Peroxidasin anticorps (AA 900-1054) (Fluoro594)

N° du produit ABIN8020576

Cet anticorps anti-Peroxidasin Polyclonal Lapin conjugué à Fluoro594 (ABIN8020576) détecte spécifiquement Peroxidasin dans FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Peroxidasin anticorps (AA 900-1054) (Fluoro594) (ABIN8020576)

Antigène: Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Peroxidasin est conjugé à/à la Fluoro594

Application: Flow Cytometry (FACS)

Détail du produit anti-Peroxidasin anticorps (Fluoro594)

Épitope: AA 900-1054

Fonction: Anti-PXDN Antibody Fluoro594 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human PXDN shares 94.8% amino acid (aa) sequence identity with mouse PXDN.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human PXDN recombinant protein (Position: R900-D1054). Human PXDN shares 94.8% amino acid (aa) sequence identity with mouse PXDN.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur Peroxidasin

Antigène: Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

Autre désignation: PXDN

Sujet:

Background: 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.

Gene Full Name: peroxidasin

ID gène: 7837

UniProt: Q92626