β-thalassaemia gene mutation test kit

1. Comprehensive coverage: more comprehensive coverage of disease site detection, supplements for higher gene mutations in various regions, greatly reducing the risk of missed detection.
2. High accuracy: Detect samples with known missing types, and the results show the corresponding missing types, with an accuracy rate of over 99%.
3. Strong specificity: the detection of non-thalassemia human genomic DNA samples, the specificity is more than 99%.
4. Reliable technology: The technology platform has been recognized and verified by clinical and hospitals for many years.
5. Suitability: The conditions of use are simple and can be carried out by ordinary PCR laboratories.