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    • 35. 发明专利
    • Capture device for fruit tree stink bugs
    • 水果树皮疙瘩捕获装置
    • JP2008161090A
    • 2008-07-17
    • JP2006352235
    • 2006-12-27
    • Chiba PrefectureNational Agriculture & Food Research Organization千葉県独立行政法人農業・食品産業技術総合研究機構
    • ADACHI ISHIZUEUCHINO KEN
    • A01M1/10A01M1/02A01N49/00
    • Y02A50/374
    • PROBLEM TO BE SOLVED: To provide a capture device for fruit tree stink bugs, which has a high capture efficiency of fruit tree stink bugs, captures and recovers a large amount of fruit tree stink bugs, in a short time.
      SOLUTION: The capture device 1 for fruit tree stink bugs is equipped with a stink bug attraction part 2 for attracting fruit tree stink bugs by an aggregation pheromone agent 70 and a stink bug capture part 3 for capturing fruit tree stink bugs, the stink bug capture part 3 is arranged above the stink bug attraction part 2 and the capture device 1 has a pathway for moving fruit tree stink bugs, and the surface of the pathway is processed unevenly. The stink bug attraction part is preferably constituted by assembling a plurality of skirt boards 11. The stink bug capture part 3 is equipped with a funnel part 4 for concentrating attracted fruit tree stink bugs and a container part 5 for capturing the concentrated fruit tree stink bugs, and the container part 5 is detachably attached to the funnel part 4.
      COPYRIGHT: (C)2008,JPO&INPIT
    • 要解决的问题:为了提供果树臭虫的捕获效果高的果树臭虫的捕获装置,在短时间内捕获并回收大量的果树臭臭虫。

      解决方案:果树臭虫捕获装置1配备有臭虫吸引部分2,用于通过聚集信息素试剂70和用于捕获果树臭虫的臭虫捕获部分3来吸引果树臭虫, 臭鼬捕获部分3布置在臭臭虫吸引部分2上方,并且捕获装置1具有用于移动果树臭虫的路径,并且路径的表面被不均匀地处理。 臭臭虫吸引部优选通过组装多个裙板11构成。臭臭捕捉部3配备有用于集中吸引的果树臭臭的漏斗部4和用于捕获浓缩果树臭虫的容器部5 ,并且容器部分5可拆卸地附接到漏斗部分4.版权所有(C)2008,JPO&INPIT

    • 37. 发明专利
    • Method of screening medicine for amyotrophic lateral sclerosis
    • 筛选用于多发性前列腺切除术的药物的方法
    • JP2008061505A
    • 2008-03-21
    • JP2006239422
    • 2006-09-04
    • Chiba PrefectureHisamitsu Pharmaceut Co Inc久光製薬株式会社千葉県
    • NAKAGAWARA AKIRALIU TIAN-LINGKODA TADAYUKI
    • C12Q1/02C12N15/09C12Q1/48G01N33/15G01N33/50
    • G01N33/6896G01N2333/9121G01N2800/2814
    • PROBLEM TO BE SOLVED: To provide a method of screening therapeutic agents for familial juvenile amyotrophic lateral sclerosis (ALS2). SOLUTION: The method for screening therapeutic agents for familial juvenile amyotrophic lateral sclerosis is provided with a process for determining the substance that inhibits the expression of Tollip in cells as the medicine for the familial juvenile amyotrophic lateral sclerosis. The method for screening therapeutic agents for familial juvenile amyotrophic lateral sclerosis is provided with a process for determining a substance that promotes the transfer of Tollip from cytoplasms to cell nuclei in cells as the therapeutic agent for the familial juvenile amyotrophic lateral sclerosis. The method for screening therapeutic agents for familial juvenile amyotrophic lateral sclerosis is provided with a process for determining a substance that inhibits mutual interaction between Tollip and IRAK-1 in cells as the therapeutic agents for the familial juvenile amyotrophic lateral sclerosis. COPYRIGHT: (C)2008,JPO&INPIT
    • 待解决的问题:提供筛选家族性青少年肌萎缩性侧索硬化症(ALS2)的治疗剂的方法。 解决方案:筛选用于家族性青少年肌萎缩性侧索硬化症的治疗剂的方法具有确定抑制细胞中Tollip的表达的物质作为家族性青少年肌萎缩性侧索硬化症的药物的方法。 用于筛选家族性青少年肌萎缩性侧索硬化症的治疗剂的方法具有确定促进Tollip从细胞质转移到细胞核细胞中作为家族性青少年肌萎缩性侧索硬化症的治疗剂的物质的方法。 筛选用于家族性青少年肌萎缩性侧索硬化症的治疗剂的方法具有确定抑制作为家族性青少年肌萎缩性侧索硬化症的治疗剂的细胞中的Tollip和IRAK-1之间相互作用的物质的方法。 版权所有(C)2008,JPO&INPIT
    • 38. 发明专利
    • Method for creating chimeric adenovirus and pharmaceutical using the same
    • 使用该方法创造重型腺病毒和药物的方法
    • JP2008048621A
    • 2008-03-06
    • JP2006225392
    • 2006-08-22
    • Aristo:KkChiba Prefecture千葉県株式会社アリスト
    • TAGAWA MASATOSHIKAWAMURA KIYOKOTAKENOBU NAONORI
    • C12N7/00A61K35/14A61K35/28A61K35/76A61P35/00C12N15/09
    • C12N15/86A61K35/761C12N2710/10332C12N2710/10343C12N2810/60C12N2810/6018C12N2830/008
    • PROBLEM TO BE SOLVED: To provide a new chimeric adenovirus vector, to provide a method for efficiently creating the same, and to provide pharmaceuticals to which the new chimeric adenovirus vector is applied. SOLUTION: The new chimeric adenovirus is created from a vector DNA with the fiber knob region of type 35 adenovirus integrated in type 5 adenovirus and a second vector DNA where the expression of E1A and E1B genes of the type 5 adenovirus is made controllable by an extraneous transcriptional control region. This chimeric adenovirus, which a modified type 5 adenovirus, is such that its fiber knob region is substituted by the fiber knob region of the type 35 adenovirus and the E1A transcriptional control region is eliminated, and at the resulting site, an arbitrary extraneous transcriptional control region controlling the expression of the E1A and E1B genes is introduced. This chimeric adenovirus is capable of melting cells or tumors, thus being applicable, for example, to pharmaceuticals having high cell-damaging activity against intractable tumors. COPYRIGHT: (C)2008,JPO&INPIT
    • 待解决的问题:提供一种新的嵌合腺病毒载体,以提供有效产生该嵌合腺病毒载体的方法,并提供应用新的嵌合腺病毒载体的药物。 解决方案:新型嵌合腺病毒由载体DNA产生,其中腺病毒5型腺病毒的纤维旋钮区域集成在5型腺病毒中,第2种载体DNA使5型腺病毒E1A和E1B基因的表达可控制 通过外来的转录控制区。 这种嵌合腺病毒是修饰型5型腺病毒,使得其纤维旋钮区域被35型腺病毒的纤维旋钮区域和E1A转录控制区域取代,并且在所得位点处,任意的外来转录控制 介绍了控制E1A和E1B基因表达的区域。 该嵌合腺病毒能够融化细胞或肿瘤,因此可用于例如对难治性肿瘤具有高细胞破坏活性的药物。 版权所有(C)2008,JPO&INPIT
    • 40. 发明专利
    • Concentration measuring device and method
    • 浓度测量装置和方法
    • JP2007322268A
    • 2007-12-13
    • JP2006153521
    • 2006-06-01
    • Atago:KkChiba Prefecture千葉県株式会社アタゴ
    • TORIGOE YOSHIAKIIWAGUCHI YOSHIKAZUTANABE SHINKOBAYASHI SHOZOANZAKI YUKIKOKUBO KENJI
    • G01N27/04
    • PROBLEM TO BE SOLVED: To provide a concentration measuring device capable of measuring the concentration of a measuring object in a solid sample easily, accurately and nondestructively. SOLUTION: This concentration measuring device is equipped with a housing, including an insulating member having the first and second through holes, the first and second rod-like electrodes each of which is engaged respectively with the first and second through holes and extended from the insulating member to be inserted into the solid sample; a power source means for supplying the power between the first and second electrodes; a detection means for detecting at least either of a voltage between the first and second electrodes and a current flowing between the first and second electrodes; a temperature sensor supported by the housing to be inserted into the solid sample, together with the first and second electrodes; a calculation means for calculating the concentration of the measuring object in the solid sample, based on a current value or a voltage value detected by the detection means and a temperature of the solid sample measured by the temperature sensor; and a display means for displaying the concentration calculated. COPYRIGHT: (C)2008,JPO&INPIT
    • 要解决的问题:提供一种能够容易地,准确地且非破坏性地测量固体样品中的测量对象的浓度的浓度测量装置。 解决方案:该浓度测量装置配备有包括具有第一和第二通孔的绝缘构件的壳体,第一和第二棒状电极分别与第一和第二通孔接合并延伸 从绝缘构件插入固体样品; 用于在第一和第二电极之间提供电力的电源装置; 用于检测第一和第二电极之间的电压中的至少一个和在第一和第二电极之间流动的电流的检测装置; 由所述壳体支撑以插入所述固体样品中的温度传感器,与所述第一和第二电极一起; 计算装置,用于根据由检测装置检测的电流值或电压值以及由温度传感器测量的固体样品的温度来计算固体样品中的测量对象的浓度; 以及显示所计算的浓度的显示装置。 版权所有(C)2008,JPO&INPIT