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JJN-3 Cell Line

General Information
Organism Homo sapiens, human
Cell Line Description JJN-3 is a human plasma cell leukemia cell line derived from the bone marrow of a 57-year-old female patient suffering from plasma cell leukemia—an aggressive, terminal-stage variant of multiple myeloma. JJN-3 cells exhibit a lymphoblast-like morphology and grow in suspension as single cells or small clusters. The cell line secretes immunoglobulin light chains (Ig-kappa) and retains biological characteristics typical of advanced plasma cell malignancies. Genetically, JJN-3 harbors complex chromosomal rearrangements—including the t(14;16)(q32;q23) translocation that drives MAF oncogene overexpression—as well as mutations in the TP53 and KRAS genes. Given its aggressive tumor phenotype and distinct genomic alterations, JJN-3 has become a valuable in vitro model for studying the pathogenesis of multiple myeloma and plasma cell malignancies, evaluating novel therapeutic agents, investigating mechanisms of drug resistance, and screening targeted anti-myeloma drugs.
Tissue Bone marrow
Disease Plasma Cell Leukemia; Multiple Myeloma
Morphology Lymphoblast-like
Gender Female
Age 57 years
Product Format Frozen
Growth Mode Suspension
Biosafety Level 1 (Biosafety classification is based on U.S. Public Health Service Guidelines)
Applications 1. Biological research on multiple myeloma and plasma cell leukemia;
2. Research on MAF oncogene regulation and KRAS/TP53 pathway signaling;
3. Evaluation of novel anti-myeloma compounds and targeted immunotherapeutic strategies;
4. High-throughput screening and functional genomics research on mechanisms of drug resistance.
Shipped In Dry ice
Storage Temperature −196°C
Characteristics
Karyotype Hyperdiploid / Aneuploid
Tumorigenic Yes, forms tumors in immunocompromised mice
Genetic Profile t(14;16)(q32;q23) translocation (IGH/MAF fusion); TP53 mutation; KRAS mutation
Expression Markers Secretes immunoglobulin light chains (Ig-kappa); CD38 positive; CD138 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 × 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 × 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
Cat.No.Product NamePrice
CSC-RR01199 Nluc Reporter Cell Line - JJN-3 Inquiry

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