Mycoplasma pneumoniae detection device and detection method
A technology of Mycoplasma pneumoniae and a detection device, applied in the field of genetic engineering, can solve problems with high requirements, and achieve the effects of satisfying rapid detection, improving convenience, and improving generalizability
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[0067] ERA / CRISPR-Cas12a double detection was performed on 62 suspected positive samples and 30 negative samples, and the sequences were extracted with QIAmpDNA Mini Kits. The above samples have been renumbered out of order to protect patient privacy. All tests were repeated three times, and the qPCR results were used as the gold standard to evaluate the coincidence rate (PPA / NPA) of the ERA / CRISPR-Cas12a dual system for clinical specimens.
[0068] The extracted DNA was subjected to real-time PCR with qPCR kit and amplified with ABI7500. The system is as follows: 38L of reaction solution, 2L of enzyme mixture, and 0.4L of internal standard substance are configured into enzyme mixture according to the reaction ratio. Add 10L of the sample to be tested into the amplification reaction tube, let it stand for 10 minutes, add 40L of enzyme mixture, and put it on the amplification instrument after spotting. The amplification program was: 50°C for 2 minutes; 94°C for 5 minutes; the...
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