Platform
pixCells
pixCells - Overview
Wild-type Cells
pixHep™
Primary-like hepatocytes engineered for accurate liver function and toxicity studies.
pixStellate™
iPSC-derived hepatic stellates for modeling fibrogenesis and liver inflammation.
Co-Culture Models
Integrated hepatocyte–stellate systems modeling disease from steatosis to fibrosis.
pixIO™
Intestinal organoids combining epithelial complexity with absorption and metabolism profiling.
Disease Models
MASLD
Human iPSC derived hepatocytes recapitulating steatosis, insulin resistance, and inflammatory signatures.
A1ATD
Alpha-1 antitrypsin deficiency iPSC-derived hepatocytes modeled from disease-matched genotypes.
PFIC2
iPSC-derived hepatocyte cholestatic models capturing bile transport and hepatocyte polarity defects.
UCD
Hyperammonemia modeled in iPSC-derive hepatocytes to study urea cycle enzyme dysfunction.
Other
Custom
Fully tailored models—from donor selection to CRISPR engineering—to match your study design.
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