ATPase, Cu++ Transporting Alpha Polypeptide (ATP7a)
MK; MNK; MC1; Menkes Syndrome; Copper pump 1; Copper-transporting ATPase 1; Menkes disease-associated protein
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ATP7A provides instructions to make a protein that is important for regulating copper levels in the body. This protein is found in most tissues, but it is absent from the liver. In the small intestine, the ATP7A protein helps control the absorption of copper from food. In other organs and tissues, the ATP7A protein has a dual role and shuttles between two locations within the cell. The protein normally resides in a cell structure called the Golgi apparatus, which modifies and transports newly produced enzymes and other proteins. Here, the ATP7A protein supplies copper to certain enzymes that are critical for the structure and function of bone, skin, hair, blood vessels, and the nervous system. If copper levels in the cell environment are elevated, however, the ATP7A protein moves to the cell membrane and eliminates excess copper from the cell.
Organism species: Homo sapiens (Human)
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Organism species: Mus musculus (Mouse)
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Organism species: Rattus norvegicus (Rat)
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- Customized Service n/a CLIA Kit for ATPase, Cu++ Transporting Alpha Polypeptide (ATP7a) CLIA Kit Customized Service Offer
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