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21.发明授权
公开(公告)号：KR100246126B1
公开(公告)日：2000-03-15
申请号：KR1019970064030
申请日：1997-11-28
Applicant: 한국과학기술연구원
Abstract: 본 발명은 암세포 조직에서 특이적으로 발현되는 N-아세틸글루코사민 전이효소Ⅲ(N-acetylglucosaminyl transferase Ⅲ)에 대한 단일클론 항체, 이를 생산하는 융합세포주 및 그들의 제조방법에 관한 것이다. 구체적으로, 본 발명은 간질환 환자의 간세포 및 암세포에서 그 활성이 증가하는 인간 N-아세틸글루코사민 전이효소Ⅲ를 특이적으로 인식하는 단일클론 항체에 대한 것으로서, 상기의 단일클론 항체는 혈액이나 조직내의 N-아세틸글루코사민 전이효소Ⅲ 항원을 검색하여 암세포 및 간질환을 진단하는데 유용하게 사용될 수 있다.
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公开(公告)号：KR1019990086029A
公开(公告)日：1999-12-15
申请号：KR1019980018811
申请日：1998-05-25
Applicant: 한국과학기술연구원
IPC: C07K16/08
Abstract: 본 발명은 돼지 전염성 위장염 바이러스의 침단백질에 대한 생쥐 단일클론항체와 이를 생산하는 하이브리도마 세포주 및 이들의 제조방법에 관한 것이다.
본 발명은 돼지에서 유행성 설사질환을 유발하는 돼지 전염성 위장염 바이러스의 침단백질을 특이적으로 인식하는 단일클론항체에 대한 것으로서 본 발명의 단일클론항체는 제조하기 간편하고 대량생산이 가능할 뿐만 아니라 돼지의 분비물에서 돼지 전염성 위장염 바이러스를 조기 진단할 수 있는 뛰어난 효과가 있다.-
Patent Agency Ranking
公开(公告)号：KR100129488B1
公开(公告)日：1998-04-08
申请号：KR1019940004070
申请日：1994-03-03
Applicant: 한국과학기술연구원
IPC: G01N33/493
Abstract: Automatic system of urine test and decipherment is applied as follows; (a) After comparing the measuring value of reflection light with the standard value to save that comparative value in RAM(17), and analyze qualitatively and quantitatively the comparative value saved in RAM(17) according to the program saved in ROM(16) to output the value to a printer(13). (b) Micro-controller(10) discriminates whether measuring result by each item is positive or negative, and if the result is positive, radiate a luminous diode(12) with red, when negative, radiate it with green. (c) In case the output of urine measuring result is finished, discriminate whether the result is the last measuring item or not, and if the result is the last item, finish urine decipherment process.
Abstract translation: 尿液检查和解密的自动系统应用如下： （a）将反射光的测量值与标准值进行比较以将该比较值保存在RAM（17）中，并根据保存在ROM（16）中的程序定期和定量地分析存储在RAM（17）中的比较值， 以将该值输出到打印机（13）。 （b）微控制器（10）鉴别每个项目的测量结果是正还是负，并且如果结果为正，则用红色辐射发光二极管（12），否则将其用绿色辐射。 （c）尿液测定结果的输出结束后，判断结果是否为最后一个测量项目，如果结果为最后一项，则完成尿液解密处理。
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公开(公告)号：KR1019970010983B1
公开(公告)日：1997-07-05
申请号：KR1019930020973
申请日：1993-10-09
Applicant: 한국과학기술연구원
IPC: G01N33/53
Abstract: Dry testing paper for simultaneous detection of various narcotics by using the immunity analysis method and a manufacturing method thereof are provided, in which the dry testing paper for simultaneous detection of various narcotics by using the immunity analysis method includes a first membrane which is temporarily fixed with one or more kinds of colored corpuscle-antibiotic of narcotics, and a second membrane which is connected to the first membrane in a longitudinal direction and permanently fixed with one or more narcotics-protein conjugates, wherein the corpuscles of the colored corpuscle-antibiotic of narcotics have different colors per the antibiotic of narcotics so that one or more narcotics may be discriminated at once with naked eyes and the testing paper is convenient for carrying out.
Abstract translation: 提供了通过使用免疫分析方法及其制造方法同时检测各种麻醉剂的干试纸，其中通过使用免疫分析方法同时检测各种麻醉剂的干试纸包括第一膜，其临时固定有 一种或多种毒品的有色微粒抗生素，以及第二膜，其沿纵向方向连接到第一膜并且与一种或多种麻醉剂 - 蛋白质缀合物永久固定，其中所述毒品的着色小体抗生素的小体 每种麻醉品的抗生素有不同的颜色，以便用肉眼可以一次鉴别一种或多种麻醉剂，并且测试纸便于进行。
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公开(公告)号：KR1019950002926B1
公开(公告)日：1995-03-28
申请号：KR1019910017544
申请日：1991-10-07
Applicant: 한국과학기술연구원
IPC: G01N33/50
Abstract: The method produce a drug detecting paper that is mostly composed of tetra-Bromophenolphthalein-ester (TBPE) and methylene chloride. The drug detecting paper deliberately and accurately detects methamphetamine, methoxyphenamine, DL-methylephedrine, amphetamine, ephedrine, and norephedrine which are contained in urine. Generally, the production method of drug detecting paper is divided into two catagories: a dry method and a wet method. This method follows the dry production method of drug detecting papers. The dry method comprises the steps of: dipping a filter paper in methylene chloride solution in which tetra-Bromophenophthlein-ethyl-ester is solved; drying the filter paper; dipping the filter paper in 10% borax solution; and drying the paper.
Abstract translation: 该方法生产大部分由四溴苯酚酯（TBPE）和二氯甲烷组成的药物检测纸。 药物检测纸故意准确检测尿液中含有的甲基苯丙胺，甲氧基苯胺，DL-甲基麻黄素，苯丙胺，麻黄碱和去甲麻黄碱。 一般来说，药物检测纸的生产方法分为干法和湿法两大类。 该方法遵循药物检测纸的干法生产方法。 干法包括以下步骤：将滤纸浸入其中溶解四溴酚酞 - 乙酯的二氯甲烷溶液中; 干燥滤纸; 将滤纸浸入10％硼砂溶液中; 并干燥纸张。
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