http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Kim, Hee-Sue,Lee, Hee-Gu,Lim, Jong-Seok,Lee, Ki-Young,Kim, Jae-Wha,Chung, Kyeong-Soo,Choe, Yong-Kyung,Choe, In-Seong,Chung, Tai-Wha,Kim, Kil-Hyoun Korean Society for Biochemistry and Molecular Biol 1995 Journal of biochemistry and molecular biology Vol.28 No.6
The purpose of this study was to establish an in vitro culture method of tumor-specific T cells, and determine the efficacy of the cultured tumor-specific cytotoxic T-lymphocytes (CTL) as an agent of anti-tumor immunotherapy against a murine lymphoma, TIMI.4. Tumor-specific T-lymphocytes derived from C57BL/6 mice (thy-1.2) immune to TIMI.4 were activated by in vitro stimulation with the irradiated TIMI.4 cells, and expanded by restimulation with TIMI.4 in the presence of the concanavalin A-stimulated rat spleen culture supernatant, and splenic antigen-presenting cells. In vitro restimulation enhanced markedly the proportion of $CD8^+$, a predominant surface marker of CTL and the cytotoxic activity in the cultured immune T cell population. The resulting TIMI.4-specific T cells were adoptively transferred into nude mice. The tumor cells residing in the host after 7 days of adoptive transfer to B6.PL (thy-1.1) mice were quantified by use of an antibody directed to the thy-1.2 allele. The TIMI.4 cells in the recipient nude mice were decreased in a dose-dependent manner. Anti-tumor activity of the TIMI.4-specific T cells was also demonstrated by a survival test, where the tumor-bearing nu/nu mice which received the activated T-cells survived about 30% longer than the control mice which received the tumor cells alone. These suggest that adoptive transfer of TIMI.4-specific T cells could be a candidate for effective therapy of the murine lymphoma.
구재회(Gu, Jae-Hoi),김수현(Kim, Su-Hyun),김문현(Kim, Mun-Hyun),최종혜(Choi, Jong-Hyea),허수정(Heo, Su-Jung),윤기수(Yoon, Ki-Soo),김성현(Kim, Soung-Hyoun) 한국신재생에너지학회 2008 한국신재생에너지학회 학술대회논문집 Vol.2008 No.05
The 3 ton/day-scale pilot plant consists of waste press, feed channel, fixed bed type gasification & melting furnace, quench scrubber, syngas refinery facility and flare stack. H₂/CO ratio of gasification syngas using the solid waste and sludge in the 3 ton/day gasifier showed about 1. Gasification melting furnace was operated 1,300{sim}1,600?C. H₂/CO ration control system was obtained H₂/CO ratio 2 and 3.
해석 프로그램을 이용한 72W급 LED 등기구의 광분석과 열해석
고제현(Je-Hyun Ko),박재현(Jae-hyoun Park),김현종(Hyun-jong Kim),김현지(Hyun-ji Kim),김정환(Jung-hwan Kim),김범석(Bum-suk Kim),김정렬(Jeong-ryul Kim),오세준(Sea-June Oh),김진구(Jin-Gu Kim) 대한기계학회 2014 대한기계학회 춘추학술대회 Vol.2014 No.11
In recently, LED light device is used for various purposes according to the efficiency and performance of the respective accessories. Among the LED light devices using in marine are satisfied with the inadequate condition of circumstances more than that of land. For example, the tests of sea water, electromagnetic wave and explosion proof should be taken. So this study deal with the basic analysis of heat and optic on the LED light device to satisfy the KS standard.
마우스(H-2K^(b))에서 간염 바이러스 핵 항원에 의한 CTL유도
김재화,이희구,이기영,임종석,김용호,박순희,최용경,정태화,최인성,김길현 大韓免疫學會 1996 大韓免疫學會誌 Vol.18 No.2
Recently reported viral peptides from virus-infected cells that are bound to class I MHC molecules showed 8-lOmer sequences and typical dominant anchor residues. Using the mutant tumor line RMA-S, which expresses its surface H-2K' molecules devoid of peptides, we investigated the specific CTL epitopes on the hepatitis B viral surface and core proteins that were isolated from hepatitis B virus-infected patients. This was done by examining the ability of randomly trypsinized protein to bind to H-2K' or Db molecule on RMA-S cells. The trypsin-treated proteins enhanced the expression of H-2b molecules on RMA-S cells. We have analyzed the digested proteins by high performance liquid chromatography, and binding assays with respective peptide fractions showed the presence of H-2' binding epitopes on hepatits B viral protein. These findings suggest that it is possible to determine the epitope sequences directly by measuring their binding to class I molecules followed by analyzing their amino acid sequences.