Device for detecting oral lichen planus precancerous lesions
A technology for oral lichen planus and precancerous lesions, applied in the field of biotechnology and diagnosis, can solve problems such as metastasis, incurable cancer, and poor overall prognosis, and achieve the effect of predicting risks
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Embodiment 1
[0037] A detection device for precancerous lesions of oral lichen planus, including Golli-MPB, STIM1, FGF19, FGFR4 four protein markers and a kit using the four markers as detection targets, according to the four markers The development stage of precancerous lesions of lichen planus can be judged by the expression level of the mRNA of the substance, and the kit includes fluorescent quantitative PCR reagent, Western-blot western blot, reverse transcription reagent and DAB chromogenic reagent.
[0038] The fluorescent quantitative PCR reagent, Western-blot and reverse transcription reagent detect two proteins, Golli-MPB and STIM1, and the DAB chromogenic reagent detects two proteins, FGF19 and FGFR4.
Embodiment 2
[0040] Excluding patients with other oral diseases, autoimmune diseases, taking immune preparations and taking drugs that may cause lichenification, 50 adult patients with OLP were selected as the experimental group, and 50 healthy adults were selected as the control group. Neither was statistically significant.
[0041]Fluorescent quantitative PCR: (1) Extraction of total RNA from the sample: transfer the purified peripheral blood lymphocytes to an enzyme-free and pyrogen-free tube, centrifuge, discard the supernatant, add 1ml Trizol to mix, and let stand on ice for 10 minutes; Chloroform, mix well, let stand on ice for 2-5min, and centrifuge at 12000r / min for 15min at 4°C; Centrifuge at 12000r / min for 10min at 4°C for 10min; discard the supernatant, wash the pellet gently with 75% ethanol, then centrifuge at 12000r / min for 10min at 4°C; discard the supernatant, and dry the RNA pellet in a fume hood 2-3min; after the dried RNA precipitate was dissolved in DEPC water, reverse...
Embodiment 3
[0044] On the basis of Example 2, combined with figure 1 and figure 2 , the results of real-time fluorescence quantification showed that the expression level of Golli-MPB mRNA in the experimental group was significantly higher than that in the normal control group, P<0.001, and the expression level of STIM1 mRNA in the OLP group was significantly higher than that in the normal control group, P<0.001. According to the Western blot results, the expression levels of Golli-MPB and STIM1 proteins in the experimental group were also significantly higher than those in the normal control group.
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