90 results about "Ascorbate Oxidase" patented technology

A fuel cell is provided with an anode and a cathode. The anode is in electrical communication with an anode enzyme and the cathode is in electrical communication with a cathode enzyme. The anode enzyme is preferably an oxidase or a dehydrogenase. The cathode enzyme is a copper-containing enzyme, such as a laccase, an ascorbate oxidase, a ceruloplasmine, or a bilirubin oxidase. Preferably, the cathode enzyme is operable under physiological conditions. Redox polymers serve to wire the anode enzyme to the anode and the cathode enzyme to the cathode. The fuel cell can be very small in size because it does not require a membrane, seal, or case. The fuel cell can be used in connection with a biological system, such as a human, as it may operate at physiological conditions. By virtue of its size and operability at physiological conditions, the fuel cell is of particular interest for applications calling for a power source implanted in a human body, such as a variety of medical applications.

The invention provides an electrochemical uric acid test strip comprising an insulating substrate (1), a working electrode (2) and a counter electrode (3), wherein the working electrode (2) and the counter electrode (3) are arranged at a first end of the insulating substrate (1) side by side at an interval; the working electrode (2) is provided with an anti-interference reagent layer; the components of the reagent layer comprise an ascorbic acid oxidase, a macromolecular compound and a buffering solution; and the components of the working electrode (2) comprise a non-aqueous redox electron transfer mediator. The invention further provides a manufacturing method of the electrochemical uric acid test strip. The test strip provided by the invention utilizes the non-water-soluble electron transfer mediator and combines an interference-removing enzyme layer, so that the effect of removing ascorbic acid is obvious. In a test, the interference of the ascorbic acid on uric acid test is very small.

The invention discloses a detection kit for determining the content of creatinine in serum by an enzymic method. The detection kit comprises a reagent R1 and a reagent R2, wherein the reagent R1 contains 3-10g/L of buffering solution with the pH value being 7.5-8.0, 0.2-0.5g/L of EDTA, 0.5-2g/L of N-ethyl-N-(2-hydroxyl-3-sulfopropyl) m-toluidine sodium salt, 1 per mill-5 per mill of a surface active agent, 0.2-1g/L of sarcosine oxidase, 1-5KU/L of ascorbate oxidase, 2-5KU/L of creatinase and 0.5-1g/L of a stabilizing agent; the reagent R2 contains 3-10g/L of buffering solution with the pH value being 7.5-8.0, 0.1-0.5g/L of 4-aminoantipyrine, 0.1-0.4g/L of potassium ferricyanide, 2-8g/L of creatininase amidohydrolase, 1-6KU/L of peroxidase and 0.5-2g/L of a preservative. The detection kit disclosed by the invention is excellent in stability, strong in interference resistance and high in clinical application value.

The invention relates to a stable kit for measuring NEFA (non-esterified fatty acid) through an enzymic method. The kit comprises two separate liquid reagents, namely, a reagent 1 and a reagent 2 which are respectively placed, and is good in stability and anti-interference performance. The enzymic method is adopted to measure NEFA, and the method is easy, convenient and easy to operate. According to the kit, novel chromogen is selected, and anti-interference agents such as ascorbic acid oxidase and potassium ferrocyanide are added into the formula at the same time, so that the reagent has the characteristics of being high in sensitivity and anti-interference performance; a liquid stabilization technology is adopted, and a series of special stabilizers, chelating agents and enzymatic protective agents are added, so that the reagent is good in stability, and can be widely applied to most semi/full automatic biochemical analyzers, and used for monitoring human body fat metabolic status, lipid level, and the like, and clinical popularization is facilitated.

The invention discloses a detection kit for LDL (low-density lipoprotein) cholesterol and a use method of the detection kit, relates to the field of biochemical detection and aims to provide a detection kit, having high stability, accuracy and precision as well as low toxicity, for LDL cholesterol and a use method of the detection kit. The kit comprises a reagent 1 and a reagent 2, wherein the reagent 1 is prepared from a surfactant, polyethylene glycol, SDS (sodium dodecyl sulfate), Emulgen A9 series, CHOD (cholesterol oxidase), CHER (cholesterol esterase), ascorbic acid oxidase, CAT (catalase), 4-AAP (4-aminoantipyrine) and the like; the reagent 2 is prepared from octylphenyl polyethylene glycol, cholate, a compound stabilizer, bovine serum albumin, POD (peroxidase), TOPS (sodium 3-(N-ethyl-3-methylanilino)propanesulfonate) and the like. The proclin series added to the kit is a novel biological preservative, has good compatibility with various enzymes, better stability and low toxicity, and the stability of the reagents is maintained.

The invention discloses a detection reagent for triglyceride and test paper for the triglyceride. The detection reagent comprises 18-25KU/L lipoprotein lipase, 20-30KU/L glycerol kinase, 3-5KU/L glycerine triphosphate oxidase, 7.5-9.0KU/L horse radish peroxidase, 3-5KU/L ascorbic acid oxidase, 0.20-0.35g/L 4-amino-antipyrineand 0.2-0.30g/L color material. The detection reagent contains multiple specific enzymes for particular proportioning, so that the targets that detection is fast and relatively accurate are achieved. The test paper comprises a reaction base layer, a reaction layer, a blood filtering layer and a hydrophillic layer, and a siphon system is formed by superposing the reaction base layer, the reaction layer, the blood filtering layer and the hydrophilic layer, so that fast detection and relatively accurate detection are further ensured.

The invention discloses a total cholesterol detection reagent and total cholesterol detection paper. The total cholesterol detection reagent comprises 6-9 KU/L cholesterol esterase, 3-5 KU/L cholesterol oxidase, 15-20 KU/L horseradish peroxidase, 3-5 KU/L ascorbic acid oxidase, 0.20-0.35 g/L 4-ampyrone, and 0.20-0.30 g/L color-showing matter. The detection reagent contains a plurality of specific enzymes in a specific ratio, and can achieve the purposes of rapid detection and relatively accurate detection. The detection paper comprises a reaction base layer, a reaction layer, a blood filtering layer and a hydrophilic layer, which are overlapped to form a siphon system, thereby further ensuring rapid detection and relatively accurate detection.

The invention relates to the technical field of serum 5'-ribotide hydrolase detection, in particular to a serum 5'-ribotide hydrolase detection reagent. A PIPES buffer solution is adopted, and various stabilizers are added to remarkably improve the stability of the reagent; beta-sodium glycerophosphate, bilirubin oxidase and ascorbic acid oxidase are added to effectively prevent interference caused by alkaline phosphatase, cholerythrin and ascorbic acid and greatly enhance the anti-interference capability of the reagent. Besides, a preferred novel amphoteric surfactant, dodecyl dimethyl betaine (BS-12), is added to prevent a reaction system from turbidity, enhance the stability of a substrate and improve the anti-interference capability of the reagent.

The invention relates to an enzymic uric acid detection agent with high interference preventing capacity. The agent is characterized in that an agent R1 includes a buffering solution, 4-ampyrone, sodium nitrite, an ion balancing agent, ascorbic acid oxidase, a heavy metal ion chelator, bovine serum albumin, dodecyl trimethyl betaine, triton-305 and a preservative; an agent R2 includes a bufferingsolution, F-DAOS (N-ethyl-N-(2-hydroxyl-3-sulfopropyl)-3, 5-dimethoxy-4-fluoroaniline), uricase, bovine serum albumin, peroxidase, a preservative, and other components. The agent is high in interference preventing capacity and particularly capable of accurately detecting a sample of a newborn.

The invention relates to the field of serum direct bilirubin detection technologies, in particular to a serum direct bilirubin (oxidase method) detection reagent. A reagent R1 contains a buffer solution, sodium fluoride, NAC(N-acetylcysteine), sodium 4-methylbenzenesulfonate, lipase, ascorbic acid oxidase, alpha-cyclodextrin, sucrose, trehalose, PEG-6000, fatty alcohol polyoxyethylene ether (AEO-9) and a preservative; and a reagent R2 contains a buffer solution, bilirubin oxidase, sucrose, trehalose, PEG-6000, fatty alcohol polyoxyethylene ether (AEO-9) and a preservative. Through the reagent,the specificity and accuracy of direct bilirubin testing are obviously improved, turbidity of a reaction system can be prevented, a reaction is promoted, and the stability and interference resistanceof the reagent are further improved.

The invention relates to the technical field of serum phospholipid detection and particularly relates to a serum phospholipid detecting reagent. A reagent R1 comprises a buffer solution, phospholipase D, DAOS, ascorbic acid oxidase, bilirubin oxidase, polyethylene glycol 6000, cane sugar, xanthan gum, mannitol, trehalose, BSA, glycerol propoxylate-block-ethoxylate (Pluranic L64) and an aseptic. A reagent R2 comprises the buffer solution, 4-aminoantipyrine, peroxidase, choline oxidase, the polyethylene glycol 6000, the cane sugar, the xanthan gum, the mannitol, the trehalose, the BSA, the glycerol propoxylate-block-ethoxylate (Pluranic L64) and the aseptic. The HEPES buffer solutions and a novel Trinder reaction chromogen DAOS are adopted. A plurality of stabilizers are added to obviously improve stability of the detecting reagent. The bilirubin oxidase and the ascorbic acid oxidase are added, thus effectively avoiding interference caused by bilirubin and ascorbic acid and greatly improving interference-resisting capability of the detecting reagent. In addition, addition of the glycerol propoxylate-block-ethoxylate (Pluranic L64) which is an optional nonionic surfactant prevents reaction system turbidity, enhances substrate stability and improves the interference-resisting capability of the detecting reagent.

The invention relates to the field of reagent NAG detection technologies, in particular to an N-acetyl-beta-D glucosidase reagent. The reagent R1 contains a buffer solution, VRA-NAG, bovine serum albumin, TritonX-100, ethylene glycol, ascorbic acid oxidase and a preservative. The reagent R2 contains a buffer solution and a preservative. The reagent adopts a novel substrate VRA-NAG, the substrate has better solubility in water compared with other substrates, is good in stability and is a reliable NAG substrate. The reagent uses citric acid-disodium hydrogen phosphate as the buffer solution, the buffering capacity of the reagent is greatly improved, and meanwhile a reaction system is not destroyed. The added TritonX-100 and the ethylene glycol serve as cosolvents to promote dissolution of the substrate and have an obvious solubilization assisting effect. BSA is added to serve as a stabilizer, and the stability and anti-interference capability of the reagent are greatly enhanced. The N-acetyl-beta-D glucosidase reagent is simple in configuration and low in price and is very suitable for large-area clinic popularization.

The invention belongs to the field of urine analysis and detection, relates to urine glucose test paper capable of resisting ascorbic acid interference and a preparation method thereof and solves thetechnical problem of existence of ascorbic acid interference in the detection of urine glucose in an existing dry chemistry test paper. The urine glucose test paper capable of resisting ascorbic acidinterference is formed by a substrate and filter paper fixedly arranged on the substrate. The test paper is obtained by being immersed into immersion liquid consisting of a buffer solution, glucose oxidase, peroxidase, potassium iodide, ascorbic acid oxidase, anti-interference substance xanthan gum, a surfactant, an enzyme stabilizer and a blue dye substance, so that anti-VC interference capability of the glucose test paper with potassium iodide as the substrate can be significantly improved, and sensitivity and accuracy of the detection result are enhanced; and the glucose detection result isnot influenced when the content of the VC in the sample does not exceed 3.5mmol/L. The preparation method of the urine glucose test paper capable of resisting ascorbic acid interference is simple andeasy to operate, stable in performance and accurate in test result.

The invention discloses a boron-doping diamond film based ascorbic acid oxidase sensor electrode which is composed of a boron-doping diamond film, an amino monomolecular layer and an enzyme membrane layer. The preparation method of the ascorbic acid oxidase sensor electrode comprises the steps of: firstly, depositing a boron-doping diamond film on a tantalum sheet which is subjected to a surface pre-treatment by utilizing a hot filament CVD (Chemical Vapor Deposition) device; then performing amination modification on the boron-doping diamond film; and finally fixing the ascorbic acid oxidase on the surface of the ammoniated diamond film by adopting a chemical crosslinking way, wherein the electrode can be used on an electrochemical biosensor. The boron-doping diamond film based ascorbic acid oxidase sensor electrode, disclosed by the invention, has the advantages of having the limit of detection of 1*10-11 mol/L, and having high sensitivity, good reproducibility and long service life as the electrode inherits the advantages of corrosion resistance, extremely high oxygen evolution overvoltage, wide electric potential window, high electrochemical stability and the like of the diamond.

The invention provides a homocysteine detecting kit and a using method thereof, relates to the field of biochemical detection, and aims to provide a homocysteine detecting kit which is high in stability, high in accuracy and high in precision and a using method of the homocysteine detecting kit. The homocysteine detecting kit comprises a reagent 1 and a reagent 2, wherein the reagent 1 comprises a capso buffer solution, lactic dehydrogenase (LDH), L-serine, reduced coenzyme Thio-NADH, tris((2-carboxyethyl)phosphine, mercaptoethanol, an alkylphenol polyoxyethylene series, EDTA, polyethylene glycol 300, ascorbic acid oxidase, a composite stabilizer, and a proclin series preservative; and the reagent 2 comprises a capso buffer solution, cystathionine-beta-synthase, methionine synthase, cystathionine-beta-lyase, methionine-gamma lyase, a surfactant and sodium dodecylbenzene sulfonate. By the various added mixed enzymes and methionine-gamma lyases, the accuracy of the kit on detection of homocysteine can be improved.

The invention discloses a nano copper oxide with the activity of an ascorbic acid oxidization mimic enzyme, and aims at effectively catalyzing ascorbic acid oxidization to generate dehydroascorbic acid under aerobic environment and keeping the activity of the ascorbic acid oxidization mimic enzyme under strong acid, strong base or high temperature. By utilizing an ultraviolet spectrophotometry, the influences, on the nano copper oxide as ascorbic acid oxidase, of the temperature, pH and reaction time are respectively researched. The steady-state kinetic parameters of the nano copper oxide as the ascorbic acid oxidase are equivalent to the natural ascorbic acid oxidase, and the stability of the nano copper oxide as the ascorbic acid oxidase is obviously stronger than the natural ascorbic acid oxidase. By utilizing a deoxidization experiment and a fluorescence analysis method, a mechanism of the nano copper oxide as the ascorbic acid oxidase to catalyze ascorbic acid oxidization is verified. The activity of the ascorbic acid oxidization mimic enzyme shows a relatively tempting application prospect in the technical fields of nano enzymes, nanometers and bionic.

The invention discloses a direct bilirubin detection reagent. The direct bilirubin detection reagent comprises diluents and reaction reagents. The diluents comprise a buffer 1, a surfactant, an antiseptic and ascorbate oxidase. The reaction reagents comprise a buffer 2, common salt, disodium ethylene diamine tetraacetate, hydroxylamine sulphate, etidronic acid, sodium persulfate, sulfuric acid, an antiseptic and a freeze-drying protective agent. The direct bilirubin detection reagent has good sensitivity, accuracy, precision and linearity and can satisfy clinical examination requirements.

The invention provides a glutathione reductase determination kit, and a preparation method and applications thereof, and relates to the technical field of biochemical reagent determination. The kit includes a reagent R1 and a reagent R2; the reagent R1 includes a phosphate buffer solution, ascorbic acid oxidase, pyruvate oxidase, potassium ferrocyanide, oxidized glutathione, MgCl2, FAD, a preservative and a surfactant; and the reagent R2 includes a glycine buffer solution, NADPH, the preservative and a protective agent. Through the adding of EGTA and dithiothreitol in the reagents, the linearrange of the kit can be enlarged, and the stability of the kit can be enhanced. The preparation method and applications of the kit are also provided; and the kit can accurately determine glutathione reductase.

The invention discloses test paper for measuring high density lipoprotein cholesterol and a preparation method and application thereof. The test paper comprises a red blood cell separation layer, an auxiliary separation layer and a reaction layer, wherein the red blood cell separation layer, the auxiliary separation layer and the reaction layer are prepared from a separation material, a separationmembrane and a reaction membrane through carrying out steeping by red blood cell separation solution, auxiliary separation solution and reaction solution and then carrying out drying; the red blood cell separation solution comprises the following components: buffer salt, a divalent metal ion, dextran sulfate sodium salt with a molecular weight of 30000-500000, hemagglutinin or an Anti-RBC antibody; the auxiliary separation solution comprises the following components: buffer salt, a surfactant I and polyhydric alcohol; and the reaction solution comprises the following components: buffer salt,a surfactant II, polysaccharide, cholesterol esterase, cholesterol oxidase, peroxidase, ascorbic acid oxidase, an oxidizing substance and a color developing agent. The test paper is capable of simplyand rapidly detecting the contents of high density lipoprotein cholesterol. The invention furthermore provides a preparation method and application of the test paper.

The invention relates to a reagent for quantitatively detecting the content of free fatty acid in human serum. The reagent comprises a reagent I and a reagent II which are respectively placed, wherein the reagent I comprises sodium dihydrogen phosphate, disodium hydrogen phosphate, magnesium chloride, fatty acyl-coenzyme A synthetase, ascorbic acid oxidase, coenzyme A, ATP and 4-aminoantipyrine, and the reagent II contains sodium dihydrogen phosphate, disodium hydrogen phosphate, phenoxy ethanol, fatty acyl-coenzyme A oxidase, peroxidase, chromogen and a surfactant. The kit and the detection method only need dozens of microlitres of serum without centrifugal or electrophoresis and other separation treatments, are simple and convenient to operate, can be used for meeting the requirement of full-automatic analysis, and are suitable for timely accurate detection of large-scale samples.

The invention discloses an application of ascorbic acid oxidase RIP5 to regulating and controlling of drought resistance of rice. An RIP5 gene knockout mutant is constructed by targeted mutation of anRIP5 gene through a GRISPR/Cas9 system, and the inventor finds that the drought resistance of plants can be effectively improved by inhibiting the expression quantity and/or activity of the RIP5 protein, that is, the ascorbic acid oxidase gene RIP5 of rice can negatively regulate and control the drought resistance of the plants. The invention also provides a gRNA target sequence for editing the ascorbic acid oxidase gene RIP5 of the rice, and the gRNA target sequence cooperates with a CRISPR/Cas9 gene editing system to realize targeted mutation of the coding gene of the RIP5 protein, so thatthe drought resistance of the rice can be regulated and controlled. The research of the invention provides new gene targets and resources for drought resistance genetic breeding of the plants, and knockout mutant plants obtained by editing the gene have important application value.