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NRK-49F Cell Line

General Information
Organism Rattus norvegicus, rat
Cell Line Description NRK-49F is a spontaneously immortalized rat kidney fibroblast cell line characterized by contact inhibition. This cell line originated from a specific clone derived from a normal mixed-tissue culture sample of adult rat kidney submitted by J.E. DeLarco. NRK-49F cells grow as an adherent monolayer. Because the cell line can recapitulate the fibroblast-to-myofibroblast transition upon stimulation by exogenous cytokines, it is widely used to establish models of chronic kidney disease (CKD) and renal fibrosis. Furthermore, given its non-malignant phenotype and contact inhibition, it is globally recognized as a standard tool for assaying the biological activity of transforming growth factor-alpha (TGF-α) or sarcoma growth factor (SGF).
Tissue Kidney; derived from in situ renal tissue
Cell Type Fibroblast
Breed / Strain Osborne-Mendel
Disease Normal / Non-cancerous (Spontaneously immortalized)
Morphology Fibroblast-like; elongated or spindle-shaped cells
Product Format Frozen
Growth Mode Adherent
Biosafety Level 1 (Biosafety classification aligns with global laboratory guidelines for non-infectious animal materials)
Applications 1. A direct in vitro model of renal interstitial fibrosis and extracellular matrix (ECM) accumulation;
2. A standard model for detecting TGF-β1-induced myofibroblast activation and α-smooth muscle actin (α-SMA) expression;
3. A targeted bioassay tool for validating transforming growth factor-alpha (TGF-α) activity;
4. Investigation of toxicological cascades, drug-induced nephrotoxicity, and ferroptosis pathways in renal biology;
5. Evaluation of cellular mechanisms regulating contact inhibition and viral/chemical transformation networks.
Shipped In Dry ice
Storage Temperature −196°C (Liquid nitrogen vapor phase only)
Characteristics
Tumorigenic No, natively non-tumorigenic under normal baseline cultivation. However, the cells are exceptionally sensitive to malignant transformation if treated with specific chemical mutagens or oncogenic viruses.
Growth Property Baseline Highly contact-inhibited. Warning: Maintaining the culture at complete 100% confluence for extended periods will permanently trigger spontaneous transformation, causing cells to lose their normal contact-inhibition mechanism.
Expression Markers They synthesize and express the epidermal growth factor (EGF) receptor and exhibit binding characteristics for multiplication-stimulating activity (MSA). These cells respond strongly to exogenous transforming growth factor-beta (TGF-β), upregulating fibrosis-related transcripts such as collagen and α-SMA.
Growth Kinetics Moderate to rapid adherent expansion; population doubling time spans approximately 30 to 40 hours depending on passage numbers.
Mycoplasma Test Negative
Culture Conditions and Handling
Subculturing 1. Completely remove and discard the spent complete culture medium.
2. Briefly rinse the cell monolayer with a 0.25% trypsin-0.03% EDTA solution to thoroughly remove residual serum components.
3. Aspirate the rinse solution, add 1.0 to 2.0 mL of fresh trypsin-EDTA solution, and incubate the culture vessel at room temperature (or 37°C) until the cells detach and become rounded.
4. Immediately add fresh culture medium to completely neutralize the enzymatic reaction.
5. Gently pipette the cell suspension up and down to ensure a uniform cell dispersion, then transfer the cells to a new culture flask.
6. Critical Confluence Warning: To prevent unwanted phenotypic changes, ensure that subculturing is performed before the cells reach full confluency (typically 70–80% density).
Medium Renewal 2 times per week
Culture Conditions Atmosphere: Air, 95%; CO2, 5%; Temperature: 37°C
Cryopreservation 90% Complete culture growth medium + 10% DMSO

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