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Last updated: 2016/10/23
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CYP27A1 purified MaxPab mouse polyclonal antibody (B01P)MaxPab

  • Catalog # : H00001593-B01P
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length human CYP27A1 protein.
  • Immunogen:
  • CYP27A1 (NP_000775.1, 1 a.a. ~ 531 a.a) full-length human protein.
  • Sequence:
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • CYP27A1 MaxPab polyclonal antibody. Western Blot analysis of CYP27A1 expression in human liver.
  • PDF DownloadProtocol Download
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of CYP27A1 expression in transfected 293T cell line (H00001593-T01) by CYP27A1 MaxPab polyclonal antibody.

    Lane 1: CYP27A1 transfected lysate(58.41 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:
  • 1593
  • Gene Name:
  • CYP27A1
  • Gene Alias:
  • CP27,CTX,CYP27
  • Gene Description:
  • cytochrome P450, family 27, subfamily A, polypeptide 1
  • Gene Summary:
  • This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein oxidizes cholesterol intermediates as part of the bile synthesis pathway. Since the conversion of cholesterol to bile acids is the major route for removing cholesterol from the body, this protein is important for overall cholesterol homeostasis. Mutations in this gene cause cerebrotendinous xanthomatosis, a rare autosomal recessive lipid storage disease. [provided by RefSeq
  • Other Designations:
  • 5-beta-cholestane-3-alpha, 7-alpha, 12-alpha-triol 26-hydroxylase,5-beta-cholestane-3-alpha, 7-alpha, 12-alpha-triol 27-hydroxylase,cholestanetriol 26-monooxygenase,cytochrome P-450C27/25,cytochrome P450, subfamily XXVIIA (steroid 27-hydroxylase, cerebrot
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