HEK-293 cells were subjected to SDS PAGE followed by western blot with FNab00329(GLA antibody) at dilution of 1:1500
Immunohistochemistry of paraffin-embedded mouse kidney tissue slide using FNab00329(GLA Antibody) at dilution of 1:100
Immunofluorescence analysis of HeLa cells using FNab00329(GLA antibody) at dilution of 1:50. Blue: DAPI for nuclear staining.
Background
GLA, also named as Melibiase, Agalsidas and Alpha-galactosidase A, Belongs to the glycosyl hydrolase 27 family. It hydrolysis of terminal, non-reducing alpha-D-galactose residues in alpha-D-galactosides, including galactose oligosaccharides, galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy(ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease, a lysosomal storage disease.