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AARS2 Protein (Myc-DYKDDDDK Tag)

AARS2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2714254
  • Antigène Voir toutes AARS2 Protéines
    AARS2 (Alanyl-tRNA Synthetase 2, Mitochondrial (AARS2))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    Humain
    Source
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette AARS2 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human AARS2 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product AARS2 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    AARS2 (Alanyl-tRNA Synthetase 2, Mitochondrial (AARS2))
    Autre désignation
    Aars2 (AARS2 Produits)
    Synonymes
    AARSL Protein, COXPD8 Protein, MT-ALARS Protein, MTALARS Protein, Aarsl Protein, AlaRS Protein, Gm89 Protein, alanyl-tRNA synthetase 2, mitochondrial Protein, AARS2 Protein, Aars2 Protein
    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.
    Poids moléculaire
    107.1 kDa
    NCBI Accession
    NP_065796
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