PGLYRP1 Polyclonal Antibody, 100ul Protein Expression making it a valuable asset

making it a valuable asset in any laboratory

This protein plays an essential role in microtubule organization

Allelic variations in this gene have been associated| but not causally linked| with two different forms of kidney disease: membranoproliferative glomerulonephritis type II (MPGNII) and hemolytic uraemic syndrome (HUS)

This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss

and cell adhesion

PGLYRP1 Polyclonal Antibody, 100ul Protein Expression making it a valuable assetPGLYRP1 (Peptidoglycan Recognition Protein 1) is a Protein Coding gene. Among its related pathways are TNF Signaling (sino). GO annotations related to this gene include peptidoglycan binding and N acetylmuramoyl L alanine amidase activity. An important paralog of this gene is PGLYRP4.