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    • 3. 发明申请
    • Air outlet device for vehicle cabin
    • 车厢出风装置
    • US20070066206A1
    • 2007-03-22
    • US11448995
    • 2006-06-07
    • Michio OnoMasahiro EndouKeiko Tanaka
    • Michio OnoMasahiro EndouKeiko Tanaka
    • B60H1/00
    • B60H1/3421B60H1/3428
    • In an air outlet device for a vehicle cabin, primary wind-direction adjustment plates are rotated between a parallel condition and a series condition, to thereby provide a wind distribution function of opening the outlet opening of a tubular body and adjusting the flow direction of air and a wind shutoff function of closing the outlet opening. Of the primary wind-direction adjustment plates, a certain primary wind-direction adjustment plate is configured such that its tip end edge gradually separates from an inner wall surface of the tubular body when the primary wind-direction adjustment plates are rotated so as to open the outlet opening. A secondary wind-direction adjustment plate is secured to the back of the certain primary wind-direction adjustment plate with a predetermined spacing formed therebetween. The secondary wind-direction adjustment plate rotates, together with the certain primary wind-direction adjustment plate, about the rotation center of the certain primary wind-direction adjustment plate.
    • 在车厢的出风装置中,主风向调节板在平行状态和串联状态之间旋转,从而提供打开管状体的出口的风力分配功能,并调节空气的流动方向 以及关闭出口的风切断功能。 在主风向调节板中,主风向调整板被构造为使得当主风向调节板旋转以使其开口时其顶端边缘与管状体的内壁表面逐渐分离 出口开口。 二次风向调整板以特定的间隔形成在一定的主风向调整板的背面。 二次风向调整板与某一个主风向调整板一起围绕某一主风向调整板的旋转中心旋转。
    • 6. 发明申请
    • METHOD OF DETECTING OR QUANTITATING ENDOGENOUS WHEAT DNA AND METHOD OF DETERMINING CONTAMINATION RATE OF GENETICALLY MODIFIED WHEAT IN TEST SAMPLE
    • 检测或定量内源性DNA的方法和测定样品中遗传修饰小麦污染率的方法
    • US20120208992A1
    • 2012-08-16
    • US13366190
    • 2012-02-03
    • Shinjiro IMAIKeiko Tanaka
    • Shinjiro IMAIKeiko Tanaka
    • C07H21/04
    • C12Q1/6895
    • An object of the present invention is to discover an endogenous wheat sequence satisfying the conditions of: a) it is universally present in varieties of wheat, b) the amount present (detected amount) is not affected depending on the wheat variety, c) even if other grains are present, only wheat can be detected without cross-reactivity, and d) it is amplified quantitatively by the PCR reaction. A further object of the present invention is to provide a method of accurately detecting and quantitating endogenous wheat DNA in a test sample by the polymerase chain reaction. The present invention provides replicable DNA comprising: a DNA sequence as endogenous DNA common to both genetically modified wheat and non-genetically modified wheat; and one or more DNA sequence each comprising a sequence that is specific to a strain of genetically modified wheat.
    • 本发明的目的是发现满足以下条件的内源性小麦序列:a)其在小麦品种中普遍存在,b)存在量(检测量)不受小麦品种的影响,c)均匀 如果存在其他颗粒,则只能检测到小麦不具有交叉反应性,并且d)通过PCR反应定量扩增。 本发明的另一个目的是提供通过聚合酶链式反应准确地检测和定量测试样品中的内源性小麦DNA的方法。 本发明提供可复制的DNA,其包含:作为转基因小麦和非转基因小麦共有的内源DNA的DNA序列; 和一个或多个DNA序列,每个DNA序列各自包含对转基因小麦品系特异的序列。
    • 7. 发明授权
    • Method of detecting or quantitating endogenous wheat DNA and method of determining contamination rate of genetically modified wheat in test sample
    • 检测或定量内源性小麦DNA的方法和测定样品中转基因小麦污染率的方法
    • US08173400B2
    • 2012-05-08
    • US12300973
    • 2007-05-11
    • Shinjiro ImaiKeiko Tanaka
    • Shinjiro ImaiKeiko Tanaka
    • C12P19/34C12Q1/68
    • C12Q1/6895
    • An object of the present invention is to discover an endogenous wheat sequence satisfying the conditions of: a) it is universally present in varieties of wheat, b) the amount present (detected amount) is not affected by the wheat variety, c) even if other grains are present, only wheat can be detected without cross-reactivity, and d) it is amplified quantitatively by the PCR reaction. A further object of the present invention is to provide a method of accurately detecting and quantitating endogenous wheat DNA in a test sample by the polymerase chain reaction. The present invention provides a method of detecting or quantitating endogenous wheat DNA in a test sample by the polymerase chain reaction, the method comprising: a step of using a nucleic acid molecule in the test sample or a nucleic acid molecule extracted from the test sample as a template to amplify the nucleic acid molecule of a region consisting of the nucleotide sequence identified as SEQ ID NO: 2 or a partial sequence thereof with a primer pair capable of amplifying that region; and a step of detecting or quantitating the amplified nucleic acid molecule.
    • 本发明的目的是发现满足以下条件的内源性小麦序列:a)其在小麦品种中普遍存在,b)存在量(检测量)不受小麦品种的影响,c)即使 其他颗粒存在,只有小麦可以检测到没有交叉反应性,和d)通过PCR反应定量扩增。 本发明的另一个目的是提供通过聚合酶链式反应准确地检测和定量测试样品中的内源性小麦DNA的方法。 本发明提供了通过聚合酶链式反应检测或定量测试样品中的内源性小麦DNA的方法,所述方法包括:使用测试样品中的核酸分子或从测试样品中提取的核酸分子的步骤 用于扩增由SEQ ID NO:2所鉴定的核苷酸序列组成的区域的核酸分子或其部分序列的扩增该区域的引物对的模板; 以及检测或定量扩增的核酸分子的步骤。
    • 10. 发明申请
    • METHOD OF DETECTING OR QUANTITATING ENDOGENOUS WHEAT DNA AND METHOD OF DETERMINING CONTAMINATION RATE OF GENETICALLY MODIFIED WHEAT IN TEST SAMPLE
    • 检测或定量内源性DNA的方法和测定样品中遗传修饰小麦污染率的方法
    • US20100062432A1
    • 2010-03-11
    • US12300973
    • 2007-05-11
    • Shinjiro IMAIKeiko Tanaka
    • Shinjiro IMAIKeiko Tanaka
    • C12Q1/68C07H21/04
    • C12Q1/6895
    • An object of the present invention is to discover an endogenous wheat sequence satisfying the conditions of: a) it is universally present in varieties of wheat, b) the amount present (detected amount) is not affected depending on the wheat variety, c) even if other grains are present, only wheat can be detected without cross-reactivity, and d) it is amplified quantitatively by the PCR reaction. A further object of the present invention is to provide a method of accurately detecting and quantitating endogenous wheat DNA in a test sample by the polymerase chain reaction. The present invention provides a method of detecting or quantitating endogenous wheat DNA in a test sample by the polymerase chain reaction, the method comprising: a step of using a nucleic acid in the test sample or a nucleic acid extracted from the test sample as a template to amplify the nucleic acid of a region consisting of the base sequence identified as SEQ ID NO: 2 or a partial sequence thereof with a primer pair capable of amplifying that region; and a step of detecting or quantitating the amplified nucleic acid.
    • 本发明的目的是发现满足以下条件的内源性小麦序列:a)其在小麦品种中普遍存在,b)存在量(检测量)不受小麦品种的影响,c)均匀 如果存在其他颗粒,则只能检测到小麦不具有交叉反应性,并且d)通过PCR反应定量扩增。 本发明的另一个目的是提供通过聚合酶链式反应准确地检测和定量测试样品中的内源性小麦DNA的方法。 本发明提供了通过聚合酶链式反应检测或定量测试样品中的内源小麦DNA的方法,所述方法包括:将测试样品中的核酸或从测试样品提取的核酸作为模板的步骤 以由具有鉴定为SEQ ID NO:2的碱基序列或其部分序列组成的区域的核酸与能够扩增该区域的引物对扩增; 以及检测或定量扩增的核酸的步骤。