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: BIOCHEMICAL PHARMACOLOGY (2026) IF: 5.6
DOI: 10.1016/j.bcp.2026.117809
Product Cited: NCI-H520 Cells Line, RPMI-1640 Medium, SPC-A-1 Cells Line, NCI-H1299 Cells Line, A549 Cells Line, Fetal Bovine Serum, DMEM (High glucose) Medium
Journal: AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY (2026) IF: 5.3
Product Cited: NCI-H1299 Cells Line, LLC Cells Line, NCI-H441 Cells Line
Journal: Communications Biology (2026) IF: 5.1
DOI: 10.1038/s42003-026-10004-6
Product Cited: NCI-H1299 Cells Line
Journal: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2026) IF: 4.9
DOI: 10.3390/ijms27041693
Product Cited: MDA-MB-231 Cells Line, PC-3M Cells Line, A549 Cells Line, NCI-H1299 Cells Line, Hep G2 Cells Line, LLC Cells Line
Journal: Frontiers in Pharmacology (2026) IF: 4.8
DOI: 10.3389/fphar.2026.1785207
Product Cited: RPMI-1640 Medium, 0.25% Trypsin Solution, with EDTA, dissolved in PBS, Phosphate Buffer (PBS, 1 ×) , Penicillin-Streptomycin Solution, 100 ×, NCI-H1299 Cells Line, NCI-H460 Cells Line
