126results about How to "The inspection method is simple" patented technology

The invention relates to the technical field of health toilets, in particular to a cloud health toilet capable of analyzing urine and a use method thereof. The cloud health toilet comprises a toilet body, a urine data gathering and analyzing device is arranged in the toilet body, and the cloud health toilet is further provided with an intelligent controller; the urine data gathering and analyzing device gathers urine data, analyzes and processes the gathered urine data and transmits the analyzed and processed urine detection data to the intelligent controller; the intelligent controller acquires the urine detection data of the urine data gathering and analyzing device, accesses and browses the urine detection data and performs data interaction transmission with a remote server. The cloud health toilet is capable of conveniently detecting the urine, the health condition can be realized at any time without going to the hospital, and a lot of time and energy are saved; the detection method is simple and sanitary, and the data precision is high.

The invention discloses a method for detecting a sulfanilamide medicine and a special enzyme-linked immunoassay reagent kit thereof. The enzyme-linked immunoassay reagent kit comprises a sulfanilamide medicine monoclonal antibody and the sulfanilamide medicine. The sulfanilamide medicine monoclonal antibody is secreted by the hybridoma cell line SAs of a sulfanilamide monoclonal antibody, whose preservation number is CGMCC No. 3393. In the enzyme-linked immunoassay reagent kit of the invention, an indirect competition ELISA (Enzyme-Linked Immuno Sorbent Assembly) method is mainly used for qualitatively or quantitatively detecting the content of the sulfanilamide medicine in products (especially milk, pork, chicken, eggs, honey, fish, shrimp and the like) eaten by animals or people. The reagent kit and the detection method of the invention have low requirements on the pretreatment of samples and simple pretreatment process of the samples and can detect mass samples quickly at the same time. By using the sulfanilamide medicine monoclonal antibody with high specificity, the detection method is convenient and simple, and the invention has the characteristics of high specificity, high sensibility, high precision, high accuracy and the like.

The invention provides an elisa kit for detecting cephalo-type medicine, containing: an ELIAS plate peridium of which is provided with peridium source, an enzyme label, cephalo-type medicine specific antibody working solution (contained when the peridium on the ELIAS plate is antigen and the enzyme label is enzyme label anti antibody or when the peridium on the ELIAS plate is anti antibody and theenzyme label is enzyme label antigen), ceftiofur standard solution, substrate developer, stop solution, concentrated cleaning solution and concentrated complex solution. The invention also disclosesa method applying the elisa kit for detecting cephalo-type medicine, including: firstly sample preprocessing is carried out, then the elisa kit is used for detection, and finally the detection result is analyzed. The elisa kit provided by the invention can be applied to detecting residual quantity of cephalo-type medicine in samples such as animal tissue (chicken, pork, fish and shrimp) and milk, etc, the operation is easy, the cost is low, the sensitivity is high, and the elisa kit is applied to on-site supervision and numerous sample screening.

The invention provides an enzyme-linked immunosorbent kit for inspecting sulfa drugs, comprising an ELISA plate which is coated with coating antigen, an enzyme label, sulfa drug specific antibody working liquid (being contained when the antigen is coated on the ELISA plate and the enzyme label is enzyme labeling antibody or antibody is coated on the ELISA plate and the enzyme label is enzyme labeling antigen), sulfamethoxy-isoxazole standard product solution, substrate color development solution, stop solution, concentrated washing liquid and concentrated complex solution. The invention further discloses a method which applies the enzyme-linked immunosorbent kit for inspecting the sulfa drugs, and the method comprises the steps of firstly carrying out the pre-treatment on a sample, then using the kit for inspecting and finally analyzing the inspection result. The provided enzyme-linked immunosorbent kit can be used for inspecting the residual amount of the sulfa drugs in animal tissues(chicken, pork, fish and shrimp), honey, eggs, milk, feeds and other samples, the operation is simple, the cost is low, the sensitivity is high and the enzyme-linked immunosorbent kit can be monitore d on-site and is applicable in screening mass samples.

The invention provides an ELISA (enzyme linked immunosorbent assay) kit for detecting carbofuran. The ELISA kit comprises an ELISA plate coated with a carbofuran conjugated antigen, a carbofuran monoclonal antibody, an enzyme labeled antibody, a carbofuran standard solution, a substrate color development solution, a stop buffer, a cleaning solution and a re-dissolution solution. The invention further discloses a method for applying the ELISA kit to detection of the carbofuran. The method comprises the following steps: a sample is pretreated firstly, then the kit is used for detection, and a detection result is analyzed finally. The ELISA kit can be used for detecting the content of the carbofuran in vegetables and tea leaves, the operation is simple and convenient, the cost is low, the sensitivity is high, on-site supervision can be realized, and the kit is suitable for screening of a large quantity of samples.

The invention provides an enzyme linked immune regent box to detect neomycin medicine. It includes: the enzyme labeled board which encrusts the encrusting substance, the enzyme marker, the special antibody for the neomycin, the neomycin standard solution, the substrate color solution, the stop solution, the condense washing solution, the condense recovery solution. The invention also discloses the method which includes the process: first to pre-treat the sample, then to detect by the regent box and last to analyze the detecting result. The invention is to detect the neomycin residue weight in the animal food such as the chicken, chicken liver, pork, pork liver, milk powder, egg and feedstuff. The method is simple, low cost and has high sensitivity, also it is proper for detect the mass sample.

The present invention discloses a method for detecting the erythromycin compounds and an enzyme linked immunoreaction reagent kit thereof which is specialized for the method. The enzyme linked immunoreaction reagent kit comprises an erythromycin specific antibody, a coatingen and an enzyme label. The erythromycin specific antibody is a monoclone antibody or polyclonal antibody of the erythromycin. The erythromycin compound is at least one in erythromycin, erythromycin thiocyanate and erythromycin ethylsuccinate. The erythromycin is erythromycin A. The enzyme linked immunoreaction reagent kit of the invention has the advantages of simple structure, convenient use, low cost, convenient carriage, high efficiency of the detecting method, accuracy and easiness. The on-spot monitoring can be executed. Furthermore the enzyme linked immunoreaction reagent kit is suitable for the qualitative and quantitative sieving of considerable samples, and can exert an important function in the detection to the erythromycin.

The invention provides an enzyme-linked immunosorbent kit for inspecting porcine immunoglobulin G, comprising an ELISA plate which is coated with coating antigen, an enzyme label, porcine immunoglobulin G specific antibody working liquid (being contained when the antigen is coated on the ELISA plate and the enzyme label is enzyme labeling antibody or antibody is coated on the ELISA plate and the enzyme label is enzyme labeling antigen), porcine immunoglobulin G standard product solution, substrate color development solution, stop solution, concentrated washing liquid and concentrated complex solution. The invention further discloses a method which applies the enzyme-linked immunosorbent kit for inspecting the porcine immunoglobulin G, and the method comprises the steps of firstly carrying out the pre-treatment on a sample, then using the kit for inspecting and finally analyzing the inspection result. The provided enzyme-linked immunosorbent kit can be used for inspecting the content ofthe porcine immunoglobulin G in porcine plasma protein powder and other samples, the operation is simple, the cost is low, and the enzyme-linked immunosorbent kit can be monitored on-site and is appl icable in screening mass samples.

The invention provides an enzyme linked immune regent box to detect gentamycin. It includes: the enzyme labeled board which encrusts the encrusting substance, the enzyme marker, the special antibody for the gentamycin (when the antigen is on enzyme labeled board and the enzyme marker is the enzyme labeled antiantibody or the antiantibody is in the enzyme labeled board and the enzyme marker is the enzyme labeled antigen), the gentamycin standard solution, the substrate color solution, the stop solution, the condense washing solution, the condense recovery solution. The invention also discloses the method which includes the process: first to pre-treat the sample, then to detect by the regent box and last to analyze the detecting result. The invention is to detect the gentamycin residue weight in the animal food such as the chicken, chicken liver, pork, pork liver, milk powder, egg and feedstuff. The method is simple, low cost and has high sensitivity, also it is proper for detect the mass sample.

The invention relates to a composition and a preparation process, a testing process and an application thereof. The composition comprises a therapeutically effective amount of candesartan or pharmaceutically acceptable ester or salt, a therapeutically effective amount of amlodipine or other pharmaceutically acceptable salt, 70-150 parts of mannitol or lactose, 2-5 parts of croscarmellose sodium or cross-calcium carboxymethyl cellulose and 5-40 parts of microcrystalline cellulose or corn starch. The composition is easy to prepare, low in production cost, utilizes accessories of unique prescription, and the like, can be prepared into oral preparation in forms of tablets, capsules, granules and the like by means of pharmaceutics, can be checked by different checking processes, has high quality, has functions of treating hypertension, angina pectoris and kidney diseases and has effect of myocardial protection.

The invention relates to the technical field of automobile control, in particular to a method and system for achieving steering-wheel turning angle verification based on EPS. A target turning angle command is received, and according to the target turning angle command, a motor of a steering wheel is driven so as to make the steering wheel rotate to a target angle; the actual turning angle deltaalpha of the steering wheel in a sampling time interval deltat is calculated; the turning angle deltadelta of a motor in the sampling time interval deltat is calculated; the turning angle deltadelta of amotor in the sampling time interval deltat is converted into the relative turning angle deltabeta of the steering wheel; the difference between the relative turning angle deltabeta of the steering wheel and the actual turning angle deltaalpha of the steering wheel is calculated, when the absolute value of the difference is not greater than that of phi, it is judged that a turning angle signal ofthe steering wheel is normal, and when the absolute value of the difference is greater than phi, it is judged that the turning angle signal of the steering wheel is abnormal. According to the rotary position sensor signal of a motor of the steering wheel in an electric power steering system, the relative turning angle of the steering wheel is calculated out, and the redundancy check of a steeringwheel angle signal sent by a vehicle angle sensor is achieved.

The present invention provides an enzyme-linked immunosorbent assay kit for dibutyl phthalate detection. The enzyme-linked immunosorbent assay kit comprises: a coating antigen-coated enzyme label plate, specific dibutyl phthalate antibody, an enzyme marker, a dibutyl phthalate standard substance solution, a substrate coloration solution, a stop buffer, a cleaning solution and a sample diluent, wherein the coating antigen is a conjugate formed by conjugating dibutyl phthalate to antigen, and the enzyme marker is an enzyme-labeled anti-antibody. The invention further discloses a method for applying the enzyme-linked immunosorbent assay kit to detect dibutyl phthalate, wherein the method comprises: carrying out a sample pretreatment, adopting the kit to detect, and analyzing the detection result. The enzyme-linked immunosorbent assay kit can be provided for detect the dibutyl phthalate content in the white spirit, has characteristics of simple operation, low cost and high sensitivity, can be provided for on-site monitoring, and is suitable for screening large number of samples.

The present invention discloses a method for detecting sulfaquinoxaline and its special-purpose ELIA kit. Said ELIA kit includes sulfaquinoxaline specific antibody, coating source and enzyme label. The described coating source is the conjugate of sulfaquinoxaline semiantigen and carrier protein or sulfaquinoxaline antiantibody, the described enzyme label is enzyme labeled sulfaquinoxaline antiantibody or enzyme labeled fulfaquinoxaline semiantigen. When the coating source is conjugate of the sulfaquinoxaline semiantigen and carrier protein, the described enzyme label is enzyme labeled sulfaquinoxaline antiantibody; and when the described coating source is sulfaquinoxaline antiantibody, the described cenzyme label is enzyme-labelled sulfaquinoxaline semiantigen.

The invention provides an imidacloprid detection ELISA (enzyme linked immunosorbent assay) kit which includes an ELISA plate coated with a coating antigen, a specific antibody, an enzyme marker, an imidacloprid standard solution, a substrate coloring liquid, a terminating liquid, a washing liquid and a complex solution, the coating antigen is an imidacloprid coupling antigen, and the enzyme marker is an enzyme labeled antibody. The invention also discloses an imidacloprid detection method using the ELISA kit, and the method includes first, pretreatment of a sample, then detection with the ELISA kit and final detection result analyzing. The ELISA kit can be used to detect the content of imidacloprid in vegetables and fruits, and has the advantages of being simple in operation, low in cost, high in sensitivity, capable of monitoring on site and suitable for screening a large number of samples.

The invention provides a method for inspecting gas tightness of argon pipelines of a molten steel tank, which is simple, can effectively solve the problems that the existing air pressure test or hydrostatic test is not accurate and can reduce the equipment cost. The method can be realized by the following technical scheme: pressure gas or pressure water is introduced in the argon pipeline of the molten steel tank; the method is characterized in that before the pressure gas or the pressure water is introduced in the argon pipeline of the molten steel tank, purple litmus reagent is coated at a to-be-detected part of the argon pipeline of the molten steel tank, wherein the pressure gas is CO2 gas and the pressure water is acid pressure water, and if the purple litmus reagent of the detection part of the pipeline goes red, the result indicates that the gas tightness of the detection part is poor.

The invention provides an enzyme linked immunosorbent assay kit for detecting triadimenol. The enzyme linked immunosorbent assay kit comprises an enzyme-labeled plate coated with a triadimenol coupling antigen, a triadimenol monoclonal antibody, an enzyme-labeled antibody, a triadimenol standard solution, substrate coloring liquid, a stop solution, washing liquid and reconstitution fluid. The invention further discloses a method using the enzyme linked immunosorbent assay kit to detect triadimenol residual quantity. The method includes: preprocessing a sample, detecting with the kit, and analyzing the detection result. The enzyme linked immunosorbent assay kit can be used for detecting the residual quantity of the triadimenol in tobacco and is simple to operate, low in cost, high in sensitivity, capable of achieving on-site monitoring and suitable for the screening of a large amount of samples.

The invention discloses a method for detecting maduramicin and a special enzyme-linked immunoassay reagent kit thereof. The enzyme-linked immunoassay reagent kit comprises a maduramicin monoclonal antibody. The maduramicin monoclonal antibody is secreted by the hybridoma cell line MAD of the maduramicin monoclonal antibody, whose preservation number is CGMCC No. 3391. In the enzyme-linked immunoassay reagent kit of the invention, an indirect competition ELISA (Enzyme-Linked Immuno Sorbent Assembly) method is mainly used for qualitatively or quantitatively detecting the content of the maduramicin in animal muscles and livers. The reagent kit and the detection method of the invention have low requirements on the pretreatment of samples and simple pretreatment process of the samples and can detect mass samples quickly at the same time. By using the maduramicin monoclonal antibody with high specificity, the detection method is convenient and simple, and the invention has the characteristics of high specificity, high sensibility, high precision, high accuracy and the like.

The invention provides an enzyme linked immunosorbent assay kit detecting folic acid. The enzyme linked immunosorbent assay kit comprises an elisa plate coated with a coating antigen, a folic acid antibody working solution, an enzyme marker, a folic acid standard substance solution, a substrate developing solution, a stop solution, a scrubbing solution and a compound solution. The coating antigen is a folic acid coupling antigen, and the enzyme marker is an enzyme marking antibody. The invention further discloses a method applying the enzyme linked immunosorbent assay kit detecting the folic acid. The method comprises the steps that sample pretreatment is carried out at first, then the kit is used for detection, and finally the detection result is analyzed. The enzyme linked immunosorbent assay kit can be used for detecting the content of the folic acid in finished milk, milk powder and cereals such as rice, millet, corns, soybeans and flour. The kit is easy and convenient to operate, low in cost, high in sensitivity, capable of monitoring the folic acid on site, and suitable for screening a large number of samples.

The present invention provides an enzyme-linked immunoassay kit for detecting dimethomorph. The enzyme-linked immunoassay kit contains an enzyme labeled plate coated with a dimethomorph-conjugated antigen, a dimethomorph standard substance solution, a concentrated enzyme conjugate, an enzyme conjugate working solution, a substrate chromogenic solution and a terminating solution. The invention further discloses a method for detecting dimethomorph in a sample by using the enzyme-linked immunoassay kit, wherein the method comprises: pre-treating a sample, detecting by using the kit, and analyzingthe detection result. According to the present invention, the enzyme-linked immunoassay kit can be used for detecting the residual dimethomorph in vegetable samples (raw materials, matching materialsand concentrated materials), has advantages of simple operation, low cost, high sensitivity and on-site monitoring, and is suitable for screening of a large number of samples.

The invention provides an enzyme linked immunosorbent assay (ELISA) kit for detecting vitamin B12. The enzyme linked immunosorbent assay kit comprises an ELISA plate coated with a vitamin B12 coupling antigen, an enzyme labeling ant-antibody working solution, a vitamin B12 specific antibody working solution, a vitamin B12 standard substance solution, substrate developing liquid, a stop solution, a concentration scrubbing solution and redissolution liquid. The invention also discloses a method for detecting the vitamin B12 by using the enzyme linked immunosorbent assay kit. The method comprises the following steps: firstly carrying out sample pretreatment, then detecting by using the kit, and finally analyzing detection results. The enzyme linked immunosorbent assay kit provided by the invention can be used for detecting the content of vitamin B12 in cereals (maize meal, soybean meal, millet meal and rice meal), milk and milk powder, is simple and convenient to operate, low in cost and high in sensitivity, can realize on-site monitoring and is suitable for screening lots of samples.

The invention provides an enzyme-linked immunoassay kit for detecting chlorpyrifos. The kit comprises an enzyme label board coated with chlorpyrifos coupling antigen, a chlorpyrifos monoclonal antibody, an enzyme labeling antiantibody, a chlorpyrifos standard product solution, a substrate developing solution, TMAH, a cleaning solution and a combination solution. The invention further discloses a method for detecting chlorpyrifos by means of the enzyme-linked immunoassay kit. The method includes the steps that firstly, sample pretreatment is conducted; secondly, detection is conducted by means of the kit; finally, a detection result is analyzed. The enzyme-linked immunoassay kit can be used for detecting the content of chlorpyrifos in vegetables, fruits and tea leaves, is easy to operate, low in cost, high in sensitivity, capable of achieving in-situ monitoring and suitable for screening a lot of samples.

The invention provides an enzyme linked immunosorbent assay kit for detecting nitroimidazole drugs. The kit comprises an enzyme labeling plate coated with metronidazole coupling antigen, enzyme labeling antiantibody working solution, specific antibody working solution of the nitroimidazole drugs, metronidazole standard substance solution, substrate developing solution, stop solution, concentrated washing solution and redissolving solution. The invention further discloses a method for detecting the nitroimidazole drugs by utilizing the enzyme linked immunosorbent assay kit. The method comprises the following steps of: firstly, carrying out sample preprocessing; secondly, carrying out detection by utilizing the kit; and thirdly, analyzing a detection result. The enzyme linked immunosorbent assay kit provided by the invention can be used for detecting the content of the nitroimidazole drugs in a honey sample, is simple and convenient to operate, is low in cost, can realize on-site monitoring and is suitable for screening of a large number of samples.

The present invention provides an enzyme-linked immunoassay kit for chloramphenicol detection. The enzyme-linked immunoassay kit comprises an enzyme label plate coated with coating antigen, an enzyme marker, a specific chloramphenicol antibody working solution (when the enzyme label plate is coated with antigen and the enzyme marker is enzyme-labeled anti-antibody or the enzyme label plate is coated with anti-antibody and the enzyme marker is enzyme-labeled antigen, the kit contains the specific chloramphenicol antibody working solution), chloramphenicol standard solutions, a substrate coloration solution, a termination solution, a concentration washing solution and a concentration reconstituted solution. The present invention further discloses a method for detecting chloramphenicol by using the enzyme-linked immunoassay kit. The method comprises: carrying out a sample pretreatment, adopting the kit to detect, and finally analyzing a detection result. With the enzyme-linked immunoassay kit, chloramphenicol residue in animal tissues (muscles, livers and the like), delicatessen, aquatic products, royal jelly, urine, feeds, milk and other samples can be detected, characteristics of simple operation, low cost and high sensitivity are provided, and the kit and the method can be applicable for screening and on-site monitoring of a large number of samples.

The invention provides an enzyme-linked immunosorbent assay kit for detecting diazepam. The enzyme-linked immunosorbent assay kit comprises an ELISA (Enzyme Linked Immunosorbent Assay) plate coated with a diazepam coupled antigen, a diazepam monoclonal antibody, an enzyme-labeled anti-antibody, a diazepam standard product solution, a substrate color developing solution, a stopping solution, a washing solution and a dissolution solution. The invention further discloses a method for utilizing the enzyme-linked immunosorbent assay kit to detect the diazepam. The method comprises the following steps: firstly, pre-treating a sample; secondly, detecting by utilizing the kit; finally, analyzing a detection result. The enzyme-linked immunosorbent assay kit provided by the invention can be used for detecting the content of the diazepam in animal tissues, urine, feed and water, is simple and convenient to operate, low in cost and high in sensitivity, can be monitored in field and is suitable for screening a lot of samples.

The invention provides a swine fever and porcine pseudorabies bivalent vaccine. The swine fever and porcine pseudorabies bivalent vaccine contains at least one swine fever virus antigen and at least one porcine pseudorabies virus antigen, wherein the two antigens coordinate well, are excellent in immune effect and can promote each other. The swine fever and porcine pseudorabies bivalent vaccine is simple in preparation method, is convenient and efficient in immunization and has the advantages that immunization cost is reduced, an immunization procedure is simplified and economy and reliability are realized compared with a vaccine which can be used for preventing and treating more than two diseases only when immunization is carried out in steps and at least two injections are taken and an immune method of the vaccine in the prior art. The immune effect of the swine fever and porcine pseudorabies bivalent vaccine is better than that of a single vaccine and better in safety and avoids adverse effects caused by multiple immunizations. Besides, the invention also provides a simple testing method for determining swine fever effect in the bivalent vaccine by adopting an indirect immunofluorescence method, so that quality of bivalent live vaccines in each batch is guaranteed, and economic benefit is obviously increased.

The invention discloses an enzyme immunity test agent box for testing the apurone drug, which comprises: an enzyme mark plate that coated by coat source; enzyme mark matter; apurone specific antibody working solution (when the enzyme mark plate is coated by antibody and the enzyme mark matter is the enzyme mark antibody or the enzyme mark plate is coated by the anti antibody and the enzyme mark matter is the enzyme mark antigen); apurone standard solution; base color display solution; stop solution; concentrated washing solution; and concentrated compound solution. The invention also discloses a method for using said agent box to test apurone, which comprises: processing pretreatment on the sample; then using test box to test; at last analyzing the test result. The inventive agent box can be used to test the left amount of apurone in chicken and shrimp, etc, with simple operation, lower cost, and high sensitivity.

The invention provides a color upper conversion nano material and method for preparation, wherein the nano material comprises one or more ground substance selected from the oxide and inorganic salt of yttrium, gadolinium and lanthanum, one or more activating agents selected from the oxide and inorganic salt of yttrium and thulium, one or more coactivator selected from the oxide and inorganic salt of erbium, holmium, cerium, praseodymium and magnesium, the granularity of the material is 50-900 nm. The nano material provided by the invention has strong stableness, it is easy to integrate with biochemical antibody, thus can be utilized for the quick detection of various viruses and bacteria.

The invention discloses an electrochemically active strain separating method and an electrochemical activity detecting method, relates to microorganism separating and detecting methods, and solves the problems that separating culture mediums of electrochemically active strains have simple nutrition, are unfavorable for the growth of the electrochemically active strains, and has low electrochemical activity and success ratio of the separated strains, complex detecting operations of electrochemical strain activity and long filtering period. The separating method comprises the steps of: (1) accumulation cultivation, (2) doubling dilution, (3) Hungate rolled tube separation and (4) electrochemically active strain purification. A circular voltammetry method is adopted for detecting electrochemical strain activity. A liquid culture medium of the electrochemically active strain separating method has abundant nutrition, favorable growth of the electrochemically active strains, very intuitive strain size and morpha observation and high separating success ratio; and the circular voltammetry method adopted for detecting the electrochemically active strains has simple operations and shortened filtering period.

The invention relates to the method and the system to check the fake of the electronic label video which can insert the electronic label information in the video. It can do with many different videos in a short time and many kinds of different label information. The system can search the real figure information of the goods in the production or circulation process by the electronic label information. The system supports the local search and the network search; also it has the function of fuzzy search. So it can improve the authenticity, the visibility and accurate of checking the goods and help the people to intensify the consciousness of anti fake.