NIH-3T3 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).
Essential facts about the NIH-3T3 cell line
| Description | NIH-3T3 cells are a fibroblast cell line derived from the tissue of a NIH Swiss mouse embryo. These cells are known for their spindle-shaped morphology and are widely utilized in scientific research due to their ability to grow rapidly and to a high cell density. NIH-3T3 cells are particularly noted for their utility in genetic studies, including DNA transfection experiments, where they are used to introduce foreign DNA into their genomes. This has made them a valuable tool for studying gene function and regulation. Additionally, NIH-3T3 cells are employed in oncogenic research, specifically in assays for the identification and characterization of cancer-causing genes. They have a remarkable capacity to support the propagation of various types of viruses, including sarcoma and leukemia viruses, making them integral to virology studies. One of the key features of the NIH-3T3 cell line is its spontaneous immortalization. This characteristic, combined with their genetic stability over continuous passaging, makes NIH-3T3 cells an exemplary model system for exploring cellular processes, signaling pathways, and the effects of various pharmacological treatments in mammalian cells. Characterized by a heterogeneous cell population, NIH 3T3 mouse cells underscore the intrinsic cellular heterogeneity within fibroblast subtypes, which is critical for deciphering the complex interplay between cellular composition and tissue architecture. These cells exhibit a spindle-like morphology on a chitosan surface, transitioning to an elongated form on OCMCS (oxidized cellulose) surfaces. The NIH3T3 cell line ontology encompasses various subclones, including 3T3-L1, a model for adipogenesis, and 3T3-J2, employed as a feeder layer in keratinocyte cultures, illustrating the cellular line's broad applicability across different proliferation rates and research disciplines. NIH-3T3 cells are pivotal in research for their rapid growth, spindle-shaped morphology, and versatility in genetic and oncogenic studies. Their spontaneous immortalization and genetic stability enhance their utility in exploring cellular dynamics and pharmacological effects. The diversity within this cell line, including its response to various substrates and the existence of specialized subclones like 3T3-L1 and 3T3-J2, underscores its broad applicability and critical role in advancing our understanding of cellular behavior and disease mechanisms. |
|---|---|
| Organism | Mouse |
| Tissue | Embryonic |
| Applications | Transfection host |
| Synonyms | NIH/3T3, NIH 3T3, NIH3T3, 3T3, 3T3NIH, 3T3-Swiss, Swiss-3T3, Swiss/3T3, Swiss 3T3, Swiss3T3 |
Details
| Breed/Subspecies | NIH Swiss |
|---|---|
| Age | Embryo |
| Gender | Male |
| Morphology | Spindle-like morphology, indicative of their fibroblast nature |
| Cell type | Fibroblast |
| Growth properties | Adherent |
Specifications
| Citation | NIH-3T3 (Cytion catalog number 400101) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_0594 |
Genetic profile of the fibroblast cell line
| Viruses | MAP-test: Negative. |
|---|
Culturing methods
| Culture Medium | DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | Accutase |
| Subculturing | Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium. |
| Fluid renewal | 2 times per week |
| 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 assurance of the NIH 3T3 cell line
| 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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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 400101-161224 | Certificate of Analysis | 18. Aug. 2025 | 400101 |
| 400101-1420 | Certificate of Analysis | 23. May. 2025 | 400101 |
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Required products
Required products
Antibiotic/Antimycotic Solution (100x)Product Overview
Volume: 100 ml
Storage: ≤-15°C
Sterility: Sterile-filtered
Antibiotic/Antimycotic Solution (100x) is a sterile, ready-to-use concentrate designed to reduce microbial contamination risks in cell culture and related laboratory applications. This 100x solution contains a well-established combination of penicillin, streptomycin, and amphotericin B—providing broad-spectrum antimicrobial activity against Gram-positive and Gram-negative bacteria, yeasts, and filamentous fungi. The formulation is suitable for use in eukaryotic cell cultures, bacterial media, and other contamination-sensitive systems, supporting clean and consistent lab operations.
Application and Benefits Optimized for routine research protocols, this solution is widely used to maintain aseptic conditions in cell culture workflows. It offers reliable performance in contamination-sensitive environments, helping researchers reduce the risk of microbial overgrowth without compromising cell health or experimental reproducibility. The sterile-filtered formulation eliminates the need for additional solubilization steps, supporting streamlined media preparation and reducing variability in daily lab procedures.
Usage and Compatibility To achieve standard working concentrations, dilute the solution 1:100 into your complete culture medium. The product is compatible with a broad range of mammalian cell lines and basal media. With consistent stock availability, researchers benefit from dependable supply continuity and simplified logistics planning. The solution should be stored at ≤ –15 °C and protected from repeated freeze-thaw cycles to maintain stability. For research use only. Not for use in diagnostic or therapeutic procedures. Not for use in humans or animals.USD$45.00* -
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