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| Size | Qty | Add To Basket |
|---|---|---|
| 1×48 T | ||
| 1×96 T |
| Product Description | The quantitative human KIR2DS4 (glycosylated) sandwich ELISA kit is designed to detect human killer cell immunoglobulin like receptor 2DS4 (KIR2DS4) levels. KIR2DS4 is an activating receptor expressed on natural killer (NK) cells. KIR2DS4 triggers NK cell activation upon binding to its ligand. This receptor can enhance NK cell cytotoxicity. It plays a role in immune responses to infections and tumors. The kit is suitable for various biological samples such as tissue homogenates, cell lysates. Its sensitivity is 0.855 ng/mL, which can accurately detect low concentrations of KIR2DS4 in the sample. |
| Target | KIR2DS4 |
| N-Glycosylation Site | 67, 84, 144, 178, 211 |
| Sample Types | Tissue homogenates, cell lysates |
| Sample Volume | 100 μL |
| Sensitivity | 0.855 ng/mL |
| Detection Principle | Quantitative sandwich ELISA |
| Detection Range | 2.5 ng/mL-75 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 | Killer cell immunoglobulin like receptor 2DS4 |
| Alternate Names | KIR2DS4; Killer cell immunoglobulin like receptor 2DS4; CD158I; NKAT8; PAX; Natural killer-associated transcript 8; CD158 antigen-like family member I |
| Uniprot No. | P43632 |
| Application | The quantitative human KIR2DS4 (glycosylated) sandwich ELISA kit is used to measure glycosylated KIR2DS4 levels in samples. This measurement is important in research related to immunology and NK cell functions. The kit is applied in studies of conditions such as cancer and viral infections. |
| 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, 80-95%; Plasma sample: n=4, 80-100%; |
| Standard Curve | ![]() The standard curve is for reference only, and a new standard curve should be generated for each set of samples tested. |