MEF-2C Polyclonal Antibody, 20ul Peripheral Blood Separation Tube indicates nucleotide deletion in the

indicates nucleotide deletion in the genomic sequence would result in frameshift and early termination of translation

The enzyme may localize to the endoplasmic reticulum and the Golgi

Mutations in this gene result in Bernard-Soulier syndromes and platelet-type von Willebrand disease

Induces B-cells to aggregate and improves their viability in vitro

There is a pseudogene for this gene on chromosome 2

MEF-2C Polyclonal Antibody, 20ul Peripheral Blood Separation Tube indicates nucleotide deletion in theMEF2C 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