Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Peroxisomal Biogenesis Factor 10 (PEX10) Peptide

PEX10 Reactivity: Human Host: Synthetic BP, WB, IHC
Catalog No. ABIN981595
  • Target See all PEX10 products
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    Origin
    Human
    Source
    • 4
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-PEX10 antibody (Catalog #: ARP43442_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    Synonyms
    ATPEX10 Peptide, T9J22.2 Peptide, peroxin 10 Peptide, NALD Peptide, PBD6A Peptide, PBD6B Peptide, RNF69 Peptide, AV128229 Peptide, Gm142 Peptide, peroxin 10 Peptide, peroxisomal biogenesis factor 10 Peptide, PEX10 Peptide, Pex10 Peptide
    Background
    PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.

    Alias Symbols: MGC1998, NALD, RNF69

    Protein Interaction Partner: PEX12,PEX19,PEX2,PEX5,PEX10,PEX12,PEX12,PEX19,PEX19,PEX2,PEX5

    Protein Size: 346
    Molecular Weight
    39 kDa
    Gene ID
    5192
    NCBI Accession
    NM_153818, NP_722540
You are here:
Support