Method for rapidly detecting EGFRvIII mutation
A fast, probe-based technology, applied in the fields of cancer detection and molecular biology, can solve problems such as weak correlation, achieve the effects of avoiding pollution, accurate and reliable experimental results, and streamlined operations
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Embodiment 1
[0022] A method for rapid detection of EGFRvIII mutation, comprising the following steps:
[0023] (1) extract the RNA of the tumor tissue of sample 1;
[0024] (2) Construct PCR reaction system;
[0025] (3) Real-time fluorescent quantitative PCR was carried out by TaqMan probe method;
[0026] (4) Interpretation of results.
[0027] Further, the extraction steps for sample 1 RNA are as follows: paraffin sample dewaxing: take five 7 μm sample 1 paraffin tissue sections and put them into a 1.5ml centrifuge tube, add 1ml xylene, centrifuge at 13,000xg for 1 minute, discard the supernatant, and then Add 1ml of xylene, centrifuge at 13,000xg for 1 minute, and discard the supernatant. Add 1ml of absolute ethanol to the centrifuge tube, centrifuge at 13,000xg for 1 minute, discard the supernatant, and dry it; add tissue lysate and proteinase K to the dried tissue, lyse at 56°C for 15 minutes, and transfer the centrifuge tube to Keep it at 80°C for 15 minutes and take it off. Wh...
Embodiment 2
[0039] A method for rapid detection of EGFRvIII mutation, comprising the following steps:
[0040] (1) extract the RNA of sample 1 tumor tissue;
[0041] (2) construct PCR reaction system;
[0042] (3) Real-time fluorescent quantitative PCR was carried out by TaqMan probe method;
[0043] (4) Interpretation of results.
[0044] Further, the extraction steps for sample 1 RNA are as follows: paraffin sample dewaxing: take five 7 μm sample 1 paraffin tissue sections and put them into a 1.5ml centrifuge tube, add 1ml xylene, centrifuge at 13,000xg for 1 minute, discard the supernatant, and then Add 1ml of xylene, centrifuge at 13,000xg for 1 minute, and discard the supernatant. Add 1ml of absolute ethanol to the centrifuge tube, centrifuge at 13,000xg for 1 minute, discard the supernatant, and dry it; add tissue lysate and proteinase K to the dried tissue, lyse at 56°C for 15 minutes, and transfer the centrifuge tube to Keep it at 80°C for 15 minutes and take it off. When it r...
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