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

Peroxidasin anticorps

PXDN Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7269230
  • Antigène Voir toutes Peroxidasin (PXDN) Anticorps
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Reactivité
    • 13
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 10
    • 3
    Lapin
    Clonalité
    • 11
    • 2
    Polyclonal
    Conjugué
    • 8
    • 4
    • 1
    Cet anticorp Peroxidasin est non-conjugé
    Application
    • 13
    • 4
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Fonction
    PXDN Rabbit pAb
     Réactivité croisée
    Humain, Souris
    Attributs du produit
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human PXDN.
    Isotype
    IgG
    Top Product
    Discover our top product PXDN Anticorps primaire
  • 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.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Autre désignation
    PXDN (PXDN Produits)
    Synonymes
    anticorps D2S448, anticorps D2S448E, anticorps MG50, anticorps PRG2, anticorps PXN, anticorps VPO, anticorps 2310075M15Rik, anticorps C85409, anticorps E330004E07, anticorps VPO1, anticorps mKIAA0230, anticorps peroxidasin, anticorps PXDN, anticorps Pxdn
    Sujet
    This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis.,PXN,VPO,MG50,PRG2,ASGD7,COPOA,D2S448,D2S448E,PXDN,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,PXDN
    ID gène
    7837
    UniProt
    Q92626
Vous êtes ici:
Support technique