Abstract: The embodiments of the present disclosure provide a display panel, a manufacturing method thereof, and a display device. The display panel includes a first substrate and a second substrate cell-assembled to each other, a light emitting member layer disposed between the first substrate and the second substrate and a light diffusion layer disposed on a light existing side of the light emitting member layer, the light emitting member layer includes a plurality of light emitting units and imaging holes disposed on at least two sides of each of the light emitting units, the light diffusion layer includes a reflective member configured to reflect a light ray emitted by the light emitting unit and reaching the reflective member, and the reflected light ray reflected by the reflective member exits from the imaging holes.

Abstract: The invention belongs to the field of biotechnology, in particular, relates to peptide fragment, monoclonal antibody, colloidal gold test strip and detection method thereof used for detection of stichopus oligopeptide. Sequences of the peptide fragments are KIVPGVPD and GRDGDQGPV. After identification, the peptides KIVPGVPD and GRDGDQGPV are newly discovered oligopeptides, which are exclusive peptide fragments of Stichopus oligopeptide.

Abstract: A backlight assembly and a display device including the backlight assembly are provided. The backlight assembly includes a light source unit, a peep-proof layer on a light emitting side of the light source unit, a light adjustment layer on a side of the peep-proof layer distal to the light source unit, and a plurality of first microstructures between the peep-proof layer and the light adjustment layer and spaced apart from each other.

Abstract: Disclosed herein are magnesium alloys and methods of making and use thereof. The magnesium alloys comprise: from 1 to 1.5 wt % Zn, from 1 to 1.4 wt. % Al, from 0.2 to 0.7 wt % Ca, from 0.2 to 0.4 wt % Ce, from 0.1 to 0.8 wt % Mn, and the balance comprising Mg.

Abstract: In a display method for an electronic device, on one hand, when a screen ratio of a first screen of the electronic device does not meet a preset ratio requirement, a display interface of a first application is displayed in a first area on the first screen; and a shortcut function control is displayed in a second area on the first screen, where a screen ratio of the first area meets the ratio requirement; on the other hand, the display interface of the first application is displayed on the first screen when the screen ratio of the first screen meets the ratio requirement.

Abstract: An operation method for an electronic device and an electronic device are provided, and relate to the field of electronic devices. In a split-screen display scenario, a function of quickly opening a specific interface by using an entered gesture is implemented. When a screen of the electronic device is split for display, the electronic device receives different operations for a side that is of a single window and that is closely adjacent to another window, and the electronic device may execute a corresponding event only for the window, for example, display a previous-level interface of a current interface in the window, display a desktop in the window, or display a task list interface in the window, and an interface displayed in the another window remains unchanged.

Abstract: The present disclosure relates, according to some embodiments, to methods for preparing a library for sequencing. For example, a method may comprise (a) in a coupled reaction, (i) contacting a population of nucleic acid fragments with a tailing enzyme to produce tailed fragments, and (ii) ligating to the tailed fragments a sequencing adapter with a ligase to produce adapter-tagged fragments; and/or separating adapter-tagged fragments from the tailing enzyme and the ligase to produce separated adapter-tagged fragments and, optionally, separated tailing enzyme and/or separated ligase. In some embodiments, a tailing enzyme and/or a ligase used in library preparation may be immobilized enzymes.

Abstract: Disclosed are compounds, compositions and methods for treating diseases, disorders, or medical conditions that are affected by the modulation of DHODH. Such compounds are represented by Formula (I) as follows: wherein R1, R2, R3, R4, X, and Y are defined herein.

Abstract: An antibody or antigen binding fragment thereof that binds to a Fn14, wherein the antibody or antigen binding fragment thereof is an antagonist and non-agonist of Fn14.

Abstract: Provided are a novel bile acid derivative for treating fatty liver disease, a pharmaceutical composition thereof, and a use in the preparation of a medicine for treating and improving diseases and symptoms mediated or caused by FXR or TGR5. The bile acid derivative of the present invention inhibits or delays the metabolism of bile acid by bacterial BSH/7? dehydroxylase in the intestine and greatly prolongs the effective survival time of bile acid in the intestine. The bile acid derivative and the pharmaceutical composition thereof can significantly stimulate bile acid membrane receptor TGR5, promote the secretion of glucagon-like peptide 1 from enteroendocrine cells, reduce liver fat accumulation, significantly improve liver function and increase glucose tolerance, thereby having an excellent effect on the treatment of fatty liver disease.

Abstract: Disclosed herein are magnesium alloy based objects and methods of making and use thereof. For example, disclosed herein are methods of making a magnesium alloy based object, the methods comprising: heating an object comprising a preliminary magnesium alloy at a first temperature for a first amount of time, the preliminary magnesium alloy comprising a first intermetallic phase, a second intermetallic phase, and an alloy phase, to thereby substantially dissolving the first intermetallic phase into the alloy phase to form an object comprising an intermediate magnesium alloy, the intermediate magnesium alloy comprising the second intermetallic phase and the alloy phase; and heating the object comprising the intermediate magnesium alloy at a second temperature for a second amount of time to thereby substantially dissolving the second intermetallic phase into the alloy phase and minimizing incipient melting of the alloy phase to form the magnesium alloy based object.

Abstract: Provided are high concentration stable formulations of anti-CSF1R/CSF1 antibodies. An example formulation includes 105 to 250 mg/mL of the antibody, 100 mM to 200 mM of arginine glutamate or arginine HCl, 10 mM to 50 mM histidine, and 0.015 to 0.035 w/v % of polysorbate 80, at a pH of 5.4 to 5.6. Also provided are methods of using the formulations for treating diseases.

Abstract: Disclosed is a magnetic compression anastomosis system for laparoscopic cholangioenterostomy, including an emission gun, daughter and parent magnetic rings, and an assisting rod, wherein the parent magnetic ring is positioned at the stump of a common bile duct in a purse string suture manner, the relative position is fixed by the assisting rod, the emission gun is loaded with the daughter magnetic ring and makes the same in butt joint with the parent magnetic ring by an intestinal cavity channel of an intestinal tube, the distance between the daughter magnetic ring and the parent magnetic ring is continuously shortened by a push rotary button of the emission gun, and when the relative distance between the daughter and the parent magnetic rings is shortest and mutual attraction is realized, separating the daughter magnetic ring from the emission gun is achieved by an activation mechanism of the emission gun, realizing laparoscopic cholangioenterostomy.

Abstract: A user interface display method includes that when an electronic device displays an interactive interface element in an unreachable area of a display of the electronic device, the electronic device displays the interactive interface element in a reachable area of the display in response to a gesture entered by a user on the display.

Abstract: A display panel configured to display images is provided, each image including a plurality of image pixels and each image pixel including a plurality of sub-pixels of different colors, respectively, the display panel including: a base substrate; and a plurality of sub-beam generation components on the base substrate, each sub-beam generation component being configured to generate at least one sub-pixel in at least one image pixel of the image pixels and including: a group of light-emitting units comprising at least one light-emitting unit and corresponding to at least one sub-pixel; and a beam-expanding layer, which is arranged on a light emergent side of the group of light-emitting units and configured to expand light beams emitted from the group of light-emitting units; an orthogonal projection of the beam-expanding layer on the base substrate at least partially overlapping with an orthogonal projection of the group of light-emitting units on the base substrate.

Abstract: The present disclosure provides an electronic device. The electronic device includes a body and a display screen. The display screen is fixed to the body. A back of the body includes a spacing area not covered by the display screen, the spacing area including a conductor layer. The electronic device further includes an antenna of the electronic device disposed in the spacing area to emit or receive radio frequency signals. The antenna includes the conductor layer.

Abstract: The present disclosure provides a modified catalyst, and preparation method and a method for producing aromatic hydrocarbons by aromatization of olefins using the modified catalyst. The modified catalyst comprises an acidic molecular sieve and an olefin aromatization active metal component, the total acid amount of the catalyst as measured by NH3-TPD method is not higher than 0.35mmo1/g, and ratio of the strong acid to weak acid is within a range of 0.8-1.2.

Abstract: Provided herein is a thermolabile proteinase and methods of using the same. In some embodiments, the thermolabile proteinase may comprise an amino acid sequence that is at least 90% identical to any of SEQ ID NOs:1-11 and at least one amino acid substitution in helix 3. The thermolabile proteinase is active at a temperature in the range of 4° C.-40° C. and is inactivated by raising the temperature to above 50° C., where the proteinase is substantially inactive at 65° C.

Abstract: The present disclosure provides a method of manufacturing a bonding structural test block with defects. The method of manufacturing the bonding structural test block with defects includes: providing a first plate and a second plate; applying an adhesive on an upper surface of the first plate to form an adhesive layer; heating and curing at least partial region of the adhesive layer for the first time; placing the second plate on the adhesive layer; and heating and curing the adhesive layer for the second time to form a boding structural test block. According to the present disclosure, the at least partial region of the adhesive layer is heated and cured for the first time and chemical reaction occurs, so that the at least partial region forms a defect, and controllable manufacturing of the defect is realized. The test block with the defect is subjected to mechanical detection to simulate the actual defective product.

Abstract: A calibration method includes: acquiring eight error models obtained after a preliminary calibration of a Terahertz frequency band system; based on the eight error models, determining a first mathematical model according to a first S parameter related to a first calibration piece, the first mathematical model comprising parallel crosstalk terms between probes, and determining a second mathematical model according to a second S parameter related to a second calibration piece, the second mathematical model comprising series crosstalk terms between the probes; determining a third mathematical model according to a third S parameter related to a measured piece; and solving and obtaining a Z parameter of the measured piece based on the first mathematical model, the second mathematical model and the third mathematical model, and acquiring an S parameter of the measured piece according to the Z parameter of the measured piece.