Active chemiluminescent protein chip
A technology of chemiluminescence and protein chips, applied in chemiluminescence/bioluminescence, analysis through chemical reactions of materials, scientific instruments, etc. problem, to achieve the effect of improving sensitivity and simple structure
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Embodiment 1
[0037] (1) Fix the nitrocellulose membrane 4 coated with the rubella virus antigen microarray on the base 3, place the cuvette 1 on the base 3 to press the nitrocellulose membrane 4 in advance, and place the locking ring 2 along the The outer wall of the cuvette 1 slides down, and the elastic tightening piece 6 contracts inwardly under the extrusion force from the clamping groove 7. After the top surface is in contact, the elastic tightening piece 6 is tightly attached to the outer wall of the base 3 to grasp the base 3, and the locking ring 2 completes the clamping and fixing work of the cuvette 1 and the base 3;
[0038] (2) Connect the small opening at the bottom of the base 3 to the peristaltic pump;
[0039] (3) Add 200 μL of the sample to be tested into cuvette 1 at room temperature (the sample has been diluted at a ratio of 1:10);
[0040] (4) Turn on the peristaltic pump, set the reaction speed of the peristaltic pump to 0.1 rpm, and the sample to be tested in the cuv...
Embodiment 2
[0047] The difference between embodiment 2 and embodiment 1 is only in step (3), and all the other steps are the same:
[0048] (3) Add 200 μL of the sample to be tested into cuvette 1 at room temperature (the sample has been diluted at a ratio of 1:100);
Embodiment 3
[0050] The difference between embodiment 3 and embodiment 1 is only in step (3), and all the other steps are the same:
[0051] (3) Add 200 μL of the sample to be tested into cuvette 1 at room temperature (the sample has been diluted at a ratio of 1:1000);
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