Detection method and correlated detection probe and kit for prostatic cancer related fusion gene Fish
A prostate cancer and fusion gene technology, applied in biochemical equipment and methods, microbe measurement/inspection, etc., can solve rare problems and achieve the effects of intuitive detection, simple operation, and ingenious design
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[0122] 1. source of sample material
[0123] Samples of prostate cancer tissue slices and normal prostate samples were obtained from the hospital.
[0124] 2. Dewaxing and Hydration
[0125] Deparaffinize the samples in xylene for 5 min in 1 repeat. Then hydrate in 95% ethanol and 70% ethanol twice for 5 minutes each.
[0126] 3. hybridization pretreatment
[0127] The samples were bathed in boiling water at 95°C for 10 minutes, transferred to 1×PBS and equilibrated for 5 minutes, and repeated once.
[0128] Remove the sample and digest it with pepsin for 5-15 minutes. Transfer to 1x PBS to equilibrate for 5 min.
[0129] Remove samples and fix with 1% formaldehyde for 1 min. Transfer to 1x PBS to equilibrate for 5 min.
[0130] The samples were dehydrated with 75%, 85%, and 95% graded ethanol for 5 minutes each, and dried in the air.
[0131] 4. Denaturation of tissue sections
[0132] The samples were denatured in a preheated denaturing solution at 70°C for 5 mi...
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