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- 抗原 See all AGLU 抗体
- AGLU (alpha-Glucosidase (AGLU))
- 抗原表位
- AA 173-203, N-Term
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This AGLU antibody is un-conjugated
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应用范围
- Western Blotting (WB), Enzyme Immunoassay (EIA), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 特异性
- This antibody recognizes Human Alpha-glucosidase (N-term).
- 纯化方法
- Protein A column, followed by peptide affinity purification
- 免疫原
- conjugated synthetic peptide between 173-203 amino acids from the N-terminal region of Human Alpha-glucosidase Genename: GAA
- 亚型
- Ig Fraction
- Top Product
- Discover our top product AGLU Primary Antibody
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anti-alpha-Glucosidase (AGLU) antibody
AGLU 适用: 人 WB 宿主: 小鼠 Monoclonal 43G7 unconjugated
anti-alpha-Glucosidase (AGLU) antibodyAGLU 适用: 人 IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-alpha-Glucosidase (AGLU) (AA 860-1090) antibodyAGLU 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- Optimal working dilution should be determined by the investigator.
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.25 mg/mL
- 缓冲液
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
- 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 freezing and thawing.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- 抗原
- AGLU (alpha-Glucosidase (AGLU))
- 别名
- alpha-Glucosidase (AGLU 产品)
- 别名
- MG antibody, MGA antibody, SPAC56F8.01 antibody, SPAC922.02c antibody, CG11909 antibody, CT33098 antibody, Dmel\\CG11909 antibody, GB19017 antibody, 6030407P20Rik antibody, maltase-glucoamylase antibody, alpha-glucosidase (predicted) antibody, alpha-glucosidase antibody, glucosidase, alpha, acid antibody, target of brain insulin antibody, sucrase-isomaltase antibody, MGAM antibody, SPAC30D11.01c antibody, LMOf2365_0194 antibody, SPAC1039.11c antibody, Gaa antibody, tobi antibody, SI antibody, Hbg3 antibody, Mgam antibody
- 背景
- This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene.Synonyms: Acid maltase, Aglucosidase alfa, GAA, LYAG, Lysosomal alpha-glucosidase
- 分子量
- 105319 Da
- 基因ID
- 2548
- NCBI登录号
- NP_000143
- 途径
- Cellular Glucan Metabolic Process
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