Eight-joint detection kit for vaginitis
A kit and vaginitis technology, applied in the field of in vitro diagnostic reagents, can solve the problem of inability to simultaneously detect aerobic bacterial vaginitis, bacterial vaginosis, trichomonal vaginitis and fungal vaginitis, and the lack of detection accuracy of the kit, etc. problems, to achieve the effect of solving solubility problems, small proportion, and increasing firmness
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Embodiment 1
[0043] Such as Figure 1-Figure 2 A vaginitis eight joint detection kit is shown, including a reaction plate 1, the reaction plate has a reaction well 2 for detecting the following indicators: β-glucuronidase, coagulase, hydrogen peroxide, sialidase, leukocyte ester Enzyme, acetylamino-β-glucosidase, proline aminopeptidase, pH; (2) diluent;
[0044] The substrate reaction reagent of the β-glucuronidase reaction well 2 is an absolute ethanol solution of 0.1-5g / L 5-bromo-4-chloro-3-indole glucuronide, and the β-glucuronidase The stabilizer protection solution of the reaction well is an aqueous solution of 20-50 g / L trehalose.
[0045] The substrate reaction reagent of the coagulase reaction well is glycyl-arginyl-4-methoxy-β-naphthylamide hydrochloride 0.2-4g / L, and the solvent is PBS buffer; the stability of the coagulase reaction well is The agent protection solution is an aqueous solution of 20-50g / L trehalose.
[0046] The substrate reaction reagents of the hydrogen perox...
Embodiment 2
[0058] The solvent of the β-glucuronidase reaction well is ethylene glycol, and the other is the same as in Example 1. The test activity is 1U / mL of β-glucuronidase quality control substance. The comparison results with Example 1 are shown in Table 1.
Embodiment 3
[0060] No HRP enzyme stabilizer is added to the reaction reagent of the hydrogen peroxide reaction well, and the others are the same as in Example 1. The comparison results are shown in Table 2. Table 2 shows the activity of the hydrogen peroxide reaction well under different storage times.
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