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| Product Name | Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) ELISA Detection Kit |
| Catalog No. | DDGD-QCY-0054 |
| Description | This kit is specifically designed for detecting the cystic fibrosis transmembrane conductance regulator (CFTR) in human samples. CFTR gene mutations are the primary cause of cystic fibrosis. This kit assists in the clinical diagnosis of cystic fibrosis, genetic counseling, and research into related pathogenesis. |
| Application | This kit is designed to detect the levels of cystic fibrosis transmembrane conductance regulator (CFTR) in samples, providing analytical data for research into cystic fibrosis-related genetic disease. |
| Target Disease | Cystic fibrosis (CF) |
| Species | Homo sapiens (Human) |
| Assay Type | Double-antibody sandwich |
| Samples | Tissue homogenates, cell lysates and other biological fluids |
| Detection Range | 0.156-10 ng/mL |
| Sensitivity | 0.059 ng/mL |
| Test Time | 3 h |
| Storage | Store at 2-8°C away from light. |
For research use only, not for clinical use.
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