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58 results about "Anaphase" patented technology

Anaphase (from the Greek ἀνά, "up" and φάσις, "stage"), is the stage of mitosis after the metaphase, when replicated chromosomes are split and the newly-copied chromosomes (daughter chromatids) are moved to opposite poles of the cell. Chromosomes also reach their overall maximum condensation in late anaphase, to help chromosome segregation and the re-formation of the nucleus.

Automated segmentation, classification, and tracking of cell nuclei in time-lapse microscopy

InactiveUS20060127881A1Efficient dynamic cell imaging studyIncrease capacityImage enhancementImage analysisAutomated segmentationInterphase Cell
Methods and apparatus are provided for the automated analysis of images of living cells acquired by time-lapse microscopy. The new methods and apparatus can be used for the segmentation, classification and tracking of individual cells in a cell population, and for the extraction of biologically significant features from the cell images. Based upon certain extracted features, the inventive image analysis methods can characterize a cell as mitotic or interphase and / or can classify a cell into one of the following mitotic phases: prophase, metaphase, arrested metaphase, and anaphase with high accuracy.
Owner:THE BRIGHAM & WOMENS HOSPITAL INC

Telegenesis and oosperm hatching technique for whitebait

The invention relates to the technical field of fish propagating, in particular to a technique of artificial insemination and hatching zygote for whitebait and is provided with 1. artificial insemination process: extruding semen and an egg granule in a container, adding normal saline of 0.004 to 0.008 percent, stirring and standing for 2 to 3 minutes; 2. fertilized egg hatching process and prophase hatching: the fertilized eggs are arranged in a hatching chamber and is poured into a hatching tray after sterilized by the normal saline of 0.004 to 0.008 percent and hatched by adding purifying water; the temperature of the hatching chamber is 16 to 20 DEG C, avoiding air, lighting and avoiding from being directly irradiated by sunshine and changing water as well as controlling the water temperature; anaphase management: after the fertilized eggs begin to emerge, stopping changing water and sterilizing, adding purifying water and arranging the fries beginning to swim flatly into a culture pool after 48 to 72 hours. The technique of the invention adopts a reasonable and scientific method and has the processes of sterilizing, water quality control, temperature control, appliance control and environment control, etc., which greatly improves the yield and quality of the fries.
Owner:江苏太滆水产科技有限公司

Cultivation method for promoting rapid accumulation of oil producing microalgae cells and grease

The invention discloses a cultivation method for promoting rapid accumulation of oil producing microalgae cells and grease. At first, under heterotrophic culture condition, the cells are stimulated to grow rapidly by utilizing fulvic acid; when the microalgae cells grow to the anaphase of logarithmic phase, cell concentration reaches 6.63g L<-1> at the moment; supernatant is removed through centrifugation so as to serve as a seed solution required in a subordinate phase. A 1000mgL<-1> fulvic acid mother solution is prepared by using pure water, and the fulvic acid mother solution is added in kuh1 culture mediums, so that the concentrations of the fulvic acidare 5, 25, 125, and 625mg L<-1> respectively. Then the obtained seed solution is added in the kuh1 culture mediums containing the fulvic acid of different concentrations, and the initial concentration of the seed solution is 2.3g L<-1>. Then the algae solution is subjected to continuous illumination cultivation, and sampling is performed every two other days for measuring biomass and grease content. The cultivation method disclosed by the invention is simple and feasible, and low in cost; the cultivation time is greatly shortened and the grease content is remarkably increased, and great significance is put forth for the industrialization of microalgae biodiesel production.
Owner:KUNMING UNIV OF SCI & TECH

Method for producing L-tyrosine through enzyme method

The invention discloses a method for producing L-tyrosine through an enzyme method. The method comprises the following steps of adopting a fermentation method to produce pyruvic acid, adding beta-tyrosinase, phenol and NH4Cl at the fermentation anaphase of the pyruvic acid, converting the generated pyruvic acid into the L-tyrosine, and obtaining fermentation liquor containing the L-tyrosine; heating the fermentation liquor containing the L-tyrosine to be 70 DEG C to 90 DEG C, and acidifying until L-tyrosine crystals are completely dissolved; adding activated carbon to decolor, after decoloring, filtering by utilizing a ceramic membrane, removing bacteria, albumen and the activated carton, carrying out secondary filtering on obtained clear liquid through an acid-resisting liquid cartridge filter; adjusting the pH of the secondary filtered clear liquid to be 5.0 to 7.0, cooling to crystallize, centrifuging, and obtaining the L-tyrosine. According to the method for producing the L-tyrosine through the enzyme method provided by the invention, the process is simplified, the production efficiency is improved, the obtained L-tyrosine is high in purity and yield, the purity of the obtained tyrosine is remarkably improved and reaches to 98.0 percent or above compared with a traditional extraction method, and various tyrosine drug standards are met.
Owner:SHANDONG YANGCHENG BIOLOGY TECH CO LTD

Method for efficiently regenerating Sapium sebiferum leaf disc

The invention discloses a method for efficiently regenerating a Sapium sebiferum leaf disc. The method comprises the following steps: cutting leaves of aseptic Sapium sebiferum seedlings into leaf discs, and conducting induction culturing on the leaf discs through a cluster bud induction culture medium to form cluster buds; conducting micropropagation and elongation on the cluster buds in a micropropagation and elongation culture medium; and after the buds grow to 2-3cm, transferring into a rooting culture medium for rooting culturing, thus obtaining strong Sapium sebiferum test-tube plantlets after 25-30 days. Compared with the prior art, the method has the following advantages that raw materials are easily available and abundant, the regeneration efficiency is high, the culture period is short, hormone components added to the culture mediums are simple, the operation is convenient, and the like, and the method can realize fast propagation of excellent wild single plants, and keep the germplasm characteristics of a female parent, thus realizing the breeding of variety, laying a foundation for the genetic transformation of Sapium sebiferum, being beneficial to quickening the genetic improvement of Sapium sebiferum, and providing technical support for the fast propagation of excellent anaphase Sapium sebiferum plant systems in the later period.
Owner:HEFEI INSTITUTES OF PHYSICAL SCIENCE - CHINESE ACAD OF SCI

Experimental apparatus for in-vitro circulating perfusion and digestion of liver tissues

The invention discloses an experimental apparatus for in-vitro circulating perfusion and digestion of liver tissues. The experimental apparatus comprises an incubator 1 and a perfusion loop arranged in the incubator 1, wherein the perfusion loop comprises a liver-tissue container 2, a peristaltic pump device 4, a three-way pipe 5, a filtering device 6 and an aseptic pipeline 7 which are connected in sequence; the peristaltic pump device 4 comprises a peristaltic pump 3 and a flexible pipeline 11 corresponding to the peristaltic pump 3; the flexible pipeline 11 bypasses the corresponding peristaltic pump 3 and the two ends of the flexible pipeline 11 are respectively communicated with the liver-tissue container 2 and the three-way pipe 5. The experimental apparatus disclosed by the invention can be applied to separation of various cells in the liver tissues, can digest collagenous tissues in the liver tissues by a circulating digestion mode to enable the cells to be dispersed, and collect the cells for the following culture and realizes related experimental research on the biological characteristics of various cells in the liver tissues; since the cells are separated out in shorter time, the activity of the separated-out cells is higher and the success ratio of anaphase culture is increased.
Owner:GUIYANG MEDICAL UNIVERSITY

Fertilization method under the condition of drip irrigation under film film

InactiveCN102282950AIncrease profitGive full play to absorptionFertilising methodsShort rootDrip irrigation
The invention discloses a fertilization method under the condition of drip irrigation cultivation under corn film, which belongs to the field of agricultural planting technology. The method is: mechanical fertilization, the fertilizer applicator is set with three fertilization ports, three rows of fertilizer are applied on each large ridge, and the middle row of fertilizer is applied to the ridge In the middle, the distance between the fertilization openings on the outermost two sides is 50-55cm; apply 60% fertilizer in the middle, and 20% fertilizer on each side; apply 15-17cm deep in the middle, and 8-10cm deep on both sides place. The beneficial effects are as follows: 1. Cross-layer fertilization. In the early stage of corn growth, its root system is short and can absorb shallow fertilizer, while in the middle and late stages of corn growth, its root system is longer and can absorb deep fertilizer; 2. Fertilize on both sides. There are fertilizers on both sides of the corn plant, and the closest distance to the fertilization belt is 5cm, which fully exerts the absorption of the fertilizer by the whole plant and improves the utilization rate of the fertilizer; 3. Fertilize on demand. Corn needs more fertilizer at the jointing and booting stage. At this time, the root system is longer and can absorb deep-level fertilizers, and the deep-level fertilizers account for a large proportion, which can just meet the needs of corn for fertilizers.
Owner:吉林省农业广播电视学校

Fry anaphase intermediate formation method adapated for seashell of shallows-tidal-flat area

It relates to an method of intermediate rearing mussel germchits during later period in shallows. When the germchits are cultivated during later period at natural cultivating sea zones, the germchitsare cultivated in string bags, and hanged at buoyant rafts and cultivated. The method comprises: transferring juvenile mollusks with the 0.4??.5mm shells in length into string bags, 5,000í½11,000 juvenile mollusks in a string bag, assembling 6í½10 bags into a bundle, assembling 10-15 bundles into a string, the distance between strings is 15í½30cm; the distance between the string ropes is 1.0í½1.5mú
Owner:INST OF OCEANOLOGY - CHINESE ACAD OF SCI

Chromosome preparation method, as well as required culture medium and preparation method thereof

The invention discloses a chromosome preparation method, as well as a required culture medium and a preparation method thereof, and is used for solving karyotype analysis problem of chromosome. The culture medium consists of RPMI (Roswell Park Memorial Institute) 1640, heparin sodium, HEPES (2-[4-(2-Hydroxyethyl)-1-piperazinyl]ethanesulfonic acid), L-glutamine, NaHCO3, benzylpenicillin potassium, streptomycin sulphate, bovine serum and phytohemagglutinin (PHA). The detection method comprises the following steps: implanting 0.3 to 0.4ml of human peripheral blood into the culture medium; adding colchicinamide in 2-4 hours before culture is terminated to realize that the cell is terminated in anaphase; culturing the cell after 68 to 72 hours to harvest the cell; performing hypotonicity for 40 minutes, three times of fixation, banding, dyeing and other treatments; and performing chromosome analysis under a microscope to determine whether the peripheral blood supplier has a phenomenon of chromosome abnormality. The culture medium disclosed by the invention has convenience for use, simpleness in operation, low cost and low patient detection fee, and is suitable for genetic diagnosis, infertility and prenatal diagnosis in each level of hospitals.
Owner:苏州苏大赛尔免疫生物技术有限公司

Baby pig forced supplementary feeding method

InactiveCN101331865AAlleviate Early Weaning SyndromeReduce disease rateAnimal husbandryTraining periodAnimal science
The invention discloses a grice forcing supplementary feeding method and relates to the technical field of scientific cultivation. The grice forcing supplementary feeding method is a wholly new supplementary feeding method which is designed for the purposes of accurately controlling the quantity and time of grice supplementary feeding, achieving the ideal supplementary feeding effect and reducing the harm caused by the 'early ablactation syndrome' of grice. The technical points are that the grice supplementary feeding period is 8-21 age in days, in the supplementary feeding period, 'free feeding and forcing supplementary feeding' are carried out, the 'teaching feedstuff' with high quality is selected as the supplementary feedstuff, the times of supplementary feeding is 4 times every day, and the total amount of supplementary feeding is 290g. The supplementary feeding course is divided into three stages: 8-11 age in days is the training period, the dosage is increased from less to more and is 10g per day averagely; 12-16 age in days is the middle period, and the dosage is 20g per day averagely; 17-21 age in days is the anaphase, the dosage is 30g per day averagely. By adopting the method provided by the invention, the 'early ablactation syndrome' can be alleviated obviously, disease rate and death rate of the grice can be reduced, and the growth state of the grice can be improved.
Owner:张明海

Eustoma grandiflorum cultivation method

The invention discloses a eustoma grandiflorum cultivation method comprising the following steps: selecting field, soil working, applying fertilizer, disinfecting soil, and applying fertilizer; removing underground insects; using a single-particle-sing-hole mode to sow eustoma grandiflorum seeds into deep hole trays filled with a sowing matrix, wherein the sowing matrix is excellent in draining performance; examining seedlings when the eustoma grandiflorum seedling grows to 3cm above the ground, removing a film and transplanting the seedlings when the eustoma grandiflorum seedlings grow to 5-10cm in height and the roots grow to 8-10cm in depth; weeding when the seedlings grow to 12cm, and weeding in every two months; topdressing; timely removing top buds when the seedlings grow to 10cm. The method can improve the eustoma grandiflorum germination capacity, and the produced eustoma grandiflorum seedlings are stronger, thus improving the seedling transplanting survival rate; the anaphase growth vigor is fast, and the product quality is good; cut flower eustoma grandiflorum anaphase growth consistency is good, and the flower leaves are tidy; the eustoma grandiflorum is strong in disease resistance, thus reducing insect diseases, improving cut flow yield, and improving the economic benefits.
Owner:石林怡和农业产业开发有限公司

Strategy for producing acetoin through efficient fermentation based on AR/BDH enzymatic properties of bacillus subtilis

The invention relates to a strategy for producing acetoin through efficient fermentation based on AR / BDH enzymatic properties of bacillus subtilis and belongs to the field of genetic engineering and fermentation engineering. Shown by researches on the AR / BDH enzymatic properties of a strain B. subtilis JNA, which is independently screened by our laboratory, has independent intellectual property and can produce acetoin at high yield, the conditions that the optimal pH in the reduction direction of AR / BDH is 6.5 and the optimal pH of the oxidation direction of AR / BDH is 8.5 are discovered for the first time. Based on the enzymatic properties and according to the fermentation strategy, the strain is in the optimal growth pH (6.5) condition at the prophase of fermentation and in the optimal transformation pH (8.0) condition at the anaphase of fermentation, 150g / L glucose can be transformed into 56.8g / L acetoin, the yield of 2,3-butanediol is only 6.1g / L, and the production rate of acetoin reaches 0.59g / (L.h) and is increased by nearly 84%; recombinant B. subtilis which overexpresses AR / BDH consumes 180g / L glucose under the regulation and control of the same fermentation strategy, the yield of acetoin is increased to 73.6g / L, and the production rate finally reaches 0.77g / (L.h), so that the capability of producing acetoin through the anaphase reverse transformation of the target strain is enhanced, and a basis is provided for producing acetoin through microbial industrialized fermentation.
Owner:JIANGNAN UNIV
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