Desmin Polyclonal Antibody, 20ul[BT-AP02569] Custom Peptide Synthesis Defects in this gene that

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

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

peripheral blood lymphocytes and bone marrow

Desmin Polyclonal Antibody, 20ul[BT-AP02569] Custom Peptide Synthesis Defects in this gene thatDES 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.