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    • 1. 发明申请
    • PLANT-BASED RECOMBINANT BUTYRYLCHOLINESTERASE PRODUCTION METHODS
    • 基于植物的重组丁基胆碱酯酶生产方法
    • WO2015050627A1
    • 2015-04-09
    • PCT/US2014/049387
    • 2014-08-01
    • POGUE, GregHIATT, ErnieKANDZIA, RomyWERNER, StefanTHIEME, FrankMOR, Tsafrir
    • POGUE, GregHIATT, ErnieKANDZIA, RomyWERNER, StefanTHIEME, FrankMOR, Tsafrir
    • C12N9/00
    • C12N9/18A61K38/465C12Y301/01008
    • A new, reliable, easily scalable and reproducible method for the production of recombinant butyrylcholinesterase (rBuChE) is provided. Through the utilization of a plant transfection procedure, various plant strains have been shown to generate effective and scalable amounts of rBuChE under acceptable manufacturing processes to permit reliable levels of such enzymes for desired nerve agent protection requirements (including tetrameric products). As well, such methods in engineered plant lines have shown suitable production of these enzymes in tetramer form with glycan formation and sialyalation (for terminal groups) to allow for optimal potency against organophosphorus agent exposure as well as proper immunogenic response within the plant sources. The overall production method, including the transfection and production within mammalian cells, as well as the process steps involved for such a reliable sourcing platform from plants is thus encompassed within the invention.
    • 提供了一种用于生产重组丁酰胆碱酯酶(rBuChE)的新的,可靠的,易于扩展和重现的方法。 通过利用植物转染方法,已经显示各种植物菌株在可接受的制造过程中产生有效和可缩放量的rBuChE,以允许可靠水平的这些酶用于所需的神经药物保护要求(包括四聚物产品)。 同样,工程化植物品系中的这些方法已经显示出以四聚体形式合适地生产这些酶,其中聚糖形成和sialyalation(用于末端基团)以允许针对有机磷剂暴露的最佳效力以及在植物来源内的适当的免疫原性反应。 因此,包括哺乳动物细胞内的转染和生产的总体生产方法以及从植物获得这种可靠的采购平台所涉及的工艺步骤。
    • 2. 发明申请
    • ROGOWSKI-SENSOR UND VERFAHREN ZUM MESSEN EINES STROMES
    • ROGOWSKI传感器和方法测量当前
    • WO2008077798A1
    • 2008-07-03
    • PCT/EP2007/063834
    • 2007-12-12
    • SIEMENS AKTIENGESELLSCHAFTERMISCH, JochenHERING, UweTHIEME, FrankVOLKMAR, Ralf-Reiner
    • ERMISCH, JochenHERING, UweTHIEME, FrankVOLKMAR, Ralf-Reiner
    • G01R15/18
    • G01R15/181
    • Die Erfindung bezieht sich u. a. auf einen Rogowski-Sensor (10) zum Messen eines Stromes (I1(t)) eines Stromleiters (90) mit einer einen elektrischen Wicklungswiderstand (Rr) aufweisenden Rogowskispule (20) und einer mit der Rogowskispule in Verbindung stehenden Integrationseinrichtung zum Erzeugen eines Ausgangssignals (Ua(t)), das zu dem von dem Rogowski-Sensor zu messenden elektrischen Strom (I1(t)) proportional ist. Erfindungsgemäß ist vorgesehen, dass die Integrationseinrichtung durch den Wicklungswiderstand (Rr) der Rogowskispule (20) und einen mit den beiden Wicklungsanschlüssen (50, 60) der Rogowskispule in Verbindung stehende Kapazität (Ci) gebildet ist und das Ausgangssignal der Integrationseinrichtung durch die an der Kapazität (Ci) anliegende Spannung (Ua(t)) gebildet wird.
    • 本发明涉及Ú。 一。 罗氏传感器(10),用于一个电流导体(90)具有电绕组电阻(RR),其具有罗氏线圈(20)和与所述罗柯夫斯基线圈的集成相关的装置,用于产生一输出信号的测量的电流(I1(t))的( UA(t))的与所述罗戈夫斯基传感器的测量电流相关联的(I1(t))的成比例。 根据本发明,它提供了集成的罗果夫斯基线圈(20)和一个在与所述绕组电阻(RR)通信罗果夫斯基线圈的两个绕组端子(50,60)的装置由在容量形成电容(Ci)与积分装置的输出信号 (次)形成施加的电压(Ua的(t))的。
    • 3. 发明申请
    • METHOD AND DEVICE FOR MEASURING CURRENT
    • 方法和设备用于测量电流
    • WO1998016839A1
    • 1998-04-23
    • PCT/DE1997002348
    • 1997-10-14
    • SIEMENS AKTIENGESELLSCHAFTERMISCH, JochenSTEPHAN, UweTHIEME, FrankBAUERSCHMIDT, Peter
    • SIEMENS AKTIENGESELLSCHAFT
    • G01R15/14
    • G01R15/146
    • In order to accurately measure currents with high dynamic range, specially in a gas-isolated power switchgear, a first signal (A1) of a first low-power measuring transducer (6) and a second signal (A2) of a second magnet-free measuring transducer (8), for instance, working according to the principle of a Rogowski coil or the Faraday effect, are compared. Depending on the degree of accuracy, one of the two signals (A1, A2) is selected and further processed. The deviation of both signals (A1, A2), specially their gradient, is used as comparison criteria. Both different type measuring transducers (6, 8) are connected to a common processing module (12) to process the signal in a corresponding device.
    • 为电流的具有高动态范围的精确测量,特别是在一个气体绝缘开关柜,是第一信号的第一低功率换能器的(A1)(6)和第二磁体 - 自由,例如第二信号(A2) 根据一个罗柯夫斯基线圈或法拉第效应的原理工作的,换能器(8)进行比较。 在这种情况下根据两个信号(A1,A2)和进一步处理的准确度被选择。 作为比较的标准是两个信号(A1,A2)彼此的偏差,特别是所使用的梯度。 与具有共同的处理模块(12)的不同类型被连接用于信号处理的两个测量换能器的适当装置(6,8)。
    • 4. 发明申请
    • PROCESS OF CLEAN CLONING
    • 清洁过程
    • WO2010040531A3
    • 2010-07-01
    • PCT/EP2009007237
    • 2009-10-08
    • ICON GENETICS GMBHMARILLONNET SYLVESTREWERNER STEFANENGLER CAROLAKANDZIA ROMYTHIEME FRANKWEBER ERNST
    • MARILLONNET SYLVESTREWERNER STEFANENGLER CAROLAKANDZIA ROMYTHIEME FRANKWEBER ERNST
    • C12N15/09C12N15/10
    • C12N15/64C12N15/66
    • A process of inserting a nucleic acid sequence of interest into an acceptor nucleic acid, comprising the following steps: amplifying by PCR a DNA comprising in the following order a sequence segment U, a nucleic acid sequence segment of known nucleotide sequence K2 and a nucleic acid sequence segment of known sequence K3 using a forward primer defining a first end of the amplified DNA and a reverse primer defining a second end of the amplified DNA, said reverse primer terminating at its 3'-end in a nucleotide sequence of nucleic acid sequence segment K3; treating the linear double-stranded DNA molecules contained in the PCR product obtained in the previous step with an exonuclease to obtain a single-stranded overhang at the first end of the DNA and a single-stranded overhang comprising nucleic acid segments K2 and K3 at the second end of the DNA; and annealing the product of the previous step to a linearized double-stranded acceptor nucleic acid having at a first end thereof a single-stranded overhang complementary to the single-stranded overhang of the first end of the DNA and at a second end thereof a single- stranded overhang complementary to the single-stranded sequence segment K2 of the second end of the DNA.
    • 包括以下步骤:通过PCR扩增包含以下顺序的DNA序列的已知核苷酸序列K2的核酸序列片段和核酸的方法 已知序列K3的序列片段使用限定扩增DNA第一末端的正向引物和限定扩增DNA第二末端的反向引物,所述反向引物在其核酸序列片段的核苷酸序列的3'末端终止 K3; 用外切核酸酶处理前一步骤中获得的PCR产物中包含的线性双链DNA分子,以在DNA的第一端获得单链突出端,并且在第一端包含核酸片段K2和K3的单链突出端 DNA的第二端; 并将前述步骤的产物退火到线性双链受体核酸,其在第一端具有与DNA的第一末端的单链突出部互补的单链突出端,并且在其第二端具有单链突出端 - 与DNA的第二末端的单链序列片段K2互补的双链突出端。
    • 5. 发明申请
    • PROCESS OF CLEAN CLONING
    • 清洁克隆过程
    • WO2010040531A2
    • 2010-04-15
    • PCT/EP2009/007237
    • 2009-10-08
    • ICON GENETICS GMBHMARILLONNET, SylvestreWERNER, StefanENGLER, CarolaKANDZIA, RomyTHIEME, FrankWEBER, Ernst
    • MARILLONNET, SylvestreWERNER, StefanENGLER, CarolaKANDZIA, RomyTHIEME, FrankWEBER, Ernst
    • C12N15/09C12N15/10
    • C12N15/64C12N15/66
    • A process of inserting a nucleic acid sequence of interest into an acceptor nucleic acid, comprising the following steps: amplifying by PCR a DNA comprising in the following order a sequence segment U, a nucleic acid sequence segment of known nucleotide sequence K2 and a nucleic acid sequence segment of known sequence K3 using a forward primer defining a first end of the amplified DNA and a reverse primer defining a second end of the amplified DNA, said reverse primer terminating at its 3'-end in a nucleotide sequence of nucleic acid sequence segment K3; treating the linear double-stranded DNA molecules contained in the PCR product obtained in the previous step with an exonuclease to obtain a single-stranded overhang at the first end of the DNA and a single-stranded overhang comprising nucleic acid segments K2 and K3 at the second end of the DNA; and annealing the product of the previous step to a linearized double-stranded acceptor nucleic acid having at a first end thereof a single-stranded overhang complementary to the single-stranded overhang of the first end of the DNA and at a second end thereof a single- stranded overhang complementary to the single-stranded sequence segment K2 of the second end of the DNA.
    • 将感兴趣的核酸序列插入受体核酸中的方法,包括以下步骤:通过PCR扩增包含以下顺序的DNA的序列:序列区段U,核酸序列片段 使用限定扩增的DNA的第一末端的正向引物和限定扩增的DNA的第二末端的反向引物的已知核苷酸序列K2和已知序列K3的核酸序列区段,所述反向引物在其3'末端终止于 核酸序列片段K3的核苷酸序列; 用外切核酸酶处理在前一步骤中获得的PCR产物中所含的线性双链DNA分子,以在DNA的第一末端获得单链突出端和单链突出端,所述单链突出端包含位于第一端的核酸片段K2和K3 DNA的第二末端; 和将前一步骤的产物退火成线性化双链受体核酸,所述线性化双链受体核酸在其第一末端具有与DNA第一末端的单链突出端互补的单链突出端,并且在其第二末端具有单一突出端 - 与DNA第二末端的单链序列片段K2互补的多余突出端。