Blood agar plate and preparation method thereof
A blood agar plate and agar technology are applied in the field of blood agar plate and its preparation, which can solve the problems of caking, entrapped air bubbles, and difficulty in detection, and achieve the effects of improving separation rate, promoting growth and comprehensive nutrition.
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[0029] The embodiment of the present invention also provides a kind of preparation method of above-mentioned blood agar plate, it comprises:
[0030] S1. Mix tryptone, soybean peptone, sodium chloride, yeast extract powder, beef heart extract powder, agar, and water, heat to dissolve, and obtain a culture solution.
[0031] S2. Sterilize the culture medium at 120-125°C for 20-40 min.
[0032] S3. Cool down the sterilized culture solution to 80-90°C, continue heating for 5-10 minutes, then cool to 40-45°C;
[0033] S4. Mix the preheated defibrated sheep blood with the cooled culture medium evenly, pour it into a plate for further cooling, and obtain a blood agar plate.
[0034] Further, tryptone, soybean peptone, yeast extract powder, and beef heart extract powder provide suitable carbon and nitrogen sources for microorganisms. Sodium chloride can maintain the balance of bacterial osmotic pressure. Agar is the medium coagulant. At room temperature, the dissolution of the ab...
Embodiment 1
[0042] This embodiment provides a blood agar plate, which is obtained by mixing culture fluid and defibrated sheep blood, cooling and solidifying. Wherein, in parts by weight, the culture solution includes:
[0043] 8 parts of tryptone, 10 parts of soybean peptone, 4 parts of sodium chloride, 4 parts of yeast extract powder, 1 part of beef heart extract powder, 13 parts of agar, and 1000 parts of water;
[0044] The volume ratio of culture medium and defibrated sheep blood is 1:0.06.
[0045] The preparation method of this blood agar plate is as follows:
[0046] S1. Mix tryptone, soybean peptone, sodium chloride, yeast extract powder, beef heart extract powder, agar, and water, heat to 90°C to dissolve to obtain a culture medium, and adjust the pH of the culture medium to 7.2.
[0047]S2. Sterilize the culture medium at 120°C for 40 min.
[0048] S3. Cool down the sterilized culture solution to 90°C, continue heating for 5 minutes, then cool to 40°C;
[0049] S4. Mix the ...
Embodiment 2
[0053] This embodiment provides a blood agar plate, which is obtained by mixing culture fluid and defibrated sheep blood, cooling and solidifying. Wherein, in parts by weight, the culture solution includes:
[0054] 12 parts of tryptone, 6 parts of soybean peptone, 6 parts of sodium chloride, 2 parts of yeast extract powder, 3 parts of beef heart extract powder, 18 parts of agar, and 900 parts of water;
[0055] The volume ratio of culture medium and defibrated sheep blood is 1:0.04.
[0056] The preparation method of this blood agar plate is as follows:
[0057] S1. Mix tryptone, soybean peptone, sodium chloride, yeast extract powder, beef heart extract powder, agar, and water, heat to 80°C to dissolve to obtain a culture medium, and adjust the pH of the culture medium to 7.4.
[0058] S2. Sterilize the culture medium at 125°C for 20 min.
[0059] S3. Cool down the sterilized culture solution to 80°C, continue heating for 10 minutes, then cool to 45°C;
[0060] S4. Mix th...
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