Test strip for quantitatively detecting prostate-specific antigen as well as preparation method and test paper card
A prostate-specific and quantitative detection technology, applied in the field of in vitro test strip detection, can solve problems such as easy errors, achieve high accuracy, improve fluorescence intensity, and reduce quenching effects
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Embodiment 1
[0043] Such as figure 1 As shown, a test strip for simultaneous detection of free and total prostate-specific antigen includes a base plate 1 and absorbent paper 3, nitrocellulose membrane 2, and binding pad 5 sequentially adhered to the base plate 1 along the length direction of the base plate 1 and sample pad 4;
[0044] The nitrocellulose membrane 2 is adhered to the middle part of the bottom plate 1, and the two ends overlap with the absorbent paper 3 and the binding pad 5 respectively; the other end of the binding pad 5 partially overlaps with the sample pad 4;
[0045] A first detection zone 7, a second detection zone 8 and a quality control zone 6 are sequentially arranged on the nitrocellulose membrane 2 at intervals;
[0046] The surface of the binding pad 5 is sprayed with anti-compound prostate-specific antigen antibody and anti-free prostate-specific antigen antibody, and both the anti-compound prostate-specific antigen antibody and the anti-free prostate-specific...
Embodiment 2
[0051] A method for preparing a test strip for simultaneously detecting free and total prostate-specific antigens, comprising the following steps:
[0052] (1) Antibody pretreatment:
[0053] Dialyze the commercial composite PSA scratching antibody and the free PSA scratching antibody overnight at 4°C with 0.05mol / L phosphate buffer solution with a pH of 7.2-7.6;
[0054] (2), preparation of bonding pad 5:
[0055] Add carbodiimide (EDC) (the final concentration of EDC is 20mmol / L) and step (1) pretreated composite prostate-specific antigen delimiting antibody in the nanometer microsphere solution of lanthanide rare earth ion, nanometer microsphere The mass ratio to the pretreated antibody is 50:1, react at room temperature for 2 hours, centrifuge, remove the supernatant, add sample diluent (0.05 mol / L of BSA containing 1% mass fraction, phosphoric acid at pH 7.2 Salt buffer solution) until the microsphere concentration is 1.0ug / L, stand-by;
[0056] Add carbodiimide (EDC) ...
Embodiment 3
[0062] Such as figure 2 As shown, a test paper card for quantitative detection of prostate specific antigen comprises a test paper strip for quantitative detection of prostate specific antigen and a casing covering the test strip; the casing includes a base and a card cover 9, and the card cover 9 is provided with a Expose the local area observation port 11 and sample addition port 10 of the test strip; wherein, the sample addition port 10 is located above the sample pad 4 to expose part or all of the sample pad 4 area, and the observation port 11 is located on the nitrocellulose The upper part of the prime film 2 to expose the first detection zone 7 , the second detection zone 8 and the quality control zone 6 . Both the base and the card cover 9 are made of plastic.
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