Mouse Anti-Human GAFP Monoclonal Antibody (EX023)

Astrocytes can be uniquely identified by the expression of the intermediate filament protein glial acidic fibrillary protein (GFAP). Mutations in this gene can cause Alexander disease, a rare astrocyte disease of the central nervous system. Exosomes derived from glioma cells transpoRoom Temperature a series of bioMolecules and mediate cell-to-cell communication. Studies have shown that serum from patients with glioma is rich in CD9+ exosomes with GFAP on their surface.