CL-0214
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Product Introduction
| Cell Name | SK-N-SH |
| Synonyms | SK N SH;SKN-SH;SK-NSH;SKNSH;NSH |
| Cellosaurus Accession | CVCL_0531 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | neuroblastoma cells |
| Tissue | Brain; derived from metastatic site: bone marrow |
| Age | 4Y |
| Sex | Female |
| 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 | MEM, with NEAA [PM150410]+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 | 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 | The SK-N-SH cell line was established by J.L. Biedler. In contrast to SK-N-MC cells, SK-N-SH cells exhibit a longer doubling time and higher dopamine-β-hydroxylase activity. SK-N-SH cells are widely used as a target cell line in cell-mediated cytotoxicity assays. |
| Antigen Expression | Blood Type A; Rh+ |
| Gene Expression | plasminogen activator, shows increased expression of M-CSF after treatment with amyloid-beta peptide. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: JOURNAL OF VIROLOGY (2022) IF: 6.549
DOI: 10.1128/jvi.01318-22
Product Cited: SK-N-SH Cell Complete Medium, SK-N-SH Cells Line
Journal: Frontiers in Oncology (2022) IF: 5.738
Product Cited: SK-N-SH Cells Line, SH-SY5Y [SHSY-5Y] Cells Line
Journal: International Immunopharmacology (2022) IF: 5.6
DOI: 10.1016/j.intimp.2021.108464
Product Cited: SK-N-SH Cells Line, SK-N-SH Cells Complete Medium
Journal: Bioengineered (2022) IF: 4.9
DOI: 10.1080/21655979.2022.2042999
Product Cited: Human Umbilical Vein Endothelial cells, SH-SY5Y [SHSY-5Y] Cells Line, SK-N-SH Cells Line, SK-N-AS Cells Line, SK-N-BE (2) Cells Line
Journal: Frontiers in Oncology (2022) IF: 4.7
Product Cited: SK-N-SH Cells Line, SH-SY5Y [SHSY-5Y] Cells Line
