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    • 1. 发明专利
    • Method and device for wavelength conversion using nonlinear optical element, and laser system
    • 使用非线性光学元件和激光系统进行波长转换的方法和装置
    • JPH11271820A
    • 1999-10-08
    • JP7613998
    • 1998-03-24
    • Nidek Co LtdRikagaku Kenkyusho株式会社ニデック理化学研究所
    • TASHIRO HIDEOWADA TOMOYUKIYAMADA TAKESHI
    • G02F1/35G02F1/37
    • G02F1/3501G02F2001/3505
    • PROBLEM TO BE SOLVED: To stably maintain wavelength conversion characteristics of nonlinear optical crystal for a long period by making laser light incident on cerium lithium borate crystal arranged under a vacuum and performing wavelength conversion.
      SOLUTION: The nonlinear optical crystal 12 as a wavelength converting element such as cerium lithium borate crystal is arranged in a metallic vacuum container 11, made of stainless steel, in the wavelength converting device 10. A light beam enters the vacuum container 11 through its input-side optical window 13a having specific transmissivity and has its wavelength converted by interacting with the nonlinear optical crystal 12 and is emitted from the output-side optical window 13b. For the optical windows 13a and 13b, quartz, etc., having no light absorption in a wavelength range of 200 to 3,000 nm is used. A vacuum sealing valve 14 is provided to the upper part of the vacuum container 11. The part formed of the main body of the vacuum container 11, optical windows 13a and 13b, and vacuum sealing valve 14 is sealed with O rings 15a, 15b, and 15c and a vacuum of about 10
      0 to 10
      2 Torr is held in the vacuum container 11.
      COPYRIGHT: (C)1999,JPO
    • 要解决的问题:通过使入射在真空下布置的硼酸铈锂晶体上进行激光并进行波长转换,来长时间稳定地保持非线性光学晶体的波长转换特性。 解决方案:作为波长转换元件如硼酸锂硼酸盐晶体的非线性光学晶体12在波长转换装置10中布置在由不锈钢制成的金属真空容器11中。光束通过其输入端进入真空容器11 具有特定透射率的光学窗口13a,并且通过与非线性光学晶体12相互作用而将其波长转换并从输出侧光学窗口13b发射。 对于光学窗口13a和13b,使用在200〜3000nm的波长范围内没有光吸收的石英等。 在真空容器11的上部设有真空密封阀14.由真空容器11的主体,光学窗口13a,13b,真空密封阀14构成的部分用O形环15a,15b密封, 并且在真空容器11中保持15c至大约10至10 2 Torr的真空。
    • 2. 发明专利
    • Method for analyzing biochip, and system for automatic analysis of the same
    • 生物分析方法及其自动分析系统
    • JP2011013000A
    • 2011-01-20
    • JP2009155249
    • 2009-06-30
    • Consonal Biotechnologies Co LtdInstitute Of Physical & Chemical Research株式会社コンソナルバイオテクノロジーズ独立行政法人理化学研究所
    • TASHIRO HIDEOITO YOSHIHIRO
    • G01N33/53G01N21/76G01N33/543G01N35/04G01N37/00
    • PROBLEM TO BE SOLVED: To provide a method for analyzing a biochip capable of rapidly obtaining a measuring result, by automating a reaction detection process of a specimen and an antigen after the specimen is sampled, using the biochip loaded with antigens of many kinds of allergens which are mutually independent, that is, isolated spots, and to provide a system for automatic analysis of biochip.SOLUTION: A consistent system for automatic analysis of biochip is provided with the biochip 2 loaded with the antigen as the spot 6; a prefilter for removing serum component from a sampled blood specimen and a reagent cassette 4a becoming a pair along with the biochip 2, can rapidly obtain an analysis and measurement result, by automating the respective processings from the reaction of the biochip 2, to which the specimen is added, with the antigen, the reaction with an antibody, cleaning and the addition of a detection reagent to the detection of chemoluminescence, shortens the analysis and measurement time and attains micronization of an installation area.
    • 要解决的问题:提供一种用于分析能够快速获得测量结果的生物芯片的方法,通过使样本采集后的样品和抗原的反应检测过程自动化,使用装载有多种过敏原抗原的生物芯片 这是相互独立的,也就是孤立斑点,并提供生物芯片自动分析系统。解决方案:将生物芯片2作为斑点6装载抗生素的生物芯片2,提供一个生物芯片自动分析系统。 用于从取样的血液样本中除去血清成分的预过滤器和与生物芯片2一起成为一对的试剂盒4a可以通过使生物芯片2的反应自动化,从而快速获得分析和测量结果, 加入标本,用抗原,与抗体反应,清洗和添加检测试剂以检测化学发光,缩短分析和测量时间,达到安装区域的微粉化。
    • 4. 发明专利
    • Method for detecting nucleic acid, and genotyping method
    • 检测核酸的方法和基因分型方法
    • JP2008199927A
    • 2008-09-04
    • JP2007037885
    • 2007-02-19
    • Institute Of Physical & Chemical Research独立行政法人理化学研究所
    • KONDO YASUMITSUTASHIRO HIDEO
    • C12Q1/68C12N15/09G01N21/78G01N37/00
    • PROBLEM TO BE SOLVED: To provide a new genotyping method capable of quickly performing genotyping and a new nucleic acid detection method which can be utilized in the genotyping method.
      SOLUTION: The nucleic acid detection method comprises (1) a step of preparing a supporting member, having at least one kind of nucleic acid probe fixed to the member; (2) a step of preparing a labeled nucleic acid complementary to at least a part of the sequence of at least a part of the nucleic acid probe; (3) a step of keeping the labeled nucleic acid and a specimen nucleic acid in a specimen, in a hybridizable state; (4) a step of keeping the nucleic acid mixture, obtained by the step 3 and the nucleic acid probe fixed to the supporting member, in a hybridizable state; and (5) a step of measuring the labeled nucleic acid on the support member.
      COPYRIGHT: (C)2008,JPO&INPIT
    • 要解决的问题:提供能够快速进行基因分型的新的基因分型方法和可用于基因分型方法的新的核酸检测方法。 解决方案:核酸检测方法包括(1)制备支撑构件的步骤,其具有固定到构件上的至少一种核酸探针; (2)制备与核酸探针的至少一部分序列的至少一部分互补的标记核酸的步骤; (3)将标记的核酸和标本核酸保持在可检测状态的步骤; (4)将通过步骤3获得的核酸混合物和固定在支撑构件上的核酸探针的核酸混合物保持在可混合状态的步骤; 和(5)测量载体上标记的核酸的步骤。 版权所有(C)2008,JPO&INPIT
    • 8. 发明专利
    • Method for manufacturing biomolecule microarray and spot apparatus
    • 制造生物分子微量元素和点阵装置的方法
    • JP2003057236A
    • 2003-02-26
    • JP2001243930
    • 2001-08-10
    • Inst Of Physical & Chemical ResThk Co LtdThk株式会社理化学研究所
    • TASHIRO HIDEOKITSUNAI TOKUJIKONDO YASUMITSUSHIRAI TAKEKINAKAZAWA TOJIIIMURA AKIHIRO
    • G01N33/53C12Q1/68G01N37/00
    • PROBLEM TO BE SOLVED: To provide a method and an apparatus for manufacturing a quantitative biomolecule microarray which accurately spots a solution containing probe biomolecules to solid-phase parts for receiving the probe biomolecules.
      SOLUTION: A substrate with a plurality of the solid-phase parts for receiving the probe biomolecules (referred to as solid-phase parts, in the following), capable of specifically and quantitatively receiving the probe biomolecules in their surfaces is prepared. The solution containing the probe biomolecules is spotted to the solid-phase parts, and the probe biomolecules contained in the solution are immobilized to the solid-phase parts (the spotting of the solution is performed, in such a way that all the surface of one solid-phase part is covered with one droplet of the solution, and the one droplet contains the number of the probe biomolecules that the one solid-phase part is capable of receiving or more) in the method for manufacturing the biomolecule microarray and the apparatus used for the method. The substrate comprises alignment marks in its surface for the positioning of the substrate. The solid-phase parts are positioned with location relation to the alignment marks. The spotting of the solution is performed to the solid-phase parts positioned with locational relation to the alignment marks.
      COPYRIGHT: (C)2003,JPO
    • 要解决的问题:提供一种用于制造定量生物分子微阵列的方法和装置,其将含有探针生物分子的溶液精确地定位到用于接收探针生物分子的固相部分。 解决方案:制备具有多个用于接收能够在其表面上特异性和定量地接收探针生物分子的探针生物分子(以下称为固相部分)的固相部分的基底。 将含有探针生物分子的溶液点样固相,将溶液中包含的探针生物分子固定在固相部分(以溶液的点样,以一个 在制造生物分子微阵列的方法和使用的装置的方法中,固相部分被一滴溶液覆盖,并且一个液滴包含一个固相部分能够接收的多个探针生物分子) 为方法。 衬底包括其表面中的对准标记用于衬底的定位。 固相部分与定位标记位置关系定位。 对与定位标记有定位关系的固相部分进行溶液的点样。