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C10orf2 anticorps

C10ORF2 Reactivité: Souris WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7256978
  • Antigène Voir toutes C10orf2 (C10ORF2) Anticorps
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Reactivité
    • 42
    • 13
    • 12
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Souris
    Hôte
    • 40
    • 2
    Lapin
    Clonalité
    • 40
    • 2
    Polyclonal
    Conjugué
    • 15
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp C10orf2 est non-conjugé
    Application
    • 25
    • 19
    • 17
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    A synthetic peptide of human C10orf2 (NP_068602.2).
    Isotype
    IgG
    Top Product
    Discover our top product C10ORF2 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Autre désignation
    C10orf2 (C10ORF2 Produits)
    Synonymes
    anticorps ATXN8, anticorps IOSCA, anticorps MTDPS7, anticorps PEO, anticorps PEO1, anticorps PEOA3, anticorps SANDO, anticorps SCA8, anticorps TWINL, anticorps C6H10orf2, anticorps D19Ertd626e, anticorps Twinl, anticorps twinkle mtDNA helicase L homeolog, anticorps twinkle mtDNA helicase, anticorps twnk.L, anticorps TWNK, anticorps Twnk
    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.
    Poids moléculaire

    Observed_MW: 77 kDa

    Calculated_MW: 60 kDa/66 kDa/77 kDa

    ID gène
    56652
    UniProt
    Q96RR1
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