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GCS1 抗体 (AA 60-320)

MOGS 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6143945
发货至: 中国
  • 抗原 See all GCS1 (MOGS) 抗体
    GCS1 (MOGS) (Mannosyl-Oligosaccharide Glucosidase (MOGS))
    抗原表位
    • 15
    • 7
    • 7
    • 5
    • 3
    • 1
    AA 60-320
    适用
    • 40
    • 14
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 41
    克隆类型
    • 41
    多克隆
    标记
    • 17
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GCS1 antibody is un-conjugated
    应用范围
    • 41
    • 18
    • 13
    • 13
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB)
    序列
    RWVLAWYRAR RAVTLHSAPP VLPADSSSPA VAPDLFWGTY RPHVYFGMKT RSPKPLLTGL MWAQQGTTPG TPKLRHTCEQ GDGVGPYGWE FHDGLSFGRQ HIQDGALRLT TEFVKRPGGQ HGGDWSWRVT VEPQDSGTSA LPLVSLFFYV VTDGKEVLLP EVGAKGQLKF ISGHTSELGD FRFTLLPPTS PGDTAPKYGS YNVFWTSNPG LPLLTEMVKS RLNSWFQHRP PGAPPERYLG LPGSLKWEDR GPSGQGQGQF L
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Polyclonal Antibodies
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 60-320 of human MOGS (NP_006293.2).
    亚型
    IgG
    Top Product
    Discover our top product MOGS Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000
    说明

    HIGH QUALITY

    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    GCS1 (MOGS) (Mannosyl-Oligosaccharide Glucosidase (MOGS))
    别名
    MOGS (MOGS 产品)
    背景
    This gene encodes the first enzyme in the N-linked oligosaccharide processing pathway. The enzyme cleaves the distal alpha-1,2-linked glucose residue from the Glc(3)-Man(9)-GlcNAc(2) oligosaccharide precursor. This protein is located in the lumen of the endoplasmic reticulum. Defects in this gene are a cause of type IIb congenital disorder of glycosylation (CDGIIb). Two transcript variants encoding different isoforms have been found for this gene.,MOGS,CDG2B,CWH41,DER7,GCS1,MOGS
    分子量
    80 kDa/91 kDa
    基因ID
    7841
    UniProt
    Q13724
    途径
    SARS-CoV-2 Protein Interactome
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