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  4. WDR60 Antibody, FITC conjugated

WDR60 Antibody, FITC conjugated

  • 中文名稱：
    WDR60兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA845154HC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) WDR60 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    WDR60
  • 別名：
    WDR60WD repeat-containing protein 60 antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human WD repeat-containing protein 60 protein (1-200AA)
  • 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：
    Acts as one of several non-catalytic accessory components of the cytoplasmic dynein 2 complex (dynein-2 complex), a motor protein complex that drives the movement of cargos along microtubules within cilia and flagella in concert with the intraflagellar transport (IFT) system. DYNC2I1 plays a major role in retrograde ciliary protein trafficking in cilia and flagella. Requires also to maintain a functional transition zone.
  • 基因功能參考文獻：
    1. exome analysis allowed to identify mutations not previously reported in the DYNC2H1 (MIM 603297) and WDR60 (MIM 615462) genes, both codifying for ciliary intraflagellar transport components whose mutations are known to cause Jeune syndrome PMID: 26874042
    2. These findings show that WDR60 mutations can cause skeletal ciliopathies and suggest a role for WDR60 in ciliogenesis. PMID: 23910462
  • 相關疾病：
    Short-rib thoracic dysplasia 8 with or without polydactyly (SRTD8)
  • 亞細胞定位：
    Cell projection, cilium. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome.
  • 組織特異性：
    Expressed in chondrocytes (at protein level).
  • 數據庫鏈接：

    HGNC: 21862

    OMIM: 615462

    KEGG: hsa:55112

    STRING: 9606.ENSP00000384290

    UniGene: Hs.389945



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