In-situ detection method of honeysuckle flower tannin
An in-situ detection and honeysuckle technology, which is applied in the direction of measuring devices, test plant materials, and preparation of test samples, can solve the problems of inability to display the position of tannins and in-situ analysis, and achieve the effect of saving time
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Embodiment 1
[0018] The in-situ detection method of tannin in this example honeysuckle fresh sample comprises the following steps:
[0019] In the first step, the different tissues of flower buds are cut into small pieces or slices (less than 1.0 mm × 1.0 mm) with double-sided blades, soaked in 1 ml of 2% glutaraldehyde solution (prepared with pH 6.8 phosphate buffer) for 2 Hours, the container is a 1.5 ml capped centrifuge tube, and the temperature is room temperature. During the period, use a vacuum pump to pump air;
[0020] In the second step, suck out the glutaraldehyde solution in the tube, soak it with pH 6.8 phosphate buffer solution for 3 times, each time for 20 minutes, then add 0.3 ml of 1% osmium tetroxide aqueous solution, and soak the sample in it for 2 hours , the temperature is room temperature;
[0021] The third step is to suck out the osmium tetroxide solution and dehydrate it with a gradient of 10% alcohol series, starting from 30% alcohol until 100% alcohol, 1 ml per...
Embodiment 2
[0026] The in-situ detection method of tannin in the honeysuckle dried sample of this example comprises the following steps:
[0027] In the first step, the dried flower buds are fully hydrated in phosphate buffer solution, and different tissues are cut into small pieces or small pieces (less than 1.0 mm × 1.0 mm) with a double-sided blade, and mixed in 1 ml of 2% glutaraldehyde solution (with a pH of 6.8 Prepared in phosphate buffer solution) for 2 hours, the container is a 1.5 ml centrifuge tube with a cover, and the temperature is room temperature. During the period, use a vacuum pump to pump air;
[0028] In the second step, suck out the glutaraldehyde solution in the tube, soak it with pH 6.8 phosphate buffer solution for 3 times, each time for 20 minutes, then add 0.3 ml of 1% osmium tetroxide aqueous solution, and soak the sample in it for 2 hours , the temperature is room temperature;
[0029] The third step is to suck out the osmium tetroxide solution and dehydrate ...
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