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Last updated: 2016/10/16
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ALDH6A1 MaxPab mouse polyclonal antibody (B01)MaxPab

  • Catalog # : H00004329-B01
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length human ALDH6A1 protein.
  • Immunogen:
  • ALDH6A1 (NP_005580.1, 1 a.a. ~ 535 a.a) full-length human protein.
  • Sequence:
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Storage Buffer:
  • No additive
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • For IHC and IF applications, antibody purification with Protein A will be needed prior to use.
  • Publication Reference
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • ALDH6A1 MaxPab polyclonal antibody. Western Blot analysis of ALDH6A1 expression in human liver.
  • PDF DownloadProtocol Download
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of ALDH6A1 expression in transfected 293T cell line (H00004329-T01) by ALDH6A1 MaxPab polyclonal antibody.

    Lane 1: ALDH6A1 transfected lysate(58.85 KDa).
    Lane 2: Non-transfected lysate.
  • PDF DownloadProtocol Download
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 4329
  • Gene Name:
  • ALDH6A1
  • Gene Alias:
  • Gene Description:
  • aldehyde dehydrogenase 6 family, member A1
  • Gene Summary:
  • This protein belongs to the aldehyde dehydrogenases family of proteins. This enzyme plays a role in the valine and pyrimidine catabolic pathways. The product of this gene, a mitochondrial methylmalonate semialdehyde dehydrogenase, catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids. [provided by RefSeq
  • Other Designations:
  • aldehyde dehydrogenase 6A1,mitochondrial acylating methylmalonate-semialdehyde dehydrogenase
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