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- 抗原 See all GBA 抗体
- GBA (Glucosidase, Beta, Acid (GBA))
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适用
- 人, 小鼠
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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 GBA antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Synthetic peptide of human GBA
- 亚型
- IgG
- Top Product
- Discover our top product GBA Primary Antibody
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anti-Glucosidase, Beta, Acid (GBA) (AA 146-235) antibody
GBA 适用: 人 WB, ELISA, IHC (p), IF 宿主: 小鼠 Monoclonal 2E2 unconjugated
anti-Glucosidase, Beta, Acid (GBA) (AA 117-214) antibodyGBA 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) antibodyGBA 适用: 小鼠, 大鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) (AA 334-498) antibodyGBA 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) (C-Term) antibodyGBA 适用: 人 WB, ICC, IHC (p), IF 宿主: 兔 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) (AA 255-509) antibodyGBA 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) (AA 215-343) antibodyGBA 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) (AA 1-536) antibodyGBA 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) (AA 1-536) antibodyGBA 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Glucosidase, Beta, Acid (GBA) (AA 146-235) antibodyGBA 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2H4 unconjugated
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- 应用备注
- WB 1:500-1:2000, IHC 1:50-1:100, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1.56 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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.
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- 抗原
- GBA (Glucosidase, Beta, Acid (GBA))
- 别名
- GBA (GBA 产品)
- 背景
- This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.
- 分子量
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Observed_MW: Refer to figures
Calculated_MW: 60 kDa
- UniProt
- P04062
- 途径
- Cellular Glucan Metabolic Process
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