Test strip for detecting pepsinogen I and pepsinogen II as well as detection method and application of test strip
A technology of pepsinogen and test strips, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve problems such as prone to errors, and achieve the effects of high precision, accurate ratio results, and small errors
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Embodiment 1
[0037] Such as figure 1 with 2 As shown, a test strip for detecting pepsinogen I and II of this embodiment includes a bottom plate 1, and absorbent paper 3 and nitrocellulose sequentially adhered to the bottom plate 1 along the length direction of the bottom plate 1. The plain film 2, the binding pad 5, and the sample pad 4; wherein the nitrocellulose film 2 is adhered to the middle part of the bottom plate 1, the absorbent paper 3, the nitrocellulose film 2, and the binding pad 5 and the sample pad 4, which are sequentially in contact with and only with adjacent parts and partially overlap; the nitrocellulose membrane 2 is provided with spaced first sprayed pepsinogen I monoclonal antibody I Detection zone 7, the second detection zone 8 of the pepsinogen II monoclonal antibody II, and the quality control zone 6 sprayed with rabbit anti-mouse polyclonal antibody. The binding pad 5 is sprayed with the surface modified pepsinogen I monoclonal antibody Antibody I and pepsinogen II...
Embodiment 2
[0043] On the basis of Example 1, this example further provides a preparation method of the test strip described in Example 1, including the following steps:
[0044] (1) Antibody pretreatment: select commercial pepsinogen I monoclonal antibody I and pepsinogen II monoclonal antibody II, use 0.05mol / L, pH 7.2-7.6 phosphate buffer at 4℃ Dialysis overnight.
[0045] (2) Preparation of binding pad 5: Add carbodiimide (EDC) (final concentration 20mmol) and pretreated pepsinogen I monoclonal antibody I (microsphere quality: antibody) to the polymer nanosphere solution Mass=50:1), react at room temperature for 2 hours, centrifuge, remove the supernatant, add sample diluent (0.05mol / L containing 1% BSA, pH 7.2 phosphate buffer) to the microsphere concentration of 1.0 mg / ml, to be used. Add carbodiimide (EDC) (final concentration 20mmol) and pretreated pepsinogen II monoclonal antibody I (microsphere mass: antibody mass = 50:1) into the polymer nanosphere solution, and react at room temp...
Embodiment 3
[0049] Such as image 3 As shown, on the basis of Example 1, this example further provides a test paper card for detecting pepsinogen I and II, which includes the test paper strip described in Example 1 and the test strip coated The housing; the housing includes a base and a card cover 9, the card cover 9 is provided with a partial area observation port 11 for exposing the test strip and a sample port 10; wherein the sample port 10 is provided in the Above the sample pad 4 to expose part or all of the sample pad 4 area, the observation port 11 is provided on the upper part of the nitrocellulose membrane 2 to expose the first detection zone 7 and the second detection zone 8 and the quality control belt 6. In this embodiment, the test paper card with a shell is not only convenient for storage and carrying, but also convenient for detection operations during operation; and the setting of the sample addition port 10 is convenient for adding sample liquid during the operation, and t...
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