Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

MPZ anticorps

Cet anticorps anti-MPZ est un anticorps Polyclonal produit chez le Lapin, détectant MPZ dans WB. Convient pour Humain.
N° du produit ABIN1513218
-15% Promotion 2026
272,00 €
320,00 €
Économisez 48,00 € (-15 %)
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 8 à 10 jours ouvrables

Aperçu rapide pour MPZ anticorps (ABIN1513218)

Antigène

Voir toutes MPZ Anticorps
MPZ (Myelin Protein Zero (MPZ))

Reactivité

  • 41
  • 28
  • 25
  • 15
Humain

Hôte

  • 49
  • 7
  • 3
  • 1
Lapin

Clonalité

  • 53
  • 7
Polyclonal

Conjugué

  • 28
  • 5
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MPZ est non-conjugé

Application

  • 49
  • 25
  • 20
  • 13
  • 13
  • 7
  • 7
  • 7
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB)
  •  Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Immunogène

    Recombinant protein of human MPZ

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,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.

    Conseil sur la manipulation

    Avoid freeze / thaw cycles

    Stock

    -20 °C

    Stockage commentaire

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

    MPZ (Myelin Protein Zero (MPZ))

    Autre désignation

    MPZ

    Sujet

    This gene is specifically expressed in Schwann cells of the peripheral nervous system and encodes a type I transmembrane glycoprotein that is a major structural protein of the peripheral myelin sheath. The encoded protein contains a large hydrophobic extracellular domain and a smaller basic intracellular domain, which are essential for the formation and stabilization of the multilamellar structure of the compact myelin. Mutations in this gene are associated with autosomal dominant form of Charcot-Marie-Tooth disease type 1 (CMT1B) and other polyneuropathies, such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN). A recent study showed that two isoforms are produced from the same mRNA by use of alternative in-frame translation termination codons via a stop codon readthrough mechanism.,MPZ,CHM,CMT1,CMT1B,CMT2I,CMT2J,CMT4E,CMTDI3,CMTDID,DSS,HMSNIB,MPP,P0,Neuroscience,Cell Type Marker,Neurodegenerative Diseases,Neuron marker,Axon marker,MPZ

    Poids moléculaire

    27 kDa/34 kDa

    ID gène

    4359

    UniProt

    P25189
Vous êtes ici:
Chat with us!