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AGA 抗体 (Middle Region)

AGA 适用: 人, 大鼠, Pig, Cow, 犬, 豚鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2788660
发货至: 中国
  • 抗原 See all AGA 抗体
    AGA (Aspartylglucosaminidase (AGA))
    抗原表位
    • 6
    • 1
    • 1
    • 1
    • 1
    Middle Region
    适用
    • 19
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 大鼠, Pig, Cow, 犬, 豚鼠, 马
    宿主
    • 19
    • 1
    克隆类型
    • 20
    多克隆
    标记
    • 9
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AGA antibody is un-conjugated
    应用范围
    • 10
    • 7
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    序列
    SMGFINEDLS TTASQALHSD WLARNCQPNY WRNVIPDPSK YCGPYKPPGI
    预测反应
    Cow: 86%, Dog: 79%, Guinea Pig: 85%, Horse: 79%, Human: 100%, Pig: 86%, Rat: 79%
    产品特性
    This is a rabbit polyclonal antibody against AGA. It was validated on Western Blot.
    纯化方法
    Affinity Purified
    Top Product
    Discover our top product AGA Primary Antibody
  • 应用备注
    Optimal working dilutions should be determined experimentally by the investigator.
    说明

    Antigen size: 336 AA

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    Lot specific
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent 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
    Aspartylglucosaminidase 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. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.
    Alias Symbols: AGU, ASRG, GA
    Protein Interaction Partner: FBXO6, ALB, AGA, IGF2R,
    Protein Size: 336
    分子量
    36 kDa
    基因ID
    175
    NCBI登录号
    NM_001171988, NP_001165459
    UniProt
    P20933
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