Cj Cheiljedang Corporation

Gwangju Institute of Science and Technology

Samsung Electronics Co., Ltd.

California Institute of Technology

Chonnam National University

Korea Basic Science Institute

Nanobiz Co., Ltd.

Sung Jae Yang

Seong Bo Kim

Young Mi Lee

Seung Won Park

Hyun Kug Cho

Il Hyang Park

Yang Hee Kim

Min Hae Kim

Chan-Hyoung Lee

Eun Jung Choi

Taek Beom Kim

Sun Mi Shin

Ran Young Yoon

Alexander Zhbanov

Seung Hwan Kim

Seung Hyun Cho

Jin Ha Kim

Kun Sun Eom

Myoung Hoon Jung

Chang Gyeom Kim

In Seok Oh

Eul-Soo Park

Hyun June Park

Sang Youl Yoon

Ye Sung Lee

Taek Eon Jeong

Kyong Yeon Cho

Jae Hong Han

Yu Gyung Jung

Kwang Soo Kim

Jong Hyun Kim

James R Heath

Jin Won Kim

Songming Peng

Joseph Kwon

Sun Kyu Lee

Seung Yeob Lee

Suk In Jung

Hyun Suk Min

Hye Jung Yang

Byung-sam Son

Jong-Soon Choi

Do Kyun Woo

Alphonsus Hon-Chung Ng

Sung Ki Nam

Sung Sik Yun

Sang Young Yoon

Jae Hyeon Ahn

Byung-Sam Son

Jong Chan Choi

Myounggon Kim

Su Heon Jeong

Yang-Jun Kang

William Chour

Jung Kyun Kim

Byung Jun Kim

Jongchan Choi

Eul Soo Park

Du-Woon Kim

Sung A Hong

Ji-Chul Hyun

Sung-A Hong

Ji Chul Hyun

Heemin Lee

Young Ran Yun

So-hyeong Kim

Minkook Son

Ii Hyang Park

The present application relates to a psicose-6-phosphate phosphatase, a microorganism comprising the same, and a method for producing psicose using the same.

Psicose-6-phosphate phosphatase, composition for producing psicose comprising the same, and method for producing psicose using the same

The present application relates to a psicose-6-phosphate phosphatase comprising motif A and motif B, a composition for producing D-psicose comprising the enzyme, and a method for producing D-psicose using the enzyme.

Psicose-6-phosphate phosphatase, composition for producing psicose including said enzyme, method for producing psicose using said enzyme

The present invention relates to a multi-microorganism detection system, and more particularly, to a multi-microorganism detection system using a dielectrophoresis force. Provided is a rapid and accurate multi-microorganism detection system. Microorganisms are concentrated at a high throughput using DEP after synthesizing the microorganisms and fluorescent magnetic particles, and when a complex in which the fluorescent magnetic particles are bound to the microorganisms passes through a detection unit by moving only the microorganisms to the detection unit after separating the magnetic particles from the complex (i.e., the microorganisms to which the magnetic particles are bound) using a DEP force, a fluorescence signal of a specific wavelength band is generated according to the type of the fluorescent magnetic particle and the concentration of the microorganisms according to the type of microorganism is measured by measuring and analyzing the fluorescence signal.

Multi-microorganism detection system

The present disclosure relates to a microorganism detection apparatus using a dielectrophoresis (DEP) force. A microorganism detection apparatus according to one embodiment of the present disclosure may include a detection unit that detects microbial particles using a DEP force corresponding to latex particles combined with the microbial particles.

Microorganism detection apparatus using dielectrophoresis force

An apparatus for analyzing a biological material component may include an impedance sensor comprising a first electrode having a first contact surface that contacts an analysis target, and a second electrode having a second contact surface that contacts the analysis target and that faces the first contact surface. The apparatus may include an impedance measurement assembly configured to measure impedance of the analysis target using the first electrode and the second electrode. The apparatus may include a processor configured to model the measured impedance as an equivalent circuit, and analyze a biological material component based on a modeling result.

Apparatus and method for analyzing biological material component, and apparatus for measuring impedance

The present invention relates to a blood diagnostic device, which includes one or more blood input parts into which blood is injected, a deterministic lateral displacement separation part which communicates with the blood input part to form a blood flow path along which the blood flows and separates white blood cells from remaining blood components, a first microchannel which communicates with the deterministic lateral displacement separation part so that the white blood cells separated through the deterministic lateral displacement separation part flow therein, one or more second microchannels which communicate with the deterministic lateral displacement separation part so that the remaining blood components separated through the deterministic lateral displacement separation part flow therein, a first discharge part which communicates with the first microchannel so that the white blood cells flowing in the first microchannel are discharged therethrough, and a second discharge part which communicates with the second microchannel.

Blood diagnostic device

Provided are a fructose-4-epimerase variant having tagatose conversion activity, and a method of preparing tagatose using the same.

Fructose-4-epimerase and method of producing tagatose using the same

Provided are a composition for producing tagatose, comprising fructose-6-phosphate 4-epimerase, and a method of producing tagatose using the same.

Composition for producing tagatose and method of producing tagatose using the same

A diagnosis kit is disclosed. The diagnosis kit according to an embodiment of the present invention includes a concentration channel into which a sample containing a methylated DNA is introduced, a concentration chamber connected to the concentration channel, wherein the methylated DNA is concentrated by an ion concentration polarization (ICP) phenomenon and moves to the concentration chamber, a sensing chamber connected to the concentration chamber to allow the methylated DNA inside the concentration chamber to move, allow the methylated DNA moved from inside of the concentration chamber to be hybridized, and allow a methylated DNA binding protein to be bound to the hybridized methylated DNA, and a sensor configured to acquire a first electrochemical signal inside the sensing chamber when the methylated DNA is hybridized and acquire a second electrochemical signal inside the sensing chamber when the methylated DNA binding protein is bound.

Diagnostic kit, diagnostic method, and diagnostic apparatus

Provided are a tagatose-bisphosphate aldolase variant having tagatose conversion activity, and a method of preparing tagatose using the same.

An apparatus for analyzing an in vivo component is provided. The apparatus for analyzing an in vivo component may include an impedance sensor including a first electrode and a second electrode configured to contact a fluid channel of a fluid to be analyzed. The apparatus may include an impedance measurement device configured to apply a current to the first electrode and the second electrode, measure a voltage between the first electrode and the second electrode based on applying the current, and measure an impedance of the fluid based on the measured voltage. The apparatus may include a processor configured to model the measured impedance using an equivalent circuit; and analyze the in vivo component based on modeling the measured impedance using the equivalent circuit.

Apparatus and method for analyzing in vivo component and impedance measuring apparatus

The present disclosure relates to a composition for producing tagatose, comprising fructose-6-phosphate-4-epimerase, and a method of producing tagatose using the same.

Composition for producing tagatose from fructose-6-phosphate and method of producing tagatose from fructose-6-phosphate using the same

Provided are a hexuronate C4-epimerase variant with improved activity in converting D-fructose by D-tagatose of hexuronate C4-epimerase and a method for production of D-tagatose using them.

Nucleic acid encoding hexuronate C4-epimerase variant having improved D-tagatose conversion activity, and D-tagatose production method using same

Provided are a fructose-4-epimerase variant having tagatose conversion activity, and a method of producing tagatose using the same.

Fructose-4-epimerase and method of preparing tagatose using the same

Disclosed herein are methods and devices for antigen-specific T cell identification or neoantigen identification. Also disclosed herein are devices for separating and isolating antigen-specific T cells or other particles of a certain size from a population of particles of different sizes. Also describe herein are methods and devices for the separation and isolation of barcoded T cells from other nanoparticles containing barcodes for subsequent analysis and further processing of a viable T cell.

Microfluidic devices and methods for purifying rare antigen-specific T cell populations

Growing community of inventors

Suwon, South Korea

Sung Jae Yang