Transfected Stable Cell Lines
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Cat. No. : CSC-RI0207
Host Cell : HEK293 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RI0207 |
| Description | This cell line is engineered to stably express mouse transient receptor potential cation channel, subfamily V, member 1 (TRPV1) in HEK293 cells. |
| Target Gene | TRPV1 |
| Gene Species | Mus musculus (Mouse) |
| 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 | Trpv1 transient receptor potential cation channel, subfamily V, member 1 [ Mus musculus ] |
| Gene Symbol | Trpv1 |
| Synonyms | Vr1; VR-1; OTRPC1; TRPV1beta; TRPV1alpha |
| Gene Description | transient receptor potential cation channel, subfamily V, member 1 |
| GeneID | 193034 |
| Uni ProtID | Q704Y3 |
| mRNA Refseq | NM_001001445.1 |
| Protein Refseq | NP_001001445.1 |
| Chromosome Location | 11 44.1 cM; 11 B3 |
| Function | ATP binding; calcium activated cation channel activity; calcium channel activity; calcium-dependent protein kinase C activity; calmodulin binding; cation channel activity; cation channel activity; cation transmembrane transporter activity; chloride channel regulator activity; ion channel activity; nucleotide binding; |
| Pathway | Neuroactive ligand-receptor interaction, organism-specific biosystem; Neuroactive ligand-receptor interaction, conserved biosystem; serotonin and anxiety, organism-specific biosystem; |
Transient Receptor Potential Vanilloid 1 (TRPV1) is a non-selective cation channel predominantly expressed in sensory neurons and plays a crucial role in the detection of noxious stimuli, particularly heat and capsaicin. Its discovery in 1997 marked a significant milestone in understanding thermosensation and pain transduction mechanisms. Subsequently, the development of stable cell lines expressing Mouse TRPV1 in Human Embryonic Kidney 293 (HEK293) cells has provided a valuable tool for investigating TRPV1 pharmacology and function. This cellular model, established through stable transfection techniques, allows for controlled and reproducible studies on TRPV1-mediated signaling pathways and drug interactions. The availability of Mouse TRPV1 Stable Cell Line - HEK293 has greatly facilitated research into pain modulation, thermoregulation, and the development of TRPV1-targeted therapeutics.
The TRPV1 ion channel plays a critical role in detecting both thermal and chemical pain sensations. Researchers demonstrate TRPV1's role in thermal and chemical pain sensation. TRPV1 activation leads to Ca2+-dependent desensitization, including acute desensitization and tachyphylaxis. They reveal that the strength of stimulation regulates whole-cell TRPV1 tachyphylaxis. Using light-sheet microscopy and pH-sensitive sensor pHluorin, they observe TRPV1 endocytosis and exocytosis trafficking, linking tachyphylaxis to TRPV1 recycling to the plasma membrane. This activity-dependent trafficking, associated with distinct Ca2+ signals, involves synaptotagmin 1 and 7-mediated recycling routes, influen cing TRPV1 surface expression and nociceptive response.
Figure 1. TRPV1's role in synaptotagmin-mediated regulation of recycling was investigated by researchers. Syt1 facilitated TRPV1 recovery during capsaicin-induced tachyphylaxis. Low capsaicin-evoked TRPV1 recycling was facilitated by Syt1, not Syt7, in HEK cells expressing TRPV1 and Syt1. (Tian Q, et al., 2019)
Using Creative Biogene's Mouse TRPV1 Stable Cell Line - HEK293 in similar experiments could offer several improvements. Firstly, employing a stable cell line ensures consistent expression levels of TRPV1 across experiments, reducing variability. This stability allows for more reliable and reproducible results compared to transient transfections. Furthermore, the use of a stable cell line saves time and resources by eliminating the need for repeated transfections and selection processes, thereby streamlining experimental workflows.
1. Pain research: Assessing the analgesic potential of novel compounds by measuring TRPV1-mediated calcium influx in response to thermal or chemical stimuli.
2. Pharmacological studies: Evaluating the effects of TRPV1 agonists or antagonists on cellular signaling pathways implicated in pain transmission or inflammation.
3. Inflammatory response assays: Examining the impact of TRPV1 activation on cytokine release or immune cell recruitment in inflammatory conditions such as arthritis or colitis.
4. Drug delivery research: Assessing the efficacy of TRPV1-targeted drug delivery systems for site-specific pain relief or localized treatment of inflammatory disorders.
5. Functional characterization: Investigating the physiological roles of TRPV1 in sensory neurons or other cell types by analyzing its activation kinetics and downstream signaling events.
6. Disease modeling: Generating disease-specific TRPV1 mutant cell lines to mimic pathological conditions and explore potential therapeutic interventions.
7. Toxicity testing: Assessing the safety profiles of pharmaceutical compounds by monitoring TRPV1-mediated cytotoxicity or adverse effects on cellular viability.
A: HEK293 cells were likely selected for their robust expression machinery and suitability for heterologous expression of ion channels like TRPV1, enabling studies on its functional properties and pharmacology.
A: Stability was likely confirmed through methods such as calcium imaging, patch-clamp electrophysiology, or functional assays assessing TRPV1 activation by capsaicin or other ligands, with continuous selection pressure applied.
A: Characterization may involve analysis of TRPV1 subcellular localization, sensitivity to temperature and ligands, ion channel properties, and functional implications in pain perception and sensory signaling.
A: Quality control likely included screening for mycoplasma contamination, confirmation of stable transgene integration, and assessment of phenotypic stability and consistency.
A: Comparative analysis with sensory neurons or animal models helps validate the relevance of TRPV1 expression in pain pathways and its potential as a target for analgesic drugs or thermoregulatory agents.
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Exceptional quality! The Mouse TRPV1 Stable Cell Line in HEK293 cells has been a cornerstone in my pain research. Its stable expression of TRPV1 has provided reliable and reproducible results, facilitating detailed investigations into pain signaling pathways.
Reliable and consistent! The stable expression of TRPV1 in HEK293 cells has ensured the accuracy and precision of my experiments, allowing me to confidently explore the role of TRPV1 in pain perception and nociception.
Streamlining my studies! With the Mouse TRPV1 Stable Cell Line, I've been able to conduct high-throughput screening assays with ease. Its robust TRPV1 expression has simplified data interpretation and accelerated the pace of my research.
Impressive performance! The Mouse TRPV1 Stable Cell Line has exceeded my expectations in terms of reliability and efficiency. Its stable expression of TRPV1 has been invaluable in elucidating the molecular mechanisms underlying thermal and chemical pain sensations.
A valuable research tool! The Mouse TRPV1 Stable Cell Line has significantly advanced my understanding of TRPV1-mediated pain signaling. Its consistent performance has been instrumental in unraveling the complexities of pain perception and sensitization.
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