Method for detecting inflammatory markers and kit for detecting inflammatory markers
A detection kit and detection method technology are applied in the detection of inflammatory markers and the field of inflammatory marker detection kits, which can solve the problems of narrow detection range of inflammatory markers, low sensitivity, and requirements for manual operation of climate conditions, etc. Stable test results, high accuracy and sensitivity, and easy operation
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Embodiment 1
[0114] Example 1: Simultaneous detection of three markers SAA / PCT / CRP
[0115] 1. Prepare
[0116] 1.1 Select different codable magnetic fluorescent microspheres according to different projects
[0117] SAA→No.8 Microspheres
[0118] PCT→No.1 microsphere
[0119] CRP → No. 15 microspheres;
[0120] 1.2 Take 1 mg of the prepared No. 1 / 8 / 15 microspheres respectively, and wash them with MES buffer (50 mM) at pH 5.5;
[0121] 1.3 Use 0.1M pH6.2Na 2 HPO 4 The solution was activated and vortexed for 20s; after that, 100 μg of NHS and EDC were added respectively (NHS and EDC were dissolved in 50 mM MES buffer solution with pH 5.5, which is now used and prepared), vortexed for 20s, and room temperature for 30 minutes;
[0122] 1.4 Use a magnetic separation plate for magnetic separation, and absorb the supernatant; add 500 μL of MES buffer solution (50 mM) at pH 5.5, vortex the microspheres for 20 seconds, perform magnetic separation with a magnetic separation plate, and absorb t...
Embodiment 2
[0148] Example 2: Simultaneous detection of three markers PCT / SAA / CRP
[0149] 1. Prepare
[0150] 1.1 Select different codable magnetic fluorescent microspheres according to different projects
[0151] PCT→16 microspheres
[0152] SAA→24 microspheres
[0153] CRP → No. 26 microspheres;
[0154] 1.2 Take 1 mg of the prepared No. 16 / 24 / 26 microspheres respectively, and wash them with MES buffer (20 mM) at pH 5.0;
[0155] 1.3 Use 0.1M pH6.2Na 2 HPO 3 The solution was activated and vortexed for 20s; after that, 100 μg of NHS and EDC were added respectively (NHS and EDC were dissolved in 20 mM MES buffer with pH 5.0, and prepared immediately after use), vortexed for 20s, and 30 minutes at room temperature.
[0156] 1.4 Use a magnetic separation plate for magnetic separation, and absorb the supernatant; add 500 μL of MES buffer solution (20 mM) at pH 5.0, vortex the microspheres for 20 seconds, perform magnetic separation with a magnetic separation plate, and absorb the supern...
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