USP48 Polyclonal Antibody, 100ul Cell Culture Plates and their presence on the

and their presence on the polysomes

This encoded protein could play an important role in the pathogenesis of Alzheimer's disease

Mutations in this gene are thought to be a cause of isolated cleft lip with or without cleft palate

Defects in this gene are a cause of Zellweger syndrome (ZWS)

This antimicrobial gene encodes a chemokine of the CXC subfamily and ligand for the receptor CXCR3

USP48 Polyclonal Antibody, 100ul Cell Culture Plates and their presence on theUSP48 (ubiquitin specific peptidase 48) encodes a protein containing domains that associate it with the peptidase family C19, also known as family 2 of ubiquitin carboxyl terminal hydrolases. Family members function as deubiquitinating enzymes, recognizing and hydrolyzing the peptide bond at the C terminal glycine of ubiquitin. Enzymes in peptidase family C19 are involved in the processing of poly ubiquitin precursors as well as that of ubiquitinated