
    Short-rib thoracic dysplasia 10 with or without polydactyly (SRTD10); Retinitis pigmentosa 71 (RP71)
  • 亞細胞定位：
    Cell projection, cilium. Note=Localized to the axoneme and around the base of the cilium.
  • 蛋白家族：
    IFT172 family
  • 數據庫鏈接：

    HGNC: 30391

    OMIM: 607386

    KEGG: hsa:26160

    STRING: 9606.ENSP00000260570

    UniGene: Hs.127401



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