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  4. ZNF644 Antibody, FITC conjugated

ZNF644 Antibody, FITC conjugated

  • 中文名稱：
    ZNF644兔多克隆抗體, FITC偶聯(lián)
  • 貨號：
    CSB-PA026914LC01HU
  • 規(guī)格：
    ￥880
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱：
    Rabbit anti-Homo sapiens (Human) ZNF644 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    ZNF644
  • 別名：
    BM005 antibody; KIAA1221 antibody; RGD1306805 antibody; Zep-2 antibody; Zep2 antibody; Zinc finger motif enhancer binding protein 2 antibody; Zinc finger motif enhancer-binding protein 2 antibody; Zinc finger protein 644 antibody; Zinc finger protein 644, isoform 2 antibody; ZN644_HUMAN antibody; ZNF644 antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Zinc finger protein 644 protein (752-913AA)
  • 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(chǎn)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(chǎn)品評價

靶點詳情

  • 功能：
    May be involved in transcriptional regulation.
  • 基因功能參考文獻：
    1. Our data suggested that genetic variants in GRM6 are associated with high myopia. The mechanism of GRM6 in the development of high myopia need to be further investigated. PMID: 27034204
    2. ZNF644 is associated with high myopia in a cohort from a Chinese population. PMID: 24991186
    3. Two novel variants in ZNF644 are associated with high-grade myopia in a US cohort. PMID: 22539872
    4. ZNF644 might be a causal gene for high myopia in a monogenic form. PMID: 21695231
  • 相關疾?。?/div>
    Myopia 21, autosomal dominant (MYP21)
  • 亞細胞定位：
    Nucleus.
  • 蛋白家族：
    Krueppel C2H2-type zinc-finger protein family
  • 組織特異性：
    Expressed in liver, placenta, retina and retinal pigment epithelium.
  • 數(shù)據(jù)庫鏈接：

    HGNC: 29222

    OMIM: 614159

    KEGG: hsa:84146

    STRING: 9606.ENSP00000337008

    UniGene: Hs.173001



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