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C10orf2 anticorps

Cet anticorps anti-C10orf2 est un anticorps Lapin Polyclonal détectant C10orf2 dans WB. Adapté pour Souris.
N° du produit ABIN7256978

Aperçu rapide pour C10orf2 anticorps (ABIN7256978)

Antigène

Voir toutes C10orf2 (C10ORF2) Anticorps
C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))

Reactivité

  • 40
  • 13
  • 12
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Souris

Hôte

  • 38
  • 2
Lapin

Clonalité

  • 38
  • 2
Polyclonal

Conjugué

  • 18
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp C10orf2 est non-conjugé

Application

  • 23
  • 15
  • 14
  • 3
  • 2
  • 2
  • 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
  • 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

    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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