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| Size | Qty | Add To Basket |
|---|---|---|
| 1×48 T | ||
| 1×96 T |
| Product Description | The quantitative human MFSD2A (glycosylated) sandwich ELISA kit is designed to detect human major facilitator superfamily domain containing protein 2A (MFSD2A) levels. MFSD2A is a transporter that is involved in the transport of lipids. MFSD2A is particularly important for transporting lipids across the blood-brain barrier. The kit is suitable for various biological samples such as tissue homogenates, cell lysates. Its sensitivity is 0.258 ng/mL, which can accurately detect low concentrations of MFSD2A in the sample. |
| Target | MFSD2A |
| N-Glycosylation Site | 230, 240 |
| Sample Types | Tissue homogenates, cell lysates |
| Sample Volume | 100 μL |
| Sensitivity | 0.258 ng/mL |
| Detection Principle | Quantitative sandwich ELISA |
| Detection Range | 2 ng/mL-40 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 | Major facilitator superfamily domain containing protein 2A |
| Alternate Names | MFSD2A; Major facilitator superfamily domain containing protein 2A; NLS1; Sodium-dependent lysophosphatidylcholine symporter 1 |
| Uniprot No. | Q8NA29 |
| Application | The quantitative human MFSD2A (glycosylated) sandwich ELISA kit is used to determine MFSD2A concentrations in biological specimens. This measurement is crucial for studies investigating lipid transport. It also contributes to understanding the role of MFSD2A in brain lipid metabolism. Furthermore, it is valuable in research exploring neurological diseases and blood-brain barrier functions. |
| 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. |