Patents
Literature
Patsnap Copilot is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Patsnap Copilot

77results about How to "Increase fixed amount" patented technology

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

Electrochemical immune sensor for phosphating protein

The invention relates to an electrochemical immune sensor for phosphating protein. In the electrochemical immune sensor, a magnetic nanometer-antibody composition MPs-p53<15>Ab1 is used as an adsorbent to separate the phosphating protein, a carbon nanometer sphere CNS is used as a carrier, lead phosphate-apoferritin (LPA) and a phosphating protein antibody p5315Ab2 are modified on the surface of the CNS, and thus, LPA-p53<15>Ab2-CNS nanometer complexing agent is prepared for detecting signal amplification. According to the sandwich immunoassay principle, the content of the phosphating protein to be detected is in proportion to the captured LPA-p5315Ab2-CNS, and the content of lead ions encapsulated in LPA is detected according to a dissolving volt-ampere method to measure the concentration of the phosphating protein in a sample. The method has the advantages of simplicity and convenience for operation and simple and efficient separation, and the advantage that an integral immunologic reaction is finished in an epoxy (EP) tube; a large number of LPA signal molecules are introduced by taking the CAN as the carrier, and each LPA molecule contains a large number of Pb<2+>, so the sensitivity of detection is improved; and the dissolved Pb<2+> is used as a detection signal without adding an enzyme substrate, so the electrochemical immune sensor is a reagent-free sensor. In the electrochemical immune sensor for the phosphating protein, the linear concentration range of the phosphating protein phosphor-p53<15> is from 0.02 to 20 ng mL<-1>, and the detection limit is 0.01 ng mL<-1>.
Owner:HUAZHONG NORMAL UNIV

Paper element micro-fluidic chip proteolysis reactor and preparation method thereof

InactiveCN104911101AAchieving covalent bond immobilizationLow costLaboratory glasswaresEnzyme production/based bioreactorsFiberEngineering
The invention belongs to the technical field of a micro-fluidic chip, and particularly relates to a paper element micro-fluidic chip proteolysis reactor and a preparation method thereof. The preparation method comprises the following steps: cutting a piece of filter paper into strips or a needed shape, wetting the filter paper, then adhering the filter paper onto a thermoplastic transparent plastic sheet which is cut into the size of a chip, airing the filter paper, covering the filter paper with a piece of plastic sheet in the same size with solution connection holes, and clamping the filter paper between two glass sheets, and then pressing by utilizing a clamp; and heating for 5 to 15 minutes in a drying oven with temperature of 110 to 180 DEG C, encapsulating a paper element between two plastic sheets, and obtaining a paper element micro-fluidic chip with a paper fiber filling channel, wherein the width of the channel with the paper element is 0.5mm to 3mm; and then filling the channel with a periodic acid solution, oxidizing cellulose in the paper element into aldehyde groups, cleaning, and injecting such a protease solution as trypsin solution so as to fix the protease by covalent bonds to obtain a proteolysis micro-fluidic chip. The reactor is simple and convenient to process, short in enzymolysis time and small in sample dosage.
Owner:FUDAN UNIV

Microorganism sample rapid detection method and detection device thereof

The invention discloses a microorganism sample rapid detection method and a detection device thereof, which is realized by a mesoporous biochip. The detection method comprises the following steps: firstly fixing antibodies on micropore tunnel surfaces of a mesoporous biochip, allowing a test sample to flow through the chip micropore tunnels with the antibodies fixed so as to realize separation and enrichment of pathogenic microorganisms or other biological substances by the chip, then injecting a solution containing a fluorescence-labeled or an enzyme-labeled antibody into the chip micropore tunnel to form a sandwich-type antibody-antigen-labeled antibody immune complex, and detecting the pathogenic microorganisms or other biological substances by detecting the fluorescence intensity of the fluorescence-labeled antibody or the light absorption or chemiluminiscence intensity of the product of the enzymic catalytic reaction so as to realize the detection of the microorganisms to be detected. The mesoporous biochip has a great number of micropore tunnels, which greatly increases the reaction area, and thus when used for microorganism sample detection, the detection method and the detection device of the invention have the characteristics of high detection sensitivity and high detection speed.
Owner:SICHUAN UNIV

Inorganic carrier used for cell immobilization and immobilized nitrobacteria prepared by same

The invention provides a cheap inorganic porous adsorption carrier capable of being used for cell immobilization. Clay is fired to prepare the carrier; the carrier has the characteristics of porosity, high mechanical strength, stable properties, low price, large cell immobilization quantity and the like, is simple in cell immobilization operation, is non-toxic for microbial cells and can be reused; and the carrier can be used for industrial-scale cell immobilization. The carrier is used to immobilize nitrobacteria so as to prepare immobilized nitrobacteria used for converting ammonium in a water body to nitrate; and the conversion speed of the obtained immobilized nitrobacteria to ammonium is high, and the efficiency is high. The method for converting ammonium with the immobilized nitrobacteria comprises the following steps: the immobilized nitrobacteria are placed in a netted container, the netted container is placed in an ammonium sulfate solution or ammonium-containing water body, and after a certain time period, the immobilized nitrobacteria can convert ammonium to nitric nitrogen. The immobilized nitrobacteria in the netted container can be reused. After the immobilized nitrobacteria are respectively placed in a 5g/L ammonium sulfate solution and a 20g/L ammonium sulfate solution for 4h, the average conversion rates of ammonium nitrogen are respectively 79.7%-83.6% and 86.5%-86.7%. After being stored for half a year at 4 DEG C, the nitrification ability of the immobilized nitrobacteria is not reduced.
Owner:NORTHWEST A & F UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products