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| Size | Qty | Add To Basket |
|---|---|---|
| 1×48 T | ||
| 1×96 T |
| Product Description | The quantitative human CD1A (glycosylated) sandwich ELISA kit is designed to detect human T-cell surface glycoprotein CD1A (CD1A ) levels. CD1A is a non-classical MHC class I molecule that presents lipid antigens to T cells, particularly NKT cells, playing a role in immune surveillance and lipid-mediated immune responses. The kit is suitable for various biological samples such as tissue homogenates, cell lysates, serum, plasma. Its sensitivity is 0.086 ng/mL, which can accurately detect low concentrations of CD1A in the sample. |
| Target | CD1A |
| N-Glycosylation Site | 37, 60, 74, 145 |
| Sample Types | Tissue homogenates, cell lysates, serum, plasma |
| Sample Volume | 100 μL |
| Sensitivity | 0.086 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 | T-cell surface glycoprotein CD1A |
| Alternate Names | CD1A ; T-cell surface glycoprotein CD1A; CD1; FCB6; T6; T-cell surface antigen T6/Leu-6 |
| Uniprot No. | P06126 |
| Application | The quantitative human CD1A (glycosylated) sandwich ELISA kit is valuable in research investigating lipid antigen presentation, NKT cell biology, and diseases involving CD1A-expressing cells, such as Langerhans cell histiocytosis and certain T cell lymphomas. Researchers utilize this ELISA to quantify CD1A levels, providing insights into its role in immune responses and potential diagnostic or therapeutic applications. |
| 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, 85-100%; Plasma sample: n=4, 80-95%; |
| Standard Curve | ![]() The standard curve is for reference only, and a new standard curve should be generated for each set of samples tested. |