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MOGS Antibody

  • 中文名稱：
    MOGS兔多克隆抗體
  • 貨號(hào)：
    CSB-PA014713GA01HU
  • 規(guī)格：
    ￥3,900
  • 其他：

產(chǎn)品詳情

  • Uniprot No.：
  • 基因名：
  • 別名：
    EC 3.2.1.106 antibody; glucosidase I antibody; Mannosyl oligosaccharide glucosidase antibody; Mannosyl-oligosaccharide glucosidase antibody; Mogs antibody; MOGS_HUMAN antibody; Processing A glucosidase I antibody; Processing A-glucosidase I antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human,Mouse,Rat
  • 免疫原：
    Human MOGS
  • 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 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA,WB
  • Protocols：
  • 儲(chǔ)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(píng)價(jià)

靶點(diǎn)詳情

  • 功能：
    Cleaves the distal alpha 1,2-linked glucose residue from the Glc(3)Man(9)GlcNAc(2) oligosaccharide precursor in a highly specific manner.
  • 基因功能參考文獻(xiàn)：
    1. A shortened immunoglobulin half-life was determined to be the mechanism underlying the hypogammaglobulinemia in congenital disorder of glycosylation type IIb (CDG-IIb). PMID: 24716661
    2. Perturbation of free oligosaccharide trafficking in endoplasmic reticulum glucosidase I-deficient and castanospermine-treated cells. PMID: 11942856
    3. MafF/NFE2 hetrodimers act as weak transcriptional activators, and, in particular, are able to stimulate activity of the GCS1 promoter. PMID: 12490281
    4. identification of sequence motifs responsible for endoplasmic reticulum localization PMID: 12626409
  • 相關(guān)疾?。?/div>
    Type IIb congenital disorder of glycosylation (CDGIIb)
  • 亞細(xì)胞定位：
    Endoplasmic reticulum membrane; Single-pass type II membrane protein.
  • 蛋白家族：
    Glycosyl hydrolase 63 family
  • 數(shù)據(jù)庫鏈接：

    HGNC: 24862

    OMIM: 601336

    KEGG: hsa:7841

    STRING: 9606.ENSP00000233616

    UniGene: Hs.516119