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

C10ORF2 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN5672122
  • Target See all C10orf2 (C10ORF2) products
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Protein Region
    C-Term
    Origin
    Human
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Sequence
    KARLKKIKDD TGPVAKKPSS GKKGATTQNS EICSGQAPTP DQPDTSKRSK
    Characteristics
    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.
  • Application Notes
    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.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Synonyms
    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
    Background
    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: PEO, PEO1, SCA8, ATXN8, IOSCA, PEOA3, SANDO, TWINL, MTDPS7, PRLTS5, C10orf2

    Protein Size: 684
    Gene ID
    56652
    NCBI Accession
    NM_001163812, NP_001157284
    UniProt
    Q96RR1
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