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AGA 抗体

AGA 适用: 人, 小鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6294189
发货至: 中国
  • 抗原 See all AGA 抗体
    AGA (Aspartylglucosaminidase (AGA))
    适用
    • 20
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    人, 小鼠
    宿主
    • 20
    • 1
    克隆类型
    • 21
    多克隆
    标记
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AGA antibody is un-conjugated
    应用范围
    • 11
    • 7
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human AGA
    亚型
    IgG
    Top Product
    Discover our top product AGA Primary Antibody
  • 应用备注
    WB 1:500 - 1:1000
    IF 1:50 - 1:100
    限制
    仅限研究用
  • 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 -20C. Avoid freeze / thaw cycles.
  • 抗原
    AGA (Aspartylglucosaminidase (AGA))
    别名
    AGA (AGA 产品)
    别名
    AGU antibody, ASRG antibody, GA antibody, AW060726 antibody, aspartylglucosaminidase antibody, AGA antibody, Aga antibody
    背景
    This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. This enzyme is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. Mutations in this gene are associated with the lysosomal storage disease aspartylglycosaminuria that results in progressive neurodegeneration. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is subject to proteolytic processing.
    分子量
    37.208 kDa
    基因ID
    175
    UniProt
    P20933
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