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| Size | Qty | Add To Basket |
|---|---|---|
| 1×48 T | ||
| 1×96 T |
| Product Description | The quantitative human TRPM8 (glycosylated) sandwich ELISA kit is designed to detect human transient receptor potential cation channel subfamily M, member 8 (TRPM8) levels. TRPM8 is an ion channel protein that is activated by cold temperatures and cooling agents like menthol. This channel is expressed in sensory neurons and plays a crucial role in cold sensation. The kit is suitable for various biological samples such as tissue homogenates, cell lysates. Its sensitivity is 0.133 ng/mL, which can accurately detect low concentrations of TRPM8 in the sample. |
| Target | TRPM8 |
| N-Glycosylation Site | 934 |
| Sample Types | Tissue homogenates, cell lysates |
| Sample Volume | 100 μL |
| Sensitivity | 0.133 ng/mL |
| Detection Principle | Quantitative sandwich ELISA |
| Detection Range | 0.55 ng/mL-15 ng/mL |
| Detection Time | 1 h-5 h |
| Detection Wavelength | 450 nm |
| Storage | Store at 2-8°C for long term storage. |
| Species | Human |
| Full Name | Transient receptor potential cation channel subfamily M, member 8 |
| Alternate Names | TRPM8; Transient receptor potential cation channel subfamily M, member 8; LTRPC6; TRPP8; CMR1; Long transient receptor potential channel 6; Transient receptor potential p8 |
| Uniprot No. | Q7Z2W7 |
| Application | The quantitative human TRPM8 (glycosylated) sandwich ELISA kit is designed for the quantitative measurement of glycosylated TRPM8 levels in biological samples. The kit is applicable in studies of sensory biology, cold sensation, and pain. It is useful in fields such as neurobiology and pharmacology. |
| Kit Components | Pre-coated ELISA plate; Lyophilized standard; Biotin-labeled antibody; HRP-avidin; Various diluents; Wash buffer; TMB chromogenic substrate; Stop solution |
| Precision | Intra-Assay: n=20, CV <8%; Inter-Assay: n=20, CV <10%; |
| Recovery | Serum sample: n=5, 95-110%; Plasma sample: n=4, 85-100%; |
| Standard Curve | ![]() The standard curve is for reference only, and a new standard curve should be generated for each set of samples tested. |