MEF-2C(Phospho Ser396) Polyclonal Antibody, 100ul Buffer Solutions Mutations at this locus have

Mutations at this locus have been associated with susceptibility to hemolytic uremic syndrome

such as GPR81

The 26 S proteasome may be involved in trinucleotide repeat expansion| a phenomenon which is associated with many hereditary neurological diseases

This enzyme is a tetramer that may be composed of different subunits encoded by distinct genes in different tissues

F2RL3 is activated by thrombin and trypsin

MEF-2C(Phospho Ser396) Polyclonal Antibody, 100ul Buffer Solutions Mutations at this locus haveThis locus encodes a member of the MADS box transcription enhancer factor 2 (MEF2) family of proteins, which play a role in myogenesis. The encoded protein, MEF2 polypeptide C, has both trans activating and DNA binding activities. This protein may play a role in maintaining the differentiated state of muscle cells. Mutations and deletions at this locus have been associated with severe mental retardation, stereotypic movements, epilepsy, and cerebral