Tyrosine Hydroxylase Polyclonal Antibody, 20ul Buffers & Solutions |subunit:Interacts with AATF

|subunit:Interacts with AATF

Mutations in CYC1 may cause mitochondrial complex III deficiency

thereby allowing them to fold correctly

Alternatively spliced transcript variants encoding distinct isoforms have been reported for this gene

Several genes of the C-type lectin superfamily

Tyrosine Hydroxylase Polyclonal Antibody, 20ul Buffers & Solutions |subunit:Interacts with AATFThe protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.