Kit for detecting susceptibility of hebephrenic schizophrenia
A schizophrenia and susceptibility technology, applied in the direction of microbial determination/examination, biochemical equipment and methods, etc., can solve the problem of undiscovered susceptibility gene of adolescent schizophrenia, and achieve good therapeutic effect, significant symptoms, The effect of inhibiting disease progression
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Embodiment 1
[0043] 1. Select candidate genes and SNPs
[0044] 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. 11 chromosome, through NCBI (http: / / www.ncbi.nlm.nih.gov / mapviewer) database, access to DRD2 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
[0045] 2. Materials and methods
[0046] 2.1 Research object
[0047] The present invention takes 320 cases of juvenile schizophre...
Embodiment 2
[0088] Validation test: Using this kit, randomly select 20 samples of adolescent schizophrenia patients and 20 samples of the control group, and detect the polymorphism of DRD2 gene rs1800497 by PCR sequencing.
[0089] 1. PCR amplification:
[0090] The PCR amplification conditions are: 1. 94°C for 5min, 2. 96°C for 45s, 60°C for 60s, 72°C for 60s for 3 cycles, 3. 95°C for 45s, 59°C for 65s, 72°C for 60s for 5 cycles, 4. 94°C for 45s, 57°C for 60s, 72°C for 60s, 32 cycles, 5, 72°C for 10min, take 5uL of PCR product and electrophoresis on 1.5% agarose gel, using DNAmarker as the molecular weight standard.
[0091] 2. Identification of genotype by restriction endonuclease digestion
[0092] The enzyme digestion reaction system is 20uL, including 10uL PCR product, 0.5uL restriction endonuclease TaqI, 2uL enzyme digestion buffer, placed in a 37°C incubator for 4 hours, and subjected to 3% agarose gel electrophoresis to determine the gene according to the enzyme digestion map ty...
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