Abstract:
This system takes in raw cellular material collected using a provided swab, blood collection device, urine collection device, or other sample collection device and transforms that biological material into a digital result, identifying the presence, absence and/or quantity of nucleic acids, proteins, and/or other molecules of interest.
Abstract:
Provided is a composite cover plate including a substrate body, wherein the substrate body includes two surfaces that are arranged opposite, at least one surface is provided with an antistatic film layer; the antistatic film layer includes a perfluoropolyether mixture and a silane coupling agent. Further provided is a method for preparing a composite cover plate, including: providing a substrate body with two surfaces that are arranged opposite, and spraying an antistatic film layer on at least one surface of the substrate body; wherein the antistatic film layer includes a perfluoropolyether mixture and a silane coupling agent. Further provided is a display device including a display module and a composite cover plate covering the surface of the display module, wherein the composite cover plate is any composite cover plate provided herein, an antistatic film layer is arranged on a side of the composite cover plate away from the display module.
Abstract:
A thermosetting powder coating material includes powder particles containing a thermosetting resin, a thermosetting agent, and a surfactant. The amount of the surfactant is about 0.1 ppm or more and about 8.0 ppm or less on a mass basis.
Abstract:
A method for forming a multilayer coating film includes applying an aqueous first base coating composition (A) onto a cured electrodeposition coating film, applying an aqueous second base coating composition (B) without preheating, performing preheating, further applying a clear coating composition (C), and simultaneously heat-curing the first base coating film, the second base coating film, and the clear coating film. The aqueous first base coating composition contains a specific aqueous polyester resin, a specific aqueous acrylic resin, a specific aqueous urethane resin and a melamine resin. A breaking energy of a coating film formed of the aqueous first base coating composition and a peel strength between the coating film and the cured electrodeposition coating film are controlled to specific values.
Abstract:
Devices, systems, and methods for detecting molecules of interest within a collected sample are described herein. In certain embodiments, self-contained sample analysis systems are disclosed, which include a reusable reader component, a disposable cartridge component, and a disposable sample collection component. The reader component may communicate with a remote computing device for the digital transmission of test protocols and test results. In various disclosed embodiments, the systems, components, and methods are configured to identify the presence, absence, and/or quantity of particular nucleic acids, proteins, or other analytes of interest, for example, in order to test for the presence of one or more pathogens or contaminants in a sample.
Abstract:
Devices, systems, and methods for detecting molecules of interest within a collected sample are described herein. In certain embodiments, self-contained sample analysis systems are disclosed, which include a reusable reader component, a disposable cartridge component, and a disposable sample collection component. In some embodiments, the reader component communicates with a remote computing device for the digital transmission of test protocols and test results. In various disclosed embodiments, the systems, components, and methods are configured to identify the presence, absence, and/or quantity of particular nucleic acids, proteins, or other analytes of interest, for example, in order to test for the presence of one or more pathogens or contaminants in a sample.
Abstract:
Devices, systems, and methods for detecting molecules of interest within a collected sample are described herein. In certain embodiments, self-contained sample analysis systems are disclosed, which include a reusable reader component, a disposable cartridge component, and a disposable sample collection component. In some embodiments, the reader component communicates with a remote computing device for the digital transmission of test protocols and test results. In various disclosed embodiments, the systems, components, and methods are configured to identify the presence, absence, and/or quantity of particular nucleic acids, proteins, or other analytes of interest, for example, in order to test for the presence of one or more pathogens or contaminants in a sample.
Abstract:
Fiber-containing composites are described that contain woven or non-woven fibers, and a cured binder formed from a binder composition that includes (1) a reducing sugar and (2) a crosslinking agent that includes a reaction product of a urea compound and a polycarbonyl compound. Exemplary reaction products for the crosslinking agent may include the reaction product of urea and an α,β-bicarbonyl compound or an α,γ-bicarbonyl compound. Exemplary fiber-containing composites may include fiberglass insulation.
Abstract:
Method for forming a transparent article comprising: heating a polymer sheet 40 to form a heated sheet; creating a pressure differential across the heated sheet; pushing the heated sheet onto the contoured surface 20 to form a shaped article; and releasing the shaped article from the mold 12. Also included herein are articles made therefrom.
Abstract:
Devices, systems, and methods for detecting molecules of interest within a collected sample are described herein. In certain embodiments, self-contained sample analysis systems are disclosed, which include a reusable reader component, a disposable cartridge component, and a disposable sample collection component. In some embodiments, the reader component communicates with a remote computing device for the digital transmission of test protocols and test results. In various disclosed embodiments, the systems, components, and methods are configured to identify the presence, absence, and/or quantity of particular nucleic acids, proteins, or other analytes of interest, for example, in order to test for the presence of one or more pathogens or contaminants in a sample.