Kit for detecting glypican-3 and detection method
A technology of phosphatidylinositol and proteoglycan, which is applied in the detection kit and detection field of phosphatidylinositol proteoglycan 3, can solve problems such as poor stability, troublesome preparation of biological enzymes, and enzyme denaturation, and achieve high cost, Good effect, simple method effect
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Embodiment 1
[0028] Embodiment 1: the catalytic property of copper ion and its application
[0029] Preparation of antibody-functionalized copper oxide nanoprobes:
[0030] Add 1mg copper oxide (particle size less than 50nm) to 1mL phosphate buffer (10mM, pH7.4) and ultrasonically disperse evenly. Slowly add 50 μL of 150 μg / mL GPC3 antibody (1G12, Santa Cruz Biotechnology, Inc.), and shake for 3 hours. Add BSA to a final concentration of 1%, and block for 1 h to obtain antibody-functionalized copper oxide nanoprobes (CuO NPs-Ab).
[0031] Meanwhile, copper oxide nanoprobes (CuO NPs-BSA) that only blocked BSA were obtained as a reference according to the above method, omitting the step of antibody modification.
[0032] Catalytic properties of copper ions:
[0033] figure 1 It is the verification diagram of copper ion catalytic activity, a is TMB solution, b is TMB plus H 2 o 2 solution, c is the solution of TMB plus copper ions, d is the solution of TMB plus H 2 o 2 solution with c...
Embodiment 2
[0039] Example 2: Detection of Glypican 3 (GPC3)
[0040] (1) Solution preparation
[0041]Protein coating diluent: 6.7mM phosphate buffer (pH7.4);
[0042] Washing solution: 50mM phosphate buffer (pH7.4) + 135mM sodium chloride + 2.7mM potassium chloride + 0.05% (w / w) Tween-20;
[0043] Blocking solution: 1% (w / w) BSA solution;
[0044] Chromogenic solution: 0.2M acetate buffer (pH4.0)+1.33mM TMB+1.33M H 2 o 2 ;
[0045] Stop solution: 2M sulfuric acid solution.
[0046] (2) Detection method
[0047] Coating: Dissolve and dilute 50 μg of the protein sample to be tested with 200 μL coating diluent, add 50 μL to a 96-well plate and place at 37 °C for 2 hours, discard the liquid in the well, and wash 3 times with washing solution;
[0048] Blocking: Add 200 μL of blocking solution to each reaction well and place at 37°C for 2 hours, and wash 3 times with washing solution after blocking;
[0049] Incubation of nanobiological probes: Dilute the prepared antibody-functional...
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