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  4. TGDS Antibody

TGDS Antibody

  • 中文名稱：
    TGDS兔多克隆抗體
  • 貨號：
    CSB-PA023444GA01HU
  • 規格：
    ￥3,900
  • 其他：

產品詳情

  • Uniprot No.：
  • 基因名：
    TGDS
  • 別名：
    6-dehydratase antibody; dTDP D glucose 4,6 dehydratase antibody; dTDP-D-glucose 4 antibody; Growth inhibiting protein 21 antibody; SDR2E1 antibody; TDP glucose 4,6 dehydratase antibody; TDPGD antibody; TGDS antibody; TGDS_HUMAN antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human,Mouse,Rat
  • 免疫原：
    Human TGDS
  • 免疫原種屬：
    Homo sapiens (Human)
  • 抗體亞型：
    IgG
  • 純化方式：
    Antigen Affinity purified
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產品提供形式：
    Liquid
  • 應用范圍：
    ELISA,WB,IHC
  • Protocols：
  • 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

  • 基因功能參考文獻：
    1. Our findings widen the phenotype spectrum caused by TGDS mutations and underline the phenotypic overlap with Temtamy preaxial brachydactyly syndrome. This improves our understanding of the prenatal development and the pathogenetic mechanism of Catel-Manzke syndrome. PMID: 28422407
    2. By using haplotype reconstruction we showed that the mutation c.298G>T is probably a founder mutation. Due to the spectrum of the amino acid changes, we suggest that loss of function in TGDS is the underlying mechanism of Catel-Manzke syndrome. PMID: 25480037
  • 相關疾病：
    Catel-Manzke syndrome (CATMANS)
  • 蛋白家族：
    NAD(P)-dependent epimerase/dehydratase family, dTDP-glucose dehydratase subfamily
  • 數據庫鏈接：

    HGNC: 20324

    OMIM: 616145

    KEGG: hsa:23483

    STRING: 9606.ENSP00000261296

    UniGene: Hs.12393



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