SW480-Luc
CAD$1,072.26*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
General information
| Description | SW480-Luc is a bioluminescent derivative of the human SW480 colon adenocarcinoma cell line, engineered to stably express a firefly luciferase reporter gene. The parental SW480 cell line was established from a primary colon adenocarcinoma of a 51-year-old Caucasian male patient and is widely used as a model of primary colorectal cancer. SW480 cells exhibit epithelial-like morphology and harbor key oncogenic mutations including KRAS G12V, TP53 R273H and P309S, and APC truncation, making this line a relevant model for studying the role of Wnt/β-catenin and KRAS signaling in colorectal cancer. Importantly, SW480 was derived from the same patient as SW620 but represents the primary tumor, allowing comparative studies of primary versus metastatic colorectal cancer biology. The stable luciferase integration in SW480-Luc enables sensitive, quantitative bioluminescence imaging (BLI) of tumor burden in subcutaneous and orthotopic xenograft models using immunocompromised hosts. The emitted luminescent signal correlates with viable tumor cell number, supporting noninvasive longitudinal monitoring of tumor engraftment, growth kinetics, and therapeutic response. SW480-Luc is widely used for in vivo evaluation of KRAS-targeted agents, Wnt pathway inhibitors, and chemotherapeutic regimens in colorectal cancer, as well as for comparative studies with the matched metastatic SW620 line. SW480-Luc retains the established molecular characteristics of the parental SW480 line, including KRAS, TP53, and APC mutations. The luciferase modification substantially enhances experimental throughput and sensitivity for in vivo pharmacodynamic studies. Researchers should verify luciferase activity, mutational profile, and growth kinetics under their specific experimental conditions prior to large-scale preclinical use. |
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| Organism | Human |
| Tissue | Colon |
| Disease | Colon adenocarcinoma |
Characteristics
| Age | 51 years |
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| Gender | Male |
| Ethnicity | Caucasian |
| Morphology | Epithelial-like |
| Growth properties | Adherent |
Regulatory Data
| Citation | SW480-Luc (Cytion catalog number 305698) |
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| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_C8Y1 |
| GMO Status | GMO-S1: This cell line contains a stably integrated firefly luciferase reporter cassette (Luc2, codon-optimized) introduced via replication-incompetent lentiviral transduction. The resulting polyclonal cell population was maintained under puromycin selection (1–5 µg/mL). S1 containment is required. This classification applies only within Germany and may differ elsewhere. |
Biomolecular Data
| Receptors expressed | Epidermal growth factor (EGF), keratin (immunoperoxidase staining). Matrilysin, a metalloproteinase associated with tumor invasiveness, is not expressed. |
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| Protein expression | P53 protein; Luc2 (firefly, codon-optimized) |
| Antigen expression | HLA A2, B8, B17, blood type A, Rh+. Luc2 (firefly, codon-optimized) |
| Isoenzymes | G6PD, B, PGM1, 2, PGM3, 1, 6PGD, A, PEP-D, 1, ES-D, 1 |
| Tumorigenic | Yes, in nude mice |
| Viruses | Reverse transcriptase negative |
| Virus susceptibility | Human immunodeficiency virus (HIV, LAV) |
| Products | Carcinoembryonic antigen (CEA) 0.7 ng/106 cells/10 days, keratin, TGF-β. The cells have been reported to produce GM-CSF. |
| Mutational profile | Mutation: p.Gln1338Ter, Homozygous; Mutation: p.Gly12Val, Homozygous; Mutation: p.Arg273His, Heterozygous; Mutation: p.Pro309Ser, Heterozygous |
Handling
| Culture Medium | DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a) |
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| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | Accutase |
| Subculturing | Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium. |
| Split ratio | 1 to 3 |
| Seeding density | 1 to 3 x 104 cells/cm2 |
| Fluid renewal | 2 to 3 times per week |
| Freeze medium | As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability. |
| Thawing and Culturing Cells |
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| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| Shipping Conditions | Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage. |
| Storage Conditions | For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen. |