CL-0790
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Product Introduction
| Cell Name | AC16 |
| Cellosaurus Accession | CVCL_4U18 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Tissue | Heart; Ventricle |
| 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 | DMEM/F12, with HEPES [PM150310]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:2-1:4 |
| 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 | AC16 Human Cardiomyocytes can be serially passaged and can differentiate when cultured in mitogen-free medium. The cells may be used to study developmental regulation of cardiomyocytes. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: JOURNAL OF MOLECULAR STRUCTURE (2025) IF: 4.7
DOI: 10.1016/j.molstruc.2025.144175
Product Cited: AC16 Cells Line
Journal: Frontiers in Cell and Developmental Biology (2025) IF: 4.3
DOI: 10.3389/fcell.2025.1628915
Product Cited: RPMI-1640 Medium, Penicillin-Streptomycin Solution, 100 ×, DMEM/F12, with HEPES Medium, THP-1 Cells Line, AC16 Cells Line, Fetal Bovine Serum
Journal: JOURNAL OF MOLECULAR MEDICINE-JMM (2025) IF: 4.2
DOI: 10.1007/s00109-025-02605-1
Product Cited: AC16 Cells Line
Journal: RSC Medicinal Chemistry (2025) IF: 4.1
DOI: 10.1039/D4MD00926F
Product Cited: MCF7 [MCF-7] Cells Line, A549 [A-549] Cells Line, HGC-27 Cells Line, MKN-28 Cells Line, 4T1 Cells Line, AC16 Cells Line, 293T [HEK-293T] Cells Line, BEL-7404 Cells Line, MDA-MB-468-06 Cells Line, SMMC-7721 Cells Line, MKN-45 Cells Line, HuH-7 Cells Line
Journal: Journal of Inflammation Research (2025) IF: 4.1
DOI: 10.2147/JIR.S523124
Product Cited: AC16 Cells Line, TNF-α/ TNFA/ TNFSF2, Human, Recombinant
