Catalog Number: HSC-003
pixStellate iPSC-derived Stellate Cells
Human iPSC-derived stellate cells for modeling fibrosis and hepatic inflammation.
- Express key fibrotic and activation markers (COL1A1, ACTA2, PDGFRβ)
- Respond to TGF-β and LPS stimulation for fibrosis induction studies
- Donor-matched Co-culture compatible with pixHep for MASLD and steatohepatitis modelling
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pixStellate™ are iPSC-derived stellate cells that maintain hallmark markers (α-SMA, desmin, GFAP) and activate under fibrogenic stimuli.
They can be used alone or paired with pixHep™ to model fibrosis progression, MASLD-to-NASH transitions, or chronic liver injury.
Quiescent in baseline culture; responsive to injury cues.
Express hallmark stellate markers confirmed via immunostaining.
Upregulate pro-fibrotic genes upon activation.
Available from healthy or disease donor lines.
Compatible with custom genetic engineering
Technical Data & Functional Validation
pixlbio iPSC-derived Hepatic Stellate Cells (pixStellate) express key HSC markers at gene and protein level

Key HSC Markers (mRNA)

Key HSC Markers (Protein)

Quiescent Phenotype

pixStellate Activation


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