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Peroxisomal Biogenesis Factor 10 (PEX10) Peptid

PEX10 Reaktivität: Human Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN981595
  • Target Alle PEX10 Produkte
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    Spezies
    Human
    Quelle
    • 4
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Produktmerkmale
    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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
    Synonyme
    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
    Hintergrund
    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
    Molekulargewicht
    39 kDa
    Gen-ID
    5192
    NCBI Accession
    NM_153818, NP_722540
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