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NAD-ME antibody (AA 26-584)

The Rabbit Polyclonal anti-NAD-ME antibody is suitable to detect NAD-ME in samples from Human, Mouse, Rat and Monkey. It has been validated for WB, ELISA, IF and IHC (p).
Catalog No. ABIN7873011
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for NAD-ME antibody (AA 26-584) (ABIN7873011)

Target

See all NAD-ME Antibodies
NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

Reactivity

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  • 18
  • 6
  • 2
  • 2
  • 2
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  • 1
  • 1
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Human, Mouse, Rat, Monkey

Host

  • 38
  • 3
Rabbit

Clonality

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  • 12
Polyclonal

Conjugate

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  • 1
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This NAD-ME antibody is un-conjugated

Application

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  • 1
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  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 8
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    • 5
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    • 1
    • 1
    • 1
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    AA 26-584

    Purpose

    ME2 Antibody / NAD-ME

    Purification

    Affinity purified

    Immunogen

    Recombinant human protein (amino acids K26-E584) was used as the immunogen for the ME2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the ME2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the ME2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

    Alternative Name

    ME2

    Background

    NAD-dependent malic enzyme, mitochondrial is a protein that in humans is encoded by the ME2 gene. It is mapped to 18q21.2. 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.

    UniProt

    P23368

    Pathways

    Production of Molecular Mediator of Immune Response
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