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NAD-ME anticorps (AA 26-584)

L’anticorps anti-NAD-ME Polyclonal Lapin est utilisé pour la détection de NAD-ME dans des échantillons de Humain, Souris, Rat et Singe. Il a été validé pour WB, ELISA, IF et IHC (p).
N° du produit ABIN7873011
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour NAD-ME anticorps (AA 26-584) (ABIN7873011)

Antigène

Voir toutes NAD-ME Anticorps
NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

Reactivité

  • 40
  • 18
  • 6
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat, Singe

Hôte

  • 38
  • 3
Lapin

Clonalité

  • 29
  • 12
Polyclonal

Conjugué

  • 23
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp NAD-ME est non-conjugé

Application

  • 34
  • 17
  • 17
  • 14
  • 7
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Épitope

    • 8
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 26-584

    Fonction

    ME2 Antibody / NAD-ME

    Purification

    Affinity purified

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

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

    Autre désignation

    ME2

    Sujet

    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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