AGA 抗体
(Aspartylglucosaminidase (AGA))
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. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jan 2010].
| Catalog no. | 产品 | 适用 | 宿主 / 克隆类型 | 应用 | 价格和交货时间 |
|---|---|---|---|---|---|
| AGA 抗体 (Alexa Fluor 594) | 人, 小鼠 | 兔 Polyclonal |
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| AGA 抗体 (Alexa Fluor 488) | 人, 小鼠 | 兔 Polyclonal |
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| AGA 抗体 | 人, 小鼠, 大鼠 | 兔 Polyclonal |
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| AGA 抗体 (AA 206-346) | 人, 小鼠 | 兔 Polyclonal |
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Primary Antibody
- WB (Western Blotting: 所列应用)
- ELISA (ELISA: 所列应用)
- 适用
- 人, 小鼠
- 宿主
- 兔
- 克隆形成能力
- Polyclonal
- 标记
- unconjugated
- 抗体亚型
- IgG
- 抗原表位
- AA 206-346
Aliases for AGA 抗体
aspartylglucosaminidase (AGA) 抗体aspartylglucosaminidase (Aga) 抗体
AGU 抗体
ASRG 抗体
AW060726 抗体
GA 抗体
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