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PCR Kit For Gene Detection of α-Thalassemia Deletions TELLGEN Life Science is dedicated in the developing of Thalassemia related diagnostic test kits for clinical and research use.
Thalassemia is the name of a group of genetic blood disorders. Hemoglobin is the oxygen-carrying component of the red blood cells. It consists of two different proteins, an alpha and a beta. If the body doesn't produce enough of either of these two proteins, the red blood cells do not form properly and cannot carry sufficient oxygen. People whose hemoglobin does not produce enough alpha protein have alpha thalassemia. People whose hemoglobin does not produce enough beta protein have beta thalassemia.
PCR Kit For Gene Detection of α-Thalassemia Deletions α-Thalassemia is a common single-gene disease, which is characterized by a reduction or complete absence of α-globin gene expression. As the majority of α-thalassemia is mainly caused by a few common deletions such as - α 3.7, -α 4.2, --SEA. PCR Kit For Gene Detection of α-Thalassemia Deletions, is specially designed for the qualitative analysis of most common deletions of α-globin gene expressions (- α 3.7, - α 4.2, --SEA). The Assay Kit use three pairs of primers and one inter-control according to the Gap-PCR principle. Each pair of primers amplified a segment of chromosome deletion. Then the PCR amplification band detected through Electrophoresis. OPTIMIZED 4 STEP ASSAYS 1. Genomic DNA Extraction 2. PCR Amplification 3. Electrophoresis 4. Result analysis
Ordering Instructions Cat.NO./SIZE | NAME | ITEM | PG010012/20T | PCR Kit For Gene Detection of α-Thalassemia Deletions | - α3.7, -α4.2, --SEA |
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