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| Size | Qty | Add To Basket |
|---|---|---|
| 1×48 T | ||
| 1×96 T |
| Product Description | The quantitative human MCP1 (glycosylated) sandwich ELISA kit is designed to detect human monocyte chemotactic protein 1 (MCP1) levels. MCP1 is a chemokine that attracts monocytes, macrophages, and T lymphocytes to sites of inflammation. It plays a crucial role in various inflammatory and immune responses. The kit is suitable for various biological samples such as tissue homogenates, cell lysates, serum, plasma. Its sensitivity is 6.956 pg/mL, which can accurately detect low concentrations of MCP1 in the sample. |
| Target | MCP1 |
| N-Glycosylation Site | 37 |
| Sample Types | Tissue homogenates, cell lysates, serum, plasma |
| Sample Volume | 100 μL |
| Sensitivity | 6.956 pg/mL |
| Detection Principle | Quantitative sandwich ELISA |
| Detection Range | 25 pg/mL-1000 pg/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 | Monocyte chemotactic protein 1 |
| Alternate Names | MCP1; Monocyte chemotactic protein 1; CCL2; GDCF2; MCAF; Chemokine C-C-motif ligand 2; Monocyte chemotactic and activating factor |
| Uniprot No. | P13500 |
| Application | The quantitative human MCP1 (glycosylated) sandwich ELISA kit is valuable in research investigating inflammatory diseases, such as atherosclerosis, rheumatoid arthritis, and inflammatory bowel disease, as well as in studies of cancer and fibrosis. Researchers utilize this ELISA to quantify MCP1 levels, providing insights into inflammatory processes 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, 90-105%; |
| Standard Curve | ![]() The standard curve is for reference only, and a new standard curve should be generated for each set of samples tested. |