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NAD-ME Antikörper

NAD-ME Reaktivität: Human, Maus WB, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7003513
  • Target Alle NAD-ME Antikörper anzeigen
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Reaktivität
    • 37
    • 13
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 35
    • 2
    Kaninchen
    Klonalität
    • 35
    • 2
    Polyklonal
    Konjugat
    • 17
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser NAD-ME Antikörper ist unkonjugiert
    Applikation
    • 25
    • 20
    • 17
    • 8
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human ME2
    Isotyp
    IgG
    Top Product
    Discover our top product NAD-ME Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.78 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Andere Bezeichnung
    ME2 (NAD-ME Produkte)
    Synonyme
    ODS1 antikoerper, AW120568 antikoerper, D030040L20Rik antikoerper, NAD-ME antikoerper, zgc:100941 antikoerper, malic enzyme 2 antikoerper, malic enzyme 2, NAD(+)-dependent, mitochondrial antikoerper, malic enzyme 2, NAD(+)-dependent, mitochondrial S homeolog antikoerper, ME2 antikoerper, Me2 antikoerper, me2.S antikoerper, me2 antikoerper
    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

    Observed_MW: Refer to figures

    Calculated_MW: 65 kDa

    UniProt
    P23368
    Pathways
    Production of Molecular Mediator of Immune Response
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