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Abnova/ACADM (Human) IP-WB Antibody Pair/1kit/H00000034-PW2
  • Abnova/ACADM (Human) IP-WB Antibody Pair/1kit/H00000034-PW2

Abnova/ACADM (Human) IP-WB Antibody Pair/1kit/H00000034-PW2

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货号: H00000034-PW2
品牌: Abnova
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  • 详情
  • 使用说明
  • 常见问题
      • Specification
      • Product Description:
      • This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.
      • Reactivity:
      • Human
      • Quality Control Testing:
      • Immunoprecipitation-Western Blot (IP-WB)QC Testing of H00000034-PW2Immunoprecipitation of ACADM transfected lysate using rabbit polyclonal anti-ACADM and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-ACADM.
      • Supplied Product:
      • Antibody pair set content:1. Antibody pair for IP: rabbit polyclonal anti-ACADM (300 ul)2. Antibody pair for WB: mouse purified polyclonal anti-ACADM (50 ug)
      • Storage Instruction:
      • Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
      • Interspecies Antigen Sequence:
      • Mouse (87); Rat (86)
      • Datasheet:
      • PDF DownloadDownload
      • Applications
      • Immunoprecipitation-Western Blot
      • PDF DownloadProtocol Download
      • Application Image
      • Immunoprecipitation-Western Blot
      • Gene Information
      • Entrez GeneID:
      • 34
      • Gene Name:
      • ACADM
      • Gene Alias:
      • ACAD1,FLJ18227,FLJ93013,FLJ99884,MCAD,MCADH
      • Gene Description:
      • acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain
      • Omim ID:
      • 201450, 607008
      • Gene Ontology:
      • Hyperlink
      • Gene Summary:
      • This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
      • Other Designations:
      • OTTHUMP00000011345,medium-chain specific acyl-CoA dehydrogenase
      • Gene Pathway
      • beta-Alanine metabolism
      • Fatty acid metabolism
      • Metabolic pathways
      • PPAR signaling pathway
      • Propanoate metabolism
      • Valine, leucine and isoleucine degradation
      • Related Disease
      • Cardiovascular Diseases
      • Death, Sudden
      • Deficiency Diseases
      • Diabetes Mellitus, Type 2
      • Edema
      • Epilepsy
      • Genetic Predisposition to Disease
      • Hypoglycemia
      • Lipid Metabolism, Inborn Errors
      • Metabolism, Inborn Errors
      • Seizures
      • Sleep Stages
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