Two phase Roe's culture medium and preparation method thereof
A technology similar to Roche culture medium and Roche culture medium, applied in the field of medical testing, can solve the problems of time-consuming, inability to meet clinical diagnosis and treatment and disease prevention, low positive rate, etc., to promote rapid growth, facilitate rapid preliminary identification, The effect of improving the positive rate of culture
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Embodiment 1
[0033] Embodiment 1: The Roche medium in the present invention is the modified Roche medium commonly used at home and abroad at present, and 4-6ml of 0.1% chromogenic agent TTC solution is added (or not added) to 1000ml of the modified Roche medium; liquid medium It consists of basal medium, growth promoters and bacteriostatic agents.
[0034] The composition of the basal medium is as follows: copper sulfate 0.001 g, zinc sulfate 0.001 g, calcium chloride 0.001 g, magnesium sulfate 0.01 g, oleic acid 0.01 g, ferric ammonium citrate 0.05 g, sodium citrate 0.1 g, ammonium sulfate 0.2 g, sodium pyruvate 0.5 g, Tween-80 0.5 g, asparagine 1 g, potassium dihydrogen phosphate 1 g, sodium dihydrogen phosphate 2 g, neutral glycerin 8 ml, distilled water 1000 ml. The preparation method is as follows: firstly dissolving the above-mentioned components in double distilled water, then sterilizing in high pressure at 115°C-121°C for 10-15 minutes, cooling, and storing in a 4°C refrigerator a...
Embodiment 2
[0039] The composition of the basal medium is as follows: copper sulfate 0.0015 g, zinc sulfate 0.0015 g, calcium chloride 0.0016 g, magnesium sulfate 0.018 g, oleic acid 0.016 g, ferric ammonium citrate 0.07 g, sodium citrate 0.15 g, ammonium sulfate 0.3 g, sodium pyruvate 0.7 g, Tween-80 0.7 g, asparagine 1.3 g, potassium dihydrogen phosphate 1.5 g, sodium dihydrogen phosphate 3 g, neutral glycerin 10 ml, distilled water 1000 ml. The preparation method is as follows: firstly dissolving the above-mentioned components in double distilled water, then sterilizing in high pressure at 115°C-121°C for 10-15 minutes, cooling, and storing in a 4°C refrigerator after sterility test.
[0040] The composition of the growth promoter is as follows: 0.015 g of pyridoxine hydrochloride, 0.015 g of biotin, 0.15 g of coenzyme A, 0.15 g of adenosine triphosphate, 0.15 g of catalase, 0.15 g of α-naphthalene acetic acid, 1.5 g of peptone, glucose, 15 g gram, bovine serum albumin V5 factor 150 gr...
Embodiment 3
[0042] Example 3: The composition of the basal medium is as follows: copper sulfate 0.002 g, zinc sulfate 0.003 g, calcium chloride 0.002 g, magnesium sulfate 0.02 g, oleic acid 0.02 g, ferric ammonium citrate 0.1 g, sodium citrate 0.2 g g, ammonium sulfate 0.4 g, sodium pyruvate 1 g, Tween-80 1 g, asparagine 2 g, potassium dihydrogen phosphate 2 g, sodium dihydrogen phosphate 4 g, neutral glycerin 12 ml, distilled water 1000 ml. The preparation method is as follows: firstly dissolving the above-mentioned components in double distilled water, then sterilizing in high pressure at 115°C-121°C for 10-15 minutes, cooling, and storing in a 4°C refrigerator after sterility test.
[0043] The composition of the growth promoter is as follows: 0.02 g of pyridoxine hydrochloride, 0.02 g of biotin, 0.2 g of coenzyme A, 0.2 g of adenosine triphosphate, 0.2 g of catalase, 0.2 g of α-naphthalene acetic acid, 2 g of peptone, 20 g of glucose, Bovine Serum Albumin V5 Factor 200g. The preparat...
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