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FARS2 Protein (Myc-DYKDDDDK Tag)

FARS2 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2720874
  • Target Alle FARS2 Proteine anzeigen
    FARS2 (Phenylalanine-tRNA Synthetase 2 (Mitochondrial) (FARS2))
    Protein-Typ
    Recombinant
    Spezies
    • 4
    • 1
    • 1
    Human
    Quelle
    • 4
    • 2
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses FARS2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human FARS2 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product FARS2 Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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.
  • Target
    FARS2 (Phenylalanine-tRNA Synthetase 2 (Mitochondrial) (FARS2))
    Andere Bezeichnung
    Fars2 (FARS2 Produkte)
    Synonyme
    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
    Hintergrund
    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.
    Molekulargewicht
    48.4 kDa
    NCBI Accession
    NP_006558
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