METHOD FOR MEASURING THE NUMBER OF ORAL LACTOBACILLUS, AND A PCR PRIMERS-PROBE SET USED FOR THE SAME
    1.
    发明申请
    METHOD FOR MEASURING THE NUMBER OF ORAL LACTOBACILLUS, AND A PCR PRIMERS-PROBE SET USED FOR THE SAME 有权
    用于测量口腔乳杆菌数量的方法和用于其的PCR引物探针

    公开(公告)号:US20090111103A1

    公开(公告)日:2009-04-30

    申请号:US12057789

    申请日:2008-03-28

    CPC classification number: C12Q1/686

    Abstract: There is provided a real-time PCR assay capable of measuring the number of lactobacillus present in an oral cavity, in a short time. The object can be solved by a method for measuring the number of oral lactobacillus using a combination of a forward primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 1 to 4 and a reverse primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 5 to 7; and a probe for measuring the number of oral lactobacillus, comprising a oligonucleotide part of at least 10 sequential bases in the base sequence any one of SEQ ID NO: 8 to 15.

    Abstract translation: 提供了能够在短时间内测量存在于口腔中的乳杆菌数量的实时PCR测定。 该目的可以通过使用包含SEQ ID NO:1至4中任一个的碱基序列中的至少15个连续碱基的寡核苷酸部分的正向引物和反向引物的方法来测量口服乳酸杆菌的数量的方法 包含SEQ ID NO:5至7中任一个的碱基序列中至少15个连续碱基的寡核苷酸部分; 以及用于测量口服乳杆菌数量的探针,其包含SEQ ID NO:8至15中任一个的碱基序列中至少10个连续碱基的寡核苷酸部分。

    METHOD FOR MEASURING THE NUMBER OF ORAL STREPTOCOCCI AND A PCR PRIMERS-PROBE SET USED FOR THE SAME
    2.
    发明申请
    METHOD FOR MEASURING THE NUMBER OF ORAL STREPTOCOCCI AND A PCR PRIMERS-PROBE SET USED FOR THE SAME 审中-公开
    用于测量口腔粘膜数量的方法和用于其的PCR引物探针

    公开(公告)号:US20080182265A1

    公开(公告)日:2008-07-31

    申请号:US12023448

    申请日:2008-01-31

    Applicant: Yuko MATSUMOTO

    Inventor: Yuko MATSUMOTO

    CPC classification number: C12Q1/689 C12Q2600/156

    Abstract: There is provided a real time PCR assay capable of calculating a ratio of the number of mutans streptococci to the number of oral streptococci present in an oral cavity, in a short time.The object can be solved by a method for measuring the number of oral streptococci using the combination of a forward primer comprising a primer oligonucleotide part of at least 15 sequential bases in the base sequence of SEQ ID NO: 1 and a reverse primer comprising a probe oligonucleotide part of at least 15 sequential bases in the base sequence of SEQ ID NO: 2; and a probe for measuring the number of oral streptococci, comprising a nucleotide part consisting of at least 10 sequential bases in the base sequence of SEQ ID NO: 3 or 4.

    Abstract translation: 提供了能够在短时间内计算变形链球菌数目与口腔中存在的口服链球菌数目的比率的实时PCR测定法。 该目的可以通过使用包含SEQ ID NO:1的碱基序列中的至少15个连续碱基的引物寡核苷酸部分的正向引物和包含探针的反向引物的组合来测量口服链球菌数的方法来解决 SEQ ID NO:2的碱基序列中至少15个连续碱基的寡核苷酸部分; 以及用于测量口服链球菌数目的探针,其包含由SEQ ID NO:3或4的碱基序列中的至少10个连续碱基组成的核苷酸部分。

    Method of driving organic EL device and display device
    3.
    发明申请
    Method of driving organic EL device and display device 有权
    驱动有机EL器件和显示器件的方法

    公开(公告)号:US20060197462A1

    公开(公告)日:2006-09-07

    申请号:US11361364

    申请日:2006-02-24

    Abstract: According to one aspect of the present invention, it is possible to sufficiently perform the discharging of charge without lowering the light emitting efficiency of an organic EL device and hence, the device can exhibit the light emitting efficiency higher than a conventional organic EL device and, at the same time, can prevent the degradation of the device. As an organic EL device to which the present invention is applied, on a glass transparent substrate, a transparent electrode, a hole injection layer and a hole transport layer which function as a hole transport function layer, a light emitting layer, an electron transport function layer, and a metal electrode are formed sequentially, and a drive power sources are connected to the transparent electrode and the metal electrode. Further, from the drive power source, as an applying voltage, a voltage which is obtained by overlapping any one of a sine wave, a pulse wave, a triangle wave and a sawtooth wave having two cycles or more to a drive signal or a voltage which is obtained by overlapping a sine wave having two cycles or more to the drive signal is supplied.

    Abstract translation: 根据本发明的一个方面,可以在不降低有机EL器件的发光效率的情况下充分地进行电荷的放电,因此该器件可以表现出高于常规有机EL器件的发光效率, 同时可以防止设备的劣化。 作为应用本发明的有机EL器件,在玻璃透明基板上,透明电极,空穴注入层和作为空穴传输功能层的空穴传输层,发光层,电子传输功能 层和金属电极,并且驱动电源连接到透明电极和金属电极。 此外,从驱动电源,作为施加电压,通过将具有两个周期以上的正弦波,脉波,三角波和锯齿波中的任一个与驱动信号或电压重叠而获得的电压 提供通过使具有两个周期以上的正弦波与驱动信号重叠而获得的。

    Liquid crystal display device and manufacturing method thereof
    7.
    发明授权
    Liquid crystal display device and manufacturing method thereof 有权
    液晶显示装置及其制造方法

    公开(公告)号:US08692970B2

    公开(公告)日:2014-04-08

    申请号:US12943190

    申请日:2010-11-10

    CPC classification number: G02F1/133788 G02F2001/1316 G02F2001/133354

    Abstract: Disclosed is a manufacturing method of a liquid crystal display device which is a manufacturing method of a liquid crystal display device including a liquid crystal alignment film to which an alignment regulating force is imparted by a photo-alignment treatment, including: a film forming step of forming a film containing a polymer whose main chain is cleaved by irradiation with light; a photo-alignment step of imparting an alignment regulating force to the film formed in the film forming step by irradiation of the film with light in an atmosphere of a temperature lower than 100° C.; and a removing step of removing a low-molecular weight component generated by cleaving the main chain of the polymer through the light irradiation after the light irradiation. Also disclosed is a liquid crystal display device manufactured by the manufacturing method.

    Abstract translation: 公开了一种液晶显示装置的制造方法,该液晶显示装置是包括通过光取向处理赋予取向调节力的液晶取向膜的液晶显示装置的制造方法,包括:成膜步骤 形成含有主链通过光照射而被切割的聚合物的膜; 光学对准步骤,通过在低于100℃的气氛中用光照射膜,在成膜步骤中形成的膜施加取向调节力; 以及去除在光照射后通过光照射分解聚合物主链而产生的低分子量成分的除去步骤。 还公开了通过该制造方法制造的液晶显示装置。

    Manufacturing Method of Display Device
    9.
    发明申请
    Manufacturing Method of Display Device 有权
    显示设备制造方法

    公开(公告)号:US20130095720A1

    公开(公告)日:2013-04-18

    申请号:US13707029

    申请日:2012-12-06

    Abstract: A method of manufacturing an organic EL display device that includes an element substrate on which a first organic luminescent material and a second organic luminescent material are formed, includes forming the first organic luminescent material by dripping the first organic luminescent material from an inkjet nozzle on the element substrate while relatively moving the inkjet nozzle and the element substrate in a first direction, and forming the second organic luminescent material by dripping the second organic luminescent material from an inkjet nozzle on the element substrate while relatively moving the inkjet nozzle and the element substrate in a direction perpendicular to the first direction.

    Abstract translation: 一种制造有机EL显示装置的方法,所述有机EL显示装置包括其上形成有第一有机发光材料和第二有机发光材料的元件基板,包括通过从所述第一有机发光材料从所述喷嘴喷嘴滴下所述第一有机发光材料来形成所述第一有机发光材料 同时沿着第一方向相对地移动喷墨喷嘴和元件基板,并且通过在元件基板上的喷墨喷嘴中滴下第二有机发光材料来形成第二有机发光材料,同时使喷墨喷嘴和元件基板在 垂直于第一方向的方向。

    Method for measuring the number of oral Lactobacillus, and a PCR primers-probe set used for the same
    10.
    发明授权
    Method for measuring the number of oral Lactobacillus, and a PCR primers-probe set used for the same 有权
    用于测量口服乳杆菌的数量的方法和用于其的PCR引物 - 探针组

    公开(公告)号:US08133677B2

    公开(公告)日:2012-03-13

    申请号:US12057789

    申请日:2008-03-28

    CPC classification number: C12Q1/686

    Abstract: There is provided a real-time PCR assay capable of measuring the number of lactobacillus present in an oral cavity, in a short time. The object can be solved by a method for measuring the number of oral lactobacillus using a combination of a forward primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 1 to 4 and a reverse primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 5 to 7; and a probe for measuring the number of oral lactobacillus, comprising a oligonucleotide part of at least 10 sequential bases in the base sequence any one of SEQ ID NO: 8 to 15.

    Abstract translation: 提供了能够在短时间内测量存在于口腔中的乳杆菌数量的实时PCR测定。 该目的可以通过使用包含SEQ ID NO:1至4中任一个的碱基序列中的至少15个连续碱基的寡核苷酸部分的正向引物和反向引物的方法来测量口服乳酸杆菌的数量的方法 包含SEQ ID NO:5至7中任一个的碱基序列中至少15个连续碱基的寡核苷酸部分; 以及用于测量口服乳杆菌数量的探针,其包含SEQ ID NO:8至15中任一个的碱基序列中至少10个连续碱基的寡核苷酸部分。

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