UFD1 Polyclonal Antibody, 50ul RNA Synthesis A mutation in the serine-rich

A mutation in the serine-rich region of the protein is thought to be associated with hyperuricemia (PMID: 21594610)

known as SL1

The activity of this receptor is coupled to the formation of inositol 1

A similar enzyme in mouse can catalyze the degradation of O-phospho-homoserine to a-ketobutyrate

tissue specificity:Widely expressed with highest levels in the heart

UFD1 Polyclonal Antibody, 50ul RNA Synthesis A mutation in the serine-richThe protein encoded by this gene forms a complex with two other proteins, nuclear protein localization 4 and valosin containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial