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    • 13. 发明公开
    • B형 간염 검사용 PCR 프라이머 세트 및 이를 포함하는 B형 간염 검사 키트
    • 用于检测乙型肝炎病毒的PCR检测装置将检测时间减少到30分钟,并提高检测重现性和用于检测乙型肝炎病毒B的方法
    • KR1020050018511A
    • 2005-02-23
    • KR1020030056432
    • 2003-08-14
    • 삼성전자주식회사
    • 이영선한정임황정주김미경조윤경임희균김영아
    • C12Q1/68
    • C12Q1/706C12Q2565/629C12Q2565/543C12Q2531/113
    • PURPOSE: A PCR primer set for detection of hepatitis B and a method for detecting hepatitis B using the same primer set are provided, thereby reducing the detection time to 30 minutes and improving the detection reproductivity by optimizing the PCR condition and using specific PCR primer set. CONSTITUTION: The PCR primer set for detection of hepatitis B is selected from the group consisting of: (a) a set of primers having the nucleotide sequences of SEQ ID NO:1 and SEQ ID NO:2; (b) a set of primers having the nucleotide sequences of SEQ ID NO:1 and SEQ ID NO:3; (c) a set of primers having the nucleotide sequences of SEQ ID NO:4 and SEQ ID NO:5; (d) a set of primers having the nucleotide sequences of SEQ ID NO:4 and SEQ ID NO:6; (e) a set of primers having the nucleotide sequences of SEQ ID NO:4 and SEQ ID NO:7; (f) a set of primers having the nucleotide sequences of SEQ ID NO:7 and SEQ ID NO:8; (g) a set of primers having the nucleotide sequences of SEQ ID NO:9 and SEQ ID NO:10; (h) a set of primers having the nucleotide sequences of SEQ ID NO:11 and SEQ ID NO:12; (i) a set of primers having the nucleotide sequences of SEQ ID NO:13 and SEQ ID NO:14; (j) a set of primers having the nucleotide sequences of SEQ ID NO:15 and SEQ ID NO:16; (k) a set of primers having the nucleotide sequences of SEQ ID NO:17 and SEQ ID NO:18; (l) a set of primers having the nucleotide sequences of SEQ ID NO:19 and SEQ ID NO:20; (m) a set of primers having the nucleotide sequences of SEQ ID NO:21 and SEQ ID NO:22; (n) a set of primers having the nucleotide sequences of SEQ ID NO:23 and SEQ ID NO:24; (o) a set of primers having the nucleotide sequences of SEQ ID NO:25 and SEQ ID NO:26; (p) a set of primers having the nucleotide sequences of SEQ ID NO:27 and SEQ ID NO:28; (q) a set of primers having the nucleotide sequences of SEQ ID NO:29 and SEQ ID NO:30; (r) a set of primers having the nucleotide sequences of SEQ ID NO:31 and SEQ ID NO:32; (s) a set of primers having the nucleotide sequences of SEQ ID NO:33 and SEQ ID NO:34; (t) a set of primers having the nucleotide sequences of SEQ ID NO:35 and SEQ ID NO:36; (u) a set of primers having the nucleotide sequences of SEQ ID NO:37 and SEQ ID NO:38; and (a) a set of primers having the nucleotide sequences of SEQ ID NO:39 and SEQ ID NO:40.
    • 目的:提供用于检测乙型肝炎的PCR引物组和使用相同引物组检测乙型肝炎的方法,从而将检测时间缩短到30分钟,并通过优化PCR条件并使用特异性PCR引物组来提高检测繁殖力 。 构成:用于检测乙型肝炎的PCR引物组选自:(a)一组具有SEQ ID NO:1和SEQ ID NO:2的核苷酸序列的引物; (b)具有SEQ ID NO:1和SEQ ID NO:3的核苷酸序列的一组引物; (c)具有SEQ ID NO:4和SEQ ID NO:5的核苷酸序列的一组引物; (d)具有SEQ ID NO:4和SEQ ID NO:6的核苷酸序列的一组引物; (e)具有SEQ ID NO:4和SEQ ID NO:7的核苷酸序列的一组引物; (f)具有SEQ ID NO:7和SEQ ID NO:8的核苷酸序列的一组引物; (g)具有SEQ ID NO:9和SEQ ID NO:10的核苷酸序列的一组引物; (h)具有SEQ ID NO:11和SEQ ID NO:12的核苷酸序列的一组引物; (i)具有SEQ ID NO:13和SEQ ID NO:14的核苷酸序列的一组引物; (j)具有SEQ ID NO:15和SEQ ID NO:16的核苷酸序列的一组引物; (k)具有SEQ ID NO:17和SEQ ID NO:18的核苷酸序列的一组引物; (1)具有SEQ ID NO:19和SEQ ID NO:20的核苷酸序列的一组引物; (m)具有SEQ ID NO:21和SEQ ID NO:22的核苷酸序列的一组引物; (n)具有SEQ ID NO:23和SEQ ID NO:24的核苷酸序列的一组引物; (o)具有SEQ ID NO:25和SEQ ID NO:26的核苷酸序列的一组引物; (p)一组具有SEQ ID NO:27和SEQ ID NO:28的核苷酸序列的引物; (q)具有SEQ ID NO:29和SEQ ID NO:30的核苷酸序列的一组引物; (r)具有SEQ ID NO:31和SEQ ID NO:32的核苷酸序列的一组引物; 一组具有SEQ ID NO:33和SEQ ID NO:34的核苷酸序列的引物; (t)具有SEQ ID NO:35和SEQ ID NO:36的核苷酸序列的一组引物; (u)具有SEQ ID NO:37和SEQ ID NO:38的核苷酸序列的一组引物; 和(a)具有SEQ ID NO:39和SEQ ID NO:40的核苷酸序列的一组引物。
    • 19. 发明公开
    • 분리막, 이의 제조 방법 및 분리막을 포함하는 수처리 장치
    • 膜,其制造方法和包括其的水处理装置
    • KR1020130011899A
    • 2013-01-30
    • KR1020120020423
    • 2012-02-28
    • 삼성전자주식회사
    • 한정임공혜영한성수
    • B01D69/12B01D69/10B01D71/06C02F1/44
    • Y02A20/131B01D69/12B01D61/002B01D69/10B01D71/08C02F1/445
    • PURPOSE: A separation layer, a manufacturing method thereof, and a water treatment device using the same are provided to have an excellent durability with a high strength property, to minimize polarization of an inside concentration, to have an excellent salt removal rate, and to have a simple and economical manufacturing process. CONSTITUTION: A separation film comprises a supporting layer including a polymer with the structure unit represented by chemical formula 1, and a polymer matrix layer. In chemical formula 1, R1-R6 is independently hydrogen, or a substituted or non-substituted C1-C30 alkyl group, a substituted or non-substituted C3-C30 cycloalkyl group, a substituted or non-substituted C2-C30 heterocycloalkyl, a substituted or non-substituted C6-C30 aryl group, a substituted or non-substituted C2-C30 heteroaryl group, a substituted or non-substituted C7-C30 alkylaryl group, a substituted or non-substituted C7-C30 arylalkyl group, or -COR7. In chemical formula 1, R7 is a substituted or non-substituted C1-C30 alkyl group, a substituted or non-substituted C3-C30 cycloalkyl group, a substituted or non-substituted C2-C30 heterocycloalkyl, a substituted or non-substituted C6-C30 aryl group, a substituted or non-substituted C2-C30 heteroaryl group, a substituted or non-substituted C7-C30 alkylaryl group, or a substituted or non-substituted C7-C30 arylalkyl group. However, at least one among R1-R3 and at least one among R4-R6 are identical to or different from -COR7.
    • 目的:提供一种分离层及其制造方法以及使用其的水处理装置,具有优异的耐久性,具有高强度特性,使内部浓度的极化最小化,具有优异的除盐率, 有一个简单而经济的制造工艺。 构成:分离膜包括包含具有由化学式1表示的结构单元的聚合物的支撑层和聚合物基质层。 在化学式1中,R 1 -R 6独立地为氢,或取代或未取代的C 1 -C 30烷基,取代或未取代的C 3 -C 30环烷基,取代或未取代的C 2 -C 30杂环烷基,取代的 取代或未取代的C 6 -C 30芳基,取代或未取代的C 2 -C 30芳基,取代或未取代的C 7 -C 30烷基芳基,取代或未取代的C 7 -C 30芳烷基或-COR 7。 在化学式1中,R 7为取代或未取代的C 1 -C 30烷基,取代或未取代的C 3 -C 30环烷基,取代或未取代的C 2 -C 30杂环烷基,取代或未取代的C 6 -C 30烷基, C30芳基,取代或未取代的C2-C30杂芳基,取代或未取代的C7-C30烷基芳基,或取代或未取代的C7-C30芳烷基。 然而,R 1 -R 3中的至少一个和R 4 -R 6中的至少一个与-COR 7相同或不同。
    • 20. 发明授权
    • 생분자 동정 방법
    • 一种生物分子标记方法
    • KR100882554B1
    • 2009-02-12
    • KR1020070113958
    • 2007-11-08
    • 삼성전자주식회사
    • 한정임심저영정원석남궁각
    • G01N33/48G01N27/26G01N27/00
    • G01N27/4145
    • A method for indentifying a biomolecule is provided to indentify each DNA from one sample although various kinds of DNAs are PCR-amplified at the same time by indentifying A and B which are PCR products by utilizing transition temperature property. A biomolecule detecting apparatus having a field effect transistor(FET) is used in order to indentify a biomolecule. A method for indentifying a biomolecule comprises steps of: (a) heating a sample including the biomolecule into a biomolecule detecting apparatus in which the sample is injected; (b) measuring current flowing to a channel formed between a source region and a drain region of the field effect transistor; (c) calculating transition temperature which is temperature when current change amount is maximum from current data measured in the step (b); and (d) indentifying the biomolecule using the transition temperature.
    • 提供了用于鉴定生物分子的方法,虽然通过利用转变温度性质通过鉴定作为PCR产物的A和B同时PCR扩增各种DNA,但是从一个样品中鉴定每个DNA。 使用具有场效应晶体管(FET)的生物分子检测装置,以识别生物分子。 用于鉴定生物分子的方法包括以下步骤:(a)将包含生物分子的样品加热到注射样品的生物分子检测装置中; (b)测量流向形成在场效应晶体管的源极区域和漏极区域之间的沟道的电流; (c)计算当在所述步骤(b)中测量的当前数据当前变化量最大时的温度的转变温度; 和(d)使用转化温度鉴定生物分子。