M-1 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).
General information
| Description | The M-1 cell line is a well-characterized epithelial model derived from the kidney of a transgenic adult mouse. Specifically, M-1 cells originate from the cortical collecting duct epithelium and retain many differentiated features of this nephron segment. These cells express markers typical of cortical collecting duct cells, including epithelial sodium channels (ENaC), aquaporins, and tight junction proteins, making them a widely used in vitro model for renal physiology, ion transport, and epithelial polarity studies. Functionally, M-1 cells exhibit high transepithelial resistance and vectorial ion transport properties, which are critical for studying aldosterone-regulated sodium reabsorption and vasopressin-mediated water transport. According to the foundational characterization by Stoos et al., M-1 cells form polarized monolayers on permeable supports and show appropriate responsiveness to hormonal stimuli, such as dexamethasone and aldosterone, that regulate transport protein expression and activity. These features make M-1 cells particularly valuable in dissecting mechanisms of electrolyte handling and cellular signaling in kidney epithelial cells. Moreover, M-1 cells have been validated in more recent studies, including genetic authentication using STR profiling for mouse cell lines. This underscores their continued relevance and reliability in contemporary renal physiology research. Their ability to recapitulate in vivo-like behaviors under controlled conditions has established them as a standard in studies on epithelial function, nephrotoxicity, and renal disease modeling. |
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| Organism | Mouse |
| Tissue | Kidney, cortical collecting duct |
| Synonyms | M1-CCD |
Characteristics
| Breed/Subspecies | Tg(SV40E)Bri/7 transgenic |
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| Age | Unspecified |
| Gender | Unspecified |
| Morphology | Epithelial |
| Growth properties | Adherent |
Regulatory Data
| Citation | M-1 (Cytion catalog number 305261) |
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| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_8786 |
| GMO Status | GMO-S1: This murine collecting duct cell line (M-1) contains the early region of SV40 from a transgenic mouse line (Tg(SV40E)Bri7), supporting stable immortalization. The construct is endogenously integrated in the transgenic background. This classification applies only within Germany and may differ elsewhere. |
Biomolecular Data
| Viruses | Simian virus 40 (SV40) |
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Handling
| 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) |
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| Supplements | Supplement the medium with 5% FBS, 5 µM dexamethasone |
| 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. |
| 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 Control & Molecular Analysis
| 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 |
|---|---|---|---|
| 305261-060924 | Certificate of Analysis | 23. May. 2025 | 305261 |