Abstract: A device cold plasma sterilization includes a housing, a base, a conveying assembly, a plurality of core modules, a transformer, a control cabinet, a distribution box, a shielding door, and a controller. The housing is disposed on the base. The plurality of core modules is disposed in the housing along a moving direction of the conveying assembly and are spaced apart from each other. The plurality of core modules each include a plurality of electrode assemblies spaced from one another by equal distance and arranged in a row. The transformer, the control cabinet, and the distribution box are disposed in a lower part of the base and are connected to the plurality of electrode assemblies. The conveying assembly is disposed in a middle part of the base. The base includes an inlet for entry and an outlet for exit of a package to be sterilized.

Abstract: The present disclosure provides an electrode assembly and a secondary battery. The electrode assembly includes a first electrode plate, a second electrode plate and a separator. The first electrode plate, the second electrode plate and the separator are wound to a flat structure, and the flat structure comprises a main region and corner regions, the corner regions are provided at two ends of the main region along a width direction of the main region. The first electrode plate and the second electrode plate each are wound to turns. A gap is provided between two adjacent turns of the first electrode plate, the gap includes a first gap and a second gap. The first gap corresponds to the corner region in position, the second gap corresponds to the main region in position, and a dimension of the first gap is larger than a dimension of the second gap.

Abstract: A sterilizer includes a cold plasma generator; an ultraviolet (UV) light generator; and an airflow circulation system. The cold plasma generator and the UV light generator are disposed in the airflow circulation system. The cold plasma generator is configured to generate a cold plasma airflow; the UV light generator is configured to emit an UV light; the UV light generator is disposed in a downstream of the cold plasma airflow of the cold plasma generator, so that the cold plasma airflow is exposed to the UV light to form a disinfecting airflow that is then sprayed on a surface of a sample contaminated with a pathogen comprising coronavirus.

Abstract: The present invention discloses a high-voltage electric field low-temperature plasma cold sterilization system circuit and apparatus, and belongs to the field of frequency converter power source circuit technologies. The present invention including a power source module, a voltage/current/power adjustment module, a switch module, and a transformer module. The power source module includes a single-phase frequency converter and a first-stage inductance.

Abstract: The present disclosure relates to, inter alia, a method of quantitating an amount of an antibody molecule from a mixture comprising two or more antibody molecules, comprising separating each of the two or more antibody molecules from the mixture by hydrophobic interaction chromatography high performance liquid chromatography (HIC-HPLC) and quantitating an amount of each antibody molecule, wherein the molecular weight of each antibody molecule is within 15 kDa of any other antibody molecule in the mixture and either each antibody molecule is different from another antibody molecule in the mixture by more than about 0.25 unit on the Kyte & Doolittle hydropathy scale or each of the antibody molecules when run alone on HIC-HPLC elutes at distinct run time with little overlap from the other antibody molecules in the mixture, or both.

Abstract: A rearview mirror system for a vehicle providing a direct reflection of scenes in good light and an enhanced display of scenes in bad lighting includes a housing defining an opening, a display screen arranged at the opening, a camera, a fill light lamp, and a controller. The display screen is light-pervious at only one side. The camera and the fill light lamp are arranged on the housing. An image processing chip and the controller are arranged between the display screen and the housing. When ambient brightness is below a preset brightness value, the camera and the fill light lamp are activated, the camera captures images of side and rear scenes of the vehicle and generates an optical signal, the image processing chip, based on the optical signal, outputs an enhanced image on the display screen for better driving safety. A vehicle including the rearview mirror system is also disclosed.

Abstract: The present disclosure relates to, inter alia, a method of quantitating an amount of an antibody molecule from a mixture comprising two or more antibody molecules, comprising separating each of the two or more antibody molecules from the mixture by hydrophobic interaction chromatography high performance liquid chromatography (HIC-HPLC) and quantitating an amount of each antibody molecule, wherein the molecular weight of each antibody molecule is within 15 kDa of any other antibody molecule in the mixture and either each antibody molecule is different from another antibody molecule in the mixture by more than about 0.25 unit on the Kyte & Doolittle hydropathy scale or each of the antibody molecules when nm alone on HIC-HPLC elutes at distinct run time with little overlap from the other antibody molecules in the mixture, or both.

Abstract: This application provides a secondary battery, a battery module, and a device using a secondary battery as a power supply. The secondary battery includes an electrode assembly, a cap assembly, and current collection members. The electrode assembly includes a main body and tabs that extend from the main body. The cap assembly includes a cap plate, electrode terminals, and an insulation baffle. The electrode terminals are disposed on the cap plate. The insulation baffle is connected to a side of the cap plate, where the side is close to the main body. The current collection members are at least partly located between the insulation baffle and the main body, and each of the current collection members includes a tab connection portion connected to one of the tabs. The insulation baffle contains a first recess.

Abstract: The present disclosure relates to, inter alia, a method of quantitating an amount of an antibody molecule from a mixture comprising two or more antibody molecules, comprising separating each of the two or more antibody molecules from the mixture by hydrophobic interaction chromatography high performance liquid chromatography (HIC-HPLC) and quantitating an amount of each antibody molecule, wherein the molecular weight of each antibody molecule is within 15 kDa of any other antibody molecule in the mixture and either each antibody molecule is different from another antibody molecule in the mixture by more than about 0.25 unit on the Kyte & Doolittle hydropathy scale or each of the antibody molecules when run alone on HIC-HPLC elutes at distinct run time with little overlap from the other antibody molecules in the mixture, or both.

Abstract: An electrode assembly and a battery cell is disclosed. The electrode assembly includes a first electrode plate and a second electrode plate. The first electrode plate includes a first current collector and a first active material layer, the first current collector includes a first main body and a first tab, and the first tab extends from one end of the first main body in a longitudinal direction. The second electrode plate includes a second current collector and a second active material layer, the second current collector includes a second main body and a second tab, the second tab extends from one end of the second main body in the longitudinal direction, and the second active material layer is applied on a surface of the second main body.

Abstract: A prokaryotic expression system or a recombinant adenovirus system is used to highly efficiently express VZV envelope gE glycoprotein and the flagellin fusion protein thereof. The produced recombinant gE protein, gE flagellin fusion protein and recombinant adenovirus vector, or composition thereof is used to immunize a mouse so as to promote the body to generate gE and VZV-specific antibody titer, as well as gE-specific and VZV-specific cell immunity.

Abstract: A medication dispenser includes a base seat, a circuitry unit and an outer casing. The base seat includes a mouthpiece. The circuitry unit includes a first circuit board, a battery, and first and second switches disposed on the first circuit board. The outer casing is movable relative to the base seat between a close position where the outer casing covers the mouthpiece and where the first switch is actuated such that electric power is prevented from being supplied from the battery to the first circuit board, and an open position where the outer casing uncovers the mouthpiece and where the second switch is actuated such that electric power is supplied from the battery to the first circuit board.

Abstract: The present disclosure relates to, inter alia, a method of quantitating an amount of an antibody molecule from a mixture comprising two or more antibody molecules, comprising separating each of the two or more antibody molecules from the mixture by hydrophobic interaction chromatography high performance liquid chromatography (HIC-HPLC) and quantitating an amount of each antibody molecule, wherein the molecular weight of each antibody molecule is within 15 kDa of any other antibody molecule in the mixture and either each antibody molecule is different from another antibody molecule in the mixture by more than about 0.25 unit on the Kyte & Doolittle hydropathy scale or each of the antibody molecules when nm alone on HIC-HPLC elutes at distinct run time with little overlap from the other antibody molecules in the mixture, or both.

Abstract: This application provides a current collecting member, a secondary battery, and a fabrication method. The secondary battery includes an electrode assembly, a housing, a top cover assembly and current collecting members. The electrode assembly includes a main body portion and a first tab extending from an end of the main body portion along a transverse direction. The top cover assembly includes a top cover plate and a first electrode terminal disposed on the top cover plate connected to the housing. The current collecting member is connected to the first tab and the first electrode terminal. The current collecting member includes a substrate and a support plate, the substrate being provided at a side of the main body portion along a transverse direction, the support plate extending from an end part of the substrate in a longitudinal direction, and the first tab being connected to the support plate.

Abstract: The present disclosure provides stable pharmaceutical formulations comprising a human antibody that specifically binds to Ebola Virus (EBOV). In certain embodiments, the formulations contain, in addition to an anti-EBOV antibody, a buffer, an amino acid, a non-ionic surfactant, and a stabilizer. The pharmaceutical formulations of the present disclosure exhibit a substantial degree of antibody stability upon stress, for example, agitation during transport, and storage, for example, storage at temperatures greater than 40° C.

Abstract: Embodiments of the present disclosure provides an ultrasonic image analysis system which includes an image collection unit which receives and transmits an ultrasonic waveform and obtains two sets of three-dimensional ultrasonic image data; an image analysis unit which registers the two sets of three-dimensional ultrasonic image data to obtain a registration mapping relationship between the two sets of three-dimensional ultrasonic image data; a user interface unit which responds to a treatment done on the two sets of three-dimensional ultrasonic image data by a user through an external hardware device; an image display unit which displays the two sets of three-dimensional ultrasonic image data according to the registration mapping relationship and a result of the treatment of the user interface unit; and an image store unit for storing the two sets of three-dimensional ultrasonic image data and the registration mapping relationship.

Abstract: Provided is an artificial intelligence (AI) computing device applied to an industrial automation system. The AI computing device is connected to a field bus via a field bus interface and is communicated with a controller. The AI computing device processes data sent by the controller by using a built-in AI computing architecture, analyzes the data, and sends the analysis result to the controller. Also provided are a corresponding method and apparatus, an engineer station, and an industrial automation system.

Abstract: A medication dispenser includes a base seat, a circuitry unit and an outer casing. The base seat includes a mouthpiece. The circuitry unit includes a first circuit board, a battery, and first and second switches disposed on the first circuit board. The outer casing is movable relative to the base seat between a close position where the outer casing covers the mouthpiece and where the first switch is actuated such that electric power is prevented from being supplied from the battery to the first circuit board, and an open position where the outer casing uncovers the mouthpiece and where the second switch is actuated such that electric power is supplied from the battery to the first circuit board.

Abstract: The present disclosure relates to, inter alia, a method of quantitating an amount of an antibody molecule from a mixture comprising two or more antibody molecules, comprising separating each of the two or more antibody molecules from the mixture by hydrophobic interaction chromatography high performance liquid chromatography (HIC-HPLC) and quantitating an amount of each antibody molecule, wherein the molecular weight of each antibody molecule is within 15 kDa of any other antibody molecule in the mixture and either each antibody molecule is different from another antibody molecule in the mixture by more than about 0.25 unit on the Kyte & Doolittle hydropathy scale or each of the antibody molecules when nm alone on HIC-HPLC elutes at distinct run time with little overlap from the other antibody molecules in the mixture, or both.