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1. 发明申请

US20130195658A1 AIRCRAFT ICE PROTECTION SYSTEM AND AIRCRAFT PROVIDED WITH THE SAME 有权
标题翻译：飞机冰保护系统和飞机提供
公开(公告)号：US20130195658A1
公开(公告)日：2013-08-01
申请号：US13816562
申请日：2011-08-30
申请人： Isao Saito , Tatsuo Ishiguro , Shigeki Abe , Hideaki Tanaka , Toru Takasu , Motohiro Atsumi , Masakazu Nakanishi , Minoru Kamogari
发明人： Isao Saito , Tatsuo Ishiguro , Shigeki Abe , Hideaki Tanaka , Toru Takasu , Motohiro Atsumi , Masakazu Nakanishi , Minoru Kamogari
IPC分类号： F01D25/02
CPC分类号： F01D25/02 , B64D15/04
摘要： An aircraft ice protection system is provided for preventing ice accretion on a wing of an aircraft or removing the accreted ice. Bleed air extracted from a main engine of the aircraft and air introduced from an air intake installed on an airframe and heated by a heat source of the airframe of the aircraft are selectively supplied to a hot air chamber formed inside the wing, thereby carrying out ice protection.
摘要翻译：提供了一种飞机防冰系统，用于防止飞机机翼上的积冰或排除积冰。从飞机的主发动机抽出的排出的空气和从安装在机身上的进气引入并由飞机的机体的热源加热的空气被选择性地供应到形成在机翼内部的热空气室，从而进行冰保护。

2. 发明申请

US20060234253A1 Method for detecting a target substance by using a nucleic acid probe 审中-公开
标题翻译：通过使用核酸探针检测目标物质的方法
公开(公告)号：US20060234253A1
公开(公告)日：2006-10-19
申请号：US11244045
申请日：2005-10-06
申请人： Yasushi Hasui , Shigeki Abe , Motonari Daito , Koichi Yamagata
发明人： Yasushi Hasui , Shigeki Abe , Motonari Daito , Koichi Yamagata
IPC分类号： C12Q1/68 , C07H21/04
CPC分类号： C12Q1/6834 , C12Q2565/519 , C12Q2537/1373 , C12Q2537/125 , C12Q2537/1376
摘要： A method for detecting a target substance is described, which comprises the steps of: forming a first complex comprising (a) a first nucleic acid probe immobilized on a first solid phase and having a single-strand portion, (b) a nucleic acid ligand which has a binding section as a base sequence hybridizable with the single-strand portion of the first nucleic acid probe and which has a target-binding substance capable of binding to the target substance, (c) the target substance, and (d) a labeling substance capable of binding to the target substance; separating, from the first complex, a second complex comprising the nucleic acid ligand, the target substance and the labeling substance; and detecting the target substance on the basis of the labeling substance in the second complex.
摘要翻译：描述了用于检测目标物质的方法，其包括以下步骤：形成第一配合物，其包含（a）固定在第一固相上并具有单链部分的第一核酸探针，（b）核酸配体其具有与第一核酸探针的单链部分杂交的碱基序列的结合部分，其具有能够结合目标物质的靶结合物质，（c）靶物质，和（d）能够结合目标物质的标记物质; 从第一复合物中分离出包含核酸配体，靶物质和标记物质的第二复合物; 并基于第二配合物中的标记物质检测目标物质。

3. 发明授权

US07114795B2 Data processing apparatus, data processing method, program, and ink jet printing system 有权
标题翻译：数据处理装置，数据处理方法，程序和喷墨打印系统
公开(公告)号：US07114795B2
公开(公告)日：2006-10-03
申请号：US10647204
申请日：2003-08-26
申请人： Norio Shimura , Masaya Kikuta , Tetsushi Kohno , Takeaki Nakano , Hirokazu Kameda , Masaaki Endo , Shigeki Abe , Manabu Kuchiki , Masanori Echigo , Munetaka Yamaguchi
发明人： Norio Shimura , Masaya Kikuta , Tetsushi Kohno , Takeaki Nakano , Hirokazu Kameda , Masaaki Endo , Shigeki Abe , Manabu Kuchiki , Masanori Echigo , Munetaka Yamaguchi
IPC分类号： B41J2/165
CPC分类号： B41J11/0065 , G06K15/181
摘要： An ink jet printing system is provided which has an ink jet printing apparatus and a host and which alleviates a data processing load on the ink jet printing apparatus, prevents a reduction in a printing operation speed, and realizes a cost reduction. The ink jet printing apparatus of this invention has an ink receiving member for receiving waste ink ejected onto an overrunning area outside edges of a print medium and an accumulated value memory section for storing an accumulated value equivalent to waste ink volumes ejected onto the ink receiving member. The host includes a waste ink volume setting section for obtaining a value equivalent to a waste ink volume and a data sending section for sending data to the ink jet printing apparatus. The accumulated value memory section of the ink jet printing apparatus stores the accumulated value equivalent to waste ink volumes obtained by the host.
摘要翻译：提供一种喷墨打印系统，其具有喷墨打印设备和主机，并且其减轻了喷墨打印设备上的数据处理负担，防止了打印操作速度的降低，并且实现了成本降低。本发明的喷墨打印设备具有用于接收喷射到打印介质外边缘的超越区域上的废墨的墨接收部件和用于存储与喷墨到墨接收部件上的废墨量相当的累积值的累积值存储部。主机包括用于获得与废墨量相当的值的废墨量设置部分和用于向喷墨打印设备发送数据的数据发送部分。喷墨打印装置的累积值存储部存储与主机获得的废墨量相当的累积值。

4. 发明授权

US08465924B2 Treatment solution for preparing sample solution for nucleic acid amplification reaction and method for detecting nucleic acid by using treatment solution 有权
标题翻译：用于制备用于核酸扩增反应的样品溶液的处理溶液和使用处理溶液检测核酸的方法
公开(公告)号：US08465924B2
公开(公告)日：2013-06-18
申请号：US11294545
申请日：2005-12-06
申请人： Yasuhiro Otomo , Kazuhiko Takeda , Shigeki Abe , Kazuki Nakabayashi
发明人： Yasuhiro Otomo , Kazuhiko Takeda , Shigeki Abe , Kazuki Nakabayashi
IPC分类号： C12Q1/68 , C12P19/34
CPC分类号： C12N15/1003 , C12Q1/6806 , C12Q1/6846
摘要： A treatment solution for preparing a sample solution for nucleic acid amplification reaction is described. The treatment solution comprises dimethyl sulfoxide and aqueous solvent. The sample solution prepared by treating a biological sample with the treatment solution is used in the amplification reaction of a nucleic acid, whereby the nucleic acid can be efficiently recovered from a biological sample, and the influence of an inhibitor during nucleic acid amplification can be effectively reduced.
摘要翻译：描述了用于制备用于核酸扩增反应的样品溶液的处理溶液。处理液包含二甲基亚砜和含水溶剂。通过用处理溶液处理生物样品而制备的样品溶液用于核酸的扩增反应，从而可以从生物样品有效地回收核酸，并且可以有效地在核酸扩增过程中抑制剂的影响减少

5. 发明授权

US08076080B2 Nucleic acid amplification primers for detecting cytokeratins and examination method with the use of the primers 有权
标题翻译：用于检测细胞角蛋白的核酸扩增引物和使用引物的检查方法
公开(公告)号：US08076080B2
公开(公告)日：2011-12-13
申请号：US10514776
申请日：2003-05-20
申请人： Sachiyo Tada , Yasumasa Akai , Yasuyuki Imura , Shigeki Abe , Harumi Minekawa
发明人： Sachiyo Tada , Yasumasa Akai , Yasuyuki Imura , Shigeki Abe , Harumi Minekawa
IPC分类号： C12Q1/68 , C12P19/34 , C07H21/04
CPC分类号： C12Q1/6844 , C12Q1/686 , C12Q1/6886 , C12Q2600/112 , C12Q2531/119 , C12Q2527/101
摘要： It is intended to provide novel primers to be used in gene amplification reactions for detecting human cytokeratins (Human CK). A primer containing an oligonucleotide comprising a base sequence which is selected from among the the 270- to 1375-th regions of the base sequence represented by SEQ ID NO:1 and the regions of complementary strands thereof and represented by, for example, any of SEQ ID NOS:2 to 341 is constructed. Further, a primer containing an oligonucleotide comprising a base sequence which is selected from among the 270- to 930-th regions of the base sequence represented by SEQ ID NO:342 and the regions of complementary strands thereof and represented by, for example, any of SEQ ID NOS:343 to 434 is constructed. Furthermore, a primer containing an oligonucleotide comprising a base sequence which is selected from among the 340 to 490-th regions or the 495- to 1050-th regions of the base sequence represented by SEQ ID NO:435 and the regions of complementary strands thereof and represented by, for example, any of SEQ ID NOS:436 to 474 is constructed.
摘要翻译：旨在提供用于检测人细胞角蛋白（Human CK）的基因扩增反应中使用的新引物。一种含有寡核苷酸的引物，其包含选自SEQ ID NO：1所示的碱基序列的270〜1375位的碱基序列及其互补链的区域，构建SEQ ID NOS：2至341。此外，含有包含选自SEQ ID NO：342所示的碱基序列的270〜930区域的碱基序列的寡核苷酸的引物及其互补链的区域，例如任何构建为SEQ ID NO：343〜434。此外，含有选自SEQ ID NO：435表示的碱基序列的340〜490个区域或495〜1050个区域的碱基序列的寡核苷酸的引物及其互补链的区域并且由例如SEQ ID NO：436至474中的任一个表示。

6. 发明授权

US06955413B2 Printing apparatus and method for printing an image 失效
标题翻译：用于打印图像的打印装置和方法
公开(公告)号：US06955413B2
公开(公告)日：2005-10-18
申请号：US10648917
申请日：2003-08-27
申请人： Tetsushi Kohno , Masaya Kikuta , Norio Shimura , Takeaki Nakano , Hirokazu Kameda , Masaaki Endo , Shigeki Abe , Manabu Kuchiki , Masanori Echigo , Munetaka Yamaguchi
发明人： Tetsushi Kohno , Masaya Kikuta , Norio Shimura , Takeaki Nakano , Hirokazu Kameda , Masaaki Endo , Shigeki Abe , Manabu Kuchiki , Masanori Echigo , Munetaka Yamaguchi
IPC分类号： B41J2/01 , B41J11/42 , B41J13/00 , B41J29/48 , B41J29/393
CPC分类号： B41J13/0009
摘要： A printing apparatus of the invention acquires a velocity and an acceleration of a printing medium when a rear end of the printing medium passes through a detection lever. A correction amount for the rear end of the printing medium is determined in accordance with the velocity and the acceleration of the printing medium. The correction amount is a transportation amount of the printing medium during a physical return time after the rear end of the printing medium passes through the detection lever until the detection lever is detected by a sensor. A remaining region from a printing position of a print head up to the rear end of the printing medium is controlled in accordance with the correction amount for the rear end of printing medium.
摘要翻译：当打印介质的后端通过检测杆时，本发明的打印装置获取打印介质的速度和加速度。根据打印介质的速度和加速度确定打印介质的后端的校正量。校正量是在打印介质的后端通过检测杆直到检测杆被传感器检测到的物理返回时间之前的打印介质的传送量。根据打印介质的后端的校正量来控制从打印头的打印位置到打印介质的后端的剩余区域。

7. 发明申请

US20060094008A1 Nucleic acid amplification primers for detecting cytokeratins and examination method with the use of the primers 有权
标题翻译：用于检测细胞角蛋白的核酸扩增引物和使用引物的检查方法
公开(公告)号：US20060094008A1
公开(公告)日：2006-05-04
申请号：US10514776
申请日：2003-05-20
申请人： Sachiyo Tada , Yasumasa Akai , Yasuyuki Imura , Shigeki Abe , Harumi Minekawa
发明人： Sachiyo Tada , Yasumasa Akai , Yasuyuki Imura , Shigeki Abe , Harumi Minekawa
IPC分类号： C12Q1/68 , C07H21/04 , C12P19/34
CPC分类号： C12Q1/6844 , C12Q1/686 , C12Q1/6886 , C12Q2600/112 , C12Q2531/119 , C12Q2527/101
摘要： It is intended to provide novel primers to be used in gene amplification reactions for detecting human cytokeratins (Human CK). A primer containing an oligonucleotide comprising a base sequence which is selected from among the the 270- to 1375-th regions of the base sequence represented by SEQ ID NO:1 and the regions of complementary strands thereof and represented by, for example, any of SEQ ID NOS:2 to 341 is constructed. Further, a primer containing an oligonucleotide comprising a base sequence which is selected from among the 270- to 930-th regions of the base sequence represented by SEQ ID NO:342 and the regions of complementary strands thereof and represented by, for example, any of SEQ ID NOS:343 to 434 is constructed. Furthermore, a primer containing an oligonucleotide comprising a base sequence which is selected from among the 340 to 490-th regions or the 495- to 1050-th regions of the base sequence represented by SEQ ID NO:435 and the regions of complementary strands thereof and represented by, for example, any of SEQ ID NOS:436 to 474 is constructed.
摘要翻译：旨在提供用于检测人细胞角蛋白（Human CK）的基因扩增反应中使用的新引物。一种含有寡核苷酸的引物，其包含选自SEQ ID NO：1所示的碱基序列的270〜1375位的碱基序列及其互补链的区域，构建SEQ ID NOS：2至341。此外，含有包含选自SEQ ID NO：342所示的碱基序列的270〜930区域的碱基序列的寡核苷酸的引物及其互补链的区域，例如任何构建为SEQ ID NO：343〜434。此外，含有选自SEQ ID NO：435表示的碱基序列的340〜490个区域或495〜1050个区域的碱基序列的寡核苷酸的引物及其互补链的区域并且由例如SEQ ID NO：436至474中的任一个表示。

8. 发明授权

US08967543B2 Aircraft ice protection system and aircraft provided with the same 有权
标题翻译：飞机防冰系统和飞机提供的相同
公开(公告)号：US08967543B2
公开(公告)日：2015-03-03
申请号：US13816562
申请日：2011-08-30
申请人： Isao Saito , Tatsuo Ishiguro , Shigeki Abe , Hideaki Tanaka , Toru Takasu , Motohiro Atsumi , Masakazu Nakanishi , Minoru Kamogari
发明人： Isao Saito , Tatsuo Ishiguro , Shigeki Abe , Hideaki Tanaka , Toru Takasu , Motohiro Atsumi , Masakazu Nakanishi , Minoru Kamogari
IPC分类号： B64D15/02 , F01D25/02 , B64D15/04
CPC分类号： F01D25/02 , B64D15/04
摘要： An aircraft ice protection system is provided for preventing ice accretion on a wing of an aircraft or removing the accreted ice. Bleed air extracted from a main engine of the aircraft and air introduced from an air intake installed on an airframe and heated by a heat source of the airframe of the aircraft are selectively supplied to a hot air chamber formed inside the wing, thereby carrying out ice protection.
摘要翻译：提供了一种飞机防冰系统，用于防止飞机机翼上的积冰或排除积冰。从飞机的主发动机抽出的排出的空气和从安装在机身上的进气引入并由飞机的机体的热源加热的空气被选择性地供应到形成在机翼内部的热空气室，从而进行冰保护。

9. 发明申请

US20090004749A1 METHOD AND KIT FOR DETERMINING THE AMOUNT OF DNA BINDING PROTEIN 审中-公开
标题翻译：用于测定DNA结合蛋白质量的方法和试剂盒
公开(公告)号：US20090004749A1
公开(公告)日：2009-01-01
申请号：US12163431
申请日：2008-06-27
申请人： Koichi Yamagata , Shigeki Abe
发明人： Koichi Yamagata , Shigeki Abe
IPC分类号： G01N33/00
CPC分类号： G01N33/5308 , G01N33/6872
摘要： A kit for determining a quantity of a target DNA binding protein in a liquid sample by using a fluorescence correlation spectroscopy, comprising a first measuring reagent including a fluorescent-labeled nucleic acid probe and a first unlabeled nucleic acid probe, a second measuring reagent including the fluorescent-labeled nucleic acid probe and a second unlabeled nucleic acid probe, wherein the target DNA binding protein is capable of binding to the fluorescent-labeled nucleic acid probe and the first unlabeled nucleic acid probe, and is not capable of binding to the second unlabeled nucleic acid probe; and a method for determining a quantity of a target DNA binding protein in a liquid sample is also disclosed.
摘要翻译：一种用于通过使用荧光相关光谱测定液体样品中的靶DNA结合蛋白的量的试剂盒，其包括含有荧光标记的核酸探针和第一未标记的核酸探针的第一测定试剂，包含第荧光标记的核酸探针和第二个未标记的核酸探针，其中靶DNA结合蛋白能够结合荧光标记的核酸探针和第一个未标记的核酸探针，并且不能结合第二个未标记的核酸探针核酸探针; 还公开了一种用于测定液体样品中目标DNA结合蛋白的量的方法。

10. 发明申请

US20060121515A1 Treatment solution for preparing sample solution for nucleic acid amplification reaction and method for detecting nucleic acid by using treatment solution 有权
公开(公告)号：US20060121515A1
公开(公告)日：2006-06-08
申请号：US11294545
申请日：2005-12-06
申请人： Yasuhiro Otomo , Kazuhiko Takeda , Shigeki Abe , Kazuki Nakabayashi
发明人： Yasuhiro Otomo , Kazuhiko Takeda , Shigeki Abe , Kazuki Nakabayashi
IPC分类号： C12Q1/68 , C12N1/08
CPC分类号： C12N15/1003 , C12Q1/6806 , C12Q1/6846
摘要： A treatment solution for preparing a sample solution for nucleic acid amplification reaction is described. The treatment solution comprises dimethyl sulfoxide and aqueous solvent. The sample solution prepared by treating a biological sample with the treatment solution is used in the amplification reaction of a nucleic acid, whereby the nucleic acid can be efficiently recovered from a biological sample, and the influence of an inhibitor during nucleic acid amplification can be effectively reduced.

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