Enzyme linked immunosorbent assay kit for detecting human epididymis secretory protein 4
A technology for epididymis secreted protein and human detection, which is applied in the field of enzyme-linked immunosorbent assay kits, can solve the problems of high false positive rate, and achieve the effects of high detection sensitivity and accuracy, convenient detection method, and strong reliability
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Embodiment 1
[0014] Component preparation of embodiment 1 ELISA kit
[0015] 1. Preparation of human HE4 protein mouse monoclonal antibody:
[0016] 1) Animal immunity
[0017] Balb / c mice were used as immunized animals, and the biologically active recombinant human HE4 protein produced by Beijing Yiqiao Shenzhou Biotechnology Co., Ltd. was used as the immunogen, and the immunization dose was 50 μg / mouse. Complete Freund's adjuvant to make emulsifier, abdominal subcutaneous injection in multiple points, take the same dose of immunogen and equal amount of incomplete Freund's adjuvant to make emulsifier at intervals of 2-3 weeks, boost immunization twice, and measure serum after three times of immunization For titer, mice with high serum titer were taken for intraperitoneal booster immunization once, and splenocytes were taken for fusion after 4 days.
[0018] 2) Cell fusion and cloning
[0019] Splenocytes from immunized mice were mixed with SP2 / 0 myeloma cells at a ratio of 4:1, and fus...
Embodiment 2
[0033] Example 2 The formation of the ELISA kit for detecting human HE4
[0034] Set up an enzyme-linked immunosorbent assay kit for detecting human HE4, including the following reagents:
[0035] 1) Mouse anti-human HE4 monoclonal coating antibody;
[0036] 2) HRP-labeled rabbit polyclonal antibody;
[0037] 3) Recombinant human HE4 protein standard;
[0038] 4) The coating buffer is pH7.4, 0.1mol / L phosphate buffer;
[0039] 5) The blocking solution is a phosphate buffer containing 2% bovine serum albumin;
[0040] 6) The sample diluent is a phosphate buffer containing 0.1% bovine serum albumin;
[0041] 7) The concentrated washing solution is a Tris buffer containing 2% Tween or a phosphate buffer containing 2% Tween washing solution;
[0042] 8) Color developing solution A and color developing solution B are composed, and color developing solution A is hydrogen peroxide or carbamide peroxide, and color developing solution B is tetramethylbiphenyl;
[0043] 9) The sto...
Embodiment 3
[0044] Example 3 Preparation of ELISA Kit for Detecting Human HE4
[0045] 1. Explore the optimal antibody concentration of the enzyme-linked immunosorbent immunoassay kit by using orthogonal experiments
[0046]According to the ultraviolet spectrophotometer method, the concentration of antibody and antigen was determined. Using the orthogonal test method, the anti-HE4 monoclonal antibody was diluted to a concentration of 4 μg / ml, 2 μg / ml, and 1 μg / ml, and the recombinant HE4 protein concentration was diluted to 1000 pg / ml, 100 pg / ml, and 0 pg / ml. HE4 rabbit polyclonal antibody was diluted to 2μg / ml, 1μg / ml, 0.5μg / ml, 0.25μg / ml. Considering the background and the light absorption value of the recombinant protein, the coating concentration of the selected antibody was 2 μg / ml, and the working concentration of the HRP-labeled antibody was 0.5 μg / ml.
[0047] 2. Batch preparation of kits
[0048] 1) Coating microtiter plate: use phosphate coating buffer (weigh 8g of sodium chl...
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