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公开(公告)号：KR101444196B1
公开(公告)日：2014-09-26
申请号：KR1020120129111
申请日：2012-11-14
Applicant: 대한민국(관리부서:국립수산과학원)
Abstract: 본 발명은 신규한 미생물 바실러스 코아귤란스(
Bacillus
coagulans ) KM-1, 이를 이용한 발효대두박 및 양어용 사료에 관한 것으로, 보다 상세하게는 알파-갈락토시다제 효소활성을 가지며 난소화성 탄수화물 분해활성이 우수한 신규한 미생물 바실러스 코아귤란스 KM-1 균주를 이용하여 대두박을 고온발효시킴으로써 기존의 대두박보다 소화율이 향상된 양어용 사료를 제조하는 방법에 관한 것이다.-
公开(公告)号：KR101437381B1
公开(公告)日：2014-09-11
申请号：KR1020130099031
申请日：2013-08-21
Applicant: 대한민국(관리부서:국립수산과학원)
CPC classification number: C12N15/11 , C12Q1/6844
Abstract: To provide an economical and effective method for discerning pacific oyster triploids, the present invention provides a multiplex kit for discerning pacific oyster triploids, wherein the multiplex kit comprises three or more primer sets selected from the group including: a primer set 1 which consists of a forward primer having a nucleic acid sequence represented by sequence number 1 and a reverse primer represented by sequence number 2; a primer set 2 which consists of a forward primer having nucleic acid sequence represented by sequence number 5 and a reverse primer having a nucleic acid sequence represented by sequence number 6; a primer set 3 which consists of a forward primer having a nucleic acid sequence represented by sequence number 7 and a reverse primer having a nucleic acid sequence represented by sequence number 8; a primer set 4 which consists of a forward primer having a nucleic acid sequence represented by sequence number 15 and a reverse primer having a nucleic acid sequence represented by sequence number 16; a primer set 5 which consists of a forward primer having a nucleic acid sequence represented by sequence number 19 and a reverse primer having a nucleic acid sequence represented by sequence number 20; and a primer set 6 which consists of a forward primer having a nucleic acid sequence represented by sequence number 21 and a reverse primer having a nucleic acid sequence represented by sequence number 22.
Abstract translation: 为了提供一种用于鉴别太平洋牡蛎三倍体的经济有效的方法，本发明提供了一种用于鉴别太平洋牡蛎三倍体的多重试剂盒，其中所述多重试剂盒包含三个或更多个选自以下的引物组：引物组1，其由 具有由序列号1表示的核酸序列的正向引物和由序列号2表示的反向引物; 引物组2，其由具有由序列号5表示的核酸序列的正向引物和具有由序列号6表示的核酸序列的反向引物组成; 引物组3，其由具有由序列号7表示的核酸序列的正向引物和具有由序列号8表示的核酸序列的反向引物组成; 引物组4，其由具有由序列号15表示的核酸序列的正向引物和具有由序列号16表示的核酸序列的反向引物组成; 引物组5，其由具有由序列号19表示的核酸序列的正向引物和具有由序列号20表示的核酸序列的反向引物组成; 和引物组6，其由具有由序列号21表示的核酸序列的正向引物和具有由序列号22表示的核酸序列的反向引物组成。
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公开(公告)号：KR101374194B1
公开(公告)日：2014-03-13
申请号：KR1020130055554
申请日：2013-05-16
Applicant: 대한민국(관리부서:국립수산과학원)
IPC: C07K14/435 , C12N15/12 , C12N15/63 , A61K38/17
Abstract: The present invention relates to a peptide representing serine protease inhibition activity and firstly separated from Fenneropenaeus chinensis, and proved anti-trypsin activity and anticoagulant activity. According to an embodiment of the present invention, a novel serine protease inhibitor is separated from Fenneropenaeus chinensis and identified, and the present invention proves effects of anti-trypsin activity and anticoagulant activity thereof, thereby efficiently applying the same as an active ingredient of anticoagulants. [Reference numerals] (AA) Anticoagulant activity(Prolongation of APTT(s))
Abstract translation: 本发明涉及一种代表丝氨酸蛋白酶抑制活性的肽，首先从中华ensis ensis分离，证明了抗胰蛋白酶活性和抗凝血活性。 根据本发明的一个实施方案，将新的丝氨酸蛋白酶抑制剂从中华龙胆中分离出来，鉴定出来，本发明证明了抗胰蛋白酶活性和抗凝血活性的作用，从而有效地将其作为抗凝剂的活性成分施用。 （参考号）（AA）抗凝血活性（延长APTT）
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公开(公告)号：KR1020120085538A
公开(公告)日：2012-08-01
申请号：KR1020110006928
申请日：2011-01-24
Applicant: 부산대학교 산학협력단 , 대한민국(관리부서:국립수산과학원)
CPC classification number: C12Q1/6813 , C12Q1/6837 , C12Q2563/155
Abstract: PURPOSE: A DNA hybridization detection method using gold nanoparticles is provided to enhance speed, accuracy, and sensitivity of DNA hybridization detection and to reduce time and cost due to reduced reaction time. CONSTITUTION: A DNA hybridization detection method comprises: a step of reacting target DNA conjugated with gallic acid to a probe DNA to induce hybridization; a step of removing the target DNA to which unhybridized gallic acid is conjugated; and a step of adding gold ions to the probe DNA which was hybridized with the target DNA and measuring the generation of gold nanoparticles.
Abstract translation: 目的：提供使用金纳米颗粒的DNA杂交检测方法，以提高DNA杂交检测的速度，准确度和灵敏度，并减少反应时间缩短的时间和成本。 构成：DNA杂交检测方法包括：将与没食子酸缀合的靶DNA与探针DNA反应以诱导杂交的步骤; 除去未杂交的没食子酸的靶DNA的步骤; 以及向与靶DNA杂交的探针DNA中添加金离子并测定金纳米粒子的产生的步骤。
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Patent Agency Ranking
公开(公告)号：KR101770966B1
公开(公告)日：2017-08-24
申请号：KR1020160137414
申请日：2016-10-21
Applicant: 대한민국(관리부서:국립수산과학원)
IPC: C12Q1/68
CPC classification number: C12Q1/6888 , C12Q2537/143 , C12Q2565/125 , C12Q2600/124 , C12Q2600/16
Abstract: 본발명은형태학적으로구분하기어려운넙치의유전적성(sex)을신속하고정확하게판별할수 있는단일염기다형성(SNP) 마커를제공한다.
Abstract translation: 本发明提供了一种单核苷酸多态性（SNP）标记，其能够快速且准确地区分难以在形态上区分的牙鲆的遗传性别。
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公开(公告)号：KR1020170062559A
公开(公告)日：2017-06-08
申请号：KR1020150145265
申请日：2015-10-19
Applicant: 대한민국(관리부서:국립수산과학원)
IPC: C07K7/08 , C07K14/435 , A23L3/3526 , A61K8/64 , A61K38/08
Abstract: 본발명은항균특성및 새로운생리학적활성으로서항암특성을가지는펩타이드, 이펩타이드를코딩하는핵산및 이펩타이드또는핵산의응용에관한것이다. 본발명에따라합성된펩타이드, 또는이 펩타이드를코딩하는핵산이삽입된벡터를유효성분으로사용하여, 항균및/또는항암조성물, 예를들어약학적조성물, 화장품조성물및/또는식품첨가제로활용될수 있다.
Abstract translation: 本发明涉及一种新的抗菌性能和生理活性的核酸编码的肽，具有抗癌特性和肽或核酸的应用的肽。 或通过使用的载体核酸，其编码的肽作为活性成分，抗微生物和/或抗肿瘤组合物中的插入件在根据本发明合成的肽，例如，它被用作药物组合物，化妆品组合物和/或食品添加剂 有。
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公开(公告)号：KR101508693B1
公开(公告)日：2015-04-07
申请号：KR1020130120993
申请日：2013-10-11
Applicant: 대한민국(관리부서:국립수산과학원)
IPC: C07K14/435 , C12N15/12 , A61K38/17 , A23K20/195
Abstract: 본발명은항미생물성펩타이드에관한것으로서, 어류병원성미생물에대하여효율적인항미생물활성을나타낼뿐만아니라, 적혈구에대한용혈활성은거의없기때문에, 양식어류에대한사료첨가제로사용되거나, 항생제대체제로사용되더라도어류및 인체의건강에대한위협요소를제공하지않는다.
Abstract translation: 本发明涉及一种抗菌肽，其具有对来自鱼类的病原微生物有效的抗微生物活性，对红细胞无溶血活性，因此可用作养鱼的饲料添加剂，并且对人和鱼无害，即使 抗菌肽用作抗生素替代品。
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公开(公告)号：KR101423293B1
公开(公告)日：2014-07-24
申请号：KR1020140051791
申请日：2014-04-29
Applicant: 대한민국(관리부서:국립수산과학원)
Abstract: The present invention relates to an EP feedstuff composition for halibuts which can be a substitute for a moisture pellet (MP) feedstuff. A protein base material of the feedstuff composition is adjusted so that the feedstuff composition can have a low feed coefficient while retaining nutrients a moisture pellet (MP) feedstuff has. The feedstuff composition is manufactured by mixing 66 weight% of brown fish powder, 5 weight% of hydrolyzed fish protein, 1 weight% of krill powder, 1 weight% of squid powder, 2 weight% of a fermented soybean meal, 1 weight% of concentrated soybean protein, 2 weight% of wheat gluten, 16 weight% of wheat flour, 3 weight% of fish oil, and 3 weight% of inorganic materials and additives. When compared to the moisture pellet (MP) feedstuff, the EP feedstuff composition has similar breeding results of growing and fattening halibuts and has similar feedstuff efficiency. Meanwhile, the EP feedstuff has an outstandingly low feed coefficient and thus can contribute to development of an aquaculture industry.
Abstract translation: 本发明涉及一种可以代替水分颗粒（MP）饲料的用于大戟的EP饲料组合物。 调节饲料组合物的蛋白质基料，使得饲料组合物可以具有低的饲料系数，同时保持水分颗粒（MP）饲料具有的营养物质。 饲料组合物通过混合66重量％的棕色鱼粉，5重量％的水解鱼蛋白，1重量％的磷虾粉，1重量％的鱿鱼粉，2重量％的发酵豆粕，1重量％ 浓缩大豆蛋白，2重量％的小麦面筋，16重量％的小麦粉，3重量％的鱼油和3重量％的无机材料和添加剂。 当与水分颗粒（MP）饲料相比时，EP饲料组合物具有与生长和育肥的大比目鱼相似的育种结果，具有相似的饲料效率。 同时，EP饲料饲料系数显着降低，有利于水产养殖业的发展。
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40.发明授权돌기해삼의 체색변이 종인 홍해삼과 청해삼의 유전학적 구별 방법 및 이에 이용되는 대립유전자 특이적 프라이머 有权US US OF OF OF OF OF OF METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD METHOD
公开(公告)号：KR101083015B1
公开(公告)日：2011-11-22
申请号：KR1020110056799
申请日：2011-06-13
Applicant: 대한민국(관리부서:국립수산과학원)
CPC classification number: C12Q1/6858
Abstract: PURPOSE: A genetic method for distinguishing colour variant in Stichopus japonicus Selenka and to improve accuracy of distinguishing. CONSTITUTION: A genetic method for distinguishing colour variant Stichopus japonicus Selenka using allele-specific PCR comprises: a step of isolating genome DNA of HSP70 from variants in Stichopus japonicus Selenka; a step of adding a primer set of sequence numbers 2 and 3 and an allele-specific primer of sequence number 4 to the isolated DNA for performing PCR; and a step of determining the species. The primer of sequence number 4 is used for allele-specific PCR amplification to distinguish the color of Stichopus japonicus Selenka.
Abstract translation: 目的：区分ic ishing ishing ishing ishing ishing ishing。。。。。。。。。。。。。。。。。。。。。。。 构成：使用等位基因特异性PCR区分色变St us us A A A A A A A A A;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;; 将序列号2和3的引物组和序列号4的等位基因特异性引物加入分离的DNA进行PCR的步骤; 并确定物种的一个步骤。 序列号4的引物用于等位基因特异性PCR扩增，以区分日本j the的颜色。
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