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  4. FRYL Antibody, FITC conjugated

FRYL Antibody, FITC conjugated

  • 中文名稱：
    FRYL兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA009007LC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) FRYL Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    FRYL
  • 別名：
    2010313D22Rik antibody; 2310004H21Rik antibody; 2510002A14Rik antibody; 9030227G01Rik antibody; AF4P12 antibody; AI930088 antibody; ALL fused gene from chromosome 4p12 antibody; ALL1-fused gene from chromosome 4p12 protein antibody; DKFZp686E205 antibody; FLJ161772 antibody; FRY like antibody; FRYL antibody; FRYL_HUMAN antibody; Furry homolog like (Drosophila) antibody; Furry homolog like antibody; Furry like antibody; KIAA0826 antibody; mKIAA0826 antibody; Protein furry homolog-like antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Protein furry homolog-like protein (42-739AA)
  • 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：
    Plays a key role in maintaining the integrity of polarized cell extensions during morphogenesis, regulates the actin cytoskeleton and plays a key role in patterning sensory neuron dendritic fields by promoting avoidance between homologous dendrites as well as by limiting dendritic branching. May function as a transcriptional activator.
  • 基因功能參考文獻：
    1. Thus, t(4;11)(p12;q23) with MLL and FRYL involvement represents a new recurring 11q23 translocation, to date seen only in therapy-related acute leukemias. PMID: 17854671
  • 相關疾病：
    A chromosomal aberration involving FRYL is found in treatment-related acute lymphoblastic leukemia (ALL). Translocation t(4;11)(p12;q23) that forms a KMT2A/MLL1-FRYL fusion protein.
  • 蛋白家族：
    Furry protein family
  • 組織特異性：
    Widely expressed with higher expression in colon, placenta, brain and cells of lymphoid origin.
  • 數據庫鏈接：

    HGNC: 29127

    KEGG: hsa:285527

    STRING: 9606.ENSP00000351113

    UniGene: Hs.595553



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