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81results about How to "Test results have no effect" patented technology

Production method of molecular engram membrane electrode for detecting endocrine interference in trace amount surroundings and detecting method thereof

The invention discloses a method for detecting an electrode of a molecular imprinting membrane of EDCs and the EDCs; the preparing method of the molecular imprinting membrane electrode comprises the following steps: a functional monomer is selected; template molecule of the EDCs, the functional monomer, a crosslinker, a porosity-making agent, an initiating agent and organic solvent are mixed evenly according to a certain molar ratio so as to prepare MIPs solution; nanometer material solution is prepared; the nanometer material and molecular imprinting polymer MIPs are modified on the surface of the electrode of a sensor by using the electrode surface modifying technology; a method for detecting trace amount of the EDCs comprises the following steps: the electrode of the molecular imprinting membrane is connected with an electrochemical working station and detects the EDCs in the environment sample extract; the electrode of the molecular imprinting membrane of the invention has strong specificity and high sensitivity which can reach ng level; a basic detection process is completed by only 1 to 2 minutes; the cost is low and the detection of one sample needs only a plurality of cents; the method for detecting the secretion in the environment by the electrode of the molecular imprinting membrane has fast and simple operation and the reaction and result are completed and recorded automatically by instruments.
Owner:UNIV OF JINAN

Study and application of quantum dot molecular imprinting microsphere quartz fluorescent sensor for detecting trace multicomponent food additives quickly on site

The invention discloses a quantum dot molecular imprinting microsphere quartz fluorescent sensor for detecting multicomponent food additives simultaneously and a method for detecting the food additives by the quantum dot molecular imprinting microsphere quartz fluorescent sensor. A method for preparing a quantum dot molecular imprinting microsphere comb quartz plate comprises the following steps of: selecting functional monomers corresponding to the food additives; preparing quantum dots and preparing quantum dot molecular imprinting microspheres according to the literature; and modifying thesurfaces of different probes of the comb quartz plate with the imprinting microspheres of different food additives by utilizing layer-upon-layer accumulated surface modification technology. The method for detecting the trace multicomponent food additives simultaneously (which is shown as the figure) comprises the following steps of: immersing the modified quartz plate into simply-pulpified food solution, arranging the quartz plate on a sealing quartz vessel, and detecting the food additives in a sample. The quantum dot molecular imprinting microsphere quartz fluorescent sensor has high specificity and sensitivity, short detection time and low cost; and in a method for detecting pesticide residues by fluorescent light, the operation is simple and quick, and reactions and results are completed and recorded automatically by instruments.
Owner:UNIV OF JINAN

Trace amount environment incretion jam object molecular imprinting film substrate and preparation method and application thereof

The invention provides an endocrine interferent molecularly imprinted membrane substrate in a trace environment with rapid detection speed and high sensitivity, the preparation method and the application thereof. The molecularly imprinted membrane substrate comprises a gold quartz crystal substrate, and multi-layer nano-materials that alternate with each other and environmental endocrine interferent molecularly imprinted polymer are formed on the surface of the gold quartz crystal substrate. The preparation method comprises the following steps: selecting functional monomer that can be synthesized with the environmental endocrine interferent into the molecularly imprinted polymer; preparing the molecularly imprinted polymer solution; and modifying the nano-material and the molecularly imprinted polymer on the surface of the gold quartz crystal substrate. The invention applies the surface modification technology to the preparation of the molecularly imprinted membrane substrate, so as to allow the controllability over the preparation of the nano-scale synergetic EDCs molecularly imprinted membrane substrate. A method for detecting the environmental endocrine is rapid and simple, and the reaction and the result are automatically recorded and completed by an instrument with good repeatability, thereby facilitating the on-site detection.
Owner:UNIV OF JINAN

Electrochemical immunosensor for detecting toxoplasma gondii IgM antibody and preparation method thereof

The invention belongs to the technical field of analytical chemistry and chemical sensors and discloses an electrochemical immunosensor for detecting a toxoplasma gondii IgM (Immunoglobulin m) antibody (Tg-IgM) of a gravida and a preparation method of the electrochemical immunosensor. The immunosensor is prepared by sequentially modifying graphene, polythionine, gold nanoparticles and capture antigen to the surface of a glassy carbon electrode. An enzyme-functionalized nano-composite detection probe with an electrical signal amplifying function is prepared by assembling enzyme and a second antibody with high proportions on an Au-Fe3O4 surface. According to the sandwich immunoassay principle, the concentration of Tg-IgM is determined by using an electrochemical signal generated by catalysis of enzyme to a substrate. According to the electrochemical immunosensor, the specificity of immunoreaction is combined with the sensitivity of electrochemical detection; the transmission of electronics is promoted by using the graphene, the polythionine, the gold nanoparticles, Au-Fe3O4 and other material; and the sensitivity of the detection is improved. The electrochemical immunosensor has the advantages of simplicity and convenience for operation, favorable regeneration performance and detection cost reduction. The electrochemical immunosensor prepared on the basis can be also used for detecting other immunological markers and has favorable application prospect in medical diagnosis.
Owner:CHONGQING MEDICAL UNIVERSITY

Flexible, simple and convenient loading device for anti-seismic property test

The invention relates to a flexible, simple and convenient loading device for an anti-seismic property test. The device comprises constraint units for fixing test pieces to ground beams, a horizontal loading unit for applying a horizontal load to the test pieces and a vertical loading unit for applying a vertical load to the test pieces; the vertical loading unit comprises vertical jacks, vertical flexible pull rods and reaction beams located over the test piece, the lower ends of the vertical flexible pull rods are fixed with the ground beams, the upper ends of the vertical flexible pull rods are connected with the reaction beams, and the vertical jacks are fixed to the bottoms of the reaction beams and apply vertical loads to the top of the test pieces. According to the device, the vertical flexible pull rods are thin and long rod parts with the certain flexibility, when the test pieces generate horizontal displacement deformation under the action of the horizontal load, the vertical flexible pull rod can generate the certain curvature, and therefore the upper ends of the vertical flexible pull rods can horizontally move along with the reaction beams and the vertical jacks, that is to say, the relative positions between the vertical loading unit and the test piece do not change. The device is simple in structure and easy to install.
Owner:HEFEI UNIV OF TECH

Fluorescent quantitative PCR primer, probe, kit and detection method for detecting avian influenza subtype

The invention provides a multiplex fluorescent quantitative PCR primer and a probe for detecting H5, H7 and H9 subtype avian influenza viruses. With adoption of the primer and the probe, multiplex fluorescent quantitative PCR can be adopted to simultaneously detect which subtypes the H5, H7 and H9 subtype avian influenza viruses concretely are, no influences exist among the primers of different subtypes, the specificity is strong, the detection sensitivity is 10-50 copy numbers, a target sequence can be accurately detected quantitatively and qualitatively, the repeatability is good, and the reliability is high. The invention provides a multiplex fluorescent quantitative PCR kit for simultaneously detecting the H5, H7 and H9 subtype avian influenza viruses. The kit has the detection sensitivity being 10-50 copy numbers and is high in sensitivity and strong in specificity. The invention also provides a detection method which is good in stability. With adoption of plasmids with gene fusion as a positive standard substance, tedious operation of changing the positive standard substance for multiple times is avoided, the detection time is greatly shortened, the detection times are greatly reduced, and detection of a sample can be finished within 2h.
Owner:NANJING AGRICULTURAL UNIVERSITY

Research and application of molecular identification-based fluorescence nanocrystal quartz fluorescent sensor for high-selectivity multicomponent saccharide detection

The invention discloses a fluorescence nanocrystal quartz fluorescent sensor for molecular identification-based multicomponent simultaneous saccharide detection and a method for detecting saccharides by using the same. The invention provides a preparation method of a molecular identification-based fluorescence nanocrystal comb quartz plate, which comprises the following steps: selecting an identifier corresponding to the saccharides; preparing a fluorescence nanocrystal, and carrying out surface modification on the fluorescence nanocrystal according to the literature; and modifying the modified fluorescence nanocrystal onto surfaces of different probes of the comb quartz plate by using layer-by-layer accumulation surface modification technique. The invention also provides a method for multicomponent simultaneous saccharide detection, which comprises the following steps: immersing the modified quartz plate into a food sample solution which is simply pulpified, installing the quartz plate onto a sealed silica dish, and detecting the saccharides in the sample. The invention has the advantages of strong specificity, high sensitivity, short detection time and low cost. The saccharide fluorescence detection method has a quick and simple operation process, and the reaction and the result are automatically completed and recorded by instruments.
Owner:UNIV OF JINAN

Method for quick quantitative determination of active bifidobacteria

The invention discloses a method for quickly and quantificationally detecting live bifidobacterium and relates to a quick and quantificational detection method for the live bifidobacterium in products containing bifidobacterium. A detection technology of the bifidobacterium is divided into the prior detection with plate bacterial colony counting as a base and various detections with molecular biology as a base. The method comprises the following steps that: a sample is taken, is diluted up to 10 times, and is subjected to EMA treatment, DNA of the sample is extracted, the molecular beacon-real-time PCR detection is performed, the content of the bifidobacterium is calculated according to a standard curve, wherein, the extraction process of the DNA is that: the sample which is subjected to the EMA treatment is added with 18 percent sodium citrate and 1M NaOH and is centrifugated for 10min at a rotating speed of 10,000rpm, somatic cells are collected and are washed by ultrapure water, a bacterial suspension is taken, is added into a Tritox-100 liquid with a concentration of 2 percent, is subjected to water bath treatment for 10min at a temperature of 100 DEG C, and then is cooled immediately, and supernate is used for molecular beacon-real-time PCR amplification. The method is used for quantitative detection of the live bifidobacterium in the products containing the bifidobacterium.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Preparation method of voltage-controllable multiplex multichannel sensing paper chip for detecting antibiotic residues by molecular imprinting electroluminescence

The invention discloses a preparation method of a voltage-controllable multiplex multichannel sensing paper chip for detecting antibiotic residues by molecular imprinting electroluminescence. The preparation method comprises the following steps of self-preparing a transformer and a multiplexer switch, preparing a multichannel printing electrode on paper, preparing a molecular imprinting (MIPs) sol of antibiotic residues, preparing carbon dots and silicon dioxide pellets coated by the carbon dots, preparing a graphene nano-material, and modifying the surface of the multichannel printing electrode on paper by the graphene nano-material, the silicon dioxide pellets coated by the carbon dots and the MIPs sol by an electrode surface modification technology. The preparation method also comprises the following steps that through the modified multichannel printing electrode, a chemiluminescent analyzer, the transformer and the multiplexer switch, antibiotic residues in sample extract are detected. The voltage-controllable multiplex multichannel sensing paper chip has strong singularity, high sensitivity reaching the ng grade and a low cost, can be operated fast and simply, and realizes automatic reactions and result recording by apparatuses.
Owner:UNIV OF JINAN

Glycosyl functional bacterial toxin molecularly imprinted membrane substrate as well as preparation method and application thereof

The invention relates to a glycosyl functional bacterial toxin molecularly imprinted membrane substrate as well as a preparation method and an application thereof. The molecularly imprinted membrane substrate forms a reaction layer on the surface of a gold quartz crystal substrate by taking a glycosyl functional bacterial toxin molecularly imprinted polymer as a recognition element. The preparation method comprises the following steps: selecting a carbohydrate molecule functional monomer which can carry out specificity recognition with bacterial toxin and compound the corresponding molecularly imprinted polymer; preparing a glycosyl functional molecularly imprinted polymer solution; and modifying the glycosyl functional molecularly imprinted polymer on the surface of the gold quartz crystal substrate by a substrate surface modifying technology to form a reaction layer. The glycosyl functional molecularly imprinted membrane substrate prepared by the method is connected to a piezoelectric quartz crystal microbalance to detect bacterial toxin in an environmental sample extracting solution. The molecularly imprinted membrane substrate has favorable molecular recognition performance and greatly improves the sensitivity and the selectivity for detecting the bacterial toxin.
Owner:UNIV OF JINAN

Method for preparing glycosyl functional molecularly imprinted membrane electrode for detecting bacterial toxin and application thereof

The invention relates to a method for preparing a glycosyl functional molecularly imprinted membrane electrode for detecting bacterial toxin, which comprises the following steps: (1) selecting a functional monomer which can compound a glycosyl functional molecularly imprinted polymer with the bacterial toxin; (2) uniformly mixing a bacterial toxin template molecule, the functional monomer, a cross-linking agent, a porogenic agent, an initiating agent and an organic solvent to prepare a glycosyl functional molecularly imprinted polymer solution according to a certain molar ratio; and (3) modifying the glycosyl functional molecularly imprinted polymer on the surface of an electrode of a sensor by an electrode surface modifying technology. The method for detecting trace bacterial toxin comprises the following steps: connecting the glycosyl functional molecularly imprinted membrane electrode prepared by the method to an electrochemical workstation and detecting the bacterial toxin in an environmental sample extracting solution. The glycosyl functional bacterial toxin molecularly imprinted membrane electrode has high specificity, sensitivity and detecting sped, can realize high flux screening of a plurality of samples in short time and reduces the detecting cost.
Owner:UNIV OF JINAN

Immunity test strip based on fluorescent microsphere for detecting infectious pleural pneumonia antibody of goat as well as preparation and detection method

The invention relates to an immunity test strip based on a fluorescent microsphere for detecting an infectious pleural pneumonia antibody of a goat as well as a preparation and detection method, whichbelong to the detection field of immunity. The test strip comprises a shell and a test strip, wherein the test strip comprises a bottom plate as well as a water absorption pad, a detection pad, a combination pad and a sample pad which are successively lapped and adhered onto the bottom plate; a nitrocellulose membrane is provided with a quality control line C and a detection line T, the quality control line C covers a His tag monoclonal antibody, and the detection line T covers a goat mycoplasma pneumonia recombinant protein; the combination pad is a glass cellulose membrane coating with thegoat mycoplasma pneumonia recombinant protein marked by time resolution fluorescent microspheres; and the sample pad is a dry glass cellulose membrane after being soaked in sample treatment liquid. The test strip prepared by the invention has better stability and higher sensitivity, and can achieve a purpose of rapid semi-quantitative detection by virtue of the fluorescent signal analysis.
Owner:LUOYANG LAIPSON INFORMATION TECH +1

Sample preparation method used for determining abundance of <15>N isotope of nitrite

The invention relates to a sample preparation method used for determining abundance of a <15>N isotope of nitrite. The sample preparation method comprises the following steps: loading a sample, namelyloading a <15>N-labeled to-be-prepared sample and aqueous solution of a reducing agent into a first bulb of a double bulb reaction tube, and loading an acidic material into a second bulb of the double bulb reaction tube; preparing a <15>NO gas, namely maintaining vacuum degree, and adding the acidic material in the second bulb into the first bulb, so that the <15>NO gas is generated; detecting, namely after the vacuum degree of a pipeline between a vacuum plug valve and a gas isotope ratio mass spectrometer is reduced to be below 2*10<-5>Pa, opening the vacuum plug valve, and introducing the<15>NO gas in the first bulb into the gas isotope ratio mass spectrometer; setting detection parameters of the gas isotope ratio mass spectrometer, detecting a relative intensity when mass numbers are30 and 31, and performing a parallel test for multiple times; and calculating an abundance value of the <15>N isotope. Compared with the prior art, the sample preparation method provided by the invention has the advantages that an operation process is safe and reliable, sample pretreatment time is greatly shortened, economic cost is low and test data accuracy and precision are high.
Owner:SHANGHAI RES INST OF CHEM IND

Lanthanide metal europium ion complex probe-based method for detecting pH value

The invention discloses a lanthanide metal europium ion complex probe-based method for detecting a pH value. The detection method mainly comprises the following steps: firstly, carrying out fluorescence intensity scanning on a to-be-detected sample A including lanthanide metal europium ion complexes and solutions with different pH values; observing the change of the fluorescence intensity, and carrying out quantitative detection on the pH values of the solutions, so as to obtain a linear interval between the pH values and the fluorescence intensity; and detecting the fluorescence intensity of a to-be-detected sample B including the lanthanide metal europium ion complexes and a to-be-detected water body sample, so as to obtain the pH value of the to-be-detected water body sample. The method disclosed by the invention is capable of achieving the detection effect of a traditional method, and has good selectivity, high response speed, short detection time, simplicity of operation and low price; a time-resolved fluorescence signal is strong and stable; and the repeatability of an experimental method and the recognizable degree of the fluorescence signal in a complicated environment are ensured, so that the ultimate practicability of the detection method is powerfully guaranteed.
Owner:SOUTH CHINA INST OF ENVIRONMENTAL SCI MEP

Kit for simultaneously detecting and tracing a plurality of environmental endocrine disruptors and application thereof

The invention relates to the field of environmental endocrine disruptors, and provides a kit for simultaneously detecting a plurality of environmental endocrine disruptors and application thereof. The kit is made by adopting the following steps: respectively preparing potassium permanganate solution, HCL solution and polysorbate-80 solution; uniformly mixing template molecules, a functional monomer, a cross-linking agent, a porogenic agent, an initiator and organic solvent in a certain molar rate to prepare molecularly imprinted sol-gel of the environmental endocrine disruptors; modifying the molecularly imprinted sol-gel on the inner surface of a microporous plate, sealing the inner surface by a preservative film for hours; soaking the modified microporous plate in eluant for eluting; and inserting ports of a sample injector of the microporous plate into luminescence reagent solution to obtain the kit for simultaneously detecting a plurality of environmental endocrine disruptors. The kit is connected to a multifunctional analyzer on the microporous plate to detect the environmental endocrine disruptors in an environmental sample extracting solution. The kit has the advantages of simple operation, less dosage of reagent, economy and practicality, low price and accessibility of chemical luminescent reagent, high sensitivity and simple operation.
Owner:UNIV OF JINAN

Nanometer synergistic glycosyl group functionalized bacterial toxin molecular engram film substrate as well as preparation method and application thereof

The invention relates to a nanometer synergistic glycosyl group functionalized bacterial toxin molecular engram film substrate as well as a preparation method and an application thereof. The nanometersynergistic bacterial toxin molecular engram film substrate is to form a plurality of layers of mutually-alternating nanometer materials and glycosyl group functionalized bacterial toxin molecular engram polymers on a gold quartz crystal substrate by taking the glycosyl group functionalized bacterial toxin molecular engram polymers as coupling agents. The preparation method is realized as follows: selecting sugar molecule functional monomers which can recognize the specificity of bacterial toxin and synthesize corresponding molecular engram polymers; preparing molecular engram polymer solution; and modifying the nanometer materials and the molecular engram polymers on the surface of the gold quartz crystal substrate. The molecular engram substrate is connected to a piezoelectric quartz crystal microbalance to detect the bacterial toxin in an environment sample extraction solution. The invention has simple operation and high specificity and sensitivity for detecting the bacterial toxin.
Owner:UNIV OF JINAN

Testing method of contact heat resistance between circular section one-dimensional nanostructures

The invention discloses a testing method of contact heat resistance between circular section one-dimensional nanostructures. The method comprises the following steps: breaking a circular section one-dimensional nanostructure into two sections by using a micro manipulator under an optical microscope or a scanning electron microscope, wherein two sections are respectively lapped at a heat source anda heat sink of an overhead microdevice; enabling two sections of specimens to form parallel contact between the heat source and the heat sink; testing the sample by adopting a heat bridge method, thereby obtaining apparent heat resistance Rtot1; changing two sections of specimens as cross contact from parallel contact by using the microdevice under the optical microscope or the scanning electronmicroscope, testing the sample by adopting the heat bridge method so as to obtain the apparent heat resistance Rtot2, wherein the contact heat resistance of the unit area between two sections of specimens can be approximate as RCA=(Rtot2-Rtot1)*Ac2, wherein the AC2 is the contact area of the cross contact between two sections of specimens. The testing successful rate is improved, the specimen quality consistency requirement is reduced, and the testing precision is improved.
Owner:SOUTHEAST UNIV

Preparation method and application of nano-synergistic carbohydrate functionalized molecularly imprinted column for detecting bacterial toxins

The invention relates to a preparation method of a nano-synergistic carbohydrate functionalized molecularly imprinted column for detecting bacterial toxins, comprising the following steps: selecting a carbohydrate functional monomer which can be used for synthesizing a carbohydrate functionalized molecularly imprinted polymer with the bacterial toxins; preparing solution of the carbohydrate functionalized molecularly imprinted polymer; preparing nano solution; and modifying nano materials and the carbohydrate functionalized molecularly imprinted polymer on the inner surface of a glass tube column. A method for detecting trace bacterial toxins of the invention is characterized by connecting the carbohydrate functionalized molecularly imprinted column prepared by the above method with a chemiluminescence analyzer, respectively pumping chemiluminescence system solution and sample solution into the chemiluminescence analyzer and detecting the bacterial toxins in the samples. The preparation method of the invention has controllability and improves the sensitivity and accuracy of the column. The prepared molecularly imprinted column features strong specificity, high sensitivity and rapid detection speed, can realize high throughout screening of vast samples in short time and lower the detection cost.
Owner:UNIV OF JINAN
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