Method for correcting human genome damage through micro nutrient substances according to genetic background
A genome damage and nutrient technology, applied in the fields of nutritional genomics and medical genetics, can solve the problems that have not been seen before, and achieve the effect of maintaining stability and preventing cardiovascular diseases.
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Embodiment 1
[0062] A method for correcting human genome damage with micronutrients based on genetic background, comprising the steps of:
[0063] (1) Detection of blood folic acid level:
[0064] S1. Acquisition of serum: collect individual peripheral blood with a coagulation-promoting tube, then put it at 4°C for coagulation for 1 hour, centrifuge at 2500 rpm for 15 minutes, and the yellow supernatant is serum, which is divided into 300 μl each, and stored at -20°C in the dark;
[0065] S2. Detection of serum folic acid level: After the serum sample was thawed at room temperature for half an hour, the sample was added to the BECKMANAccess2 automatic immune analyzer for detection, and the serum folic acid value of the tested sample was obtained;
[0066] S3. Red blood cell acquisition: collect individual peripheral blood with EDTA-anticoagulant tube, centrifuge at 1000rpm for 5min to separate red blood cells, wash red blood cells three times with normal saline, centrifuge at 1000rpm for 5...
Embodiment 2
[0113]A method for correcting human genome damage with micronutrients based on genetic background, comprising the steps of:
[0114] (1) Detection of blood folic acid level:
[0115] S1. Acquisition of serum: Collect individual peripheral blood with a coagulation-promoting tube, then place it at 4°C for coagulation for 1 hour, centrifuge at 2500 rpm for 20 minutes, and the yellow supernatant is serum, which is divided into 300 μl each, and stored at -20°C in the dark;
[0116] S2. Detection of serum folic acid level: After the serum sample was thawed at room temperature for half an hour, the sample was added to the BECKMANAccess2 automatic immune analyzer for detection, and the serum folic acid value of the tested sample was obtained;
[0117] S3. Red blood cell acquisition: collect individual peripheral blood with EDTA-anticoagulant tube, centrifuge at 1000rpm for 10min to separate red blood cells, wash red blood cells three times with normal saline, centrifuge at 1000rpm for...
Embodiment 3
[0164] A method for correcting human genome damage with micronutrients based on genetic background, comprising the steps of:
[0165] (1) Detection of blood folic acid level:
[0166] S1. Serum acquisition: collect individual peripheral blood with a coagulation-promoting tube, then put it at 4°C for coagulation for 1 hour, centrifuge at 2500rpm for 18 minutes, and the yellow supernatant is serum, which is divided into 300 μl each, and stored at -20°C in the dark;
[0167] S2. Detection of serum folic acid level: After the serum sample was thawed at room temperature for half an hour, the sample was added to the BECKMANAccess2 automatic immune analyzer for detection, and the serum folic acid value of the tested sample was obtained;
[0168] S3. Red blood cell acquisition: collect individual peripheral blood with EDTA-anticoagulant tube, centrifuge at 1000rpm for 7min to separate red blood cells, wash the red blood cells three times with normal saline, centrifuge at 1000rpm for 5...
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