Anion diagnosis marker for osteoporosis and detection method thereof
A diagnostic marker and osteoporosis technology, which is applied in the field of osteoporosis negative ion diagnostic markers and its detection, can solve the problems of limited detection and achieve a wide range of applications
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Embodiment 1
[0026] A negative ion diagnostic marker for osteoporosis, including two kinds of serum polar negative ions, the two serum polar negative ions are respectively 4-hydroxyproline and 3-[3-(sulfoxyl)phenyl]propionic acid, The detection method of this marker is as follows:
[0027] (1) Take 50 μL serum sample and place it in a 96-well plate, add 200 μL methanol / acetonitrile (1:1, v / v);
[0028] (2) Vortex for 5 minutes, let stand at 4°C for 10 minutes, then centrifuge in a plate centrifuge at 5010g for 20 minutes at 4°C;
[0029] (3) After transferring 200 μL of the supernatant to a new 96-well plate, freeze-dry in a freeze dryer for 2-3 hours;
[0030] (4) sealed and stored at low temperature for mass spectrometry analysis;
[0031] (5) Reconstitute the lyophilized supernatant with 80 μL of acetonitrile-water (1:3, v / v), vortex for 3 minutes, centrifuge at 5010 g for 20 minutes at 4°C, and then take 70 μL of the supernatant for testing , the specific detection process is: using...
Embodiment 2
[0034] A negative ion diagnostic marker for osteoporosis, including two kinds of serum polar negative ions, the two serum polar negative ions are respectively 4-hydroxyproline and 3-[3-(sulfoxyl)phenyl]propionic acid, The detection method of this marker is as follows:
[0035] (1) Take 50 μL serum sample and place it in a 96-well plate, add 200 μL methanol / acetonitrile (1:1, v / v);
[0036] (2) Vortex for 5 minutes, let stand at 4°C for 10 minutes, then centrifuge at 4800g for 20 minutes at 5°C in a plate centrifuge;
[0037] (3) After transferring 200 μL of the supernatant to a new 96-well plate, place it in a freeze dryer for 2 hours to freeze-dry;
[0038] (4) sealed and stored at low temperature for mass spectrometry analysis;
[0039] (5) Reconstitute the lyophilized supernatant with 80 μL of acetonitrile-water (1:3, v / v), vortex for 3 minutes, centrifuge at 5000 g for 15 minutes at 4°C, and then take 70 μL of the supernatant for sample detection , the specific detectio...
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