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PXDN


Official Full Name
peroxidasin
Organism
Homo sapiens
Gene ID
7837
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
PXN; VPO; MG50; PRG2; ASGD7; COPOA; D2S448; D2S448E; hsPxd01

Cat.No. Product Name Price
SHH387284 shRNA set against Human PXDN (NM_012293.1) Inquiry
SHH387288 shRNA set against Mouse PXDN (NM_181395.2) Inquiry
Cat.No. Product Name Price
CDFH015647 Human PXDN cDNA Clone(NM_012293.1) Inquiry
MiUTR1H-08511 PXDN miRNA 3'UTR clone Inquiry
CDCB182545 Rabbit PXDN ORF clone (XM_002723811.2) Inquiry
CDCH067626 human PXDN ORF clone (NM_012293.1) Inquiry
CDCR275517 Mouse Pxdn ORF Clone(NM_181395.2) Inquiry
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