ACADL 抗体 (AA 201-300) (Biotin)
Quick Overview for ACADL 抗体 (AA 201-300) (Biotin) (ABIN708403)
抗原
See all ACADL 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 201-300
- 
                                            预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit
- 
                                            纯化方法
- Purified by Protein A.
- 
                                            免疫原
- KLH conjugated synthetic peptide derived from human ACADL
- 
                                            亚型
- IgG
 
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    - 
                                            应用备注
- 
                        IHC-P 1:200-400
 IHC-F 1:100-500
- 
                                            限制
- 仅限研究用
 
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    - 
                                            状态
- Liquid
- 
                                            浓度
- 1 μg/μL
- 
                                            缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 
                                            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.
- 
                                            储存条件
- -20 °C
- 
                                            储存方法
- Store at -20°C for 12 months.
- 
                                            有效期
- 12 months
 
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    - ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
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                                            别名
- ACADL
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                                            背景
- 
                        Synonyms: mitochondrial, ACAD4, ACADL, ACADL_HUMAN, Acyl Coenzyme A dehydrogenase long chain, FLJ94052, LCAD, Long chain acyl CoA dehydrogenase, Long-chain specic acyl-CoA dehydrogenase. Background: The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq]. 
- 
                                            基因ID
- 33
- 
                                            途径
- Monocarboxylic Acid Catabolic Process
 抗原
- 
                    
 
                                     
                                     
                                    