Biomarker for detecting plateau hypoxia and application thereof
A technology of biomarkers and detection markers, applied in biological testing, material inspection products, etc., to achieve the effect of facilitating the progress of hypoxic injury and being easy to accept
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Embodiment 1
[0018] Example 1 Animals simulate high altitude hypoxia exposure
[0019] 1. Select qualified experimental animals C57BL / 6 mice, male, purchased from Beijing Weitong Lihua Laboratory Animal Technology Co., Ltd., raised in a constant temperature (23±2℃), constant humidity animal room, 12 / 12h day and night cycle every day, can be Free food and water. The hypobaric and hypoxic animal experimental cabin simulating the plateau environment was purchased from Guizhou Fenglei Aviation Ordnance Co., Ltd., model: DYC-DWI. The cabin is connected with two air pumps, which can continuously pump the gas in the cabin out of the cabin, thereby simulating a low-pressure and low-oxygen environment at a certain altitude; at the same time, an electronic display screen and an oxygen sensor probe are connected (real-time display of the location in the cabin). altitude and oxygen concentration).
[0020] 2. 18 mice were randomly divided into three groups, control group, hypobaric hypoxia group for...
Embodiment 2
[0022] Embodiment 2 IL-5 content detection
[0023] The detection method of IL-5 in serum is carried out according to the following steps:
[0024] (1) Take out the required slats from the aluminum foil bag after equilibrating at room temperature for 20 minutes, and seal the remaining slats in a self-sealing bag and put them back at 4°C;
[0025] (2) Set standard wells (concentrations are 0, 5, 10, 20, 40, 80 pg / ml in sequence) and sample wells, and add 50 μl of standard with different concentrations to each standard well;
[0026] (3) First add 10 μl of the sample to be tested to the sample well, and then add 40 μl of the sample diluent; the blank well is not added;
[0027] (4) In addition to the blank wells, add 100 μl of horseradish peroxidase (HRP)-labeled detection antibody to each well of the standard wells and sample wells, seal the reaction wells with a sealing film, and incubate at 37°C for 60 minutes;
[0028] (5) Discard the liquid, pat dry with absorbent paper, ...
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