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| Product Name | Human Lysosomal Acid Alpha-Glucosidase (GAA) ELISA Kit |
| Catalog No. | DDGD-QCY-0042 |
| Description | This kit employs enzyme-linked immunosorbent assay technology to quantitatively detect lysosomal acid alpha-glucosidase (GAA) in human samples. GAA deficiency leads to lysosomal storage disorders such as Pompe disease. This kit provides a crucial tool for diagnosing these diseases, monitoring disease progression, and investigating their pathogenesis. |
| Application | This kit can be used to quantify the levels of human lysosomal acid alpha-glucosidase (GAA) in samples, providing diagnostic data for research into genetic disease associated with GAA deficiency, such as Pompe disease. |
| Target Disease | Pompe disease |
| Species | Homo sapiens (Human) |
| Assay Type | Sandwich |
| Samples | Serum, plasma, tissue homogenates, cell lysates |
| Detection Range | 25-1600 pg/mL |
| Sensitivity | 6.25 pg/mL |
| Test Time | 1-5 h |
| Storage | Store at 2-8°C. |
For research use only, not for clinical use.
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