Lipase A 抗体
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北京 101111
Quick Overview for Lipase A 抗体 (ABIN1108046)
抗原
See all Lipase A (LIPA) 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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特异性
- This antibody reacts to LAL.
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交叉反应 （详细）
- Species reactivity (tested):Human.
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纯化方法
- Purified
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亚型
- IgG2a
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anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (AA 1-399) antibody
LIPA 适用: 人 WB, ELISA, IP 宿主: 小鼠 Monoclonal 1F9 unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (AA 22-399) antibodyLIPA 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (Center) antibodyLIPA 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (AA 1-399) antibodyLIPA 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (AA 32-201) antibodyLIPA 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (AA 32-358) antibodyLIPA 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (AA 1-399) antibodyLIPA 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (AA 42-91) antibodyLIPA 适用: 人, 大鼠, 马, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) antibodyLIPA 适用: 人 ELISA 宿主: 小鼠 Monoclonal 9G7F12 unconjugated
anti-Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA) (N-Term) antibodyLIPA 适用: 人, 大鼠, 马, Pig, Cow, 兔, 绵羊 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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缓冲液
- PBS, 0,03 % sodium azide
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储存液
- Sodium azide
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注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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- Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))
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别名
- LIPA
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背景
- Lysosomal acid lipase (LAL), with 378-amino acid protein( 43-54 kDa), functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides which are taken up by receptor-mediated endocytosis. An inherited deficiency or low activity of human lysosomal acid lipase results in the intralysosomal storage of the respective lipid substrates. So it is also responsible for the rare conditions of Wolman disease and cholesteryl ester storage disease (CESD). As the enzyme is synthesized by all nucleated cells, lipid-laden cells are found in all organs, particularly in liver, spleen, the adrenal and the hemopoietic system, and in the intestine as well as in the lymph nodes, lungs, testes, and ovaries.Synonyms: Acid cholesteryl ester hydrolase, Cholesteryl esterase, EC=3.1.1.13, LAL, LIPA, Lipase A, Lysosomal acid lipase/cholesteryl ester hydrolase, Sterol esterase
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基因ID
- 3988
抗原
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