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626 results about "Semi quantitative" patented technology

A semi-quantitative analysis would be used to determine the number of tires produced every day since a manufacturing plant began production. A semi-quantitative analysis would be used by a meteorologist to ascertain the annual average temperature of a specific location.

Method and system for rapid biomolecular recognition of amino acids and protein sequencing

Methods, compositions, kits, and apparatus are provided wherein the aminoacyl-tRNA synthetase system is used to analyze amino acids. The method allows very small devices for quantitative or semi-quantitative analysis of the amino acids in samples or in sequential or complete proteolytic digestions. The methods can be readily applied to the detection and/or quantitation of one or more primary amino acids by using cognate aminoacyl-tRNA synthetase and cognate tRNA. The basis of the method is that each of the 20 synthetases and/or a tRNA specific for a different amino acid is separated spatially or differentially labeled. The reactions catalyzed by all 20 synthetases may be monitored simultaneously, or nearly simultaneously, or in parallel. Each separately positioned synthetase or tRNA will signal its cognate amino acid. The synthetase reactions can be monitored using continuous spectroscopic assays. Alternatively, since elongation factor Tu:GTP (EF-Tu:GTP) specifically binds all AA-tRNAs, the aminoacylation reactions catalyzed by the synthetases can be monitored using ligand assays. Microarrays and microsensors for amino acid analysis are provided. Additionally, amino acid analysis devices are integrated with protease digestions to produce miniaturized enzymatic sequenators capable of generating either N- or C-terminal sequence and composition data for a protein or peptide. The possibility of parallel processing of many samples in an automated manner is discussed.
Owner:NANOBIODYNAMICS

Method and system for rapid biomolecular recognition of amino acids and protein sequencing

Methods, compositions, kits, and apparatus are provided wherein the aminoacyl-tRNA synthetase system is used to analyze amino acids. The method allows very small devices for quantitative or semi-quantitative analysis of the amino acids in samples or in sequential or complete proteolytic digestions. The methods can be readily applied to the detection and / or quantitation of one or more primary amino acids by using cognate aminoacyl-tRNA synthetase and cognate tRNA. The basis of the method is that each of the 20 synthetases and / or a tRNA specific for a different amino acid is separated spatially or differentially labeled. The reactions catalyzed by all 20 synthetases may be monitored simultaneously, or nearly simultaneously, or in parallel. Each separately positioned synthetase or tRNA will signal its cognate amino acid. The synthetase reactions can be monitored using continuous spectroscopic assays. Alternatively, since elongation factor Tu:GTP (EF-Tu:GTP) specifically binds all AA−tRNAs, the aminoacylation reactions catalyzed by the synthetases can be monitored using ligand assays. Microarrays and microsensors for amino acid analysis are provided. Additionally, amino acid analysis devices are integrated with protease digestions to produce miniaturized enzymatic sequenators capable of generating either N- or C-terminal sequence and composition data for a protein or peptide. The possibility of parallel processing of many samples in an automated manner is discussed.
Owner:NANOBIODYNAMICS

Rapid detection method employing ultrasensitive quantum dot microsphere immunity-chromatograph test paper strips

InactiveCN101893623AHigh sensitivityPrecise and efficient quantitative detection resultsMaterial analysisMicrosphereCentrifugation
The invention relates to a detection method, in particular to a rapid detection method employing ultrasensitive quantum dot microsphere immunity-chromatograph test paper strips. The prior art has the disadvantage that the detection sensitivity is unable to satisfy demands of users because of high detection limit of samples, complex composition of the samples and great pretreatment difficulty. The rapid detection method of the invention comprises the steps of: preparing silicon dioxide nanoparticles, incubating the amino silicon dioxide nanoparticles with antibody for 1-10 hours in the presence of a condensation agent at 37 DEG C, and removing the antibody and the condensation agent which are failed to bond 1-4 times through high-speed centrifugation, redissolving precipitates obtained after centrifugation, adding the condensation agent and carboxylic water-soluble quantum dots, and removing free quantum dots and the condensation agent through high-speed centrifugation; preparing a silica/quantum dot composite microsphere probe; and constructing an immunity-chromatograph test paper strip system. The invention has the advantages of simple and convenient detection method, accurate and visual results, high sensitivity, low price, and wide application and can be used for semi-quantitative detection and quantitative detection.
Owner:SHANGHAI NORMAL UNIVERSITY

On-site quick detection method for organic pollutants in water

The invention relates to the technical field of environmental protection or chemistry analysis, which is an on-site quick detection method for organic pollutants in water; wherein on-site quick separation is carried out on various types of organic pollutants in a polluted water sample to be detected with thin layer chromatography, and on-site quick detection is carried out on the organic pollutants by using surface enhancement Raman spectroscopy technology. The method comprises the following steps of: firstly, preparing the active base of a high-density surface reinforced Raman spectrum; secondly, establishing a characteristic-peak strength-density standard curve map; thirdly, separating the organic pollutants which are stabilized on a chromatographic sheet; fourthly, obtaining the surface reinforced Raman spectrum map of the organic pollutants; and fifthly, carrying out contrast and detection. The method has the following benefits: the method has high detection and analysis speed, high sensitivity, wide detection range, low sample dosage and convenience for instrument carrying and operation; and the on-site quick qualitative analysis and semi-quantitative detection can be carried out on the organic pollutants, wherein the detective sensitivity can be less than 1 ppm.
Owner:EAST CHINA UNIV OF SCI & TECH

Method for semi-quantitatively detecting pathogenic nucleic acid by adding internal control nucleic acid

InactiveCN101957373AAvoid diagnostic problems that are prone to false negativesAvoid problems prone to false negativesMicrobiological testing/measurementMaterial analysisTest sampleQuality control
The invention belongs to the field of nucleic acid detection and discloses a method for semi-quantitatively detecting pathogenic nucleic acid by adding internal control nucleic acid. Corresponding internal control is added in the whole process of extracting and amplifying target nucleic acid and testing by using a test paper, so that the internal control and a target segment are parallelly operated, and the semi-quantitative detection is performed finally through color development and intensity contrast of three strips, namely a detection line, an internal control line and a quality control line on the test paper. In the method, in the whole process of processing the target nucleic acid, the corresponding internal control is taken as a positive contrast, and false negative results due to links such as extraction, amplification or sample application errors are avoided in the processing of detecting by using the test paper. Meanwhile, by comparing color development intensity of the internal control line and a sample line and introducing the semi-quantitative function on the basis of the qualitative function of the immunochromatographic test paper to estimate the copy number of tested samples, the detection results are more detailed, accurate and reliable. The method has the advantages of convenient and quick operation and capacity of meeting the actual clinical requirement.
Owner:HUADONG RES INST FOR MEDICINE & BIOTECHNICS

Preparation of hydrophilic polymer and application thereof in detecting mercury ions based on change of fluorescence and color

The invention discloses preparation of hydrophilic polymer and application thereof in detecting mercury ions based on the change of fluorescence and color, particularly a rhodamine B hydrazide grafted hydrophilic polymer probe applied to the detection of mercury ions in aqueous medium based on the change of fluorescence and color and a kit and test paper applied to the detection of the mercury ions by using the probe, belonging to the technical field of material preparation and heavy metal ion detection. The polymer containing a rhodamine chromophore is prepared by subjecting rhodamine B hydrazide and propylene oxide on the side chain of polyvinylpyrrolidone-glycidyl methacrylate which is a water-soluble polymer to ring-opening reaction, has good water solubility and can be applied to selectively detecting the mercury ions by using visual colorimetry and fluorescence detection. The probe realizes the high-sensitivity and high-selectivity rapid quantitative or semi-quantitative detection of the trace mercury ions in the aqueous medium, has a simple synthetic route, low cost and convenience of use, is applicable to amplified synthesis and actual production and has great application prospects in the field of medicine, biology and environmental science and the like.
Owner:JIANGNAN UNIV

Geological logging explanation evaluating method

InactiveCN101183154AAccurate Geological ParametersReliable geological parametersSeismic signal processingFluorescenceSlurry
The invention relates to a geological logging interpretation and evaluation method for oil drilling exploration. The method is based on wellbore information and collects drilling time, oil and gas characteristics of rock samples, fluorescence characteristics, gas measurement parameters, mud tank surface conditions, storage 20 parameters of 6 categories of layer electrical measurement parameters are stored in the corresponding table, and then the scoring method is used to assign specific points to each parameter item; geological analysis experts make interpretation and evaluation conclusions based on the above parameter information to guide on-site personnel to judge the underground The properties of the reservoir fluid can achieve the goal of protecting oil and gas layers and safe drilling, and provide accurate and reliable geological parameters in time to provide a basis for the next step of work measures or construction plan formulation. The geological interpretation and evaluation method provided by the present invention analyzes and defines the parameters reflecting reservoir characteristics and fluid properties, so that qualitative data can be transformed into quantitative or semi-quantitative interpretation, and from a single evaluation to a comprehensive analysis and evaluation of multiple parameters, which can make Reservoir interpretation and evaluation results or conclusions are more scientific and rational.
Owner:LIAOHE GASOLINEEUM EXPLORATION BUREAU

Quick detection method of tea polyphenol contents on basis of micro-fluidic paper chip technology

The invention provides a quick detection method of tea polyphenol contents on the basis of a micro-fluidic paper chip technology. The quick detection method comprises the following steps: arranging a symmetrical hydrophilic channel network on a micro-fluidic paper chip, wherein the symmetrical hydrophilic channel network comprises a center area and a plurality of hydrophilic channels around the center area, one end of each hydrophilic channel is communicated with the center area, one end, far away from the center area, of each hydrophilic channel is provided with a reaction detection area, and the plurality of hydrophilic channels have the same length and width and form point symmetry; in each reaction detection area, dropwise adding a foline-phenol reagent and carrying out sample introduction, dropwise adding sodium carbonate solution in the center area, diffusing to each detection area through the hydrophilic channels, carrying out developing reaction for 1-10min, and carrying out semi-quantitative measurement or quantitative measurement of tea polyphenol. According to the method, a symmetrical multi-channel detection array of the micro-fluidic paper chip is used for carrying out parallel developing reaction and integral data acquisition, and a foline-phenol developing-detecting array with highly-consistent reaction time is obtained, so that accurate colorimetric determination can be realized at any time point in a developing reaction process, and time required for detection is greatly shortened.
Owner:TEA RES INST CHINESE ACAD OF AGRI SCI

Colloidal gold test strip for semi-quantitative detection of progesterone and preparation method thereof

InactiveCN102297966ASimple Breeding SituationPromote reproductionMaterial analysisNitrocelluloseControl line
The invention relates to a colloidal gold test strip for semi-quantitative detection of progesterone and a preparation method thereof. The invention belongs to the technical field of dairy cow pregnancy diagnosis. Colloidal gold test strip for semi-quantitative detection of progesterone, the sample pad, the gold pad containing gold-labeled progesterone antibody complex, and the nitrocellulose membrane are pasted end to end on the bottom plate; there are detection lines and control lines on the nitrocellulose membrane . Preparation of test strips: preparation of colloidal gold: prepared from chloroauric acid and trisodium citrate; preparation of purified polyclonal antibody: preparation of artificial antigen of dairy cow progesterone by dicyclohexylcarbodiimide coupling method; artificial antigen of progesterone was then used Immune mice to prepare progesterone polyclonal antibody; prepare gold-labeled antibody: colloidal gold and antibody adsorption, centrifugal purification; colloidal gold test strip preparation: soak gold-labeled pad with Tween-containing PB solution, gold-labeled antibody perfusion glass fiber Membrane; nitrocellulose membrane Spray bovine progesterone artificial antigen and goat anti-mouse secondary antibody into 2 lines with a film dispenser. The invention is simple in operation, convenient and practical, efficient and fast, and easy to popularize.
Owner:TIANJIN AGRICULTURE COLLEGE

Color RGB (red, green and blue)-component-based urine analysis device and processing method thereof

The invention discloses a color RGB (red, green and blue)-component-based urine analysis device, which is characterized by comprising a processor, a serial communication unit, a temperature measuring unit, a light intensity control unit and a color sensor unit, wherein the processor controls the light intensity of a white LED (light-emitting diode) lamp through the light intensity control unit, light emitted from the white LED lamp shines on a urinalysis test strip on a sampling platform, a color RGB component of reflected light of each reagent area of the urinalysis test strip is acquired by using the color sensor unit, and the processor determines a semi-quantitative value of a corresponding detection index of each reagent area according to the color RGB components and temperatures. The device and the method disclosed by the invention have the remarkable effects that the circuit structure is simple, and the cost is low; through the coordination of the color sensor unit and the temperature detection unit, a calculation coefficient of each detection index is fitted by using an experience numerical value of the existing precision instrument, so that a microprocessor can calculate an accurate measurement index by using the coefficients; the device is high in equipment precision and wide in temperature application range.
Owner:CHONGQING MEDICAL UNIVERSITY

Preparation of carbamide detection test paper for dairy food and carbamide detection method

The invention provides a preparation method of urea detection test paper in dairy and a detection method of urea; urease source powder is taken and mixed with pH indicator with the pKHIn more than 6.8; the mixture is diluted by deioned water and the filter solution or the upper suspension liquid after natural deposition is taken, uniformly fixed on a carrier with good water absorption by the forms of coating, printing or soaking, and dried subsequently, thus forming the urea detection test paper; the detection method of the dairy comprises the steps as follows: firstly, common pH test paper is used for detecting the dairy to be detected; whether the dairy to be detected is in normal pH range 6.3-6.8 or not is checked; if so, the urea detection is directly carried out; if not, the pH value is adjusted to the normal pH range and the urea detection is carried out subsequently; one piece of urea detection test paper dips the dairy to be detected and the color change of the test paper is observed; if the color of the test paper is not changed, the dairy is qualified; if the color of the test paper changes, the dairy is mixed with the urea, thus carrying out qualitative judgment on the dairy; and the displayed color is compared with a standard colorimetric card, so as to carry out semi-quantitative detection of the urea in the dairy.
Owner:XI AN JIAOTONG UNIV
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