Trita^® Thalassemia Detection Kit

• Applying the fast and easy method of QF-PCR for simultaneous diagnosis of prenatal aneuploidy and beta thalassemia in a short time after sampling.
• Simultaneous amplification of 13 loci including STR and SD marker on chromosomes 13, 18, 21, X & Y as well as 4 STR markers with high heterozygosity in upstream and downstream of human beta-globin gene (HBB)
• Determining the status of being Beta-thalassemia carrier or patient in unborn child based on haplotype mapping
• Uses extracted DNA from amniotic fluid (AF), Chorionic villus sampling (CVS) or human peripheral blood
• Marker detection based on five-dye fluorescent system technology
• Result analysis by professional softwares such as GeneMapper® or GeneMarker®