ACADV Polyclonal Antibody, 20ul Hepatocytes In humans and rabbits

In humans and rabbits

|Contains 1 MH1 (MAD homology 1) domain

Defects in this gene are a cause of Rubinstein-Taybi syndrome and may also play a role in epithelial cancer

including Rho

which is associated with the fragile X mental retardation syndrome (MIM 300624)

ACADV Polyclonal Antibody, 20ul Hepatocytes In humans and rabbitsThe protein encoded by this gene is targeted to the inner mitochondrial membrane where it catalyzes the first step of the mitochondrial fatty acid beta oxidation pathway. This acyl Coenzyme A dehydrogenase is specific to long chain and very long chain fatty acids. A deficiency in this gene product reduces myocardial fatty acid beta oxidation and is associated with cardiomyopathy. Alternative splicing results in multiple transcript variants encoding