Product Browser

Last updated: 2016/10/16

Product Compare

Product Compare Cancel Click this icon to add products to compare list. Select up to 10 products.

Quick Order (Tutorial)

Input Catalog #,
place order here!
Catalog # :
  • Where to buy
  • Choose your location

PEX19 (Human) Matched Antibody Pair

  • Catalog # : H00005824-AP11
  • Visit Frequency :
  • Countries :
  • Specification
  • Product Description:
  • This antibody pair set comes with matched antibody pair to detect and quantify protein level of human PEX19.
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Standard curve using recombinant protein ( H00005824-P01 ) as an analyte.

    QC Testing of H00005824-AP11
    Sandwich ELISA detection sensitivity ranging from 0.3 ng/ml to 100 ng/ml.
  • Supplied Product:
  • Antibody pair set content:
    1. Capture antibody: rabbit MaxPab® affinity purified polyclonal anti-PEX19 (100 ug)
    2. Detection antibody: mouse monoclonal anti-PEX19, IgG2a Kappa (20 ug)
    *Reagents are sufficient for at least 1-2 x 96 well plates using recommended protocols.
  • Storage Instruction:
  • Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
  • Applications
  • Application Image
  • ELISA Pair (Recombinant protein)
  • Gene Information
  • Entrez GeneID:
  • 5824
  • Gene Name:
  • PEX19
  • Gene Alias:
  • 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
  • RSS
  • YouTube
  • Linkedin
  • Facebook