267 results about "Basic research" patented technology

The invention provides a photovoltaic active distribution network voltage out-of-limit problem tracing method comprising the following steps: receiving research data and carrying out multi-scale feature analysis to obtain a standardized multi-dimensional feature matrix and a time-space incidence matrix; constructing an initial causal graph based on basic research data and power grid physical constraints, and constructing a multi-layer causal network by calculating causal intensity; extracting a dynamic feature sequence, analyzing propagation features, and generating a propagation path set and a path weight matrix; performing tensor completion and state estimation on the research data to obtain a state estimation matrix and estimation uncertainty; and outputting an out-of-limit source position, an out-of-limit risk score and early warning information based on pattern matching analysis and risk assessment. According to the invention, through combination of multi-dimensional feature analysis and a multi-layer causal network, accurate positioning and risk early warning of a voltage out-of-limit source are realized, and traceability accuracy and analysis efficiency are improved.

The invention discloses a silver carp 20K liquid phase chip and application thereof, the liquid phase chip comprises a probe combination of 20,909 SNP molecular markers covering a whole genome, the physical positions of the 20,909 SNP molecular markers are determined based on sequence alignment of the silver carp genome (GCA041475455.1), and the site information of the 20,909 SNP molecular markers is shown in the specification table 1. The invention provides a silver carp first type whole genome SNP liquid phase breeding chip, which effectively reduces the application cost of silver carp in genetic diversity analysis, QTL positioning, GWAS analysis and the like in scientific research, solves the problem that no applicable product exists in silver carp molecular auxiliary breeding and whole genome selective breeding, accelerates the progress of silver carp basic research and breeding, and has a wide application prospect. The method is of great significance in improving the utilization efficiency of silver carp germplasm resources, accelerating the breeding process of excellent characters and improving the economic value and environmental adaptability of bred varieties.

The invention belongs to the technical field of microbial medicine, and provides a primary multidrug resistance human far-end bile duct cancer cell line CBC3T-6 Homo sapiens and application thereof.The human far-end bile duct cancer cell line CBC3T-6 Homo sapiens is separated from differentiated adenocarcinoma in a far-end bile duct, the human far-end bile duct cancer cell line CBC3T-6 Homo sapiens is already subcultured to 50 generations at present, the long-term in-vitro culture character is stable, and on the premise that the biological characteristics of bile duct cancer are reserved, the human far-end bile duct cancer cell line CBC3T-6 Homo sapiens can be used for preparing the primary multidrug resistance human far-end bile duct cancer cell line CBC3T-6 Homo sapiens. The compound has the characteristics of short multiplication time, high mouse subcutaneous tumor formation rate and the like, and has different degrees of drug resistance to gemcitabine, 5-fluorouracil, oxaliplatin and cis-platinum in first-line anti-cancer drugs for bile duct cancer. The method not only enriches an extrahepatic bile duct cancer cell bank, provides a new cell model for basic research and clinical drug research and development of bile duct cancer, but also provides powerful scientific research data for research developed based on the genetic background of Chinese population. Therefore, the primary multidrug resistant cell line has higher scientific research and clinical application values.

The invention belongs to the technical field of biological industry, and particularly relates to a spike protein antigen epitope peptide of porcine acute diarrhea syndrome coronavirus as well as a monoclonal antibody and application of the spike protein antigen epitope peptide. The invention provides an antibody or an antigen binding fragment thereof. A nucleotide sequence of a heavy chain variable region of the antibody or the antigen binding fragment thereof is as shown in SEQ ID NO. 2; the nucleotide sequence of the light chain variable region of the monoclonal antibody is shown as SEQ ID NO. 4. The amino acid sequence of the minimum binding epitope is as shown in SEQ ID NO.22. The antigen epitope is highly conserved in a plurality of different subtypes of SADS-CoV. The antibody can be applied to fundamental research on an SADS-CoV invasive molecular mechanism and provides a good scientific research material for application research on SADS-CoV detection and treatment.

The invention relates to the technical field of biological detection, in particular to a miniaturized portable fluorescence microplate reader for instant fluorescence detection, and aims to provide a fluorescence detection scheme which is portable, high in sensitivity and quick in response. The detector integrates an MCU microcontroller, a voltage conversion module, a light source driving module, a motor driving module, a photoelectric detection module, an AD sampling module, an automatic temperature control module based on a PID algorithm, a signal processing system and a data processing system. High-sensitivity and high-resolution detection of a fluorescent sample can be realized, the concentration of the sample can be detected in real time, and the change process of the concentration of the sample can be presented through a kinetic curve. Through the optimization of the structure, optics and electronic circuits, the instrument is more miniaturized and has portability. Due to the advantages of portability, high sensitivity, quick response and the like, the kit has wide application prospects in multiple fields of basic research of nucleic acid, gene expression, sequence analysis, transgenic detection and the like.

The invention discloses a flood process runoff monitoring method coupled with satellite remote sensing and hydrodynamics. The flood process runoff monitoring method comprises the following steps that unmanned aerial vehicle complete river topography measurement is carried out; river upstream and downstream section hydraulic parameters are obtained; constructing a digital river channel section; batch extraction of satellite remote sensing water surface width; flow calculation parameters are obtained based on the digital river section and the water surface width data; performing remote sensing inversion on the roughness of the complete riverway; and section flow monitoring and historical data inversion. A section of complete river channel is determined as a basic research unit, flow calculation precision is remarkably improved through multi-section synchronous monitoring in combination with river channel slope and roughness change dynamically captured in real time, the flowing process of water flow in the complete river channel is finely described, and the flow calculation precision is improved. The method provides long-sequence and high-reliability flow data for parameter calibration and result verification of a hydrological model, is particularly suitable for describing the flow condition when flood comes, and enables the flow condition to be closer to reality.

The invention discloses a rock dynamic triaxial statistical damage constitutive model establishing method, and belongs to the technical field of rock dynamic constitutive model basic research of deep underground engineering. The method comprises the following steps: introducing a nonlinear Mohr-Coulomb and Hoek-Brown strength criterion, and deriving a nonlinear rock dynamic strength criterion considering a strain rate effect based on a rock dynamic strength and strain rate dependent strength criterion of a thermal activation and viscosity mechanism; constructing a rock infinitesimal strength measurement method capable of reflecting rock dynamic deformation characteristics, and establishing a rock dynamic triaxial statistical damage constitutive model; and carrying out sensitivity analysis on the rock dynamic triaxial statistical damage constitutive model. According to the method, the rock dynamic triaxial statistical damage constitutive model suitable for the high confining pressure and the high strain rate is effectively established, so that the nonlinear deformation process of the deep high confining pressure rock under the dynamic load effect is accurately simulated, and the method can be applied to the technical field of rock dynamic constitutive model basic research of deep underground engineering.

The invention discloses an application of a marker combination in prediction or diagnosis of gout, the marker combination comprises an immune cell subset and clinical data, and the immune cell subset comprises virus-specific cytotoxic NK cells and inhibitory Vdelta2 cells. The marker combination comprises immune cell subgroups and clinical data, different immune cell subgroups are matched with different clinical data when a gout attack stage and a gout remission stage are distinguished, or when the gout remission stage and a healthy subject are distinguished, and high-sensitivity and high-specificity diagnosis results are achieved. Therefore, the marker combination disclosed by the invention has a wide prospect in the aspect of predicting different processes of gout, and can provide more basic research data for health management of gout high-risk people.

The invention discloses an oyster carbon sink value evaluation method, model and equipment based on carbon sequestration amount, and a medium. The method comprises the following steps: collecting oyster breeding data in an oyster breeding process; the method comprises the following steps: respectively calculating an oyster body carbon sequestration amount, an oyster attached organism carbon sequestration amount and an oyster biological sediment carbon sequestration amount according to oyster breeding data, and summarizing the oyster body carbon sequestration amount, the oyster attached organism carbon sequestration amount and the oyster biological sediment carbon sequestration amount into a total oyster breeding carbon sink amount; and calculating the carbon sink value of the oysters according to the total carbon sink amount of the oyster culture. According to the method, a traditional culture shellfish carbon sequestration basic metering method is improved, carbon sequestration amount calculation is carried out on oyster bodies and biological sediments of attached organisms respectively, the more accurate oyster culture carbon sequestration total amount can be obtained, and the carbon sequestration income of oysters is calculated based on the carbon sequestration total amount. The method is beneficial to enriching the basic research in the field of shellfish culture carbon sink accounting, and enables the ecological service value of the shellfish culture industry to be compensated through carbon sink transaction.

The invention belongs to the technical field of gene editing, and discloses a fusion protein, a base editing system for realizing protein multimerization and application. The fusion protein provided by the invention is a Cas9 protein in which antigen epitopes are embedded or replaced; the antigen epitope is an antigen epitope in a protein collection system; the antigen epitope can realize multimerization of the fusion protein. The base editor system comprises the fusion protein and an editing enzyme fusion protein. The editing enzyme fusion protein comprises an antibody of the antigen epitope and editing enzyme. The base editor system disclosed by the invention has the characteristics of a base editing platform which can be modularized, multimerized, programmable and extensible, and brings more possibilities and selection capabilities to the field of gene editing. The base editor system can be applied to gene editing, including application in the fields of basic research, gene therapy, animal living body editing, agricultural breeding and the like.

The invention provides a lysosome extraction method. The lysosome extraction method comprises the following steps: (1) extracting cells; (2) tissue extraction; (3) crude separation of lysosome; and (4) separating the lysosome by magnetic beads. Through EDTA-free digestion optimization, lysis solution and buffer solution formula optimization, a filter membrane interception-magnetic bead purification combined technology, a double-antibody synergistic capture strategy and a competitive mild elution system, the four core problems of low purity, large activity damage, tedious operation and strong equipment dependence in a traditional lysosome separation technology are systematically solved. Experimental data show that the lysosome yield and functional integrity of the method are obviously superior to those of a density gradient centrifugation method, and the method is suitable for trace samples and conventional equipment and has high conversion value. In the future, the technical barrier can be further optimized through automation equipment integration and multi-dimensional function verification, and the application of the method in basic research and clinical diagnosis is promoted.

The invention discloses a camellia oleifera SNP (Single Nucleotide Polymorphism) molecular marker combination and application thereof. The camellia oleifera SNP molecular marker combination comprises at least one of 50 SNP molecular markers and 454 SNP molecular markers, and the physical positions of the 50 SNP molecular markers and the 454 SNP molecular markers are determined on the basis of sequence alignment of a camellia oleifera reference genome GCA039905865.1. The camellia oleifera SNP molecular marker combination can be effectively used for molecular marker breeding of camellia oleifera, the camellia oleifera SNP molecular marker combination is used for preparing a first type of whole genome liquid phase chip of camellia oleifera, and the application cost of genetic diversity analysis, QTL positioning, GWAS analysis and the like in scientific research of camellia oleifera is effectively reduced; the problem that no applicable product exists in camellia oleifera molecular auxiliary breeding and whole genome selective breeding is solved, and the process of camellia oleifera basic research and breeding is accelerated.

The invention provides a single molecule sensing array module, a quantitative analysis chip and a quantitative analysis method, which can realize excitation and sensing of high-flux parallel single molecules, and the detection sensitivity limit can reach a single molecule level; a standard curve can be formed for optical signals of ultralow-concentration target molecules, the problem that the intensity of the optical signals is not uniform and not repeated is solved through a digital processing method, accurate quantitative analysis of the ultralow-concentration molecules can be achieved, the detection sensitivity is improved, and the sensitivity grade reaches the single-molecule grade. The method has great application value in the fields of clinical medicine, life science, food detection, environmental protection, national defense, public safety, basic research and the like. The method can also be applied to single-molecule immunodetection, and single-molecule immunodetection with ultralow detection limit is realized.

Next Generation DNA sequencing promises to revolutionize clinical medicine and basic research. However, while this technology has the capacity to generate hundreds of billions of nucleotides of DNA sequence in a single experiment, the error rate of approximately 1% results in hundreds of millions of sequencing mistakes. These scattered errors can be tolerated in some applications but become extremely problematic when “deep sequencing” genetically heterogeneous mixtures, such as tumors or mixed microbial populations. To overcome limitations in sequencing accuracy, a method Duplex Consensus Sequencing (DCS) is provided. This approach greatly reduces errors by independently tagging and sequencing each of the two strands of a DNA duplex. As the two strands are complementary, true mutations are found at the same position in both strands. In contrast, PCR or sequencing errors will result in errors in only one strand. This method uniquely capitalizes on the redundant information stored in double-stranded DNA, thus overcoming technical limitations of prior methods utilizing data from only one of the two strands.

The invention provides a pharmaceutical composition for treating MSS intestinal cancer, and belongs to the technical field of biological medicine, the pharmaceutical composition is used for deeply researching a treatment scheme for effectively inhibiting the MSS intestinal cancer, carrying out basic research from protein purification, proteomics, siRNA libraries and the like, and trying to develop a brand new treatment scheme and a treatment mode using nitixinone, sorafenib and PD1 antibodies; the three medicines are combined for use, so that a remarkable synergistic effect is achieved, and the tumor is successfully changed from cold to hot. The pharmaceutical composition provided by the invention has an important clinical value, breaks through the current difficulty in treatment of MSS intestinal cancer, and opens a brand new direction of application of immunotherapy in clinical advanced metastatic colorectal cancer.

The invention relates to a science and technology development stage identification and prediction method based on a life cycle matrix. The method comprises the steps of determining a direction involved in the science and technology field; scientific and technological papers and patent literatures are retrieved, time sequence data of the publication quantity of the scientific and technological papers and the application quantity of patents are obtained, S curve fitting is carried out, and time nodes of the scientific and technological field in the germination stage, the growth stage, the mature stage and the decline stage of basic research and technology application are identified; taking the basic research stage and the technical application stage as horizontal and vertical coordinates, and constructing a life cycle matrix according to a time overlapping region division result of the basic research stage and the technical application stage; and according to the life cycle matrix and the duration of each stage, an evolution trend curve of the fundamental research and technology application stage is drawn, and field growth pattern recognition and development law prediction are carried out. According to the method, the interaction relationship between the basic research and the technical application in the scientific and technological development process is demonstrated, and guidance is provided for identifying and predicting the scientific and technological development stage and trend.

The invention provides an immunofluorescence detection method and system for dynamically detecting mouse uterus structure development based on multiple time points, and immunofluorescence staining comprises the steps of sheet unfolding, dewaxing, repairing, cell membrane punching, sealing, primary antibody treatment and secondary antibody treatment. The system comprises a sample pretreatment control module, a multi-channel confocal microscope imaging module and a data analysis module integrating fluorescence intensity calculation, Pearson co-localization analysis and a Western blot data integration algorithm. Through a multi-time-point and multi-index immunofluorescence detection method, dynamic and systematic data support is provided for mouse uterus development mechanism research, and an application basis is provided for fundamental research of reproductive biology and construction of related disease models.

The invention discloses a method for establishing a hemophagocytic syndrome in-vitro cell disease model, and belongs to the technical field of biology. Based on human PBMC construction, the reaction of a human immune system can be truly reflected, experimental result deviation caused by species difference in an animal model is avoided, and a more accurate model basis is provided for research of human diseases. In addition to T cell over-activation, the HLH model of the present application has a clear key feature of NK cell reduction, which is HLH, accompanied by up-regulation of cytokines such as interferon-gamma and IL-10. The establishment process of the model is rapid and efficient, the experimental period is remarkably shortened, a large number of samples or drugs can be rapidly screened, the research efficiency is improved, and the conversion process from basic research to clinical application is accelerated. The method can be used for researching various mechanisms related to the HLH, is beneficial to more comprehensive understanding of pathogenesis of the HLH, and provides a theoretical basis for developing preliminary screening of targeted drugs.

The invention discloses a textile dyeing and finishing large model copied based on dyeing and finishing reaction conditions and application thereof, relates to the technical field of textile dyeing and finishing, and aims to solve the technical problem that the dyeing and finishing process has great uncertainty due to the fact that a data source is lacked and reaction conditions are difficult to effectively copy by means of scientific data in the prior art. Comprising a basic research module, a standard reaction condition copying module, a dyeing and finishing digital module and a dyeing and finishing large model application module. Various reaction tank tests are carried out through the basic research module, physical and chemical reaction standard data of different cloth types on auxiliaries and dyes are obtained, an accurate data source is provided for a large dyeing and finishing model, reaction conditions with high yield and good quality can be effectively copied and customized, and a proper dyeing and finishing formula and process sheet are generated. The method is beneficial to improving the quality of dyed and finished products, guarantees the production efficiency, enables the dyeing and finishing process to be more scientific and normative, and reduces defective products caused by poor conditions.

According to the application of the HTATSF1 gene in regulation and control of cattle muscle growth and development and breeding, the influence of the HTATSF1 gene on muscle growth and development and the correlation between HTATSF1-CNV and cattle growth traits are verified, a reliable molecular marker is provided for cattle seed selection and breeding, and help is provided for cattle variety improvement. A foundation is laid for association between copy number variation and growth traits of the cattle HTATSF1 gene, cattle molecular marker-assisted selection breeding work can be accelerated, the method is simple, rapid and convenient to popularize and apply, and a complete solution from fundamental research to industrial application is provided for improvement of cattle germplasm resources.

The invention belongs to the field of basic research of sandstone type uranium ore associated resource evaluation, and particularly relates to a method for judging the existence form of associated gallium in a sandstone type uranium deposit, which comprises the following steps of: measuring the contents of major elements and trace elements of a plurality of uranium ore samples, and judging whether gallium meets the lowest grade requirement of associated resources of the uranium deposit; for uranium ore samples exceeding the lowest grade requirement of gallium associated resources, correlation analysis of gallium elements, main elements and trace elements is carried out, and possible key mineral types closely related to gallium are preliminarily speculated; carrying out slice analysis, and circling an approximate range of speculated possible key mineral types; carrying out scanning electron microscope and energy spectrum analysis combined observation, and determining the existence form of gallium in the uranium deposit; the position exceeding the associated grade gallium is determined through laser in-situ analysis; the gallium-related mineral type is directly determined through electron probe analysis; and comprehensively judging the existence form of gallium in the uranium deposit. According to the method, the existence form of associated gallium in the sandstone type uranium deposit can be accurately and quickly judged.

This application discloses a method for offline analysis of powder ionization conditions, comprising the following steps: placing a silicon wafer on a target plate of a plasma device; generating a plasma beam under preset powder ionization conditions using the plasma device; injecting powder into the plasma device so that the plasma beam bombards the powder until powder injection is complete; detecting whether a first condition and a second condition are met, wherein the first condition includes at least 70% of the powder injected into the plasma device ablation and brightening upon bombardment by the plasma beam and / or forming a coating on the silicon wafer; the second condition includes the coating containing chemical bonds formed by elements of the powder and / or detecting spectral lines generated by ionization of the powder upon bombardment by the plasma beam. If the first and second conditions are met, the powder is determined to be effectively ionized. Otherwise, the powder is determined to be ineffectively ionized. The method of this application can obtain basic research data on the boronization of boron powder.

The present invention provides a method for determining the surface deformation of a CFG pile composite foundation under reverse fault dislocation. Combined with the fault rupture mode in the site cover layer, a method for analyzing the site stress of the fault rupture zone and a calculation formula are given to solve the problem of calculating the deformation of a vertical reinforced composite foundation adjacent to or across a strong earthquake surface rupture zone in an actual engineering project. (1) Combined with the fault rupture mode in the site cover layer, determine the calculation range of the site's surface uneven deformation, 1, 2, 3, j...n; (2) Calculate the deformation D of the surface point j caused by the bedrock dislocation j ; (3) Calculate the deformation of the composite foundation under the load of the building itself#imgabs0#(4) Calculate the foundation deformation S when the soil of the composite foundation is broken due to strong earthquake dislocation jQ ; (5) Calculate the total deformation T of the surface at point j j The present invention provides a parameter basis for the anti-fracture design of composite foundations of buildings on engineering sites across fault rupture zones, and provides basic research data for the safe use and toughness requirements of buildings in strong earthquake rupture zones.

The invention discloses an antibody for specifically recognizing 1147th acetylation of ribosome biosynthetic factor 1 protein as well as a preparation method and application of the antibody. According to the protein sequence and the modification type of the ribosome biosynthetic factor 1, two modified antigen polypeptides A and B are designed, and through detection, the antibody obtained by immunizing animals with the two polypeptides has high specificity and affinity, can accurately recognize the acetylation modification form of the 1147th site of BMS1, and avoids recognition of an unmodified form or other modification sites. The antibody is suitable for various immunological detection methods, is high in repeatability and low in background, has mass production potential, can realize industrialization, not only can be used for evaluating the cis-platinum drug resistance condition in esophageal cancer treatment, but also can be used for various scenes such as basic research, disease mechanism analysis, biomarker development and drug target screening, and is wide in application range.

Next Generation DNA sequencing promises to revolutionize clinical medicine and basic research. However, while this technology has the capacity to generate hundreds of billions of nucleotides of DNA sequence in a single experiment, the error rate of approximately 1% results in hundreds of millions of sequencing mistakes. These scattered errors can be tolerated in some applications but become extremely problematic when “deep sequencing” genetically heterogeneous mixtures, such as tumors or mixed microbial populations. To overcome limitations in sequencing accuracy, a method Duplex Consensus Sequencing (DCS) is provided. This approach greatly reduces errors by independently tagging and sequencing each of the two strands of a DNA duplex. As the two strands are complementary, true mutations are found at the same position in both strands. In contrast, PCR or sequencing errors will result in errors in only one strand. This method uniquely capitalizes on the redundant information stored in double-stranded DNA, thus overcoming technical limitations of prior methods utilizing data from only one of the two strands.

The invention discloses application of baclofen in preparation of a medicine for treating glioma, and belongs to the technical field of biological medicine. Through systematic in-vitro and in-vivo experiments, it is proved for the first time that baclofen (especially R-configuration) has a remarkable anti-tumor effect on glioma including temozolomide (TMZ) drug resistance. The invention not only provides a brand-new clinical strategy for treating TMZ drug-resistant glioma, but also shows important value in the field of scientific research: baclofen can be used as a valuable tool compound and is used for exploring a new function of a GABAB receptor signal channel in glioma progress and drug resistance; meanwhile, a key tool is provided for constructing a stable TMZ drug-resistant model, the high-throughput drug screening and evaluation efficiency can be remarkably improved, and the TMZ drug-resistant monoclonal antibody can serve as a positive control drug to accelerate the conversion process from basic research of glioma to clinical application and has wide scientific research application prospects and conversion potential.

The present invention discloses a method for culturing wild Ganoderma curtisii. Using a puncher, 7-mm mycelial blocks are obtained by punching at the same radius on a petri dish covered with mycelia of wild Ganoderma curtisii strains, and then inoculated on a culture medium petri dish and cultured in the dark in a constant temperature incubator at 15-30 °C. Compared with the prior art, the optimal culture conditions for the wild Ganoderma curtisii of the present invention are: carbon source starch, nitrogen source yeast powder, pH 9.0, temperature 30 °C. Under such culture conditions, the wild Ganoderma curtisii grows fastest with the best growth vigor and prefers to grow in a slightly alkaline environment; it provides basic research data for the further development and utilization of Ganoderma curtisii resources and also provides basic data reference for the research on the biological characteristics and domestication cultivation of related species of this genus.

The invention discloses a heteronuclear cerium-germanium complex and a preparation method and application thereof, and belongs to the technical field of organic synthesis.The heteronuclear cerium-germanium complex is a cerium-germanium complex A, a cerium-germanium complex B or a cerium-germanium complex C. Cerium and germanium centers of the complexes are in a specific space adjacent state; the cerium-germanium complex A, the cerium-germanium complex B and the cerium-germanium complex C have unique structures, so that the cerium-germanium complex A, the cerium-germanium complex B and the cerium-germanium complex C become an ideal fundamental research carrier. The method can be used for in-depth exploration of electron interaction or spin coupling possibly existing between cerium and germanium through a ligand skeleton; the two independent metal centers have synergistic reaction activity in a limited space; such structures have potential properties in molecular magnetic or luminescent materials. Therefore, the invention not only enriches the structure types of the rare earth-main group element complex, but also provides a new platform with accurate structure and adjustable performance for the basic research of multi-center metal organic chemistry, and has definite scientific significance and potential application exploration value.

The invention provides a quality detection method and application of a liver-warming decoction, and belongs to the technical field of medicine detection.The quality detection method comprises the steps that the liver-warming decoction is used for preparing a test solution, acetonitrile (A)-0.08 wt%-0.12 wt% formic acid aqueous solution (B) serves as a mobile phase, gradient elution is adopted, and the quality of the liver-warming decoction is detected through ultra-high performance liquid chromatography-tandem mass spectrometry; the obtained detection result can be used for quality evaluation or control of the whole process of research / development / production / clinical application of the liver-warming decoction. According to the present invention, the UPLC-Q-TOF-MS method is adopted to perform qualitative analysis on the substance-based chemical components of the liver-warming decoction, such that the scientific basis is provided for the substance-based material basic research of the liver-warming decoction, and the main chemical components are clarified;

A testing system for internal strain field in rock mass physical simulation test involves the testing field of stress field in physical simulation test in geotechnical engineering, and can improve the installation efficiency and testing accuracy of strain bricks in rock mass physical simulation test. The present invention is composed of three parts: a sample stabilization system, a soil cutting system, and a motor system, wherein the sample stabilization system includes an outer frame column, a base plate, a base plate track, a transverse slide rail, and a longitudinal slide rail; the soil cutting system includes a disc, a rotating pressure rod, a pressure plate, a soil bucket, a fixed rod, a rotating bearing, a soil cutting line fixed rod, a soil cutting line fixed rod jack, and a soil cutting line; the motor system includes a motor and a motor controller. The present invention utilizes the synchronous deformation of strain bricks and simulated rock mass to study the changes in the internal stress and strain of the simulated rock mass under the action of external force, summarizes the changing laws of the internal stress field and strain field of the rock mass, and provides experimental references for basic research on related topics in rock mass physical simulation.