Embossing method for bacterium sampling
An embossing method and bacterial technology, applied in the direction of biological material sampling method, microbial measurement/inspection, biochemical equipment and methods, etc., can solve the problems of cumbersome and complicated procedures, heavy workload, and inaccurate sampling results, and achieve Accurate analysis results, improved work efficiency, and high promotional value
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Embodiment 1
[0034] The described imprinting method for hand bacterial sampling comprises the following steps:
[0035] (1) To prepare a neutralizing solution, add soybean lecithin, Tween 80, peptone, sodium chloride, sodium thiosulfate and glycine into water, then add sodium hydroxide solution to adjust the pH to 7.3 to obtain a neutralizing solution.
[0036] In the neutralizing solution, the percentages of each component in the mass of water are: 0.3% soybean lecithin, 0.3% Tween 80, 1% peptone, 0.5% sodium chloride, 0.1% sodium thiosulfate, and 0.3% glycine.
[0037] (2) After mixing the neutralizing solution and the dissolved nutrient agar evenly, put it in a high-pressure steam sterilizer for sterilization to obtain a mixed solution.
[0038] (3) Cool the mixed solution to 42° C., pour it into a culture dish, and cool it for later use. The cooled mixed solution becomes a culture medium.
[0039] (4) Press the medium surface on the culture dish directly from the base of the palm to t...
Embodiment 2
[0043] The described imprinting method for sampling bacteria on the surface of an object comprises the following steps:
[0044] (1) To prepare a neutralizing solution, add soybean lecithin, Tween 80, peptone, sodium chloride, sodium thiosulfate and glycine into water, then add dilute hydrochloric acid solution to adjust the pH to 7.2 to obtain a neutralizing solution.
[0045] In the neutralizing solution, the percentages of each component in the mass of water are: soybean lecithin 0.2%, Tween 80 0.4%, peptone 0.8%, sodium chloride 0.6%, sodium thiosulfate 0.15%, glycine 0.4%.
[0046] (2) After mixing the neutralizing solution and the dissolved nutrient agar evenly, put it in a high-pressure steam sterilizer for sterilization to obtain a mixed solution.
[0047] (3) Cool the mixed solution to 45°C, pour it into a culture dish, and cool it for later use. The cooled mixed solution becomes a culture medium.
[0048] (4) During detection, press the surface of the culture dish o...
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