Hej,

I am looking for an alternative read-out for phenotypical consequences of Wilson's Disease in cellular models such as HepG2 - apart from mislocalised ATP7B and Cu levels.

Would it make sense to determine Ceruloplasmin activity or iron levels? Or is VLDL measurement in HepG2 feasible i.e. do these cells produce measurable amounts of VLDL without any extra stimulation?

Thanks for your help!

Katharina

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