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DLD anticorps

L’anticorps Lapin Polyclonal anti-DLD a été validé pour IHC et ELISA. Il convient pour détecter DLD dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7241168

Aperçu rapide pour DLD anticorps (ABIN7241168)

Antigène

Voir toutes DLD Anticorps
DLD (Dihydrolipoamide Dehydrogenase (DLD))

Reactivité

  • 46
  • 27
  • 26
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 53
  • 6
Lapin

Clonalité

  • 49
  • 10
Polyclonal

Conjugué

  • 37
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DLD est non-conjugé

Application

  • 55
  • 23
  • 22
  • 14
  • 13
  • 10
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human DLD

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Autre désignation

    DLD

    Sujet

    This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants.

    UniProt

    P09622

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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