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78results about How to "Morphologically normal" patented technology

Fresh amnion preservation fluid, fresh amnion preservation method and application thereof

The invention discloses a fresh amnion preservation fluid, a fresh amnion preservation method and application thereof. The fresh amnion preservation fluid is made by adding water for injection to 9.0-12.0g of DMEM culture medium, 10.0-25.0g of chondroitin sulfate, 0.5-1.0g of sodium hyaluronate, 4.0-5.0g of HEPES, 10.0-15.0g of dextran, 1.0-6.0ml of gentamycin, 24.0-30.0mg of dexamethasone, 10.0-15.0ml of non-essential amino acid, 0.50-0.95g of glutathione, 0.0-50.0ml of fetal calf serum to 1000ml. The fresh amnion preservation method comprises the following steps: separating the amnion by a blunt, rinsing the amnion clean, and then processing the amnion by an antibiotic; cutting and packaging the amnion into a container with the amnion preservation fluid; storing the amnion preservation fluid in a refrigerator with the temperature of 4 DEG C, and rinsing hands clean with aseptic phosphate buffer before use. The fresh amnion preservation fluid has the following advantages: 1. the amnion preservation fluid is only stored in the refrigerator with the temperature of 4 DEG C; 2. the shelf life is prolonged to at least 20-30 days; 3. the amnion preservation fluid can be in batch processing and centralized storage, and 4. the amnion preservation fluid can be applied to various amnion transplantation repairs, for example (1) ocular surface reconstruction as a conjunctival substitute, (2) amnion transplantation for treating symblepharon, and (3) treatment of corneal ulcer caused by various reasons and the like.
Owner:天津市医药科学研究所

Mesenchymal stem cell preservation liquid, and preparation method and application thereof

ActiveCN102365933AProlong the duration of activityEasy to prepareDead animal preservationCord blood stem cellMedicine
The invention belongs to the field of biologic medicines and discloses mesenchymal stem cell preservation liquid, and a preparation method and application thereof. The mesenchymal stem cell preservation liquid contains AB cord blood plasma which is 5-15% of the volume of the preservation liquid and low molecular weight heparin calcium which is 70-80 AXaIU / ml. The AB cord blood plasma and mesenchymal stem cells come from the same provider. By means of the mesenchymal stem cell preservation liquid provided by the invention, the activity maintaining time of the mesenchymal stem cells can be prolonged (above 90% of activity is kept at 4-15 DEG C for 72 h); after the mesenchymal stem cells are preserved in the preservation liquid for 72h, the cells are normal in form, the proliferation and amplification capability of the cells cannot be influenced, and the phenotypic characteristics of the mesenchymal stem cells cannot be influenced; the mesenchymal stem cell preservation liquid disclosed by the invention is safe and reliable for clinical application; and, because the AB cord blood plasma and the cord mesenchymal stem cells come from the same placenta and belong to auto-plasma, the possibility of exogenous virus pollution is reduced.
Owner:广州市天河诺亚生物工程有限公司

Heat treatment method for U71MnH steel rail welding joint

ActiveCN109022748ANormal tissue morphologyImprove performance statusIncreasing energy efficiencyFurnace typesHardnessCooling speed
The invention relates to a heat treatment method for a U71MnH steel rail welding joint, and belongs to the technical field of steel rail welding. The problem that harmful structures such as martensites are generated to influence the joint hardness due to the fact that the local cooling speed is higher than the critical transition temperature when an existing steel rail welding joint is cooled in the heat treatment process is solved. The heat treatment method for the U71MnH steel rail welding joint comprises the steps that a U71MnH steel rail welding joint welding seam area which is cooled to 300 DEG C or below after being welded is heated to 915-935 DEG C, then heating is stopped, air spraying cooling is adopted and stopped after the steel rail joint tread temperature is lowered to 405-432DEG C, and natural cooling is conducted till the room temperature is achieved. By adopting the method, it is guaranteed that the joint structure is normal while the hardness of the U71MnH steel railflash welding joint is effectively controlled.
Owner:PANZHIHUA IRON & STEEL RES INST OF PANGANG GROUP

Porphyra zebra tps gene and its application in improving rice salt tolerance

The invention discloses a PyTPS (porphyra yezoensis ueda trehalose-6-phosphate synthase) gene which is cloned to construct a plant expression vector of the gene, and the plant expression vector is transferred into the agrobactrium tumefaciens strain, so that an engineering strain is obtained. A rice variety is transformed by utilizing agrobacterium-mediated transformation, so that genetically modified rice is obtained; after growing and acclimatization, a T0 individual plant is obtained, and a T1 seed is collected; a seedling germinated from the T1-generation genetically modified seed receives PCR (polymerase chain reaction) detection and a salt tolerance assay, so that a T1-generation genetically modified salt-resistant strain is obtained, a T2 generation receives a kanamycin resistance assay, PCR detection and Southern hybridization, and results indicate that the PyTPS gene is already integrated into the genome of the genetically modified strain. The PyTPS gene in the invention has a TPS domain as well as a TPP (thiamine pyrophosphate) domain; the PyTPS gene source is safe; the development of the plant morphology of the PyTPS genetically modified rice is normal; the PyTPS gene can be stably inherited in genetically modified plants; and moreover, the transformation system is highly effective.
Owner:QINGDAO AGRI UNIV

Reagent capable of preventing and eliminating pollution of mammalian cells

ActiveCN106047796AGood compatibilityRemoval of bacterial and mycoplasma contaminationCulture processVertebrate cellsAmino acid compositionAntibiotics
The invention provides a reagent capable of preventing and eliminating pollution of mammalian cells, and belongs to the field of microbial pollution control in mammalian cell culture. A polypeptide having a sequence of SEQ ID NO:1 can be used for preventing and eliminating pollution of the mammalian cells; the reagent is composed of the polypeptide having the sequence of SEQ ID NO:1 and amino acid and does not contain any antibiotic component. The product is prepared in accordance with the concentration required for prevention and elimination of pollution, microbial pollution in the mammalian cells can be effectively prevented and eliminated, and the defects of use restriction of antibiotic components in a conventional product and longer cell treatment period are overcome; and the product is good in stability and easy to preserve.
Owner:GENLOCI BIOTECH

Polyploidy induction method for fiber linum usitatissimum under isolated culture condition

InactiveCN102119662ARaise the ratioPolyploid plants are morphologically normalPlant tissue cultureHorticulture methodsBudLinum
The invention relates to a polyploidy induction method for fiber linum usitatissimum under an isolated culture condition, wherein the method comprises the following steps of: selecting health and full fiber linum usitatissimum seeds; sterilizing the seeds and then culturing into seedling; processing the stem tip with colchicines to induce polyploid; transforming into a stem tip extending culture media for culturing; identifying the ploidy of the stem tip chromosome; culturing the stem section which is identified to be a tetraploid plant in a callus and bud induction culture medium to obtain lots of tetraploid sterile seedlings; and then transforming to an extending growing culture medium to grow; performing rooting culture in a rooting culture medium, and then transferring to a sterilized substrate for manging; and finally identifying the ploidy of chromosome of the root tip. The method can obtain higher inductivity than that of a method which processes the fiber linum usitatissimum seeds; the inductivity can be up to 25.5%; the pure tetraploid ratio is high; the polyploidy plant has normal shape, and high transplanting survival rate; the method can realize quick breeding under the isolated condition to obtain a large amount of tetraploid tissue-cultured seedlings in a short time.
Owner:HEILONGJIANG BAYI AGRICULTURAL UNIVERSITY

Medicine for treating hepatitis and cirrhosis ascites and its preparation method

InactiveCN101057912APromotes liver cell recoveryImprove body immunityDigestive systemAntiviralsBorneolHepatocyte
The invention relates to a traditional Chinese medicament for treating hepatitis and cirrhosis ascites which is prepared from the following raw materials (by weight portion): red ginseng 60-100 parts, white atractylodes rhizome 50-80 parts, borneol 30-50 parts, chicken's gizzard-skin 30-50 parts, red peony root 20-30 parts, blood clam shell 80-100 parts, centipede 40-50 parts, ligumaloes 20-30 parts, earthworm 80-100 parts and polyporus umbellatus 55-80 parts. The medicament is prepared through mixing, grinding into fines, sieving, and can be prepared into powders, tablets, capsules or pills.
Owner:张兆君

Method for acquiring suspension cell line with hypocotyl of cabbage type rape as explant and application of suspension cell line

InactiveCN108064687ASimple and time-saving operation stepsHigh callus induction efficiencyPlant tissue cultureHorticulture methodsNutrientCellular level
The invention specifically relates to a method for acquiring a suspension cell line with the hypocotyl of cabbage type rape as explant and application of the suspension cell line, belonging to the technical field of plant cell culture. According to the invention, the aseptic hypocotyl of cabbage type rape is used as explant and subjected to induction of embryonic callus, culture of suspension cells and the like so as to construct the suspension cell line of the cabbage type rape; and the suspension cell line is used for research on and comparison of the different morphologies and activities ofsuspension cells under the conditions of normal supply of essential micronutrient elements and shortage of the essential micronutrient elements. The prepared suspension cells of the cabbage type rapeare high in activity, stable and uniform in morphology, short in culture period, not limited by natural environmental factors like season and climate, and applicable to research on the cell development of the cabbage type rape at a single cell level and the cell growth, morphology, transmembrane nutrient transport, physiological and biochemical metabolism and gene expression of the cabbage type rape under the condition of abiotic stress.
Owner:HUAZHONG AGRICULTURAL UNIVERSITY

Nutrition-enhanced culture medium for preparing 2-KGA through fermentation and method thereof for preparing 2-KGA

The invention relates to a culture medium in the technical fields of fermentation engineering and biology, in particular to a nutrition-enhanced culture medium for preparing 2-KGA through fermentation, and the nutrition-enhanced culture medium comprises a conventional culture medium and a nutrition enhancer, wherein sorbitol or sorbose is used as a substrate of the conventional culture medium. Meanwhile, the invention also relates to a method for preparing the 2-KGA by applying the enhanced culture medium. The nutrition-enhanced culture medium can promote the growth of small bacteria, enablesthe small bacteria to be disengaged from the dependence on associated bacteria, establishes independent growth and provides a foundation for the improvement of a 2-KGA fermentation process.
Owner:仪宏

Traditional Chinese medicine decoction for treating severe acute pancreatitis

The invention relates to a traditional Chinese medicine decoction for treating severe acute pancreatitis and belongs to the technical field of traditional Chinese herbal medicine preparations for treating pancreatitis. The traditional Chinese medicine decoction is decocted by nineteen traditional Chinese herbal medicines such as gypsum, rheum officinale, mirabilite and rhizoma anemarrhenae. The traditional Chinese medicine decoction is used for treating the severe acute pancreatitis with the comprehensive synergistic effect of the nineteen traditional Chinese herbal medicines according to the theory of traditional Chinese medical recipe based on the traditional Chinese medicine principle of research and treatment on pathogenesis of severe acute pancreatitis. The traditional Chinese medicine decoction has the functions of clearing heat and removing toxicity, invigorating pulse-beat and defecating feces excretion and regulating qi to remove blood stasis, is few in side effects on the human body, simple in treatment method, low in cost, convenient to take and free of toxic and side effects, and is safe and effective. The whole recipe of the traditional Chinese medicine decoction has the functions of clearing heat and removing toxicity, invigorating pulse-beat and defecating feces excretion, regulating qi to remove blood stasis and treating both symptoms and root causes; and the effective rate of treatment on the severe acute pancreatitis reaches over 87.5%.
Owner:GONGAN COUNTY HOSPITAL OF TRADITIONAL CHINESE MEDICINE

Tissue culture and rapid propagation method of caladium bicolor suitable for industrialized production

The invention belongs to the technical field of tissue culture, and relates to a tissue culture and rapid propagation research method suitable for industrialized production. The method is summarized and concluded on the basis of experimental research and production for two years on the basis of a new variety of caladium bicolor introduced by Thai, has strong operability and can be completely used for guiding production. According to the invention, the complete rapid induction, multiplication, rooting and seedling hardening propagation method which has high inductivity and propagation multiple and is suitable for industrial production is established for the first time, a batch rapid propagation situation is formed, and the propagation generations, the hormone concentration of a culture medium and the proportion are controlled to change along with the change of the generations, stability, activity and the proliferation coefficient of seedlings are ensured, and the yield and quality are improved; and according to the method, a production manner of simultaneously propagating and rooting is adopted, so that the production cost is reduced, the production progress is accelerated, the propagation coefficient is ensured, the quality of rooted seedlings is ensured, the method is completely suitable for large-scale industrialized production, and the breeding efficiency of the caladium bicolor is greatly improved.
Owner:ZHANJIANG SUGARCANE RES CENT GUANGZHOU SUGARCANE RES INST

Design method of large-curvature cable-membrane structure

The invention discloses a design method of a large-curvature cable-membrane structure, and aims to solve the technical problems that the existing cable-membrane structure is easy to generate larger deformation to change the shape size or loosen, and the analysis and design theory of the cable-membrane structure at home and abroad is not completely mature. The design method comprises the following steps: (1) carrying out performance analysis on a membrane material to be used by the large-curvature cable membrane structure; (2) adopting ANSYS software to carry out shape finding analysis on the large-curvature cable membrane structure; (3) selecting a membrane material with a proper thickness; (4) optimizing a reinforcing cable net in the large-curvature cable membrane structure; (5) carrying out technical verification and hardware optimization on the large-curvature cable membrane structure; and (6) designing proper light transmittance of the membrane material. According to the design method, a collaborative stress system of the steel cable, the membrane material, the hardware and the cable membrane support steel structure is optimized, the overall stress stability of the structure and the applicability of the component are improved on the premise that the material performance is brought into full play, and the building body art is perfectly expressed.
Owner:CHINA RAILWAY CONSTR ENG GROUP

A kind of mesenchymal stem cell preservation solution and its preparation method and application

The invention belongs to the field of biomedicine and discloses a mesenchymal stem cell preservation solution and its preparation method and application. The mesenchymal stem cell preservation solution contains human AB type umbilical cord blood plasma and 70- 80AXaIU / ml calcium low molecular weight heparin; the human AB type umbilical cord blood plasma and mesenchymal stem cells come from the same provider. The mesenchymal stem cell preservation solution of the present invention can prolong the activity maintenance time of mesenchymal stem cells (maintain more than 90% of the activity for 72 hours at 4-15°C), and the mesenchymal stem cells are stored in the preservation solution of the present invention for 72 hours. , the cell morphology is normal, does not affect its proliferation and expansion ability, and does not affect the phenotypic characteristics of mesenchymal stem cells. The mesenchymal stem cell preservation solution of the present invention is safe and reliable in clinical application, and the AB-type umbilical cord blood plasma and umbilical cord mesenchymal stem cells are derived from the same placenta and belong to autologous plasma, which reduces the possibility of exogenous virus contamination.
Owner:广州市天河诺亚生物工程有限公司

Infection enhancing culture medium and method for improving cell lentivirus infection rate

The invention discloses an infection enhancing culture medium and method for improving the cell lentivirus infection rate, and relates to the field of MDA-MB-231 cell transfection. The enhanced infection culture medium is used for improving the lentivirus infection rate of the MDA-MB-231 cell, and the enhanced infection culture medium is prepared from the following components: a Leibovitz's L-15 culture medium, an RPMI-1640 culture medium, fetal calf serum, non-essential amino acid and an epidermal growth factor; according to the volume percentage of the total raw materials, the addition amount of the fetal calf serum is 10%, and the addition amount of the non-essential amino acid is 1%; the addition amount of the epidermal growth factor is 2-3ng/ml. By adopting the enhanced infection culture medium disclosed by the invention, the MDA-MB-231 cells can be normally cultured in the conventional environment of 37 DEG C and 5% CO2, and the infection efficiency of the lentivirus on the MDA-MB-231 cells is more remarkably improved, so that the gene editing efficiency of the MDA-MB-231 cells becomes higher, and the problem that the lentivirus infection rate of the MDA-MB-231 cells is low at present is solved.
Owner:广州源井生物科技有限公司
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