eEF2K(Phospho Ser359) Polyclonal Antibody, 100ul Buffers & Solutions Mutations in EPHA2 are the

Mutations in EPHA2 are the cause of certain genetically-related cataract disorders

Some EDG receptors (e

The isoforms type 1 and type 2 are functional receptors and are able to mediate the endocytosis of modified low density lipoproteins (LDLs)

Impairment of the interaction between these two proteins may contribute to the disease

All ETS proteins contain an ETS DNA-binding domain that binds to DNA sequences containing the consensus 5'-CGGA[AT]-3'

eEF2K(Phospho Ser359) Polyclonal Antibody, 100ul Buffers & Solutions Mutations in EPHA2 are theThis gene encodes a highly conserved protein kinase in the calmodulin mediated signaling pathway that links activation of cell surface receptors to cell division. This kinase is involved in the regulation of protein synthesis. It phosphorylates eukaryotic elongation factor 2 (EEF2) and thus inhibits the EEF2 function. The activity of this kinase is increased in many cancers and may be a valid target for anti cancer treatment.