Prostatitis Joint Detection Kit
A prostatitis and reagent kit technology, applied in the field of biochemical detection, can solve the problems of not being able to meet the needs of clinical quickness and simplicity, cumbersome operation, and long detection time of detection methods, and achieve the effects of easy promotion, avoiding missed detection, and simple operation
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Embodiment 1
[0024] The prostatitis joint detection kit according to the present invention includes a sample diluent, a chromogenic solution, and a detection card body provided with seven reaction wells. The solid reagent of phospholipid body, citric acid, zinc, acid phosphatase and elastase, the solid reagent is a reagent pad made of cotton pulp paper, filter paper, glass fiber or plastic and other carriers containing detection reagents. The specific manufacturing method of the reagent pads in the seven reaction wells is as follows:
[0025] 1. Solid reagent pad for detecting pH value: Take 10 μL of the solution prepared by 0.5~100g / L bromothymol blue sodium salt and 20 times of purified water, and apply it on a carrier with a diameter of 5.5mm, dehumidify and dry (temperature 18~ 25℃, humidity≤30%);
[0026] 2. Solid reagent pad for detecting leukocyte esterase: prepared by Tris-HCl buffer, sugar and 5-bromo-4-chloro-3-indole acetate solution, coated on the carrier, dehumidified and dri...
Embodiment 2
[0051] The prostatitis joint detection kit according to the present invention includes a sample diluent, a chromogenic solution, and a detection card body provided with seven reaction wells. The solid reagent of phospholipid body, citric acid, zinc, acid phosphatase and elastase, the solid reagent is a reagent pad made of cotton pulp paper, filter paper, glass fiber or plastic and other carriers containing detection reagents. The specific manufacturing method of the reagent pads in the seven reaction wells is as follows:
[0052] 1. Solid reagent pad for detecting pH value: Take 10 μL of the solution prepared by 0.5~100g / L bromothymol blue sodium salt and 20 times of purified water, and apply it on a carrier with a diameter of 5.5mm, dehumidify and dry (temperature 18~ 25℃, humidity≤30%);
[0053] 2. Solid reagent pad for detecting leukocyte esterase: prepared by Tris-HCl buffer, sugar and 5-bromo-4-chloro-3-indole acetate solution, coated on the carrier, dehumidified and dri...
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