ACADL 抗体 (AA 201-300) (Biotin)
-
- 抗原 See all ACADL 抗体
- ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
-
抗原表位
- AA 201-300
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This ACADL antibody is conjugated to Biotin
-
应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 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
- Top Product
- Discover our top product ACADL Primary Antibody
-
-
- 应用备注
-
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
-
- 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
- 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
-
- 抗原
- ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
- 别名
- ACADL (ACADL 产品)
- 别名
- zgc:55656 antibody, ACAD4 antibody, LCAD antibody, ACOADA antibody, AA960361 antibody, AU018452 antibody, C79855 antibody, acyl-CoA dehydrogenase long chain antibody, acyl-CoA dehydrogenase, long chain antibody, acyl-CoA dehydrogenase, long chain L homeolog antibody, acyl-Coenzyme A dehydrogenase, long-chain antibody, acadl antibody, ACADL antibody, Acadl antibody, acadl.L antibody
- 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
-