Treatment method of scanning electron microscope samples of insect tentacles and appendages
A scanning electron microscope and sample processing technology, applied in the field of scanning electron microscope sample processing, can solve the problems of inability to remove insect antennae and appendage wax layer, incomplete removal of antennae and appendage scales, incomplete cleaning of sample surface, etc., and achieve a balance. The osmotic pressure is unstable, the effect of overcoming the deformation effect, and the low price
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Embodiment 1
[0040] The steps of scanning electron microscope sample preparation for the adult antennae of Spodoptera ervata are as follows:
[0041] (1) Preparation of sample fixing solution, cleaning solution and anesthesia solution
[0042] Prepare phosphate buffer: dissolve potassium dihydrogen phosphate KH in 800 mL of distilled water 2 PO 4 1.4g, disodium hydrogen phosphate dihydrate Na 2 HPO 4 2H 2 O 1.8g, sodium chloride 0.58g and potassium chloride 0.7g, then add 1mol / L hydrochloric acid to adjust the pH to 7.4, and store in a refrigerator at 4°C after high-temperature and high-pressure sterilization.
[0043] The preparation of sample fixing solution: use above-mentioned phosphate buffer solution and the glutaraldehyde solution of commercially available mass concentration 25% and the formaldehyde solution of commercially available mass concentration 38% to be configured into glutaraldehyde-formaldehyde phosphate buffer saline, make glutaraldehyde The mass percentage content...
Embodiment 2
[0055] The steps of scanning electron microscope sample preparation for the adult antennae of Spodoptera ervata are as follows:
[0056] (1) Preparation of sample fixing solution, cleaning solution and anesthesia solution
[0057] Prepare phosphate buffer: dissolve potassium dihydrogen phosphate KH in 500 mL of distilled water 2 PO 4 4.2g, disodium hydrogen phosphate dihydrate Na 2 HPO 4 2H 2 O 5.4g, sodium chloride 1.74g and potassium chloride 2.1g, then add 1 mol / L hydrochloric acid to adjust the pH to 7.2, sterilize at high temperature and high pressure and store in a refrigerator at 4°C.
[0058] The preparation of sample fixing solution: use above-mentioned phosphate buffer solution and the glutaraldehyde solution of commercially available mass concentration 25% and the formaldehyde solution of commercially available mass concentration 38% to be configured into glutaraldehyde-formaldehyde phosphate buffer saline, make glutaraldehyde The mass percentage content is 3%...
Embodiment 3
[0070] The steps of scanning electron microscope sample preparation for the adult antennae of Spodoptera ervata are as follows:
[0071] (1) Preparation of sample fixing solution, cleaning solution and anesthesia solution
[0072] Prepare phosphate buffer: dissolve potassium dihydrogen phosphate KH in 700 mL of distilled water 2 PO 4 7.0g, disodium hydrogen phosphate dihydrate Na 2 HPO 4 2H 2 O 9.0g, sodium chloride 2.9g and potassium chloride 3.5g, then add 1mol / L hydrochloric acid to adjust the pH to 7.0, put it in a refrigerator at 4°C after high-temperature and high-pressure sterilization.
[0073] The preparation of sample fixing solution: use above-mentioned phosphate buffer solution and the glutaraldehyde solution of commercially available mass concentration 25% and the formaldehyde solution of commercially available mass concentration 38% to be configured into glutaraldehyde-formaldehyde phosphate buffer saline, make glutaraldehyde The mass percentage content is ...
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