公开(公告)号：KR100809551B1

公开(公告)日：2008-03-04

申请号：KR1020050019227

申请日：2005-03-08

Applicant: 재단법인서울대학교산학협력재단

Inventor： 이재홍 ,  유치훈

IPC: H03M13/29

CPC classification number: H03M13/25 ,  H03M13/2957 ,  H03M13/63 ,  H04L1/0066 ,  H04L1/0068 ,  H04L1/0625 ,  H04L1/0675

Abstract: 본 발명은 복수개의 안테나를 구비하는 디지털 이동 통신 시스템에서 시공간 터보 부호로 메시지를 부호화하여 송신하는 장치 및 방법에 있어서, 채널 이득 또는 위상에 대한 귀환 정보를 갖는 귀환 비트를 이용하여 메시지를 부호화하여 송신하는 장치 및 방법에 관한 것이다. 본 발명에 따른 귀환 형태를 사용하는 시공간 터보 부호는 종래의 시공간 터보 부호보다 더 우수한 성능을 나타낸다.

公开(公告)号：KR100809056B1

公开(公告)日：2008-03-03

申请号：KR1020060066439

申请日：2006-07-14

Applicant: 재단법인서울대학교산학협력재단

Inventor： 현택환 ,  박원철 ,  장영진

IPC: B82B3/00 ,  B82Y40/00

Abstract: 본 발명은 수용액 상에서 블록 공중합체를 이용하여 균일한 팔라듐 나노 입자를 제조하는 방법에 관한 것이다.
본 발명에 따른 제조방법에 의해 제조된 팔라듐 나노 입자는 그 조건에 따라서 몇 나노미터 에서 몇 십 나노미터 크기를 보이고 있으며, 입자의 크기 분포가 매우 균일하여 화학 반응의 촉매로 사용되어 높은 촉매 활성을 나타내는 장점이 있다.
블록 공중합체, 팔라듐 나노입자, 촉매

公开(公告)号：KR100808753B1

公开(公告)日：2008-02-29

申请号：KR1020060130091

申请日：2006-12-19

Applicant: 재단법인서울대학교산학협력재단 ,  삼성전자주식회사

Inventor： 김대식 ,  이광걸 ,  김현우

IPC: G01B21/00 ,  B82Y35/00

CPC classification number: G01Q60/22

Abstract: A device and a method for measuring an electric field vector, and a microscope including the device are provided to precisely measure and research characteristic of light generated from a quantum dot and a fluorescent material and interaction between the quantum dot and the fluorescent material. A device for measuring an electric field vector includes an imperforate probe(92), an object lens(93), an optical iris(94), a polarizing plate(95), a first beam split member(96), a second beam split member(97), and an electric field vector obtaining unit(99). The first beam split member splits a first split light from incident light. The second beam split member splits a second split light from light passing through a sample(90), the imperforate probe, the object lens, the optical iris, and the polarizing plate one by one. The object lens measures interference characteristic of the first and the second split lights. The object lens determines a relative phase difference between the first and the second split lights.

Abstract translation: 提供了用于测量电场矢量的装置和方法以及包括该装置的显微镜，以精确地测量和研究由量子点和荧光材料产生的光的特性以及量子点和荧光材料之间的相互作用。 用于测量电场矢量的装置包括无孔探针（92），物镜（93），光学虹膜（94），偏振片（95），第一光束分割构件（96），第二光束分割 构件（97）和电场矢量获取单元（99）。 第一光束分离构件分裂来自入射光的第一分裂光。 第二光束分离部件从通过样品（90），无孔探针，物镜，光学虹膜和偏振片的光中逐个分割第二分离光。 物镜测量第一和第二分光灯的干涉特性。 物镜确定第一和第二分光灯之间的相对相位差。

公开(公告)号：KR1020080018619A

公开(公告)日：2008-02-28

申请号：KR1020060081022

申请日：2006-08-25

Applicant: 재단법인서울대학교산학협력재단

Inventor： 노동영 ,  이정언 ,  김종빈 ,  한원식

IPC: C12N5/07 ,  C12N5/00

Abstract: A multipotential cell line II derived from cancer tissue is provided to differentiate into other cells such as epidermal cell and nerve cell except cells in the cancer tissue, and separate cancer stem cell, so that it is useful for treatment of various diseases. A method for preparing the multipotential cell line II(KCLRF-BP-00138) comprises the steps of: (1) separating cancer cells from the previously separated cancer tissue; (2) culturing the separated cancer cells in a suspension medium; (3) collecting the cells in a suspension state from the cultured medium; (4) subculturing the collected cells in a suspension medium to separate the multipotential cell line; and (5) optionally culturing the separated multipotential cell line in medium for adhesion. A multipotential cell line II(KCLRF-BP-00138) derived from cancer tissue and being cultured in a suspension state does not express markers of breast cancer diagnosis receptor(ER, PR, C-erBb2), and express markers of breast stem cell(CK19, CK5, CK6), a marker of breast cancer resistant drug(ABCG2), markers of epidermal cell(CK14, vimentin, CK18) and markers of nerve cell(nestin, Tuj-1). Further, the cancer tissue is breast cancer.

Abstract translation: 提供衍生自癌组织的多能细胞系II，以分化成其他细胞，如癌组织中除细胞外的表皮细胞和神经细胞，以及分离的癌干细胞，因此可用于治疗各种疾病。 制备多潜能细胞系II（KCLRF-BP-00138）的方法包括以下步骤：（1）从先前分离的癌组织分离癌细胞; （2）在悬浮介质中培养分离的癌细胞; （3）从培养基中收集处于悬浮状态的细胞; （4）将收集的细胞在悬浮培养基中传代培养以分离多潜能细胞系; 和（5）任选地在培养基中培养分离的多能细胞系以进行粘附。 衍生自癌组织并以悬浮状态培养的多能细胞系II（KCLRF-BP-00138）不表达乳腺癌诊断受体（ER，PR，C-erBb2）的标志物，并且表达乳腺干细胞的标志物 CK19，CK5，CK6），乳腺癌抗药物标记物（ABCG2），表皮细胞标志物（CK14，波形蛋白，CK18）和神经细胞标记物（nestin，Tuj-1）。 此外，癌组织是乳腺癌。

公开(公告)号：KR100807184B1

公开(公告)日：2008-02-27

申请号：KR1020060129755

申请日：2006-12-19

Applicant: 재단법인서울대학교산학협력재단

Inventor： 정진하 ,  방옥선 ,  강성환

IPC: C12N9/50 ,  C12N15/09

Abstract: A Ufm1-specific protease 1(UfSP1) is provided to be able to show the protein decomposing activity on Ufm1 acting on an important mechanism in a cell, thereby being widely utilized for investigating the important mechanism in the cell where the Ufm1 involves. A Ufm1-specific protease 1(UfSP1) includes an amino acid sequence of SEQ ID : NO. 1. An expression plasmid includes a gene having a sequence of SEQ ID : NO. 2 AND encoding the UfSP1 and is pMAL-c2X-UfSP1. A method for preparing the UfSP1 comprises the steps of: (a) culturing a transformant prepared by transforming E. coli BL21 using the expression plasmid; and (b) obtaining the UfSP1 from the cultured fungus bodies.

Abstract translation: 提供Ufm1特异性蛋白酶1（UfSP1）能够显示Ufm1上的蛋白质分解活性，作用于细胞中的重要机制，从而广泛用于研究Ufm1所涉及的细胞中的重要机制。 Ufm1特异性蛋白酶1（UfSP1）包含SEQ ID NO：1的氨基酸序列。 表达质粒包含具有SEQ ID NO：1的序列的基因。 2编码UfSP1并且是pMAL-c2X-UfSP1。 制备UfSP1的方法包括以下步骤：（a）培养使用表达质粒转化大肠杆菌BL21制备的转化体; 和（b）从培养的真菌体获得UfSP1。

公开(公告)号：KR1020080017239A

公开(公告)日：2008-02-26

申请号：KR1020070028905

申请日：2007-03-23

Applicant: 삼성전자주식회사 ,  재단법인서울대학교산학협력재단

Inventor： 이병옥 ,  이광복 ,  박창순

IPC: H04B7/04 ,  H04B7/26

CPC classification number: H04B7/0617 ,  H04B7/0632

Abstract: An apparatus and a method for transceiving feedback information in a multi-user multiple transceiving antenna system, and a system for the same are provided to transmit only the activation and/or inactivation of a channel by stream even when a receiver receives plural streams from the transmitter, thereby reducing the amount of the entire feedback information. A transmitter for transmitting feedback information in a multiple transceiving antenna system comprises a channel state recognizing unit(110) and a control unit(120). The channel state recognizing unit transmits reference CQI(Channel Quality Information) to a receiver, and if channel setting information is received from the receiver, recognizes a channel state of the receiver through the received channel setting information. The control unit controls the beamforming of plural antennas by using the recognized channel state.

Abstract translation: 提供了一种用于在多用户多收发天线系统中收发反馈信息的装置和方法，以及用于其的系统，用于仅通过流仅发送信道的激活和/或失活，即使当接收机从 发射机，从而减少整个反馈信息的数量。 用于在多收发天线系统中发送反馈信息的发射机包括信道状态识别单元（110）和控制单元（120）。 信道状态识别单元向接收机发送参考CQI（信道质量信息），如果从接收机接收到信道设定信息，则通过所接收的信道设定信息来识别接收机的信道状态。 控制单元通过使用识别的信道状态来控制多个天线的波束形成。

公开(公告)号：KR100806868B1

公开(公告)日：2008-02-22

申请号：KR1020060089267

申请日：2006-09-14

Applicant: 재단법인서울대학교산학협력재단

Inventor： 박봉균 ,  이철승

IPC: C12Q1/68

CPC classification number: C12Q1/686 ,  C12Q2537/143

Abstract: A multiplex PCR primer set specific to PRV(pseudorabies virus), PCMV(cytomegalovirus) and PCV(circovirus) is provided to detect rapidly and accurately porcine virus pathogens relating to xenograft with high sensitivity and specificity. A multiplex PCR primer set specific to PRV, PCMV and PCV comprises a primer set for amplifying a gF(glycoprotein G) gene of the PRV including a G1 primer having a nucleotide sequence of SEQ ID : NO. 1 and a G2 primer having a nucleotide sequence of SEQ ID : NO. 2; a primer set for amplifying a gB(glycoprotein B) gene of the PCMV including a B1 primer having a nucleotide sequence of SEQ ID : NO. 3 and a B2 primer having a nucleotide sequence of SEQ ID : NO. 4; and a primer set for amplifying an ORF1(open reading frame 1) gene of the PCV including a pcv1 primer having a nucleotide sequence of SEQ ID : NO. 5 and a pcv2 primer having a nucleotide sequence of SEQ ID : NO. 6. A method for detecting the existence or nonexistence of at least one virus selected from the group consisting of the PRV, PCMV and PCV in a sample comprises the steps of: (a) extracting a virus genome DNA from the sample including the virus; and (b) performing a multiplex PCR using the obtained genome DNA as a template and the multiplex PCR primer set as a primer. A kit for detecting the existence or nonexistence of at least one virus selected from the group consisting of the PRV, PCMV and PCV comprises the multiplex primer set, a mixture of dNTP(dATP, dCTP, dGTP, dTTP), a heat-resistant polymerase and a PCR buffer solution.

Abstract translation: 提供特异于PRV（伪狂犬病毒），PCMV（巨细胞病毒）和PCV（圆环病毒）的多重PCR引物组，以高灵敏度和特异性迅速和准确地检测与异种移植相关的猪病毒病原体。 对PRV，PCMV和PCV特异性的多重PCR引物组包括用于扩增PRV的gF（糖蛋白G）基因的引物组，其包含具有SEQ ID NO：1的核苷酸序列的G1引物。 1和具有SEQ ID NO：1的核苷酸序列的G2引物。 2; 用于扩增PCMV的gB（糖蛋白B）基因的引物组，其包含具有SEQ ID NO：1的核苷酸序列的B1引物。 3和具有SEQ ID NO：1的核苷酸序列的B2引物。 4; 以及用于扩增PCV的ORF1（开放阅读框1）基因的引物组，其包含具有SEQ ID NO：1的核苷酸序列的pcv1引物。 5和具有SEQ ID NO：5的核苷酸序列的pcv2引物。 6.一种用于检测样品中存在或不存在选自PRV，PCMV和PCV的至少一种病毒的方法，包括以下步骤：（a）从包含病毒的样品中提取病毒基因组DNA; 和（b）使用获得的基因组DNA作为模板进行多重PCR，并设置多重PCR引物作为引物。 用于检测选自PRV，PCMV和PCV的至少一种病毒的存在或不存在的试剂盒包括多重引物组，dNTP（dATP，dCTP，dGTP，dTTP），耐热聚合酶 和PCR缓冲液。

公开(公告)号：KR100804584B1

公开(公告)日：2008-02-20

申请号：KR1020050022325

申请日：2005-03-17

Applicant: 재단법인서울대학교산학협력재단

Inventor： 김영식 ,  김완석 ,  전경진

IPC: C12N15/70 ,  C12N9/24

Abstract: 본 발명은 글리코사미노글리칸 분해효소(glycosaminoglycan lyase)의 정제방법에 관한 것이고, 구체적으로는 글리코사미노글리칸의 일종인 헤파린을 분해하는 헤파리나제 Ⅰ, 헤파란 황산을 분해하는 헤파리나제 Ⅲ 및 콘드로이틴 황산을 분해하는 콘드로이티나제 ABC의 정제방법에 관한 것이다. 본 발명의 정제방법은 기존의 방법에 비하여 정제된 글리코사미노글리칸 분해효소의 수율과 활성이 높으므로 의학적 가치가 높은 글리코사미노글리칸 분해효소를 경제적으로 대량생산하는데 이용될 수 있다.
글리코사미노글리칸, 헤파리나제, 콘드로이티나제

公开(公告)号：KR100804738B1

公开(公告)日：2008-02-19

申请号：KR1020070004973

申请日：2007-01-16

Applicant: 삼성전자주식회사 ,  재단법인서울대학교산학협력재단

Inventor： 고형수 ,  박병국 ,  홍승범 ,  박철민 ,  최우영 ,  김종필 ,  송재영 ,  김상완

IPC: H01L21/66 ,  H01L21/336 ,  H01L29/78

CPC classification number: H01L29/0847 ,  H01L29/66636 ,  H01L29/66659 ,  H01L29/78 ,  G01R1/067

Abstract: A semiconductor probe using an impact-ionization semiconductor device is provided to remarkably improve the limit of sensitivity of a resistive probe and easily adjust the quantity of charges capable of being detected by a probe by developing a new probe structure for easily adjusting the band energy of a source. One tilted surface of a probe is formed by an anisotropic etch process using a first etch mask pattern formed on a silicon substrate. After impurities are doped into the exposed substrate to form a first semiconductor electrode region(16), the first etch mask pattern is removed. A second etch mask pattern opposite to the direction of the first etch mask pattern is formed on the silicon substrate. Space layers are formed on the sidewalls of the second etch mask pattern. After the exposed silicon substrate is anisotropically etched to form an opposite tilted surface of the probe, the second etch mask pattern is removed. Impurities are doped into the exposed substrate to form a second semiconductor electrode region(18), and the second etch mask pattern is removed. A silicon oxide layer pattern is formed on the resultant structure by a known method. Space layers are formed on both sidewalls of the silicon oxide layer pattern. By using the space layer, a predetermined depth of the silicon substrate is etched by a photolithography process, and the space layer is removed. The first semiconductor electrode region can be a source terminal, and the second semiconductor electrode region can be a drain terminal.

Abstract translation: 提供使用冲击电离半导体器件的半导体探针，以显着提高电阻式探头的灵敏度极限，并且通过开发新的探针结构容易地调节能够由探针检测的电荷量，从而容易地调节带电能 来源。 通过使用形成在硅衬底上的第一蚀刻掩模图案的各向异性蚀刻工艺形成探针的一个倾斜表面。 在将杂质掺杂到暴露的衬底中以形成第一半导体电极区域（16）之后，去除第一蚀刻掩模图案。 在硅衬底上形成与第一蚀刻掩模图案的方向相反的第二蚀刻掩模图案。 空间层形成在第二蚀刻掩模图案的侧壁上。 在暴露的硅衬底被各向异性蚀刻以形成探针的相对的倾斜表面之后，去除第二蚀刻掩模图案。 将杂质掺杂到暴露的衬底中以形成第二半导体电极区域（18），并且去除第二蚀刻掩模图案。 通过已知的方法在所得结构上形成氧化硅层图案。 空间层形成在氧化硅层图案的两个侧壁上。 通过使用空间层，通过光刻工艺蚀刻硅衬底的预定深度，并且去除空间层。 第一半导体电极区域可以是源极端子，第二半导体电极区域可以是漏极端子。

公开(公告)号：KR1020080012474A

公开(公告)日：2008-02-12

申请号：KR1020060073329

申请日：2006-08-03

Applicant: 재단법인서울대학교산학협력재단

Inventor： 박태성 ,  이은경

IPC: G06F17/10

CPC classification number: G06F17/15 ,  G06F17/16

Abstract: A method and a system for analyzing microarray data are provided to analyze quality of the microarray data objectively which is generated from a plurality of treatments by using a chip correlation coefficient according to the same or different treatment. A correlation module(10) generates a plurality of reference vectors according to treatments and treatment repetitions, generates the reference vector for m-th repetition of n-th treatment by using intensity of a plurality of genes included in the m-th repetition of the n-th treatment, and calculates a correlation coefficient between two reference vectors among a plurality of reference vectors. An analyzing module(20) analyzes microarray data by using the correlation coefficient. The analyzing module compares the quality of the first and second treatments by comparing the correlation coefficient of a correlation group in the repeated treatments of the first treatment with the correlation coefficient of the correlation group in the repeated treatments of the second treatment.

Abstract translation: 提供了一种用于分析微阵列数据的方法和系统，用于通过使用根据相同或不同处理的码片相关系数，从多个处理中客观地分析微阵列数据的质量。 相关模块（10）根据处理和处理重复产生多个参考矢量，通过使用包含在第m次重复中的多个基因的强度来生成第n次处理的第m次重复的参考矢量 并且计算多个参考矢量中的两个参考矢量之间的相关系数。 分析模块（20）通过使用相关系数分析微阵列数据。 分析模块通过将第一次处理的重复处理中的相关组的相关系数与第二次处理的重复处理中相关组的相关系数进行比较，来比较第一和第二处理的质量。