该POMGNT1 Polyclonal Antibody. This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described.
应用类型
IHC
免疫原
Recombinant fusion protein of human POMGNT1 (NP_060209.3).
