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  4. RSPH9 Antibody, FITC conjugated

RSPH9 Antibody, FITC conjugated

  • 中文名稱：
    RSPH9兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA867129LC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) RSPH9 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    RSPH9
  • 別名：
    C6orf206 antibody; Chromosome 6 open reading frame 206 antibody; CILD12 antibody; FLJ30845 antibody; Mitochondrial ribosomal protein S18A like 1 antibody; MRPS18AL1 antibody; Radial spoke head 9 homolog antibody; Radial spoke head protein 9 homolog antibody; RSPH 9 antibody; rsph9 antibody; RSPH9_HUMAN antibody; Uncharacterized protein C6orf206 antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Radial spoke head protein 9 homolog protein (62-171AA)
  • 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：
    Component of the axonemal radial spoke head which plays an important role in ciliary motility. Essential for both the radial spoke head assembly and the central pair microtubule stability in ependymal motile cilia. Required for motility of olfactory and neural cilia and for the structural integrity of ciliary axonemes in both 9+0 and 9+2 motile cilia.
  • 基因功能參考文獻：
    1. Mutations in RSPH9 leads to ultrastructural cilia defects and ciliary dyskinesia. PMID: 22448264
    2. Study focused on an extended 5 generation Bedouin family, analysed mutation segregation, and calculated the age of the mutated allele in 2 families based on haplotypes and haplotype+microsatellite in an attempt to define the source of the mutation. PMID: 20070851
  • 相關疾病：
    Ciliary dyskinesia, primary, 12 (CILD12)
  • 亞細胞定位：
    Cytoplasm, cytoskeleton, cilium axoneme. Cell projection, cilium, flagellum. Cell projection, kinocilium.
  • 蛋白家族：
    Flagellar radial spoke RSP9 family
  • 數據庫鏈接：

    HGNC: 21057

    OMIM: 612648

    KEGG: hsa:221421

    UniGene: Hs.534585



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