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    • 11. 发明申请
    • DEVICE AND METHOD FOR SCANNING AN OBJECT AND A MICROSCOPE
    • 用于扫描对象和显微镜的装置和方法
    • US20130044370A1
    • 2013-02-21
    • US13578608
    • 2011-02-11
    • Volker SeyfriedBernd WidzgowskiHolger Birk
    • Volker SeyfriedBernd WidzgowskiHolger Birk
    • G02B21/33
    • G02B21/33G02B21/0036
    • The invention relates to a device for scanning an object comprising a focusing lens system (30) which focuses an illuminating light beam (24) onto a region of the object to be analyzed. An actuator assembly is coupled to the focusing lens system (30) and moves the focusing lens system (30) in accordance with a predefined scanning pattern transversely to the cecenternter axis of the illumination light beam (24) in a reference position of the illumination light beam (24). A front glass (38) is disposed downstream of the focusing lens system (30) viewed in the direction of the illuminating light beam (24). An internal immersion medium (40) is disposed between the focusing lens system (30) and the front glass (38). An external immersion medium (48) can be introduced between the front glass (38) and the object.
    • 本发明涉及一种用于扫描物体的装置,包括聚焦透镜系统(30),其将照明光束(24)聚焦在被分析物体的区域上。 致动器组件联接到聚焦透镜系统(30)并且在照明光的参考位置中根据预定的扫描图案横向于照明光束(24)的入射角轴线移动聚焦透镜系统(30) 梁(24)。 从照明光束(24)的方向观察,配置在聚焦透镜系统(30)的下游的前玻璃(38)。 在聚焦透镜系统(30)和前玻璃(38)之间设置内部浸没介质(40)。 可以在前玻璃(38)和物体之间引入外部浸没介质(48)。
    • 15. 发明申请
    • Method and Device for Light-Microscopic Imaging of a Sample Structure
    • 用于样品结构的光显微镜成像的方法和装置
    • US20130222568A1
    • 2013-08-29
    • US13806047
    • 2011-06-27
    • Marcus DybaVolker Seyfried
    • Marcus DybaVolker Seyfried
    • G02B21/36
    • G02B21/365G01N21/6428G01N21/6458G02B21/16G02B21/367G02B27/58
    • A method for light-microscopy imaging of a sample structure (2, 34) is described, having the following steps: preparing the sample structure (2, 34) with markers that are transferrable into a state imageable by light microscopy, generating a sequence of individual-image data sets by sequential imaging of the sample structure (2, 34), in such a way that for each image, only a subset of the totality of the markers is in each case transferred into the state imageable by light microscopy, the markers of the respective subset having an average spacing from one another which is greater than the resolution limit of light-microscopy imaging which determines the extent of a light distribution representing one of the respectively imaged markers, generating at least two data blocks in which multiple successive individual-image data sets are respectively combined, superposing the individual-image data sets contained in the respective data block to yield a superposed-image data set, identifying an image offset between the superposed-image data sets, correcting the individual-image data sets that are contained in at least one of the superposed-image data sets on the basis of the identified image offset, determining center point positions of the light distributions representing the imaged markers, and assembling the center point positions into an offset-corrected overall image.
    • 描述了一种用于样品结构(2,34)的光学显微镜成像的方法,具有以下步骤:用可转移到可通过光学显微镜成像的状态的标记物制备样品结构(2,34),产生序列 通过对样本结构(2,34)进行顺序成像,通过对每个图像进行顺序成像的单个图像数据集,只有标记的全部子集在每种情况下都转移到通过光学显微镜可成像的状态, 相应子集的标记具有彼此之间的平均间隔,其大于光学显微镜成像的分辨率极限,其确定表示分别成像的标记之一的光分布的程度,生成至少两个数据块,其中多个连续 分别组合各个图像数据集,将包含在各个数据块中的各个图像数据集叠加以产生叠加图像数据集,识别 叠加图像数据组之间的图像偏移,基于所识别的图像偏移来校正包含在至少一个叠加图像数据集中的各个图像数据集,确定表示所述图像偏移的光分布的中心点位置 成像标记,以及将中心点位置组装成偏移校正的整体图像。
    • 16. 发明授权
    • Confocal microscope and method for detecting by means of a confocal microscope
    • 共聚焦显微镜和共聚焦显微镜检测方法
    • US07817271B2
    • 2010-10-19
    • US12044951
    • 2008-03-08
    • Volker SeyfriedFrank Schreiber
    • Volker SeyfriedFrank Schreiber
    • G01J3/28
    • G02B21/0064
    • The invention relates to a confocal microscope which illuminates a sample (15) by means of at least one light source. A detection light beam (17) is emitted from the sample (15). The detection light beam (17) is spectrally split up in a spatial manner by the dispersive element (20) and subsequently formed on a photosensor chip (19) by means of a detection optical system (22). At least one expanding optical system (23) is arranged in front of the dispersive element (20) in the direction of the detection light beam (17). The expanding optical system (23) is embodied in such a manner that the numerical aperture of the detection optical system (22) is independent from the numerical aperture of the detection light beam (17) on the detection apertured diaphragm (18).
    • 本发明涉及通过至少一个光源照射样品(15)的共聚焦显微镜。 从样品(15)发射检测光束(17)。 检测光束(17)通过色散元件(20)以空间方式进行光谱分离,随后通过检测光学系统(22)形成在光电传感器芯片(19)上。 至少一个扩展光学系统(23)沿着检测光束(17)的方向布置在色散元件(20)的前面。 扩展的光学系统(23)以使得检测光学系统(22)的数值孔径独立于检测孔径隔膜(18)上的检测光束(17)的数值孔径的方式实现。