FO-1 (MEL-CLS-1) Cells
1 104,00 CAD$*
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).
Renseignements généraux
| Description | The FO-1 cell line, also known as MEL-CLS-1, is a human amelanotic melanoma line derived from a metastatic site, specifically the iliac lymph node of a Caucasian patient. This cell line was established from a xenograft, further ensuring its utility in research focused on metastatic melanoma. Amelanotic melanoma, from which FO-1 originates, is characterized by the absence of melanin pigment, making it particularly valuable for studying melanoma subtypes that lack the typical pigmentation associated with these tumors. The FO-1 cell line exhibits a doubling time of approximately 38 hours, particularly noted at the 49th passage. This relatively fast growth rate makes it suitable for experiments requiring rapid cell proliferation. FO-1 cells are known for their differential sensitivity to various treatments, including their responsiveness to the differentiating and antiproliferative effects of interferon-beta (IFN-β) and 12-O-tetradecanoyl-phorbol-13-acetate (TPA), making them a critical model for studying the modulation of melanoma-associated antigens and HLA antigen expression under various experimental conditions. |
|---|---|
| Organisme | Human |
| Tissu | Skin |
| Maladie | Amelanotic melanoma |
| Site métastatique | Iliac lymph node |
| Synonymes | FO-1, FO #1, FO 1, MEL-CLS-1 |
Caractéristiques
| Âge | 54 years |
|---|---|
| Genre | Female |
| Origine ethnique | Caucasian |
| Propriétés de croissance | Adherent |
Données réglementaires
| Référence | FO-1 (MEL-CLS-1) (Cytion catalog number 300175) |
|---|---|
| Niveau de biosécurité | 1 |
| NCBI_Numéro d'identification fiscale | 9606 |
| Cellosaurus - Numéro d'enregistrement | CVCL_5619 |
Données biomoléculaires
| Expression des protéines | P53(+) |
|---|---|
| Tumorigène | Yes, in nude mice |
| Virus | Negative for: Sendai, Ectromelia, Polyoma, K-Virus, Kilham, Reo 3, PVM, LCM, M.pulmonis, MVM, Theiler's GD VII, Toolan's H-1, MHV, LDV, RCV/SDA, M-Adenovirus, B.piliformis. |
| Profil mutationnel | BRAF V600Emut |
| Caryotype | Modal number 51, range 38-56 |
Manipulation
| Milieu de culture | 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) |
|---|---|
| Suppléments | Supplement the medium with 10% FBS |
| Réactif de dissociation | Accutase |
| Repiquage | 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. |
| Densité de semis | 1 x 104 cells/cm2 |
| Renouvellement des fluides | Every 3 days |
| Rétablissement après le dégel | After thawing, plate the cells at 5 x 104 cells/cm2 and allow the cells to recover from the freezing process and to adhere for at least 24 hours. |
| Milieu de congélation | 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. |
| Décongélation et culture des cellules |
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| Atmosphère d'incubation | 37°C, 5% CO2, humidified atmosphere. |
| Conditions d'expédition | 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. |
| Conditions d'entreposage | 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. |
Contrôle de la qualité et analyse moléculaire
| Stérilité | 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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Certificat d'analyse (CoA)
| Numéro de lot | Type de certificat | Date | Numéro de catalogue |
|---|---|---|---|
| 300175-513 | Certificat d'analyse | 05. Dec. 2025 | 300175 |