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30results about How to "Complete three-dimensional structure" patented technology

Monoamine oxidase activity determination method and monoamine oxidase diagnostic kit

The invention relates measuring method of monoamine oxidase activity and its diagnostic kit. The invention comprises the following steps: using the monoamine oxidase to hydrolyze benzylamine, p-toluidine red-ª‰-azo naphthol, butyl amine, amyl amine, ª‰-phenylethylamine, tyramine and other aminated compounds to produce the ammonia, then the ammonia carried out coupling reaction with glutamate dehydrogenase to turn the oxidation type coenzyme to reduction type coenzyme, detecting the reducing velocity of absorbance of main wavelength 340nm to reflect the activity of monoamine oxidase in sample by definite quantity. The method has high specificity and good accuracy. The diagnostic kit is made to double agents or tri-agent to reduce the across impact and keep the agent stability and be good for long term storage. The method can be rapidly detected by the ultra-violet / visible light analysis meter or semi-automatic / full-automatic biochemical analysis meter, so the method is easy to spread and use.
Owner:SUZHOU ANJ BIOTECHNOLOGY CO LTD

Monoamine oxidase activity determination method and monoamine oxidase diagnostic kit

The invention relates measuring method of monoamine oxidase activity and its diagnostic kit. The method comprises the following steps: carrying out reaction with benzylamine, tyramine and monoamine oxidase to produce the hydrogen dioxide, then taking it with peroxidase to carry out enzyme coupling reaction, oxygenizing the achromatic color reduction type chromogen to become the quinone imines chromogen or indamine chromogen dye, detecting the change of absorbance of main wavelength 400-600nm to reflect the activity of monoamine oxidase in sample by definite quantity. The method has high specificity and good accuracy. The diagnostic kit is made to double agents or tri-agent to reduce the across impact and keep the agent stability and be good for long term storage. The method can be rapidly detected by the ultra-violet / visible light analysis meter or semi-automatic / full-automatic biochemical analysis meter, so the method is easy to spread and use.
Owner:SUZHOU ANJ BIOTECHNOLOGY CO LTD

Determination of magnesium ion content from enzyme method and magnesium ion diagnostic reagent kit

The invention is about the enzyme method of measuring magnesium ion and its diagnosis reagent box. Making use of the peculiarity that magnesium ion in the sample of plasma or serum and so on can activate the activation of glycerokinase, and producing glycerol-3-phosphoryl by reacting glycerol under the existence of adenosine triphosphate, and then causing coupled reaction with glycerol-3-phosphoryl dehydrogenase, hydroperoxide enzyme and aldehyde dehydrogenase and transferring oxidized coenzyme to reduced coenzyme. Testing the ascending range of dominant wave-length 340nm absorbance and finally measuring the content of magnesium ion in the sample. This method has high specificity and would not be contaminated by material of internal and exogenous sources, and the result is precise and accurate. Diving the diagnosis reagent box into double-dose or three-dose can reduces the cross interaction of each element, keeps the stability of the reagent and deposits chronically. Using this method can realize the fast testing in common ultraviolet / visible light analyzer or semiautomatic / automatic analyzer and doesní»t require special or additional apparatus, so the cost is low. Thus, this method can be easily promoted and applied in the whole industry.
Owner:SUZHOU ANJ BIOTECHNOLOGY CO LTD

Determination of magnesium ion content from enzyme method and magnesium ion diagnostic reagent kit

The invention is about the enzyme method of measuring magnesium ion and its diagnosis reagent box. Making use of the peculiarity that magnesium ion in the sample of plasma or serum and so on can activate the activation of glycerokinase, and producing glycerol-3-phosphoryl by reacting glycerol under the existence of adenosine triphosphate, and then causing coupled reaction with glycerol-3-phosphoryl dehydrogenase, peroxidase and oxidating the colorless reduced chromogen combination to quinoneimine chromogen or indamide chromogen dyer with color, testing the ascending range of 400ú¡600nmabsorbance and finally measuring the content of Inorganic Phosphates This method has high specificity and would not be contaminated by material of internal and exogenous sources, and the result is precise and accurate. Diving the diagnosis reagent box into double-dose or three-dose can reduces the cross interaction of each element, keeps the stability of the reagent and deposits chronically. Using this method can realize the fast testing in common ultraviolet/ visible light analyzer or semiautomatic/automatic analyzer and doesní»t require special or additional apparatus, so the cost is low. Thus, this method can be easily promoted and applied in the whole industry.
Owner:SUZHOU ANJ BIOTECHNOLOGY CO LTD

Preparation method and application of dopamine/calcium phosphate hybrid micron flower

The invention provides a preparation method and application of a dopamine / calcium phosphate hybrid micron flower. The diameter of the dopamine / calcium phosphate hybrid micron-flower material is 3-10 microns, the dopamine / calcium phosphate hybrid micron-flower material is composed of regular porous nanosheets with the thickness of about 20 nanometers and the width of about 300-800 nanometers, and the dopamine / calcium phosphate hybrid micron-flower material has a complete three-dimensional structure, an extremely high specific surface region and high porosity. The material can be used as a drug carrying material or a drug carrier for preparing a drug delivery system. The drug delivery system has high drug loading rate, and can controllably release drugs under different pH conditions.
Owner:INST OF CHEM CHINESE ACAD OF SCI

Determination of inorganic phosphorus and its diagnostic reagent kit

The invention is about the measuring method of Inorganic Phosphates and its diagnosis reagent box. Producing carbon dioxide by reacting pyruvate oxidase with pyruvate under the activation ofInorganic Phosphates in the sample of plasma or serum and so on, and producing oxaloacetic acid by reacting carbon dioxide and phosphoenolpyruvate under the existence of phosphoenolpyruvate carboxylase, and then transferring oxidized coenzyme to reduced coenzyme by reacting oxaloacetic acid and malic acid dehydrogenase. Testing the descending range of dominant wave-length340nm absorbance and finally measuring the content of Inorganic Phosphates. This method has high specificity and would not be contaminated by material of internal and exogenous sources, and the result is precise and accurate. Diving the diagnosis reagent box into double-dose or three-dose can reduces the cross interaction of each element, keeps the stability of the reagent and deposits chronically. Using this method can realize the fast testing in common ultraviolet/ visible light analyzer or semiautomatic/automatic analyzer and doesní»t require special or additional apparatus, so the cost is low. Thus, this method can be easily promoted and applied in the whole industry.
Owner:SUZHOU ANJ BIOTECHNOLOGY CO LTD

Determination of magnesium ion content from enzyme method and magnesium ion diagnostic reagent kit

The invention is about the enzyme method of measuring magnesium ion and its diagnosis reagent box. Making use of the peculiarity that magnesium ion in the sample of plasma or serum and so on can activate the activation of hexokinase, and producing glucose-6-phosphate by reacting glucose under the existence of adenosine triphosphate, and then causing coupled reaction with phosphoglucose dehydrogenase, 6-phosphogluconic acid lactone enzyme and phosphogluconate dehydrogenase, and transferring dimolecule oxidized coenzyme to dimolecule reduced coenzyme. Testing the ascending range of dominant wave-length340nm absorbance and finally measuring the content of magnesium ion in the sample. This method has high specificity and would not be contaminated by material of internal and exogenous sources, and the result is precise and accurate. Diving the diagnosis reagent box into double-dose or three-dose can reduces the cross interaction of each element, keeps the stability of the reagent and deposits chronically. Using this method can realize the fast testing in common ultraviolet / visible light analyzer or semiautomatic / automatic analyzer and doesní»t require special or additional apparatus, so the cost is low. Thus, this method can be easily promoted and applied in the whole industry.
Owner:SUZHOU ANJ BIOTECHNOLOGY CO LTD

Determination of inorganic phosphorus and its diagnostic reagent kit

The invention is about the measuring method of Inorganic Phosphates and its diagnosis reagent box. Producing hypoxanthine by reacting nucleoside phosphorylase with carnine under the activation ofInorganic Phosphates in the sample of plasma or serum and so on, and producing hydroperoxide by reacting hypoxanthine and xanthine oxidase, and producing acetaldehyde by reacting hydroperoxide with alcohol under the existence of hydroperoxide enzyme, and then transferring oxidized coenzyme to reduced coenzyme by reacting acetaldehyde and aldehyde dehydrogenase. Testing the ascending range of dominant wave-length340nm absorbance and finally measuring the content of Inorganic Phosphates. This method has high specificity and would not be contaminated by material of internal and exogenous sources, and the result is precise and accurate. Diving the diagnosis reagent box into double-dose or three-dose can reduces the cross interaction of each element, keeps the stability of the reagent and deposits chronically. Using this method can realize the fast testing in common ultraviolet / visible light analyzer or semiautomatic / automatic analyzer and doesní»t require special or additional apparatus, so the cost is low. Thus, this method can be easily promoted and applied in the whole industry.
Owner:SUZHOU ANJ BIOTECHNOLOGY CO LTD

An administer orally mixed nucleus glycosides as well as its preparing technics

The invention belongs to the biology and pharmaceutical technical field, and relates to oral mixed nucleoside and the preparation process thereof. The invention mainly provides the oral mixed nucleoside and the preparation process thereof in order to overcome the problems existing in the prior art that the spatial structure of the product is damaged to a certain degree, the production cycle is longer, the operation is difficult, and the integrated cost is high. In order to overcome the problems existing in the prior art, the invention has the technical proposal that the oral mixed nucleoside is obtained through the following preparation processes, and the preparation processes comprise the steps that step one, malt roots are prepared; step two, pre-treatment: the malt roots are extracted through water, and filtered, after being preheated, phosphatase liquid is added to be prepared to be used; step three, hydrolytic reaction: purified water is preheated, and ribonucleic acid is added into the purified water, the pH value is adjusted, the mixed fluid in the step two is added into the purified water, the pH value is adjusted again, and the purified water is insulated and reacts; stepfour, the fluid is inactivated, the pH value is adjusted, and the fluid is filtered; step five, the fluid is concentrated and dried.
Owner:西安万隆制药股份有限公司

Method for displaying three-dimensional structure of silicon-rich phase in aluminum-silicon coating by metallographic method

The invention belongs to the technical field of metal coating detection, and provides a method for displaying a three-dimensional structure of a silicon-rich phase in an aluminum-silicon coating by a metallographic method, which comprises the steps of sample preparation, chemical corrosion and microscope observation, and specifically comprises the following steps: (1) sample preparation: taking an aluminum-silicon coating steel plate, cutting a part of the aluminum-silicon coating steel plate as a sample, and then sequentially carrying out embedding and polishing treatment on the sample; (2) chemical corrosion: putting the sample prepared in the step (1) into a corrosive liquid for chemical corrosion, wherein the corrosive liquid is prepared from a hydrochloric acid aqueous solution and a sodium chloride aqueous solution; and (3) microscope observation: after the chemical corrosion is completed, washing and drying the sample, and observing by using a ZISS metallographic microscope. According to the method provided by the invention, a complete and clear three-dimensional structure of the silicon-rich phase can be obtained, the growth condition of the silicon-rich phase can be fully displayed, and the method has the characteristics of low detection cost, rapidness and simplicity.
Owner:TANGSHAN IRON & STEEL GROUP +1
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