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Last updated: 2016/12/4
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PEX7 polyclonal antibody (A01)

  • Catalog # : H00005191-A01
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a partial recombinant PEX7.
  • Immunogen:
  • PEX7 (NP_000279, 2 a.a. ~ 99 a.a) partial recombinant protein with GST tag.
  • Sequence:
  • SAVCGGAARMLRTPGRHGYAAEFSPYLPGRLACATAQHYGIAGCGTLLILDPDEAGLRLFRSFDWNDGLFDVTWSENNEHVLITCSGDGSLQLWDTAK
  • Host:
  • Mouse
  • Reactivity:
  • Human, Mouse
  • Quality Control Testing:
  • Antibody Reactive Against Recombinant Protein.

    QC Testing of H00005191-A01
    Western Blot detection against Immunogen (36.89 KDa) .
  • Storage Buffer:
  • 50 % glycerol
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • PEX7 polyclonal antibody (A01), Lot # 051122JC01. Western Blot analysis of PEX7 expression in Raw 264.7.
  • PDF DownloadProtocol Download
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Western Blot (Recombinant protein)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 5191
  • Gene Name:
  • PEX7
  • Gene Alias:
  • PTS2R,RCDP1,RD
  • Gene Description:
  • peroxisomal biogenesis factor 7
  • Gene Summary:
  • This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one 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 have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000017277,peroxin-7,peroxisomal PTS2 receptor,peroxisome targeting signal 2 receptor
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