Jiyoye Cells
USD$395.00*
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 | The Jiyoye cell line is an extensively studied model derived from a human Burkitt lymphoma. Burkitt lymphoma is a type of non-Hodgkin lymphoma that predominantly affects B cells, and the Jiyoye cell line retains many of the key characteristics of this malignancy. The cells exhibit the typical chromosomal translocation between the c-MYC gene and immunoglobulin gene loci, which is a hallmark of Burkitt lymphoma. This translocation leads to the overexpression of the c-MYC oncogene, driving the proliferative and aggressive nature of the tumor cells. As such, the Jiyoye cell line is an invaluable tool for studying the molecular and genetic mechanisms underlying lymphomagenesis, especially in the context of MYC-driven cancers. Jiyoye cells grow in suspension and are characterized by their high proliferation rate, which makes them suitable for a variety of experimental applications, including drug screening, gene expression studies, and apoptosis assays. The cell line is also frequently used in research focusing on Epstein-Barr virus (EBV), as Burkitt lymphoma cells, including Jiyoye, often harbor this virus, which is implicated in the pathogenesis of the disease. This makes Jiyoye particularly useful for investigating the interplay between viral oncogenes and cellular pathways in B cell malignancies. Given its origin and characteristics, the Jiyoye cell line is a critical model for oncological research, particularly in understanding the pathophysiology of B cell lymphomas. |
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| Organism | Human |
| Tissue | Lymphatic System |
| Disease | B-cell Non-Hodgkin-Lymphoma |
| Metastatic site | B-Lymphocyte |
| Applications | Analysis of B cell surface antigens, testing of cytotoxic drugs, mutational analysis, analysis of apoptotic mechanisms, haplotype standard. |
| Synonyms | JIYOYE, Jijoye, JIJOYE, P-2003, P3 (Jiyoye), P-3-Jijoye, P3-Jiyoye, P-3J, P3J, Jiyoye(P-2003), Jiyoye (P-2003), JiyoyeP-2003, OB2, GM04678 |
Characteristics
| Age | 7 years |
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| Gender | Male |
| Ethnicity | African |
| Cell type | B lymphocyte |
| Growth properties | Suspension |
Regulatory Data
| Citation | Jiyoye (Cytion catalog number 300366) |
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| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_1317 |
Biomolecular Data
| Antigen expression | CD10+, CD19+ |
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| Karyotype | 46, hypodiploid |
Handling
| Culture Medium | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
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| Supplements | Supplement the medium with 10% FBS |
| Subculturing | Maintain cultures by periodically adding or replacing the medium. Initiate cultures with a density of 5 x 105 cells/ml and keep the cell concentration within the range of 3 x 105 to 1 x 106 cells/ml for optimal growth. |
| Seeding density | 3 x 105 cells/ml |
| Fluid renewal | 2 to 3 times per week |
| Post-Thaw Recovery | Fast (48 hours) |
| 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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