Integral detection reaction plate and protein chip kit of hapetitis and cirrhosis
A technology integrating detection and reaction plates, applied in the field of in vitro clinical testing and biochips, can solve problems such as difficulty in meeting the inspection market, unfavorable routine physical examination, popularization of civilians, and cost.
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Embodiment 1
[0043] Preparation of detection reaction plate
[0044] Take a 96-well plate and set 42-84 sample wells and 1-8 standard wells. A solid phase support (NC membrane or PDVF membrane) is placed at the bottom of each reaction well, and the solid phase support is coated with six kinds of antigens such as anti-HBsAg, HCVAg, anti-AFP, anti-AFU, anti-MAO, and anti-HA. Antibody protein microarray ( figure 1 ).
Embodiment 2
[0046] kit preparation
[0047] Prepare a test kit containing six indicators integrated detection of hepatitis B and C, liver cirrhosis and liver cancer, which contains one reaction well plate (8-200 people) of embodiment 1, 1 bottle of washing concentrate, 1 bottle of enzyme-labeled working solution One bottle of detection solution A, one bottle of detection solution B, and a standard bottle.
[0048] Washing Concentrate, Enzyme Label Working Solution, Detection Solution A, Detection Solution B
Embodiment 3
[0050] Integrated detection of six indicators of hepatitis B and C, liver cirrhosis and liver cancer
[0051] Test each blood sample according to the following method:
[0052] 1. Add test blood or standard products to corresponding reaction wells, 100ul / well.
[0053] 2. Add enzyme-labeled working solution, 75ul / well.
[0054] 3. Incubate and shake at 30°C for 60 minutes.
[0055] 4. Wash 4-6 times with lotion, 5 minutes each time, vibrate.
[0056] 5. Add detection solution 40ul / well, so that the detection solution is evenly distributed on the bottom of the well.
[0057] 6. CCD detection, exposure for 3-20 seconds depending on the intensity of the luminescent signal.
[0058] Result judgment:
[0059] According to the CutOff value of different indicators, refer to the gradient curve of the standard to determine the negative or positive of the sample serum.
[0060] At the same time, the serum samples tested were routinely tested by conventional methods. The result sh...
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