该SGSH Polyclonal Antibody. This gene encodes one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.
应用类型
IHC
免疫原
Recombinant fusion protein of human SGSH (NP_000190.1).
