HGC-27 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 | HGC-27 is a human gastric carcinoma cell line derived from the metastatic site of an adult patient. The cell line exhibits an epithelial morphology and is commonly used in the study of gastric cancer pathogenesis and the cellular responses to various chemotherapy agents. HGC-27 cells have been utilized in numerous studies to investigate mechanisms of cancer cell proliferation, apoptosis, and metastasis. They serve as a valuable model for understanding the complex molecular interactions and pathways involved in gastric cancer, including the response to therapeutic compounds and the investigation of novel drug targets. These cells are also instrumental in studying the role of various genetic and epigenetic modifications in gastric cancer progression. Research using HGC-27 has contributed to insights into cellular processes like epithelial-to-mesenchymal transition (EMT), a critical event in cancer metastasis. Additionally, the cell line has been used to explore receptor signaling pathways and their impact on cancer cell behavior, providing crucial data for the development of targeted therapies. Overall, HGC-27 is an important tool in the advancement of gastric cancer research, helping to pave the way for new therapeutic strategies and improving our understanding of disease mechanisms. |
|---|---|
| Organism | Human |
| Tissue | Gastric |
| Disease | Gastric adenocarcinoma |
| Metastatic site | Lymph node |
| Synonyms | HGC 27, HGC27 |
Characteristics
| Age | Unspecified |
|---|---|
| Gender | Unspecified |
| Morphology | Epithelial-like, polygonal or short spindle-shaped |
| Growth properties | Monolayer, adherent |
Regulatory Data
| Citation | HGC-27 (Cytion catalog number 300436) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_1279 |
Biomolecular Data
| Protein expression | P53 negative |
|---|---|
| Tumorigenic | Yes |
Handling
| Culture Medium | DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | Accutase |
| Doubling time | 17 hours |
| 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 | 1 to 2 x 104 cells/cm2 |
| Fluid renewal | 2 to 3 times per week |
| Post-Thaw Recovery | Start culture from cryovial at a cell density of 2 to 3 x 104 cells/cm2. The cells will recover within 24 to 48 hours. |
| 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 |
|---|---|---|---|
| 300436-614 | Certificate of Analysis | 23. May. 2025 | 300436 |
| 300436-613 | Certificate of Analysis | 05. Dec. 2025 | 300436 |
| 300436-510 | Certificate of Analysis | 23. May. 2025 | 300436 |