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Valyl-tRNA Synthetase 2, Mitochondrial (VARS2) protein (Myc-DYKDDDDK Tag)

VARS2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2735162
  • Antigène Voir toutes Valyl-tRNA Synthetase 2, Mitochondrial (VARS2) Protéines
    Valyl-tRNA Synthetase 2, Mitochondrial (VARS2)
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Myc-DYKDDDDK Tag
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Valyl-tRNA synthetase 2, mitochondrial (putative) (VARS2), nuclear gene encoding mitochondrial protein 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 VARS2 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
    Valyl-tRNA Synthetase 2, Mitochondrial (VARS2)
    Autre désignation
    Valyl-Trna Synthetase 2, Mitochondrial (Putative) (Vars2) (VARS2 Produits)
    Synonymes
    VARS2 Protein, G7a Protein, VARS2L Protein, VARSL Protein, Vars2l Protein, Varsl Protein, 1190004I24Rik Protein, mKIAA1885 Protein, valyl-tRNA synthetase 2, mitochondrial Protein, VARS2 Protein, Vars2 Protein
    Sujet
    This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants.
    Poids moléculaire
    118.3 kDa
    NCBI Accession
    NP_065175
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