Probe group for diagnostic gene methylation and application of probe group
A technology of methylation and probe group, which is applied in the direction of recombinant DNA technology, microbial measurement/inspection, biochemical equipment and methods, etc., can solve the problem of ineffective detection, inability to match bisulfite modified products, and inability to form non-methylation Base probe pairing and other issues
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Embodiment 1
[0057] Embodiment 1, the methylation level detection example of MGMT gene
[0058] In this example, methylation probes were designed using the method of the present invention, combined with fluorescent PCR technology, to detect the methylation of the O6-methylguanine-DNA-methyltransferase (MGMT) gene. The MGMT gene is located at 10q26 on chromosome 10, and its function is to remove O6-guanine adducts from DNA and repair damaged DNA. When the CpG site in the promoter region of the MGMT gene is methylated, MGMT transcription stops, and the transfer of the methyl group on guanine-O6 fails, resulting in the inability to effectively repair DNA alkylation damage, which is closely related to tumorigenesis. The results of the study showed that: MGMT promoter methylation is closely related to the clinical effect of the first-line chemotherapy drug Temozolomide. It is generally believed that tumor cells with MGMT methylation are effective against alkylating agents, while non-methylatio...
Embodiment 2
[0086] Embodiment 2, the detection example of three kinds of fluorescent PCR systems to brain glioma sample
[0087] 80 cases of paraffin tissue samples of clinically confirmed glioma were taken, and 5-10um slices were made. Take 3-5 slices into a 1.5mL centrifuge tube, after deparaffinization with xylene, add 180μl DNA extraction solution and 20μl proteinase K solution, digest at 56°C until no visible tissue pieces; add 300μl GDT buffer, mix well after 70 Incubate at ℃ for 10 minutes; add 300 μl absolute ethanol, mix well, transfer to a spin column, centrifuge for 1 minute, discard the filtrate in the collection tube; add 700 μl washing solution PW, centrifuge at 8000 rpm for 1 minute, discard the filtrate; Add 700 μl washing solution WA, centrifuge at 8000 rpm for 1 minute, discard the filtrate; dry the residual liquid in the spin column (centrifuge at 12000 rpm for 2 minutes); add 100 μl DNA eluent to the center of the membrane in the spin column, and place at room temperat...
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