FOXP3 Polyclonal Antibody, 50ul[BT-AP15673] Metabolic enzymes tool compounds a unique N terminus

a unique N terminus

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

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

which is activated by nitric oxide

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

FOXP3 Polyclonal Antibody, 50ul[BT-AP15673] Metabolic enzymes tool compounds a unique N terminusThe 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.