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DLD anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement DLD dans WB, IHC et IF. Il présente une réactivité envers Humain.
N° du produit ABIN7266766

Aperçu rapide pour DLD anticorps (ABIN7266766)

Antigène

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

Reactivité

  • 46
  • 28
  • 27
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 53
  • 6
Lapin

Clonalité

  • 50
  • 9
Monoclonal

Conjugué

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

Application

  • 54
  • 23
  • 23
  • 13
  • 13
  • 10
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Fonction

    DLDH/DLD Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human DLDH/DLD

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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. [provided by RefSeq, Jan 2014],DLDD, DLDH, E3, GCSL, LAD, PHE3,Amino acid metabolism,Cancer,Carbohydrate metabolism,Endocrine & Metabolism,Signal Transduction,DLD

    Poids moléculaire

    56kDa

    ID gène

    1738

    UniProt

    P09622

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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