Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-SC016682-1
Host Cell : HEK293 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-SC016682-1 |
| Description | HEK293-TRPM4 cell line is engineered to stably overexpress human TRPM4 gene. |
| Target Gene | TRPM4 |
| Gene Species | Homo sapiens (Human) |
| Host Cell | HEK293 |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1. Gene expression studies 2. Signaling pathway research 3. Drug screening and toxicology 4. Channelopathies research |
| Size | >1x106 frozen cells/vial |
| Stability | Validated for at least 10 passages |
| Quality Control | Negative for bacteria, yeast, fungi and mycoplasma. |
| Storage | Liquid nitrogen |
| Shipping | Dry ice |
| Revival | Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media. |
| Media Type | Cells were cultured in DMEM supplemented with 10% fetal bovine serum. |
| Growth Properties | Cells are cultured as a monolayer at 37°C in a humidified atmosphere with 5% CO2. Split at 80-90% confluence, approximately 1:3-1:6. |
| Freeze Medium | Complete medium supplemented with 10% (v/v) DMSO |
| Mycoplasma | Negative |
| Format | One frozen vial containing millions of cells |
| Storage | Liquid nitrogen |
| Safety Considerations |
The following safety precautions should be observed. 1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum. 2. No eating, drinking or smoking while handling the stable line. 3. Wash hands after handling the stable line and before leaving the lab. 4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells. 5. All waste should be considered hazardous. 6. Dispose of all liquid waste after each experiment and treat with bleach. |
| Ship | Dry ice |
| Gene Name | TRPM4 transient receptor potential cation channel, subfamily M, member 4 [ Homo sapiens ] |
| Gene Symbol | TRPM4 |
| Synonyms | TRPM4; transient receptor potential cation channel, subfamily M, member 4; transient receptor potential cation channel subfamily M member 4; FLJ20041; LTrpC4; hTRPM4; melastatin-4; long transient receptor potential channel 4; calcium-activated non-selective cation channel 1; PFHB1B; TRPM4B; |
| GeneID | 54795 |
| Uni ProtID | Q8TD43 |
| mRNA Refseq | BC132727 |
| Chromosome Location | 19q13.3 |
| Function | ATP binding; calcium activated cation channel activity; calcium channel activity; calmodulin binding; ion channel activity; nucleotide binding; |
| MIM | 606936 |
The TRPM4 gene encodes the transient receptor potential melastatin 4 protein, a calcium-activated non-selective cation channel that conducts monovalent cations such as sodium and potassium while being impermeable to calcium ions. This channel is widely expressed in cardiac tissue, pancreatic beta cells, immune cells, and neuronal populations, where it regulates membrane depolarization and calcium signaling dynamics. The Human TRPM4 Stable Cell Line - HEK293 is generated by transfecting the human TRPM4 gene into the HEK293 host cell line, followed by antibiotic selection to establish a homogenous population that stably and reproducibly expresses functional TRPM4 channels at the plasma membrane. This stable cell line eliminates the need for repeated transfections and provides consistent channel expression levels across passages, making it a reliable and convenient tool for TRPM4-related research.
This cell product is primarily designed for use in ion channel drug discovery and pharmacological profiling. Researchers can employ the Human TRPM4 Stable Cell Line - HEK293 in manual or automated patch-clamp electrophysiology studies to characterize channel kinetics, voltage dependence, and calcium sensitivity, as well as to screen compound libraries for novel TRPM4 inhibitors or activators. The stable expression system also supports fluorescence-based membrane potential assays using dyes, enabling high-throughput functional screening in a multi-well plate format. Beyond drug discovery, this cell line is valuable for investigating TRPM4-mediated signaling pathways, including its role in calcium influx regulation, cell volume control, and excitability modulation in heterologous expression systems. It can also be used to study disease-associated TRPM4 mutations identified in conditions such as progressive familial heart block or immune disorders, providing a defined cellular background for structure-function analysis. Additionally, the line may serve as a positive control for TRPM4 antibody validation or Western blotting workflows, and it can support downstream applications such as co-immunoprecipitation to identify channel-interacting proteins.
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The cells performed consistently in our TRPM4 functional studies and adapted well to our routine culture workflow. This stable expression system has been useful for channel characterization and preliminary compound evaluation.
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