FOXP3 Polyclonal Antibody, 50ul[BT-AP15673] Metabolic enzymes tool compounds The protein is found predominantly

The protein is found predominantly in the nucleus| although it is also present in the cytoplasm

The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins

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

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

turnover and recycling of cytoplasmic constituents in eukaryotic cells

FOXP3 Polyclonal Antibody, 50ul[BT-AP15673] Metabolic enzymes tool compounds The protein is found predominantlyThe 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.