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NAD-ME antibody

NAD-ME Reactivity: Human, Mouse WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7003513
  • Target See all NAD-ME Antibodies
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Reactivity
    • 37
    • 13
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 35
    • 2
    Rabbit
    Clonality
    • 35
    • 2
    Polyclonal
    Conjugate
    • 17
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NAD-ME antibody is un-conjugated
    Application
    • 25
    • 20
    • 17
    • 8
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human ME2
    Isotype
    IgG
    Top Product
    Discover our top product NAD-ME Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))
    Alternative Name
    ME2 (NAD-ME Products)
    Synonyms
    ODS1 antibody, AW120568 antibody, D030040L20Rik antibody, NAD-ME antibody, zgc:100941 antibody, malic enzyme 2 antibody, malic enzyme 2, NAD(+)-dependent, mitochondrial antibody, malic enzyme 2, NAD(+)-dependent, mitochondrial S homeolog antibody, ME2 antibody, Me2 antibody, me2.S antibody, me2 antibody
    Background
    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.
    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 65 kDa

    UniProt
    P23368
    Pathways
    Production of Molecular Mediator of Immune Response
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