CURRENT INTERRUPTING DEVICE AND CURRENT INTERRUPTING METHOD

    公开(公告)号:US20220360067A1

    公开(公告)日:2022-11-10

    申请号:US17761083

    申请日:2020-09-15

    Abstract: A current interrupting device includes: a current limiting element provided on a power supply path from a predetermined power supply to a load device, the current limiting element being configured to exhibit a current limiting action when current flowing the power supply path exceeds a first current threshold value; a current diversion path switch capable of switching on and off of an electric conduction of a current diversion path, the current diversion path switch being connected in parallel with the power supply path; and a controller configured to control on and off of the current diversion path switch, wherein, the controller is configured to: switch the current diversion path switch on from an off state when it is detected that current flowing the current limiting element is limited to a second current threshold value after the current flowing the current limiting element has exceeded the first current threshold value; and switch the current diversion path switch off again after a predetermined switched-on holding time has elapsed since the current diversion path switch has been switched on.

    LIGAND HAVING THREE FINGER STRUCTURE AND A METHOD FOR DETECTING A MOLECULE BY USING THEREOF
    48.
    发明申请
    LIGAND HAVING THREE FINGER STRUCTURE AND A METHOD FOR DETECTING A MOLECULE BY USING THEREOF 有权
    具有三个手指结构的配对和使用该方法检测分子的方法

    公开(公告)号:US20150031564A1

    公开(公告)日:2015-01-29

    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.

    Abstract translation: 本发明通过cDNA显示方法改进了来自筛选cDNA的mRNA的体外病毒合成效率和稳定性,以通过分子进化工程技术提高肽生产的效率和可靠性。 提供了一种配体,其包括由反平行和平板形成的三个指状物和插入在反平行晶片之间的环区域,其中由每个指状物的环区域形成的至少指尖部分与靶分子结合 ,并且其中配体包含SEQ ID NO:1的氨基酸序列。在SEQ ID NO:1的氨基酸序列中,X7表示构成每个手指的指尖部分的任意氨基酸残基,每个数字 表示氨基酸残基的数目,X7和X4不是彼此相同的氨基酸残基组成。

    Deformation measuring method and apparatus using electronic speckle pattern interferometry
    49.
    发明申请
    Deformation measuring method and apparatus using electronic speckle pattern interferometry 审中-公开
    使用电子斑纹图案干​​涉测量的变形测量​​方法和设备

    公开(公告)号:US20040059526A1

    公开(公告)日:2004-03-25

    申请号:US10358285

    申请日:2003-02-05

    Abstract: A deformation measuring method using electronic speckle pattern interferometry comprises the steps of subtracting an average intensity from the intensity in a time domain at each point of a speckle pattern image so as to compute the cosine component of intensity; subjecting the cosine component to Hilbert transform in a temporal domain so as to compute the sine component of intensity; determining the arctangent of the ratio between thus computed sine and cosine components so as to determine an object phase; carrying out an unwrapping operation; and outputting three-dimensional deformation distribution data in a displayable mode.

    Abstract translation: 使用电子散斑图案干涉测量的变形测量​​方法包括以下步骤:从斑点图案图像的每个点处的时域中的强度减去平均强度,以计算强度的余弦分量; 在时域中对余弦分量进行希尔伯特变换,以计算强度的正弦分量; 确定所计算的正弦和余弦分量之间的比率的反正切,以便确定目标相位; 进行展开操作; 并输出可显示模式的三维变形分布数据。

    Liposome binding peptide, construct for manufacturing the liposome binding peptide, and liposome

    公开(公告)号:US12152086B2

    公开(公告)日:2024-11-26

    申请号:US17315041

    申请日:2021-05-07

    Abstract: The purpose of the present invention is to provide a method for producing a peptide that interacts with a lipid bilayer, and a lipid-bilayer-penetrating peptide obtained through the method. Provided is a lipid-bilayer-penetrating peptide constructed from 10 to 100 amino acids, the peptide having an amino acid sequence that penetrates the lipid bilayer at the C-terminal, and having an amino acid sequence with at least six contiguous arginine at the N-terminal. Also provided is a construct for producing a lipid-bilayer-penetrating peptide, the construct including, from the 5′ end toward the 3′ end, a tag region 1, a region 1 for incorporating a fluorescent protein gene sequence, a fluorescent protein gene region, a region 2 for incorporating a fluorescent protein gene sequence, a random region, and a stop codon region, and the construct being such that the random region has the aforementioned sequences.

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