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    • 32. 发明公开
    • 자궁경부암 진단 방법 및 그 진단용 키트
    • 一种诊断子宫颈癌及其套件的方法
    • KR1020150010526A
    • 2015-01-28
    • KR1020130085702
    • 2013-07-19
    • 주식회사 옵티팜연세대학교 원주산학협력단
    • 이혜영박광화이동섭왕혜영김성현김연
    • C12Q1/68C12N15/11
    • C12Q1/6886C12Q1/6851C12Q2600/158
    • The present invention relates to a novel method for diagnosing a uterine cervical cancer and to a diagnosing kit of the same. Provided in the present invention is a method for providing information for diagnosing a uterine cervical cancer, which comprises the steps of: a) isolating a whole RNA from cells obtained from the blood of a patient; b) synthesizing cDNA from the whole RNA isolated; c) performing real time-PCR of the synthesized cDNA by using one or more primer pair and a probe selected from a group consisting of a primer pair and a probe which can amplifying HPV type 16, 35, 31, 58, 33, and 52, a primer pair and a probe which can amplifying HPV type 18, 45, 39, 68, and 59, and a primer pair and a probe which can amplifying HPV type 53, 56, 66, 51, 69, 26, and 30; and d) comparing the expressed amount with the expressed amount of a normal person.
    • 本发明涉及一种用于诊断子宫颈癌的新方法及其诊断试剂盒。 本发明提供了一种提供子宫颈癌诊断信息的方法,包括以下步骤:a)从患者血液中获得的细胞中分离全RNA; b)从分离的整个RNA合成cDNA; c)通过使用一种或多种引物对和选自引物对和探针的探针进行合成cDNA的实时PCR,所述引物对和探针可以扩增HPV 16,18,35,53,32和52的HPV ,可以扩增HPV 18,185,39,68和59的引物对和探针,以及可以扩增HPV56,56,69,26,30的HPV的引物对和探针。 和d)将表达的量与正常人的表达量进行比较。
    • 37. 发明公开
    • 정원세포를 이용한 조류 카이메라의 생산방법 및 조류 카이메라
    • 使用从成熟的粉丝中大量获得的微生物细胞生产亚利桑那的方法,以及当它们被转运到其中产生的蛋白质和AVIAN CHIMERA时,大量生产的GERMLINE CHIMERA的方法
    • KR1020050017850A
    • 2005-02-23
    • KR1020030055326
    • 2003-08-11
    • 주식회사 옵티팜재단법인서울대학교산학협력재단
    • 한재용임정묵이영목김진남홍영호한범구
    • A01K67/00
    • C12N15/873A01K67/0271A01K2217/05A01K2227/30C12N5/061C12N2500/44C12N2501/105C12N2501/115C12N2501/235
    • PURPOSE: A method for producing avian chimera using spermatogonial cells and avian chimera produced therefrom are provided, thereby reducing the production time and improving production efficiency than using embryo stem cells because the spermatogonial cells are easily obtained in a large quantity from matured fowls, and mass-produce germline chimera when they are transplanted into the testicle. CONSTITUTION: The method for producing avian chimera using spermatogonial cells comprises the steps of: (a) obtaining the testicle from a donor fowl; (b) isolating the testis cell population from the testicle by treating the testicle tissue with collagenase, trypsin or a mixture thereof; (c) culturing the testis cell population in a medium containing cell growth factor to obtain the spermatogonial cell population; and (d) injecting the cultured spermatogonial cell population or testis cell population into the avian testicle, wherein the cell growth factor is selected from fibroblast growth factor, insulin-like growth factor-1, stem cell factor and a combination thereof.
    • 目的:提供使用精原细胞和禽类嵌合体生产鸟类嵌合体的方法,与使用胚胎干细胞相比,减少了生产时间并提高了生产效率,因为精原细胞很容易从成熟的家禽获得,质量 - 将种系嵌合体移植到睾丸中时产生。 构成:使用精原细胞生产禽嵌合体的方法包括以下步骤:(a)从供体家禽获得睾丸; (b)通过用胶原酶,胰蛋白酶或其混合物处理睾丸组织从睾丸分离睾丸细胞群; (c)在含有细胞生长因子的培养基中培养睾丸细胞群以获得精原细胞群; 和(d)将培养的精原细胞群或睾丸细胞群注射到禽睾丸中,其中细胞生长因子选自成纤维细胞生长因子,胰岛素样生长因子-1,干细胞因子及其组合。
    • 38. 发明公开
    • 조류의 원시생식기 유래 원시생식세포의 분리방법 및생식선 키메라 조류의 제조방법
    • 分离群体性原始细胞的方法及其制备GERMLINE CHIMERIC AVES的方法
    • KR1020040073174A
    • 2004-08-19
    • KR1020030009167
    • 2003-02-13
    • 주식회사 옵티팜
    • 한재용김진남김미아박태섭임정묵
    • C12N15/00
    • PURPOSE: A method for isolating gonadal primordial germ cells and a method for preparing germline chimeric aves are provided, thereby improving purity and isolation yield of gonadal primordial germ cells, and improving preparation efficiency of germline chimeric aves. CONSTITUTION: The method for isolating gonadal primordial germ cells comprises the steps of: (a) treating gonadal primordial germ tissue cells isolated from embryos of aves with a primordial germ cell-specific first antibody; (b) treating the antibody-bound gonadal primordial germ tissue cells with microbeads bound with a second antibody which has magnetism and binds with the first antibody; and (c) cleansing the resulting product of step (b) and separating the gonadal primordial germ cell-second antibody-microbead complex. The method for preparing germline chimeric aves comprises the steps of: (a) treating gonadal primordial germ tissue cells isolated from embryos of aves with a primordial germ cell-specific first antibody; (b) treating the antibody-bound gonadal primordial germ tissue cells with microbeads bound with a second antibody which has magnetism and binds with the first antibody; (c) cleansing the resulting product of step (b) and separating the gonadal primordial germ cell-second antibody-microbead complex; (d) introducing the isolated gonadal primordial germ cells into the embryo of a recipient egg; and (e) culturing and hatching the egg.
    • 目的:提供一种分离性腺原始生殖细胞的方法和制备种系嵌合抗体的方法,从而提高性腺原始生殖细胞的纯度和分离产量,提高种系嵌合抗体的制备效率。 构成:分离性腺原始生殖细胞的方法包括以下步骤:(a)用原始生殖细胞特异性第一抗体处理从禽类胚胎分离的性腺原始胚芽组织细胞; (b)用与具有磁性并与第一抗体结合的第二抗体结合的微珠处理抗体结合的性腺原始细菌组织细胞; 和(c)清洗步骤(b)的所得产物并分离性腺原始生殖细胞 - 第二抗体 - 微珠复合物。 用于制备种系嵌合抗体的方法包括以下步骤:(a)用原始生殖细胞特异性第一抗体处理从禽类胚胎分离的性腺原始胚芽组织细胞; (b)用与具有磁性并与第一抗体结合的第二抗体结合的微珠处理抗体结合的性腺原始细菌组织细胞; (c)清洗步骤(b)的所得产物并分离性腺原始生殖细胞 - 第二抗体 - 微珠复合物; (d)将分离的性腺原始生殖细胞引入受体卵的胚胎; 和(e)培养和孵化蛋。
    • 39. 发明公开
    • 조류 콕시듐증을 유발하는 에이메리아 종의 포자소체 표면항원에 대한 scFv 재조합 항체
    • 特异性针对EIMERIA SPP的SPOROZOITE SURFACE抗原的重组SCFV抗体。 负责治疗
    • KR1020030018684A
    • 2003-03-06
    • KR1020010052934
    • 2001-08-30
    • 주식회사 옵티팜
    • 김진규한재용송기덕김성원민원기손은정릴레호즈,현순릴레호즈,에릭피터
    • C07K14/455
    • C07K16/20C07K2317/622Y10S530/822
    • PURPOSE: Recombinant ScFv antibodies specific to a sporozoite surface antigen of Eimeria spp. responsible for coccidiosis are provided. The recombinant ScFv antibodies has improved tissue-penetrating activity, can be mass-produced from a prokaryotic host cell such as Escherichia coli, and can be used in passive immunization of coccidiosis. CONSTITUTION: The variable regions of heavy chains in antibodies specific to the sporozoite surface antigen of Eimeria spp. have the amino acid sequence selected from SEQ ID NOs: 18, 20, 22, 24 and 38. The variable regions of light chains in antibodies specific to the sporozoite surface antigen of Eimeria spp. have the amino acid sequence selected from SEQ ID NOs: 26, 28, 30, 32 and 40. The genes encoding the variable regions of heavy chains in antibodies specific to the sporozoite surface antigen of Eimeria spp. having the amino acid sequence selected from SEQ ID NOs: 18, 20, 22, 24 and 38 have the nucleotide sequence selected from SEQ ID NOs: 17, 19, 21, 23 and 37. The genes encoding the variable regions of light chains in antibodies specific to the sporozoite surface antigen of Eimeria spp. having the amino acid sequence selected from SEQ ID NOs: 26, 28, 30, 32 and 40 have the nucleotide sequence selected from SEQ ID NOs: 25, 27, 29, 31 and 39.
    • 目的:针对艾美球虫属的子孢子表面抗原特异的重组ScFv抗体。 负责球虫病的提供。 重组ScFv抗体具有改善的组织穿透活性,可以从原核宿主细胞如大肠杆菌大量生产,并可用于球虫病的被动免疫。 构成:艾美球虫亚种子孢子表面抗原特异抗体的重链可变区。 具有选自SEQ ID NO:18,20,22,24和38的氨基酸序列。特异于艾美球虫属的子孢子表面抗原的抗体中的轻链的可变区。 具有选自SEQ ID NO:26,28,30,32和40的氨基酸序列。编码艾美球虫属的子孢子表面抗原特异性抗体的重链可变区的基因。 具有选自SEQ ID NO:18,20,22,24和38的氨基酸序列具有选自SEQ ID NO:17,19,21,23和37的核苷酸序列。编码轻链的可变区的基因 对艾美球虫亚种子孢子表面抗原特异的抗体。 具有选自SEQ ID NO:26,28,30,32和40的氨基酸序列具有选自SEQ ID NO:25,27,29,31和39的核苷酸序列。