CL-0441
$ 460.00
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1×10^6Cells/Vial×2Vials
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Product Introduction
General information
| Cell Name | SK-N-BE(2) |
| Synonyms | SK-N-BE2;SKNBE(2);SKNBE-2;SKNBE2;SK-N-BE;SKNBE |
| Cellosaurus Accession | CVCL_0528 |
| Organism | Human |
| Growth Properties | Semi-adherent and semi-suspension |
| Morphology | Neuroblast-like |
| Disease | neuroblastoma cells |
| Tissue | Brain; derived from metastatic site: bone marrow |
| Age | 2Y |
| Sex | Male |
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. |
| Complete Medium | MEM/F12 [PM151220]+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 | 1-2 min |
| Subculturing Procedure | 1. This cell line displays mixed adherent and suspended phenotypes. Although suspended cells remain viable, their density is low and they may be aspirated and discarded directly. 2. Rinse the adherent cells with PBS, then add 1–2 mL of 0.25% Trypsin-EDTA to the culture flask. Incubate at 37°C. Once the cells round up and detach from the vessel surface, add 4–6 mL of complete medium to terminate digestion. Gently pipette to generate a single-cell suspension, then harvest cells by centrifugation. 3. Seed the cells into fresh culture vessels at the recommended split ratio. |
| 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. |
Reference materials
| Background | The SK-N-BE(2) neuroblastoma cell line was established in November 1972 from a bone marrow biopsy taken from a child with disseminated neuroblastoma after repeated courses of chemotherapy and radiotherapy. SK-N-BE(2) cells exhibit moderate levels of dopamine-β-hydroxylase activity. It has been reported that the saturation density of SK-N-BE(2) cells exceeds 1 × 10⁶ cells/cm². The morphology of SK-N-BE(2) cells is variable, with some cells possessing long processes and others exhibiting an epithelioid appearance. The cells aggregate, form clumps, and float in the culture medium. |
| Tumorigenic | Yes, an inoculum of 1×10⁷ cells produced tumors in cortisonized hamster cheek pouches with 18% frequency. |
| Biosafety Level | BSL-1 |
Documents
Publications
Silencing of long chain noncoding RNA paternally expressed gene (PEG10) inhibits the progression of neuroblastoma by regulating microRNA-449a (miR-449a)/ribosomal protein S2 (RPS2) axis
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
HMGB3 is Associated With an Unfavorable Prognosis of Neuroblastoma and Promotes Tumor Progression by Mediating TPX2
Journal: Frontiers in Cell and Developmental Biology (2021) IF: 5.5
DOI: 10.3389/fcell.2021.769547
Product Cited: SK-N-SH Cells Line, SH-SY5Y [SHSY-5Y] Cells Line, SK-N-BE (2) Cells Line
