Joint detection kit for alpha,beta-thalassemia associated mutant genes
A technology for thalassemia and mutant genes, applied in the field of alpha, which can solve problems such as alpha that have not yet appeared
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[0064] 1. Preparation of gene chip for detection of α, β-thalassemia
[0065] 1-1. Probe design
[0066] α-thalassaemia is commonly seen in three α-globin gene deletions (-- SEA , -α 4.2 , -α 3.7 ) and 2 mutant types (Hb QS, Hb CS); β-thalassaemia is commonly found in 16 β-globin gene mutations (-28(A-G), -29(A-G), Cap(-AAAC), Int(T-G ), CD14 / 15(+G), CD17(A-T), βE(G-A), CD27 / 28(+C), CD31(-C), CD41 / 42(-TTCT), CD43(G-T), CD71 / 72 (+A), IVS-I-1(G-T, G-A), IVS-I-5(G-C), IVS-II-654(C-T)), in order to detect the above common mutation types of α, β-thalassaemia, this The inventors designed 31 probes in total, and the specific probes are SEQ ID Nos: 1-31.
[0067] 1-2. Spotting and Immobilization of DNA Probes
[0068] (1) Spotting and arrangement of probes
[0069] In the immobilization of direct oligonucleotide DNA probes, the DNA probes were first diluted with probe diluent (0.5M Na at pH 8.4 2 CO 3 and 0.5M NaHCO 3 solution) mixed and sampled. After the synthesis of the ...
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