CL-0451
$ 360.00
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1×10^6Cells/Vial×2Vials
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Product Introduction
General information
| Cell Name | SW-13 |
| Cellosaurus Accession | CVCL_0542 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | renal carcinoma cells |
| Tissue | Adrenal gland; Cortex |
| Age | 55Y |
| Sex | Female |
Handling information
| 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. 3. Leibovitz's L-15 medium is recommended for this cell line. CO₂ supplementation is not recommended for Leibovitz's L-15 medium, as this may cause cytotoxicity. 4. If a CO₂-free incubator is not available, DMEM may be used as an alternative to Leibovitz's L-15. When using DMEM medium, 5% CO₂ can be supplied normally. |
| Complete Medium | Leibovitz's L-15 [PM151010]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 100% |
| 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. |
Reference materials
| Background | The SW-13 cell line was established in August 1971 from a 55-year-old Caucasian female patient with adrenal cortical carcinoma. The pathological diagnosis was primary grade IV small cell carcinoma of the adrenal cortex. Electron microscopy demonstrated numerous bulbous gap junctions (BGJ) in SW-13 cells. |
Documents
Publications
N7-methylguanosine regulatory genes well represented by METTL1 define vastly different prognostic, immune and therapy landscapes in adrenocortical carcinoma
Journal: American Journal of Cancer Research (2023) IF: 5.3
DOI: PMID:36895966
Product Cited: NCI-H295R Cells Line, SW-13 Cells Line
CDK1 serves as a therapeutic target of adrenocortical carcinoma via regulating epithelial–mesenchymal transition, G2/M phase transition, and PANoptosis
Journal: Journal of Translational Medicine (2022) IF: 8.4
DOI: 10.1186/s12967-022-03641-y
Product Cited: NCI-H295R Cells Line, SW-13 Cells Line, , NCI-H295R Cells Complete Medium
Identification of Seven Aberrantly Methylated and Expressed Genes in Adrenocortical Carcinoma
Journal: Frontiers in Endocrinology (2019) IF: 5.2
Product Cited: SW-13 Cells Line, NCI-H295R Cells Line
