Hep-53.4 Cells
CAD$897.00*
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 | Hep-53.4 cells are a mouse-derived cell line originating from hepatocellular carcinoma in a C57BL/6J mouse model. These cells are particularly useful in the study of hepatocellular carcinoma, one of the most common types of liver cancer. By providing a consistent, reproducible model system, Hep-53.4 cells allow researchers to delve into the intricacies of cancer biology specific to the liver. This includes the exploration of oncogenic pathways, the effects of genetic modifications, and the cellular environment's role in cancer progression. |
|---|---|
| Organism | Mouse |
| Tissue | Liver |
| Disease | Hepatocellular carcinoma |
| Synonyms | HEP-53.4, 53.4 |
Characteristics
| Breed/Subspecies | C57BL/6J |
|---|---|
| Age | Adult |
| Gender | Male |
| Morphology | Epithelial-like |
| Growth properties | Adherent |
Regulatory Data
| Citation | Hep-53.4 (Cytion catalog number 400200) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_5765 |
Biomolecular Data
| Tumorigenic | Yes, in C57BL/6J mice |
|---|---|
| Mutational profile | P53 wt |
Handling
| Culture Medium | DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS |
| 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. |
| Fluid renewal | Every 3 to 5 days |
| 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 |
|---|---|---|---|
| 400200-091224 | Certificate of Analysis | 19. Jan. 2026 | 400200 |
| 400200-230226 | Certificate of Analysis | 26. Mar. 2026 | 400200 |
| 400200-060423 | Certificate of Analysis | 19. Jan. 2026 | 400200 |