[Cytes Biotechnology] Primary Human Hepatic Stellate Cells
HuSC-P1 | Stellate cells, passage 1 | 100.000 500.000 |
HuSC-P2 | Stellate cells, passage 2 | 100.000 500.000 |
HuSC-P3 | Stellate cells, passage 3 | 100.000 500.000 |
HuSCP | Plated Stellate cells | 1 plate |
Human Hepatic stellate cells Charaterization
- Charaterization I
- Cell number and viability after thawing
Morphological analysis of cells over time
- Cell number and viability after thawing
- Charaterization II
Cytes Biotechnology uses key antibodies by immunofluorescence to characterize stellate cells showing their expression at the quiescent and activated state of the cells.
Common Uses
Cell Based Assays
- Toxicity
- Drug screening
- Metabolism
Useful tool to study
- Liver function
- Physiology
- Liver diseases (Fibrotic Models)
Human hepatic stellate cells have the ability to switch to their activated phase and transdifferentiate into myofibroblast-like cells, which are involved in the pathogenesis of liver fibrosis.
In addition, activated stellate cells can proliferate, contract and regulate chemotaxis, becoming the main source of extracellular matrix production during liver injury.
extracellular matrix production during liver injury. This leads to collagen secretion that provides a scaffold for hepatocytes to repopulate during tissue regeneration and can lead to cirrhosis.
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