Primer probe and kit for detecting oncogene of cervical cancer and detection method for non-detection disease purpose
A technology of oncogenes and detection methods, applied in biochemical equipment and methods, microbe determination/inspection, DNA/RNA fragments, etc.
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Embodiment 1
[0152] HeLa cells were used to design three gradients, the original gradient was 100cells / μL, the secondary gradient was 50cells / μL, and the final gradient was 25cells / μL. All three gradients have the same volume. Schematic diagram of 96-microwell plate simulation layout figure 1 shown.
[0153] Sampling: Before sampling, wipe the mucus and blood on the surface of the cervix with a cotton swab, and gently insert the bristle part of the front of the sampler deep into the channel of the cervix, so that the bristles at the back can fully touch the transition of the cervix, and gently move forward Hold the sampler and turn the sampler 3-5 full circles in the same clockwise direction.
[0154] Sample processing: set the incubator to the temperature required for lysis at 65°C; match the number of the centrifuge tube and the sample to confirm that it is correct; mix the liquid in the sample tube and transfer it to the centrifuge tube, centrifuge at 3000rpm for 5min, pour off the su...
Embodiment 2
[0191] Sampling: Before sampling, wipe the mucus and blood on the surface of the cervix with a cotton swab, and gently insert the bristle part of the front of the sampler deep into the channel of the cervix, so that the bristles at the back can fully touch the transition of the cervix, and gently move forward Hold the sampler and turn the sampler 3-5 full circles in the same clockwise direction.
[0192] Sample processing: set the incubator to the temperature required for lysis at 65°C; match the number of the centrifuge tube and the sample to confirm that it is correct; mix the liquid in the sample tube and transfer it to the centrifuge tube, centrifuge at 3000rpm for 5min, pour off the supernatant, and add 2ml to the centrifuge tube. Ionized water, suspended sediment, 3000rpm, 5min centrifugation, discard the supernatant; add 200μL lysate, 400μL deionized water, 5μL proteinase K to each sample, mix well, put it in an incubator at 65°C for 1 hour, and mix it once in a while. ...
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