Kit and method for detecting horizontal in situ hybridization of MICRORNA-372 at the early pathological evolution stage of a variety of cancers and application thereof
A detection kit and detection method technology, applied in the field of related detection technology, can solve the problems of imperfect design ideas of anticancer drugs, unscientific design of animal models, and non-decreasing mortality rate, etc.
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Embodiment 1
[0051] The in situ hybridization kit of this example was prepared according to conventional methods, and the kit included a hybridization probe designed with MICRORNA-372, a label, and instructions, wherein: the probe label of this example was digoxin.
[0052] Kit hybridization solution composition:
[0053] digestive juice 100μL / tube 1 tube / box colorless transparent liquid protective fluid 100μL / tube 1 tube / box colorless transparent liquid Pre-hybridization solution 1300μL / tube 2 tubes / box colorless transparent liquid Right-sense hybridization solution 10μL / tube 1 tube / box colorless transparent liquid antisense hybridization solution 10μL / tube 1 tube / box colorless transparent liquid blocking solution 1000μL / tube 1 tube / box colorless transparent liquid Alkaline phosphatase antibody 1 μL / tube 1 tube / box colorless transparent liquid Chromogen A 175μL / tube 1 tube / box yellow liquid Chr...
Embodiment 2
[0061] The implementation process of applying nucleic acid in situ hybridization detection method to the expression level of MICRORNA-372 in blood samples of each group:
[0062] 1).Take two specimens to be tested;
[0063] 2). Add 50 ml of digestive solution (100 μL of digestive solution plus 99.9 ml of 1× buffer Ⅰ, which is the concentration used) in a glass tank, preheat in a water bath at 37°C for 10 minutes, put 16 slides in, and treat at 37°C for 12 minutes , and then washed with 1× buffer I for 5 min;
[0064] 3). Use 0.2% protection solution (protection solution 1ml plus 1× buffer , 99ml is the concentration used), washed for 10 minutes, washed with three-distilled water for 5 minutes (the above process was carried out in a glass tank), took out the slide, and let it dry naturally;
[0065] 4). Put the slides into a humidifying box, add 25 μL / slice of pre-hybridization solution (add to the place where there are cells), cover with a cover glass, cover the humidifying...
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