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| Size | Qty | Add To Basket |
|---|---|---|
| 1×48 T | ||
| 1×96 T |
| Product Description | The quantitative human CXCR6 (glycosylated) sandwich ELISA kit is designed to detect human chemokine C-X-C-motif receptor 6 (CXCR6) levels. CXCR6 is a G protein-coupled receptor that binds to the chemokine CXCL16, playing a role in cell migration, adhesion, and immune responses. It is involved in various physiological and pathological processes, including inflammation and cancer metastasis. The kit is suitable for various biological samples such as tissue homogenates, serum, plasma. Its sensitivity is 0.125 ng/mL, which can accurately detect low concentrations of CXCR6 in the sample. |
| Target | CXCR6 |
| N-Glycosylation Site | 16 |
| Sample Types | Tissue homogenates, serum, plasma |
| Sample Volume | 100 μL |
| Sensitivity | 0.125 ng/mL |
| Detection Principle | Quantitative sandwich ELISA |
| Detection Range | 1 ng/mL-10 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 | Chemokine C-X-C-motif receptor 6 |
| Alternate Names | CXCR6; Chemokine C-X-C-motif receptor 6; CD186; STRL33; G-protein coupled receptor STRL33 |
| Uniprot No. | O00574 |
| Application | The quantitative human CXCR6 (glycosylated) sandwich ELISA kit is valuable for researchers studying inflammatory diseases, cancer, and HIV infection, where CXCR6 plays a significant role in cellular trafficking and disease progression. By quantifying CXCR6 levels, researchers can gain insights into its involvement in disease pathogenesis and explore potential therapeutic targets. |
| 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, 90-110%; Plasma sample: n=4, 90-110%; |
| Standard Curve | ![]() The standard curve is for reference only, and a new standard curve should be generated for each set of samples tested. |