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PEX26 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00055670-T01
  • Visit Frequency :
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-PEX26 full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 33.9
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-PEX26 antibody (H00055670-B01) by Western Blots.
    Western Blot
    QC Testing of H00055670-T01
    Lane 1: PEX26 transfected lysate ( 33.9 KDa)
    Lane 2: Non-transfected lysate.
    SDS-PAGE Gel
    QC Testing of H00055670-T01
    PEX26 transfected lysate.
  • Storage Buffer:
  • 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Application Image
  • Western Blot
  • 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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