FOXP3 Polyclonal Antibody, 50ul[BT-AP15673] Metabolic enzymes tool compounds Mutations in this gene cause

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

Retinal dehydrogenase 1 encoded by ALDH1A1 belongs to the aldehyde dehydrogenase family

turnover and recycling of cytoplasmic constituents in eukaryotic cells

ABCB7 encodes a half-transporter involved in the transport of heme from the mitochondria to the cytosol

Thyroglobulin (Tg) is a glycoprotein homodimer produced predominantly by the thryroid gland

FOXP3 Polyclonal Antibody, 50ul[BT-AP15673] Metabolic enzymes tool compounds Mutations in this gene causeThe protein encoded by this gene is a member of the forkhead winged helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X linked syndrome (IPEX), also known as X linked autoimmunity immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.