Peroxidasin antibody (AA 900-1054)

Catalog No. ABIN7825669

The Rabbit Polyclonal anti-Peroxidasin antibody has been validated for WB, IHC and ELISA. It is suitable to detect Peroxidasin in samples from Human.

Quick Overview for Peroxidasin antibody (AA 900-1054) (ABIN7825669)

Target: Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Peroxidasin antibody is un-conjugated

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

Product Details anti-Peroxidasin Antibody

Binding Specificity: AA 900-1054

Purpose: Anti-PXDN Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins

Characteristics: Anti-PXDN Antibody catalog # A06456-1. 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.

Immunogen: 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

Application Details

Application Notes: 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

Handling

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.

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for Peroxidasin

Target: Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

Alternative Name: PXDN

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.

Molecular Weight: 165 kDa

Gene ID: 7837

UniProt: Q92626