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JVM2 Cell Line

General Information
Organism Homo sapiens, human
Cell Line Description JVM-2 is a human mantle cell lymphoma (MCL) cell line derived from the peripheral blood of a 63-year-old female patient presenting with the leukemic phase of the disease. JVM-2 cells exhibit a lymphoblast-like morphology and grow primarily in suspension or as loose aggregates. Genetically, the cell line harbors the characteristic t(11;14)(q13;q32) chromosomal translocation, which juxtaposes the *CCND1* gene with the immunoglobulin heavy chain locus, resulting in the overexpression of cyclin D1. JVM-2 is unique among MCL models because it carries wild-type TP53 and is EBV-negative, making it a valuable model for studying B-cell lymphoproliferative disorders with functional TP53. Due to its stable growth characteristics and distinct molecular phenotype, JVM-2 is widely used to investigate the mechanisms of cyclin D1-mediated tumorigenesis, study B-cell receptor signaling pathways, evaluate targeted therapies such as BTK inhibitors, and conduct high-throughput drug screening.
Tissue Peripheral blood / Bone marrow
Disease Mantle Cell Lymphoma (MCL); Prolymphocytic Leukemia
Morphology Lymphoblast-like
Gender Female
Age 63 years
Product Format Frozen
Growth Mode Suspension
Biosafety Level 1 (Biosafety classification is based on U.S. Public Health Service Guidelines)
Applications 1. Research on the pathogenesis of mantle cell lymphoma (MCL) and the cyclin D1 signaling pathway;
2. Study on the response of TP53 wild-type B-cell malignancies to targeted therapies;
3. In vitro screening of BTK inhibitors, BCL-2 inhibitors, and novel chemotherapeutic agents;
4. Functional genomic analysis, target validation, and signal transduction profiling.
Shipped In Dry ice
Storage Temperature −196°C
Characteristics
Karyotype Aneuploid
Tumorigenic Yes, forms tumors in immunocompromised mice
Genetic Profile t(11;14)(q13;q32) translocation (CCND1/IGH fusion); CCND1 overexpression; TP53 wild-type
Expression Markers Cyclin D1 positive; CD19 positive; CD20 positive; CD23 positive; CD5 weak/positive; surface Ig (IgM/IgD) positive
Mycoplasma Test Negative
Culture Conditions and Handling
Subculturing 1. Maintain the culture by adding fresh medium or replacing the medium.
2. Establish the culture by centrifuging (1,000 rpm, 5 minutes) and resuspending the cells (at a density of 2 × 10⁵ to 4 × 10⁵ viable cells/mL).
3. Do not allow the cell concentration to exceed 1.5 × 10⁶ cells/mL.
4. Gently resuspend the cells to prepare a single-cell suspension before subculturing into a new culture vessel.
Medium Renewal Every 2 to 3 days
Subcultivation Ratio Maintain cell density between 2 × 10⁵ and 1.5 × 10⁶ cells/mL (split ratio approximately 1:2 to 1:4)
Culture Conditions Atmosphere: Air, 95%; CO2, 5%; Temperature: 37°C
Cryopreservation Complete growth medium supplemented with 5% to 10% (v/v) DMSO
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CSC-RO02654 Cas9 Stable Cell Line - JVM2 Inquiry

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* For research use only. Not intended for any clinical use.
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