CL-0505
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Product Introduction
| Cell Name | AN3 CA |
| Synonyms | AN3 CA;AN3 Ca;AN3CA;AN-3;AN3, AN3-CA |
| Cellosaurus Accession | CVCL_0028 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Tissue | Endometrium; derived from metastatic site: lymph node |
| Age | 55Y |
| 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 | MEM (ATCC modified) [PM150467]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:3-1:4 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 2-3 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 | The AN3 CA cell line was established in 1964. It was derived from a lymph node metastasis of a patient with endometrial cancer. It exhibits the basic characteristics of cancer cells, can be stably subcultured in vitro for long periods, and forms visible tumors when inoculated into experimental animals. However, the biological characteristics and ultrastructure of AN3 CA cells have not been fully characterized; only the absence of melanocyte-stimulating hormone synthesis has been reported. AN3 CA cells are commonly used in studies on the cell biology of human endometrial cancer and its related properties. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: ONCOLOGY RESEARCH (2026) IF: 4.1
Product Cited: AN3 CA Cells Line, HEC-1-B Cells Line, MEM, with NEAA
Journal: JOURNAL OF BIOLOGICAL CHEMISTRY (2026) IF: 3.9
DOI: 10.1016/j.jbc.2026.111447
Product Cited: Ishikawa Cells Line, AN3 CA Cells Line
Journal: BIOCHEMICAL GENETICS (2026) IF: 1.6
DOI: 10.1007/s10528-025-11309-7
Product Cited: RL95-2 Cells Line, KLE Cells Line, Ishikawa Cells Line, THP-1 Cells Line, AN3 CA Cells Line, Human Endometrial Epithelial Cell Complete Medium, HEC-1-A Cells Line
Journal: Cell Death & Disease (2025) IF: 9.6
DOI: 10.1038/s41419-025-07776-w
Product Cited: RL95-2 Cells Line, Human Endometrial Epithelial Cells, HEC-1-A Cells Line, AN3 CA Cells Line
Journal: CANCER SCIENCE (2025) IF: 4.5
DOI: 10.1111/cas.70015
Product Cited: Penicillin-Streptomycin Solution, 100 ×, Fetal Bovine Serum, DMEM (High glucose) Medium, HEC-1-A Cells Line, AN3 CA Cells Line, Ishikawa Cells Line, RL95-2 Cells Line
