Application of naturally-sourced and/or self-assembled biological membrane, closed structure or cell compartment with biological membrane property as medical high polymer material
A self-assembly technology, a technology of polymer materials, applied to other methods of inserting foreign genetic materials, recombinant DNA technology, medical preparations of non-active ingredients, etc., to achieve high safety, rich technical support, and high utilization.
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[0042] Example 1 Extraction and purification of biofilm
[0043] Use density gradient centrifugation to extract and purify the desired biofilm. The specific process is as follows:
[0044] (1) The New Zealand white rabbits fasted for 18-24 hours were sacrificed to take the liver, after removing the large blood vessels, the liver was cut into 2mm 3 The left and right small pieces, and rinse with normal saline until the tissue pieces turn white;
[0045] (2) Preparation of homogenate: 1mmol / L CaCl 2 , 50mmol / L HEPES (pH 7.4), 1mmol / L PMSF, 2μg / mL aprotinin, 2μg / mL Antipain;
[0046] (3) Add the liver tissue and homogenate to 8 times the volume of the homogenate in a mass:volume ratio, and homogenize it with an electric homogenizer at 15,000 rpm in an ice bath environment until the tissue is liquefied;
[0047] (4) Filter the homogenate through four layers of gauze, centrifuge the filtrate at 1,000×g, 10min, 4℃, and collect the precipitate;
[0048] (5) Sucrose solution A for precipitatio...
Example Embodiment
[0050] Example 2 Extraction and purification of biofilm
[0051] A two-phase partition method is used to extract and purify the desired biofilm. The specific process is as follows:
[0052] (1) Screen full and consistent normal corn seeds, soak and disinfect them in 1% NaClO for 10 minutes, rinse them, and germinate for 72 hours at a constant temperature of 25°C in the dark;
[0053] (2) Take corn epicotyls and add 2 times the volume of extraction buffer (5mmol / L EDTA, 25mmol / L Tris, 0.25mmol / L sucrose, 1mmol / L MgSO) in a mass:volume ratio 4 , 0.2% (W / V) BSA, 0.5% (W / V) PVP-10, 10% (W / V) glycerol, 15mmol / L β-mercaptoethanol, 1mmol / L PMSF, 1mmol / L DTT), ice Bath grind to liquefaction;
[0054] (3) Filter the grinding liquid through four layers of gauze, centrifuge the filtrate at 12,000×g, 15min, 4℃, and take the supernatant;
[0055] (4) Centrifuge the supernatant at 80,000×g, 30min, 4℃, and collect the precipitate;
[0056] (5) Suspension for precipitation (25mmol / L Tris, 0.25mmol / L ...
Example Embodiment
[0058] Example 3 Extraction and purification of biofilm
[0059] Use differential centrifugation to extract and purify the required biofilm. The specific process is as follows:
[0060] (1) Antarctic ice algae ( Chlamydomonas subcaudata ) Is isolated and purified from Antarctic sea ice;
[0061] (2) Inoculate Antarctic ice algae into the culture medium at a ratio of 1:100 (each 10L medium contains 21.2g NaCl, 3.6g NaSO 4 , 0.6g KCl, 0.3g NaHCO 3 , 0.1g KBr, 0.1g H 3 BO 3 , 0.1g NaF, 9.6g MgCl 2 ·6H 2 O, 1.0g CaCl 2 , 0.1g SrCl 2 ·6H 2 O), placed in a controlled light incubator for cultivation. Cultivate for 14 days under conditions of -4℃, light intensity of 1300~1900lx, light cycle of 12 bright / 12 dark, shaking 4~5 times a day;
[0062] (3) Centrifuge the ice algae culture solution at 4,000 rpm, 20 min, 4°C, collect the ice algae precipitate, and quickly rinse twice with pre-cooled distilled water to remove the extracellular viscous material, surface salt and impurities in the cul...
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