CL-0300
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Product Introduction
| Cell Name | NCI-H661 |
| Synonyms | H661;H-661;NCIH661 |
| Cellosaurus Accession | CVCL_1577 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | lung cancer cells |
| Tissue | Lung |
| Age | 43Y |
| Sex | Male |
| 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 | RPMI-1640 [PM150110]+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 | General Freezing Medium [PB180436] |
| 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 | NCI-H661 cells were derived from a lymph node of a 43-year-old Caucasian male with large cell lung carcinoma. The cells show no ultrastructural or biochemical evidence of mucin production or squamous differentiation. NCI-H661 cells express readily detectable p53 mRNA at levels significantly higher than those in normal lung cells, while lacking gross structural DNA aberrations, suggesting the presence of point mutations or minor variants. The cells stain positive for keratin and vimentin filaments and negative for neurofilament triplet protein. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: CANCER LETTERS (2026) IF: 10.1
DOI: 10.1016/j.canlet.2026.218241
Product Cited: NCI-H661 Cells Line, NCI-H520 Cells Line, RPMI-1640, with HEPES Medium, Penicillin-Streptomycin Solution, 100 ×, HCC827 Cells Line, Fetal Bovine Serum, A549 Cells Line
Journal: CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS (2025) IF: 2.4
Product Cited: LTEP-a-2 Cells Line, NCI-H661 Cells Line
Journal: Evidence-based Complementary and Alternative Medicine (2022) IF: 2.7
DOI: 10.1155/2022/5049116
Product Cited: A549 [A-549] Cells Line, NCI-H1299 Cells Line, NCI-H460 [H460] Cells Line, SK-MES-1 Cells Line, NCI-H226 [H226] Cells Line, NCI-H661 Cells Line, BEAS-2B Cells Line, 16HBE Cells Line
