Abstract:
본 발명은 TREM-2(Triggering Receptor Expressed on Myeloid cells-2) 유전자 또는 단백질을 포함하는 GA733-2 항원의 발현 억제 또는 검출용 조성물 및 방법, 및 이를 포함하는 형질전환 동물, 특히 형질전환 마우스 및 이의 사용방법에 관한 것으로서, 암, 특히 대장암의 원인 규명은 물론 그의 진단, 특히 조기진단 및 치료제 개발에 크게 기여할 수 있다. TREM-2, GA733-2, 암, 대장암, 형질전환, 동물 모델, 마우스
Abstract:
A composition for differentiation of a mature natural killer(NK) cell and a method for production of the same mature natural killer cell are provided to produce a large quantity of mature natural killer cell to increase cancer-killing effects of the mature natural killer cell. The composition for differentiation of the mature natural killer cell from a precursor natural killer cell(pNK) comprises a ligand of Axl receptor tyrosine kinase. The method for producing the mature natural killer cell comprises the steps of: treating a hematopoietic stem cell with IL-7(interleukine 7), SCF(stem cell factor) and Flt3L(fms-related tyrosine kinase 3 ligand) to differentiate the hematopoietic stem cell into a precursor natural killer cell; and treating the precursor natural killer cell with the ligand of Axl receptor tyrosine kinase, wherein the mature killer cell is useful for treatment of cancers including large intestine cancer, breast cancer, non-Hodgikin's lymphoma and acute ymphocytic leukemia.
Abstract:
A method for production of natural killer(NK) cells is provided to treat cancers without side effects using the natural killer cells by using an Axl gene capable of promoting differentiation from hematopoietic stem cells into natural killer cells. The adult natural killer cells are produced by treating hematopoietic stem cells with IL-7(interleukine 7), SCF(stem cell factor) and Flt3L(fms-related tyrosine kinase 3 ligand), so as to differentiate them into NK precursor cells, and treating the NK precursor cells with the Axl gene, wherein the hematopoietic stem cells are isolated from human cord blood. A recombinant vector pLXSN-Axl contains the Axl gene. A transformant is produced by transforming a host cell, mouse RAW264.7 macrophage, with the recombinant vector pLXSN-Axl.
Abstract:
PURPOSE: A manufacturing method of a natural dye solution is provided to provide a natural dye solution capable of manufacturing various natural dye-sensitive solar batteries for requiring growth of plants. CONSTITUTION: A manufacturing method of a natural dye solution comprises a step of preparing a natural dye powder (400); a step of forming a natural dye solution by mixing the natural dye powder, pH controller, and solvent; and a step of forming a natural dye solution by mixing the natural dye powder, pH controller, and solvent. The natural dye solution has a wavelength selectivity for promoting or inhibiting growth of plant. The natural dye is Carthami Flos xanthophyll, lac color, alive side, red cabbage pigment, gardenia red, gardenia blue, rdenia Yellow, cacao, cochineal, henna, or monascus red. The manufacturing method is provided to control wavelength range by using the pH controller.
Abstract:
A chimeric protein consisting of nontoxic CTB(cholera toxin B subunit) of Vibrio cholerae and HPV16 E7(human papilloma virus type 16 E7) protein and use thereof are provided to induce an antibody specific to HPV16 E7 and simultaneously induce mucosa immune response for promoting mucosa permeability of the antibody, so that the protein is useful as an effective ingredient of a vaccine for preventing and treating cervical cancer. The chimeric protein consisting of nontoxic CTB of Vibrio cholerae whose signal peptide region is deleted, and HPV16 E7 protein has the amino acid sequence of SEQ ID NO:6. A gene encoding the chimeric protein has the nucleotide sequence of SEQ ID NO:5. A method for producing the chimeric protein comprises the steps of: constructing a recombinant vector E7-CTB/pET29a containing the chimeric gene; transforming Escherichia coli with the vector to produce E. coli BL21(DE3):E7-CTB/pET29a(KCTC 10894BP); culturing the transformed E. coli; and separating the chimeric protein from the cultured E. coli, and purifying and removing endotoxin from the chimeric protein.
Abstract translation:提供由霍乱弧菌无毒CTB(霍乱毒素B亚基)和HPV16 E7(人乳头瘤病毒16型E7)蛋白组成的嵌合蛋白及其用途,以诱导对HPV16 E7特异性的抗体,同时诱导促进粘膜的粘膜免疫应答 抗体的渗透性,使得该蛋白质可用作预防和治疗子宫颈癌的疫苗的有效成分。 由信号肽区域缺失的霍乱弧菌无毒CTB组成的嵌合蛋白质和HPV16E7蛋白质具有SEQ ID NO:6的氨基酸序列。 编码嵌合蛋白的基因具有SEQ ID NO:5的核苷酸序列。 制备嵌合蛋白的方法包括以下步骤:构建含嵌合基因的重组载体E7-CTB / pET29a; 用载体转化大肠杆菌以产生大肠杆菌BL21(DE3):E7-CTB / pET29a(KCTC 10894BP); 培养转化的大肠杆菌; 并从培养的大肠杆菌中分离嵌合蛋白质,并从嵌合蛋白质中纯化和去除内毒素。
Abstract:
A chimeric protein consisting of nontoxic CTB(cholera toxin B subunit) of Vibrio cholerae and HPV16 E6(human papilloma virus type 16 E6) protein and use thereof are provided to produce vaccine effectively absorbed to a mucosa for preventing and treating cervical cancer by using cervical cancer treating effects of HPV16 E6 protein and mucosa-penetrating ability of CTB. The chimeric protein consists of nontoxic CTB(cholera toxin B subunit) of Vibrio cholerae wherein the signal peptide region is deleted to remove toxicity, and HPV16 E6 protein, has the amino acid sequence of SEQ ID NO:6, is encoded by a gene having the nucleotide sequence of SEQ ID NO:5, and is produced by preparing a vector E6-CTB/pET29a containing the chimeric protein gene, transforming Escherichia coli with the vector to produce Escherichia coli BL21:E6-CTB/pET29a(KCTC 10892BP), culturing Escherichia coli BL21:E6-CTB/pET29a(KCTC 10892BP), separating the chimeric protein from the cultured transformed microorganism and removing endotoxin from the separated chimeric protein.
Abstract translation:提供由霍乱弧菌无毒CTB(霍乱毒素B亚单位)和HPV16 E6(人乳头瘤病毒16型E6)蛋白组成的嵌合蛋白及其用途,以产生有效吸收到粘膜以预防和治疗宫颈癌的疫苗,方法是使用子宫颈 HPV16 E6蛋白的癌症治疗效果和CTB的粘膜穿透能力。 嵌合蛋白由霍乱弧菌的无毒CTB(霍乱毒素B亚基)组成,其中信号肽区缺失以消除毒性,HPV16E6蛋白具有SEQ ID NO:6的氨基酸序列,由具有SEQ ID NO:6的基因编码, SEQ ID NO:5的核苷酸序列,通过制备含有嵌合蛋白质基因的载体E6-CTB / pET29a,用载体转化大肠杆菌来产生大肠杆菌BL21:E6-CTB / pET29a(KCTC 10892BP), 培养大肠杆菌BL21:E6-CTB / pET29a(KCTC 10892BP),从培养的转化微生物中分离嵌合蛋白质,并从分离的嵌合蛋白中除去内毒素。
Abstract:
A chimeric protein consisting of LTB(Escherichia coli heat-labile enterotoxin B subunit) and HPV16 E6(human papilloma virus type 16 E6) protein and use thereof are provided to induce an antibody specific to HPV16 E6 protein and mucosal immune response simultaneously, so that the chimeric protein is useful for production of a vaccine for preventing and treating cervical cancer. The chimeric protein consisting of LTB wherein the signal peptide region is deleted and HPV16 E6 protein has the amino acid sequence of SEQ ID NO:6 and is encoded by a gene having the nucleotide sequence of SEQ ID NO:5. A vector E6-LTB/pET29a contains the chimeric protein gene and is used for production of a transformed Escherichia coli BL21:E6-LTB/pET29a(KCTC 10893BP). The chimeric protein consisting of LTB and HPV16 E6 protein is produced by culturing the transformed Escherichia coli BL21:E6-LTB/pET29a(KCTC 10893BP), separating the chimeric protein from the cultured transformed microorganism and removing endotoxin from the separated chimeric protein.
Abstract translation:提供由LTB(大肠杆菌热不稳定肠毒素B亚基)和HPV16 E6(人乳头瘤病毒16型E6)蛋白组成的嵌合蛋白及其用途,以同时诱导HPV16E6蛋白特异性抗体和粘膜免疫应答,从而 该嵌合蛋白质可用于生产用于预防和治疗子宫颈癌的疫苗。 由LTB组成的嵌合蛋白,其中信号肽区被缺失,HPV16E6蛋白具有SEQ ID NO:6的氨基酸序列,并由具有SEQ ID NO:5的核苷酸序列的基因编码。 载体E6-LTB / pET29a含有嵌合蛋白基因,用于生产转化大肠杆菌BL21:E6-LTB / pET29a(KCTC 10893BP)。 通过培养转化的大肠杆菌BL21:E6-LTB / pET29a(KCTC 10893BP),从培养的转化微生物中分离嵌合蛋白质并从分离的嵌合蛋白质中除去内毒素,产生由LTB和HPV16 E6蛋白组成的嵌合蛋白质。
Abstract:
A method for production of a natural killer(NK) cell is provided to avoid side effects in cancer therapy by using a natural killer cell differentiated from a hematopoietic stem cell instead of a matured natural killer cell. The adult natural killer cell is produced by treating the hematopoietic stem cell with IL-7(interleukine 7), SCF(stem cell factor) and Flt3L(fms-related tyrosine kinase 3 ligand) to differentiate the hematopoietic stem cell into a NK precursor cell, and treating the NK precursor cell with the Axl receptor and its ligand Gas6. The hematopoietic stem cell is isolated from the human cord blood; the Axl is a recombinant Axl produced from a transformant containing a recombinant vector pLXSN-Axl; the host cell of the transformant containing the recombinant vector pLXSN-Axl is a mouse RAW264.7 macrophage; the recombinant Gas6 is produced from a transformant containing a recombinant vector pcDNA3.1(+)-GAS6; and the host cell of the transformant containing the recombinant vector pcDNA3.1(+)-GAS6 is a mouse OP9 cell line.
Abstract:
A dye-sensitized solar cell using a copolymer binder including a hydroxy group and a carboxyl group and a manufacturing method thereof are provided to increase an open circuit voltage and short circuit current by using the copolymer. A relative electrode includes a light-transmitting material(10), a conductive light-transmitting layer(20), and a platinum layer(30). An optical electrode includes a copolymer binder comprising a hydroxy group and a carboxyl group, a mixture layer comprising a transition metal oxide, and a conductive light-transmitting layer. An electrolyte solution(50) is positioned between the relative electrode and the optical electrode. The copolymer binder comprising the hydroxy group and the carboxyl group is composed of a styrene-based monomer comprising a vinyl group, an acrylate-based monomer comprising the hydroxy group, and a methacrylic acid-based monomer including the carboxyl group.
Abstract:
염료감응 태양전지용 천연염료 용액 제조방법 및 이를 이용한 천연염료 감응 태양전지 제조방법을 제공한다. 염료감응 태양전지용 천연염료 용액 제조방법은 천연염료 분말을 준비하는 단계; 및 상기 천연염료 분말, pH 조절제 및 용매를 혼합하여 천연염료 용액을 형성하는 단계를 포함하고, 상기 천연염료 용액은 식물 생장의 촉진 또는 억제를 위한 파장 선택성을 갖는 것을 특징으로 하는 염료감응 태양전지용 천연염료 용액 제조방법을 포함한다. 따라서, 흡수파장대가 다른 천연염료 용액을 조합하여 제조된 파장선택용 칵테일 용액을 적용하여 식물의 생장에 필요한 파장대에 적합한 천연염료 감응 태양전지를 다양하게 제조할 수 있다.