BTD 抗体 (AA 401-500) (AbBy Fluor® 594)
Quick Overview for BTD 抗体 (AA 401-500) (AbBy Fluor® 594) (ABIN2810462)
抗原
See all BTD 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 401-500
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交叉反应
- 大鼠
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预测反应
- Human,Mouse,Dog,Cow,Sheep,Horse,Chicken,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human Biotinidase
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亚型
- IgG
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anti-Biotinidase (BTD) (AA 284-543) antibody
BTD 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Biotinidase (BTD) antibodyBTD 适用: 人, 大鼠, 小鼠 IHC 宿主: 兔 Polyclonal unconjugated
anti-Biotinidase (BTD) (AA 1-543) antibodyBTD 适用: 人 WB, ELISA, IP 宿主: 小鼠 Monoclonal 3B10-2B3 unconjugated
anti-Biotinidase (BTD) antibodyBTD 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Biotinidase (BTD) (AA 42-271) antibodyBTD 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Biotinidase (BTD) (AA 322-397) antibodyBTD 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Biotinidase (BTD) (AA 1-543) antibodyBTD 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- BTD (Biotinidase (BTD))
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别名
- BTD/Biotinidase
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背景
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Synonyms: Biotinase, Biotinidase, Btd, BTD_HUMAN, EC 3.5.1.12.
Background: Biotin, also known as vitamin B7, is an essential water-soluble vitamin that is a cofactor in glucogenesis and in the metabolism of fatty acids and leucine. Biotinidase is a 523 amino acid enzyme that catalyzes the hydrolysis of biocytin to biotin and lysine. Secreted into extracellular space, biotinidase is expressed in liver, heart, placenta, brain, skeletal muscle, pancreas and kidney. Biotinidase contains one carbon-nitrogen hydrolase domain, which is involved in the reduction of organic nitrogen compounds and ammonia production. Defects in the gene encoding biotinidase are the cause of biotinidase deficiency, which is characterized by skin rash, ataxia, seizures, hearing loss, hypotonia and optic atrophy. These symptoms are due to the individual?s inability to reutilize biotin and can, therefore, typically be treated with the addition of free biotin.
抗原
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