Method for extracting abalone hepatopancreas metabolites
A technology of hepatopancreas and metabolites, applied in the field of molecular biology, can solve problems such as being unsuitable for high-throughput, large-scale use, ineffective removal of polysaccharides and pigments, affecting the quantification of important metabolites, etc., to eliminate polysaccharides and pigments. The effect of interference, high recovery rate and low cost
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Embodiment 1
[0033] Example 1 Using the method of the present invention to extract abalone hepatopancreas metabolites
[0034] The specific method includes the following steps:
[0035] S1. Weigh 300 mg abalone hepatopancreas and place in a 5 mL centrifuge tube;
[0036] S2. Add 1.2 mL of methanol and 0.6 mL of water to the centrifuge tube in step S1, and add steel balls, and then place it in a low-temperature tissue grinder and vibrate at 4 °C to break;
[0037] S3. Add 1.2 mL of chloroform and 1.2 mL of water to the centrifuge tube in step S2, vortex at a speed of 2500 rpm for 1 min, and place it on ice for 10 min;
[0038] S4. Centrifuge at 10000 g for 10 min at 4 °C after standing still, and transfer the upper layer solution to another centrifuge tube;
[0039] S5. Put the upper layer solution obtained in step S4 into a freeze-dried powder by vacuum freeze-drying in a vacuum freeze dryer at -80°C after quick-freezing with liquid nitrogen;
[0040] S6. Add 0.9 mL methanol and 0.1 mL ...
Embodiment 2
[0047] Example 2 Using the method of the present invention to extract hepatopancreatic metabolites from abalone
[0048] The specific method includes the following steps:
[0049] S1. Weigh 300 mg abalone hepatopancreas and place in a 5 mL centrifuge tube;
[0050] S2. Add 1.2 mL of methanol and 0.6 mL of water to the centrifuge tube in step S1, and add steel balls, and then place it in a low-temperature tissue grinder and vibrate at 4 °C to break;
[0051] S3. Add 1.2 mL of chloroform and 1.2 mL of water to the centrifuge tube in step S2, vortex at a speed of 2500 rpm for 1 min, and place it on ice for 10 min;
[0052] S4. Centrifuge at 10000 g for 10 min at 4 °C after standing still, and transfer the upper layer solution to another centrifuge tube;
[0053] S5. Put the upper layer solution obtained in step S4 into a freeze-dried powder by vacuum freeze-drying in a vacuum freeze dryer at -80°C after quick-freezing with liquid nitrogen;
[0054] S6. Add 0.9 mL methanol and ...
Embodiment 3
[0061] Example 3 Using the method of the present invention to extract abalone hepatopancreas metabolites
[0062] The specific method includes the following steps:
[0063] S1. Weigh 300 mg abalone hepatopancreas and place in a 5 mL centrifuge tube;
[0064] S2. Add 1.2 mL of methanol and 0.6 mL of water to the centrifuge tube in step S1, and add steel balls, and then place it in a low-temperature tissue grinder and vibrate at 4 °C to break;
[0065] S3. Add 1.2 mL of chloroform and 1.2 mL of water to the centrifuge tube in step S2, vortex at a speed of 2500 rpm for 1 min, and place it on ice for 10 min;
[0066] S4. Centrifuge at 10000 g for 10 min at 4 °C after standing still, and transfer the upper layer solution to another centrifuge tube;
[0067] S5. Put the upper layer solution obtained in step S4 into a freeze-dried powder by vacuum freeze-drying in a vacuum freeze dryer at -80°C after quick-freezing with liquid nitrogen;
[0068] S6. Add 0.9 mL methanol and 0.23 mL...
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