Hepatitis B and C and multiple tumor marker protein chip inspecting reagent unit
A technology for hepatitis C and B and C, which is applied in the field of in vitro clinical testing and biochips, can solve the problems of laborious, expensive, unfavorable routine physical examination, popularization of civilians, etc.
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Embodiment 1
[0036] Preparation of detection reaction plate
[0037] Take a 48-well plate, set 42 sample wells and 6 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 anti-HBsAg, HCVAg, anti-AFP, anti-CEA, anti-CA199, anti-CA125, anti-PSA and anti- Protein microarrays of eight antigens or antibodies such as fPSA ( figure 1 ).
Embodiment 2
[0039] kit preparation
[0040] Prepare a test kit containing eight indicators of hepatitis B and C and various tumor diseases for integrated detection. It contains one reaction well plate (24-48 people) of Example 1, one bottle of washing concentrate, and one enzyme-labeled working solution. One bottle of detection solution A, one bottle of detection solution B, and a standard bottle.
[0041] Washing Concentrate, Enzyme Label Working Solution, Detection Solution A, Detection Solution B
Embodiment 3
[0043] Integrated detection of eight indicators of hepatitis B and C and various tumor diseases
[0044] Test each blood sample according to the following method:
[0045] 1. Add test blood or standard substance to the corresponding reaction well, 75ul / well.
[0046] 2. Add enzyme-labeled working solution, 75ul / well.
[0047] 3. Incubate and shake at 37°C for 60 minutes.
[0048] 4. Wash 4-6 times with lotion, 2 minutes each time, vibrate.
[0049] 5. Add detection solution 20ul / well, so that the detection solution is evenly distributed at the bottom of the well.
[0050] 6. CCD detection, exposure for 30-60 seconds depending on the strength of the luminescent signal.
[0051] Result judgment:
[0052] 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.
[0053] At the same time, the serum samples tested were routinely tested by conventional methods. The result show...
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