Human ATPase, Cu++ Transporting Beta Polypeptide (ATP7b) ELISA Kit

Built around the copper-transporting P-type ATPase implicated in Wilson's disease, this Assay Genie kit provides quantitative measurement of ATP7b in tissue homogenates from human samples. ATP7b normally resides in hepatocyte membranes, where it loads copper onto ceruloplasmin and pumps excess copper into bile; loss-of-function variants cause hepatic copper overload, with secondary deposition in brain and cornea.

The 96-assay format supports research into copper homeostasis, hepatology, and Wilson's disease, with in vitro research use only. Refrigerated storage preserves antibody performance across repeated freeze-thaw cycles.

Investigators working on metal-ion transport disorders, copper-related neurodegenerative conditions, and Wilson's disease biomarkers can apply this kit to profile ATP7b levels in patient liver specimens and disease-model systems.