Detection method for AMACR auto-antibody and its application in prostatic cancer diagnosis
A technology of autoantibodies and detection methods, which is applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of low concentration and unsuitability for prostate cancer markers, and achieve the effects of high purity, low detection cost, and simple and easy operation
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[0038] 1. Preparation of reagents
[0039] (1) Coating buffer (0.05M, pH9.6): 1.59g Na 2 CO 3 , 2.93g NaHCO 3 , add ultrapure water to 1000mL;
[0040] (2) Phosphate buffer solution (PBS, 0.15M, pH7.4): 8.0g NaCl, 0.2gKCl, 2.9gNa 2 HPO 4 12H 2 O, 0.2g KH 2 PO 4 , adjust the pH to 7.4, add ultrapure water to make the volume to 1000mL;
[0041] (3) Phosphate-Tween buffer solution (PBST, 0.15M, pH7.4): 8.0g NaCl, 0.2gKCl, 2.9gNa 2 HPO 4 12H 2 O, 0.2g KH 2 PO 4 , 0.5ml Tween-20, adjust the pH to 7.4, add ultrapure water to make the volume to 1000mL;
[0042](4) Blocking solution: 1.0g gelatin was dissolved in 100ml phosphate buffered saline (PBS, 0.15M, pH7.4);
[0043] (5) Substrate buffer (0.05M, pH5.6): 39.8g Na 2 HPO 4 12H 2 O, 6.3g citric acid, add ultrapure water and be constant to 1000mL;
[0044] (6) Chromogenic solution: 10 mL pH5.6 substrate buffer, 0.1 mL 1% tetramethylbenzidine (10 mg tetramethylbenzidine dissolved in 1 mL dimethyl sulfoxide) and 32 μ...
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