||Full length native Human Ceruloplasmin purified from human plasma.
||The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities.
||Expressed by the liver and secreted in plasma.
||Lyophilised:Reconstitute with distilled water. Please contact Abcam for lot-specific recommended volume.
||>95% by SDS-PAGE
||Preservative: NoneConstituents: 50mM Potassium phosphate, 5mM EDTA, 20mM EACA, 100mM Potassium chloride, pH 6.8
||Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.
||Belongs to the multicopper oxidase family.Contains 3 F5/8 type A domains.Contains 6 plastocyanin-like domains.