| National University Corporation University of Toyama Patent applications |
| Patent application number | Title | Published |
|---|
| 20110218558 | TISSUE PIECE FORMING DEVICE AND TISSUE PIECE FORMING METHOD - A tissue piece forming device suitable for forming a tissue piece required in the process of fabricating a novel tissue array chip having many benefits such as the one that the tissue array chip can be fabricated even if the tissue included in a tissue block has a small thickness. The tissue piece forming device ( | 09-08-2011 |
| 20110213041 | METHOD FOR MANUFACTURING UNSATURATED HYDROCARBON AND OXYGENATED COMPOUND, CATALYST, AND MANUFACTURING METHOD THEREFOR - The method for manufacturing an unsaturated hydrocarbon and an oxygen-containing compound according to the present invention comprises: a first step of dispersing a catalyst in poly-α-olefin and reducing the catalyst with carbon monoxide or synthesis gas, wherein the catalyst is prepared by supporting iron on a support containing manganese and having an average pore size of 2 to 100 nm; and a second step of bringing the catalyst after reduction in the first step into contact with synthesis gas under the conditions of a reaction temperature of 100 to 600° C. and a reaction pressure of 0.1 to 10 MPa to obtain a reaction product containing an unsaturated hydrocarbon and an oxygen-containing compound. | 09-01-2011 |
| 20110129816 | DEVICE FOR DETECTION OF INFLUENZA VIRUS - A device for detecting or quantifying influenza viruses in a sample, which comprises a detection region having a human anti-influenza virus nucleoprotein antibody immobilized onto a support, a sample supply region, and a sample-migrating region; and a kit for detecting or quantifying influenza viruses, which comprises a solid phase in which a human anti-influenza virus nucleoprotein antibody is fixed onto a carrier. | 06-02-2011 |
| 20110117609 | Homologous Recombination Method, Cloning Method, and Kit - Disclosed is a method which can achieve the homologous recombination of a gene of interest selectively. Also disclosed is a recombinant DNA molecule produced by the method. Specifically disclosed is a homologous recombination method which uses a PCR product and a linearized vector. The PCR product comprises a sequence for a target gene and amplification primer sequences P | 05-19-2011 |
| 20110020879 | REACTION DEVICE, REACTION METHOD AND METHOD OF SYNTHESIZING cDNA - The present invention provides a device and a method whereby plural kinds of reaction operations and washing operations can be conducted in parallel without washing or replacing an instrument used in transferring a solution and the like in each operation. A reaction device having a plurality of projecting barriers provided in a line on one surface of a substrate, wherein the projecting barrier has at least one cutoff portion and an inner space capable of holding a droplet, and at least the face holding the droplets of the substrate surface has a contact angle to pure water of from 90 to 150 degrees. A reaction method using the above reaction device wherein a substance immobilized on magnetic beads is sequentially transferred in and between droplets of a solution containing a surface tension reducing agent that are held in the spaces for holding a droplet defined by the above-described projecting barriers by means of a magnet located on the opposite surface of the substrate to the surface having the projecting barriers to thereby conduct reactions and washings. | 01-27-2011 |
| 20100280398 | LASER DOPPLER BLOOD FLOW MEASURING METHOD AND DEVICE - [Subject] To provide laser Doppler blood flow measuring method and device which achieve multi-dimensional measurement efficiently at a high degree of accuracy over a wide range with a simple optical system and device. | 11-04-2010 |
| 20100274511 | SIGNAL ANALYSIS METHOD, SIGNAL ANALYSIS DEVICE AND SIGNAL ANALYSIS PROGRAM - Provided is a signal analysis device that has a high frequency resolution not depending on an analysis window length and can analyze a frequency with considerably high accuracy. When the signal analysis device inputs therein an analysis object signal to be analyzed, the device obtains a frequency f′, amplitude A′ and an initial phase φ′ such that the sum of squares of a difference between the analysis object signal and a sinusoidal model signal expressed by a phase using the frequency f′ and the initial phase φ′ and by the amplitude A′ is a minimum value. | 10-28-2010 |
| 20100145052 | FUSED TRICYCLIC COMPOUND HAVING ALDOSE REDUCTASE INHIBITORY ACTIVITY - A fused tricyclic compound having aldose reductase inhibitory activity and shown by the following formula, | 06-10-2010 |
| 20100087333 | PROCESS OF FABRICATING TISSUE ARRAY BLOCK, PROCESS OF FABRICATING TISSUE ARRAY SHEET, TISSUE ARRAY BLOCK, TISSUE ARRAY CHIP, SYSTEM OF FABRICATING TISSUE ARRAY BLOCK AND SYSTEM OF FABRICATING TISSUE ARRAY SHEET - [Task] A process of fabricating a tissue array block; a process of fabricating a tissue array sheet; a tissue array block; a tissue array chip; a system of fabricating a tissue array block; and a system of fabricating a tissue array sheet are proposed, in which the tissue array block can be fabricated even in the case of that having a small thickness, is little affected by tissue hardness and, when having been processed into a tissue array chip, does not suffer any defect in a piece of tissue or at a site of interests, enables the collection of pieces of tissue from a dispersed area, also enables the establishment of positional relationship between the inside of a tissue piece and the inside of a tissue block, and scarcely affects the utilization of the tissue block remaining after collecting the pieces of tissue. | 04-08-2010 |
| 20100079219 | PLANAR STRUCTURE MICROWAVE SIGNAL MULTI-DISTRIBUTOR - In a conventional Bagley polygon power divider of a planar configuration, a length of transmission lines from an input port to output ports adjacent thereto on both sides is determined to be a quarter wavelength and a geometry thereof is an odd regular polygon with each side being a length equal to half of a wavelength at a designed frequency, which is large in size. Since the output ports are located at vertices of the regular polygon, inconvenience can be caused, e.g., in arrangement of the output ports. | 04-01-2010 |
| 20100025672 | THIN-FILM LAMINATE AND ORGANIC TRANSISTOR USING THE SAME - An organic transistor includes a semiconductor section that includes a thin-film laminate in which a first organic thin film and a second organic thin film are alternately stacked. The thin-film laminate includes at least two layers of the first organic thin film. The first organic thin film is a pentacene thin film, and the second organic thin film is an amorphous organic thin film. The pentacene thin film may be a pentacene bilayer thin film, and the amorphous organic thin film may be a tetraaryldiamine thin film. The tetraaryldiamine thin film may be an α-NPD thin film. The organic transistor has improved transistor characteristics (e.g., mobility, ON/OFF ratio, or threshold value control). | 02-04-2010 |
| 20090232339 | DIGITAL MICROPHONE - A digital microphone comprises a ΔΣ modulator. The ΔΣ modulator has a resonator including a membrane which vibrates by receiving a sound wave and a wiring pattern disposed opposite to the membrane, an oscillator, including the resonator, for outputting an FM signal according to the vibration of the membrane, and a one-bit quantizer for outputting a one-bit quantized signal by sampling the FM signal with a high-frequency clock. | 09-17-2009 |
| 20090061446 | METHOD FOR QUICKLY IDENTIFYING PATHOGENIC BACTERIA RESPONSIBLE FOR INFECTION - A system rapidly detects and identifies pathogenic bacteria responsible for infection (particularly septicemia), and selects an appropriate antimicrobial drug. A method according to the present invention for detecting and identifying pathogenic bacteria includes performing gene amplification such as real-time PCR, and analyzing the combination of the melting temperatures (Tm values) determined by gene amplification product melting curve analysis or the difference between the Tm values. Specifically, real-time PCR is performed using 4 to 16 primer sets including 1 to 7 primer sets for the 16S ribosomal RNA of bacteria, 1 to 6 primer sets for the 18S ribosomal RNA of fungi, and one primer set respectively for the spa gene and the mecA gene specific to MRSA, and the combination of the Tm values of the amplification product or the combination of the differences between the Tm values is compared with a database to identify pathogenic bacteria responsible for septicemia. Pathogenic bacteria responsible for infection (particularly septicemia) can be rapidly detected and identified using the method according to the invention so that a rapid septicemia diagnosis method and evidence-based medicine in septicemia treatment are implemented. | 03-05-2009 |
