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FGGY Antibody，FITC conjugated

  • 中文名称：
    FGGY兔多克隆抗体，FITC偶联
  • 货号：
    CSB-PA853393LC01HU
  • 规格：
    ￥880
  • 其他：

产品详情

  • 产品名称：
    Rabbit anti-Homo sapiens (Human) FGGY Polyclonal antibody
  • Uniprot No.：
    Q96C11
  • 基因名：
    FGGY
  • 别名：
    FGGYFGGY carbohydrate kinase domain-containing protein antibody; EC 2.7.1.- antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Recombinant Human FGGY carbohydrate kinase domain-containing protein (1-244AA)
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    FITC
  • 克隆类型：
    Polyclonal
  • 抗体亚型：
    IgG
  • 纯化方式：
    >95%, Antigen Affinity purified & Affinity purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 产品提供形式：
    Liquid
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    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.

产品评价

靶点详情

  • 功能：
    Catalyzes ATP-dependent phosphorylation of D-ribulose at C-5 to form D-ribulose 5-phosphate. Postulated to function in a metabolite repair mechanism by preventing toxic accumulation of free D-ribulose formed by non-specific phosphatase activities. Alternatively, may play a role in regulating D-ribulose 5-phosphate recycling in the pentose phosphate pathway. Can phosphorylate ribitol with low efficiency.
  • 基因功能参考文献：
    1. S. cerevisiae Ydr109c and human FGGY could act as metabolite repair enzymes, serving to re-phosphorylate free d-ribulose generated by promiscuous phosphatases from d-ribulose 5-phosphate. In human cells, FGGY can additionally participate in ribitol metabolism. PMID: 27909055
    2. Single-nucleotide polymorphism in FGGY is not associated with amyotrophic lateral sclerosis in a large Chinese cohort. PMID: 24439956
    3. The result of this study suggested that FLJI0986 that do not modulate the risk for SALS in the German population. PMID: 19464757
    4. This study indicated that mutations in fggy genes are unlikely to be a common cause of ALS in the French and French Canadian populations. PMID: 20001489
    5. Results suggest that common genetic variation in FGGY is not associated with susceptibility to sporadic ALS in genetically homogeneous populations from northern Europe. PMID: 19922138
    6. Variants of FLJ10986 may confer susceptibility to sporadic ALS (amyotrophic lateral sclerosis). PMID: 17671248

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  • 相关疾病：
    Amyotrophic lateral sclerosis (ALS)
  • 蛋白家族：
    FGGY kinase family
  • 组织特异性：
    Expressed in kidney, lung and small intestine and to a lower extent in liver and detected in cerebrospinal fluid (at protein level).
  • 数据库链接：

    HGNC: 25610

    OMIM: 105400

    KEGG: hsa:55277

    STRING: 9606.ENSP00000360262

    UniGene: Hs.444301