Method for detecting plasticizer by nematode larvae
A technology of plasticizers and nematodes, which is applied in the direction of biological testing, material inspection products, etc., can solve the problems of complex operation, high instrument dependence, and high cost, and achieve the effect of convenient experimental operation, low cost, and easy mastery
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specific Embodiment approach 1
[0016] Specific embodiment one: In this embodiment, the method of using nematode larvae to detect plasticizers is as follows:
[0017] 1. Weigh 1.0 g of cholesterol, dissolve it in absolute ethanol, and prepare a cholesterol ethanol solution with a concentration of 10 mg / ml;
[0018] 2. Preparation of phosphate buffer: weigh 13.6g KH 2 PO 4 , 1.8g KOH, add distilled water to 100mL, adjust the pH value to 6.0;
[0019] 3. Mix 15-20g agar powder, 2-3g peptone, 0.10-0.12g CaCl 2 , 0.11~0.13g MgSO 4 Add 2~3g NaCl and 2~3g NaCl into a 1000mL beaker, add 1ml cholesterol ethanol solution and 25mL phosphate buffer, and distill the volume to 1000ml with distilled water;
[0020] 4. Seal the beaker, put it in a high-pressure steam sterilizer at 120°C for 15-25 minutes, then cool it down to 50-60°C, add 0.5-5ml of white wine to be tested under a sterile environment, and then put the mixture in a sterile Pour it into a petri dish under the environment, and dry it in a sterile environ...
specific Embodiment approach 2
[0022] Specific embodiment two: the difference between this embodiment and specific embodiment one is that in step two, 16~19g agar powder, 2g peptone, 0.10g CaCl 2 , 0.11g MgSO 4 and 2g NaCl were added to a 1000mL beaker. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0023] Specific embodiment three: what this embodiment is different from specific embodiment one is that in step 2, 15g agar powder, 2g peptone, 0.10g CaCl 2 , 0.11g MgSO 4 and 2g NaCl were added to a 1000mL beaker. Others are the same as in the first embodiment.
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