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Last updated: 2017/3/26

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PEX26 polyclonal antibody

  • Catalog # : PAB18622
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of PEX26.
  • Immunogen:
  • A synthetic peptide corresponding to amino acids at internal region of human PEX26.
  • Sequence:
  • C-QKPNLEGSVSHK
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 33
  • Reactivity:
  • Human
  • Specificity:
  • Reported variants represent identical protein: NP_060399.1, NP_001121121.1.
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Recommend Usage:
  • ELISA (1:64000)
    Western Blot (0.5-1.5 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In 0.5 mg/mL Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • PEX26 polyclonal antibody (Cat # PAB18622) (0.5 ug/mL) staining of human kidney lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • ELISA
  • 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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