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AARS2 anticorps

AARS2 Reactivité: Humain, Souris, Rat WB, IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7234729
  • Antigène Voir toutes AARS2 Anticorps
    AARS2 (Alanyl-tRNA Synthetase 2, Mitochondrial (AARS2))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 23
    • 1
    Lapin
    Clonalité
    • 24
    Polyclonal
    Conjugué
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp AARS2 est non-conjugé
    Application
    • 13
    • 13
    • 7
    • 7
    • 5
    • 5
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human AARS2
    Isotype
    IgG
    Top Product
    Discover our top product AARS2 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000, IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    AARS2 (Alanyl-tRNA Synthetase 2, Mitochondrial (AARS2))
    Autre désignation
    AARS2 (AARS2 Produits)
    Synonymes
    anticorps AARSL, anticorps COXPD8, anticorps MT-ALARS, anticorps MTALARS, anticorps Aarsl, anticorps AlaRS, anticorps Gm89, anticorps alanyl-tRNA synthetase 2, mitochondrial, anticorps AARS2, anticorps Aars2
    Sujet
    The protein encoded by this gene belongs to the class-II aminoacyl-tRNA synthetase family. Aminoacyl-tRNA synthetases play critical roles in mRNA translation by charging tRNAs with their cognate amino acids. The encoded protein is a mitochondrial enzyme that specifically aminoacylates alanyl-tRNA. Mutations in this gene are a cause of combined oxidative phosphorylation deficiency 8. Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction: alanine is first activated by ATP to form Ala-AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged tRNA(Ala) via its editing domain
    Poids moléculaire
    107 kDa
    UniProt
    Q5JTZ9
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