BLOCK COPOLYMER, MULTILAYER STRUCTURE, SOLID POLYMER FILM, FUEL CELL, PRODUCTION METHOD FOR MULTILAYER STRUCTURE, AND PRODUCTION METHOD FOR MULTILAYER STRUCTURE CONTAINING INORGANIC NANOPARTICLES

    公开(公告)号:US20190169420A1

    公开(公告)日:2019-06-06

    申请号:US16321083

    申请日:2017-08-01

    Inventor: Hiroshi YABU

    Abstract: The problem addressed by the present invention is to provide a block copolymer that can be used in a neutral solvent atmosphere and can produce a solid polymer membrane including nanoparticles.The problem is solved by a block copolymer represented by formula (1) below. wherein in the formula, R1 represents a C1-20 linear, branched, or cyclic alkyl group, C6-20 aryl group, or C7-20 aralkyl group; R2 represents a group having a functional group having an acid dissociation constant pKa of from 0.5 to 7; R3, R4, and R5 each show H or a C1-20 linear, branched, or cyclic alkyl group; R6, R7, and R8 each represent a hydrogen, hydroxyl group, nitro group, carboxy group, or carbonyl group; X represents an amide or ester, but may not be included; Y represents an amide or ester, but may not be included; p represents an integer of 1-10, but may not be included; n represents an integer of 3-1000; m represents an integer of 3-1000; and t represents an integer of 3-1000, but n may not be included; the arrangement of n, m, and t is arbitrary, but n and m are adjacent when n is included.

    Method of amplifying circular DNA
    63.
    发明授权

    公开(公告)号:US10301672B2

    公开(公告)日:2019-05-28

    申请号:US15527560

    申请日:2015-11-18

    Abstract: The present invention provides a method for easily and exponentially amplifying circular DNA, particularly long chain circular DNA, in a cell-free system. Specifically, the present invention provides a method for amplifying circular DNA in which circular DNA having a replication origin sequence (origin of chromosome (oriC)) is mixed with a reaction solution containing the following enzyme groups to form a reaction mixture, which is then reacted under an isothermal condition, the enzyme groups being: (1) a first enzyme group that catalyzes replication of circular DNA; (2) a second enzyme group that catalyzes an Okazaki fragment maturation and synthesizes two sister circular DNAs constituting a catenane; and (3) a third enzyme group that catalyzes a separation of two sister circular DNAs.

    Data editing device and data editing method

    公开(公告)号:US10296496B2

    公开(公告)日:2019-05-21

    申请号:US14342264

    申请日:2012-07-05

    Inventor: Hiroshi Deguchi

    Abstract: A data storage unit of a data editing apparatus stores both a base indicating a data attribute and a data value in association with each other as data to be edited. A code acquisition unit acquires a user code, which is a code described in a first program language for describing data editing details by intensive notation and which describes editing details for the data to be edited that are based on the base. A code generation unit generates, in accordance with a predetermined correspondence relationship between a second program language for describing data editing details by extensive notation and the first program language, an execution code described in the second program language based on the user code. An editing processing unit edits the data to be edited in accordance with the execution code.

    TUMOR CELL MALIGNANT TRANSFORMATION SUPPRESSOR AND ANTI-TUMOR AGENT

    公开(公告)号:US20190062751A1

    公开(公告)日:2019-02-28

    申请号:US15569559

    申请日:2016-04-22

    Abstract: The present invention provides an anti-tumor agent and a suppressor for suppressing malignant transformation such as acquisition of metastatic ability or acquisition of apoptosis resistance of a tumor cell. The present invention provides a tumor cell malignant transformation suppressor, including a substance suppressing or inhibiting Zic5 gene functions as an active ingredient to suppress or inhibit acquisition of metastatic ability or acquisition of apoptosis resistance of a tumor cell; a method of suppressing tumor cell malignant transformation of animals other than humans, including suppressing or inhibiting Zic5 gene functions to suppress or inhibit acquisition of metastatic ability or acquisition of apoptosis resistance of a tumor cell; an anti-tumor agent including a substance suppressing or inhibiting Zic5 gene functions as an active ingredient, in which the agent is used in prostate cancer therapy; and a marker for tumor cell malignancy consisting of the expression level of Zic5 gene.

    IRRADIATION DEVICE, LASER MICROSCOPE SYSTEM, IRRADIATION METHOD, AND LASER MICROSCOPE DETECTION METHOD

    公开(公告)号:US20190041620A1

    公开(公告)日:2019-02-07

    申请号:US16076627

    申请日:2017-02-09

    Abstract: Provided are an irradiation device, a laser microscope system, an irradiation method, and a laser microscope detection method which can further widen a bandwidth of detection light as a multiplexed signal. Laser light beams are separated and enter a first AOD (24) and a second AOD (34) so that a plurality of first diffracted light beams and a plurality of second diffracted light beams with deflection angles and sizes of frequency shifts different from each other are generated. The first diffracted light beams and the second diffracted light beams are superposed by a beam splitter (19) so as to generate a plurality of interference light beams with beat frequencies different from each other. An objective lens (52) is formed by aligning a plurality of irradiation spots of interference light beam linearly in a main scanning direction and irradiates a sample (T) with the interference light beam. The irradiation spot is moved by oscillation of a scanning mirror (47a) in a sub scanning direction orthogonal to the main scanning direction. Fluorescence emitted from the sample (T) by irradiation of each interference light beam is detected by a light detection unit (13).

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