1911 results about "Tris" patented technology

The invention discloses a preparation method of injectable nano composite hydrogel for relieving osteoarthritis, which comprises the following steps: firstly, synthesizing nano rod-like hydroxyapatite with the length of 150-300 nm and the diameter of 10-15 nm, and the hydroxyapatite is hydrophilic hydroxyapatite doped with strontium and europium ions; the preparation method comprises the following steps: by taking Ca (NO3) 2, Sr (NO3) 2, Eu (NO3) 3 and soluble phosphate as main raw materials, carrying out hydrothermal reaction to prepare strontium and europium ion co-doped hydrophobic hydroxyapatite, dispersing the strontium and europium ion co-doped hydrophobic hydroxyapatite in a Tris-HCl buffer solution, adding tannic acid, stirring, centrifugally collecting precipitate, and drying to obtain strontium and europium ion doped hydrophilic hydroxyapatite; the preparation method comprises the following steps: taking chondroitin sulfate and adipic dihydrazide as main raw materials, stirring, dialyzing, freeze-drying, and dissolving in a buffer solution to obtain the chondroitin sulfate solution grafted with the hydrazide group; the preparation method comprises the following steps: taking hyaluronic acid, 3-aminophenylboronic acid and sodium periodate as main raw materials, stirring, dialyzing, freeze-drying, and dissolving in a buffer solution to obtain the phenylboronic acid group grafted oxidized hyaluronic acid solution; the preparation method comprises the following steps: blending hydrophilic hydroxyapatite doped with strontium and europium ions, a chondroitin sulfate solution grafted with a hydrazide group, an oxidized hyaluronic acid solution grafted with a phenylboronic acid group and a recombinant collagen solution, and stirring to obtain the injectable nano composite hydrogel. The injectable nano composite hydrogel obtained by the invention has good biocompatibility, and a favorable local immune microenvironment can be created to immunomodulate macrophages so as to relieve osteoarthritis and promote subchondral bone repair.

The invention discloses a polyrotaxane covalent organic framework material capable of regulating interlayer spacing through cyclodextrin and application of the polyrotaxane covalent organic framework material, and belongs to the technical field of biological medicine. The polyrotaalkylated covalent organic framework material is obtained by taking a cyclodextrin aromatic multi-amino inclusion compound and a (multi-aldehyde bipyridine) ruthenium (II) complex as structural units and carrying out copolymerization; the cyclodextrin aromatic polyamine inclusion compound is a beta-cyclodextrin p-phenylenediamine inclusion compound with a hydroxyl group or without a hydroxyl group; the (multi-aldehyde dipyridyl) ruthenium (II) complex is tris (4, 4 '-diformaldehyde-2, 2'-dipyridyl) ruthenium (II). The interlayer spacing of the polyrotaxane covalent organic framework material is greatly increased by utilizing a cavity of gamma-cyclodextrin, and meanwhile, the material has excellent photo-thermal and photodynamic activity, is positively charged, and can better adsorb negatively charged bacteria; and the hydrogel is good in biocompatibility and free of toxic and side effects, and has an excellent treatment effect on wounds infected with staphylococcus aureus.

The invention discloses tris (dimethylamino) cyclopentadienyl hafnium and a preparation process thereof.The preparation process of the tris (dimethylamino) cyclopentadienyl hafnium comprises the following steps that S1, an n-hexane solution of n-butyllithium and dimethylamine are subjected to a reaction, and a lithium dimethylamino emulsion is obtained; s2, adding hafnium tetrachloride into the lithium dimethylamino emulsion for reaction, and separating to obtain a liquid-phase product; s3, the liquid-phase product is heated, a tetra (dimethylamino) hafnium concentrated solution is obtained, and the volume of the tetra (dimethylamino) hafnium concentrated solution is 20%-30% of the volume of the liquid-phase product; and S4, obtaining cyclopentadiene, adding the cyclopentadiene into the tetra (dimethylamino) hafnium concentrated solution to react, and filtering to obtain tris (dimethylamino) cyclopentadienyl hafnium. According to the preparation process of the tris (dimethylamino) cyclopentadienyl hafnium, complex solvent components are not needed, the preparation efficiency is improved, and the use amount of the solvent and the preparation cost are reduced.

The invention provides a kit and a detection method for detecting Alzheimer disease related proteins in human blood. The kit comprises a microsphere solution coupled with a p-Tau-217 capture antibody, a microsphere solution coupled with a p-Tau-231 capture antibody, a fluorescein PE coupling detection antibody solution and a diluent, the diluent is prepared from tris (hydroxymethyl) aminomethane, Triton X-100, sodium chloride and Proclin300; according to the kit provided by the invention, the accuracy of detecting the p-Tau-217 protein and the p-Tau-231 protein is improved by designing the microspheres, specifically detecting the p-Tau-217 protein and the p-Tau-231 protein and using a double-antibody sandwich detection method, clinical detection application is more convenient, and the kit is high in specificity, high in sensitivity, good in repeatability and relatively good in application prospect.

The invention discloses high-performance unsaturated polyester resin, and relates to the field of polyester resin. When the high-performance unsaturated polyester resin is prepared, diatomite and a silver nitrate solution are uniformly mixed to obtain silver-loaded diatomite; then, the silver-loaded diatomite is subjected to a reaction with 3-aminopropyltrimethoxysilane and 3-allyl salicylaldehyde in sequence, and modified diatomite is obtained; the preparation method comprises the following steps: reacting tris (dimethylaminopropyl) amine with 3-chloropropene to obtain a cross-linking monomer; 2-formyl pyridine and 3-aminopropane phosphoric acid are subjected to a reaction, and a flame-retardant monomer is obtained; reacting terephthalic acid, fumaric acid, 1, 3-propylene glycol and a flame-retardant monomer to obtain modified unsaturated polyester resin; and uniformly mixing the modified unsaturated polyester resin, the modified diatomite and a crosslinking monomer to obtain the high-performance unsaturated polyester resin. The prepared high-performance unsaturated polyester resin has excellent flame retardance, antibacterial property, antistatic property, anti-aging property and self-repairing property.

The invention relates to the field of heat shrinkage films, in particular to an antistatic PETG heat shrinkage film. The PETG heat shrink film comprises the following components in parts by weight: 100 parts of PETG resin, 2-6 parts of an anti-adhesion agent, 2-5 parts of a lubricant, 1-5 parts of an antistatic modifier, 1-2 parts of an antioxidant and 0.5-1 part of a light stabilizer. In the preparation process of the PETG heat shrink film, a novel borate antistatic agent is introduced, and the antistatic agent is synthesized by taking tris (2-carboxyethyl) isocyanurate and 4-aminophenylboronic acid pinacol ester as raw materials, so that compared with a traditional antistatic agent, the antistatic property is better, the heat stability is obviously improved, and the service life of the heat shrink film is prolonged. And the phenomenon of local deformation or poor arc-shaped shrinkage of the PETG heat shrinkage film when the PETG heat shrinkage film shrinks at a non-uniform interface is reduced.

The invention discloses a synthetic method of tris (isopropyl cyclopentadienyl) lanthanum. The synthetic method comprises the following steps: preparing a lanthanum trichloride tetrahydrofuran complex; synthesis of isopropyl cyclopentadiene is carried out; and synthesis of tri (isopropyl cyclopentadienyl) lanthanum. According to the technical scheme, the lanthanum trichloride tetrahydrofuran complex is prepared firstly and then reacts with lithium dimethylamino and isopropyl cyclopentadiene in sequence, and the target product is obtained. Reaction raw materials are simple and easy to obtain, operation is convenient, the safety coefficient is high, the yield is high, and the method is suitable for industrial large-scale production.

The invention relates to a preparation method of a cultivation material for cultivating selenium-rich black fungus, which comprises the following steps: respectively preparing a slow-release sodium chlorate composite material and a slow-release selenium-containing mineral material, and then mixing with carbon nutrition, nitrogen nutrition and mineral nutrition to obtain the cultivation material. The slow-release selenium mineral material is a polymer-coated slow-release selenium mineral material prepared by the following steps: preparing a selenium mineral core material from selenium powder, gypsum, calcium superphosphate, monopotassium phosphate, calcium sulfate, diatomite, nano silicon dioxide and a surfactant OP-10, preparing a coating material, adding the selenium mineral core material, and soaking with a Bis-Tris buffer solution. Sodium chlorate and selenium are respectively prepared into specific slow release systems, and are slowly released in the cultivation material to react to generate a seleninic acid component which can be easily absorbed and utilized by the black fungus, so that the concentration of seleninic acid in the cultivation material is regulated, the growth of the black fungus is promoted, the yield of the black fungus is increased, the quality of the black fungus is remarkably improved, and the cultivation cost is reduced. The selenium content and the amino acid content in the black fungus are obviously increased.

The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2,2′,2″-(1,3,5,2,4,6-trioxatriborinane-2,4,6-triyl)tris(3-fluorophenol), useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

The invention belongs to the technical field of biology, and particularly relates to a reagent combination and a kit for extracting nucleic acid through a paramagnetic particle method and application of the reagent combination and the kit. The reagent combination or the kit does not adopt beta-mercaptoethanol with pungent smell or dithiothreitol needing to be stored at low temperature as an antioxidant, but adopts tris (2-formylethyl) phosphine hydrochloride and / or metabisulfite as an antioxidant, belongs to common salt chemical reagent powder, can be stored at normal temperature, and can be used for preparing a reagent for the first time. Manual addition by experimenters before an experiment is not needed, so that nucleic acid (RNA) released by splitting decomposition can be effectively prevented from being oxidized and denatured, and the integrity of extracted nucleic acid (total RNA) fragments is ensured; especially, the metabisulfite is commonly used in food additives, does not cause harm to the body, and is non-toxic and non-volatile.

The invention relates to a hyaluronic acid-polyurethane composite material based on a double dynamic network and a preparation method and application thereof, and the preparation method comprises the following steps: carrying out hydrophobic modification reaction on hyaluronic acid and aminophenylboronic acid to obtain aminophenylboronic acid modified hyaluronic acid; the preparation method comprises the following steps: mixing polytetrahydrofuran ether glycol, polyethylene glycol and isophorone diisocyanate, carrying out a primary reaction, adding trimethylolpropane tri (3-mercaptopropionic acid) ester, carrying out a secondary reaction, adding tannic acid, and carrying out a third reaction to obtain tannic acid-terminated dynamic thionocarbamate polyurethane; and mixing the amino phenylboronic acid modified hyaluronic acid with the tannic acid terminated dynamic thionocarbamate polyurethane for reaction to obtain the hyaluronic acid-polyurethane composite material with the double dynamic networks. Compared with the prior art, by introducing a'thionocarbamate-borate 'double-dynamic network, high toughness, high strength, good self-repairability and repeatable processability in an extreme environment are realized, and the material is particularly suitable for manufacturing and repairing of key components in an LNG ship body and a heat insulation system thereof.

The invention relates to the technical field of polyurethane adhesives, and provides a heat-conducting polyurethane structural adhesive and a preparation and use method thereof.The heat-conducting polyurethane structural adhesive comprises a first component and a second component, and the first component comprises modified bio-based polyol, polythiol, heat-conducting filler, a first water removal agent, a thixotropic agent, a first catalyst and a second catalyst; the second component comprises epoxy resin, diisocyanate, polyisocyanate, a heat-conducting filler, a coupling agent, a second dewatering agent, a dispersing agent and a retarder; the modified bio-based polyol is selected from at least one of modified castor oil polyol, modified grease polyol and modified cashew nut shell oil polyol; the polythiol is selected from at least one of trimethylolpropane tri (3-mercaptopropionic acid ester), pentaerythritol tetra (3-mercaptopropionic acid ester), butanediol mercaptopropionic acid ester and polythiol. Through the arrangement, the heat-conducting polyurethane structural adhesive has relatively long openable time, and is rapidly cured at room temperature within a short time to generate relatively high initial curing strength.

The invention discloses a nitrite electrochemical sensor based on a graphene oxide and polytromethamine composite material and a preparation method and application thereof, and belongs to the field of electrochemical method detection, the preparation method comprises the following steps: uniformly dispensing a graphene oxide suspension on the surface of a glassy carbon electrode, and airing to obtain GO / GCE; putting the GO / GCE, a saturated calomel electrode and a platinum wire electrode into an electrolyte containing tromethamine with a certain concentration, and carrying out electropolymerization by adopting a cyclic voltammetry to obtain Poly (Tris) / GO / GCE; a saturated calomel electrode is used as a reference electrode, a platinum wire electrode is used as a counter electrode, Poly (Tris) / GO / GCE is used as a working electrode, and the nitrite electrochemical sensor is constructed and is more accurate and sensitive in nitrite detection, the linear detection range is 2 * 10 <-6 >-6 * 10 <-3 > mol / L, and the detection limit is 1.00 * 10 <-7 > mol / L.

The invention relates to a rapid detection kit for large yellow croaker pyramidal worm, and belongs to the field of pathogen biological diagnosis in aquaculture. The kit comprises a nucleic acid releasing agent and further comprises a primer and a probe which are used for detecting the large yellow croaker pyramidal worm. The kit comprises a nucleic acid releaser; the formula of the nucleic acid releasing agent comprises tris (hydroxymethyl) aminomethane hydrochloride with the final concentration of 100 mM, sodium chloride with the final concentration of 100 mM, sodium dodecyl sulfate with the final concentration of 1 wt%, sodium alpha-olefin sulfonate with the final concentration of 3 wt%, sodium lauroyl glutamate with the final concentration of 1.2 wt%, betaine with the final concentration of 1 wt% and water as a solvent. The sequences of the primer and the probe for detecting the Pseudosciaena crocea pyramidal are 5 '-TATGGGCAATTCTGAATCCT-3', 5 '-TCTTTTCTGATCCCTGAAT-3' and 5 '-FAM-GTCGGTGGAGTGATTTGTTTG-3'. The kit disclosed by the invention is simple to operate, provides a tool for diagnosis, prevalence monitoring, prevention and control of the Pseudosciaena crocea pyramidal, and has a very high application value.

The invention belongs to the field of novel environment-friendly materials, and particularly relates to a modified covalent organic framework material for simultaneously adsorbing multiple heavy metal ions as well as a preparation method and application of the modified covalent organic framework material. The preparation method of the material comprises the following steps: dissolving 1, 3, 5-tri (4-aminophenyl) benzene and 2, 5-dihydroxy terephthalaldehyde in a mixed solvent, and standing and reacting at room temperature to obtain a mixed solution; adding scandium trifluoromethanesulfonate into the obtained mixed solution, carrying out standing reaction at room temperature, after the reaction is finished, separating insoluble substances from the reaction solution, and washing and drying the insoluble substances to obtain a covalent organic framework base material; a covalent organic framework base material prepared by adopting a neutral solution is subjected to ultrasonic modification treatment, and then the modified base material is washed and dried to obtain the modified covalent organic framework material. The material modified by the neutral solution shows a good adsorption effect on multiple heavy metal mixed ions in water, and has a good application prospect in the aspect of adsorbing and removing heavy metal ions in a water environment.

The invention discloses a preparation method of a polyurethane material with a shape memory function, biocompatibility and degradability, which comprises the following steps: (1) melting and mixing hydroxyl-terminated polyether or polyester polyol and isosorbide in a nitrogen atmosphere, and then adding diisocyanate for prepolymerization; (2) adding hexahydro-1, 3, 5-tris (hydroxyethyl)-s-triazine into the pre-polymerized solution, stirring, dissolving and reacting, and then pouring the mixed solution into a mold; and (3) placing the mold under the condition of 80 DEG C to volatilize the solvent, and curing to obtain the polyurethane film. The polyurethane film prepared by the invention has excellent mechanical properties. Meanwhile, the polyurethane film has good biocompatibility, a shape memory function and dual degradability. Compared with the traditional polyurethane material, the polyurethane material prepared by the method disclosed by the invention takes the biomass-based compound isosorbide as a raw material, integrates excellent comprehensive performance, functionality and degradability, and is a novel sustainable material with wide application.

The present invention relates to the field of water treatment technology, and more particularly to a kind of reverse osmosis membrane and preparation method thereof.The preparation method of the reverse osmosis membrane includes:Basement membrane is soaked in aqueous phase solution, after taking out surface drying, oil phase solution is coated on basement membrane and carries out interfacial polymerization reaction, after solidification, coating modifier solution, after drying, obtain reverse osmosis membrane;The modifier includes 2,4,6-tris (4-aminophenyl) ‑1,3,5-triazine ‑1,3,5-tris (4-methylphenyl) benzene.The COFs successfully grafted by the present invention can improve the water permeability of membrane to a certain extent, and can also improve the anti-pollution property, acid resistance and oxidation resistance of membrane, and then improve the service life of membrane.The present invention further compares the different effects that the same type of imino COFs are introduced into reverse osmosis membrane, so as to highlight the excellence of the imino COFs selected by the present invention.

The invention relates to a non-aqueous electrolyte composition having a solvent system which comprises a first component which comprises a first organo carbonate-based solvent and a second organo carbonate-based solvent; and a second component which comprises one or more performance additives that includes tris(trimethylsilyl) borate (TMSB). Devices, methods and uses including electrolytes compositions are also disclosed.

The invention discloses a 3-ketosteroid-delta1-dehydrogenase mutant and application thereof in synthesis of prednisone acetate, the mutant with high catalytic activity on cortisone acetate is obtained through screening, and a methanol-water phase (Tris-HCl buffer solution) system is adopted to increase the solubility of a substrate so as to improve the biological catalytic efficiency. In a single water phase system (Tris-HCl buffer solution) without methanol, the conversion efficiency is only 64.8% for 60g / L of cortisone acetate, and under the condition that other conditions are the same, the conversion rate in the Tris-HCl buffer solution system with methanol is increased to 92.1%, and the conversion rate is increased by 1.42 times.

The invention relates to an aromatic soluble polymer microneedle as well as a preparation method and application thereof. The preparation method comprises the following steps: adding a zinc acetate hexahydrate aqueous solution and a Tris buffer solution into a eugenol-curcumin mixed ethanol solution to obtain self-assembled carrier-free nanoparticles containing eugenol and curcumin; and dissolving the nano-particles in a soluble hyaluronic acid solution, drying in a microneedle mold, and demolding to obtain the aromatic soluble polymer microneedle. The structure of the aromatic soluble polymer microneedle is that self-assembled carrier-free nanoparticles are wrapped in a soluble hyaluronic acid microneedle. Compared with the prior art, the aromatic soluble polymer microneedle prepared by the invention can overcome skin barrier and quickly absorb moisture and dissolve so as to promote the transdermal absorption effect of active substances; a perfume delivery system is constructed by using the soluble polymer microneedle, so that the biocompatibility is improved, the slow release control capability of the perfume can be effectively enhanced, and a new path is opened up for clinical application of inflammatory diseases.

The invention relates to the technical field of metal working fluids, in particular to a degradable environment-friendly vegetable oil-based semi-synthetic cutting fluid and a preparation method thereof. The cutting fluid comprises 20-30 parts of vegetable lubricating oil, 10-20 parts of an alkali storage agent, 2-5 parts of a corrosion inhibitor, 3-5 parts of a coupling agent, 5-8 parts of a surfactant and 6-11 parts of a composite anti-rust agent, the composite anti-rust agent comprises an anti-rust agent A and an anti-rust agent B, the anti-rust agent A comprises N-[3-(dimethylamino) propyl]-N, N-dimethylformamide, and the anti-rust agent B comprises N-[3-(dimethylamino) propyl]-N, N-dimethylformamide. The antirust agent A comprises at least one of N, N ', N'-trimethyl-1, 3-propanediamine, benzotriazole, sebacic acid and 2, 4, 6-tri (aminocaproic acid)-1, 3, 5-triazine, and the antirust agent B comprises at least one of an imidazoline compound and fatty acid sarcosine ester. The cutting fluid provided by the invention has excellent corrosion resistance, rust resistance, defoaming property, biodegradability and storage stability, and has a good application prospect.

The invention provides a hydrogen bond organic framework material, a preparation method and application of the hydrogen bond organic framework material in dopamine detection, the preparation method of the hydrogen bond organic framework material comprises the following steps: S1, dissolving 1, 3, 5-tri (4-carboxyphenyl) benzene in an organic solvent to obtain an organic solution; and S2, dropwise adding an alcohol solvent into the organic solution to react to obtain turbid liquid, and drying to obtain the hydrogen bond organic framework material. The hydrogen bond organic framework material HOF-BTB prepared by the invention is a porous material, has two-dimensional (2D) pi-pi stacked hexagonal lamellas and complex eight interpenetration, generates a one-dimensional channel in the framework, and is simple in preparation process, mild in synthesis condition, low in cost, good in biocompatibility and low in cytotoxicity; and due to rigid organic construction molecules, the compound shows excellent fluorescence performance. The HOF-BTB material has high selectivity due to differential recognition of binding sites, and can be effectively applied to detection of dopamine.

The invention discloses a reaction buffer solution for improving endotoxin detection sensitivity of a recombinant tachypleus amebocyte lysate, a kit containing the reaction buffer solution and application of the reaction buffer solution. The reaction buffer solution comprises the following components: a Tris-HCl buffer solution, magnesium ions, sodium chloride, cane sugar, ethylene glycol diethyl ether diamine tetraacetic acid, a nonionic surfactant and cyclodextrin or a derivative thereof. The invention also discloses a preparation method of the reaction buffer solution and a kit containing the reaction buffer solution. When the reaction buffer solution or the kit is used for detecting the endotoxin of the recombinant tachypleus amebocyte lysate, the sensitivity of the recombinant tachypleus amebocyte lysate for detecting the endotoxin can be improved by one order of magnitude, the lowest detection limit can reach 0.0005 EU / ml, the reaction buffer solution or the kit has strong anti-interference capability and short reaction time, and the detection efficiency is greatly improved.

The invention belongs to the technical field of membrane materials, and relates to a PDA / TA / FeOOH-PVDF self-cleaning membrane and a preparation method and application thereof.The preparation method comprises the steps that firstly, membrane pretreatment is conducted, and a pretreated PVDF membrane is obtained; 2, dopamine hydrochloride is dissolved in a Tris-HCl solution, then FeCl3. 6H2O and tannic acid are added to prepare a solution, then the pretreated PVDF membrane is placed in the solution, and the PDA / TA / Fe (III)-PVDF membrane is obtained after uniform mixing; 3, FeCl3. 6H2O is dissolved in water, then the PDA / TA / Fe (III)-PVDF membrane is added for in-situ mineralization, and a target product is obtained. According to the PDA / TA / FeOOH-PVDF self-cleaning membrane provided by the invention, the technical problems that PVDF is low in hydrophilicity and easy to pollute can be solved; the method is used for separating traditional Chinese medicine volatile oil and has excellent separation efficiency.

The invention discloses an antistatic protective glove and a preparation method thereof, and relates to the technical field of protective gloves. The antistatic protective glove is prepared from the following raw materials in parts by weight: 50 to 60 parts of natural latex, 40 to 50 parts of neoprene latex, 0.4 to 2 parts of potassium hydroxide, 1.2 to 1.8 parts of peregal O, 1.5 to 3 parts of sulfur, 1 to 2 parts of accelerant BZ, 3.5 to 5 parts of antistatic agent, 0.5 to 1 part of sodium carboxymethyl cellulose and 1.2 to 1.8 parts of anti-aging agent. The preparation method of the antistatic agent comprises the following steps: firstly, reacting 1, 3, 5-tri (2, 3-epoxypropoxy) benzene with N1, N7 dimethyl heptane-1, 7-diamine to obtain a hyperbranched polymer, and then carrying out quaternization on the hyperbranched polymer and chlorinated octadecane to obtain the antistatic agent. The antistatic protective glove provided by the invention has excellent antistatic performance and anti-aging performance.

The invention relates to the technical field of nucleic acid extraction and purification, in particular to a DNA and RNA co-extraction reaction reagent and an extraction method, the reaction reagent comprises a nucleic acid protective agent RP, a sample lysis binding solution LB, a protein washing solution WB1, a nucleic acid rinsing solution WB2 and a nucleic acid eluent EB; the nucleic acid protective agent RP comprises DTT, mercaptoethanol, TCEP and sodium hydroxide; the sample cracking binding solution LB comprises Tris-HCl, benzenesulfonic acid, sodium citrate, guanidine hydrochloride, guanidine isothiocyanate, guanidine thiocyanate, urea, triton 100, SDS, potassium chloride, sodium chloride, bromhexine, N-acetylcysteine, ambroxol hydrochloride, isopropanol and absolute ethyl alcohol; the protein washing liquid WB1 comprises Tris-HCl, benzenesulfonic acid, sodium citrate, guanidine hydrochloride, guanidine isothiocyanate, guanidine thiocyanate, urea, triton 100, sodium chloride, isopropanol and absolute ethyl alcohol; the nucleic acid rinsing liquid WB2 is prepared from Tris-HCl, sodium chloride, isopropanol and absolute ethyl alcohol; and the nucleic acid eluent EB is nuclease-free water. The reaction reagent can be used for rapidly and sufficiently enriching and purifying DNA and RNA of a sample at the same time.

The invention relates to a method for constructing a C-N bond or a C-C bond through an insertion reaction of oxygen-sulfur ylide and aromatic amine. According to the method, tris (pentafluorophenyl) borane is taken as a catalyst, oxygen-sulfur ylide and aromatic amine are taken as raw materials, and N-H or C-H insertion reaction is carried out under different temperatures and solvents. According to the method, the defect that a metal catalyst or an oxidizing agent is used traditionally is overcome, and on the basis of the method, various alpha-amino-acid ester derivatives or diaryl acetate derivatives can be obtained by using different aromatic amines and oxygen-sulfur ylide as substrates. According to the method, the raw materials are easy to obtain, the operation is simple, the use of a catalyst and an oxidizing agent is avoided, and the method is a mild, effective, feasible and environment-friendly method for preparing the alpha-amino-acid ester and the diaryl acetate and has important application value.

A method for preparing exosomes is provided. The method includes preparing a human platelet, treating the human platelet with a buffer to obtain a platelet solution, centrifuging the platelet solution, and collecting supernatant of the centrifuged platelet solution to obtain an exosome solution. The buffer is calcium ion buffer, phosphate buffered saline (PBS), tris(hydroxymethyl)aminomethane hydrochloride (Tris-HCl) buffer, or 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid (HEPES) buffer.

The invention belongs to the technical field of oil exploitation, and particularly relates to an acid liquor thickening agent as well as a preparation method and application thereof. The synthesis method comprises the following steps: adding butylene glycol, 4, 4 '-diaminostilbene-2, 2'-disulfonic acid, (2-acrylamido ethyl) phosphonic acid, monopotassium phosphate and deionized water into a first reactor, uniformly stirring, and adjusting the pH value to 7-8; (3-acryloyloxypropyl) tri (trimethylsiloxy) silane, deionized water, hydroxypropyl methyl cellulose, OP-10 and monopotassium phosphate are sequentially added into a second reactor, and the pH is adjusted to be 7-8; adding an initiator into a high-position dropwise adding tank, dropwise adding the initiator into a second reactor, quickly adding the mixed liquid in the first reactor when the viscosity begins to rise, heating, and carrying out heat preservation reaction to obtain viscous liquid; and drying and granulating to obtain the product. The invention has the advantages of simple synthesis, high apparent viscosity, strong shear resistance, good salt-resistant and hardness-resistant effects, and good drag reduction effect.

The invention belongs to the technical field of molecular diagnosis, and particularly discloses a high-risk HPV16 rapid detection system based on RPA-CRISPR / Cas12a, which is prepared by the following steps: (1) mixing a nucleic acid lysis solution containing Tris (pH = 8.0), NaHCO3, polyvinylpyrrolidone and Tween-20 with Proteinase K to treat a sample, and performing pyrolysis at room temperature for 5 minutes to obtain a nucleic acid template; (2) an RPA reaction system contains an RNA inhibitor, a reverse transcriptase and an RPA reaction essential enzyme, and after the template and the starting agent in the step (1) are added, RPA amplification is carried out at 37 DEG C; (3) dropping the reaction liquid on a colloidal gold test strip subjected to position exchange and transformation of a sample pad and a water absorption pad, and carrying out result interpretation; and (4) adding the RPA product into a CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) reaction system containing the LbCas12a protein, the specific gRNA and the probe. According to the scheme, a rapid, high-sensitivity and cross-reaction-free detection system of the HPV16 is realized by optimizing a nucleic acid lysis solution formula, designing a specific primer and gRNA and modifying a test strip for detection.