ACADL rabbit pAb

    • 货号:YT6498
    • 应用:WB
    • 种属:Human;Mouse;Rat
      • 靶点:
      • ACADL
      • 简介:
      • >>Fatty acid degradation;>>Metabolic pathways;>>Fatty acid metabolism;>>PPAR signaling pathway
      • 基因名称:
      • ACADL
      • 蛋白名称:
      • ACADL
      • Human Gene Id:
      • 33
      • Human Swiss Prot No:
      • P28330
      • Mouse Swiss Prot No:
      • P51174
      • 免疫原:
      • Synthesized peptide derived from human ACADL AA range: 258-308
      • 特异性:
      • This antibody detects endogenous levels of ACADL at Human/Mouse/Rat
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500-2000
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 分子量:
      • 47kD
      • 背景:
      • 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, Jul 2008],
      • 功能:
      • catalytic activity:Acyl-CoA + acceptor = 2,3-dehydroacyl-CoA + reduced acceptor.,cofactor:FAD.,disease:Impaired ACADL activity results in non-ketotic hypoglycemia, hypotonia, muscle weakness and episodes of cardiorespiratory arrest associated with fasting [MIM:201460].,miscellaneous:A number of straight-chain acyl-CoA dehydrogenases of different substrate specificities are present in mammalian tissues.,pathway:Lipid metabolism; mitochondrial fatty acid beta-oxidation.,similarity:Belongs to the acyl-CoA dehydrogenase family.,subunit:Homotetramer.,
      • 细胞定位:
      • Mitochondrion matrix .

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      Identification and Verification of Hub Mitochondrial Dysfunction Genes in Osteoarthritis Based on Bioinformatics Analysis Journal of Immunology Research Hui Niu WB Human 1:1000 Chondrocytes
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      • 产品图片
      • Western blot analysis of lysates from A549 cells, primary antibody was diluted at 1:1000, 4°over night