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NAD-ME anticorps

NAD-ME Reactivité: Humain, Souris WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7003513
  • Antigène Voir toutes NAD-ME Anticorps
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Reactivité
    • 37
    • 13
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 35
    • 2
    Lapin
    Clonalité
    • 35
    • 2
    Polyclonal
    Conjugué
    • 17
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp NAD-ME est non-conjugé
    Application
    • 25
    • 20
    • 17
    • 8
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of human ME2
    Isotype
    IgG
    Top Product
    Discover our top product NAD-ME Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.78 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Autre désignation
    ME2 (NAD-ME Produits)
    Synonymes
    anticorps ODS1, anticorps AW120568, anticorps D030040L20Rik, anticorps NAD-ME, anticorps zgc:100941, anticorps malic enzyme 2, anticorps malic enzyme 2, NAD(+)-dependent, mitochondrial, anticorps malic enzyme 2, NAD(+)-dependent, mitochondrial S homeolog, anticorps ME2, anticorps Me2, anticorps me2.S, anticorps me2
    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

    Observed_MW: Refer to figures

    Calculated_MW: 65 kDa

    UniProt
    P23368
    Pathways
    Production of Molecular Mediator of Immune Response
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