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Peroxisomal Biogenesis Factor 10 (PEX10) Peptide

PEX10 Reactivité: Humain Hôte: Synthetic BP, WB, IHC
N° du produit ABIN981595

Aperçu rapide pour Peroxisomal Biogenesis Factor 10 (PEX10) Peptide (ABIN981595)

Antigène

PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Origine

Humain

Source

  • 4
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Attributs du produit

    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
  • Indications d'application

    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.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène

    PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

    Sujet

    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

    Poids moléculaire

    39 kDa

    ID gène

    5192

    NCBI Accession

    NM_153818, NP_722540
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