Deletion beta thalassemia detection primers and beta thalassemia detection kit based on SNP analysis and application of deletion beta thalassemia detection kit
A thalassemia and detection kit technology, applied in the field of genetic engineering, can solve the problems of high requirements on instruments and equipment, unsuitable for routine application in grassroots units, cumbersome operation, etc., to achieve the effect of optimizing the reaction system and conditions
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Embodiment 1
[0054] The present invention establishes a method for detecting deletion mutation of β-globin gene cluster based on SNP analysis. The present invention screens out a group of six SNP sites for detection of beta globin gene cluster deletion mutations through bioinformatics analysis and sequencing data of a large number of population samples. Based on the principle of four-primer amplification hindered mutation PCR, specific primers for the above SNP sites were designed, and the typing detection of the six SNP sites was integrated into two multiplex PCR systems. At the same time, the primers were optimized, and the multiplex PCR amplification reaction system was optimized.
[0055] The genome template used in the present invention is obtained by extracting the genome from peripheral blood, and the peripheral blood samples are collected from Guangdong Province.
[0056] (1) SNP site screening
[0057] Based on the principle that the deletion of DNA fragments can lead to the los...
Embodiment 2
[0106] Peripheral blood samples from 10 patients with deletion mutations in the β-globin gene cluster were taken, including Chinese G γ( Aγδβ) 0 3 cases of -Thal deletion type, 2 cases of Yunnanese deletion type, 2 cases of Cantonese deletion type, 3 cases of (SEA)-HPFH deletion type; another 5 normal human peripheral blood samples without β-globin gene cluster deletion mutation were collected, The gene mutation types of all samples were verified by Gap-PCR or MLPA. The DNA of the above 15 samples was extracted and amplified with the following system, and the SNP typing results were compared with the sequencing method.
[0107] 3.1. Preparation of Multiplex PCR Amplification System
[0108] Reaction system A: The composition of each 50 μL reaction system is as follows: Premix LA Taq TM Master mix 25 μL, primers SNP1-in-F 0.2 μL, SNP1-in-R 1 μL, SNP3-in-F 0.2 μL, SNP3-in-R 1 μL, SNP5-in-F 1 μL, SNP5-in-R at a concentration of 10 μM 0.6 μL, 1 μL of OUT-F and 1 μL of OUT-R; ...
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