Dual-mode immunoassay method of ovarian cancer tumor marker
A tumor marker and immune analysis technology, which is applied in the field of dual-mode immune analysis of ovarian cancer tumor markers, to achieve the effect of improving photoelectric conversion efficiency and electrical conductivity
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Embodiment 1
[0032] A dual-mode immunoassay for ovarian cancer tumor markers (e.g. figure 1 shown):
[0033] (1) Indium tin oxide (ITO) electrode pretreatment of indium tin oxide (ITO) electrode: first put the indium tin oxide (ITO) electrode in an ultrasonic water bath to clean until it is clean, and then use ethanol, dilute acid and Wash thoroughly with water;
[0034] (2) Add dropwise 0.6mL of carbon nanohorn suspension with a concentration of 3mg / ml on the surface of a clean ITO electrode, dry under infrared light, and cool to room temperature;
[0035] (3) 0.6 mL of anatase TiO with a concentration of 3 mg / mL was sequentially modified on the surface of the above electrode 2 Mesoscopic crystal suspension and 0.6 mL of rutile TiO at a concentration of 3 mg / mL 2 The mesoscopic crystal suspension was dried under an infrared lamp and cooled to room temperature, and this was repeated three times to obtain a CNHs / Anatase / Rutile modified electrode;
[0036] (4) Mix the mercaptophenylboron...
Embodiment 2
[0045] A dual-mode immunoassay method for ovarian cancer tumor markers, the steps are as follows:
[0046] (1) The three-electrode system was used for the measurement. The CNHs / Anatase / Rutile / Cu NCs / Ab / Ag modified electrode prepared in Example 1 was used as the working electrode, Ag / AgCl was used as the reference electrode, and the platinum wire electrode was used as the counter electrode. Use a photoelectrochemical workstation for detection, set the voltage to 0.1V, switch the lamp every 10s, and the monochromatic light excitation light emitted by the xenon lamp is filtered by the monochromator before use;
[0047] (2) In a PBS solution with a concentration of 0.3mol / L at pH=7.5, detect 1×10 by photoelectrochemical workstation -6 ng / mL–10 ng / mL a series of lipolysis-activated lipoprotein receptor standard solutions with different concentrations, and draw the working curve by recording the different current signals generated before and after switching the light. Figure 2 A is...
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