CL-0022
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Product Introduction
| Cell Name | AGS |
| Cellosaurus Accession | CVCL_0139 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | gastric cancer |
| Tissue | Stomach |
| Age | 54Y |
| Sex | Female |
| Instructions | 1. Check all containers for leakage or breakage. 2. Remove the frozen cells from the dry ice packaging and immediately transfer them to liquid nitrogen (liquid or vapor phase) for long-term cryopreservation. |
| Complete Medium | Ham's F-12 [PM150810]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:3-1:6 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 4-5 min |
| Subculturing Procedure | 1. Remove the culture medium from the T25 cell culture flask. 2. Add approximately 2 mL of PBS. Gently tilt the flask side to side until the PBS covers the entire bottom, then aspirate and discard the PBS. 3. Add 1 mL of 0.25% trypsin solution (containing EDTA). Gently tilt the flask side to side until the trypsin solution covers the entire bottom of the flask. 4. Incubate the cells at 37°C. Observe the cells under an inverted microscope and terminate digestion once the cells round up and detach. To avoid clumping, do not agitate the cells by tapping or shaking the flask during detachment. 5. Add 3 mL of complete culture medium to terminate digestion and disperse into a single cell suspension. 6. Collect the cell suspension and centrifuge at 1200 rpm (approximately 250 ×g) for 3 minutes. Carefully aspirate and discard the supernatant. 7. Add fresh complete culture medium, pipette gently several times to resuspend the cells, and seed them at the appropriate ratio into a new culture flask. Loosen the cap or use a vented cap for incubation. |
| Freeze Medium | Freezing Medium (Serum-free & animal origin-free) [PB180438] |
| Storage Conditions | For long-term cryopreservation, cryovials should be stored in liquid nitrogen at −150°C to −196°C. Storage at −80°C is restricted to short-term interim use only. |
| Background | AGS cells were derived from an untreated, resected tumor fragment. The plating efficiency of AGS cells has been reported to be 34%. |
| Tumorigenic | Yes, in athymic BALB/c mice. |
| Biosafety Level | BSL-2 |
Documents
Publications
Journal: PHYTOMEDICINE (2025) IF: 8.3
DOI: 10.1016/j.phymed.2025.157585
Product Cited: AGS Cells Line, MKN-45 Cells Line
Journal: SENSORS AND ACTUATORS B-CHEMICAL (2025) IF: 7.7
DOI: 10.1016/j.snb.2025.139061
Product Cited: AGS Cells Line, GES-1 Cells Line, MKN-28 Cells Line
Journal: JOURNAL OF MEDICINAL CHEMISTRY (2025) IF: 6.8
DOI: 10.1021/acs.jmedchem.5c00086
Product Cited: AGS Cells Line, HCT 116 Cells Line, Panc02 Cells Line, MCF7 [MCF-7] Cells Line, MDA-MB-231 Cells Line, A549 [A-549] Cells Line, MCF-7/ADM Cells Line, A549/DDP Cells Line, HL-7702 [L-02; LO2] Cells Line, AGS/DDP Cells Line, B16-F10 Cells Line, 3T3-L1 Cells Line
Journal: JOURNAL OF MEDICINAL CHEMISTRY (2025) IF: 6.8
DOI: 10.1021/acs.jmedchem.5c01034
Product Cited: DMEM (High glucose) Medium, Ham's F-12 Medium, Donor Equine Serum, Ham's F-12K Medium, DMEM/F12 Medium, IMDM Medium, GP2d Cells Line, Penicillin-Streptomycin Solution, 100 ×, CFPAC-1 Cells Line, Fetal Bovine Serum, AGS Cells Line, RPMI-1640 Medium
Journal: International Journal of Nanomedicine (2025) IF: 6.5
DOI: 10.2147/IJN.S523766
Product Cited: GES-1 Cells Line, AGS Cells Line, Human Umbilical Vein Endothelial Cells, HGC-27 Cells Line
