Desmin Polyclonal Antibody, 20ul[BT-AP02569] Custom Peptide Synthesis cholesterol

cholesterol

Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD)

ABHD2 encodes a protein (abhydrolase domain containing 2) containing an alpha/beta hydrolase fold

Members of this family play important roles in apoptosis

Cerebellin 3 is not able to form homomeric complexes

Desmin Polyclonal Antibody, 20ul[BT-AP02569] Custom Peptide Synthesis cholesterolDES encodes a muscle specific class III intermediate filament. Homopolymers of desmin form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in DES are associated with desmin related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies.