Preparation method of core-shell magnetic conductive polymer microspheres and application thereof
A conductive polymer and polymer technology, applied in the direction of DNA preparation, recombinant DNA technology, etc., can solve the problems of increasing production costs and unfriendly environment
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Embodiment 1
[0055] Example 1: Core-shell Fe 3 o 4 Preparation of / PANI composite microspheres
[0056] To a 100mL three-neck flask, add 0.1g Fe 3 o 4 , 40mL 0.1mol / L hydrochloric acid, ultrasonically dispersed at room temperature for 5min, sealed and placed in a 5°C thermostat for 12h, magnetic separation to remove the hydrochloric acid aqueous solution and retain the magnetic core; then add 15mL absolute ethanol, 0.1 g re-distilled aniline, ultrasonically dispersed for 5 minutes, and placed in a 5°C thermostat for 12 hours.
[0057] Place the flask in an ultrasonic cleaner, and control the water temperature of the ultrasonic cleaner to 5-10°C. Dissolve 0.25mL of 12mol / L hydrochloric acid in 45mL of distilled water, then add 0.28g of ammonium persulfate to dissolve, slowly add the oxidant solution dropwise, and control the dropping time to 0.5h; keep stirring for 3h under the assistance of ultrasound.
[0058] Magnetic separation of solid and liquid, washing with water for several ti...
Embodiment 2
[0059] Example 2: Core-shell Fe 3 o 4 Preparation of / PPy composite microspheres
[0060] The aniline in embodiment 1 is replaced with pyrrole, and 0.28g ammonium persulfate is used 0.40g FeCl 3 ·6H 2 O is replaced, and other operations remain unchanged, and Fe can be obtained 3 o 4 / PPy samples.
Embodiment 3
[0061] Embodiment 3: utilize Fe 3 o 4 / PANI Composite Microspheres Separation and Purification of Escherichia coli (E.coli DH5α) Plasmid DNA
[0062] Take 10mg of dedoped Fe 3 o 4 / PANI magnetic balls were placed in a 1.5mL sterile centrifuge tube, ultrasonicated and sterilized twice with 1mL 70% (v / v) ethanol solution, then transferred to another sterile centrifuge tube, and 40μL E.coli DH5α was added in sequence Plasmid DNA crude extract and 1mL Tris-HCl (10mmol / L, pH 7.8) buffer, shake well, place at room temperature for 20min until the DNA is adsorbed on the surface of the magnetic ball, collect the magnetic ball under a magnetic field, and discard the supernatant. The magnetic balls were washed twice with 1 mL of 70% ethanol solution, magnetically separated, the supernatant was discarded, and the magnetic balls that adsorbed DNA were placed at room temperature to volatilize the ethanol.
[0063] Add 0.4mL of 2mol / L NaCl solution to the centrifuge tube containing the m...
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