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| Size | Qty | Add To Basket |
|---|---|---|
| 1×48 T | ||
| 1×96 T |
| Product Description | The quantitative human FAM132A (glycosylated) sandwich ELISA kit is designed to detect human family with sequence similarity 132, member A (FAM132A) levels. FAM132A is a member of the FAM132 protein family. Studies suggest it may be involved in cellular signaling pathways and potentially play a role in regulating cell growth or differentiation. The kit is suitable for various biological samples such as tissue homogenates, cell lysates. Its sensitivity is 0.063 ng/mL, which can accurately detect low concentrations of FAM132A in the sample. |
| Target | FAM132A |
| N-Glycosylation Site | 43 |
| Sample Types | Tissue homogenates, cell lysates |
| Sample Volume | 100 μL |
| Sensitivity | 0.063 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 | Family with sequence similarity 132, member A |
| Alternate Names | FAM132A; Family with sequence similarity 132, member A; C1QTNF12; Adipolin; Complement C1q tumor necrosis factor-related protein 12 |
| Uniprot No. | Q5T7M4 |
| Application | The quantitative human FAM132A (glycosylated) sandwich ELISA kit is used to determine FAM132A concentrations in biological samples. It proves valuable in exploratory research investigating the protein's role in cellular processes. This kit finds application in fields such as cell biology, proteomics, and potentially in studies related to diseases where FAM132A expression is altered. |
| 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, 80-90%; |
| Standard Curve | ![]() The standard curve is for reference only, and a new standard curve should be generated for each set of samples tested. |