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DPYSL3 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement DPYSL3 dans WB. Il présente une réactivité avec des échantillons de Rat.
N° du produit ABIN7880630
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour DPYSL3 anticorps (ABIN7880630)

Antigène

Voir toutes DPYSL3 Anticorps
DPYSL3 (Dihydropyrimidinase-Like 3 (DPYSL3))

Reactivité

  • 55
  • 25
  • 16
  • 1
  • 1
  • 1
  • 1
  • 1
Rat

Hôte

  • 53
  • 4
Lapin

Clonalité

  • 44
  • 13
Polyclonal

Conjugué

  • 21
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DPYSL3 est non-conjugé

Application

  • 35
  • 17
  • 15
  • 13
  • 13
  • 13
  • 12
  • 11
  • 6
  • 4
  • 1
  • 1
Western Blotting (WB)
  • Fonction

    Crmp4 Antibody / Dpysl3 / Drp-3

    Purification

    Antigen affinity purified

    Immunogène

    Amio acids DAVKIVSAKNHQSVA were used as the immunogen for the Crmp4 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the Crmp4 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 Crmp4 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

    DPYSL3 (Dihydropyrimidinase-Like 3 (DPYSL3))

    Autre désignation

    Crmp4

    Sujet

    Dihydropyrimidinase-related protein 3 is an enzyme that in humans is encoded by the DPYSL3 gene. This gene encodes a protein that belongs to the TUC (TOAD-64/Ulip/CRMP) family of proteins. Members of this family are phosphoproteins that function in axonal guidance and neuronal differentiation during development and regeneration of the nervous system. A mutation in the human gene is associated with amyotrophic lateral sclerosis. Alternative splicing results in multiple transcript variants encoding different isoforms.

    UniProt

    Q62952
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