METHOD FOR AMINO ACID ANALYSIS AND SYSTEM FOR AMINO ACID ANALYSIS

    公开(公告)号:US20200217826A1

    公开(公告)日:2020-07-09

    申请号:US16721185

    申请日:2019-12-19

    Inventor: Masami SHIBUKAWA

    Abstract: The present invention provides a highly versatile method for amino acid analysis, the method enabling separation and analysis of amino acids in a sample with high precision in a shorter time. This method is a method for amino acid analysis, the method including a step of allowing a sample containing a plurality of amino acids to flow together with an eluent 2 through a separation column 4 packed with a cation exchange resin, thereby separating the amino acids, and a step of detecting the separated amino acids, wherein the eluent 2 is an eluent containing a divalent or higher inorganic acid, a cation source, and water, and having a pH of 5.0 or lower, and the sample is allowed to flow through the separation column 4 heated by applying a temperature gradient including a temperature region of 100° C. or higher.

    SUBSTRATE MANUFACTURING METHOD
    63.
    发明申请

    公开(公告)号:US20190105739A1

    公开(公告)日:2019-04-11

    申请号:US16149631

    申请日:2018-10-02

    Abstract: A substrate manufacturing method capable of easily obtaining a thin magnesium oxide single crystal substrate is provided. Performed is a first step of disposing a laser condensing means on a surface of a magnesium oxide single crystal substrate (20) of magnesium oxide to be irradiated in a non-contact manner, the laser condensing means being for condensing a laser beam. Then, a second step of causing planar peeling from a surface side of the magnesium oxide single crystal substrate (20) to be irradiated is performed. In this second step, a laser beam (B) is irradiated to the surface of the single crystal substrate (20) and the laser beam (B) is condensed into an inner portion of the single crystal substrate (20) under designated irradiation conditions. Simultaneously with the irradiation and the condensation, the laser condensing means (14) and the single crystal substrate (20) are two-dimensionally moved relatively to each other. In this way, processing mark lines (LK), each of which is composed in such a manner that processing marks (K) formed by thermal processing are formed in line at an inner portion of a single crystal member, are formed in parallel to one another. At this time, overlapped line portions (DK) in which the processing marks (K) overlap one another are formed in at least a part of the processing mark lines (LK), whereby the planar peeling is caused from the irradiated surface (20r) side.

    ELASTIC MECHANISM
    64.
    发明申请
    ELASTIC MECHANISM 审中-公开

    公开(公告)号:US20190024746A1

    公开(公告)日:2019-01-24

    申请号:US15757413

    申请日:2016-08-05

    Inventor: Masato Saitoh

    Abstract: In the spring mechanism, the negative spring mechanism biasing the loading plate to the positive side in the z-direction has the spring shaft and interspring. The spring shaft is rotatably connected to the fixed part and is connected through the slider with respect to the loading plate so that it can rotate and can move in the x-direction. The connection part with the loading plate is positioned on the positive side in the z-direction and on the positive side in the x-direction relative to the connection part with the fixed part. An elastic force countering the compression is generated by the spring shaft. The interspring is connected to the loading plate and is connected through the slider to the spring shaft. It generates an elastic force countering the displacement to the positive side in the x-direction of the connection part of the spring shaft with the loading plate.

    Ligand having three finger structure and a method for detecting a molecule by using thereof

    公开(公告)号:US09982254B2

    公开(公告)日:2018-05-29

    申请号:US14279788

    申请日:2014-05-16

    CPC classification number: C12N15/1062 C07K14/435 C07K14/4702

    Abstract: The present invention improves in vitro virus synthesis efficiency and stability of mRNA derived from screened cDNA in a cDNA display method to improve the efficiency and reliability of the production of a peptide by a molecular evolutionary engineering technique. Provided is a ligand which comprises three fingers formed from antiparallel β-sheets and a loop region intercalated between the antiparallel β-sheets, wherein at least a fingertip part formed by the loop region of each of the fingers is bound to the target molecule, and wherein the ligand comprises the amino acid sequence of SEQ ID NO: 1. In the amino acid sequence of SEQ ID NO: 1, X7 represents an arbitrary amino acid residue that constitutes the fingertip part of each of the fingers, each numeric character represents the number of amino acid residues, and X7 and X4 are not composed of the same amino acid residues as each other.

    MAGNETIC LEVITATION DEVICE AND METHOD FOR CONTROLLING SAME

    公开(公告)号:US20170093307A1

    公开(公告)日:2017-03-30

    申请号:US15311616

    申请日:2015-02-23

    Inventor: Takeshi Mizuno

    CPC classification number: H02N15/00

    Abstract: A magnetic levitation device includes a pair of magnets, a displacement detection means, and a control means. The pair of magnets generate magnetic force for supporting a ferromagnet in a noncontact manner. The displacement detection means detect the displacement of the ferromagnet in a lateral shift direction. The control means suppresses the vibration of the ferromagnet in a lateral shift direction. The control means controls the pair of magnets so that a stronger magnetic force acts on the ferromagnet that is displaced in a direction departing from the center of the vibration than when the ferromagnet is displaced in a direction returning to the center of the vibration.

    METHOD FOR GENERATING CELL CONDENSATE FOR SELF-ORGANIZATION
    69.
    发明申请
    METHOD FOR GENERATING CELL CONDENSATE FOR SELF-ORGANIZATION 审中-公开
    用于生成自组织细胞凝聚的方法

    公开(公告)号:US20170067014A1

    公开(公告)日:2017-03-09

    申请号:US15121934

    申请日:2015-02-26

    Abstract: The present invention finds out find out the requirements necessary for preparing a cell condensate in vitro from a large number of cells (several ten thousand to several million cells) and provides a method of forming a cell condensate for self-organization which is capable of realizing complex higher structures (such as liver and kidney) and interactions with other organs.A method of preparing a cell condensate in vitro, comprising culturing a mixture of cells and/or tissues of a desired type in a total cell count of 400,000 or more and 100,000 to 400,000 mesenchymal cells to form a cell condensate of 1 mm or more in size. A cell condensate prepared by the above-described method. A method of preparing a three-dimensional tissue structure, comprising allowing self-organization of a cell condensate prepared by the above-described method to form a three-dimensional tissue structure that has been provided with higher structures. A gel-like support wherein the side on which culture is to be performed has a U- or V-shaped cross-section.

    Abstract translation: 一种在体外制备细胞冷凝物的方法,包括在总细胞计数为40万个或更多至100,000至400,000个间充质细胞中培养所需类型的细胞和/或组织的混合物以形成1mm以上的细胞冷凝物 尺寸。 通过上述方法制备的细胞冷凝物。 一种制备三维组织结构的方法,包括允许通过上述方法制备的细胞冷凝物的自组织以形成具有较高结构的三维组织结构。 凝胶状载体,其中要进行培养的一面具有U形或V形横截面。

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