SNU-398 Cells
759,00 CAD$*
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).
Renseignements généraux
| Description | The SNU-398 cell line is derived from a hepatocellular carcinoma (HCC) of a human adult. This cell line is extensively used in liver cancer research to study the molecular mechanisms underlying hepatocarcinogenesis, tumor progression, and the development of therapeutic strategies. Hepatocellular carcinoma is a prevalent and deadly form of liver cancer, and SNU-398 cells provide a relevant model for investigating the genetic and epigenetic changes associated with this disease. SNU-398 cells exhibit an epithelial morphology and express markers characteristic of liver cancer, such as alpha-fetoprotein (AFP) and cytokeratins. They harbor genetic mutations and alterations typical of HCC, including mutations in the TP53 gene, which is commonly associated with many cancers. Researchers utilize SNU-398 cells to explore various signaling pathways involved in liver cancer, such as the Wnt/β-catenin, PI3K/Akt, and MAPK pathways. These cells are also employed in drug screening assays to evaluate the efficacy of chemotherapeutic agents and targeted therapies, as well as in studies investigating resistance mechanisms to conventional treatments. The SNU-398 cell line's importance in hepatocellular carcinoma research lies in its ability to model liver cancer biology and to contribute to the development of more effective therapies for liver cancer patients. |
|---|---|
| Organisme | Human |
| Tissu | Liver |
| Maladie | Adult hepatocellular carcinoma |
| Synonymes | SNU398, NCI-SNU-398 |
Caractéristiques
| Âge | 42 years |
|---|---|
| Genre | Male |
| Origine ethnique | Korean |
| Morphologie | Epithelial |
| Propriétés de croissance | Adherent |
Données réglementaires
| Référence | SNU-398 (Cytion catalog number 305274) |
|---|---|
| Niveau de biosécurité | 1 |
| NCBI_Numéro d'identification fiscale | 9606 |
| Cellosaurus - Numéro d'enregistrement | CVCL_0077 |
Données biomoléculaires
| Antigènes de surface | Blood Type 0, Rh + |
|---|---|
| Virus | Transformant: Hepatitis B virus (HBV) |
| Profil mutationnel | Mutation: CTNNB1, p.Ser37Cys (c.110C>G), heterozygous; Mutation: TP53, p.Ser215Ile (c.644G>T), heterozygous |
Manipulation
| Milieu de culture | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
|---|---|
| Suppléments | Supplement the medium with 10% heat-inactivated FBS, 25 mM HEPES |
| Réactif de dissociation | Accutase |
| Repiquage | 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. |
| Renouvellement des fluides | 2 to 3 times per week |
| Milieu de congélation | 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. |
| Décongélation et culture des cellules |
|
| Atmosphère d'incubation | 37°C, 5% CO2, humidified atmosphere. |
| Conditions d'expédition | 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. |
| Conditions d'entreposage | 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. |
Contrôle de la qualité et analyse moléculaire
| Stérilité | 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. |
|---|
Certificat d'analyse (CoA)
| Numéro de lot | Type de certificat | Date | Numéro de catalogue |
|---|---|---|---|
| 305274-280824 | Certificat d'analyse | 26. May. 2025 | 305274 |
| 305274-250326 | Certificat d'analyse | 04. May. 2026 | 305274 |
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