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44 results about "Mixed group" patented technology

Mixed Group. Jump to navigation Jump to search. Mixed Group (Italian: Gruppo Misto, GM) is a parliamentary group active in both houses of the Italian Parliament, the Chamber of Deputies and the Senate. The groups comprise all the deputies and the senators, respectively, who are not members of any other parliamentary group.

Microfluidic particle-analysis systems

The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or detection of particles, such as cells and/or beads. The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or analysis of particles, such as cells, viruses, organelles, beads, and/or vesicles. The invention also provides microfluidic mechanisms for carrying out these manipulations and analyses. These mechanisms may enable controlled input, movement/positioning, retention/localization, treatment, measurement, release, and/or output of particles. Furthermore, these mechanisms may be combined in any suitable order and/or employed for any suitable number of times within a system. Accordingly, these combinations may allow particles to be sorted, cultured, mixed, treated, and/or assayed, among others, as single particles, mixed groups of particles, arrays of particles, heterogeneous particle sets, and/or homogeneous particle sets, among others, in series and/or in parallel. In addition, these combinations may enable microfluidic systems to be reused. Furthermore, these combinations may allow the response of particles to treatment to be measured on a shorter time scale than was previously possible. Therefore, systems of the invention may allow a broad range of cell and particle assays, such as drug screens, cell characterizations, research studies, and/or clinical analyses, among others, to be scaled down to microfluidic size. Such scaled-down assays may use less sample and reagent, may be less labor intensive, and/or may be more informative than comparable macrofluidic assays.
Owner:STANDARD BIOTOOLS INC

Microfluidic particle-analysis systems

The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or detection of particles, such as cells and/or beads. The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or analysis of particles, such as cells, viruses, organelles, beads, and/or vesicles. The invention also provides microfluidic mechanisms for carrying out these manipulations and analyses. These mechanisms may enable controlled input, movement/positioning, retention/localization, treatment, measurement, release, and/or output of particles. Furthermore, these mechanisms may be combined in any suitable order and/or employed for any suitable number of times within a system. Accordingly, these combinations may allow particles to be sorted, cultured, mixed, treated, and/or assayed, among others, as single particles, mixed groups of particles, arrays of particles, heterogeneous particle sets, and/or homogeneous particle sets, among others, in series and/or in parallel. In addition, these combinations may enable microfluidic systems to be reused. Furthermore, these combinations may allow the response of particles to treatment to be measured on a shorter time scale than was previously possible. Therefore, systems of the invention may allow a broad range of cell and particle assays, such as drug screens, cell characterizations, research studies, and/or clinical analyses, among others, to be scaled down to microfluidic size. Such scaled-down assays may use less sample and reagent, may be less labor intensive, and/or may be more informative than comparable macrofluidic assays.
Owner:STANDARD BIOTOOLS INC

Microfluidic particle-analysis systems

The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and / or detection of particles, such as cells and / or beads. The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and / or analysis of particles, such as cells, viruses, organelles, beads, and / or vesicles. The invention also provides microfluidic mechanisms for carrying out these manipulations and analyses. These mechanisms may enable controlled input, movement / positioning, retention / localization, treatment, measurement, release, and / or output of particles. Furthermore, these mechanisms may be combined in any suitable order and / or employed for any suitable number of times within a system. Accordingly, these combinations may allow particles to be sorted, cultured, mixed, treated, and / or assayed, among others, as single particles, mixed groups of particles, arrays of particles, heterogeneous particle sets, and / or homogeneous particle sets, among others, in series and / or in parallel. In addition, these combinations may enable microfluidic systems to be reused. Furthermore, these combinations may allow the response of particles to treatment to be measured on a shorter time scale than was previously possible. Therefore, systems of the invention may allow a broad range of cell and particle assays, such as drug screens, cell characterizations, research studies, and / or clinical analyses, among others, to be scaled down to microfluidic size. Such scaled-down assays may use less sample and reagent, may be less labor intensive, and / or may be more informative than comparable macrofluidic assays.
Owner:FLUIDIGM CORP

Microfluidic particle-analysis systems

The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and / or detection of particles, such as cells and / or beads. The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and / or analysis of particles, such as cells, viruses, organelles, beads, and / or vesicles. The invention also provides microfluidic mechanisms for carrying out these manipulations and analysis. These mechanisms may enable controlled input, movement / positioning, retention / localization, treatment, measurement, release, and / or output of particles. Furthermore, these mechanisms may be combined in any suitable order and / or employed for any suitable number of times within a system. Accordingly, these combinations may allow particles to be sorted, cultured, mixed, treated, and / or assayed, among others, as single particles, mixed groups of particles, arrays of particles, heterogeneous particle sets, and / or homogeneous particle sets, among others, in series and / or in parallel. In addition, these combinations may enable microfluidic systems to be reused. Furthermore, these combinations may allow the response of particles to treatment to be measured on a shorter time scale than was previously possible. Therefore, systems of the invention may allow a broad range of cell and particle assays, such as drug screens, cell characterizations, research studies, and / or clinical analysis, among others, to be scaled down to microfluidic size. Such scaled-down assays may use less sample and reagent, may be less labor intensive, and / or may be more informative than comparable macrofluidic assays.
Owner:STANDARD BIOTOOLS INC

Breed protection and selection method of Muscovy ducks

InactiveCN105766799AEarly sexual maturityConsiderable egg productionAnimal husbandryAdult femaleMixed group
The invention belongs to the technical field of livestock and poultry breeding and particularly relates to a breed protection and selection method of Muscovy ducks. The method includes the steps of firstly, selecting the Muscovy ducks conforming to the variety features of Yongchun Muscovy ducks for cultivation so as to obtain adult male ducks and adult female ducks, selecting and eliminating the Muscovy ducks which do not conform to the variety features of the Yongchun Muscovy ducks from the adult male ducks and the adult female ducks and selecting the population conforming to the variety features of the Yongchun Muscovy ducks through a series of cultivation, selection, eliminating and cultivation; secondly, selecting the adult male ducks and the adult female ducks to build an underlying group; thirdly, building generation zero, to be more specific, in the underlying group, randomly selecting dozens of the adult male ducks and the adult female ducks to form a family, and performing breeding of several families; fourthly, performing subculture breeding, to be more specific, giving wing tags to the newborn ducks in the third step, making pedigree records, and performing mixed-group feeding. By the breed protection and selection method, the problem that the preservation of the Yongchun Muscovy ducks is severely affected due to the fact that existing Yongchun Muscovy ducks raisers blindly import hybridization and improvement is solved.
Owner:YONGCHUN YUNHE WHITE MUSCOVY DUCK CONSERVATION BREEDING CO LTD

Method for setting parallel incomplete disassembly line for disassembling waste products

The invention discloses a method for setting a parallel incomplete disassembly line for disassembling waste products. The method comprises the following steps of: (1) constructing a mathematical modelaiming at minimizing the disassembly depth, the number of workstations, the idle time balance index of the workstations and the number of disassembly resources; (2) generating an initial population;(3) obtaining neighborhood individuals of the initial population; (4) comparing the target function value of a mixed group composed of the neighborhood individuals and the population individuals through Pareto, updating the population, and outputting a Pareto optimal solution to an external file; (5) performing simulated annealing operation on the population updated in the step (4) to obtain a newpopulation; (6) comparing a target function value of a mixed group consisting of the group subjected to simulated annealing operation and an external file by adopting Pareto, and outputting a Paretooptimal solution to the external file; (7) repeating the steps (3)-(6) according to the set number of times; and (8) outputting a Pareto optimal solution in the external file as a disassembly task allocation scheme. The method is easy to implement and high in search capacity.
Owner:SOUTHWEST JIAOTONG UNIV

Frequency-domain self-adaptation wavelet multi-mode blind equalization method for immune artificial shoal optimization

The invention discloses a frequency-domain self-adaptation wavelet multi-mode blind equalization method for immune artificial shoal optimization. The frequency-domain self-adaptation wavelet multi-mode blind equalization method for the immune artificial shoal optimization comprises the following steps that an immune artificial shoal is a mixed group of an artificial shoal and an immune system antibody shoal, position vectors of the artificial shoal and antibody vectors of an immune system of a set of immune artificial shoal are initialized in a random mode, the position vectors and the antibody vectors serve as decision variables of an immune artificial shoal method, input signals of an orthogonal wavelet converter serve as input signals of the immune artificial shoal method, a fitness function of the immune artificial shoal is determined by a cost function of the frequency-domain self-adaptation wavelet multi-mode blind equalization method, and initialization weight vectors of the frequency-domain self-adaptation wavelet multi-mode blind equalization method are determined by an immune artificial shoal optimization method. The frequency-domain self-adaptation wavelet multi-mode blind equalization method for the immune artificial shoal optimization is high in rate of convergence, low in steady-state error, low in complexity and good in practicability when the frequency-domain self-adaptation wavelet multi-mode blind equalization method for the immune artificial shoal optimization is used for processing high-order QAM signals.
Owner:NANJING UNIV OF INFORMATION SCI & TECH

Universal infusion head with automatic infusion continuing function

ActiveCN104383622ARealize automatic bottle changeSimple structureInfusion devicesMixed groupBottle
The invention relates to a universal infusion head with an automatic infusion continuing function. The infusion head comprises an infusion head body, two infusion passages and an automatic infusion continuing control chamber. A partition is disposed in the middle of the automatic infusion continuing control chamber to separate the automatic infusion continuing control chamber into a first floating valve chamber and a second floating valve chamber. The bottoms of the first floating valve chamber and the second floating valve chamber are communicated. The first floating valve chamber and the second floating valve chamber respectively correspond to the two infusion passages. A floater valve switch is disposed in each of the first floating valve chamber and the second floating valve chamber. The first floating valve chamber is connected with a liquid inlet tube, and the second floating valve chamber is connected with a liquid outlet tube. The floater valve switch in the two floating valve chambers moves upwards to block the infusion passage of a current bottle or bag by the buoyancy of liquid medicine entering through the liquid inlet tube, and the infusion passage of the current bottle or bag is smooth when the no liquid medicine enters from the liquid inlet tube, air enters the liquid inlet tube, and the floater valve switches naturally fall. The universal infusion head has the advantages that the physical principles of liquid, gas and the floater switches are utilized to achieve automatic infusion continuing of multi-form infusion groups including an infusion bag group, an infusion bottle group or an infusion bottle-bag mixed group, and the application range of continuous infusion devices is widened.
Owner:刘玮

Two-bee-specie dual queen mixed group construction, mixed royal jelly and production method thereof

The invention discloses a two-bee-specie dual queen mixed group construction, and mixed royal jelly and a production method thereof. The two-bee-specie dual queen mixed group construction method includes: S1, selecting an Apis mellifera group or an Apis cerana group as an original bee group; and selecting an Apis cerana comb adjustment group and an Apis mellifera comb adjustment group; S2, putting a sealed sub comb to the original bee group, and allowing bees in the selected sealed sub comb and a sealed sub comb of the original bee group to naturally fly out of the combs; S3, adjusting the proportion of the number of Apis cerana worker bee individuals and the number of Apis mellifera worker bee individuals; and S4, putting an Apis cerana queen and an Apis mellifera queen to the whole bee group, and acquiring an Apis cerana and Apis mellifera mixed group. The Apis cerana and Apis mellifera mixed group can be effectively established, and has two queens of the two bee species; a strong group can be maintained for long time, and respective advantage roles of the Apis cerana and the Apis mellifera can be fully played; various kinds of mixed royal jelly can be produced, the production efficiency of the mixed royal jelly can be improved, and the quality of the mixed royal jelly is ensured.
Owner:JIANGXI AGRICULTURAL UNIVERSITY

A kind of multi-component composite eccentric fiber and its preparation method

The invention relates to a multi-component composite eccentric fiber. The fiber is a skin-core type composite fiber with an eccentric structure spun by using different components for the skin layer and the core layer. The skin layer component is PA6 and modified PA6, and the core layer is PA6. The layer component is a two-component mixed component composed of PP component and modified PP or EVA component; or the core layer component is a three-component mixed component composed of PP component, low melting point PA6 component and modified PP or EVA component . A method for preparing multi-component composite eccentric fibers. After drying the two components of the skin layer component and the core layer separately, the skin layer component and the core layer component are respectively melted and mixed by a screw, and then enter the eccentric skin-core composite spinning assembly After spinning and winding, multi-component composite eccentric fibers are obtained. The invention solves the problem of poor compatibility between the skin layer and the core layer in the eccentric sheath-core composite fiber, and obtains a composite fiber capable of producing permanent crimp elasticity. The post-processing and dyeing is simple, the obtained fabric is light and soft, and the production cost of the fabric is reduced. At the same time, it can save energy and reduce sewage discharge.
Owner:DONGHUA UNIV +1

Method for preparing pannage with blackberry pomace

The invention provides a method for preparing pannage with blackberry pomace, relating to the technical field of preparing feedstuff. The method takes pomace which is produced by juicing fresh blackberry as raw materials, and adopts a second mixing technology to prepare the pannage. The method specifically comprises the following steps: mixing blackberry pomace powder, corn powder, soybean meal powder or fish powder according to a certain proportion to obtain a previously-mixed group A; mixing wheat bran, sodium chloride or calcium hydrophosphate according to a certain proportion to obtain a previously-mixed group B; mixing the previously-mixed group A, the previously-mixed group B and plant oil with a certain proportion; and packing to prepare blackberry pomace compound feedstuff or concentrated feedstuff. The method has the following characteristics: the blackberry pomace feedstuff has low cost, simple manufacture technology, universal equipment, less investment, easy operation and control, abundant nutrition, stable quality and easy digestion, and is easy in large-scale industrial production. The perpetration of the blackberry pomace feedstuff not only can recycle waste, but also can remove environment pollution during processing the blackberry.
Owner:INST OF BOTANY JIANGSU PROVINCE & CHINESE ACADEMY OF SCI

Method for identifying silkworm silk color in larval stage

The invention belongs to the field of biotechnology, and discloses a method for identifying a silkworm silk color in a larval stage. The method provided by the invention comprises the following steps of: extracting the ribonucleic acid (RNA) of a silkworm silk gland of a 5th instar stage to be detected by utilizing a genetic engineering technology; performing reverse transcription to synthesize complementary deoxyribonucleic acid (cDNA); taking the obtained cDNA as a template, performing reverse transcription-polymerase chain reaction (RT-PCR) amplification reaction by using a specific primer; judging whether a silkworm spins yellow silk or green silk or white silk by detecting the type and the length of a PCR amplification product by agarose electrophoresis; and further judging whether the silkworm which spins the yellow silk is a homozygous yellow silk spinning silkworm or a heterozygous yellow silk spinning silkworm, and other silkworms spin green silk or white silk by analyzing the content of the RT-PCR amplification product relative to an electrophoresis gel product. By the method provided by the invention, the pedigree with consistent internal cocoon color and external cocoon color and high color fastness also can be identified and separated from a mixed group with different cocoon layer colors and chromaticities. The identification method provided by the invention is simple, convenient and rapid to operate; and the accuracy for identifying the color of the silkworms is high.
Owner:SUZHOU UNIV

Method for artificially cultivating soft-shell blue crabs

The invention provides a method for artificially cultivating soft-shell blue crabs, which relates to a method of breeding blue crabs. By using the method, the soft-shell crabs can be obtained quickly and the survival rate of the soft-shell crab can be improved. The method comprises the following steps: dividing the blue crabs into three classes, and choosing the blue crabs in the first and second classes as the cultivated objects of the soft-shell crabs; putting a single blue crab in the first class in a crab pot, stacking and binding 3 to 5 crab pots together to be a group of crab pots, and then putting the groups of crab pots into a cultivating pool for intensive cultivation; during the cultivation period, transferring the whole group of crab pots to a black barrel or a small pond in which a natural shell-removing agent is added to soak every day; putting the crab pots into calcium hydroxide solution to soak and disinfect and promote calcium absorption and shell removal, and then putting the blue crabs subjected to socking into the original cultivating pool again; timely selecting out the blue crabs which just remove shells and transferring, then carrying out low-temperature paralysis fresh preservation or cryopreservation on the selected blue crabs; carrying out mixed group cultivation on the blue crabs in the second class in a cultivating pool, after the state of the blue crab in the second class in the shell removing cycle enters the state of the blue crab in the first class, selecting out and transferring the blue crabs to the crab pots, then cultivating the blue crabs to be the soft-shell crabs.
Owner:XIAMEN UNIV

Method for artificially cultivating soft-shell blue crabs

The invention provides a method for artificially cultivating soft-shell blue crabs, which relates to a method of breeding blue crabs. By using the method, the soft-shell crabs can be obtained quickly and the survival rate of the soft-shell crab can be improved. The method comprises the following steps: dividing the blue crabs into three classes, and choosing the blue crabs in the first and secondclasses as the cultivated objects of the soft-shell crabs; putting a single blue crab in the first class in a crab pot, stacking and binding 3 to 5 crab pots together to be a group of crab pots, and then putting the groups of crab pots into a cultivating pool for intensive cultivation; during the cultivation period, transferring the whole group of crab pots to a black barrel or a small pond in which a natural shell-removing agent is added to soak every day; putting the crab pots into calcium hydroxide solution to soak and disinfect and promote calcium absorption and shell removal, and then putting the blue crabs subjected to socking into the original cultivating pool again; timely selecting out the blue crabs which just remove shells and transferring, then carrying out low-temperature paralysis fresh preservation or cryopreservation on the selected blue crabs; carrying out mixed group cultivation on the blue crabs in the second class in a cultivating pool, after the state of the blue crab in the second class in the shell removing cycle enters the state of the blue crab in the first class, selecting out and transferring the blue crabs to the crab pots, then cultivating the blue crabs to be the soft-shell crabs.
Owner:XIAMEN UNIV
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