CL-0165
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Product Introduction
| Cell Name | NCI-H1299 |
| Synonyms | H1299;H-1299;NCIH1299 |
| Cellosaurus Accession | CVCL_0060 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | lung cancer cells |
| Tissue | Lung; derived from metastatic site: lymph node |
| 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 | 1:3-1:6 |
| 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 | NCI-H1299 cells were derived from a lymph node metastasis of a patient who had received prior radiation therapy. The cells harbor a homozygous partial deletion of the p53 gene and lack p53 protein expression. NCI-H1299 cells can synthesize neuromedin B (NMB) at 0.1 pmol/mg protein but do not produce gastrin-releasing peptide (GRP). |
| Gene Expression | These cells stain positive for keratin and vimentin but are negative for neurofilament triplet protein. neuromedin B, The cells have a homozygous partial deletion of the p53 protein, and lack expression of p53 protein. The cells produce neuromedin B. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: iScience (2025) IF: 4.6
DOI: 10.1016/j.isci.2025.112343
Product Cited: A-375 Cells Line, NCI-H460 [H460] Cells Line, MCF7 [MCF-7] Cells Line, NCI-H1299 Cells Line, A549 [A-549] Cells Line
Journal: INTERNATIONAL JOURNAL OF ONCOLOGY (2025) IF: 4.5
Product Cited: NCI-H1299 Cells Line, A549 [A-549] Cells Line
Journal: BIOORGANIC CHEMISTRY (2025) IF: 4.5
DOI: 10.1016/j.bioorg.2025.108509
Product Cited: NCI-H1299 Cells Line, A549 [A-549] Cells Line, BEAS-2B Cells Line, NCI-H460 [H460] Cells Line
Journal: Frontiers in Pharmacology (2025) IF: 4.4
DOI: 10.3389/fphar.2025.1575840
Product Cited: NCI-H1299 Cells Line, 293 [HEK-293] Cells Line
Journal: CANCER BIOLOGY & THERAPY (2025) IF: 4.4
DOI: 10.1080/15384047.2025.2501780
Product Cited: A549 [A-549] Cells Line, NCI-H1299 Cells Line
