GRSF1 rabbit monoclonal antibody Staining & IHC autosomal recessive osteopetrosis

autosomal recessive osteopetrosis

nervous system development

Physical and Topological Properties of Circular DNA

Deficiencies in this protein's function are associated with Alzheimer's disease and type 2 diabetes mellitus but mutations in this gene have not been shown to be causitive for these diseases

Associated Product:

GRSF1 rabbit monoclonal antibody Staining & IHC autosomal recessive osteopetrosisSpecification Full name GRSF1 rabbit monoclonal antibody Alternative names 50 l 100 l Reactivity rabbit monoclonal Applications WB, IF Host Rabbit Clone type rabbit monoclonal Target Background The protein encoded by this gene is a cellular protein that binds RNAs containing the G rich element. The protein is localized in the cytoplasm, and has been shown to stimulate translation of viral mRNAs in vitro. Multiple transcript variants encoding different