Abstract:
The present invention relates to a microfluid control technology. That is, a method for manufacturing a microfluidic floating block according to one embodiment of the present invention produces a microfluidic floating block by repetitively spraying an adhesive on powdery materials for the microfluidic floating block, forming the shape of the microfluidic floating block by repetitively hardening the adhesive and the materials for forming the microfluidic floating block, and drying the microfluidic floating block extracted by brushing and hardening. [Reference numerals] (AA) Start; (BB) End; (S10) Microfluidic floating block; (S20) Separate to a plurality of two-dimensional planes from the bottom; (S30) Disperse materials to form the block in a powder shape; (S40) Inject adhesive on the materials in the powder shape; (S50) Cure the adhesive and the block configuration materials; (S60) Manufacture a final block shape by repeating the steps of S30-S50; (S70) Separate from non-adhered powder by black blushing; (S80) Cure by putting the separated block in a hardening agent; (S90) Dry the hardened block
Abstract:
PURPOSE: A microfluidic chip for generating polymer-based microdroplets is provided to form a large amount of microdroplets with a uniform size and shape, in which microorganisms are transduced through a multi-parallel channel process using a high density microstructure. CONSTITUTION: A microfluidic chip (110) for generating polymer-based microdroplets comprises: three oil inlets (101,103,105) for injecting oil; two solution inlets (102,104) for injecting a solution containing water, a sample, and monomers; a droplet generation unit (110) which generates polymer-based microdroplets by connecting five channels (101',102',103',105') connected to each oil inlet and each solution inlet; and a droplet outlet (120) which discharges the polymer-based microdroplets through a droplet discharge channel (120').
Abstract:
본 발명은 카르복실기가 노출된 탄소나노튜브(carbon nanotubes; CNT)에 자기성 물질을 결합시키고, 상기 자기성 물질이 고정된 CNT를 기질 상에 위치시킨 다음, 수직 또는 수평 방향으로 자기장을 인가하여 CNT를 기질상에 어레이하는 것을 특징으로 하는 수직 또는 수평으로 정렬된 CNT 어레이의 제조방법에 관한 것이다. 본 발명은 또한, 상기의 CNT 어레이에 바이오 리셉터를 결합시키는 것을 특징으로 하는 CNT-바이오칩의 제조방법 및 이에 의해 제조된 CNT-바이오칩을 이용하는 것을 특징으로 하는 바이오 리셉터와 결합하거나 반응하는 표적 바이오물질 또는 유기화합물의 검출방법에 관한 것이다. 본 발명에 따르면, 종래의 화학합성방법(chemical vapor deposition)에 의한 성장 또는 마이크로 패턴(micro pattern)에 의한 어레이 방법에 비하여 결함이 적으면서도 고도로 CNT를 수직 또는 수평 방향으로 어레이할 수 있다. 탄소나노튜브(CNT), 어레이, 자기장, 바이오칩, 검출방법, 바이오물질
Abstract:
본 발명은 폴리하이드록시알카노이트 (PHA) 마이크로스피어에 목적단백질 또는 목적리간드가 부착되어 있는 결합체에 있어서, 목적단백질 또는 목적리간드와 PHA 마이크로스피어 사이에 PHA 분해효소의 기질결합 영역이 링커로 삽입되어 있어 목적단백질 또는 목적리간드가 상기 링커를 통해 PHA 마이크로스피어에 연결되어 있는 결합체에 관한 것이다. 본 발명에서 제공되는 PHA 마이크로스피어의 결합체는 목적단백질-반응단백질간의 반응, 목적단백질-반응리간드간의 반응, 목적리간드-반응단백질간의 반응 또는 목적리간드-반응리간드 간의 반응을 효율적으로 검출하는 데 유용하다.
Abstract:
PURPOSE: A conjugate of PHA microsphere and target protein or ligand and a method for detecting reactions are provided, thereby stably and high efficiently detecting a reaction between target protein and reaction protein, a reaction between target protein and reaction ligand, a reaction between target ligand and reaction protein or a reaction between target ligand and reaction ligand, and cheaply producing the PHA microsphere. CONSTITUTION: The conjugate of PHA microsphere and target protein or ligand contains a substrate-binding site of PHA depolymerase as a linker between the PHA microsphere and target protein or ligand, wherein the target protein is fused in the substrate-binding site of PHA depolymerase; the substrate-binding site of PHA depolymerase is fused with the C-terminal, N-terminal or intermediate of the N-C terminals of the target protein; the target protein is an enzyme or an antibody; the target ligand is low molecular weight compound, nucleic acid, peptide, carbohydrate, fatty acid or lipid which reacts with protein or peptide; the PHA is polymer, copolymer or polymer blend containing C3-C12 monomer; and the substrate-binding site of PHA depolymerase is derived from Alcaligenes faecalis. The method for detecting reactions comprises using the conjugate of PHA microsphere and target protein or ligand, wherein the reaction is detected by using fluorescence-labeled antibody.
Abstract:
PURPOSE: A protein chip using substrate specificity of polyhydroxyalkanonate depolymerase is provided, thereby inhibiting nonspecific protein binding, so that cost for production of the protein chip can be reduced. CONSTITUTION: The protein chip using substrate specificity of polyhydroxyalkanonate depolymerase comprises a substrate, PHA(polyhydroxyalkanonate) fixed on the substrate, a substrate binding domain of PHA depolymerase, and a fusion protein of a target protein, wherein the substrate is glass slide; the PHA is spin coated on the substrate; the PHA has 4 to 12 of carbon number; the binding domain of PHA depolymerase is fused with the N-terminal, C-terminal or the intermediate of N-C of a target protein; and the binding domain of PHA depolymerase is isolated from Alcaligenes faecalis.
Abstract:
PURPOSE: A protein chip for analyzing interaction between protein and substrate peptide therefor is provided, thereby rapidly and enormously analyzing interaction between protein and substrate peptide therefor by improving interaction between small molecular weight of peptides and large molecular weight of enzyme proteins, and between peptides and reactive antibodies. CONSTITUTION: The protein chip for analyzing interaction between protein and substrate peptide therefor is prepared by fixing a substrate peptide on a substrate such as aldehyde slide via a linker protein such as leptin or malic enzyme, wherein the substrate peptide is fused with the linker protein in a type of peptide monomer, dimmer of monomer-proline-monomer, or proline-linked polymer; and the peptide monomer is Camtide having the amino acid sequence set forth in SEQ ID NO: 1 or Ab1 having the amino acid sequence set forth in SEQ ID NO: 8. The method for analyzing interaction between protein and substrate peptide therefor comprises the steps of: adding a protein such as enzyme or antibody which specifically binds to the substrate peptide fixed on a protein chip into the protein chip; and detecting the interaction between the protein and substrate peptide therefor by using a fluorescence-labeled enzyme.
Abstract translation:目的:提供用于分析蛋白质与底物肽之间相互作用的蛋白质芯片,从而通过改善肽与小分子量酶蛋白之间的相互作用,以及肽和底物肽之间的相互作用,快速而极大地分析蛋白质与底物肽之间的相互作用 反应性抗体。 构成:用于分析蛋白质和底物肽之间的相互作用的蛋白质芯片通过将底物肽通过接头蛋白如瘦素或苹果酸固定在底物如醛载体上而制备,其中底物肽与接头蛋白质融合 一类肽单体,单体 - 脯氨酸单体的二聚体,或脯氨酸交联的聚合物; 并且肽单体是具有SEQ ID NO:1所示氨基酸序列的Camtide或具有SEQ ID NO:8所示的氨基酸序列的Ab1。分析蛋白质与底物肽之间相互作用的方法包括以下步骤: :将固定在蛋白质芯片上的底物肽特异性结合到蛋白质芯片中的蛋白质如酶或抗体; 并通过使用荧光标记的酶检测蛋白质和底物肽之间的相互作用。