Cardiac fatty acid binding protein detection kit and preparation method thereof
A fatty acid combination and protein detection technology, which is applied in the direction of biological testing, measuring devices, material inspection products, etc., can solve the problems of narrow detection linear range, poor reagent stability, poor anti-interference ability, etc., and achieve wide detection linear range, Accelerate the speed of immune response and improve the effect of stability
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Embodiment 1
[0053] This embodiment relates to the preparation of a H-FABP detection kit, including components and contents as follows:
[0054] Reagent R1:
[0055] components
specific type
Content description
Buffer solution with pH=7.0~7.6
Glycine buffer
120mmol / L, pH7.4
Surfactant
Tween 20
10ml / L
Chelating agent
Disodium edetate
50mmol / L
Accelerator
Dextran 8000
200mmol / L
preservative
NaN 3
1‰
[0056] Various ingredients can be added sequentially at room temperature, sealed and stored for later use. Alternatively, they are packaged individually and prepared immediately prior to testing.
[0057] Reagent R2: The preparation of latex reagent of anti-human H-FABP antibody includes the following steps.
[0058] Step 1: Acidifying the mouse anti-human H-FABP antibody in MES solution with a pH value of 4.0-6.0;
[0059] Step 2: Adjust the pH of the solution obtained in Step 1 to 7.4-8.2 wi...
Embodiment 2
[0067] The H-FABP detection kit described in this example is applicable to various types of automatic biochemical analyzers. Taking Hitachi 7170 automatic biochemical analyzer as an example, its operation is shown in Table 1. Analysis method: two-point endpoint method, that is, the dosage of reagent R1 and reagent R2 is 150ul and 50ul respectively, and the sample volume is 10ul.
[0068] Adopt kit reagent of the present invention and above-mentioned assay method, adopt the curve of the H-FABP standard substance (self-made) of 6 kinds of different contents that Hitachi 7170 biochemical analyzer records (such as figure 1 Shown), each point represents a content of the reference standard, wherein the X-axis represents the H-FABP content (ng / ml); Y-axis represents the absorbance.
[0069] Table 1
[0070]
Embodiment 3
[0071] Embodiment 3: Correlation test of detection reagent
[0072] Use the reagent of this method invention (specific formula is the same as embodiment 1) and the H-FABP latex enhanced immune turbidimetric reagent of British Landau Company of contrast reagent, adopt automatic 7170 full-automatic biochemical analyzers to 50 parts of human serum (normal and abnormal specimens) ) were measured simultaneously according to their respective parameters, and correlation analysis was carried out on the measured values.
[0073] See the test results figure 2 , X, Y axis are measured value (the content ng / ml of H-FABP), by figure 2 The results show that the correlation between the two reagents is R 2 =0.9947, the regression equation is y=0.9854x+0.3527. The result shows that the kit reagent of the present invention has good correlation with British Landau's determination of patient's serum, and has good specificity and accuracy.
[0074] In addition, the above experiments were c...
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