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    • 5. 发明授权
    • Sensorless motor driving apparatus
    • 无传感器电机驱动装置
    • US06483266B2
    • 2002-11-19
    • US09908433
    • 2001-07-18
    • Shinichi MiyazakiAkihiko Ikegami
    • Shinichi MiyazakiAkihiko Ikegami
    • H02K2300
    • H02P8/14H02P6/182H02P6/21
    • When the brushless motor 1 at rest is started, phase excitation is performed twice such that different phases are excited. A commutation reference point is set at a position at which a rotor has stopped after the second-time excitation. A position detector outputs pulse signals in response to a movement of an object driven by the brushless motor 1. The pulse signals output from the position detector are monitored and commutation is controlled on the basis of the number of pulse edges of the pulse signals as counted starting from the commutation reference point. For example, the number of pulse edges output during a period starting from the commutation reference point and ending at a point of time at which commutation should be performed is measured in advance. When the number of pulse edges with reference to the commutation reference point becomes equal to the above predetermined number, it is determined that commutation timing has reached, and commutation is performed.
    • 当静止时的无刷马达1开始时,相位激励被执行两次,使得不同的相被激励。 在转子在第二次激励之后停止的位置处设置换向参考点。 位置检测器响应于由无刷电动机1驱动的物体的移动而输出脉冲信号。监视从位置检测器输出的脉冲信号,并根据计数的脉冲信号的脉冲边缘的数量来控制换向 从换向参考点开始。 例如,在从换向参考点开始并在应该进行换向的时间点结束的时段期间输出的脉冲边缘的数量被预先测量。 当相对于换向参考点的脉冲边缘数量等于上述预定数量时,确定已经达到换向定时并且执行换向。
    • 6. 发明授权
    • Method for detecting a bacterial pathogen
    • 检测细菌病原体的方法
    • US09181592B2
    • 2015-11-10
    • US12056633
    • 2008-03-27
    • Yiping W. HanAkihiko Ikegami
    • Yiping W. HanAkihiko Ikegami
    • C12Q1/68C12Q1/04
    • C12Q1/689C12Q1/04
    • A method is provided for detecting a bacterial pathogen in a sample. One step of the method includes obtaining a sample and then subjecting the sample to nested PCR. The nested PCR is conducted in the presence of at least two outer oligonucleotide primers complementary to a target nucleotide sequence of the bacterial pathogen so that a first amplified product is produced. The target nucleotide sequence includes at least a portion of a 16S-23S ribosomal RNA sequence. The first amplified product is subjected to the nested PCR in the presence of at least two inner oligonucleotide primers complementary to the nucleotide sequence of the first amplified product so that a second amplified product is obtained. Detection of the second amplified product indicates the presence of the bacterial pathogen in the sample.
    • 提供了用于检测样品中细菌病原体的方法。 该方法的一个步骤包括获得样品,然后使样品进行巢式PCR。 在至少两个与细菌病原体的靶核苷酸序列互补的外部寡核苷酸引物的存在下进行嵌套PCR,从而产生第一个扩增产物。 靶核苷酸序列包括16S-23S核糖体RNA序列的至少一部分。 在与第一扩增产物的核苷酸序列互补的至少两个内部寡核苷酸引物的存在下,将第一扩增产物进行嵌套PCR,从而获得第二扩增产物。 第二次扩增产物的检测表明样品中存在细菌病原体。