Product Features:
1. Accurate and Reliable Results, Avoiding Missed Diagnosis:
For α-thalassemia genotypes of -α3.7/αα and -α4.2/αα (carriers of these two genes are clinically almost asymptomatic), MCV and MCH levels may be normal in routine blood tests. Genetic testing can avoid missed diagnoses in these genotypes and provide an accurate auxiliary diagnostic tool.
2. Excellent Precision and Sensitivity:
Precision tests demonstrated good intra- and inter-batch reproducibility, with consistent band positions. Analytical Detection Limit (LDL) tests indicated that this kit can stably detect genomic DNA at a minimum concentration of 2 ng/µL.
3. Automated Detection System:
Whole blood sample processing is compatible with a fully automated nucleic acid extraction system, offering simple operation and high throughput, significantly reducing time and labor costs.
4. Detection of the α-thalassemia THAI deletion gene: Detection of the rare THAI deletion genotype is crucial for genetic counseling and prenatal genetic diagnosis of α-thalassemia.
