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PEX26 purified MaxPab mouse polyclonal antibody (B01P)MaxPab

  • Catalog # : H00055670-B01P
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length human PEX26 protein.
  • Immunogen:
  • PEX26 (NP_060399.1, 1 a.a. ~ 305 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)
  • PEX26 MaxPab polyclonal antibody. Western Blot analysis of PEX26 expression in human spleen.
  • PDF DownloadProtocol Download
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of PEX26 expression in transfected 293T cell line (H00055670-T02) by PEX26 MaxPab polyclonal antibody.

    Lane 1: PEX26 transfected lysate(33.55 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
  • Gene Name:
  • PEX26
  • Gene Alias:
  • FLJ20695,PEX26M1T,Pex26pM1T
  • Gene Description:
  • peroxisomal biogenesis factor 26
  • Gene Summary:
  • This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000195598,peroxin-26,peroxisome assembly protein 26,peroxisome biogenesis disorder, complementation group 8,peroxisome biogenesis disorder, complementation group A,peroxisome biogenesis factor 26
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