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Rabbit anti-Human ME2 Polyclonal Antibody

The antibody against ME2 was raised in rabbit using the Recombinant Human NAD-dependent malic enzyme, mitochondrial protein (296-424AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, IHC.

ADC-15880A

The antibody against ME2 was raised in rabbit using the Recombinant Human NAD-dependent malic enzyme, mitochondrial protein (296-424AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, IHC.

$299.00

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Specifications


Cat.No ADC-15880A ClonalityPolyclonal
Host SpeciesRabbitTarget NameME2
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4
Purification Method>95%, Protein G purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human NAD-dependent malic enzyme, mitochondrial protein (296-424AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP23368
Background Information
  • Uniprot Id

    P23368

  • Target Species

    Human

  • Target Name

    ME2

  • Target Full Name

    NAD-dependent malic enzyme, mitochondrial

  • Target Subcellular Location

    Mitochondrion matrix.

  • Target Protein Families

    Malic enzymes family

  • Target Synonyms

    Malate dehydrogenase; Malic enzyme 2; Malic enzyme 2 mitochondrial; Malic enzyme 2 NAD(+) dependent mitochondrial; Malic enzyme mitochondrial; Malic enzyme NAD(+) dependent mitochondrial; MAOM_HUMAN; ME 2; ME2; mitochondrial; NAD dependent malic enzyme mitochondrial; NAD ME; NAD-dependent malic enzyme; NAD-ME; ODS1; Pyruvic malic carboxylase

  • Target 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.

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