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Chromosome 10 Open Reading Frame 2 (C10ORF2) (C-Term) Peptide

C10ORF2 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5511854
  • Antigène Tous les produits C10orf2 (C10ORF2)
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Protein Region
    C-Term
    Origine
    Humain
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    FRKFATDNNC HVTLVIHPRK EDDDKELQTA SIFGSAKASQ EADNVLILQD
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-PEO1 Antibody. 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.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Synonymes
    ATXN8 Peptide, IOSCA Peptide, MTDPS7 Peptide, PEO Peptide, PEO1 Peptide, PEOA3 Peptide, SANDO Peptide, SCA8 Peptide, TWINL Peptide, C6H10orf2 Peptide, D19Ertd626e Peptide, Twinl Peptide, twinkle mtDNA helicase L homeolog Peptide, twinkle mtDNA helicase Peptide, twnk.L Peptide, TWNK Peptide, Twnk Peptide
    Sujet
    This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    Alias Symbols: PEO1,C10orf2,

    Protein Size: 684
    ID gène
    56652
    NCBI Accession
    NP_068602
    UniProt
    Q96RR1
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