H-4-II-E Cells
USD$395.00*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
General information
| Description | The H-4-II-E cell line is a hepatoma-derived cell line, specifically developed from the liver tissue of an adult rat. This cell line is frequently utilized in research focused on liver physiology and pathology, particularly in studies related to hepatocellular carcinoma and liver metabolism. The H-4-II-E cells are epithelial-like in morphology and are known for their rapid growth rate and high cell density capabilities, making them a valuable model for high-throughput screening and toxicology studies. Notably, H-4-II-E cells exhibit several differentiated functions of hepatocytes, including albumin secretion, ammonia production, and the presence of cytochrome P450 enzymes. This makes them an excellent tool for studying drug metabolism, enzyme induction, and interactions that may occur in human liver disease. Moreover, these cells have been used to investigate mechanisms of liver regeneration and cancer progression, providing insights into cellular responses to various stimuli such as cytokines and growth factors. |
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| Organism | Rat |
| Tissue | Liver |
| Disease | Rat hepatocellular carcinoma |
| Synonyms | H-4-II-E, H4IIE |
Characteristics
| Breed/Subspecies | AxC |
|---|---|
| Gender | Male |
| Morphology | Epithelial |
| Growth properties | Adherent |
Regulatory Data
| Citation | H-4-II-E (Cytion catalog number 305204) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10116 |
| CellosaurusAccession | CVCL_0284 |
Biomolecular Data
Handling
| Culture Medium | EMEM (MEM Eagle), w: 2 mM L-Glutamine, w: 2.2 g/L NaHCO3, w: EBSS (Cytion article number 820100a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS and 1% NEAA |
| Dissociation Reagent | Accutase |
| Subculturing | Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium. |
| Seeding density | 2 to 4 x 104 cells/cm2 |
| Fluid renewal | 2 to 3 times per week |
| Freeze medium | As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress. |
| Thawing and Culturing Cells |
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| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| Shipping Conditions | Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage. |
| Storage Conditions | For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen. |
Quality Control & Molecular Analysis
| Sterility | Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305204-290426 | Certificate of Analysis | 24. Jun. 2026 | 305204 |