RCC-FG2 Cells
CAD$1,104.00*
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 | Established from the renal clear cell carcinoma of a 77-years-old-male, pT2a, Nx, M1/ GII. HLA-A2 positive, PAS positive, G250 positive. |
|---|---|
| Organism | Human |
| Tissue | Kidney |
| Disease | Clear cell renal cell carcinoma, pT2a, Nx, M1/GII |
| Synonyms | KTCTL-26A, KTCTL-26a, KTCTL26A, RCCFG2 |
Characteristics
| Age | 77 years |
|---|---|
| Gender | Male |
| Ethnicity | Caucasian |
| Morphology | Epithelial-like |
| Growth properties | Monolayer, adherent |
Regulatory Data
| Citation | RCC-FG2 (Cytion catalog number 300249) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_5873 |
Biomolecular Data
| Surface antigens | Cytokeratine positive 8,18,19, vimentin positive |
|---|---|
| Receptors expressed | CAIx -/+, two peaks in FACS analysis, MAB2188. |
| Protein expression | IL8 |
| Tumorigenic | In nude mice |
| Ploidy status | Aneuploid |
| MSI-status | Instable (MSI low) |
| Mutational profile | IL8 RS1126647 3-UTR SNP A>T |
| Karyotype | 47,x, -Y,del(2)(p21),del(3)(p14), t(3,13)(p23,q32), +5, +7,der(9)t(5,9)(:q15->q33::p22), +16, -21, -22 (Högemann, 1994) |
Handling
| Culture Medium | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | Accutase |
| Doubling time | 24 to 48 hours |
| 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. |
| Seeding density | 2 x 104 cells/cm2 |
| Fluid renewal | 1 to 2 times per week |
| Freeze medium | As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress. |
| 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. |
Quality Control & Molecular Analysis
| Sterility | Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 300249-220925 | Certificate of Analysis | 05. Dec. 2025 | 300249 |
| 300249-720SF | Certificate of Analysis | 23. May. 2025 | 300249 |