N-tail-end B-type brain natriuretic peptide precursor chemiluminiscence immunity quantification detecting kit and preparation method thereof
A chemiluminescence immunoassay and quantitative detection technology, applied in the field of immunoassay medicine, can solve the problems of short validity period of reagents, radioactive contamination, and narrow detection range, and achieve the effects of good stability, easy operation and high sensitivity
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Embodiment 1
[0033] Example 1: Preparation of N-terminal B-type natriuretic peptide precursor (NT-proBNP) chemiluminescence immunoquantitative detection kit
[0034] N-terminal B-type brain natriuretic peptide precursor (NT-proBNP) chemiluminescent immunoquantitative detection kit, characterized in that the kit includes: NT-proBNP antibody-coated plate, NT-proBNP antibody enzyme conjugate, NT- proBNP calibrator, NT-proBNP quality control substance, 20-fold concentrated washing solution, luminescent solution A and B.
[0035] The N-terminal B-type brain natriuretic peptide precursor chemiluminescent immunoquantitative detection kit was prepared by the following method:
[0036] 1) Preparation of NT-proBNP antibody-coated plates
[0037]Dilute the NT-proBNP antibody to 1-10ug / mL with 0.02M phosphate buffer, add it to a 96-well white microwell plate, and coat at 37°C for 2 hours; discard the liquid in the well and wash with pH7.4 PBS buffer plate, then add 0.5% BSA-containing phosphate buff...
Embodiment 2
[0061] Example 2: Preparation of N-terminal B-type BNP chemiluminescent immunoquantitative detection kit
[0062] The kit of the present invention was prepared in the same manner as in Example 1, except that the solid phase carrier was a 48-well microwell plate.
Embodiment 3
[0063] Embodiment 3: the using method of kit of the present invention
[0064] 1) Equilibrate the test kit at room temperature (18-25°C) for 30 minutes.
[0065] 2) Prepare lotion: Dilute the concentrated lotion with distilled water at 1:20 (1mL lotion plus 19mL distilled water). If the concentrated lotion has crystals, place the concentrated lotion at room temperature or 37°C until the crystals dissolve before diluting.
[0066] 3) Preparation of luminous liquid: take an appropriate amount of luminous liquid A and B liquid and mix equal volumes 5 minutes before use.
[0067] 4) Take out an appropriate amount of coated slats according to the needs of the experiment. Set up 1 well for blank control and 2 wells for each calibrator. Add 50 μL of NT-proBNP calibrator or quality control substance to each well, add 50 μL sample to the sample well, and add no calibrator or sample to the blank control.
[0068] 5) Add 50 μL of NT-proBNP enzyme conjugate to each well, except the bl...
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