FGGY Antibody,HRP conjugated
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中文名稱：FGGY兔多克隆抗體,HRP偶聯
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貨號：CSB-PA853393LB01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) FGGY Polyclonal antibody
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Uniprot No.：
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基因名：FGGY
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別名：FGGYFGGY carbohydrate kinase domain-containing protein antibody; EC 2.7.1.- antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human FGGY carbohydrate kinase domain-containing protein (1-244AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：HRP
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：>95%, Antigen Affinity purified & Affinity purified
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濃度：It differs from different batches. Please contact us to confirm it.
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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
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應用范圍：ELISA
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Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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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.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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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.
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基因功能參考文獻：
- 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
- Single-nucleotide polymorphism in FGGY is not associated with amyotrophic lateral sclerosis in a large Chinese cohort. PMID: 24439956
- The result of this study suggested that FLJI0986 that do not modulate the risk for SALS in the German population. PMID: 19464757
- 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
- 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
- Variants of FLJ10986 may confer susceptibility to sporadic ALS (amyotrophic lateral sclerosis). PMID: 17671248
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相關疾病：Amyotrophic lateral sclerosis (ALS)
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蛋白家族：FGGY kinase family
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組織特異性：Expressed in kidney, lung and small intestine and to a lower extent in liver and detected in cerebrospinal fluid (at protein level).
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數據庫鏈接：
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