Thalassemia assay kit ndαTHA-MMC

whole bloodreal-time

Alpha thalassemia (α-thalassemia) is a kind of monogenic inheritance hemopathy due to expression imbalance of peptide chain caused by alpha-globin gene mutation. It is one of the most common and most harmful inherited diseases in various provinces in the south of China. The incidence of non- deletion α-thalassemia is also high in southern China, and the common genotypes are αCSα, αQSα and αWSα. Intended Use This kit is used for in vitro qualitative detection of whether human whole blood DNA sample is with alpha thalassemia non-deleted gene, which can detect three non-deletion type alpha thalassemia (αCS α, αQS α, αWS α) simultaneously. General Specification Sample Type: anti-coagulation whole blood Precision: CV <1% LoD: 2.5 ng/μL Packing Specifications 24 tests/kit - 48 tests/kit