ACADS 抗体
Quick Overview for ACADS 抗体 (ABIN7384407)
抗原
See all ACADS (Acads) 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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纯化方法
- Affinity Purified
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亚型
- IgG
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应用备注
- WB 1:500-1:1000
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限制
- 仅限研究用
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浓度
- 300 μg/mL
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缓冲液
- 50 mM Tris-Glycine( pH 7.4), 0.15M NaCl, 40 % Glycerol, 0.01 % Sodium azide and 0.05 % BSA
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- ACADS (Acads) (Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (Acads))
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别名
- ACADS
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背景
- ACAD3,ACADS,ACADS,Acyl Coenzyme A dehydrogenase,C2 to C3 short chain,Acyl-CoA dehydrogenase,C2 to C3 short chain,Acyl-CoA dehydrogenase,short chain,Acyl-Coenzyme A dehydrogenase,short chain,AI196007,Bcd-1,Bcd1,Butyryl CoA dehydrogenase,Butyryl-CoA dehydrogenase,EC 1.3.99.2,mitochondrial,SCAD,Short chain acyl CoA dehydrogenase,Short-chain specific acyl-CoA dehydrogenase,Short-chain specific acyl-CoA dehydrogenase,mitochondrial,Unsaturated acyl CoA reductase,This gene encodes a a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with Short Chain Acyl-CoA Dehydrogenase Deficiency. It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.
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分子量
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Observed_MW: 44kDa
Calculated_MW: 44kDa
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基因ID
- 35
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UniProt
- P16219
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途径
- Monocarboxylic Acid Catabolic Process
抗原
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