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FARS2 Protein (Myc-DYKDDDDK Tag)

FARS2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2720874
  • Antigène Voir toutes FARS2 Protéines
    FARS2 (Phenylalanine-tRNA Synthetase 2 (Mitochondrial) (FARS2))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 1
    • 1
    Humain
    Source
    • 4
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette FARS2 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human FARS2 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 FARS2 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
    FARS2 (Phenylalanine-tRNA Synthetase 2 (Mitochondrial) (FARS2))
    Autre désignation
    Fars2 (FARS2 Produits)
    Synonymes
    2810431B21Rik Protein, 6720478K01Rik Protein, Fars1 Protein, COXPD14 Protein, FARS1 Protein, HSPC320 Protein, PheRS Protein, dJ520B18.2 Protein, phenylalanine-tRNA synthetase 2 (mitochondrial) Protein, phenylalanyl-tRNA synthetase 2, mitochondrial Protein, Fars2 Protein, FARS2 Protein
    Sujet
    This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    48.4 kDa
    NCBI Accession
    NP_006558
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