Thalassemia test kit dαTHA-RDB

for genotypingWhole Blood Genomicwhole blood

Alpha-thalassemia (α-thalassemia) is a kind of monogenic inheritance hemopathy due to expression imbalance of peptide chain caused by alpha -globin gene mutation of locus 16p13.3 of No. 16 chromosome. The common alpha -globin gene mutation types are three deletion types of -- SEA, -α 3.7 and -α 4.2 and three non-deletion types of αCSα, αQSα and αWSα. Intended Use This kit is used for the qualitative detection of human whole blood genomic DNA sample, which can detect the 3 common sorts of non-deletion type alpha-thalassemia gene mutation (αTthalassemia): αConstant Springα (αCSα), αQuong Szeα (αQSα) and αWestmeadα (αWSα). General Specification Sample Type: anti-coagulation whole blood Precision: CV <5% LoD: 10 ng/μL Packing Specifications 25 tests/kit (single test/tube) - 25 tests/kit (non-single test/tube) - 48 tests/lit (non-single test/tube)