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NAD-ME Protein (Myc-DYKDDDDK Tag)

NAD-ME Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2726776
  • Target Alle NAD-ME Proteine anzeigen
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Protein-Typ
    Recombinant
    Spezies
    • 3
    • 1
    Human
    Quelle
    • 2
    • 2
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses NAD-ME Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human NAD-ME 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 NAD-ME 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
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Andere Bezeichnung
    Nad-Me (NAD-ME Produkte)
    Synonyme
    ODS1 Protein, AW120568 Protein, D030040L20Rik Protein, NAD-ME Protein, zgc:100941 Protein, malic enzyme 2 Protein, malic enzyme 2, NAD(+)-dependent, mitochondrial Protein, malic enzyme 2, NAD(+)-dependent, mitochondrial S homeolog Protein, ME2 Protein, Me2 Protein, me2.S Protein, me2 Protein
    Hintergrund
    This gene encodes a mitochondrial NAD-dependent malic enzyme, a homotetrameric protein, that catalyzes the oxidative decarboxylation of malate to pyruvate. It had previously been weakly linked to a syndrome known as Friedreich ataxia that has since been shown to be the result of mutation in a completely different gene. Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy. Alternatively spliced transcript variants encoding different isoforms found for this gene.
    Molekulargewicht
    63.4 kDa
    NCBI Accession
    NP_002387
    Pathways
    Production of Molecular Mediator of Immune Response
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