Kit for determining Lp-PLA2 based on latex particle-enhanced turbidimetric immunoassay and preparation method of kit
An immunoturbidimetric and latex-enhanced technology, which is used in measurement devices, instruments, disease diagnosis, etc., can solve the problems of poor specificity and low sensitivity, achieve high accuracy, meet clinical needs, and improve sensitivity and specificity.
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[0027] In addition, the present invention also provides a method for preparing a test kit based on latex-enhanced immune turbidimetry for measuring Lp-PLA2, which includes the following steps:
[0028] S100, measure the latex microspheres with a solid content of 10%, add to the buffer, centrifuge, remove the supernatant, resuspend the latex microsphere sediment with buffer, add carbodiimide (also known as EDC) and N -Hydroxysuccinimide (aka NHS), activated. The weight ratio of carbodiimide and N-hydroxysuccinimide added in the present invention is 1:5-1:50; centrifuge again, remove the supernatant, and resuspend the latex microsphere precipitate with buffer , to prepare activated latex microspheres. There are mainly three operations in step S100: centrifugation to remove supernatant, activation, and resuspension.
[0029] S200. Take at least two kinds of monoclonal antibodies and mix them to prepare an antibody containing multiple monoclonal antibodies. In this step, by scr...
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[0036] Below in conjunction with specific embodiment, further illustrate the present invention. It should be understood that these examples are only used to illustrate the present invention and are not intended to limit the scope of the present invention. In addition, it should be understood that after reading the content of the present invention, those skilled in the art may make various changes or modifications to the present invention, and these equivalent forms also fall within the scope defined by the appended claims of the present application.
[0037] 1. Preparation of Lp-PLA2 reagent R1 (i.e. reaction solution):
[0038] Accurately weigh the chemical substances according to the ratio in List 1, place them in a beaker filled with 0.9L pure water, stir and mix well, adjust the pH value to 7.20±0.05 with 1mol / L dilute hydrochloric acid, and transfer the solution to Dilute to volume in a 1L volumetric flask, filter the solution with a 0.22-micron membrane filter, store th...
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