Primer and kit for detecting susceptibility of paranoia schizophrenia
A technology of schizophrenia and kit, which is applied in the field of schizophrenia susceptibility gene detection, to achieve the effect of fast process
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Embodiment 1
[0048] 1. Select candidate genes and SNPs
[0049] The present inventor consults literature, utilizes computer Internet and bioinformatics to obtain various aspects of schizophrenia candidate gene research, and carries out single nucleotide polymorphism (SNP) linkage disequilibrium analysis by linkage disequilibrium analysis method on No. 22 chromosome, through NCBI (http: / / www.ncbi.nlm.nih.gov / mapviewer) database, access to GNB1L gene, and through http: / / www.ncbi.nlm.nih.gov / SNP, http: / / snp.cshl. org / database to search for candidate gene SNPs that meet its conditions. The selection criteria: 1. There are relevant literature reports; 2. The minimum allele frequency of the site should be greater than 10%; 3. The selected SNPs must meet the requirements of the primer design software; 4. The selected site cannot affect the gene Typing experiment
[0050] 2. Research object
[0051] The present invention takes 451 cases of paranoid schizophrenia and 460 cases of healthy contro...
Embodiment 2
[0094] Validation test: Using this kit, randomly select 20 samples from patients with paranoid schizophrenia and 20 samples from the control group, and detect the polymorphism at rs748806 of the GNB1L gene by PCR sequencing.
[0095] 1. PCR amplification:
[0096] Amplify the partial fragment of GNB1L gene rs748806 by PCR. The PCR reaction system is: 3 μL of 10×PCR reaction buffer, 0.5 μL of 10 mM / LdNTP, 0.5 μL of TaqDNA polymerase, 0.5 μL of 10pM / L primer, 1 μL of genomic DNA, and add deionized water to 30 μL. During PCR, 20 μL of paraffin oil was added to each system to prevent the liquid from volatilizing.
[0097] The PCR reaction conditions were pre-denaturation at 95°C for 5 min, denaturation at 95°C for 30 s, annealing at 65°C for 30 s, extension at 72°C for 25 s, a total of 35 cycles, and a total extension at 72°C for 2 min.
[0098] 2. Sequencing to determine genotype
[0099] The PCR product was detected by 8% polyacrylamide gel electrophoresis, and the gel imagin...
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