Prostate cancer metabonomics marker and screening method thereof
A technology of metabolomics and prostate cancer, applied in scientific instruments, biological testing, biomaterial analysis, etc., can solve the problems of incomplete sedimentation and low sedimentation efficiency, and achieve the effects of avoiding accuracy, improving efficiency, and rapid adsorption
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Embodiment 1
[0024] A metabolomic marker of prostate cancer is obtained by removing high-abundance proteins from blood, purifying with a sedimentation agent, and then performing fluorescent staining and two-dimensional gel electrophoresis to obtain a metabolomic marker of prostate cancer.
[0025] The prostate cancer metabolomic markers were screened by the following steps:
[0026] Step S1: Shake the blue medium well, centrifuge for 5 s at a speed of 10000 r / min, remove the supernatant, add the substrate to the equilibration solution, continue centrifugation for 5 s, remove the supernatant, and add the substrate to the equilibration solution , continue centrifugation for 20s, remove the supernatant, mix the substrate and plasma evenly, incubate for 5min at a temperature of 20°C, centrifuge for 60s at a speed of 10000r / min, and continue to incubate the supernatant for 5min , centrifuge again, take the supernatant to keep warm to obtain the first sample, add the substrate to the equilibrium...
Embodiment 2
[0035] A metabolomic marker of prostate cancer is obtained by removing high-abundance proteins from blood, purifying with a sedimentation agent, and then performing fluorescent staining and two-dimensional gel electrophoresis to obtain a metabolomic marker of prostate cancer.
[0036] The prostate cancer metabolomic markers were screened by the following steps:
[0037] Step S1: Shake the blue medium well, centrifuge for 8s at a speed of 10000r / min, remove the supernatant, add the substrate to the equilibration solution, continue centrifugation for 8s, remove the supernatant, and add the substrate to the equilibration solution , continue centrifugation for 30s, remove the supernatant, mix the substrate and plasma evenly, incubate for 8min at a temperature of 23°C, centrifuge for 60s at a speed of 11000r / min, and continue to incubate the supernatant for 8min , centrifuge again, take the supernatant to keep warm to obtain the first sample, add the substrate to the equilibrium so...
Embodiment 3
[0046] A metabolomic marker of prostate cancer is obtained by removing high-abundance proteins from blood, purifying with a sedimentation agent, and then performing fluorescent staining and two-dimensional gel electrophoresis to obtain a metabolomic marker of prostate cancer.
[0047] The prostate cancer metabolomic markers were screened by the following steps:
[0048] Step S1: Shake the blue medium well, centrifuge for 10s at a speed of 10000r / min, remove the supernatant, add the substrate to the equilibration solution, continue centrifugation for 10s, remove the supernatant, and add the substrate to the equilibration solution , continue centrifugation for 40s, remove the supernatant, mix the substrate and plasma evenly, incubate for 10min at a temperature of 25°C, centrifuge for 60s at a speed of 12000r / min, and continue to incubate the supernatant for 10min , centrifuge again, take the supernatant to keep warm to obtain the first sample, add the substrate to the equilibriu...
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