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HYDIN Antibody, HRP conjugated

  • 中文名稱：
    HYDIN兔多克隆抗體, HRP偶聯(lián)
  • 貨號(hào)：
    CSB-PA670104LB01HU
  • 規(guī)格：
    ￥880
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱：
    Rabbit anti-Homo sapiens (Human) HYDIN Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    HYDIN
  • 別名：
    CILD5 antibody; Hydin antibody; HYDIN axonemal central pair apparatus protein antibody; HYDIN_HUMAN antibody; HYDIN1 antibody; HYDIN2 antibody; Hydrocephalus-inducing protein homolog antibody; PPP1R31 antibody; Protein phosphatase 1 regulatory subunit 31 antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human
  • 免疫原：
    Recombinant Human Hydrocephalus-inducing protein homolog protein (101-400AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標(biāo)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(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA
  • Protocols：
  • 儲(chǔ)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.

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

  • 功能：
    Required for ciliary motility.
  • 基因功能參考文獻(xiàn)：
    1. Three loci with high mutation frequencies, the 138665410 FOXL2 gene variant, the 23862952 MYH6 gene variant, and the 71098693 HYDIN gene variant were found to be significantly associated with sporadic Atrial Septal Defect (P<0.05); variants in FOXL2 and MYH6 were found in patients with isolated, sporadic Atrial Septal Defect (P<5x10-4). PMID: 29505555
    2. The results suggest frequent and coordinated adaptive immune responses against HYDIN variants in patients with cancer. PMID: 24777681
    3. We have found that the human HYDIN locus has been very recently duplicated, with a nearly identical 360-kb paralogous segment inserted on chromosome 1q21.1 PMID: 16938426
  • 相關(guān)疾病：
    Ciliary dyskinesia, primary, 5 (CILD5)
  • 亞細(xì)胞定位：
    Cell projection, cilium. Cytoplasm, cytoskeleton, cilium axoneme.
  • 數(shù)據(jù)庫(kù)鏈接：

    HGNC: 19368

    OMIM: 608647

    KEGG: hsa:54768

    STRING: 9606.ENSP00000314736

    UniGene: Hs.351914