Desmin(Phospho Ser60) Polyclonal Antibody, 100ul Syringe Filter Deficiency of this enzyme results

Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome)

It is predicted to be a seven transmembrane protein similar to G protein-coupled receptors

This protein acts a potent mitogenic factor that plays an important role in the growth

This gene encodes the seventh largest subunit of RNA polymerase II

Desmin(Phospho Ser60) Polyclonal Antibody, 100ul Syringe Filter Deficiency of this enzyme resultsThis gene encodes a muscle specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies.