Snu Rdb Foundation

Seoul National University

Quantamatrix Inc.

University-Industry Cooperation Group of Kyung Hee University

Celemics, Inc.

Quanta Matrix Co., Ltd.

Sung Hoon Kwon

Dong Young Kim

Su Eun Chung

Wook Park

Sung Hoon Lee

Jung Il Choi

Young Hoon Song

Ok Ju Kim

Tae Hoon Ryu

Young Joon Choi

Yong Gyun Jung

Seungah Lee

Sangkwon Han

Jung Heon Yoo

Suk Heung Song

Hyun Yong Jeong

Jisung Jang

Eun Guen Kim

Sueun Chung

Tae Geun Lim

Ji Sung Jang

Seo Hee Chang

Jun Hoi Kim

Jin Sung Noh

Yu Shin Jung

Yeong Jae Choi

Eun Geun Kim

Hyung Jong Bae

Sang Kwon Han

Hyo Ki Kim

Hyo Jun Han

Provided are a method of analyzing biological samples, an analytical chip and an analytical system comprising same, the method comprising the steps of: introducing structures for assisting the formation of bioreactors on a substrate; providing a plurality of bioreactors on the substrate by means of forming the bioreactors, which are holding biological samples, on the peripheral parts of the respective structures so as to come in contact with the structures in at least one region; and checking a change in the biological samples present in the bioreactors.

Method for analysis of biospecimen, analysis chip and analysis system based on bioreactor

Biochemical carriers are provided. Each of the biochemical carriers includes: biochemical molecules having a sequence into which digital data information is encoded; a carrier particle composed of a polymer matrix and in which the biochemical molecules are connected to the surface or inside of the polymer matrix; and an index code introduced into the carrier particle. Also provided is a method for fabricating biochemical carriers. The fabrication method includes: encoding digital data into a sequence of biochemical molecules; synthesizing the biochemical molecules based on the encoded sequence; mixing the biochemical molecules with a photocurable material; curing the mixture to obtain carrier particles including a polymer matrix; and introducing an index code into the carrier particles simultaneously with or separately from the curing. Also provided is a method for restoring digital data from the biochemical carrier. The restoration method includes: analyzing the index code of the biochemical carrier; reacquiring the biochemical molecules from the biochemical carrier based on the analytical results of the index code; sequencing the biochemical molecules; and decoding the sequencing results to restore digital data.

Biochemical carriers capable of storage, preservation and indexing and method for fabricating the same

The present invention relates to a technique for genomic library screening and provides a method for separating, capturing, analyzing, and retrieving cells and cell products by using a microstructure that can be preferentially applied to the field of antibody engineering for the development of new therapeutic antibodies and can be extensively applied to multiple genetic/phenotypic analysis of various biochemical molecules, for example, in the field of protein engineering and metabolic engineering.

Method for separating, capturing, analyzing and retrieving cells and cell products by using microstructure

Provided is a multi-well-based cell culture test device having an array structure of a plurality of aligned well units. Each of the well units includes a first sub-well adapted to accommodate a first fluid, a second sub-well adapted to accommodate a second fluid, and a barrier located between the first sub-well and the second sub-well to partition the first sub-well and the second sub-well. The first sub-well has a recess in the depth direction with respect to its bottom to accommodate a solid thin film formed by solidifying the first fluid. The barrier has such a height that the first fluid does not overflow into the second sub-well when the first fluid is loaded into the first sub-well to fill the recess.

Multi-well-based cell culture test device for rapid antibiotic susceptibility testing

A microfluidic multi-well-based cell culture testing device is provided. The multi-well-based cell culture testing device has an array structure of a plurality of aligned microfluidic well units. Each of the microfluidic well units comprises an inlet through which a first fluid enters, an accommodation compartment adapted to accommodate a second fluid therein, a microfluidic channel through which the first fluid flows, and an air outlet adapted to facilitate the entering of the first fluid.

Microfluidic multi-well-based cell culture testing device

Provided is an assay method using an encoded particle-based platform. In the assay method, first, a plurality of encoded particles having codes distinguishable from one another according to kinds of included target materials are prepared. The plurality of encoded particles are provided onto a plate including a plurality of wells by pipetting, and disposed in the plurality of wells by a self-assembly method. An analyte is provided into the plurality of wells. The codes of the plurality of encoded particles disposed in the plurality of wells are decoded. The target materials of the plurality of encoded particles are released to cause a reaction between the target materials and the analyte.

Assay method using encoded particle-based platform

A technique related with a lithography system is disclosed. The lithography system includes at least one target object disposed on a substrate, a processor configured to process an image of the target object to determine an optical pattern for a coating layer of the target object, and an exposure apparatus configured to provide light having the optical pattern determined by the processor to the substrate.

Image processing-based lithography system and method of coating target object

A method of coating a light emitting diode (LED) is provided. The method includes preparing a substrate in which a plurality of LEDs are arranged, applying a curable liquid containing a fluorescent material to the substrate and the plurality of LEDs, and selectively applying energy to the substrate to which the curable liquid is applied, to thereby pattern the curable liquid, wherein the application of the energy includes applying the energy to both surfaces of the substrate.

Uniform coating method for light emitting diode

A method of coating a light emitting device is provided. The method includes preparing a plurality of light emitting devices. The plurality of light emitting devices are coated with a first photocurable liquid. First light is selectively exposed to the first photocurable liquid to form a first coating layer on at least a partial region of a surface of each of the plurality of light emitting devices. The plurality of light emitting devices on which the first coating layer is formed are coated with a second photocurable liquid. Second light is selectively exposed to the second photocurable liquid to form a second coating layer on at least a partial region of the surface of each of the plurality of light emitting devices or a surface of the first coating layer. The first coating layer corresponds to the cured first photocurable liquid, while the second coating layer corresponds to the cured second photocurable liquid.

Method for coating light-emitting devices, light coupler, and method for manufacturing the light coupler

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Seoul, South Korea

Sung Hoon Kwon