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RBL-2H3 Cell Line

General Information
Organism Rattus norvegicus, rat
Cell Line Description RBL-2H3 is a histamine-releasing cell line derived from rat basophilic leukemia. It is widely considered the gold standard model for studying IgE-mediated degranulation, mast cell activation, and immediate-type hypersensitivity (allergy) pathways. These cells express a high-affinity IgE receptor (FcεRI) on their surface. When an antigen cross-links with the surface-bound IgE, RBL-2H3 cells rapidly undergo exocytosis, releasing histamine, β-hexosaminease, and various cytokines, among other inflammatory mediators. Due to its stable and reproducible response, this cell line is widely used in pharmacology and immunology for screening anti-allergic compounds and studying signal transduction mechanisms.
Tissue Peripheral blood
Disease Basophilic Leukemia
Morphology Fibroblastic; Epithelial-like
Gender Not specified
Age Adult
Product Format Frozen
Growth Mode Adherent
Biosafety Level 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Applications 1. Research on IgE-mediated mast cell degranulation and allergic reactions
2. Screening of antihistamines and anti-allergy drugs
3. Research on FcεRI receptor signaling and membrane transport
4. Research on calcium signaling and inflammatory mediator release
5. Development of biosensors for detecting environmental allergens
Shipped In Dry ice
Storage Temperature −196°C
Characteristics
Karyotype Aneuploid; highly variable chromosomal number
Tumorigenic Yes, in syngeneic rats
Expression Markers High-affinity IgE receptor (FcεRI); rat mast cell protease (RMCP)
Secretory Products Histamine; β-hexosaminease; leukotrienes; cytokines (e.g., TNF-α)
Mycoplasma Test Negative
Culture Conditions and Handling
Subculturing 1. Remove and discard the culture medium.
2. Briefly rinse the cell layer with PBS (without Ca2+/Mg2+) to remove all traces of serum.
3. Add 2.0 to 3.0 mL of 0.25% Trypsin - 0.53 mM EDTA solution and observe under an inverted microscope until the cell layer is dispersed (usually 5 to 10 minutes).
4. Add 6.0 to 8.0 mL of complete growth medium and gently pipette to obtain a single-cell suspension.
5. Aliquot cell suspension into new culture vessels.
Medium Renewal 2 to 3 times per week
Subcultivation Ratio A split ratio of 1:3 to 1:6 is recommended
Culture Medium MEM or DMEM supplemented with 15% Fetal Bovine Serum (FBS) and 1% Penicillin-Streptomycin.
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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* For research use only. Not intended for any clinical use.
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