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Beta - Thalassemia [Conventional PCR amplification and gel electrophoresis technique]
Introducing our cutting-edge Beta-Thalassemia PCR detection kit, a revolutionary tool designed to streamline the diagnosis of this genetic disorder. Utilizing the robust Conventional PCR amplification method coupled with gel electrophoresis technique, our kit offers unparalleled accuracy and efficiency in identifying Beta-Thalassemia mutations. With its user-friendly design and optimized protocols, healthcare professionals can swiftly detect specific genetic variations associated with Beta-Thalassemia, enabling early intervention and personalized treatment strategies. Trust in our innovative solution to empower timely diagnosis, improve patient outcomes, and revolutionize the management of Beta-Thalassemia.
- Genotyping
ORDER INFORMATION
| REF | PACKAGE |
|---|---|
| B-THALQ/WBB/25 | 25 reactions |
| B-THALQ/WBB/100 | 100 reactions |
| INTENDED USER | For research use only and NOT intended for in vitro diagnostics. |
| TECHNOLOGY | Conventional PCR amplification and gel electrophoresis technique |
| TARGET MUTATIONS | The assay detects 7 common β-globin gene mutations: IVS 1-1 (G-> T), IVS 1-5 (G-> C), CD 8/9 (+G), CD 41/42 (-TCTT), 619 base pair deletion,CD5 (-CT) and CD15 (G-A) |
| TYPE OF ANALYSIS | Qualitative |
| Detected Genotypes | Wild and mutant alleles |
| Controls | Inhibition and extraction control, negative control, positive control |
| REPORTING UNITS | detected, not detected or inconclusive |
| VALIDATED SPECIMAN | Whole blood |
| STORAGE | -20 ± 5 °C |
| INSTRUMENTS | COMPATIBLE WITH A WIDE RANGE OF REAL-TIME PCR DEVICES |