Primer probe combination for methylation detection of RASSF1A gene and P16 gene and application of primer probe combination
A primer-probe and methylation technology, applied in the field of molecular biology, can solve the problems of difficult early detection and early qualitative diagnosis, unrealistic tumor tissue detection, and difficulty in early diagnosis of liver cancer, achieving high specificity and detection operation. Simple, convenient and highly accurate results
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Embodiment 1
[0114] Example 1 Assembly of the kit
[0115] 1. The design of primer probe combination, the specific sequence is shown in Table 1 below:
[0116] Table 1 Sequence of primer probe
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[0119] 2. The reagent composition in the kit is shown in Table 2.
[0120] Table 2 Reagent composition in the kit
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[0122] Among them, the nucleotide sequences of positive control and negative control are shown in Table 3:
[0123] Table 3 Nucleotide sequence of positive control and negative control
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[0126] Put the above components, instructions and droplet generation card into the kit body.
Embodiment 2
[0127] Example 2 RASSF1A gene and P16 gene methylation detection
[0128] Using the kit in Example 1 to perform methylation detection of RASSF1A gene and P16 gene includes the following steps:
[0129] (1) Extraction of template DNA
[0130] ①Plasma separation: Collect 5mL-10mL human peripheral blood with EDTA anticoagulation tube; centrifuge the blood sample at 1600g for 10 minutes; carefully transfer the collected plasma sample to a 2mL centrifuge tube; centrifuge the plasma sample at 4℃ , 16000g, 10 minutes; carefully transfer the collected plasma sample to a new 2mL centrifuge tube; collect the completed plasma sample to save at -20℃;
[0131] ② Extraction of free DNA: Use DNA extraction reagents to extract free DNA from peripheral blood, monitor DNA quality, and select free DNA with OD260 / OD280 between 1.6 and 2.0;
[0132] ③DNA modification: The free DNA obtained in step ② is modified with sulfite according to the instructions of the kit EZ DNAMethylation-DirectTM KIT (D5020) of ...
Embodiment 3
[0151] Compared with Example 2, the PCR reaction conditions are the same as in Example 2 except that the PCR reaction conditions are pre-denaturation at 98°C for 3 minutes, 93°C for 40s; annealing at 55°C for 45s; 45 cycles, and finally at 98°C for 8 minutes.
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