3822 results about "Virus" patented technology

A platform for characterizing biomolecules, biological tissue sections, viruses, or other particles of interest in a non-invasive, high-throughput, cost-effective, and label-free manner. The platform includes a merged set of imaging modalities including and capable of interferometric microscopy and wide-field or confocal microscopy (such as, for example, a wide-field super-resolution surface enhanced Raman spectroscopy, SERS), although some aspects may be employed with data sets only received from wide-field or confocal microscopy. Related devices, systems, methods, techniques, and variations to the same are also provided.

The invention provides an electrochemical active oxygen supply device for a washing machine and a preparation method. The device comprises a shell, a single closed reaction chamber is formed in the shell, a bifunctional anode electrode and a bifunctional cathode electrode are integrated in the reaction chamber, and a compact and uniform reaction area is formed between the anode electrode and the cathode electrode. When water flows through the reaction area, hydrogen peroxide (H2O2) and / or hydroxyl radicals (OH) are / is electrochemically generated on the surface in situ by accurately adjusting the electrode potential of the difunctional anode, so that instant generation and instant utilization of active oxygen are realized. The active oxygen directly enters a washing system of the washing machine along with water flow, bacteria, viruses and fungi can be efficiently inactivated under the normal-temperature or low-temperature washing condition without additionally adding chemical disinfectants, organic stains and peculiar smell molecules are synchronously degraded, and green, efficient and intelligent healthy washing is achieved.

The invention belongs to the technical field of biology, and particularly relates to a group of paired monoclonal antibodies for resisting H9N2 subtype avian influenza viruses and a surface enhanced Raman spectroscopy rapid detection test strip established based on the antibodies. The paired monoclonal antibody comprises a labeled antibody 1E9 and a capture antibody 3C10 which are prepared by taking hemagglutinin protein of the H9N2 subtype avian influenza virus as antigens and can be specifically combined with the H9N2 subtype avian influenza virus. According to the invention, an SERS (Surface Enhanced Raman Scattering) probe Au-coated Pt-4ATP is used as a marker and is coupled with a labeled antibody 1E9 to prepare a labeled probe, and the labeled probe is paired with a capture antibody 3C10 to establish an SERS immunochromatography test strip. The test strip has a colorimetric and Raman dual interpretation mode, can be used for qualitative and quantitative detection, has the advantages of strong specificity, high sensitivity, good repeatability and stability and the like, is simple and rapid in clinical detection operation, and provides reliable technical support for on-site rapid screening of subtype viruses.

The invention relates to a primer group for detecting pangolin plague virus, a kit and application, and relates to the technical field of gene engineering. The primer group comprises a forward primer ORF1-F and a reverse primer ORF1-R. The forward primer ORF1-F and the reverse primer ORF1-R. On the basis of the primer group, the E gene in the conserved region of the pangolin plague virus can be specifically recognized, so that the primer group is combined with an RAA amplification system and a detection system, and detection is rapidly completed within a short time under the constant-temperature condition.

The application belongs to the technical field of biological detection, and particularly relates to a monoclonal antibody pair for detecting feline immunodeficiency virus p24 protein and application thereof. The monoclonal antibody pair is monoclonal antibody 1D8 and monoclonal antibody 1H10, which can specifically recognize feline immunodeficiency virus p24 protein, and the heavy chain and light chain variable region complementarity determining region sequences of 1D8 and 1H10 are clear, and are respectively shown as SEQ ID NO. 1-12. The antibody pair can effectively avoid cross reaction, and significantly improve the accuracy and sensitivity of detection; the colloidal gold detection test strip constructed based on the antibody pair is simple and fast in operation, is suitable for early antigen detection of FIV infection, solves the problem that existing antibody detection cannot distinguish natural infection and vaccine immunization, and provides a reliable technical means for on-site screening and disease prevention and control of FIV.

The invention discloses an upland cotton GhCRK29 gene as well as an encoding protein and application thereof, the GhCRK29 gene is separated from cotton, the nucleotide sequence of the GhCRK29 gene is as shown in SEQ ID No.1, and the amino acid sequence of the encoding protein of the GhCRK29 gene is as shown in SEQ ID No.2. According to the invention, a virus-induced gene silencing technology and a transgenic overexpression technology are further utilized to carry out preliminary research on the function of the cotton GhCRK29 gene in cotton verticillium wilt resistance, and a result shows that the verticillium wilt resistance of a cotton seedling plant is obviously reduced after the GhCRK29 gene in cotton is silenced; after the GhCRK29 gene is over-expressed in arabidopsis thaliana or cotton, the verticillium wilt resistance of arabidopsis thaliana or cotton is remarkably improved, and the resistance of a GhCRK29 gene forward regulation plant to verticillium dahliae is determined; the invention has application prospects in the aspects of improving the verticillium wilt resistance of plants or cultivating verticillium wilt resistant plant varieties and the like.

The invention provides application of a TaNAC42 gene in regulation and control of wheat stem rust resistance, and belongs to the technical field of gene functions. It is found for the first time that the TaNAC42 gene of wheat is related to the wheat stem rust resistance, the TaNAC42 gene is induced to be silenced through viruses, the wheat stem rust resistance can be enhanced, wheat plants are easier to resist diseases, the TaNAC42 gene is over-expressed through the agrobacterium tumefaciens-mediated transient over-expression technology, the wheat stem rust resistance can be weakened, the wheat plants are more susceptible to diseases, and the wheat plants are more susceptible to diseases. Namely, the TaNAC42 gene can negatively participate in regulating and controlling the resistance of the wheat to the Puccinia graminicola, a new target gene is provided for improved breeding of wheat Puccinia graminicola resistance molecules, and the TaNAC42 gene has important utilization value in wheat production and breeding.

A pathogen nucleic acid aerosol purification device comprises a machine shell, the machine shell comprises a frame, a front panel, a left side plate, a right side plate, a rear baffle and a top cover plate are arranged on the frame, the front panel is an arc-shaped plate with the plate face bent forwards gradually from bottom to top, the rear baffle and the top cover plate are rectangular, and an air inlet is formed in the bottom of the machine shell. The front panel, the left side plate, the right side plate, the rear baffle and the top cover plate define an air channel allowing air to circulate from bottom to top, and a plurality of centrifugal fans are arranged on the upper portion in the air channel side by side at intervals in the left-right horizontal direction. The utility model aims to provide a biological laboratory air purification device which can enable air in a biological laboratory to fully circulate without dead angles, enables the air to be free of eddy current and cross disturbance as far as possible during circulation, and can efficiently disinfect and remove nucleic acid fragments, viruses and bacterial microorganisms in aerosol in the air in the biological laboratory in an extremely short time. And the pathogen nucleic acid aerosol purification device is used for efficiently removing suspended particulate matters in air in a biological laboratory.

The application discloses a kind of carrier, kit and application for long-acting gene knockdown of animal parasitic nematode, belong to the field of animal parasitic disease prevention and control.The lentivirus vector in the application integrates specific coding sequence to the genome of the infected nematode, stably and continuously expresses short hairpin RNA (shRNA) in the nematode, efficiently produces primary single-stranded small RNA (siRNA), these siRNAs target homologous target gene mRNA to cause its degradation, realize stable and continuous gene silencing effect.The application breaks through the bottleneck of traditional animal parasitic nematode RNA interference (RNAi) technology with low efficiency and instability, significantly improves the timeliness of conventional RNAi, can be used to establish long-acting RNAi technology system of animal parasitic nematode, has application value in the research of host in vivo process such as nematode infection, parasitism and pathogenicity and animal parasitic nematode disease prevention and control.

The present invention relates to a pathogen-specific probe set capable of simultaneously detecting viruses and bacteria associated with respiratory syndromes, a composition for diagnosing respiratory syndrome comprising same, a kit for diagnosing respiratory syndrome comprising same, and a method for simultaneously detecting respiratory syndrome-associated viruses and bacteria using the probe set.

Disclosed herein are antibodies or antigen-binding fragments thereof that specifically bind to human CD19. Chimeric antigen receptors and chimeric antigen receptor transgenes comprising an antigen binding domain that specifically binds to human CD19 are also disclosed. Also described herein are immune cells, viral vectors, and other compositions containing the antibodies, the antigen binding fragments, the chimeric antigen receptors, and / or the chimeric antigen receptor transgenes.

Relating to the field of biotechnology, disclosed are a recombinant human elastin peptide with anti-aging effects and a use thereof. The recombinant human elastin peptide comprises an amino acid sequence shown in SEQ ID NO:1 or a fragment of the amino acid sequence shown in SEQ ID NO:1, the fragment comprises 30% or more of SEQ ID NO:1, or a mutant of the amino acid sequence shown in SEQ ID NO:1 or the fragment of the amino acid sequence shown in SEQ ID NO:1. A disclosed method for producing elastin peptides by using a yeast expression system enables the targeted synthesis of highly effective protein fragments with 100% homology to human proteins, while achieving low costs and facilitating large-scale production, avoiding animal-derived sources and viral risks. This makes the recombinant human elastin peptide safe for use as an anti-aging and anti-photoaging active ingredient in cosmetics, while also supporting a use thereof in the field of biomedical materials.

The present disclosure provides codon optimized GBA1 polynucleotides encoding a GCase protein, wherein a portion of the coding sequence deviates from the wild type. The disclosure also provides expression constructs, vectors, viral particles or compositions containing the disclosed polynucleotides. In addition, methods and uses of these polynucleotides, expression constructs, vectors, viral particles or compositions are also provided, including the treatment of diseases or conditions associated with GCase deficiency.

Disclosed herein is a drone docking station for deposit of items / goods delivered by a drone to a secured receptacle. Items are delivered to a receptacle at a curb, mailbox, post, porch, mobile units, and windows for a multi-parcel receptacle with a set of drawers with hot and cold sections in the station that has a specific residential / commercial address with various optional features. Features include communication systems between the station and drone; security; hot and cold temperature control and preservation of the goods before and after delivery; battery charging and exchange station; a collector to identify explosive materials, anthrax, etc.; ultraviolet system to eradicate disease, virus and harmful materials; an ozone applicator to eradicate disease, virus and harmful materials; weather monitoring; tag and track of vehicles and packages; facial recognition camera and software for pets and humans; and local two-way speakers; LED lights that strobe flash, and a flood light.

One embodiment of the invention discloses a method and device for optimizing network anti-virus indexes. The method comprises following steps: obtaining anti-virus indexes of terminals in a network, wherein the anti-virus index of each terminal in the network comprises at least one kind of information as follows: virus infection and anti-virus capability information; optimizing the anti-virus indexes of terminals in a network by means of the genetic algorithm to obtain the optimized anti-virus indexes of terminals in the network; obtaining the optimized network anti-virus indexes based on the optimized anti-virus indexes of terminals in the network. One embodiment of the invention also discloses a device for optimizing network anti-virus indexes.

The invention relates to a wheat stem rot regulatory gene Tatrx-m, and an encoding protein, a recombinant vector and an application of the wheat stem rot regulatory gene Tatrx-m. The genomic sequence of the gene is SEQ ID NO.1, the CDS sequence of the gene is SEQ ID NO.2, and thioredoxin shown as SEQ ID NO.3 is encoded. The invention further provides a specific primer pair used for gene identification, a silent vector (Tatrx-m-VIGS) and an overexpression vector (LGY-OE3-Tatrx-m) are constructed, and the function of the primer pair is verified through a virus-induced gene silencing (VIGS) technology and agrobacterium-mediated transformation of wheat. Experiments show that silence of Tatrx-m results in significant reduction of wheat stem rot resistance, and overexpression of the gene can improve resistance. Based on hypha quantification, DAB staining, H2O2 content and cell death analysis, Tatrx-m is revealed to enhance wheat resistance by regulating active oxygen removal and cell wall strengthening pathways. The gene TaTrx-m has the positive regulation effect in wheat stem rot for the first time, can be applied to disease-resistant molecular marker development, gene editing and transgenic breeding, provides core genetic resources for disease-resistant variety breeding, and has theoretical and application values.

This invention discloses a primer and probe set, a kit, and their applications for detecting Staphylococcus aureus L based on real-time fluorescence MIRA technology. The primer and probe set consists of single-stranded DNA sequences 1-3. Based on the aforementioned primer and probe set, this invention establishes and optimizes a real-time fluorescence MIRA detection method for Staphylococcus aureus L. Furthermore, the optimized real-time fluorescence MIRA method is innovatively combined with a simplified nucleic acid extraction method and a portable fluorescence detection device, significantly reducing extraction and time costs while enabling rapid on-site detection of the virus, making it particularly suitable for grassroots units and remote areas. In addition, the real-time fluorescence MIRA detection method for Staphylococcus aureus L established in this invention has advantages such as high specificity, high sensitivity, and simple operation. Moreover, the detection process does not require opening the lid, effectively avoiding aerosol contamination, providing an effective technical means for the differential diagnosis and rapid detection of Staphylococcus aureus L.

The invention discloses a potato Y virus rapid detection method based on RPA-CRISPR / Cas12a-LFA, the RPA-CRISPR / Cas12a-LFA triple technology is adopted, the RPA-CRISPR / Cas12a-LFA triple technology comprises RPA isothermal amplification, Cas12a targeted cutting and LFA visual reading, the potato Y virus can be rapidly and efficiently detected, the sensitivity is high, the specificity is high, and the operation is simple and convenient.

The invention belongs to the technical field of biological medicine, and particularly relates to an engineered cell microvesicle and a delivery system based on the engineered cell microvesicle, the system realizes efficient preparation of 1-5 [mu] m cell microvesicles, and the cell microvesicles have a large space volume and can be used for preparing the cell microvesicles. The carrier can be used for loading and delivery of target protein, polypeptide and recombinase which are specifically expressed in mother cells. The system transfects mother cells through lentivirus transfection or plasmid transfection to further produce cell microvesicles, and the microvesicles can load more goods and inherit membrane proteins of the mother cells, and can also effectively load intracellular proteins to realize effective delivery. By virtue of good structural stability, high immunogenicity and excellent biocompatibility, the cell microvesicle reduces systematic toxic and side effects of a traditional carrier, is expected to become an effective drug delivery system, and has great application potential in the field of gene therapy.

The invention discloses macromolecular antibacterial artificial leather and a preparation method thereof, and relates to the technical field of artificial leather preparation. The preparation method comprises the following steps: preparing zinc-loaded silicon dioxide with amino grafted on the surface and quaternized polyether polyurethane containing an epoxy group, mixing the zinc-loaded silicon dioxide and the quaternized polyether polyurethane to prepare antibacterial protection slurry, and bonding the zinc-loaded silicon dioxide and the quaternized polyether polyurethane through ring-opening reaction of the amino and the epoxy group during curing to form a cross-linked network, so as to obtain the antibacterial protection layer with antibacterial property, flexibility and wear resistance; zinc ions have an obvious inhibiting effect on bacteria such as gram-positive bacteria and gram-negative bacteria and fungi such as candida albicans, quaternary ammonium salt has an obvious inhibiting effect on influenza viruses, and the zinc ions and the quaternary ammonium salt have a synergistic effect, so that the antibacterial range of the artificial leather is wider, the inhibiting force on germs is stronger, and the antibacterial property of the artificial leather is further improved.

And genetic determinants conferring improved ToBRFV resistance. The present invention relates to a tomato plant resistant to tomato brown crinkled fruit virus (ToBRFV), comprising in the genome of said tomato plant the following combination: a resistant quantitative trait locus on chromosome 8 (QTL) genetically infiltrated from solanum tomentosum and conferring resistance to ToBRFV, and a resistant quantitative trait locus on chromosome 8 (QTL) genetically infiltrated from solanum tomentosum and conferring resistance to ToBRFV; and at least one QTL or Tm-1 gene on chromosome 11, which QTL, when homozygically present, confers resistance to ToBRFV to a plant leaf surface, said plant having improved resistance to ToBRFV. The invention also relates to corresponding seeds and cells, as well as various methods and uses for providing improved ToBRFV resistance based on the genetic determinant combination.

The invention relates to the technical field of biology, and particularly discloses application of OsDjA5 protein or a coding gene thereof to regulation and control of resistance of plants to southern rice black-streaked dwarf viruses. The research finds that after the expression quantity of the OsDjA5 gene is reduced, the resistance of rice to the southern rice black-streaked dwarf virus is enhanced. The invention further provides application of the OsDjA5 protein or the coding gene thereof, or a biological material containing the coding gene thereof in regulating and controlling the resistance of plants to the southern rice black-streaked dwarf virus. The invention provides a new method capable of improving the resistance of the plants to the southern rice black-streaked dwarf virus, and a new thought is provided for creating new varieties of disease-resistant plants.

The invention provides a high-throughput detection and bioinformation analysis and identification method for a human ring virus group, the method comprises the whole process from reference database construction, sample processing, high-throughput sequencing to bioinformation analysis, and the technical scheme specifically comprises the following steps: step 1, constructing a human ring virus high-quality reference database; 2, performing high-throughput sequencing on the metagenome of the human sample; and step 3, a ring virus group biological information analysis process.

The invention provides a culture method of avian encephalomyelitis virus, and belongs to the technical field of biology. According to the method, chicken lymphoma suspension cells are adopted to culture the avian encephalomyelitis virus, the titer of the obtained avian encephalomyelitis virus reaches 106.5-6.8 EID50 / 0.2 mL, and the method is short in culture period, high in production efficiency, low in cost, controllable in quality and capable of being used for large-scale industrial production.

Methods to edit genes by administering a chimeric nuclease to a cell or organism without the use of a viral vector.

The invention belongs to the technical field of external diagnosis devices, and particularly relates to a memristor for adenovirus concentration detection and a preparation method of the memristor. The memristor comprises a bottom electrode layer, a metal oxide layer, a functional layer and an upper electrode layer which are sequentially formed from bottom to top in the thickness direction, the bottom electrode layer is an FTO conductive glass layer, the metal oxide layer is tantalum pentoxide, the functional layer is a gelatin-beta cyclodextrin composite film, and the upper electrode layer is a conductive electrode layer. The gelatin-beta cyclodextrin composite film with the memristive effect serves as a functional layer, after the film makes contact with adenoviruses, the film adsorbs virus particles, then the unique resistance change characteristic of the memristor is caused, the memristive behavior of the memristor is further fed back, and the memristive effect of the memristor is improved. The method is used for recording and analyzing the electrochemical or bio-electricity signal characteristics of adenovirus solutions with different concentrations, the adenovirus solutions with different concentrations are effectively distinguished according to the electric signal difference of the adenovirus solution and the control solution, the effect is obvious, and the repeatability is good.

The invention relates to a hundred-nanoscale particle sorting control chip and device and a sorting control method, the chip comprises a micro lens, a micro-fluidic channel, a sorting outlet and a sorting inlet, the sorting outlet is a two-fork opening, and the sorting inlet is a three-fork opening and comprises a sample inflow opening and two focusing inflow openings; the sorting inlets and the sorting outlets are formed in the two ends of the micro-fluidic channel respectively, and the micro-lens is arranged at the intersection of the two sorting outlets. The device comprises a chip, a light source, an injection device and an observation platform, light emitted by the light source penetrates through a micro lens and irradiates into a micro-fluidic channel, light force is applied to particles in fluid to be sorted, the particles of different sizes enter different sorting outlets, and finally sorting is achieved. Compared with the prior art, the particle sorting device can realize quick sorting of particles with the diameter of hundreds of nanometers, has the advantages of high sorting efficiency, high control precision and the like, and has important application value in sorting and control of micro-nano-scale particles such as viruses, bacteria and the like.

Provided herein are particles comprising polynucleotide constructs for generating cells expressing anti-CD22 chimeric antigen receptor, as well as vectors, such as lentiviral vectors, comprising same, cells comprising same, and methods of using same. Some embodiments include a surface-engineered lentiviral vector. In some embodiments, the lentiviral vector further encodes a synthetic receptor protein.

The invention provides a macro virus group sequencing library construction method for removing host ribosome RNA through an enzyme method and a kit, and belongs to the technical field of biology. The method comprises the following steps: hybridizing total RNA (Ribonucleic Acid) of a sample with a DNA (Deoxyribose Nucleic Acid) probe aiming at host ribosome RNA to form a DNA / RNA hybrid chain; rNase H is used for digesting RNA in the hybrid chain, and DNase I is used for digesting the remaining DNA probe in the system; purifying to obtain virus RNA (Ribonucleic Acid); carrying out fragmentation treatment on the virus RNA; carrying out reverse transcription on the fragmented RNA to synthesize a first chain cDNA, then synthesizing a second chain cDNA, and carrying out terminal repair and dA tail addition to obtain double-chain cDNA; connecting the linker with the dT tail with the double-chain cDNA; and carrying out PCR amplification and purification on the connection product to obtain the macro virus group sequencing library. According to the construction method and the kit, the problem that the full-length sequence of the virus cannot be obtained from a low-load sample can be solved.

Disclosed herein are methods to edit genes, for example by administering a chimeric nuclease to a cell or organism without the use of a viral vector. Some methods herein include editing DNA of a cell by contacting the cell with a nuclease comprising a Cas9 sequence, where the nuclease edits the DNA of the cell.