Method for identifying varieties of residual silk of antique silk fabric based on immune trace method
A technology for silk fabrics and fragments is applied in the field of cultural relic detection, which can solve the problems of large influence of impurities and low technical sensitivity, and achieve the effects of strong fluorescence stability, full utilization of resources, and improvement of dissolution rate and extraction rate.
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Embodiment 1
[0043] 1) Preparation of fluorescent carbon dots (CDs): Weigh 2.00g sweet potato tuber fragments and 6.00g KH 2 PO 4 , add 10mL of distilled water, pour the mixed solution into a hydrothermal reaction kettle and seal it, place it in an oven at 180°C and heat it for 10 h, after cooling to room temperature, take out the reaction solution, sonicate it for 10 min, and filter it with a 0.22 μm microporous membrane to obtain a shallow Yellow fluorescent carbon dot liquid; dialyze the obtained solution with a dialysis bag (molecular weight cut-off 1000) for 24 h to remove other small molecular impurities; finally freeze-dry the purified carbon dot solution to obtain fluorescent carbon dot powder.
[0044] 2) Preparation of fluorescent carbon dot-labeled silk fibroin secondary antibody: add fluorescent carbon dots, carbodiimide and secondary antibody to 10 mmol / L PBS buffer, stir at room temperature for 2-3 h, then use The PBS buffer was used to wash and centrifuge the solution sever...
Embodiment 2
[0057] 1) Preparation of fluorescent carbon dots (CDs): Weigh 2.00g sweet potato tuber fragments and 6.00g KH 2 PO 4 , add 10 mL of distilled water, pour the mixed solution into a hydrothermal reaction kettle and seal it, place it in an oven at 200°C and heat it for 13 h, after cooling to room temperature, take out the reaction solution, sonicate it for 10 min, and filter it with a 0.22 μm microporous membrane to obtain a shallow Yellow fluorescent carbon dot liquid; dialyze the obtained solution with a dialysis bag (molecular weight cut-off 1000) for 24 h to remove other small molecular impurities; finally freeze-dry the purified carbon dot solution to obtain fluorescent carbon dot powder.
[0058] 2) Preparation of fluorescent carbon dot-labeled silk fibroin secondary antibody: add fluorescent carbon dots, carbodiimide and secondary antibody to 10 mmol / L PBS buffer, stir at room temperature for 2.5 h, then wash with PBS buffer The solution is washed and centrifuged several ...
Embodiment 3
[0071] 1) Preparation of fluorescent carbon dots (CDs): Weigh 2.00g sweet potato tuber fragments and 6.00g KH 2 PO 4 , add 10 mL of distilled water, pour the mixed solution into a hydrothermal reaction kettle and seal it, place it in an oven at 220°C and heat it for 15 h, after cooling to room temperature, take out the reaction solution, ultrasonicate for 10 min, and filter it with a 0.22 μm microporous membrane to obtain a shallow Yellow fluorescent carbon dot liquid; dialyze the obtained solution with a dialysis bag (molecular weight cut-off 1000) for 24 h to remove other small molecular impurities; finally freeze-dry the purified carbon dot solution to obtain fluorescent carbon dot powder.
[0072] 2) Preparation of fluorescent carbon dot-labeled silk fibroin secondary antibody: add fluorescent carbon dots, carbodiimide and secondary antibody to 10 mmol / L PBS buffer, stir at room temperature for 3 h, then wash with PBS buffer The solution is washed and centrifuged several ...
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