Abstract:
The present invention relates to a method for simply analyzing a sugar chain on the surface of a cell in high sensitivity only by fixing, on a substrate without additionally labelling or transforming, a live cell or a tissue cell and, more specifically, to a method for analyzing a sugar chain on the surface of a cell which is characterized by comprising the steps of: (A) fixing a cell on the surface of a substrate; (B) treating lectin binding with biotin to the cell fixed in the (A) step; (C) treating a quantum dot binding with a living particle specifically binding with the biotin on the surface after treating lectin; and (D) detecting phosphor of the quantum dot.
Abstract:
The present invention relates to a microfluidic device in which a concentration gradient and a temperature gradient are simultaneously created in a detection channel of a microchannel and, more specifically, to a microfluidic device comprising a microfluidic channel for a sample and a pair of microfluidic channels for tempreature adjustment. The microfluidic channel for a sample includes: two inlets; a gradient forming region for separating each fluid which is injected into the inlets, into multiple microchannels having a different concentration gradient; a detection channel for joining and moving the fluid separated into the multiple microchannels after passing the gradient forming region; and an outlet for discharging the fluid passed the detection channel. The pair of microfluidic channels for temperature adjustment, wherein each channel is formed in parallel on both sides of the detection channel of the microfluidic channel for a sample by being spaced out in a prefixed interval with the detection channel, and includes: an inlet; an outlet; and a microchannel through which a fluid injected into the inlet moved to the outlet, such that heating mediums having a different temperature are circulated.
Abstract:
The present invention relates to a microfluidic device for analyzing the chemotaxis of bacteria and a chemotaxis analyzing method using the same and, more specifically, to a microfluidic device which is formed by attaching a mold (61) including a microfluidic channel to a substrate (51) by comprising: a first microfluidic channel (12) which is connected to a first discharge hole (13) and a first accommodating part (11) which accommodates first solution; a second microfluidic channel (22) which is connected to a second discharge hole (23) and a second accommodating part (21) which accommodates second solution; and a detection channel (31) in which the first microfluidic channel (12) and the second microfluidic channel (22) cross. Between the detection channel (31) and the second microfluidic channel (22), a pair of air channels (43) capable of accommodating air in the upper part is arranged across a crossing channel (42) of 1-10 μm in a width direction and a diffusion channel (41) is formed to have a depth of 1-10 μm which is shallower than 1/3 of the depth of the second microfluidic channel.
Abstract:
본 발명은 살아있는 세포 또는 조직세포를 별도로 표지하거나 변형하지 않고 기판에 고정시키는 것만으로 간편하고 높은 감도로 세포 표면의 당사슬을 분석할 수 있는 방법에 관한 것르로, 보다 상세하게는 (A) 기판의 표면에 세포를 고정화하는 단계; (B) (A)단계에서 고정화된 세포에 바이오틴이 결합된 렉틴을 처리하는 단계; (C) 렉틴의 처리 후 표면에 바이오틴과 특이결합하는 생체분자가 결합된 양자점을 처리하는 단계; 및 (D) 상기 양자점의 형광을 검출하는 단계; 를 포함하여 이루어지는 것을 특징으로 하는 세포 표면의 당사슬 분석 방법에 관한 것이다.
Abstract:
본 발명은 미세유로의 검출채널에 농도구배 및 온도구배가 동시에 생성되는 미세유체장비에 관한 것으로, 보다 상세하게는 본 발명은 두 개의 주입구; 상기 주입구로 주입된 각 유체를 서로 다른 농도구배를 갖는 복수개의 미세채널로 분리하는 구배형성영역; 구배형성영역을 통과하여 복수개의 미세채널로 분리된 유체가 합류하여 이동되는 검출채널; 및 검출채널을 통과한 유체가 배출되는 배출구;를 포함하는 시료용 미세유로와 상기 시료용 미세유로의 검출채널의 양측면에 검출채널과 소정 간격을 두고 평행하게 각각 형성되며, 주입구; 배출구; 및 주입구로 주입된 유체가 배출구로 이동되는 미세유로로 구성되어 각각 다른 온도의 열매가 순환되는 한쌍의 온도조절용 미세유로;를 포함하여 구성되는 미세유체장비에 관한 것이다.
Abstract:
PURPOSE: A droplet generating micro fluid chip, a droplet reacting micro fluid chip, and a multi-droplet reacting analyzer is provided to collect multiple generation unit elements and reacting unit elements, thereby examining and analyzing various reactions based on a micro droplet by one operation. CONSTITUTION: A droplet reacting micro fluid chip comprises a main channel(210), a reaction channel array(220), and an operation channel array(230). The reaction channel array is composed of a plurality of unit reaction channels branched from the main channel. The operation channel array is arranged in one side of the unit reaction channel, and a passage of the operation channel is separated from the unit reaction channel with a separation film. Flows of fluid inside the plurality of unit reaction channels are simultaneously controlled by the unit operation channels, thereby being integrated into one fluid flow. Three unit operation channels are arranged in each unit reaction channel. A first operation channel is utilized for a droplet trap valve, and second and third operation channels are utilized for a valve adding waves to droplets.