PRPH Polyclonal Antibody, 100ul Contamination Detection & Removal Mutations in this gene cause

Mutations in this gene cause cryptogenic cirrhosis

Based on their distribution patterns| some members of this family are believed to be involved in embryogenesis| spermatogenesis| and cellular growth and division

This protein interacts with the fragile X mental retardation protein (FMRP)

including the C5 alpha chain

PRPH Polyclonal Antibody, 100ul Contamination Detection & Removal Mutations in this gene causePRPH encodes a cytoskeletal protein found in neurons of the peripheral nervous system. Peripherin is a type III intermediate filament protein with homology to other cytoskeletal proteins such as desmin, and is a different protein that the peripherin found in photoreceptors. Mutations in PRPH have been associated with susceptibility to amyotrophic lateral sclerosis.