Quantum dot-based plant hormone salicylic acid acceptor probe, its preparation method and application
A plant hormone, p-aminosalicylic acid technology, applied in chemical instruments and methods, material stimulation analysis, luminescent materials, etc., can solve the problem of no substantial breakthrough in the mechanism of plant hormone action, lack of measurable signals, complex composition of plant systems, etc. problems, to achieve the effect of stable luminous performance, low equipment requirements, and low operating costs
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Embodiment 1
[0049] (1) Preparation of NaHSe: Add 1 mL of double-distilled water, 0.0265 g (7.0×10 -4 mol)NaBH 4 (It is easy to absorb moisture, and the action should be fast when weighing), and shake the vial gently to make it completely dissolved, and then add 0.0254g (3.2×10 -4 mol) Se powder. Shake the vial until all the reactants turn from black to white, cover the stopper, place it on a magnetic stirrer, and react at a constant temperature at 4°C for 1-2 hours to obtain a NaHSe solution with a concentration of 0.32mol / L.
[0050] (2) Preparation of CdSe / MPA: Add 45mL of double-distilled water into a 100mL round bottom flask, pass nitrogen to remove oxygen, add 5mL of 7.0×10 -3 mol / L CdCl 2 Solution (3.5×10 -5 mol), add 7.6μL (density 1.2199g / mL) 3-mercaptopropionic acid (8.75×10 -5 mol), use 1mol / L NaOH to adjust the pH value of the solution to 10.0, continue to stir and blow nitrogen for 30min, then add 55μL of newly prepared 0.32mol / L NaHSe solution (1.76×10 -5 mol), refluxed...
Embodiment 2
[0057] (1) Preparation of NaHSe: same as in Example 1 step (1).
[0058] (2) Preparation of CdSe / MPA: same as step (2) of Example 1.
[0059] (3) Preparation of phytohormone salicylic acid receptor probe based on quantum dots: pipette 40ml of purified CdSe / MPA quantum dot solution (the amount of Se is 1.4×10 -5 mol), add newly prepared 228μL 0.1mol / L (2.28×10 -5 mol) carbodiimide (EDC), stirred slowly, activated at 30°C for 10min, then added 3.0ml 0.01mol / L (3.0×10 -5 mol) p-aminosalicylic acid, the molar ratio of coupling agent / salicylic acid is controlled to be 3:4, and the reaction is stirred slowly at 30°C for 3h. After the reaction, put it in the refrigerator at 5° C. overnight to terminate the reaction, and obtain the quantum dot-based plant hormone salicylic acid receptor probe.
[0060] The CdSe / MPA quantum dots prepared in step (2) and the CdSe / MPA / SA obtained in step (3) were detected by transmission electron microscopy. The results showed that both CdSe / MPA and C...
Embodiment 3
[0062] (1) Preparation of NaHSe: same as in Example 1 step (1).
[0063] (2) Preparation of CdSe / MPA: same as step (2) of Example 1.
[0064] (3) Preparation of phytohormone salicylic acid receptor probe based on quantum dots: pipette 40ml of purified CdSe / MPA quantum dot solution (the amount of Se is 1.4×10 -5 mol), add newly prepared 228μL 0.1mol / L (2.28×10 -5 mol) carbodiimide (EDC), stirred slowly, activated at 40°C for 5min, then added 6.0ml 0.01mol / L (6.0×10 -5 mol) p-aminosalicylic acid, the molar ratio of coupling agent / salicylic acid is controlled to be 3 / 8, and the reaction is stirred slowly at 40°C for 4h. After the reaction was completed, the reaction was terminated overnight in a refrigerator at 5° C. to obtain a quantum dot-based phytohormone salicylic acid receptor probe.
[0065] The CdSe / MPA quantum dots prepared in step (2) and the CdSe / MPA / SA obtained in step (3) were detected by transmission electron microscopy. The results showed that both CdSe / MPA and ...
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