Use of HDAC2 in preparation of marker for evaluating progress of hepatic inflammation of acute hepatic failure
A technology of acute liver failure and markers, applied in the field of bioengineering, to achieve highly reliable results
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Embodiment 1
[0024] Serum HDAC2 activity, serum CRP level, serum neutrophil percentage (Neu%), serum IL-1β level, serum IL-18 Level. All research subjects took 5ml of fasting cubital venous blood and placed it in a vacuum blood collection tube, and placed the blood sample in an automatic biochemical analyzer to detect the content of CRP and Neu%. The tested samples were centrifuged at 3000r / min for 3min to separate the serum. ELISA kits were used to detect serum IL-1β, IL-18, and HDAC2 levels. In the process of adding samples, blank wells, standard wells, and sample wells to be tested were respectively set. Add 100 μl of sample diluent to the blank well, and add 100 μl of standard or test sample to the remaining wells. Cover the microtiter plate and incubate at 37°C for 90 minutes. Discard the liquid, shake it dry, add 100 μl of Detection Ab working solution (prepared within 15 minutes before use) to each well, add a membrane to the microtiter plate, and incubate at 37°C for 1 hour. D...
Embodiment 2
[0026]The expression of HDAC2 in liver tissue was detected by immunohistochemical method. The cut tissues (<5mm3) were washed with normal saline, and immediately fixed in 4% paraformaldehyde (PFA) for 24 hours. After the material is fixed, it is washed with water for several hours to remove the fixation solution and crystal precipitation in the tissue. The tissues were dehydrated in 70%, 80%, and 90% ethanol solutions at various levels in turn, for 30 minutes each, and then put in 95%, 100% ethanol solutions for 2 times, each time for 20 minutes. Wet the material with a mixture of pure alcohol and xylene for 1-2 hours, and then replace it with a pure transparent agent (xylene, benzene, chloroform, n-butanol). Then put it into a mixture of xylene and paraffin, and then soak it in melted paraffin. After dipping in wax, put it into the embedding box and use paraffin for embedding. The wax block embedding the small intestine sample was cut into 3 mm slices. Endogenous peroxida...
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