Abstract: In examples, a semiconductor package comprises a substrate and multiple columns of semiconductor dies positioned approximately in parallel along a length of the substrate. The package also includes multiple passive components positioned between the multiple columns of semiconductor dies, the multiple passive components angled between 30 and 60 degrees relative to the length of the substrate, a pair of the multiple passive components having a gap therebetween that is configured to permit mold compound flow through capillary action. The package also includes a mold compound covering the substrate, the multiple columns of semiconductor dies, and the multiple passive components.

Abstract: Surface plasmon resonance (SPR) microscopy systems, methods of making SPR microscopy systems, methods of measuring and detecting the presence of one or more compounds present in a sample using the SPR microscopy system, and the like, are disclosed. In an embodiment, a surface plasmon resonance (SPR) microscopy system can include an integrated microfluidic chip that includes a plurality of layers, an SPR imaging system, and a pressure manifold to actuate flow control components in the integrated microfluidic chip.

Abstract: Surface plasmon resonance (SPR) microscopy systems, methods of making SPR microscopy systems, methods of measuring and detecting the presence of one or more compounds present in a sample using the SPR microscopy system, and the like, are disclosed. In an embodiment, a surface plasmon resonance (SPR) microscopy system can include an integrated microfluidic chip that includes a plurality of layers, an SPR imaging system, and a pressure manifold to actuate flow control components in the integrated microfluidic chip.

Abstract: An enclosed membrane-clamping (EMC) device is disclosed for running biological assays on membrane surfaces, such as Western blotting. The EMC device comprises a cover plate and a support plate, which can be coupled through a sealing mechanism. The cover plate, the support plate and the sealing mechanism are shaped such that their inner surfaces form one or more enclosed chambers. When in use, a blotting membrane is placed between the cover plate and the support plate, and clamped in the chamber formed in the EMC device. The EMC device is coupled with an assisting device to realize automation of manipulations. Liquid-phase target solutions are introduced into the chamber through its inlet and outlet to realize surface-molecular interactions between the target on the blotting membrane and the targets introduced in liquid phase. The chamber with a small vertical dimension is capable of achieving the blotting assays at a higher speed.