Method for preparing trichophyton scanning electron microscope sample
A technology for scanning electron microscopy and trichophyton, applied in the field of preparation of trichophyton scanning electron microscope samples, can solve problems such as insufficient contact of reagents, inaccurate judgment of results, health threats to experimenters, etc., and achieve good fixation effect
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[0018] Embodiment 1: the preparation of scanning electron microscope sample of Trichophyton mentagrophytes
[0019] 1 Materials and reagents:
[0020] 1.1 Experimental material: Trichophytonmentagrophytes
[0021] 1.2 Reagents: peptone, glucose, agar, phosphate buffer solution (PBS) at pH 7.2, 25% glutaraldehyde, ethanol, acetone, tert-butanol
[0022] 1.3 Main experimental instruments: ultra-clean bench, incubator, pipette, refrigerator, autoclave, freeze dryer, ion sputtering instrument, field emission scanning electron microscope (FESEM).
[0023] 1.4 Sample preparation
[0024] 1.4.1 Mycelia activation
[0025] SDA plate preparation: weigh 10g of peptone, 20g of glucose, and 18g of agar, dilute to 1L, sterilize at 121°C for 30min, pour the plate before the medium solidifies, and set aside;
[0026] Activation of strains: Inoculate the strains on a plate, culture in an incubator at 30°C for 5-7 days, and set aside.
[0027] 1.4.2 Sample preparation: inoculate the activ...
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