该MANBA Polyclonal Antibody. This gene encodes a member of the glycosyl hydrolase 2 family. The encoded protein localizes to the lysosome where it is the final exoglycosidase in the pathway for N-linked glycoprotein oligosaccharide catabolism. Mutations in this gene are associated with beta-mannosidosis, a lysosomal storage disease that has a wide spectrum of neurological involvement.
应用类型
WB,IHC
免疫原
Recombinant fusion protein of human MANBA (NP_005899.3).
