Abstract: A display device includes a display panel, a flexible circuit board, and a driving chip. The display panel includes a display area and a non-display area bent to the back of the display area. The driving chip is bonded and connected to the display panel in the non-display area. The flexible circuit board includes a bonding area bonded to the non-display area, and a first flat area, a bending area, and a second flat area arranged in sequence in a direction away from the bonding area. The flexible circuit board is at the back of the display area. The second flat area is between the first flat area and the display area. A first electromagnetic shielding layer is provided on at least a portion of the surface, close to the display area, of the second flat area.

Abstract: Provided is a display panel. The display panel is divided into a display region and a non-display region disposed on a periphery of the display region. The display panel includes: a plurality of touch units and a plurality of light-emitting devices that are within the display region; and a plurality of touch signal leads and a plurality of data signal leads that are within the non-display region, wherein the touch signal lead is electrically connected to the touch unit, and the data signal lead is electrically connected to the light-emitting device; wherein in the non-display region, a region where at least a portion of the touch signal leads are disposed and a region where the plurality of data signal leads are disposed are respectively on different sides of the display region.

Abstract: A display module includes a display panel and a peripheral region. The peripheral region includes a bendable fan-out region including a panel bonding portion and a driving chip; a flexible circuit board, including a first and a second conductive layers, and a substrate. The first conductive layer includes a first and a second bonding portions, and a connection portion; the second conductive layer is located on a side of the first conductive layer and at least partially overlaps with the first bonding portion; the first and the second conductive layers are connected through a via hole penetrating through the substrate; an end of the flexible circuit board is bonded to the panel bonding portion through the first bonding portion, and the second bonding portion is bonded to a control circuit board; and a conductive protection layer, covering the driving chip and connected to the second conductive layer.

Abstract: Provided is a support member of a flexible display module. The support member includes: a body portion and a plurality of outward protrusion portions. The plurality of outward protrusion portions are at least distributed at two opposite sides of the body portion and protrude outwards relative to the sides of the body portion. A positioning hole is formed in each of the outward protrusion portions.

Abstract: A display panel and a preparation method therefor, and a display device. The display panel comprises an active area and a peripheral area, which is arranged at the periphery of the active area and comprises a bending zone (410), wherein an edge of the peripheral area is provided with a protrusion (500), and the protrusion (500) has an alignment mark (400) for the bending zone (410).

Abstract: A display module and a display device are provided. The display module includes: a display panel including a display area and a non-display area surrounding the display area; an optical adhesive layer (2) located on a light emitting side of the display panel and covering the display area; and a cover plate, located on a side of the optical adhesive layer facing away from the display panel and covering the display panel and the optical adhesive layer. A limiting groove used for preventing an edge of the optical adhesive layer from overflowing is formed on a side of the cover plate facing the optical adhesive layer. A least the edge of the optical adhesive layer is in the limiting groove.

Abstract: A circuit board structure and a display device, the circuit board structure includes a first circuit board, a second circuit board, a filling portion and an electromagnetic shield layer. The second circuit board has a thickness greater than that of the first circuit board. At least one corner portion forms at a joint of the first circuit board and the second circuit board. A connection line forms at a joint of the second circuit board and the first circuit board. The connection line is located at the corner portion. The filling portion fills the corner portion, an extending direction of the filling portion is identical to an extending direction of the corner portion. The extending direction is identical to a direction of the connection line. A thickness of a cross section of the filling portion perpendicular to the extending direction increases as a distance from the second circuit board decreases.

Abstract: A displaying module includes a transparent cover plate, a display panel and a heat dissipating film layer; the transparent cover plate covers a first surface of the display panel, an area of the display panel is less than an area of the transparent cover plate, and the first surface refers to a surface of the display panel where a light ray exits; and the heat dissipating film layer covers a second surface of the display panel, and at least part of an edge position of the heat dissipating film layer contacts an inner surface of the transparent cover plate, wherein the second surface refers to a surface of the display panel that is opposite to the first surface, the inner surface of the transparent cover plate refers to a surface of the transparent cover plate that contacts the display panel, and the heat dissipating film layer is electrically conductive.

Abstract: In alternative embodiments, provided are compositions, including recombinant expression systems and vectors, products of manufacture and kits, and methods, for remotely-controlled and non-invasive manipulation of intracellular nucleic acid expression, genetic processes, function and activity in live cells such as T cells in vivo, for example, activating, adding functions or changing or adding specificities for immune cells, for monitoring physiologic processes, for the correction of pathological processes and for the control of therapeutic outcomes.

Abstract: An insulated thermal bag is provided, including an insulated thermal bag body, the insulated thermal bag body is mainly composed of an outer bag body and an inner container, wherein an upper end of the bag body is provided with a cover body, and the cover body is internally provided with a sponge layer, and the inner container is formed in integration by ABS resin and polyester insulation cotton. Compared with the prior art, the inner container and the bag body of the utility model adopt a detachable structure design, which greatly reduces the labor and consumption costs. In addition, the inner container of the utility model is formed in integration by ABS resin and polyester insulation cotton, which has good insulation effect.

Abstract: In alternative embodiments, provided are compositions, including products of manufacture and kits, and methods, for remotely-controlled and non-invasive manipulation of intracellular nucleic acid expression, genetic processes, function and activity in live cells, e.g., adding functions or changing or adding specificities for immune cells, for monitoring physiologic processes, for the correction of pathological processes and for control of therapeutic outcomes. In alternative embodiments, provided are ultrasound-based thermal or mechanical stimulations, and thermo- or mechano-sensitive protein, either synthetically engineered or natively (endogenously) occurring, integrated to control the production of intracellular nucleic acid and gene expression, e.g., for the expression of biological-active proteins, which can be used, in alternative embodiments, for diagnostic or therapeutic purposes.

Abstract: In alternative embodiments, provided are compositions, including products of manufacture and kits, and methods, for engineering immune effector cells, e.g., T cells, NK cells, monocytes and/or macrophages to recognize and destroy a desired target cell, which can be a cancer cell, a dysfunctional cell, or an infected cell.

Abstract: Provided are compositions, products of manufacture, kits and methods for remotely-controlled and non-invasive manipulation of intracellular nucleic acid expression, genetic processes, function and activity in live cells such as T cells in vivo, for activating, adding functions or changing or adding specificities for immune cells, for monitoring physiologic processes, for the correction of pathological processes and for the control of therapeutic outcomes. Provided are ultrasound-based stimulations and a heat-sensitive activation of proteins caused by the activation of polypeptides controlled by heat shock protein promoters to control the production of intracellular nucleic acid and gene expression, for example, for the expression of biological-active proteins such as T cell receptors, for example, chimeric antigen receptors (CARs).

Abstract: The present application provides a thin-type phone receiver, comprising a housing, a vibration membrane assembly and a coil. The vibration membrane assembly comprises a frame, a diaphragm and a sealing membrane. The coil is sealedly fixed in the mounting area and sealedly sleeved on the frame, and the spreading sealing membrane seals an entirety of a first gap between the frame and the diaphragm, thereby, the vibration membrane assembly separates a mounting cavity of the housing into two cavities that are arranged side by side and separate. When the coil is energized and an electromagnetic field generated by the coil interacts with a fixed magnetic field of the permanent magnets in the phone receiver, the entire diaphragm vibrates, thus, as the coil is sleeved on the vibration membrane assembly to form the thin-type phone receiver.

Abstract: The present application provides a thin-type phone receiver, comprising a housing, a vibration membrane assembly and a coil. The vibration membrane assembly comprises a frame, a diaphragm and a sealing membrane. The coil is sealedly fixed in the mounting area and sealedly sleeved on the frame, and the spreading sealing membrane seals an entirety of a first gap between the frame and the diaphragm, thereby, the vibration membrane assembly separates a mounting cavity of the housing into two cavities that are arranged side by side and separate. When the coil is energized and an electromagnetic field generated by the coil interacts with a fixed magnetic field of the permanent magnets in the phone receiver, the entire diaphragm vibrates, thus, as the coil is sleeved on the vibration membrane assembly to form the thin-type phone receiver.

Abstract: In alternative embodiments, provided are compositions, including products of manufacture and kits, and methods, for remotely-controlled and non-invasive manipulation of intracellular nucleic acid expression, genetic processes, function and activity in live cells, e.g., adding functions or changing or adding specificities for immune cells, for monitoring physiologic processes, for the correction of pathological processes and for control of therapeutic outcomes. In alternative embodiments, provided are ultrasound-based thermal or mechanical stimulations, and thermo- or mechano-sensitive protein, either synthetically engineered or natively (endogenously) occurring, integrated to control the production of intracellular nucleic acid and gene expression, e.g., for the expression of biological-active proteins, which can be used, in alternative embodiments, for diagnostic or therapeutic purposes.

Abstract: This invention relates to a method of extracting crude polysaccharide by microwave-assisted from Artemisia sphaerocephala seed de-oiling dregs. In particular, the invention comprising: microwave-assisted extraction, enzymatic hydrolysis, dialysis et. al. It provides a technique whereby the polysaccharide can be extracted effectively, in a relatively short period of time (20-30 min) with respect to conventional extraction methods and allows for an enhanced extraction yield (more than 30%). Furthermore, the invention also allows for the extraction of material with less solvent consumption, good reproducibility, excellent solubility, energy conservation, environmental protection, and showed great potential for efficient sample preparation and large-scale industrial application in the near future. With great resource advantage of Artemisia sphaerocephala in China, the invention has bright perspectives in promoting local economic development.

Abstract: This invention relates to a method of extracting crude polysaccharide by microwave-assisted from Artemisia sphaerocephala seed de-oiling dregs. In particular, the invention comprising: microwave-assisted extraction, enzymatic hydrolysis, dialysis et. al. It provides a technique whereby the polysaccharide can be extracted effectively, in a relatively short period of time (20-30 min) with respect to conventional extraction methods and allows for an enhanced extraction yield (more than 30%). Furthermore, the invention also allows for the extraction of material with less solvent consumption, good reproducibility, excellent solubility, energy conservation, environmental protection, and showed great potential for efficient sample preparation and large-scale industrial application in the near future. With great resource advantage of Artemisia sphaerocephala in China, the invention has bright perspectives in promoting local economic development.