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36results about How to "Stable osmotic pressure" patented technology

Medium for amplification of human mesenchymal stem cells and amplification method thereof

The invention discloses a culture medium for expanding human mesenchymal stem cells, which comprises a basic medium and an additive added to the medium, and the additive includes the following components at final concentrations: linoleic acid 2‑10 μL / mL, human Source AB type serum 5‑15 μL / mL, human transferrin 5‑15 μg / mL, etc. Using the culture medium to expand human mesenchymal stem cells includes the following steps: (1) isolating human mesenchymal stem cells from umbilical cord or placenta, or isolating mononuclear cells from bone marrow blood, umbilical cord blood or placental blood, and placing them in the culture medium (2) Place the cells separated and purified in step (1) into fresh medium for subculture. The invention adopts the culture medium of specific components and the expansion method, which can effectively speed up the cell expansion speed, shorten the expansion time, maintain the uniform shape of the cells after passaging, and reduce their differentiation, thereby ensuring the safety of human mesenchymal stem cells sex.
Owner:金时代进出口贸易重庆有限公司

Peritoneal dialysate

It is intended to provide a safe and highly stable peritoneal dialysate which causes neither peritoneal membrane disorders nor peritoneal sclerosis in frequently repeated peritoneal dialysis treatment, can protect the residual renal functions in chronic renal failure and inhibit the progress of renal damage over a long period of time, and enables peritoneal dialysis treatment in a diabetic patient. A peritoneal dialysate which contains 0.05 to 3.5 w / v% of taurine and 0.1 to 6.5 w / v% of trehalose as osmotic agents and having a pH value regulated to 6.5 to 7.5.
Owner:CHEIRON JAPAN CO

Method and system for testing rock permeability in dynamic load disturbance process

The invention provides a method and system for testing the rock permeability in a dynamic load disturbance process, and belongs to the technical field of geotechnical engineering. The method for testing the rock permeability in the dynamic load disturbance process comprises the steps of: selecting a sample, saturating the sample, applying confining pressure, applying dynamic load, applying hydraulic pressure, and calculating the permeability. The test system comprises a confining pressure chamber, a confining pressure loading device, a power loading device and a pore pressure loading device; the confining pressure chamber is hollow; the confining pressure loading device is connected with the confining pressure chamber; the power loading device and the confining pressure chamber are in abutting joint; the power loading device is used for applying dynamic load onto a rock sample along the axial direction of the rock sample; the pore pressure loading device comprises a pipeline and a hydraulic pump; the pipeline is separately communicated with the hydraulic pump and the confining pressure chamber; and the hydraulic pump is used for pumping liquid to the end part of the rock sample. Bymeans of the method and the system in the invention, the technical problems that the stress state of the rock sample is single and the security of underground engineering under the combined action ofdynamic load and water pressure cannot be reflected in the prior art can be solved.
Owner:INST OF ROCK AND SOIL MECHANICS - CHINESE ACAD OF SCI

Compound premix capable of improving content of Chinese idle muscle protein

The invention discloses a compound premix capable of enhancing the content of proteins in muscles of a grass carp. The compound premix consists of 10000g of the raw materials in weight mixing ratio: 1000g of compound vitamins, 5000g of compound mineral elements, 1000g of Beta-dextran premix agents, 500 to 1000g of taurine and unite bran. The addition of the compound premix of the invention in the formula feed for grass carp takes a weight proportion of 1 percent to ensure that the condition factor of the cultivated grass carp is larger than 2, the organ body weight proportion is smaller than the weight ratio, 11percent, and the content of the proteins in the muscles of the fish body is larger than 22 percent. The invention has the advantages that the grass carp cultivated using the compound feed of the premix has enhanced the edible part and the better meat quality. Saving the resources, the compound premix of the invention is beneficial to the environmental protection and is more beneficial to the increasing demand by the national citizens for the quality and safety of the aquatic foods.
Owner:SUN YAT SEN UNIV

Chinese sturgen artificial insemination method and used diluent

The artificial insemination method for Chinese sturgeon adopts diluent A and diluent B as insemination medium and adopts double wet method to make operation. For the first time it uses the diluent A to wash ova and remove ovarian liquid, and for the second time it uses the diluent B to activate ova and spermatozoa and make the spermatozoa be uniformly dispersed to implement insemination. The described diluent includes diluent A and diluent B. The diluent A is made up by using NaCl, Kcl, CaCl2 2H2O, MgCl 6H2O, NaHCo3, Na2Co3, NaOH, citricacid, penicillin, streptomycin and distilled water, and the diluent B is obtained by using distilled water whose volume is 25 times that of diluent A to dilute the diluent A.
Owner:YANGTZE RIVER FISHERIES RES INST CHINESE ACAD OF FISHERY SCI

Penetrating agent used for peritoneal dialysate and dialysate thereof

The invention provides a penetrating agent used for a peritoneal dialysate and a dialysate thereof, belonging to the research field of the peritoneal dialysate in peritoneal dialysis treatment of end stage renal disease. The penetrating agent is 2.5-7.5% of maltose aqueous solution, preferably 2.5%, 4.25% or 7.5% of maltose aqueous solution. Per 100 ml of the dialysate prepared by the penetrating agent comprises the following components: 2.5-7.5g of maltose, 535mg of sodium chloride, 448g of sodium lactate, 25.7mg of calcium chloride and 5.08g of magnesium chloride; and preferably, each 100ml of the dialysate comprises 2.5g, 4.25g or 7.5g of maltose. The dialysate prepared by the penetrating agent has good biocompatibility and favorable price, can maintain stable ultrafiltration effect, and generates little side effect in vivo after metabolization.
Owner:CENT SOUTH UNIV

Compound premix for livestock

The invention relates to a formula of feed for livestock, and particularly discloses a compound premix for livestock. The pecking feed part of the compound premix is prepared from the following components: barley, water, L-lysine hydrochloride, DL-methionine, ferrous sulfate, zinc sulfate, copper chloride hydroxide, manganese sulfate, sodium selenite, calcium iodate, vitamin complex for chicken, mildew preventive, magnesium sulfate, sodium bicarbonate, potassium chloride, calcium formate, calcium hydrophosphate, ethoxyquinoline, dextrin and starch. The raw materials are uniformly mixed and pressed into cake to obtain the compound premix. The compound premix has the advantages that (1) natural habits of livestock for pecking and ingesting can be met, and pickingill of chicken can be prevented; (2) the components are reasonably proportioned, the production performance of feeding chicken can be remarkably improved; (3) the ingesting time of feeding chicken can be effectively prolonged, and nutritional substances can be effectively absorbed; (4) the components in the feed cannot be layered due to proportion difference in the feeding chicken pecking process.
Owner:GUANGHAN LONGDA FEED

Heparin sodium tube sealing injection and preparation method thereof

The invention provides heparin sodium tube sealing injection, comprising heparin sodium, glucose, mannitol, sodium dihydrogen phosphate, disodium hydrogen phosphate and the balance of water, wherein the tube sealing injection of which the volume is 5ml or 10ml, the osmotic pressure is 260-320 mOsmol / Kg, and the pH value is 6-7 is prepared. By adopting the isotonic injection with low concentration, large volume and stability disclosed by the invention, untoward effects such as local irritation and haemorrhage caused by injection are reduced; the local blood coagulation and tube jamming phenomena are avoided; the anaphylaxis which can be generated by heparin sodium is reduced; meanwhile, the stability of the injection is increased; the sterile level is higher; a plurality of defects in the prior art are solved; and the security of the heparin sodium injection is greatly improved.
Owner:范克

De-host extraction kit for phlegm macrogenome

The invention provides a de-host extraction method for a sputum pathogenic microorganism metagenome. The method comprises steps of sputum pretreatment, differential lysis to remove the host and nucleic acid extraction. The invention combines DTT and protease to quickly homogenize sputum, and then uses surfactant to differentially lyse cells, reduces interference of human genes, realizes enrichmentof microbial genome, and effectively improves detection rate of metagenomic pathogens in sputum samples.
Owner:GENESEEQ TECH INC +1

Blastocyst vitrification refrigerating fluid and refrigerating method

The invention relates to a blastocyst vitrification refrigerating fluid and a refrigerating method. The vitrification refrigerating fluid comprises an equilibrium liquid, a refrigerating fluid 1 and arefrigerating fluid 2; wherein the equilibrium liquid comprises a basic equilibrium liquid and a protein additive; the refrigerating fluid 1 comprises polyvinylpyrrolidone, ethylene glycol, dimethylsulfoxide and the equilibrium liquid; the refrigerating fluid 2 comprises polyvinylpyrrolidone, ethylene glycol, dimethyl sulfoxide, trehalose, polysucrose and the equilibrium liquid. The vitrification refrigerating fluid provided by the invention can significantly improve the freeze-thaw survival rate and the recruitment rate of blastocysts, and is short in time consumption.
Owner:佛山辅康生物科技有限公司

Composition and its use, umbilical cord preservation preparation and preparation method thereof

The invention relates to the medical field, particularly to a composition and its use, an umbilical cord preservation preparation and a preparation method thereof. According to the invention, physiological saline is taken as the basic ingredient of umbilical cord preservation liquid, umbilical cord blood plasma is used as the nutritional ingredient source, as a natural substance, umbilical cord blood plasma not only provides multiple nutritional ingredients, but also can maximumly maintain the umbilical cord vitality in order to maintain a microenvironment similar to that in vivo. Lactobionic acid, hydroxyethyl starch and other macromolecular substances are added to avoid swelling death of the umbilical cord in the preservation process. The preservation liquid can be used for transportation and preservation of the preparation at low temperature. Thus, adequate nutrients are supplied to in vitro umbilical cord, and also the seed cell vitality, the original cell morphology and biological characteristics are well maintained.
Owner:GUANGZHOU SALIAI STEMCELL SCI & TECH CO LTD

Seedling raising substrate for cultivating salt resistant plant seedlings, and preparation method and application of seedling raising substrate for cultivating salt resistant plant seedlings

InactiveCN111436349AAvoid reducing growth-promoting effectReduce in quantityFungiBacteriaMicroorganismPotassium nitrate
The invention discloses a seedling raising substrate for cultivating salt resistant plant seedlings, and a preparation method and application of the seedling raising substrate for cultivating salt resistant plant seedlings. The seedling raising substrate for cultivating salt resistant plant seedlings is prepared from mushroom residues, livestock and poultry excrement and urine, vinegar residues, gypsum residues, vermiculite, functional microorganisms and plant nutrient substances. The preparation method comprises the steps of preparing thoroughly decomposed mushroom residues through stacking fermentation of the mushroom residues, the livestock and poultry excrement and urine and the vinegar residues, preparing plant nutrition element enveloping bodies through entrapping potassium nitrate and magnesium sulphate with urea-formaldehyde resins, preparing microorganism enveloping bodies through entrapping functional microorganisms of trichoderma harzinum T83 and bacillus amyloliquefaciens IAE with polyglutamic acid, and preparing the substrate through solid fermentation and compounding of raw materials. The prepared substrate has stable high-cation environment, resistance of seedlings to hyperosmosis is continuously trained, and seedling raising substrate products suitable for heavy-salt soil regions are developed. The salinity of transplanted soil, which can be borne by plant seedlings cultivated by the products, is increased by 50% to 200%.
Owner:HOHAI UNIV

Process for frozen-preserving Chinese sturgeon semen under super-low temperature

Technology for bulk preserving spermatozoa of Chinese sturgeon through freezing at ultralow temperature comprises collecting and detecting fresh spermatozoa, diluting, balancing, adding antifreeze, subpackaging, program cooling, and preserving in liquid nitrogen container of -196deg.C. Each bulk can freeze 100 mL fresh spermatozoa. when the first bulk spermatozoa is in the procedure cooling step, after 5 minute, starting diluting the second bulk spermatozoa, and repeating above steps until all spermatozoa is preserved 8-12 h before its effective time. The diluent is Tris-HCl 20-30 millimole, sucrose 30-60 mol, potassium chloride 2-10 millimole, and distilled water 1000mL, and regulating pH to 8-8.5 with HCl. The antifreeze is methanol. The invention can efficiently carry out bulk preservation of Chinese sturgeon spermatozoa through freezing at ultralow temperature and long term ultralow temperature freezing preservation, and provide enough spermatozoa resource for artificial propagation of Chinese sturgeon.
Owner:YANGTZE RIVER FISHERIES RES INST CHINESE ACAD OF FISHERY SCI

Mesenchymal stem cell preservation solution, preservation method and application thereof

The invention provides a mesenchymal stem cell preservation solution, a preservation method and application thereof, and relates to the technical field of stem cell preservation solutions. The mesenchymal stem cell preservation solution provided by the invention comprises the following components in percentage by volume: 0.1 to 0.5 percent of sodium hyaluronate, 0.2 to 0.4 percent of albumin and the balance of physiological saline. The survival rate of stem cells can reach more than 80% within 24 hours by using the preservation solution provided by the invention.
Owner:深圳市未来细胞生命科技有限公司

Swine pasteurellosis vaccine enrichment medium

The invention provides a swine pasteurellosis vaccine enrichment medium, and relates to the field of biology. The swine pasteurellosis vaccine enrichment medium is prepared from the following raw materials by weight: 20.0g of meat liver and stomach membrane digestive juice powder, 8.0g of bovine pancreas digestive juice, 10.0g of peptone, 5.0g of NaCl, 1.0g of a growth promoting factor, and purified water added to 1000ml. A preparation method of the swine pasteurellosis vaccine enrichment medium comprises the following steps: adding all the raw materials for preparing the swine pasteurellosisvaccine enrichment medium into purified water, fully dissolving the raw materials, and carrying out sterilization at 121 DEG C for 15 minutes for later use. The invention relates to an application ofa synthetic dry powder culture medium in swine pasteurellosis vaccine production. The synthetic dry powder culture medium has the beneficial effects that commercial raw materials can be selected, theculture medium is clear, the number of cultured bacteria is high, and the freeze-drying survival rate of the bacteria is increased.
Owner:青岛高科技工业园海博生物技术有限公司

Water treatment system

The invention relates to the field of water treatment, in particular to a water treatment system, which comprises an anaerobic reaction device and an aerobic reaction device, wherein the anaerobic reaction device is in fluid communication with the aerobic reaction device; the anaerobic reaction device comprises an anaerobic reaction tank body and a grid for dividing an internal space of the anaerobic reaction tank body into an isolated area and a filler area which are in fluid communication with each other; a water inlet of the anaerobic reaction device is positioned in the isolated area; a water outlet of the anaerobic reaction device is positioned in the filler area; an anaerobic reaction filler is arranged in the filler area. According to the water treatment system, systems for an A2O water treatment method can be effectively integrated, and in addition, air can float to wash the surface of a filter membrane, so that the effects of greatly reducing the energy consumption and saving an occupied area can be achieved.
Owner:上海立泉环境科技有限公司

Lactic acid bacteria stabilizer, lactic acid bacteria beverage and preparation method

The invention relates to the field of food processing and the field of biotechnology, and discloses a lactic acid bacteria stabilizer, a lactic acid bacteria beverage and a preparation method. The lactic acid bacteria stabilizer comprises low-ester pectin, medium-substitution starch phosphate, tragacanth, a metal ion regulator, a carbon source, an antioxidant and an osmotic pressure regulator. Thepreparation method of the lactic acid bacteria stabilizer comprises the following steps: firstly, adding low-ester pectin and tragacanth into water at the temperature of 75-85 DEG C, heating to 90-100 DEG C, and stirring for dissolving to obtain a mixed solution; and cooling the mixed solution to 30-40 DEG C, and adding other components to obtain the lactic acid bacteria stabilizer. The low-esterpectin, the medium-substitution starch phosphate and the tragacanth are mixed to form a copolymer, the lactic acid bacteria can be partially embedded and used in the lactic acid bacteria beverage, the stability of the lactic acid bacteria beverage can be improved, the storage stability of the lactic acid bacteria can be improved, and the survival time of the lactic acid bacteria can be prolonged.
Owner:CHAOHU UNIV

Chinese sturgen artificial insemination method and used diluent

The artificial insemination method for Chinese sturgeon adopts diluent A and diluent B as insemination medium and adopts double wet method to make operation. For the first time it uses the diluent A to wash ova and remove ovarian liquid, and for the second time it uses the diluent B to activate ova and spermatozoa and make the spermatozoa be uniformly dispersed to implement insemination. The described diluent includes diluent A and diluent B. The diluent A is made up by using NaCl, Kcl, CaCl2 2H2O, MgCl 6H2O, NaHCo3, Na2Co3, NaOH, citricacid, penicillin, streptomycin and distilled water, and the diluent B is obtained by using distilled water whose volume is 25 times that of diluent A to dilute the diluent A.
Owner:YANGTZE RIVER FISHERIES RES INST CHINESE ACAD OF FISHERY SCI

Compound premix capable of improving content of Chinese idle muscle protein

The invention discloses a compound premix capable of enhancing the content of proteins in muscles of a grass carp. The compound premix consists of 10000g of the raw materials in weight mixing ratio: 1000g of compound vitamins, 5000g of compound mineral elements, 1000g of Beta-dextran premix agents, 500 to 1000g of taurine and unite bran. The addition of the compound premix of the invention in theformula feed for grass carp takes a weight proportion of 1 percent to ensure that the condition factor of the cultivated grass carp is larger than 2, the organ body weight proportion is smaller than the weight ratio, 11percent, and the content of the proteins in the muscles of the fish body is larger than 22 percent. The invention has the advantages that the grass carp cultivated using the compound feed of the premix has enhanced the edible part and the better meat quality. Saving the resources, the compound premix of the invention is beneficial to the environmental protection and is more beneficial to the increasing demand by the national citizens for the quality and safety of the aquatic foods.
Owner:SUN YAT SEN UNIV

Mesenchymal stem cells combined with traditional Chinese medicines for activating amplification and preparation method and application of mesenchymal stem cells

The invention provides mesenchymal stem cells combined with traditional Chinese medicines for activating amplification, and a preparation method of the mesenchymal stem cells comprises the following steps: (1) pretreatment: digesting tissue pieces with pancreatin and IV collagenase, separating primary mesenchymal stem cells; (2) culture: adding the cells obtained in the step (1) to a low sugar DMEM culture medium containing components of 50-80mg / mL hemianthus micranthemoides extract, 50-80mg / mL Chinese gall extract, 1.5-3mmol / mL L-glutamine and 1.5-3ng / mL bFGF, culturing in a wet incubator of 37 DEG C with 5% CO2, changing the culture medium once every 3-4 days; and (3) collection of cells and subculture. Shown by in vitro tests, the traditional Chinese medicines activated mesenchymal stem cells can effectively inhibit reproduction of HBV and promote repair of damaged hepatic cells.
Owner:SIMPSON INT LIFE TECH (TIANJIN) CO LTD

Adipose tissue-derived stromal cell cryopreservation liquid and cryopreservation method thereof

The invention provides an adipose tissue-derived stromal cell cryopreservation liquid. The adipose tissue-derived stromal cell cryopreservation liquid is prepared from the following raw materials: a DMEM / F12 culture medium, 50 to 60 [mu] g / mL of ethylene glycol monomethyl ether, 1.5 to 4.0 mg / mL of acetylchitosamine, 25 to 30 ng / mL of bilobalide, 35 to 45 ng / mL of sodium pyrophosphate, 80 to 90 [mu] g / mL of alfalfa saponin and 100 to 110 [mu] g / mL of lipoic acid. According to the adipose tissue-derived stromal cell cryopreservation liquid provided by the invention, animal-derived serum and DMSO are not added, and the survival rate of resuscitated cells is high. The ethylene glycol monomethyl ether and the acetylchitosamine are added into the cryopreservation liquid, so that cells are not damaged, the permeability of the cells is improved, the osmotic pressure inside and outside the cells is maintained to be stable, and the activity of the cells is maintained. The bilobalide and the sodium pyrophosphate are added and compounded for use, so that denaturation and inactivation of cell protein molecules are prevented, and rapid activity recovery of cells after long-time cryopreservationis facilitated. Alfalfa saponin and lipoic acid are also added into the cryopreservation liquid, free radicals generated in the cryopreservation process are removed, and the antioxidation effect is achieved. The invention further provides a cryopreservation method of the adipose tissue-derived stromal cells, and the method is simple and convenient and easy to operate.
Owner:GUANGDONG CELL BIOTECHNOLOGY CO LTD

A device for testing the performance of forward osmosis membranes

The invention discloses a device for evaluating performance of a forward osmosis membrane. The device comprises a raw material liquid tank, a feed liquid pool, a forward osmosis membrane component, a draw solution pool, a high-concentration salt pond and a delivery tank, wherein a check valve and an overflow pipe are arranged on an overflow tank of the pool; an aeration pipe is arranged at the bottom; the forward osmosis membrane component comprises a shell; a forward osmosis membrane is arranged inside the shell, and divides the shell into upper and lower lattices, which respectively are a draw solution chamber and a feed liquid chamber; the draw solution chamber is put into a magnetic stirrer; a water inlet / outlet of the draw solution pool is connected with the draw solution chamber of the forward osmosis membrane component; a probe of a conductivity controller is put into the pool; the water outlet of the high-concentration salt pond is connected with the water inlet of the draw solution pool through a pipeline with a strong brine pump; opening and closing of the strong brine pump are controlled by a conductivity meter; the delivery tank is put on an electric scale. The device disclosed by the invention is small in volume, simple and easy to operate, stable in test result, small in required area of the forward osmosis membrane, wide in application range, and applicable to test of the forward osmosis membranes with kinds of sources.
Owner:JIANGNAN UNIV

Preparation method of thalassia hemperichii protoplast

The invention discloses a preparation method of a thalassia hemperichii protoplast and belongs to the field of plant cell engineering. The preparation method comprises the following steps: S1, takingyoung leaves of thalassia hemperichii, washing them with sterile seawater, and temporarily culturing them to obtain a raw material 1; S2, putting the raw material 1 obtained in the step S1 into a pretreatment liquid for soaking to obtain a raw material 2; S3, taking out the raw material 2 obtained in the step S2, sucking dry water, cutting them into blocks, adding enzyme liquid for enzymolysis, and obtaining enzymolysis tissues; S4, filtering the enzymolysis tissue obtained in the step S3 to obtain filtrate; S5, centrifuging the filtrate obtained in the step S4, discarding the supernatant, suspending the precipitate with a resuspension solution, centrifuging, and discarding the supernatant to obtain a precipitate; S6, suspending the precipitate obtained in S5 with a resuspension solution to obtain the thalassia hemperichii protoplast. The preparation method of the thalassia hemperichii protoplast is established for the first time, and the thalassia hemperichii protoplast obtained by the method is high in yield and high in survival rate.
Owner:HAINAN ACADEMY OF OCEAN & FISHERIES SCI

Composition and use thereof, umbilical cord preservation preparation and preparation method thereof

The invention relates to the medical field, particularly to a composition and its use, an umbilical cord preservation preparation and a preparation method thereof. According to the invention, physiological saline is taken as the basic ingredient of umbilical cord preservation liquid, umbilical cord blood plasma is used as the nutritional ingredient source, as a natural substance, umbilical cord blood plasma not only provides multiple nutritional ingredients, but also can maximumly maintain the umbilical cord vitality in order to maintain a microenvironment similar to that in vivo. Lactobionic acid, hydroxyethyl starch and other macromolecular substances are added to avoid swelling death of the umbilical cord in the preservation process. The preservation liquid can be used for transportation and preservation of the preparation at low temperature. Thus, adequate nutrients are supplied to in vitro umbilical cord, and also the seed cell vitality, the original cell morphology and biological characteristics are well maintained.
Owner:GUANGZHOU SALIAI STEMCELL SCI & TECH CO LTD

A kind of high-yielding strain of avilamycin and its breeding method

The invention provides a kind of avelamycin high-yield bacterial strain breeding method, adopts ARTP and three times 137 Csy mutagenesis mutated Streptomyces and used 2 protoplast fusions for gene recombination. The beneficial effect is: after four rounds of mutagenesis and two rounds of protoplast fusion, the fusion high-yield strain G2-31 was obtained, and its avelamycin titer reached 2842.57 mg / L, which was 4 times that of the original strain 11-10. Passage test, strain state is stable, showing high potential for industrial application.
Owner:杭州皇冠农业生物工程技术研究中心有限公司

Efficient water-soothing hydrogel mask and preparation method thereof

The invention discloses an efficient water-soothing hydrogel mask and a preparation method thereof, and relates to the technical field of cosmetics. The mask comprises the following components in percentage by weight: 1-10% of an active matter component, 0.1-7% of an oil phase component, 0.1-2% of an anti-corrosion component, 10-50% of a water phase component and the balance of water, wherein the water phase component comprises dihydroxyaluminum aminoacetate, allantoin, dipotassium glycyrrhizinate, EDTA-disodium, tartaric acid, glycerol, butanediol, and sodium polyacrylate. According to the efficient water-soothing hydrogel mask provided by the invention, under the action of body temperature and skin surface water molecules, internal physical crosslinking of solid essence is opened, essence molecules are released layer by layer and orderly permeate into the deep part of the skin, and the efficient water-soothing hydrogel mask can achieve water-soothing without irritation and is long in lasting time. Hydrogel essence is not easy to volatilize, does not suck back, always keeps stable osmotic pressure, and ensures that the essence orderly penetrates into the inner layer of the skin.
Owner:源一(杭州)生物医药发展有限公司

A kind of immune cell serum-free cryopreservation liquid and cryopreservation method

The invention discloses a serum-free cryopreservation solution for immune cells, which is characterized in that it comprises a basal medium and a cell cryopreservation protective agent, and the cell cryopreservation protective agent is composed of the following raw materials: polyethylene glycol, nonylphenol poly Oxyethylene ether-10, acacia polysaccharide, sodium carboxymethylcellulose, polyglyceryl fatty acid ester, bamboo leaf flavone. In the present invention, polyethylene glycol and nonylphenol polyoxyethylene ether-10 are used to replace DMSO to change the permeability of the cell membrane and at the same time protect the cell membrane, so that the free water in the cell can be excluded from the cell and reduce the risk of cryopreservation. The formation of ice crystals in the cells during the process damages the cells. Acacia polysaccharides, sodium carboxymethylcellulose, and polyglycerol fatty acid esters are added as osmotic pressure stabilizers to maintain a stable osmotic pressure in the extracellular environment. Added with bamboo leaf flavonoids, it helps cells recover quickly after recovery. The invention also provides a cryopreservation method for immune cells, which is simple and convenient, and meets the demands for immune cells in scientific research, medical treatment and other fields.
Owner:湖南旭智生物科技有限公司

Immune cell cryopreservation liquid and immune cell cryopreservation method

The invention discloses an immune cell cryopreservation liquid, which comprises the following components: 0.02 to 0.06 mg / mL of dimethyl sulfoxide, 1 to 6 mg / mL of cucurbitacine, 0.01 to 0.03 mL / mL of gleditsia sinensis polysaccharide, 1 to 2 mg / mL of lentinan, 1 to 5 [mu]g / mL of polyglycerol fatty acid ester, 0.01 to 0.03 mg / mL of polyethylene glycol, 10 to 16 mg / mL of non-essential amino acid and 12 to 20 mg / mL of human serum albumin. The invention discloses an immune cell cryopreservation method which comprises the following steps: uniformly mixing peripheral blood mononuclear cells with the immune cell cryopreservation liquid to obtain a cell suspension, transferring the cell suspension into a sterile cryopreservation tube, then putting the cell suspension into a cryopreservation box, carrying out programmed cooling to-70 DEG C, carrying out cryopreservation for 10-15 hours, and then transferring the cell suspension into liquid nitrogen for cryopreservation, wherein the concentration of the cells in the cell suspension is (2-4) * 10<7> cells / mL.
Owner:杭州中赢生物医疗科技有限公司

A kind of preparation method of the powdery algae protoplast

The invention discloses a preparation method of round leaf zannichelliaceae cymodocea rotundta protoplast, and belongs to the field of plant cell engineering. The preparation method comprises the stepS1 of taking spires of round leaf zannichelliaceae cymodocea rotundta, cleaning the spires with sterile seawater, and then performing temporary culture to obtain a raw material 1; the step S2 of immersing the raw material 1 obtained in the step S1 into a pretreatment solution to obtain a raw material 2; the step S3 of taking out the raw material 2 obtained in the step S2, removing the moisture, cutting the raw material into pieces and adding an enzyme solution for enzymatic hydrolysis to obtain an enzymatic hydrolysis tissue; the step S4 of filtering the enzymatic hydrolysis tissue obtained in the step S3 to obtain a filtrate; the step S5 of centrifuging the filtrate obtained in the step S4, abandoning a supernatant, conducting suspension and precipitation with a W5 solution, centrifugingand abandoning the supernatant to obtain a precipitate; the step S6 of suspending the precipitate obtained in the step S5 in an MMG solution to obtain the round leaf zannichelliaceae cymodocea rotundta protoplast. The round leaf zannichelliaceae cymodocea rotundta protoplast obtained by the method has high yield and high survival rate.
Owner:HAINAN ACADEMY OF OCEAN & FISHERIES SCI
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