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108 results about "Incubation temperature" patented technology

Incubator temperature should be maintained between 99° and 100°F. The acceptable range is 97° to 102°F. High mortality is seen if the temperature drops below 96°F or rises above 103°F for a number of hours. If the temperature stays at either extreme for several days, the egg may not hatch.

Method for screening antithrombotic drug based on magnetic bead separation

The invention discloses a method for screening an antithrombotic drug based on magnetic bead separation. According to the method, magnetic separation and chemical information collection (liquid chromatography-mass spectrometry) techniques are adopted; a target protein bonder is analyzed; the method is used for screening and evaluating the antithrombotic action of a drug. According to the method for screening the antithrombotic drug based on the magnetic bead separation, an optimal incubation temperature, an incubation time, a pH (potential of Hydrogen) value of a solution during incubation, ionic strength and a denaturizing cleaning solution are screened out through lots of experiments. A screening and evaluating method provided by the invention can be used for screening a large-scale natural product library or a combinatorial chemical library; in comparison with a conventional ultraviolet screening method, the screening efficiency can be obviously improved; a screening time is shortened; moreover, a synergistic effect between compounds can be discovered; the method for screening the antithrombotic drug based on the magnetic bead separation has the advantages of strong operability, quickness, high efficiency, accuracy, good repeatability and the like.
Owner:NANJING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE

Basal layer of soft-shelled turtle incubator

The invention discloses a basal layer of a soft-shelled turtle incubator, and relates to the technical field of aquaculture. The basal layer comprises the incubator used for incubating soft-shelled turtles and is characterized in that a basal layer body is laid at the bottom of the interior of the incubator and comprises a cobblestone layer at the bottommost, a saw dust layer is laid on the cobblestone layer, an incubation sand layer is laid at the upper portion of the saw dust layer, a covering layer is laid at the upper portion of the incubation sand layer, soft-shelled turtle eggs are embedded in the incubation sand layer, the upper ends of the soft-shelled turtle eggs are flush with the upper end of the incubation sand layer, the covering layer is a river sand layer, and a constant-temperature heater is arranged between the saw dust layer and the incubation sand layer. According to the basal layer, due to the control over the incubation temperature, the humidity of the incubator and the humidity of incubation sand, the incubation rate of the male soft-shelled turtles is 100%, and the incubation cost is reduced; operation is easy and convenient, control is easy, the male rate is high, the incubated soft-shelled turtle survival rate is high, the temperature in the incubator is convenient to control, and the air permeability is good.
Owner:安徽省淮丰园渔业科技有限公司

Injection method for single-bird egg

The invention relates to a method for injecting to a single bird egg; the operation steps are as follows: the bird egg is positioned at a position with preset direction under incubation temperature; an opening is selected by a position on the egg shell which is to be injected to be disinfected by alcohol; a disinfected solid pin is used to form small openings in the same size on the opening of the egg shell and the outer shell membrane and the inner shell membrane below the opening; the bird egg is slightly rotated, so that the position in the egg to be injected aims to the small openings on the egg shell; a disinfected disposable injection needle is extended into the small openings; materials are injected into the egg by the disposable injection needle; the temperature of the egg is reduced in the environment 1 DEG C to 10 DEG C lower than the incubation temperature; the disposable injection needle is collected; the bird egg rotates for some angles within a longitudinal section, so that the crossing of the injection needle stays from the opening of the egg shell; melted paraffin is used to seal the opening; the paraffin is solidified under the incubation temperature; the bird egg is put to the original place to be incubated. The method has the advantages of low cost, fast operation, single-egg rejection, small simulation and damage, no pollution, fixed point and quantitative injection, and direct view.
Owner:BOHAI UNIV +1

Method for inducing and cultivating tetraploid breeding of sea urchin

InactiveCN101103707AImprove farming valueExtended listing periodAnimal reproductionClimate change adaptationEmbryoSea urchin
The cultivation method of sea urchin tetraploid fingerlings has the steps that the urchin seedling is dried in shade for 0 to 40 minutes. The 0.5 to 2.0 ml 0.5 mol / L KCl solution is injected from the sea urchin membrana peristomialis for the spawing and spermiation. The urchine eggs and sperms are collected, and the hybrid fertilization is implemented. The developmental temperature of fertilized eggs is controlled between 17 to 18 DEG C. The fertilized eggs in concentration with a mix silk net are collected after 55 to 65 minutes of the fertilization, which are packed in a closed bag and disposed in a pressure vessel of a hydrostatic pressure equipment and the ambient temperature is identified between 17 to 18 DEG C. The pressure treatment is implemented after 60 to 70 minutes of the fertilization, in which the pressure is controlled between 70 to 80MPa and the processing time is controlled between 6 to 8 minutes. Afterwards the fertilized eggs are disposed inside a bin for hatching and stirred, and the incubation temperature is controlled between 16 to 18 DEG C. After floated, the embryos are selected with the proper aeration. The bait feeding is implemented during the larvae cultivation period. The water is exchanged 1 to 3 times everyday, and each time the quantity of water exchange is 1/3 to 2/3. The pond water is exchanged once every three days. The tetraploid fingerlings cultivated with the method can produce the triploid fingerlings, thus the time of processing and the time to the market are extended.
Owner:DALIAN FISHERIES UNIVERSITY

Method for hatching and breeding anser indicus

InactiveCN102388834AImprove ecological qualityWith wild habitsAnimal husbandryAnser indicusHabit
The invention discloses a method for hatching and breeding anser indicus. Aiming at the shortcomings that the hatching rate of the anser indicus by artificial hatching in the prior art is low and the method cannot be popularized in the actual breeding production, the invention provides a method for hatching and breeding the anser indicus of which the incubation hatching rate is over 90% under theconditions that the incubation temperature is 38 degrees centigrade +/- 0.1 degrees centigrade and the relative humidity is 56.0% +/- 2.0%. According to the method for artificial hatching and breeding the adult wild gooses in the invention, the adult wild gooses can be put in the breeding net to breed in open air, wherein the water area in the breeding net is 25% to 40% and the land area is 60% to 75%; the survival rate of the adult wild goose bred by the method reaches over 90%, the wild habits are good, and the ecological quality is high. The invention further provides a stereo breeding method of the anser indicus and plateau fish, which fully realizes the circulation economic model by matching a stereo breeding technology of breeding the wild gooses at the upstream and breeding the fish at the downstream with forage plant and methane utilization, and improves the overall earnings of the plateau breeding industry. The method has rational theory and simple method, and can easily control the artificial implementation conditions, so the method is suitable for popularizing the plateau area economic development.
Owner:LHASA TRINIDAD NATURAL ECOLOGICAL DEV

Method for controlling saprolegniasis of odontobutis obscura germ cells in incubation period

The invention relates to a method for controlling saprolegniasis of odontobutis obscura germ cells in incubation period. The method comprises the steps: 1, firstly, cleaning and disinfecting an artificial fish spawning nest containing germ cells, and then placing the artificial fish spawning nest into a cleaned and disinfected incubation bucket; 2, adding the aerated tap water into the incubation bucket as incubation water for incubation, controlling the incubation temperature to be 20-28 DEG C in incubation, controlling the air oxygen flow rate to be 3.5-20L/min, replacing one third to half incubation water every 4 to 7 days; and entirely covering the incubation bucket with a covering object in days, and removing the covering object at night; and 3, breaking the membrane and emerging from the germ cell after 30-40 days. Before the germ cells are transferred into the incubation bucket, the germ cells and the incubation bucket are disinfected, and incubation water used in incubation process is disinfected; and the generation of saprolegniasis of odontobutis obscura germ cells under low-temperature condition can be effectively controlled by utilizing the biological characteristic that the odontobutis obscura germ cells has larger stickiness, and through controlling the output of an aerated pump, and proper incubation conditions are created as far as possible in the incubation process.
Owner:南京市水产科学研究所

Artificial carassius auratus propagation method

The invention provides an artificial carassius auratus propagation method. The method is creatively improved in the aspects from the source of parent selection and parent fish rearing to the following aphrodisiac drug preference, incubation method design and the like, a complete technological method for artificially propagating carassius auratus is formed, and the propagation rate, the spawning rate and the incubation rate are remarkably increased. By the adoption of the preferred technical scheme, vitamin is added to fodder before parturition to promote gonad development of parent fish; the preferred temperature of water where the parent fish injected with aphrodisiac drug are located ranges from 21 DEG C to 22 DEG C, so that parent fish rutting and egg laying efficiency is further improved; the preferred incubation temperature ranges from 20 DEG C to 23 DEG C so that fertile eggs can be incubated. By the adoption of the technical scheme, a series of creative design is conducted on the technological conditions, the remarkable technical effect is achieved, the condition control angle and the condition control depth are remarkably improved or optimized compared with those in the prior art, and meanwhile the method is easy to implement, low in cost and remarkable in large-scale application prospect.
Owner:TIANJIN AGRICULTURE COLLEGE

Apparatus and method for a lysis of a sample, in particular for an automated and/or controlled lysis of a sample

The present invention provides an apparatus and a method for a lysis procedure, in particular for an automated and/or controlled lysis procedure of a sample, in particular a biological sample. The apparatus comprises at least one rotation disc (31), at least one vial holder (90) which is configured to receive a vial (100), wherein the vial holder (90) is arranged on the disc (31), at least one driving device (20) which is configured to rotate the disc (31) and the vial holder (90), at least one heating device (60) which is configured to heat the sample to a determined incubation temperature, and—at least one control device (70) which is configured to control the driving device (20) and/or the heating device (60) by means of a timing and/or step control, and/or—at least one transmitting device (80) for inductive coupling for energy and signal transmission, which is configured to transmit the energy for heating to the heating device (60), and/or—wherein the driving device (20) is configured to rotate the disc (31) in a first direction (A1) and/or with a first speed, and to rotate the vial holder (90) in a second direction (A3) and/or with a second speed. The apparatus and the method are adapted for an (automated) lysis procedure, wherein the lysis can be carried out in a safe, efficient and effective manner.
Owner:CURETIS GMBH

Prevention and treatment method of saprolegniasis in incubation period of hucho bleekeri fertilized eggs

The present invention discloses a prevention and treatment method of saprolegniasis in an incubation period of hucho bleekeri fertilized eggs. The method comprises the following steps: from the second day of incubation of the fertilized eggs, the fertilized eggs are soaked using running water containing formaldehyde every day; soaking liquid enters form the bottom of an incubator and is discharged out from the top of the incubator, a flow rate is controlled, so that the fertilized eggs do not roll over due to the excessive flow rate, the operation is continuously conducted for 30 min each time, and in the soaking process, the operation is conducted in dark place without vibration. After 30 min, normal incubation water is used to conduct running water incubation, and in the stages from the development of the fertilized eggs to early incubation (at an average incubation temperature of 7.5 DEG C and an accumulated temperature reaching 127 DEG C-170 DEG C), formaldehyde disinfection is stopped. Artificial methods are used to remove dead eggs until the fertilized eggs come out from membranes. The method is used to conduct the disinfection of the hucho bleekeri fertilized eggs, the incidence of the saprolegniasis can be reduced by 80% or more, and the deformity rate can be reduced to be 3% or below after emergence by using the method,.
Owner:FISHERIES INST SICHUAN ACADEMY OF AGRI SCI

Multiwell incubation apparatus and method of analysis using the same

A continuous temperature-gradient incubation apparatus designed to solve the problem of moving of liquid vapor generated on the high-temperature side toward the low-temperature side to thereby cause condensation.There is provided a multiwell incubation apparatus having a well-housing vessel made of a heat conducting material and, detachably housed therein, liquid-storing wells, the wells being arranged in transverse rows and longitudinal rows, the multiwell incubation apparatus being also provided with a liquid or gas flow channel or bath for supply of a gas saturated with vapor of the liquid, the multiwell incubation apparatus being capable of maintaining incubation temperatures differing between individual transverse rows of wells with a predetermined temperature difference, so as to realize a temperature series which forms a predetermined temperature difference profile along the longitudinal rows, characterized in that the multiwell incubation apparatus includes a heat source for realizing a temperature which is the lowest in the given temperature series, the heat source being disposed outside the well rows and along the transversely lined up wells close to a first side of the housing vessel; another heat source for realizing a temperature which is the highest in the given temperature series, the heat source being disposed outside the well rows and along a side opposite to the first side; and a separator provided for each transverse row of a certain temperature.
Owner:INTER UNIV RES INST RES ORG OF INFORMATION & SYST

Preparation method of oxymatrine active targeting lipidosome

InactiveCN103877023AReduce releaseCompliant with liposome requirementsOrganic active ingredientsLiposomal deliveryCholesterolPhospholipid
The invention belongs to the technical field of medicines, and discloses a preparation method of an oxymatrine active targeting lipidosome. The active targeting oxymatrine lipidosome is prepared by a pH gradient method. The optimal prescription for preparing the oxymatrine active targeting lipidosome is as follows: the ratio of medicine to lipidosome is 1:10, the ratio of phospholipid to cholesterol is 3:1 with additionally 10% mol of Lac-PE, the pH value of the outer aqueous phase is 6.8, the incubation temperature is 60 DEG C, and the average encapsulation efficiency is 55.48% under the optimal prescription. The oxymatrine active targeting lipidosome prepared by the method provided by the invention is relatively stable. In vitro drug release experiments of the active targeting lipidosome show that oxymatrine wrapped by the glycosylated lipidosome has a slow release effect. Through observation by a transmission electron microscope, the oxymatrine active targeting lipidosome prepared by the method provided by the invention is a single chamber lipidosome with the average grain size of 80nm, and meets the demand of lipidosome. In vitro dissolution experiments show that the oxymatrine active targeting lipidosome wrapped has a certain slow release feature.
Owner:CHONGQING MEDICAL UNIVERSITY

Method for screening melanin formation resistant medicines on basis of magnetic bead separation

The invention discloses a method for screening melanin formation resistant medicines on the basis of magnetic bead separation. Target protein conjugates are analyzed by the aid of magnetic separation and chemical information acquisition (liquid chromatography-mass spectrometry) technologies, and the method can be used for screening and evaluating melanin formation resisting effects of the medicines. The optimal incubation temperatures, the optimal incubation time, the optimal pH (potential of hydrogen) values of solution during incubation, the optimal ion strength and the optimal denaturation cleaning solution are screened by the aid of large quantities of experiments. Compared with the traditional methods for screening melanin formation resistant medicines, the method has the advantages that the screening efficiency can be obviously improved, and the screening time can be shortened; synergistic effects among compounds can be discovered, the method can be used for screening large-scale natural product libraries or combinatory chemical libraries, is suitable for screening the melanin formation resistant medicines (including chemically synthetic medicines and natural products) and discovering lead compounds at early stages, is speedy and accurate and is good in repeatability, and the like.
Owner:NANJING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE

Temperature-controllable incubation equipment

InactiveCN109452199AConstant internal temperatureMentioned survival rateGaseous substancesDeodrantsIncubation temperatureINCREASED EFFECT
The invention discloses temperature-controllable incubation equipment. The temperature-controllable incubation equipment comprises an incubator body, a young output basket is arranged at the bottom end inside the incubator body, a temperature control box is fixedly installed at the portion, close to one side of the young output basket, at the bottom end inside the incubator body, air inlets are formed in the two sides of the incubator body, anti-dust devices are fixedly installed at the portions, close to the outer sides of the air inlets, of the two sides of the incubator body, and a containing groove is formed in the inner wall of the incubator body. The temperature control box is arranged and used for controlling the temperature in the incubator body; a temperature sensor is arranged and used for detecting the temperature inside the incubator body; through a refrigeration pipe, an effect of reducing the temperature is achieved; heating pipes are arranged and have the temperature increasing effect, the temperature inside the incubator body is kept constant accordingly, the suitable incubation temperature is provided for bird eggs, and embryonic development of the bird eggs is facilitated; by arranging the anti-dust devices, it is avoided that impurities such as dust enter the incubator body.
Owner:台山市河东禽业有限公司

Eupolyphaga sinensis production and cultivation process

An eupolyphaga sinensis production and cultivation process comprises measures of storage of seed eggs, incubation of seed eggs, raising of larvas, management of adults and the like. The storage of seed eggs comprises putting the seed eggs in humid soil and controlling the temperature at 0-15 DEG C; the incubation of seed eggs comprises adding water into rice hull ash and fine earth which are mixed and proportioned in a ratio of 1: 1 to blend incubation soil; and putting the seed eggs in the incubation soil to be incubated, wherein the volume ratio of the seed eggs and the incubation soil is controlled at 2: 1 to 1: 1 and the incubation temperature is controlled at 28-30 DEG C; the raising of larvas comprises screening hatched larvas, putting in the larvas in an eupolyphaga sinensis pool, and adding raising soil to cover and raise the eupolyphaga sinensis once every evening till the eupolyphaga sinensis grows to adults; and the management of adults comprises selecting most male eupolyphaga sinensis to be dried in the sun after the larvas grow to adults, then adding materials to raise the eupolyphaga sinensis, screening a first batch of seed eggs three months later, screening the seed eggs once every month, and scalding female eupolyphaga sinensis by boiled water to be dried in the sun after the seed eggs are screened three times. According to the method for cultivating eupolyphaga sinensis, the eupolyphaga sinensis is high in yield and good in quality.
Owner:上海辰农生物科技有限公司
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