ACADL 抗体 (Middle Region)
(1 reference)-
- 抗原 See all ACADL 抗体
- ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
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抗原表位
- Middle Region
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适用
- 人, 小鼠, 大鼠, Pig, 兔, 马, Cow, 斑马鱼, 豚鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This ACADL antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- LPQERLLIAD VAISASEFMF EETRNYVKQR KAFGKTVAHL QTVQHKLAEL
- 预测反应
- Cow: 92%, Guinea Pig: 92%, Horse: 100%, Human: 100%, Mouse: 100%, Pig: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 77%
- 产品特性
- This is a rabbit polyclonal antibody against ACADL. It was validated on Western Blot using a cell lysate as a positive control.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the middle region of human ACADL
- Top Product
- Discover our top product ACADL Primary Antibody
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anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) antibody
ACADL 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (AA 31-210) antibodyACADL 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (AA 30-260) antibodyACADL 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (AA 1-430) antibodyACADL 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (N-Term) antibodyACADL 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (AA 214-430) antibodyACADL 适用: 人 WB, IHC, ICC 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (AA 292-319) antibodyACADL 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB22017 unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (AA 288-337) antibodyACADL 适用: 人, 小鼠, Pig, 兔, 马, 斑马鱼, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Acyl-CoA Dehydrogenase, Long Chain (ACADL) (N-Term) antibodyACADL 适用: 人, 兔, 马, 犬 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
- 说明
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Antigen size: 430 AA
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- Lot specific
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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: "Glp-1 analog, liraglutide, ameliorates hepatic steatosis and cardiac hypertrophy in C57BL/6J mice fed a Western diet." in: American journal of physiology. Gastrointestinal and liver physiology, Vol. 302, Issue 2, pp. G225-35, (2012) (PubMed).
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: "Glp-1 analog, liraglutide, ameliorates hepatic steatosis and cardiac hypertrophy in C57BL/6J mice fed a Western diet." in: American journal of physiology. Gastrointestinal and liver physiology, Vol. 302, Issue 2, pp. G225-35, (2012) (PubMed).
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- 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
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ACADL 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.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.
Alias Symbols: ACAD4, LCAD
Protein Interaction Partner: Htt, UBC,
Protein Size: 430 - 分子量
- 44 kDa
- 基因ID
- 33
- NCBI登录号
- NM_001608, NP_001599
- UniProt
- P28330
- 途径
- Monocarboxylic Acid Catabolic Process
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