Thalassemia and other Genetic Diseases

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Alpha Thalassemia Genotyping Kit -- αTHA-gapPCR

Clinical Application

The kit is used for in vitro qualitative detection of whether whole blood DNA samples carry α-thalassaemia deletion genes. The kit can detect three α-thalassemia deleted gene including --SEA, -α3.7and -α4.2.
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.

Intended Use

This kit is used for detection of whether whole blood DNA sample is with alpha-thalassemia deleted gene, which can detect three kinds of deletion types of alpha-thalassemia (-- SEA , -α3.7 , -α4.2 ) simultaneously.

General Specification

Methodology: gap-PCR
Sample Type: anti-coagulation whole blood
Precision: CV <5%
LoD: 2ng/μL

Packing Specifications

25 tests/kit

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