Rapid detective reagent strip of treponema pallidum immunoglobulin m (IgM) antibody and preparation method thereof
A technology for treponema pallidum and detection reagents, applied in measuring devices, instruments, scientific instruments, etc., to achieve the effects of simple and fast operation, high sensitivity and strong specificity
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Embodiment 1
[0027] see figure 1 , a rapid detection reagent strip for Treponema pallidum IgM antibody comprising a sample pad (1), a colloidal gold pad (2), an NC film (3), a sample suction pad (4) and a plastic plate (7), and the colloidal gold pad is marked with T1 antibody and TP fusion protein, the anti-human IgM μ chain monoclonal antibody coated on the NC membrane constitutes the T line (5) and the goat anti-mouse IgG antibody constitutes the C line (6), the sample pad, colloidal gold pad, NC membrane Paste the sample pad on the plastic plate to form a detection reagent strip.
[0028] The detection reagent strip is prepared by the following method:
[0029] 1. Preparation of Colloidal Gold Pads
[0030] Prepare the colloidal gold solution that diameter is 30-50nm with chloroauric acid-trisodium citrate reduction method, 0.2MK CO Regulate the pH of colloidal gold solution to be 8.5-9.5, then be placed on the magnetic stirrer and stir slowly, press every 100ml solution containing ...
Embodiment 2
[0038] Similar to Example 1, the difference is that the labeling and coating proteins are reversed, that is, the colloidal gold pad is labeled with an anti-human IgM μ chain monoclonal antibody, and the detection area on the NC membrane is coated with TP recombinant antigen as a T line (5), and at the same time, it is coated with the labeled plus The sample loading indicator line (8) at the sample position, for details, refer to figure 2 . When testing, first add 3 to 5ul of the standard substance to be tested on the NC membrane marking line, then add an appropriate amount of sample diluent to the sample pad, and let it stand for 20 minutes to observe the test results. The assembly of the reagent strips and the determination of the test results of the clinical samples are the same as in Example 1.
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