ACOX1 抗体
Quick Overview for ACOX1 抗体 (ABIN7111266)
抗原
See all ACOX1 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Immunogen affinity purified
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纯度
- ≥95 % as determined by SDS-PAGE
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免疫原
- acyl-Coenzyme A oxidase 1, palmitoyl
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亚型
- IgG
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anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) (AA 1-270) antibody
ACOX1 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) antibodyACOX1 适用: 人 WB, IHC, ELISA, IF 宿主: 小鼠 Monoclonal 153CT43-1-1 unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) (AA 210-409) antibodyACOX1 适用: 人 WB, IHC, ICC, IP 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) (AA 113-273) antibodyACOX1 适用: 人 IHC, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) antibodyACOX1 适用: 人 WB, IF, IHC (p) 宿主: 小鼠 Monoclonal 3C1 unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) antibodyACOX1 适用: 人, 小鼠, 大鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) (AA 1-660) antibodyACOX1 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) antibodyACOX1 适用: 人, 小鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) (AA 1-660) antibodyACOX1 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Oxidase 1, Palmitoyl (ACOX1) (AA 1-660) antibodyACOX1 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- WB: 1:500 - 1:2000, IHC: 1:100 - 1:200, IF: 1:50 - 1:200
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
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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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储存条件
- -20 °C
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储存方法
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
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有效期
- 12 months
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- ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
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别名
- ACOX1
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背景
- Synonyms:ACOX, ACOX1, AOX, PALMCOX, Palmitoyl CoA oxidase, SCOX Background:The protein encoded by this gene is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids. Alternatively spliced transcript variants encoding different isoforms have been identified.
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分子量
- 74 kDa
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基因ID
- 51
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UniProt
- Q15067
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途径
- Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
抗原
-
