In situ hybridization detection kit for lung cancer , detecting method and use thereof
An in situ hybridization and comprehensive detection technology, which is applied in biochemical equipment and methods, and microbial determination/inspection, etc., can solve problems such as imperfect design of anticancer drugs, unreported detection methods, and drug resistance of tumor cells , to achieve the effect of radically curing malignant diseases of cancer, convenient operation and strong specificity
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Embodiment 1
[0051] A lung cancer in situ hybridization comprehensive detection kit, including four sets of hybridization probes and markers, the hybridization probes respectively have the sequence table SEQ ID NO.1, SEQ ID NO.2, SEQ ID NO.3 and SEQ ID NO.3 The sequence shown in ID NO.4. For the PAX9 gene sequence, see the sequence shown in SEQ ID NO.1. For the sequence of NKX2-8 gene, see the sequence shown in SEQ ID NO.2. See the sequence shown in SEQ ID NO.3 for the sequence of the TTF1 gene. For the sequence of RhoGDI2 gene, see the sequence shown in SEQ ID NO.4. Labeled with digoxin. The composition of other liquids and specimens in the kit is as follows:
[0052] Digestive solution 100μL / tube 4 tubes / box Colorless transparent liquid
[0053] Protective solution 100μL / tube 4 tubes / box Colorless transparent liquid
[0054] Pre-hybridization solution 1300μL / tube 8 tubes / box Colorless transparent liquid
[0055] Sense hybridization solution 10μL / tube 4 tubes / box Colorless transpar...
Embodiment 2
[0102]A kind of PAX9 gene, NKX2-8 gene, TTF1 gene and RHOGDI2 gene in situ hybridization detection method and kit application thereof
[0103] 1. Specimen processing
[0104] 1. Use a 10ml centrifuge tube to fill 4.5ml of lymphocyte separation solution, then slowly add 3ml of anticoagulated blood into the centrifuge tube containing lymphocyte separation solution (blood: lymphocyte separation solution = 1:1.5), and centrifuge at 2000r / min 10min;
[0105] 2. Take the white blood cells in the middle layer into another centrifuge tube, then add about twice the amount of 1× buffer I to this tube, mix well, and centrifuge at 1500g / min for 10min;
[0106] 3. Discard the supernatant. Add about twice the 1× buffer I to the precipitate, mix well, and centrifuge at 1500g / min for 10min;
[0107] 4. Discard the supernatant, and absorb the excess liquid from the mouth of the test tube with paper towels. Then the precipitate was made into a suspension, dropped on a glass slide, and allowe...
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