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Thalassemia test kit 30071
for genes

thalassemia test kit
thalassemia test kit
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Tested parameter
for genes


CapitalBio Thalassemia Gene Mutations Detection Kit is designed for a rapid and accurate genotyping of Thalassemia. Thalassemia is one of the most common monogenic hereditary blood diseases. It is caused by the deletion of or the mutation in globin-encoding genes which leads to hemolytic anemia. Its symptoms include bone deformities, enlarged spleen, iron overload, and lowered growth rate. Thalassemia major could result in death. Approximately 4.83% of the human population are carriers of Thalassemia-related gene mutations. As many as 500,000 babies with Thalassemia major are born every year. Genetic counseling is key to the prevention of Thalassemia. Covering 25 Thalassemia-related gene mutations, CapitalBio Thalassemia Gene Mutations Detection Kit is a useful tool for genetic counseling. ● High Throughput: As many as 25 gene mutations are detected simultaneously. α-Thalassemia and β-Thalassemia do not need to be detected separately. ● Rapid Detection: It takes only 4.5 hours to finish the testing process. ● Automatic Operation: Hybridization, washing, and scanning are all finished by instruments. No developing operation is needed. Reports are generated automatically by the software. ● High Traceability: Test results can be saved permanently and therefore are highly traceable.
*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.