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NAD-ME Protein (Myc-DYKDDDDK Tag)

NAD-ME Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2726776
  • Antigène Voir toutes NAD-ME Protéines
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    Humain
    Source
    • 2
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette NAD-ME protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human NAD-ME 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 NAD-ME 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
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Autre désignation
    Nad-Me (NAD-ME Produits)
    Synonymes
    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
    Sujet
    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.
    Poids moléculaire
    63.4 kDa
    NCBI Accession
    NP_002387
    Pathways
    Production of Molecular Mediator of Immune Response
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