Samsung Electronics Co., Ltd.

Samsung Electro-mechanics Co., Ltd.

Electronics and Telecommunications Research Institute

S-printing Solution Co., Ltd.

Cj Cheiljedang Corporation

Samsung Life Public Welfare Foundation

Seoul National University

Kyungpook National University Industry-academic Cooperation Foundation

Samsung Led Co., Ltd.

Other

Lg Electronics Inc.

Hewlett-packard Development Company, L.p.

Sungkyunkwan University

Korea Atomic Energy Research Institute

Hp Printing Korea Co., Ltd.

Dong Woo Lee

Jin Young Choi

Jin Han Kim

Bo Sung Ku

Da Eun Kim

Seung Eun Chung

Seok-Mo Chang

Sung Chan Yun

Yong Jik Lee

Hyun Soo Park

Soo Hwan Bae

Dong Jin Seol

Ji Su Park

Sang Jae Lee

Hyung Cheol Shin

Su Ho Shin

Jun Tae Kim

Han Seung Lee

Hwan Mook Kim

Chong-Pyoung Chung

Jue-Yeon Lee

Tae Gyu Kim

Yoon Jeong Park

Do Hyun Nam

Sun Mi Shin

Yong Ki Son

Yoon Hee Lee

Sun Soo Kim

Don Jung Lee

Sun Hyung Lee

Sang Uk Jeon

Yu Ryang Pyun

Ho Jeong Song

In Sik Park

Sun Young Park

Sang Jin Kim

Valeriy Prushinskiy

Seung Mo Lim

Jun Young Lee

Yeonsu Kim

Jong Pil Lee

Won Ho Lee

Joon Young Jung

Su Jin Park

Il Do Kim

Dong Sik Kim

Sung Wook Kim

Hee Sook Shin

Dong-bum Choi

Sung Yong Shin

Jeong Mook Lim

Seok Mo Chang

Yong Soon Park

Jin Sook Suh

Sang Eun Bae

Moo Youn Park

Hwan Hee Kim

Hyung Sok Yeo

Il Hwan Seo

Sang Hyun Yi

Igor Ivanov

Jung Eun Kim

Ja Beom Gu

Baesun Kim

Dae Wook Park

Jei Won Yeon

Byoung Chan Kim

Il-Soo Kim

Hyun Tae Jeong

Bae Sun Kim

Ga Gue Kim

Na-ri Im

Jabeom Gu

Soo Ryong Hwang

Tae Hong Park

Sang Ho Lim

Jai Il Park

Byung Man Kang

Kun Ho Chung

Jong Seong Choi

Sungyong Shin

Hwa Kyeung Jeong

Gae Won Nam

Hee-Soo Jeong

Ji Yeon Kim

Changjoon Park

Youngil Son

Sun Keun Shim

Yeon Sook Choi

Jong Sub Na

Soo Man Yun

Gi Su Heo

Yu Jin Han

Hye Jeong Jeong

Hyun Su Jin

Wan Sik Cha

Nam Joo Kang

Hyeon Su Jin

In Hyuk Yeo

An image signal processor includes a statistic data generating unit for receiving an image signal from an external device, an image processing unit for receiving the image signal, and a direct memory access (DMA) module connected to the statistic data generating unit and the image processing unit. The statistic data generating unit performs first image pre-processing on the image signal and generates first statistic data based on the image signal subjected to the first image pre-processing. The DMA module stores the first statistic data therein and provides the stored first statistic data to the image processing unit. The image processing unit performs second image pre-processing on the image signal and performs image processing on the image signal based on the first statistic data.

Statistic generating circuit for image processing

A muscle control device includes an electromyography (EMG) electrode unit including a plurality of electrodes, and that senses an EMG signal, an EMG circuit unit that generates channel data, based on electrode signals, a control unit that receives the channel data, extracts a volitional electromyography signal, based on the channel data, and determines FES (Functional Electrical Stimulation) stimulation parameters, based on the volitional electromyography signal, an FES electrode unit that outputs a functional electrical stimulation, based on the FES stimulation parameters, and an FES circuit unit that receives the FES stimulation parameters, generates the functional electrical stimulation, based on the FES stimulation parameters, and transmits the functional electrical stimulation to the FES electrode unit, and the control unit recognizes a direction and an intensity of a motion from the volitional electromyography signal, based on the volitional electromyography signal and adjusts an intensity of the functional electrical stimulation.

Muscle control device and operation method thereof

The present invention is directed to a method of measuring cell migration by measuring the invasion ratio of cells incubated on a pillar array inserted into a well structure, the method including steps of: preparing a pillar array having a plurality of micropillars and a well structure having a plurality of microwells into which the plurality of micropillars is insertable, respectively; forming cell spheroids by incubating cells in an extracellular matrix attached to the end contact surfaces of the micropillars; allowing the cells contained in the cell spheroids to invade the end contact surfaces; staining and scanning the cell spheroids, the cells contained in the cell spheroids, and the cells that invaded the end contact surfaces; and calculating the invasion ratio of cells by the following equation through a fluorescence image of the scanned cells: wherein Arepresents the total cell area, and Arepresents the spheroid area.

Measuring method of cell migration using the rate of cell invasion

The present invention relates to a radioactive chemical waste treatment apparatus including an adsorption unit including an radioactive chemical waste adsorption member for adsorbing and separating radioactive chemical wastes from radioactive chemical waste-containing fluid, and a regeneration unit which is in fluidic communication with the adsorption unit and is for regenerating the radioactive chemical waste adsorption member by desorbing the radioactive chemical wastes from the adsorption member with the radioactive chemical wastes adsorbed thereonto, and to a radioactive chemical waste treatment method including (A) adsorbing radioactive chemical wastes onto a radioactive chemical waste adsorption member and separating the radioactive chemical wastes from a radioactive chemical waste-containing fluid, and (B) desorbing the radioactive chemical wastes from the radioactive chemical waste adsorption member with the radioactive chemical wastes adsorbed thereonto, and regenerating the radioactive chemical waste adsorption member.

Radioactive chemical waste treatment apparatus

Disclosed is a game test automation device capable of automating a game test. The game test automation device can comprise: a database for storing test procedure information, which is a combination of game scripts to be tested in a game service; and a testing unit for testing game build of the game service on the basis of the test procedure information, and creating game state information derived in the testing process and a test report on the test.

Game test automation device and method

A washing machine comprises a housing including a main inlet on a front surface thereof, a main washing unit disposed in the housing, a main door opening and closing the inlet, and a sub-washing unit disposed in the main door and provided with a pulsator. A large amount of laundry can be washed through the main washing unit and a small amount of laundry can be washed through the sub-washing unit, so that washing can be efficiently performed according to the amount of laundry.

Drum washing machine

Disclosed herein are a system and a method for volitional electromyography (vEMG) signal detection from an EMG signal when functional electrical stimulation (FES) is applied. The system for vEMG signal detection includes a receiver for receiving data from an EMG electrode when FES is applied, a memory for storing a program for detecting a vEMG signal using the received data, and a processor for executing the program, wherein the processor cuts the data received from the EMG electrode disposed at a predetermined position, calculates a difference between data for previous FES and data for current FES, and detects the vEMG signal using the calculated difference.

System and method for volitional electromyography signal detection

Provided is a method for analyzing metagenomic information using a degenerate primer which can be applied for quickly determining the utility value of a massive amount of metagenome samples. In particular, the superfamily-specific degenerate primer of the present invention is used to quickly detect the presence or absence of the genetic information of the target peptides in the metagenome by a simple method, thereby collecting a large amount of useful peptide resource information from various metagenome samples at high speed. Further, the present invention may be used for screening new peptide genes by designing and producing superfamily-specific degenerate primers of new target peptides based on the method of the present invention. In addition, the method of the present invention can be applied not only to enzymes but also to studies related to polypeptides, oligopeptides, antibiotic resistance genes, antimicrobial peptides, antifungal peptides, oligopeptides, markers, or single-nucleotide polymorphism (SNP).

Method for exploring useful genetic resources through bulk metagenome analysis and use thereof

The present invention relates to a pillar structure for a biochip, the pillar structure including: a substrate portion which has a plate-shaped structure; multiple pillar portions which protrude from one surface of the substrate portion and each of which has an end portion on which a sample is disposed; and smooth surface forming portions which are formed on the other surface of the substrate portion that defines the plate-shaped structure together with the one surface of the substrate portion, the smooth surface forming portions forming smooth surfaces each having a relatively concave groove shape at a portion corresponding to a circumferential surface of each of the pillar portions.

Pillar structure for biochip

Technology for a pillar structure for a biochip is disclosed. The pillar structure for a biochip includes: a substrate portion having a plate structure; an insertion pillar portion formed in one piece with the substrate portion and protruding downward from a lower surface of the substrate portion so as to be inserted into a well; and a compensation pillar portion formed in one piece with the substrate portion, the compensation pillar portion corresponding to the insertion pillar portion and protruding upward from an upper surface of the substrate portion. Therefore, when the pillar structure is cooled during an injection molding process, the substrate portion is prevented from being partially recessed, and when samples are analyzed using microscopic images, accuracy and reliability may be improved.

A dryer includes a main body, a drying chamber provided inside the main body and configured to accommodate objects to be dried, a conveying unit configured to convey the objects to be dried, a sensor unit configured to sense information on states of the objects to be dried, and a control unit configured to control the conveying unit to move the objects to be dried based on the information sensed by the sensor unit.

Dryer and control method thereof

A washing machine which performs a washing operation by heating water, a detergent, or a wash liquid using a dielectric heating method and a method of controlling the washing machine. The washing machine may include a water supply portion which supplies a wash liquid including water and a detergent, a power supply portion which supplies alternating current (AC) power, and an electric field forming portion which forms an electric field between a first electrode portion and a second electrode portion according to the AC power to heat the supplied wash liquid.

Washing machine and method of controlling the same

The present disclosure relates to methods of preparing an ultra-low molecular weight keratin peptide and use thereof. In particular, the present disclosure relates to a method of preparing an ultra-low molecular weight keratin peptide using culturing a microorganism having keratinolytic activity in a medium including keratin, ultrafiltration, ion exchange chromatography and gel filtration chromatography, a peptide prepared by the method, and a cosmetic and food composition for preventing or improving skin aging or skin wrinkles including the same. According to the method of preparing a keratin peptide of the present invention, it is possible to eco-friendly biologically treat waste resources and efficiently purify and recover anti-aging functional ultra-low molecular weight keratin peptides. In addition, the keratin peptide of the present disclosure breaks down collagen to have abilities to inhibit MMP-1 expression and activity, which is an enzyme that causes skin aging, which has an excellent effect on anti-skin aging and skin wrinkle improvement and has no toxicity to skin cells. It is suitable for use as a cosmetic, pharmaceutical or food composition for preventing, improving or treating skin aging or skin wrinkles, thereby being effectively used for the efficient and rapid production and development of high value-added functional cosmetic substances.

Method of preparing ultra-low molecular weight keratin peptide

Technology for a biochip pillar structure is disclosed. According to an embodiment of the present disclosure, the biochip pillar structure includes: a pillar structure including a plate-shaped first substrate portion, and pillar portions protruding from a surface of the first substrate portion; and a well structure including a plate-shaped second substrate portion, and well portions formed in a surface of the second substrate portion and having a predetermined depth to respectively receive the pillar portions of the pillar structure, wherein the well portions have a diameter within a range of 800 &#x3bc;m to 1500 &#x3bc;m, and the pillar portions configured to be inserted into the well portions have a diameter of which the ratio to the diameter of the well portions ranges from 0.3 to 0.58, thereby providing a high-density biochip and preventing bubbling in an aqueous liquid contained in the well portions when the pillar portions are inserted.

Biochip pillar structure

A fixing device comprising a fixing belt, a rotating member to be in engagement with an outer circumferential surface of the fixing belt, to form a fixing nip between the fixing belt and the rotating member, and sliding members on both ends of the fixing belt.

Fixing device and image forming device having same

Growing community of inventors

Seoul, South Korea

Dong Woo Lee