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31results about How to "Eliminates washing steps" patented technology

Method for extracting total DNAs of soil microorganisms at high purity

The invention discloses a method for extracting total DNAs of soil microorganisms at high purity. CTAB (Cetyltrimethyl Ammonium Bromide), lysozyme, protease and SDS (Sodium Dodecyl Sulfonate) act together to perform lysis of cells and simultaneously freeze and thaw the cells repeatedly; therefore, an excellent cell lysis effect is achieved; the humic acid is removed by utilizing PVP (Polyvinyl Pyrrolidone), CaC12 and BSA (Bull Serum Albumin); and the DNAs are precipitated by utilizing isopropanol so that the purity of the obtained DNAs is high. The method is simple and convenient; and without being purified, the DNAs obtained by the method can be used for subsequent PCR (Polymerase Chain Reaction) analysis and DGGE (Denaturing Gradient Gel Electrophoresis) analysis. The purity of the extracted DNAs meets the requirement for directly performing subsequent molecular biological research; the extracted DNA segments can be subjected to 16SrDNA amplification and DGGE atlas analysis; glue cutting recovery and basic group sequencing can be performed on specific stripes of the DGGE band; unknown bacteria can be identified through comparison with the conventional sequences in an RDP (Ribosomal Database Project) database or by establishing a new sequence probe; and therefore, the structural composition of the microbial community can be determined, and a foundation can be laid for researching the structural diversity and ecological functions of the soil microorganisms in the rhizosphere of the mulberry in future.
Owner:INST OF ECONOMIC CROP HUBEI ACADEMY OF AGRI SCI

Method for extracting total DNA (deoxyribonucleic acid) of mulberry rhizosphere soil microorganisms by adopting plurality of measures

The invention discloses a method for extracting total DNA (deoxyribonucleic acid) of mulberry rhizosphere soil microorganisms by adopting a plurality of measures, which can achieve a good cell lysis effect by utilizing PVP (polyvinyl pyrrolidone) prewashing to remove humic acid, the synergy of CTAB (cetyltrimethyl ammonium bromide), lysozyme, protease and SDS (sodium dodecyl sulfate) to lyse cells and repetitively freezing and thawing the cells at the same time and utilizes PEG8000 to precipitate DNA, so that the purity of the obtained DNA is high. The adopted method is simple and convenient, and the DNA can be used in subsequent PCR (Polymerase Chain Reaction) analysis and DGGE (denaturing gradient gel electrophoresis) analysis without needing to be purified. The extracted DNA is so pure as to meet the requirement of direct subsequent molecular biology research, an extracted DNA fragment can be used in the amplification and DGGE map analysis of 16SrDNA, moreover, the specific band gel extraction and base sequencing of a DGGE band can be carried out, comparison with the sequence existing in an RDP (ribosomal database project) database can be carried out, or a new sequence probe can be established to identify unknown bacteria, so that the composition of a microbial community structure can be determined, and thereby laying a foundation for the future research of the community structure diversity and the ecological functions of the mulberry rhizosphere soil microorganisms.
Owner:INST OF ECONOMIC CROP HUBEI ACADEMY OF AGRI SCI

Method for extracting total DNAs of soil microorganisms through PVP pretreatment

The invention discloses a method for extracting total DNAs (Deoxyribonucleic Acid) of soil microorganisms through PVP (Polyvinyl Pyrrolidone) pretreatment. Humic acid is removed through PVP pre-washing; CTAB (Cetyltrimethyl Ammonium Bromide), lysozyme, protease and SDS (Sodium Dodecyl Sulfonate) act together to perform lysis of cells and simultaneously freeze and thaw the cells repeatedly; therefore, an excellent cell lysis effect is achieved; and the DNAs are precipitated by utilizing isopropanol so that the purity of the obtained DNAs is high. The method is simple and convenient; and without being purified, the DNAs obtained by the method can be used for subsequent PCR (Polymerase Chain Reaction) analysis and DGGE (Denaturing Gradient Gel Electrophoresis) analysis. The purity of the extracted DNAs meets the requirement on directly performing subsequent molecular biological research; the extracted DNA segments can be subjected to 16SrDNA amplification and DGGE atlas analysis; glue cutting recovery and basic group sequencing can be performed on specific stripes of the DGGE band; and unknown bacteria can be identified through comparison with the conventional sequences in an RDP (Ribosomal Database Project) database or by establishing a new sequence probe; and therefore, the structural composition of the microbial community can be determined, a foundation can be laid for researching the structural diversity and ecological functions of the soil microorganisms in the rhizosphere of the mulberry in future.
Owner:INST OF ECONOMIC CROP HUBEI ACADEMY OF AGRI SCI

Preparation method of lithium ion battery positive electrode composite material and precursor thereof

The invention discloses a preparation method of a lithium ion battery positive electrode composite material and a precursor thereof, and in particular relates to a novel method for preparing a high-purity low-cost binary or ternary precursor and preparing a high-performance lithium ion battery binary or ternary positive electrode composite material by utilizing the precursor, belonging to the technical field of new energy materials and the preparation thereof. The method comprises the following specific steps: (1) putting salt-type solid raw materials of two or three of nickel, cobalt and manganese with crystal water into a reactor, and heating the materials to the molten state; (2) introducing ammonia under the protection of inert gas, supplementing a small amount of water or no water according to the solubility of salts at different temperatures, stirring and reacting; (3) evaporating ammonium salt after full reaction, taking the solid out, and drying so as to get the amorphous binary or ternary positive electrode composite material precursor; and (4) mixing the precursor with lithium carbonate according to a certain ratio, and further preparing the lithium ion battery positive electrode composite material through a two-section sintering method. The precursor synthetic method is simple, sodium hydroxide is avoided from being used, separation and purification are not required, and the high-purity positive electrode composite material precursor which has no impurities basically can be obtained; furthermore, no industrial waste water is discharged, and the by-product ammonium salt can further generate economic benefit; and the positive electrode composite material prepared by the precursor has excellent performances, and is convenient for industrialization.
Owner:CENT SOUTH UNIV

Method for total DNA extraction and diversity analysis of ship ballast water microorganisms

The invention discloses a method for total DNA extraction and diversity analysis of ship ballast water microorganisms. The method comprises the steps that according to the characteristics of ship ballast water, two-level filtering and refrigerating fixation is performed by using millipore filtration membranes of 3 micrometers and 0.22 micrometer, and adhering of the microorganisms to the filtration membranes is reinforced; the microorganisms are processed by using cetyltrimethyl ammonium bromide (CTAB) to enable the total DNA purity of the obtained microorganisms to meet the requirements of directly performing subsequent molecular biology study; 16SrDNA amplification and denaturing gradient gel electrophoresis (DGGE) can be performed on extracted DNA fragments, and the diversity degree of ship ballast water microorganism populations can be judged after digitalization analysis is performed on electrophoretogram; the varieties of dominant bacterial populations of the ballast water is obtained by performing rubber tapping recovering, clone sequencing and BLAST sequence alignment on special bands, and therefore the structual components of the microorganism populations are determined. According to the method, a basis is laid for studying the diversity and ecological function of the microorganisms in the ship ballast water and sediment.
Owner:SHANGHAI OCEAN UNIV

A New Method for Detection of Immune Complexes by Size-Exclusion Chromatography

ActiveCN110082526BAvoid the disadvantage of insufficient out-of-phase reactionEliminates washing stepsMaterial analysisAssayImmune complex deposition
The invention discloses a new method for detecting immune complexes by size-exclusion chromatography, which adopts a double-antigen or double-antibody sandwich method for detection, and specifically includes the following steps: 1) selecting carrier particles, and coating the surface of the carrier particles with detection antigen / Antibody, label the paired antigen / antibody with a marker; 2) Add the carrier particles coated with the detection antigen / antibody, the antigen / antibody with the marker, and the sample to be tested into the reaction container at the same time; 3) Incubation and centrifugation; 4) Detected by a detector. Compared with traditional ELISA and CLIA, the new method of size exclusion chromatography detection of immune complexes of the present invention saves washing steps, is easy to operate, and shortens the detection time; antigen and antibody belong to the same phase reaction in the microcolumn cavity, and the reaction is sufficient , to avoid the shortcomings of insufficient heterogeneous reaction of ELISA; compared with MGIA, the use of fluorescent and other immunolabeling assays amplifies the signal, greatly improves the sensitivity, and has a wider range of applications.
Owner:SUZHOU INST OF BIOMEDICAL ENG & TECH CHINESE ACADEMY OF SCI

Precise immunosensing method with adjustable linear range and portable biological resistance sensing measurement device

The invention relates to an accurate immune sensing method with an adjustable linear range and a portable biological resistance sensing measurement device.The detection device comprises a detection pipeline, one end of the detection pipeline is connected with a vacuum pump through threads, a liquid suction head is arranged at the other end of the detection pipeline, a micro-channel is formed in the detection pipeline, and a battery is arranged on the side face of the detection pipeline; the battery provides power for the concentration measurement module, two detection electrodes are arranged in the measurement module and connected to the two sides of the micro-channel respectively, a kit is arranged in the joint of the detection pipeline and the gun head, and a vibration device is arranged on the detection pipeline on the outer side of the kit. According to the present invention, the detection limit linear range is adjustable, the sensitivity is high, the stability is good, the detection cost is low, and the detection speed is fast; high pressure generated by the vacuum pump is matched with filtration of the microporous filter membrane, so that the problems of blockage of large-particle non-to-be-detected substances in the microchannel and adsorption, aggregation and blockage of to-be-detected substances in the microchannel can be well solved.
Owner:HUAZHONG AGRI UNIV

Process for producing white carbon black/solution polymerized butadiene styrene rubber nano-composite material

InactiveCN101220177BImprove methodAchieving co-agglomeration and compoundingSolventSilicon dioxide
The invention relates to a method for preparing a white carbon black / solution-polymerized styrene-butadiene rubber nano composite material. In the invention, nano white carbon black powder and silanecoupling agent are fully mixed and condensation reaction is carried out at high temperature, organic modified nano white carbon black powder is obtained and added into solution-polymerized styrene-butadiene; the mixture of the white carbon black powder and solution-polymerized styrene-butadiene is stirred and removes solvent and then dried, thus obtaining the silicon dioxide / solution-polymerized styrene-butadiene rubber nano composite material prepared by co-polymerization. The invention expands the range of methods for preparing the nano composite material with solution composition. The adopted method using the organically modified white carbon black is simple and easy for operation and the solution composite technique is fast and convenient with low cost. The prepared co-polymerized rubber can be taken as master batch and is added with the white carbon black or added with other fillings for preparing novel nano composite material. The physical and mechanical properties and dynamic mechanical property of the rubber prepared by the method are better than the properties of coordinative amount of filling prepared by mechanical mixing method and the composition speed of subsequent fillings of the rubber prepared by the method is faster than that prepared by the mechanical method.
Owner:BEIJING UNIV OF CHEM TECH

Exclusion chromatography detection new method of immune complex

ActiveCN110082526AAvoid the disadvantage of insufficient out-of-phase reactionEliminates washing stepsMaterial analysisImmune complex depositionImmune complex
The invention discloses an exclusion chromatography detection new method of an immune complex. A double antigen or double antibody sandwich method is used to carry out detection. The method comprisesthe following steps of 1) selecting carrier particles, coating detection antigens / antibodies on a surface of the carrier particles, and marking the paired antigens / antibodies with markers; 2) simultaneously adding the carrier particles coated with the detection antigens / antibodies, the antigens / antibodies with the markers, and a sample to be tested to a reaction container; 3) incubating and centrifuging; and 4) detecting through a detector. Compared with traditional ELISA and CLIA, in the exclusion chromatography detection new method of the immune complex, a washing step is omitted, operationis simple and detection time is shortened. The antigens and antibodies belong to a same phase reaction in a microcolumn cavity, the reaction is sufficient so as to avoid a disadvantage of an insufficient ELISA heterogeneous reaction. Compared with MGIA, fluorescence and other immunolabeling verification is performed, a signal is amplified, sensitivity is greatly increased and an application rangeis wide.
Owner:SUZHOU INST OF BIOMEDICAL ENG & TECH CHINESE ACADEMY OF SCI

Method for extracting total DNAs of soil microorganisms at high purity

The invention discloses a method for extracting total DNAs of soil microorganisms at high purity. CTAB (Cetyltrimethyl Ammonium Bromide), lysozyme, protease and SDS (Sodium Dodecyl Sulfonate) act together to perform lysis of cells and simultaneously freeze and thaw the cells repeatedly; therefore, an excellent cell lysis effect is achieved; the humic acid is removed by utilizing PVP (Polyvinyl Pyrrolidone), CaC12 and BSA (Bull Serum Albumin); and the DNAs are precipitated by utilizing isopropanol so that the purity of the obtained DNAs is high. The method is simple and convenient; and without being purified, the DNAs obtained by the method can be used for subsequent PCR (Polymerase Chain Reaction) analysis and DGGE (Denaturing Gradient Gel Electrophoresis) analysis. The purity of the extracted DNAs meets the requirement for directly performing subsequent molecular biological research; the extracted DNA segments can be subjected to 16SrDNA amplification and DGGE atlas analysis; glue cutting recovery and basic group sequencing can be performed on specific stripes of the DGGE band; unknown bacteria can be identified through comparison with the conventional sequences in an RDP (Ribosomal Database Project) database or by establishing a new sequence probe; and therefore, the structural composition of the microbial community can be determined, and a foundation can be laid for researching the structural diversity and ecological functions of the soil microorganisms in the rhizosphere of the mulberry in future.
Owner:INST OF ECONOMIC CROP HUBEI ACADEMY OF AGRI SCI
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