| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 141 | 폴리에틸렌 수지의 물성 평가 방법 | KR20160157722 | 2016-11-24 | KR20180058574A | 2018-06-01 | |
| 본발명은폴리에틸렌수지의물성평가방법에관한것으로, 보다상세하게는, 쉬운방법에의해단 시간내에측정가능한물성을이용하여, 실제제조되는성형제품의장기내구성을정확히도출해낼수 있는, 새로운폴리에틸렌수지의물성평가방법에관한것이다. | ||||||
| 142 | 분석용 칩 | KR1020177026514 | 2016-03-31 | KR1020170132159A | 2017-12-01 | 오츠카히로키; 우에다요지 |
| 본발명에따른분석용칩은피검물질과선택적으로결합하는선택결합성물질이고정화된복수의반응부를갖는기판본체와, 반응부가형성되어있는표면을통과하는평면을절단면으로하는단면에있어서서로다른직선또는곡선이교차하는모서리부와, 기판본체의반응부가형성된표면에발수처리를실시해서이루어지고, 상기표면이이루는외측가장자리의내부에있어서복수의반응부를구획하는구획부와, 발수성을갖고구획부의일부와모서리부사이를접속하는접속부를구비했다. | ||||||
| 143 | 미세 액체 이송 구조체 및 분석 장치 | KR1020177014314 | 2015-11-27 | KR1020170073695A | 2017-06-28 | 오누키,료지; 쿠니노리,마사히로; 이와사키,츠토무 |
| 복수의미세돌기 (60)가일렬로늘어서고, 또한인접한미세돌기 (60)의간극을액체이송로(61)로하는단위열이주기적으로배열설치되어각각의미세돌기 (60)의간격이모세관현상을일으키는간격이되도록배열하고, 단위열마다액체이송로(61) 중적어도하나를다른액체이송로 (61b)보다유동저항을상대적으로감소시킨저유동저항액체이송로(61a)로함과동시에, 저유동저항액체이송로 (61a)가소정의액체이송방향에따라배치되도록미세돌기 (60)를배열한다. 이로써액체이송방향에편향이발생하지않고액체이송방향을재현성있게임의로제어할수 있다. | ||||||
| 144 | 간암의 검출 키트 또는 디바이스 및 검출 방법 | KR1020177000870 | 2015-06-18 | KR1020170018411A | 2017-02-17 | 콘도우사토시; 노부마사히토시; 코조노사토코; 수도히로코; 카와우치준페이; 오치아이아츠시; 코지마모토히로 |
| 간암의검출용키트또는디바이스, 및검출방법을제공한다. 본발명은피험체의검체중의 miRNA와특이적으로결합가능한핵산을포함하는, 간암검출용키트또는디바이스, 및그 miRNA를 in vitro에서측정하는것을포함하는간암을검출하는방법에관한것이다. | ||||||
| 145 | 담도암 검출 키트 또는 디바이스 및 검출 방법 | KR1020177000779 | 2015-06-11 | KR1020170015509A | 2017-02-08 | 카와우치준페이; 노부마사히토시; 코조노사토코; 콘도우사토시; 수도히로코; 오치아이아츠시; 코지마모토히로 |
| 담도암검출용키트또는디바이스, 및검출방법을제공한다. 본발명은피험체의검체중의 miRNA와특이적으로결합가능한핵산을포함하는담도암검출용키트또는디바이스, 및상기 miRNA를인비트로에서측정하는것을포함하는담도암을검출하는방법에관한것이다. | ||||||
| 146 | 온라인 측정기의 켈리브레이션 방법, 이를 구현하기 위한 프로그램이 저장된 기록매체 및 이를 구현하기 위해 매체에 저장된 컴퓨터프로그램 | KR1020150022482 | 2015-02-13 | KR1020160100031A | 2016-08-23 | 유승교; 김동철; 이응선; 오권식; 이진섭; 김대희 |
| 본발명은온라인측정기의켈리브레이션방법, 이를구현하기위한프로그램이저장된기록매체및 이를구현하기위해매체에저장된컴퓨터프로그램에관한것으로서, 더욱상세하게는샘플용액에표준용액을혼합한표준용액농도에따른오염도측정값을근거로, 샘플용액자체의오염도를산출하여, 샘플용액의실시간오염도측정값을보정함으로써, 실시간으로샘플용액의오염도를측정하는온라인측정기의켈리브레이션방법, 이를구현하기위한프로그램이저장된기록매체및 이를구현하기위해매체에저장된컴퓨터프로그램을제공한다. | ||||||
| 147 | 수심별 유속제어가 가능한 배관구조를 갖는 폐쇄생태계 실험장치 | KR1020150020194 | 2015-02-10 | KR101636987B1 | 2016-07-08 | 최희락; 신유나; 김상훈; 이재윤; 노성유; 이재안; 김진필; 류덕희; 박주순 |
| 본발명에따른폐쇄생태계실험장치(1)는, 높이를달리하도록한쪽측벽에복수개의층으로유입구(31)가형성되고높이를달리하도록다른한쪽측벽에복수개의층으로유출구(32)가형성되는생태수조(30); 유입구(31)에대응하도록설치되는복수개의유입관(40); 유출구(32)에대응하도록설치되는복수개의유출관(50); 유입관(40)과유출관(50) 각각에설치되는유량조절수단(41, 51); 유입관(40)을통하여생태수조(30)에물을공급하도록설치되는분배조(20); 유출관(50)을통하여생태수조(30)에서층별로유출되는물이하나로취합되어외부배출되도록복수개의유출관(50)에연결설치되는취합유출관(80); 취합유출관(80)에서분기되도록설치되는분기관(87); 분기관(87)을통해서배출되는물을받도록설치되는수통(85); 분기관(87)이분기된부위보다뒤쪽에위치하도록취합유출관(80)에설치되는취합배출개폐밸브(82); 및분기관(87)에설치되는분기관개폐밸브(81); 을포함하여이루어지는것을특징으로한다. 본발명에의하면, 수심에따라유속을달리할수 있기때문에강, 하천, 바다등과같이흐르는물의실제생태환경에근접한조건하에생태연구가이루어지게되어매우정확하고신뢰성있게물속의생태환경을조사연구할수 있다. | ||||||
| 148 | 체외진단용 분석장치의 카트리지 | KR1020140150872 | 2014-11-03 | KR1020160051253A | 2016-05-11 | 천동철; 홍석기 |
| 본발명에따른체외진단용분석장치의카트리지는, 적어도두 개의시약을저장하는시약저장부가탑재되고, 일측에시료가주입되는시료주입구를구비하고, 일측상단에멤브레인을구비한멤브레인하우징이상기시료주입구와상기멤브레인이정렬되게탑재되도록형성된제1몸체; 및상부에홀이구비되고이 상부홀이하부의캐필러리와연통되게구성되는적어도두 개의캐필러리부가안착되도록형성되고, 하단에천공수단이형성된제2몸체;를포함하여구성되고, 상기제2몸체는상기제1몸체상단의제1위치에하부의제2위치로이동가능하게결합되고, 상기시약저장부는상단이차폐수단에의해차폐되는구조를제안함으로써, 사용자의취급을최소화하여편의성을향상시킴과동시에테스트의신뢰성및 정확도를높일수 있도록한다. | ||||||
| 149 | 센서 검사 장치 | KR2020140007068 | 2014-09-29 | KR2020160001146U | 2016-04-07 | 최진수; 구정모; 박태한; 이상섭; 이진욱 |
| 본고안은누출가스를감지하는센서의정상작동여부를확인하는센서검사장치에관한것이다. 본고안의일 실시예에따른센서검사장치는회전축, 와인드라인및 커버부재등을포함한다. 회전축은그 길이방향의중심축을중심으로회전되게제공된다. 와인드라인은회전축의회전에의해회전축의측면에감기거나풀리도록제공된다. 커버부재는와인드라인및 회전축의상부를커버한다. 따라서, 와인드라인이회전축에최대한감긴경우, 와인드라인및 회전축을외부충격또는빗물등으로부터보호함으로써, 센서검사장치의파손또는부식이방지되고, 와인드라인이회전축에감겨제공됨으로써, 직접와인드라인을직접선체에고정하는경우에비해적은수의서포트가요구된다. | ||||||
| 150 | 회전형 디지털 ＰＣＲ 공정용 마이크로 칩 및 이를 이용한 디지털 ＰＣＲ 방법 | KR1020130033734 | 2013-03-28 | KR101391066B1 | 2014-05-27 | 서태석; 박병현 |
| The present invention relates to a digital PCR, and more specifically, to a microchip for a rotary digital PCR process and a digital PCR method using the same. According to an embodiment of the present invention, the microchip includes: a capturing chamber which has an entrance and an outlet facing each other; and a plurality of capturing structures which are placed inside the capturing chamber and independently captures samples, wherein the width of the entrance is greater than the width of the outlet. | ||||||
| 151 | 테스트 미터로부터 테스트 스트립을 배출시키기 위한 형상 기억 합금 배출 기구 | KR1020127023023 | 2011-02-03 | KR1020130040774A | 2013-04-24 | 데안겔리마르코; 발세치루카 |
| 테스트 스트립 수용 포트 및 테스트 스트립과 함께 사용하기 위한 테스트 스트립 배출 기구는 프레임워크, 긴 형상 기억 합금(SMA) 스트립(예를 들어, SMA 와이어), 슬라이더 및 가열 모듈을 포함한다. SMA 스트립은 프레임워크에 부착되는 제1 및 제2 단부를 갖고, 고체 상태 전이 온도를 나타낸다. 슬라이더는 프레임워크를 따라 이동하도록 구성된다. 가열 모듈은 고체 상태 전이 온도 미만의 온도로부터 고체 상태 전이 온도 초과의 온도까지 SMA 스트립을 가열하도록 구성된다. 또한, SMA 스트립 및 슬라이더는, 형상 기억 스트립이 가열 모듈에 의해 고체 상태 전이 온도 미만의 온도로부터 고체 상태 전이 온도 초과의 온도까지 가열됨에 따라, 슬라이더가 SMA 스트립에 의해 슬라이더 상에 가해진 인가력 하에서 프레임워크를 따라 이동하도록 구성된다. 더욱이, 슬라이더는 테스트 스트립 수용 포트 내에 수용된 테스트 스트립과 결합하도록 그리고 슬라이더가 프레임워크를 따라 이동함에 따라 테스트 스트립 수용 포트로부터 테스트 스트립을 배출하도록 구성된 근위 단부를 갖는다. 테스트 스트립과 함께 사용하기 위한 테스트 미터는 테스트 스트립 수용 포트 및 테스트 스트립 배출 기구를 포함한다.
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| 152 | SINGLE-USE PRE-STERILIZED SENSORS WITH USAGE COUNT FOR USE IN BIO-PROCESSING APPLICATIONS | PCT/US2013058208 | 2013-09-05 | WO2014039640A3 | 2014-05-30 | SCHICK KARL G; UHEN DAVID |
| Single-use, pre-sterilized, and pre-calibrated, prevalidated sensors are provided. These sensors are designed to store sensor-specific information, such as calibration and production information, in a non-volatile memory chip on the sensor or in a barcode printed on the sensor. These sensors may be utilized with in-line systems, closed fluid circuits, bioprocessing systems, or systems which require an aseptic environment while avoiding or reducing cleaning procedures and quality assurance variances. The sensors exhibit both their primary sensing function such as conductivity, pH level, dissolved oxygen, pressure or temperature, as well as at least one secondary sensing function of risk management or risk mitigation. | ||||||
| 153 | MAGNETO-OPTICAL BIO-DISCS AND SYSTEMS INCLUDING RELATED METHODS | PCT/US0238021 | 2002-11-27 | WO03046511A2 | 2003-06-05 | COOMBS JAMES HOWARD; PHAN BRIGITTE CHAU; VALENCIA RAMONCITO MAGPANTAY |
| The present invention relates in general to molecular and cellular biomagnetic assays and, in particular, to molecular and cellular biomagnetic assays conducted on magneto−optical bio−discs. The invention further relates to magneto−optical bio−disc systems including the magneto−optical bio−discs and MO drives. More specifically, but without restriction to the particular embodiments hereinafter described in accordance with the best mode of practice, this invention relates to biomagnetic methods, including immunomagnetic methods, for detection and selective manipulation of specific target cells in cell populations and solutions of cell populations, using magnetic particles or beads, and to magnetically guided neurite growth, nerve regeneration, and magnetically formed neural networks using the MOBDS. | ||||||
| 154 | DETECTION OF CHROMOSOME COPY NUMBER CHANGES TO DISTINGUISH MELANOCYTIC NEVI FROM MALIGNANT MELANOMA | PCT/US0009609 | 2000-04-10 | WO0061814A9 | 2001-06-28 | BASTIAN BORIS; PINKEL DANIEL |
| The present invention provides for methods of distinguishing melanocytic nevi, such as Spitz nevi, from malignant melanoma. The methods comprise contacting a nucleic acid sample from a patient with a probe which binds selectively to a target polynucleotide sequence on a chromosomal region such as 11p, which is usually amplified in Spitz nevi. The nucleic acid sample is typically from skin tumor cells located within a tumor lesion on the skin of the patient. Using another probe which binds selectively to a chromosomal region such as 1q, 6p, 7p, 9p, or 10q, which usually show altered copy number in melanoma, the method can determine that those tumor cells with no changes in copy number of 1q, 6p, 7p, 9p, or 10q, are not melanoma cells but rather Spitz nevus cells. The finding of amplifications of chromosome 11p, particularly the presence of an 11p isochromosome would be an additional indication of Spitz nevus. An increase in copy number of chromosome 11p can also be determined by detecting the presence of an amplification of the H-RAS gene. The amplified gene can be normal or can be a mutated H-RAS gene. | ||||||
| 155 | DETECTION OF CHROMOSOME COPY NUMBER CHANGES TO DISTINGUISH MELANOCYTIC NEVI FROM MALIGNANT MELANOMA | PCT/US0009609 | 2000-04-10 | WO0061814A8 | 2001-05-25 | BASTIAN BORIS; PINKEL DANIEL |
| The present invention provides for methods of distinguishing melanocytic nevi, such as Spitz nevi, from malignant melanoma. The methods comprise contacting a nucleic acid sample from a patient with a probe which binds selectively to a target polynucleotide sequence on a chromosomal region such as 11p, which is usually amplified in Spitz nevi. The nucleic acid sample is typically from skin tumor cells located within a tumor lesion on the skin of the patient. Using another probe which binds selectively to a chromosomal region such as 1q, 6p, 7p, 9p, or 10q, which usually show altered copy number in melanoma, the method can determine that those tumor cells with no changes in copy number of 1q, 6p, 7p, 9p, or 10q, are not melanoma cells but rather Spitz nevus cells. The finding of amplifications of chromosome 11p, particularly the presence of an 11p isochromosome would be an additional indication of Spitz nevus. An increase in copy number of chromosome 11p can also be determined by detecting the presence of an amplification of the H-RAS gene. The amplified gene can be normal or can be a mutated H-RAS gene. | ||||||
| 156 | PHOTOSENSITIVE COMPOSITION FOR BIOCHIP FOR FLUORESCENCE ANALYSIS, METHOD FOR MANUFACTURING BIOCHIP FOR FLUORESCENCE ANALYSIS, AND BIOCHIP FOR FLUORESCENCE ANALYSIS | EP16864268.4 | 2016-11-09 | EP3376286A1 | 2018-09-19 | SAKURADA, Tomoaki; OBI, Masaki |
To provide a biochip whereby noise lights in fluorescence analysis are reduced. A photosensitive composition for forming a liquid repellent film on a liquid contact surface of a biochip for fluorescence analysis, said photosensitive resin composition comprising a polymer having a fluoroalkyl group which may have an etheric oxygen atom, and a polymerizable crosslinkable group, and a photoinitiator having an absorption coefficient at a wavelength of 365 nm of at most 400 [mL·g-1·cm-1]. A method for producing a biochip for fluorescence analysis, which comprises applying the photosensitive composition onto a liquid contact surface of a biochip for fluorescence analysis, followed by exposure and development. |
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| 157 | NANO-FLUID DEVICE AND CHEMICAL ANALYSIS APPARATUS | EP16857569.4 | 2016-10-21 | EP3367105A1 | 2018-08-29 | KAZOE Yutaka; PIHOSH Yuriy; KITAMORI Takehiko |
A nano-fluidic device includes: a first substrate that has a nanoscale groove on one surface; and a second substrate that is integrally provided with the first substrate by bonding one surface of the second substrate to the one surface of the first substrate and forms a nanochannel with the groove of the first substrate, in which either the first substrate or the second substrate includes at least a thin portion in a part of a position overlapping the nanochannel in plan view, and the thin portion is deformed by pressing to open and close the nanochannel. |
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| 158 | IMMUNOLOGICAL MEASUREMENT DEVICE | EP16857452.3 | 2016-10-19 | EP3367097A1 | 2018-08-29 | IWASAKI, Tsutomu; OONUKI, Ryuuji; KUNINORI, Masahiro |
In the present invention, a strong capillary action is applied to a flowpath itself so as to reliably move and mix a specimen and a labeling substance, without constituting, by use of a porous material, the flowpath to move the specimen and without excessively prolonging nor complicating the flowpath. Furthermore, it is possible to reliably and effectively improve visibility and signal strength of the labeling substance without risk of clogging the flowpath even if a particle diameter of the labeling substance is increased. The present invention comprises a micro fluid device 1 comprising a flowpath which moves a specimen subjected to immunological measurement by an antigen-antibody reaction, a labeling reagent supply unit 4 that labels the specimen and is arranged in an upstream section of the flowpath, and a detection flowpath 8 arranged downstream than the labeling reagent supply unit 4 to measure the antigen-antibody reaction of the specimen, wherein the labeling reagent supply unit 4 comprises a labeling reagent having the labeling substance in which an antigen or an antibody is solidified, to label the specimen by the antigen-antibody reaction. |
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| 159 | FLOW PATH STRUCTURE AND DEVICE FOR MEASURING MEASUREMENT OBJECT LIQUID | EP16855417.8 | 2016-10-12 | EP3364186A1 | 2018-08-22 | SAKAI, Osamu; TAGUCHI, Yoshihiro; SAMESHIMA, Kenichiro; SUZUKI, Yoshimune |
As a flow channel structure that facilitates to reduce a size of a measuring device in which the flow channel structure is embedded, there is provided a flow channel structure that includes a substrate including a supply flow channel that guides a measurement target liquid toward inside; a separation element accommodating unit that accommodates a separation element that separates a plurality of components included in the measurement target liquid, the measurement target liquid being guided by the supply flow channel; and a detector that guides the measurement target liquid that passes through the separation element accommodating unit, wherein measuring light for measuring information about the plurality of components is to be irradiated onto the measurement target liquid, wherein the detector includes a measurement flow channel part that guides the measurement target liquid, an incident part that is provided at an end of the measurement flow channel part and that guides the measuring light toward inside the measurement flow channel part, and an emission part that is provided at the other end of the measurement flow channel part and that guides the measuring light from the measurement flow channel part. |
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| 160 | ANALYTE TREATMENT CHIP, ANALYTE TREATMENT DEVICE, AND ANALYTE TREATMENT METHOD | EP16853771.0 | 2016-10-07 | EP3360953A1 | 2018-08-15 | TAGAWA, Ayato; NAKANO, Tsuyoshi; KAWAMOTO, Yasuko; YAMAWAKI, Koya; TOBIMATSU, Hiroaki |
The present specimen treatment chip includes: a first flow channel for forming a droplet containing a mixed liquid of a nucleic acid, a reagent for an amplification reaction of the nucleic acid, and a carrier to which a primer for binding to the nucleic acid is added, in a dispersion medium; a second flow channel for amplifying the nucleic acid in the droplet; and a third flow channel for mixing the droplet containing the carrier with the primer having bound to an amplification product of the nucleic acid, and a reagent for breaking down the droplet, to break down the droplet. |
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