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PEX19 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00005824-T02
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-PEX19 full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 33
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-PEX19 antibody (H00005824-B02) by Western Blots.
    SDS-PAGE Gel
    QC Testing of H00005824-T02
    PEX19 transfected lysate.
    Western Blot
    QC Testing of H00005824-T02
    Lane 1: PEX19 transfected lysate ( 33 KDa)
    Lane 2: Non-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
  • Entrez GeneID:
  • 5824
  • Gene Name:
  • PEX19
  • Gene Alias:
  • D1S2223E,HK33,PMP1,PMPI,PXF,PXMP1
  • Gene Description:
  • peroxisomal biogenesis factor 19
  • Gene Summary:
  • This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000031848,housekeeping gene, 33kD,peroxisomal farnesylated protein
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