Abstract: A high-throughput automated preprocessing method and a system are applied to a nucleic acid preprocessing apparatus including a control system, a sample transfer area, a nucleic acid extraction area, and a reagent setup area. The control system includes a user interface and guides a user to set up on the user interface. In the sample transfer area, the method includes steps of: a user selecting a sampling tube type, a test protocol and an extraction protocol on the user interface, and the control system performing a sample transfer task. In the nucleic acid extraction area, the method includes steps of: the control system performing a nucleic acid extraction task based on the selected extraction protocol. In the reagent setup area, the method includes steps of: the control system performing a reagent deployment task based on the selected test protocol, and the control system performing a nucleic acid transfer task.

Abstract: An optical module includes a first bearer and a second bearer. The first bearer includes a first bearing portion and an inclined plane, the first bearing portion is configured to carry a first optical element, and the inclined plane is disposed on a peripheral edge of a first end surface of the first bearing portion. The second bearer includes a second bearing portion and a protruding portion, the second bearing portion is configured to carry a second optical element, a second end surface of the second bearing portion faces the first end surface, and the protruding portion extends from the second end surface to the first bearing portion and is configured to contact the inclined plane. When the protruding portion contacts the inclined plane, the inclined plane does not expose the protruding portion in a direction from the first bearing portion to the second bearing portion.

Abstract: A microwell device and a method of manufacturing the same are provided. The microwell device includes a substrate and a plurality of microwells formed on the substrate. In addition, each of the microwells includes a cavity being recessed on the substrate and an opening, and the diameter of the opening is smaller than the largest inner diameter of the cavity. Furthermore, the microwells are curved.

Abstract: A microwell device and a method of manufacturing the same are provided. The microwell device includes a substrate and a plurality of microwells formed on the substrate. In addition, each of the microwells includes a cavity being recessed on the substrate and an opening, and the diameter of the opening is smaller than the largest inner diameter of the cavity. Furthermore, the microwells are curved.

Abstract: An optical module includes a first bearer and a second bearer. The first bearer includes a first bearing portion and an inclined plane, the first bearing portion is configured to carry a first optical element, and the inclined plane is disposed on a peripheral edge of a first end surface of the first bearing portion. The second bearer includes a second bearing portion and a protruding portion, the second bearing portion is configured to carry a second optical element, a second end surface of the second bearing portion faces the first end surface, and the protruding portion extends from the second end surface to the first bearing portion and is configured to contact the inclined plane. When the protruding portion contacts the inclined plane, the inclined plane does not expose the protruding portion in a direction from the first bearing portion to the second bearing portion.

Abstract: A fabricating device of a three-dimensional (3-D) scaffold comprises a bubble generator, a bubble mixing channel, a coagulating solution channel and a bubble collector. The bubble generator includes a gas channel and a gel solution channel crossing the gas channel. The bubble mixing channel is connected with a first outlet of the bubble generator. The coagulating solution channel is connected with the bubble mixing channel. The bubble collector is connected with a second outlet of the bubble mixing channel.

Abstract: A projector includes a polarization changing mechanism and a polarized beam splitter. The polarization changing mechanism is movable. A first polarized beam is configured to pass or not pass through the polarization changing mechanism. The first polarized beam transforms into a second polarized beam when the first polarized beam passes through the polarization changing mechanism. The polarized beam splitter has a light splitting surface. The first polarized beam enters the polarized beam splitter and is guided by the light splitting surface to travel in a first direction, when the first polarized beam does not pass through the polarization changing mechanism. The second polarized beam enters the polarized beam splitter and is guided by the light splitting surface to travel in the first direction or a second direction, when the first polarized beam passes through the polarization changing mechanism and transforms into the second polarized beam.

Abstract: Methods and apparatuses for using microfluidics to generate bubbles and using the generated bubbles to construct scaffolds and cell-holding structures for culturing biological samples or analytes. In one implementation, a scaffold for growing cells is provided to include a matrix of interconnected cavities formed from mixing a gas and a liquid containing a cross linkable material to produce a matrix of gas bubbles of substantially the same size and cross linking the cross linkable material to form a structure in which cells are grown. In another implementation, a scaffold apparatus for growing cells includes a ball of a cross linked material forming an exterior shell that encloses to form a hollow interior inside the ball and biological samples embedded in the external shell.

Abstract: A projector includes a polarization changing mechanism and a polarized beam splitter. The polarization changing mechanism is movable. A first polarized beam is configured to pass or not pass through the polarization changing mechanism. The first polarized beam transforms into a second polarized beam when the first polarized beam passes through the polarization changing mechanism. The polarized beam splitter has a light splitting surface. The first polarized beam enters the polarized beam splitter and is guided by the light splitting surface to travel in a first direction, when the first polarized beam does not pass through the polarization changing mechanism. The second polarized beam enters the polarized beam splitter and is guided by the light splitting surface to travel in the first direction or a second direction, when the first polarized beam passes through the polarization changing mechanism and transforms into the second polarized beam.

Abstract: An optical mechanism includes a bracket, a first polarization beam splitter, a second polarization beam splitter, a plurality of panels and a plurality of lenses. The first polarization beam splitter and the second polarization beam splitter are joined to the bracket. Light passes through the first polarization beam splitter to reach the panels and is reflected by the panels to generate image beams. The image beams are reflected by the first polarization beam splitter to enter the second polarization beam splitter. The image beams are reflected by a splitting surface of the second polarization beam splitter to pass through the lenses and projected by the lenses.

Abstract: An optical mechanism includes a bracket, a first polarization beam splitter, a second polarization beam splitter, a plurality of panels and a plurality of lenses. The first polarization beam splitter and the second polarization beam splitter are joined to the bracket. Light passes through the first polarization beam splitter to reach the panels and is reflected by the panels to generate image beams. The image beams are reflected by the first polarization beam splitter to enter the second polarization beam splitter. The image beams are reflected by a splitting surface of the second polarization beam splitter to pass through the lenses and projected by the lenses.

Abstract: A fabricating device of a three-dimensional (3-D) scaffold comprises a bubble generator, a bubble mixing channel, a coagulating solution channel and a bubble collector. The bubble generator includes a gas channel and a gel solution channel crossing the gas channel. The bubble mixing channel is connected with a first outlet of the bubble generator. The coagulating solution channel is connected with the bubble mixing channel. The bubble collector is connected with a second outlet of the bubble mixing channel.

Abstract: Methods and apparatuses for using microfluidics to generate bubbles and using the generated bubbles to construct scaffolds and cell-holding structures for culturing biological samples or analytes. In one implementation, a scaffold for growing cells is provided to include a matrix of interconnected cavities formed from mixing a gas and a liquid containing a cross linkable material to produce a matrix of gas bubbles of substantially the same size and cross linking the cross linkable material to form a structure in which cells are grown. In another implementation, a scaffold apparatus for growing cells includes a ball of a cross linked material forming an exterior shell that encloses to form a hollow interior inside the ball and biological samples embedded in the external shell.

Abstract: Methods and apparatuses for using microfluidics to generate bubbles and using the generated bubbles to construct scaffolds and cell-holding structures for culturing biological samples or analytes. In one implementation, a scaffold for growing cells is provided to include a matrix of interconnected cavities formed from mixing a gas and a liquid containing a cross linkable material to produce a matrix of gas bubbles of substantially the same size and cross linking the cross linkable material to form a structure in which cells are grown. In another implementation, a scaffold apparatus for growing cells includes a ball of a cross linked material forming an exterior shell that encloses to form a hollow interior inside the ball and biological samples embedded in the external shell.

Abstract: An automatic focus system of a projector includes a projecting module, an image catching module, a memory, a micro processor, and a focusing module. The projecting module has an image light source to provide image light, and a projecting lens to project the image light on a screen. The image catching module senses an image on the screen. The microprocessor calculates the sensed image to have a definition value of the image and save the definition value in the memory. The focusing module may move the projecting lens is moved along an optical axis under a control of microprocessor. The microprocessor compares the definition values to control the focusing module to move the cam to a position where the projector may project a clear image on the screen.

Abstract: The present invention provides a particle monolayer and a method for fabricating the same. The method comprises the following steps: providing a container; adding a solvent into said container; adding a mixture of a particle-suspension and a spreading agent into said solvent; and adding a solvent-soluble polymer to said mixture to form a particle-monolayer. By using a solvent-soluble polymer, the particle monolayer fabricated by the method is a large-area particle monolayer with ordered structure, and the method can be used for any kind of substrates.

Abstract: An optical engine is provided, including an imaging module, a driver module and a connecting unit. The imaging module includes an imaging housing with an imaging space and an imaging unit installed in the imaging space. The imaging housing is made of a conductive material. The driver module includes a driver housing with a driver space and a driver circuit board installed in the driver space. The connecting unit includes at least one of the cables is electrically connected to the imaging unit and the driver circuit board and at least a protruding module protruding from the imaging housing (or the driver housing) to contact with the driver housing (or the imaging housing). The cable is installed in the protruding module made of a conductive material.

Abstract: A method of fabricating three-dimensional scaffolds includes the steps of forming a plurality of bubbles by providing a gelatin solution and a gas stream passing through a bubble production device, gathering the bubbles, cooling the bubbles, crosslinking the bubbles by adding the agent with aldehyde group, and breaking at least some of the bubbles to be interconnected to form a three-dimensional porous materials.

Abstract: A light-filtering module includes a light-source module, a dichroic mirror and a first image unit. The light-source module outputs a light beam. The dichroic mirror divides the light beam into a first colored light and a dual colored light. The first image unit provides the first colored light with image information. The light-filtering module includes a light-filtering unit and a driving unit. The light-filtering unit is located between the dichroic mirror and the first image unit is located at a light path of the first colored light. The driving unit includes a coupling element coupled to the light-filtering unit and a driving element utilized to drive the coupling element. The driving element drives the light-filtering unit, switching between a first status and a second status by the coupling element. A wide-wavelength spectrum and a narrow-wavelength spectrum are provided when the light-filtering unit is in the first and second statuses, respectively.

Abstract: Methods and apparatuses for using microfluidics to generate bubbles and using the generated bubbles to construct scaffolds and cell-holding structures for culturing biological samples or analytes. In one implementation, a scaffold for growing cells is provided to include a matrix of interconnected cavities formed from mixing a gas and a liquid containing a cross linkable material to produce a matrix of gas bubbles of substantially the same size and cross linking the cross linkable material to form a structure in which cells are grown. In another implementation, a scaffold apparatus for growing cells includes a ball of a cross linked material forming an exterior shell that encloses to form a hollow interior inside the ball and biological samples embedded in the external shell.