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AARS2 antibody

AARS2 Reactivity: Human, Mouse, Rat WB, IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7234729
  • Target See all AARS2 Antibodies
    AARS2 (Alanyl-tRNA Synthetase 2, Mitochondrial (AARS2))
    Reactivity
    Human, Mouse, Rat
    Host
    • 28
    • 1
    Rabbit
    Clonality
    • 29
    Polyclonal
    Conjugate
    • 9
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AARS2 antibody is un-conjugated
    Application
    • 13
    • 13
    • 7
    • 7
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human AARS2
    Isotype
    IgG
    Top Product
    Discover our top product AARS2 Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    AARS2 (Alanyl-tRNA Synthetase 2, Mitochondrial (AARS2))
    Alternative Name
    AARS2 (AARS2 Products)
    Synonyms
    AARSL antibody, COXPD8 antibody, MT-ALARS antibody, MTALARS antibody, Aarsl antibody, AlaRS antibody, Gm89 antibody, alanyl-tRNA synthetase 2, mitochondrial antibody, AARS2 antibody, Aars2 antibody
    Background
    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
    Molecular Weight
    107 kDa
    UniProt
    Q5JTZ9
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