Abstract: A display panel and a display apparatus are described. The display panel includes a plurality of touch units. The touch units include first electrodes and second electrodes that are disposed in a same layer. Adjacent first electrodes along a first direction are connected through a bridge line, and adjacent second electrodes along a second direction are connected through a connecting line. The bridge line is disposed in a different layer from the first electrode, and the connecting line is disposed in a same layer as the second electrode. A display region has a through-hole, and the touch units include a first touch unit that at least partially surrounds the through-hole. The first touch unit includes at least two bridge units, the bridge unit is connected to two adjacent first electrodes along the first direction, and the bridge unit includes at least one bridge line.

Abstract: The present invention relates to the field of medical biology, and discloses a single domain antibody and derivative proteins thereof against CTLA4. In particular, the present invention discloses a CTLA4 binding protein and the use thereof, especially the use for treating and/or preventing CTLA4 relevant diseases such as tumor.

Abstract: The present disclosure provides a device for separately arranging vacuum glass supports, which comprises a base, a vibrator, a separation chamber assembly, a separation actuator, a feed tube, and a drive device. The separation chamber assembly is provided with a feed inlet, an accommodation cavity, and a dispensing outlet. The feed inlet is communicated with the accommodation cavity. The dispensing outlet is communicated with the feed tube. The separation actuator is arranged directly below the accommodation cavity and capable to move reciprocatingly with respect to the accommodation cavity. A recess capable of accommodating one support is provided at the upper edge of the separation actuator. Thus, at each reciprocating movement, the separation actuator transports one support from the accommodation cavity to the dispensing outlet via the recess, which avoid arranging multiple supports in one operation.

Abstract: Disclosed herein are methods for detecting a target protein in a sample and methods for detecting a target protein and a target nucleic acid in a sample. Kits for carrying out the methods are also disclosed.

Abstract: The present disclosure provides a display screen based on LED display panels. The display screen includes a plurality of the LED display panels, at least one installation columns, a plurality of longitudinal reference parts, a plurality of assembling and installation assemblies, and a plurality of power control boxes; several LED display panels arranged in longitudinal direction consist of one group; each group of LED display panels has been longitudinally assembled through longitudinal reference parts arranged close to two sides, of backs of a plurality of LED display panels; two transverse adjacent groups of LED display panels are arranged at two sides of one installation column which is vertically located; The transverse reference part of each assembling and installation assembly and the two adjacent longitudinal reference parts are clasped on back to back sides of the installation columns. The display screen has the advantages of being thin, flexible to use.

Abstract: The present invention relates to the field of medical biology, and discloses a single domain antibody and derivative proteins thereof against CTLA4. In particular, the present invention discloses a CTLA4 binding protein and the use thereof, especially the use for treating and/or preventing CTLA4 relevant diseases such as tumor.

Abstract: Provided are an organic light-emitting diode (OLED) device and a manufacturing method therefor. The OLED device includes a substrate and an encapsulation layer. The substrate is divided into a pixel region and an encapsulation region. The substrate and the encapsulation layer are connected by means of a sealing medium. A first electrode layer, an organic light-emitting layer and a second electrode layer are stacked at the pixel region on the substrate, and a buffer layer is provided between the first electrode layer and the substrate. In the present disclosure, the buffer layer is provided so that metal ions of a glass substrate are blocked from penetrating into the first electrode layer/auxiliary electrode.

Abstract: An air conditioning system. A first evaporator and a second evaporator are connected in parallel. A first electronic expansion valve is serially connected to the first evaporator, and a second electronic expansion valve is serially connected to the second evaporator, so that the opening degrees of the first electronic expansion valve and the second electronic expansion valve can be separately adjusted, the first electronic expansion valve and the second electronic expansion valve can perform position correction according to valve opening position information of the first electronic expansion valve and the second electronic expansion valve stored by the air conditioning system, and separately adjust target positions to calibrated target positions. Also disclosed are a control system and a control method for the air conditioning system.

Abstract: The present invention relates to the field of medical biology, and discloses a single domain antibody and derivative proteins thereof against CTLA4. In particular, the present invention discloses a CTLA4 binding protein and the use thereof, especially the use for treating and/or preventing CTLA4 relevant diseases such as tumor.

Abstract: An air conditioning system. A first evaporator and a second evaporator are connected in parallel. A first electronic expansion valve is serially connected to the first evaporator, and a second electronic expansion valve is serially connected to the second evaporator), so that the opening degrees of the first electronic expansion valve and the second electronic expansion valve can be separately adjusted, the first electronic expansion valve and the second electronic expansion valve can perform position correction according to valve opening position information of the first electronic expansion valve and the second electronic expansion valve stored by the air conditioning system, and separately adjust target positions to calibrated target positions. The air conditioning system can reduce risks of out-of-synchronization of the electronic expansion valves and optimize performance of a control system. Also disclosed are a control system and a control method for the air conditioning system.

Abstract: The present disclosure relates to a double-juxtaposed-valve-core rotary multi-functional hydraulic regulating valve driven by two motors. The hydraulic regulating valve includes a first regulating component, a second regulating component and a valve block. The first regulating component includes a first motor, a first valve core, a first connection sleeve and a first valve sleeve. The second regulating component includes a second motor, a second valve core, a second connection sleeve and a second valve sleeve. The first motor and the second motor are provided with angular displacement sensors. Both the first valve core and the second valve core include a connection portion and a cylinder portion. The cylinder portion defines a group of crossed radial through holes. Both the first valve sleeve and the second valve sleeve are of hollow cylinder structures.

Abstract: Methods for treatment of wAMD with an active CNV lesion of less than 50% of the total lesion size and pharmaceutical compositions for the use therein are disclosed.

Abstract: The present invention relates to the field of medical biology, and discloses a single domain antibody and derivative proteins thereof against CTLA4. In particular, the present invention discloses a CTLA4 binding protein and the use thereof, especially the use for treating and/or preventing CTLA4 relevant diseases such as tumor.

Abstract: The present disclosure relates to a double-juxtaposed-valve-core rotary multi-functional hydraulic regulating valve driven by two motors. The hydraulic regulating valve includes a first regulating component, a second regulating component and a valve block. The first regulating component includes a first motor, a first valve core, a first connection sleeve and a first valve sleeve. The second regulating component includes a second motor, a second valve core, a second connection sleeve and a second valve sleeve. The first motor and the second motor are provided with angular displacement sensors. Both the first valve core and the second valve core include a connection portion and a cylinder portion. The cylinder portion defines a group of crossed radial through holes. Both the first valve sleeve and the second valve sleeve are of hollow cylinder structures.

Abstract: The application discloses a dental zirconia restoration material with uniform transition of strength and color, and a preparation method thereof. The preparation method includes the following steps: (1) pouring colored zirconia powder into a dry pressing mould in accordance with a sequence of the strength from high to low and the color from dark to light for each layer, and performing dry pressing; (2) performing isostatic cool pressing after the dry pressing; (3) performing pre-sintering after the isostatic cool pressing to obtain a greenware; and (4) performing CAD/CAM cutting on the greenware, and finally performing final sintering to obtain the dental zirconia restoration material. In the present application, the strength of a restoration can gradually increase from a cut end to the neck, the wear to adjacent teeth and jaw teeth is reduced, and long-bridge restoration can be realized due to the high strength of the neck.

Abstract: This application discloses a glass pane bombardment degassing device. The glass pane bombardment degassing device comprises a vacuum box body, a glass pane carrying device, an inlet and an outlet arranged on the vacuum box body for the glass pane carrying device to enter or exit the body, a bottom plate arranged on the glass pane carrying device to stack a plurality of glass panes stacked, every two adjacent glass panes being separated from each other, and a bombardment device placed inside the vacuum box body. The bombardment device includes a first and a second electrodes arranged in an up-and-down opposite way and connected with a positive electrode of a power supply, a moving electrode arranged between the first and second electrodes and connected with a negative electrode of the power supply, to generate ion or electron streams performing bombardment degassing to glass panes.

Abstract: Methods for treatment of wAMD with an active CNV lesion of less than 50% of the total lesion size and pharmaceutical compositions for the use therein are disclosed.

Abstract: The invention provides novel 7,8-dihydro-imidazo[1,2-?]pyrazolo[4,3-e]pyrimidin-4-one compounds and 7,8,9-trihydro-[1H or 2/f]-pyrimido[1,2-a]pyrazolo[4,3-e]pyrimidin-4(5H)-one compounds, substituted at the 1 or 2 position with C2-g allcyl, C3-9 cycloalkyl, heteroarylalkyl, or substituted arylalkyl, in free, salt or prodrug form, processes for their production, their use as pharmaceuticals, particularly as PDE1 inhibitors, and pharmaceutical compositions comprising them.

Abstract: In various aspects and embodiments, the present invention is directed to versatile, label-free method for the quantitative and qualitative detection of biomarkers and/or other compounds in a fluid sample using functionalized microparticle aggregates. In these methods, micron-scale particles are functionalized to specifically interact with the biomarker being measured and added to the sample to form aggregates, the size and number of which are counted to find a volume fraction and/or number fraction of aggregates in the sample. There is a direct correlation between the volume fraction and number fraction of these aggregates and the concentration of the corresponding biomarker. By comparing the measured volume fraction and/or number fraction of aggregates in the sample to a calibration curve, the concentration of that biomarker may be determined even for biomarkers or other target compounds in samples at very low concentrations, without the need for fluorescence and enzyme labelling of antibodies.