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

Mutations in this gene cause cryptogenic cirrhosis

|PTM:Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains

Methyltransferase

including the C5 alpha chain

PPARG encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors

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.