Peroxidasin anticorps (AA 900-1054)

N° du produit ABIN7825669

L’anticorps anti-Peroxidasin Polyclonal Lapin est utilisé pour la détection de Peroxidasin dans des échantillons de Humain. Il a été validé pour WB, IHC et ELISA.

Aperçu rapide pour Peroxidasin anticorps (AA 900-1054) (ABIN7825669)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Peroxidasin est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Détail du produit anti-Peroxidasin anticorps

Épitope: AA 900-1054

Fonction: Anti-PXDN Antibody

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

Attributs du produit: Anti-PXDN Antibody (ABIN7825669). Tested in WB, IHC, ELISA applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

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: Western blot, 0.25-0.5 μg/mL, Human
Immunohistochemistry, 2-5 μg/mL, Human
ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur Peroxidasin

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

Autre désignation: 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.

Poids moléculaire: 165 kDa

ID gène: 7837

UniProt: Q92626