Wilms10T Cells
US$ 800,00*
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).
Informações gerais
| Descrição | The Wilms10T cell line was derived from a primary Wilms tumor sample obtained from a patient with Wilms tumor, a pediatric nephroblastoma. This cell line is characterized by a homozygous deletion of the WT1 gene, leading to a complete loss of WT1 function, a critical gene involved in kidney development and the maintenance of normal renal differentiation. Unlike many other Wilms tumor cell lines, Wilms10T lacks any WT1 protein expression, which is reflective of the severe genetic alterations present in this tumor subtype. Additionally, the Wilms10T cell line exhibits loss of heterozygosity (LOH) in the 11p15 chromosomal region, which includes important genes like IGF2, further contributing to its tumorigenic properties. Wilms10T cells have a stable normal karyotype with no major chromosomal rearrangements apart from the specific deletion of the WT1 region. This cell line has been utilized extensively to study the effects of complete WT1 loss on tumor biology, including its impact on cell proliferation, differentiation, and response to various signaling pathways. The cells retain mesenchymal characteristics, expressing markers such as vimentin, while lacking epithelial markers like cytokeratin, indicative of their stromal origin. Significant research has focused on the signaling pathways active in Wilms10T cells. Proteomic studies have demonstrated that these cells show activation of several receptor tyrosine kinases (RTKs) such as IGF1R, PDGFRβ, and AXL, which are known to drive tumorigenesis. Additionally, downstream signaling pathways, including the MAPK and PI3K/AKT pathways, are activated in Wilms10T cells, contributing to their aggressive tumor phenotype. The comprehensive characterization of Wilms10T makes it a valuable model for investigating the molecular underpinnings of Wilms tumor with complete WT1 loss, as well as for exploring potential therapeutic targets in this aggressive tumor subtype. |
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| Organismo | Human |
| Tecido | Kidney |
| Doença | Wilms tumor |
| Aplicações | In vitro cell culture model and biochemical studies |
| Sinônimos | Wilms10 |
Características
| Idade | 2 years |
|---|---|
| Gênero | Female |
| Etnia | Caucasian |
| Morfologia | Spindle-shaped |
| Tipo de célula | Wilms cells |
| Propriedades de crescimento | Adherent |
Dados regulatórios
| Referência | Wilms10T (Cytion catalog number 300417) |
|---|---|
| Nível de biossegurança | 1 |
| NCBI_TaxID | 9606 |
| Número de acesso do Cellosaurus | CVCL_A5SL |
Dados biomoleculares
| Perfil mutacional | WT1 mutation status: homozygous del WT1 within del11p13. LOH: no in 11p13 but UPD in 11p15. CTNNB1 mutation status: homozygous del TCT, p.DS45, UPD 3p |
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Manuseio
| Meio de cultura | MSCGM kit (from Lonza) |
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| Reagente de dissociação | Accutase |
| Tempo de duplicação | 46 hours |
| Subcultura | 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. |
| Densidade de semeadura | 4 x 104 cells/cm2 |
| Renovação de fluidos | 1 to 2 times per week |
| Meio de congelamento | 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. |
| Descongelamento e cultura de células |
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| Atmosfera de incubação | 37°C, 5% CO2, humidified atmosphere. |
| Condições de envio | 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. |
| Condições de armazenamento | 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. |
Controle de Qualidade e Análise Molecular
| Esterilidade | 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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Certificado de Análise (CoA)
| Número do lote | Tipo de certificado | Data | Número de catálogo |
|---|---|---|---|
| 300417-221 | Certificado de Análise | 23. May. 2025 | 300417 |
| 300417-131025 | Certificado de Análise | 05. Dec. 2025 | 300417 |