HDAC10 gene in-situ hybridization detection kit, detection method and application thereof
A detection kit and in situ hybridization technology, applied in the field of kits, can solve the problem of inability to simulate the function of full-length proteins, and achieve the effects of high sensitivity, strong specificity and convenient operation.
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Embodiment 1
[0046] An in situ hybridization detection kit for HDAC10 gene, comprising hybridization probes, markers and synergists, wherein the hybridization probe sequence 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] Chromogen B ...
Embodiment 2
[0097] A kind of HDAC10 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 medium, then slowly add 3 ml of anticoagulated blood into the centrifuge tube containing lymphocyte separation medium (blood: lymphocyte separation medium = 1:1.5), 2000r / min Centrifuge for 10 min;
[0100] 2. Draw the white blood cells in the middle layer to another centrifuge tube, and then add about twice the amount of 1× buffer to this tube , mix well, centrifuge at 1500g / min for 10 min;
[0101] 3. Discard the supernatant. Add about twice the amount of 1× buffer to the pellet , mix well, centrifuge at 1500g / min for 10 min;
[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 pushed to dry naturally. (Hospitals with conditions ...
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