MEF2C Polyclonal Antibody, 50ul Subcellular Fractions Stickler syndrome type I

Stickler syndrome type I

It associates with the spliceosome and contains a zinc knuckle motif that is found in other splicing factors and is involved in protein-nucleic acid and protein-protein interactions

It may also be involved in glial tumorigenesis and may provide a potential target for therapeutic intervention

There is evidence for multiple polyadenylated sites for this transcript

5 mL micro centrifuge tubes

MEF2C Polyclonal Antibody, 50ul Subcellular Fractions Stickler syndrome type IMEF2C 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