In-situ hybridization detection kit and detection method for PTEN gene, and application of kit
A detection kit and in situ hybridization technology, applied in the field of kits, can solve the problems of nutrient consumption and the like, and achieve the effects of convenient operation, radical cure of malignant diseases of cancer and high sensitivity
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Embodiment 1
[0046] An in situ hybridization detection kit for PTEN gene, comprising a hybridization probe, a marker and a synergist, wherein the sequence of the hybridization probe is shown in SEQ ID NO.1. Hybridization probes were labeled with digoxigenin. The composition of other liquids and specimens in the kit is as follows:
[0047] Digestive solution 100μl / tube 1 tube / box Colorless transparent liquid
[0048] Protective solution 100μl / tube 1 tube / box Colorless transparent liquid
[0049] Pre-hybridization solution 1300μl / tube 2 tubes / box Colorless transparent liquid
[0050]Sense hybridization solution 10μl / tube 1 tube / box Colorless transparent liquid
[0051] Antisense hybridization solution 10μl / tube 1 tube / box Colorless transparent liquid
[0052] Blocking solution 1000μl / tube 1 tube / box Colorless transparent liquid
[0053] Alkaline phosphatase antibody 1μl / tube 1 tube / box Colorless transparent liquid
[0054] Chromogen A 175μl / tube 1 tube / box Yellow liquid
[0055] Chrom...
Embodiment 2
[0097] A kind of PTEN gene in situ hybridization detection method and its kit application
[0098] 1. Specimen processing
[0099] 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;
[0100] 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;
[0101] 3. Discard the supernatant. Add about twice the 1× buffer I to the precipitate, mix well, and centrifuge at 1500g / min for 10min;
[0102] 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 allowed to dry naturally. (Hospitals with conditi...
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