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PXDN (NM_012293) Human Recombinant Protein

Product Specifications

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. [provided by RefSeq, Aug 2014]

Overview

Purified recombinant protein of Homo sapiens peroxidasin homolog (Drosophila) (PXDN)

Synonyms

ASGD7; COPOA; D2S448; D2S448E; MG50; PRG2; PXN; VPO

Gene ID

7837

UniProt

Q92626

Accession Number mRNA

NM_012293

Chromosomal Location

2p25.3

Expression System

HEK293T

Tag

C-Myc/DDK

Concentration

>50 ug/mL as determined by microplate BCA method

Purity

> 80% as determined by SDS-PAGE and Coomassie blue staining

Form

Liquid

Buffer

25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

Function

Druggable Genome, Transmembrane

Molecular Weight

165.1 kDa

Storage Conditions

Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.

Symbol

PXDN

Species

Human

Protein ID

NP_036425

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/7837

Uniprot URL

https://www.uniprot.org/uniprot/Q92626

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_012293

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_036425

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