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