会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 3. 发明授权
    • Navigation system
    • 导航系统
    • US08825372B2
    • 2014-09-02
    • US13131134
    • 2009-10-29
    • Kumi NishibashiTakashi Irie
    • Kumi NishibashiTakashi Irie
    • G01C21/26G01C21/32G01C21/34
    • G01C21/34G01C21/3629G01C21/3658G09B29/007G09B29/10
    • A navigation system includes: a map information acquiring unit 31 for acquiring map information; an HOV lane decision unit 38 for deciding whether an HOV lane is included in a road represented by the map information acquired by the map information acquiring unit 31 or not; a road number processing unit 43 for performing, when the HOV lane decision unit 38 decides that the HOV lane is included, processing of adding information representing the HOV lane to a road number of the road including the HOV lane; and a display processing unit 44 or a voice information unit 46 for causing the road number passing through the processing by the road number processing unit 43 to be displayed on the guide map or output in voice.
    • 导航系统包括:地图信息获取单元31,用于获取地图信息; HOV车道判定单元38,用于判定由地图信息获取单元31获取的地图信息表示的道路中是否包括HOV车道; 道路号处理单元43,用于当HOV车道判定单元38判定包括HOV车道时,执行表示HOV车道的信息到包括HOV车道的道路的道路号码的处理; 以及用于使通过道路号码处理单元43的处理的道路号码显示在引导地图上或以语音输出的显示处理单元44或语音信息单元46。
    • 7. 发明申请
    • Fluorescence analyzing method, fluorescence analyzing apparatus and image detecting method
    • 荧光分析方法,荧光分析装置和图像检测方法
    • US20070281315A1
    • 2007-12-06
    • US11806318
    • 2007-05-31
    • Satoshi TakahashiTakashi Irie
    • Satoshi TakahashiTakashi Irie
    • C12Q1/68G06F19/00C12M3/00
    • G01N21/6452
    • A fluorescence analyzing method includes the steps of irradiating a board, to which oligonucleotide is fixed, with light for fluorescence measurement; focusing produced fluorescence to form an image; and detecting the fluorescence with a two-dimensional sensor. Here, the board is provided with plural regions to which the oligonucleotide is fixed, and the plural regions are spaced apart from one another on the board substantially equidistantly in the vertical and horizontal directions. A fluorescent image is detected in a condition where the following equation is satisfied: dd=ds×M/n where ds denotes the interval between the regions, M denotes the imaging magnification of an optical focusing/imaging system, dd denotes the pixel pitch of the two-dimensional sensor, and n denotes an integer (n=1, 2, 3, 4, 5).
    • 荧光分析方法包括以下步骤:将固定有寡核苷酸的板与用于荧光测量的光照射; 聚焦产生荧光以形成图像; 并用二维传感器检测荧光。 这里,板上设置有寡核苷酸固定的多个区域,并且多个区域在基板上基本等距离地在垂直和水平方向上彼此间隔开。 在满足以下等式的条件下检测荧光图像:<?in-line-formula description =“In-line formula”end =“lead”?> dd = dsxM / n <?in-line-formula description =“在线公式”end =“tail”?>其中ds表示区域之间的间隔,M表示光学聚焦/成像系统的成像倍率,dd表示二维传感器的像素间距,n表示 表示整数(n = 1,2,3,4,5)。
    • 8. 发明授权
    • PCR primers and a method for deciding a base sequence thereof regarding adenylation
    • PCR引物和用于确定其关于腺苷酸化的碱基序列的方法
    • US06773901B2
    • 2004-08-10
    • US10083616
    • 2002-02-27
    • Chihiro UematsuKazunori OkanoTakashi Irie
    • Chihiro UematsuKazunori OkanoTakashi Irie
    • C12P1934
    • C12Q1/6853C12Q2525/161
    • Adenylation of a DNA fragment with a DNA polymerase occurs in the course of PCR, and thus two peaks are detected. To prevent the peak splitting, it is necessary to raise efficiency of adenylation a single peak to occur without changing reaction conditions. To this end, four types of PCR primers which, respectively, have an anchor sequence at 5′ terminus so that any of A, C, G or T is attached to at the 5′ terminus of the anchor sequence, and PCR is carried out by use of the respective primers to determine efficiencies of adenylation. Subsequently, an anchor sequence that is more likely to undergo adenylation is screened to decide an anchor sequence more likely undergo adenylation, followed by PCR by use of a primer having the decided anchor sequence.
    • 在PCR过程中DNA聚合酶的DNA片段的腺苷酸化发生,因此检测到两个峰。 为了防止峰分裂,需要提高腺苷酸化的效率,单峰发生而不改变反应条件。 为此,分别在5'末端具有锚定序列以使A,C,G或T中的任一个连接到锚定序列的5'末端的4种PCR引物,并进行PCR 通过使用各自的引物来确定腺苷酸化的效率。 随后,筛选更可能进行腺苷酸化的锚定序列以确定锚定序列更可能进行腺苷酸化,随后通过使用具有决定的锚定序列的引物进行PCR。
    • 10. 发明授权
    • Capillary electrophoresis system
    • 毛细管电泳系统
    • US06635164B1
    • 2003-10-21
    • US09696262
    • 2000-10-26
    • Takashi AnazawaTakashi IrieMasao Kamahori
    • Takashi AnazawaTakashi IrieMasao Kamahori
    • C02F140
    • G01N27/44726
    • A capillary electrophoresis system includes a plurality of capillaries arranged in parallel on a vertical plane at an identical distance from each other, each of which has a sample injection end immersed in a cathode buffer 23 and pointed downward vertically to facilitate connection between the cathode buffer 23 and a sample solution. The sample elution end is connected via a pump block 11 and a connection tube 3 to an anode buffer 24. The height is made identical between the liquid levels for buffers 23 and 24 to prevent movement of the separation medium in the capillaries. The sample introduced from the sample injection end 20 moves upward vertically via electrophoresis to the sample elution end in the capillary and is passed through and detected at the fluorescence detection position 19. The effective separation length is thus decreased to 10 cm or less to attain high throughput.
    • 毛细管电泳系统包括在垂直平面上彼此平行布置的多个毛细管,每个毛细管具有浸入阴极缓冲器23中的样品注射端,并垂直向下指向以便于阴极缓冲器23之间的连接 和样品溶液。 样品洗脱端通过泵块11和连接管3连接到阳极缓冲器24.在缓冲器23和24的液面之间的高度相同,以防止分离介质在毛细管中移动。 从样品注射端20引入的样品通过电泳向上垂直移动到毛细管中的样品洗脱端,并在荧光检测位置19处通过并检测。因此有效分离长度降低到10cm以下以达到高 吞吐量。