For research use only
| Cat No. | ABC-TC3205 |
| Product Type | Mouse Primary Cells |
| Cell Type | Liver Cell |
| Species | C57BL/6 Mouse |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Liver |
| Disease | Normal |
| Storage | Liquid Nitrogen |
C57BL/6 mouse liver cells include hepatocytes, Kupffer and stellate cells, vital for liver injury and immune response modeling in vitro and ex vivo assays.
C57BL/6 Mouse Liver Cells are primary cells isolated from the liver tissue of pathogen-free C57BL/6 mice. This heterogeneous population was characterized using immunocytochemical methods, including parenchymal hepatocytes, Kupffer cells (F4/80⁺ macrophages), hepatic stellate cells (GFAP⁺), and endothelial cells (CD34⁺). Functionally, Kupffer cells perform phagocytosis and immune surveillance, clearing pathogens and cellular debris, whereas stellate cells regulate extracellular matrix remodeling. These cells are implicated in liver injury models, including non-alcoholic fatty liver disease (NAFLD) and toxin-induced hepatitis through cytokine secretion (e.g., TNF-α, IL-6) and inflammatory responses. Due to limited expansion capacity, repeated freezing/thawing cycles should be avoided to maintain viability. This primary cell system provides a physiologically relevant platform for studying hepatic pathophysiology without genetic background variability .
| Product Code | MLIC |
| Species | C57BL/6 Mouse |
| Cat.No | ABC-TC3205 |
| Product Category | Primary Cells |
| Size/Quantity | 1 vial |
| Cell Type | Liver Cell |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Liver |
| Disease | Normal |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Mouse Primary Cells |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
Mouse liver cells, especially hepatocytes, serve as a crucial predictive model in drug development. They effectively simulate drug interactions within the liver, supporting preclinical in vitro studies on drug metabolism and pharmacokinetics. These cells are widely used to evaluate drug clearance, metabolic pathways, cellular uptake, hepatotoxicity, and drug-drug interactions. Sharing similar drug-metabolizing enzymes with human hepatocytes, particularly in biotransformation processes, mouse liver cells provide a reliable platform to predict human drug responses. Additionally, cryopreserved mouse liver cells offer a cost-effective and practical alternative to in vivo studies, available in various formats to meet diverse experimental needs, thereby accelerating drug discovery and development.
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