KU-19-19 Cells
USD$500.00*
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 | KU-19-19 is a human bladder carcinoma cell line established from an adult male patient with metastatic transitional cell carcinoma of the bladder. The cell line exhibits epithelial morphology and grows adherently under standard culture conditions. KU-19-19 has been characterized as a constitutive producer of multiple hematopoietic growth factors, demonstrating robust cytokine secretion activity in vitro. Conditioned medium derived from KU-19-19 cultures strongly stimulates proliferation of growth factor-dependent hematopoietic cell lines, indicating functional secretion of biologically active cytokines. Biochemical analyses of KU-19-19-conditioned medium have documented high levels of granulocyte colony-stimulating factor (G-CSF), exceeding 5 ng/mL, along with detectable secretion of granulocyte-macrophage colony-stimulating factor (GM-CSF), macrophage colony-stimulating factor (M-CSF), stem cell factor (SCF), interleukin-6 (IL-6), and interleukin-8 (IL-8). Functional proliferation assays using cytokine-dependent leukemia cell lines, including myeloid and megakaryocytic models, have confirmed that KU-19-19-derived factors significantly enhance DNA synthesis as measured by thymidine incorporation. The proliferative response is dose-dependent and observed across a broad panel of hematopoietic cell lines, underscoring the biological potency of secreted factors. Cytokine production in KU-19-19 cells is modulated by external stimuli. Short-term exposure to phorbol ester (TPA), interleukin-1β, or interferon-γ results in increased secretion of G-CSF, GM-CSF, and M-CSF, demonstrating that multiple regulatory signaling pathways control cytokine expression in this model. These properties make KU-19-19 a valuable in vitro system for studying tumor-derived cytokine production, tumor-hematopoietic cell interactions, and the regulation of growth factor secretion in bladder carcinoma. |
|---|---|
| Organism | Human |
| Tissue | Urinary bladder |
| Disease | Bladder carcinoma |
| Synonyms | KU 19-19, KU19-19, KU1919, Keio University-19-19 |
Characteristics
| Age | 76 years |
|---|---|
| Gender | Male |
| Ethnicity | Japanese |
| Growth properties | Adherent |
Regulatory Data
| Citation | KU-19-19 (Cytion catalog number 305517) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_1344 |
Biomolecular Data
| Mutational profile | Mutation: p.Glu17Lys, Unspecified |
|---|
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% heat-inactivated FBS |
| Doubling time | ~48 hours |
| Freeze medium | As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability. |
| Thawing and Culturing Cells |
|
| 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
Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305517-171125 | Certificate of Analysis | 08. Jan. 2026 | 305517 |