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    • 4. 发明公开
    • MICROSCOPE
    • 显微镜
    • EP3293559A1
    • 2018-03-14
    • EP17186629.6
    • 2017-08-17
    • Olympus Corporation
    • BRINKMAN, BrendanSHIMADA, Yoshihiro
    • G02B21/33G02B21/00G02B21/26
    • G02B21/33G01N21/0303G01N21/6458G01N2021/0342G01N2021/0367G02B21/006G02B21/0088G02B21/086G02B21/16G02B21/22G02B21/26G02B21/34G02B21/361
    • Highly reliable observation is achieved by preventing a liquid immersion medium from running out while still reducing the amount and replenishment frequency of the liquid immersion medium with a simple and inexpensive structure. Provided is a microscope 1 including: a chamber 5 that stores a solution W2 in which a cuvette 3 accommodating a solution W1 together with a sample S is immersed and that has an index of refraction identical to that of the solution W1; an immersion objective lens 11 that is placed outside the chamber 5 and that collects light emitted from the sample S; a camera 31 that acquires an image of the light collected by the immersion objective lens 11; a targeting section 12 that moves the immersion objective lens 11 in a direction along a detection light axis P thereof; and a movable stage 7 that supports the cuvette 3 in the chamber 5 so as to be movable in at least a direction along the detection light axis P, wherein the cuvette 3 and the chamber 5 have a transparent section 3b and a transparent section 5b that can transmit light coming from the sample S, and the immersion objective lens 11 is placed so as to face the transparent section 3b of the cuvette 3 with the transparent section 5b of the chamber 5 interposed therebetween.
    • 通过防止液体浸渍介质用完,同时通过简单和廉价的结构仍然减少液体浸渍介质的量和补充频率来实现高度可靠的观察。 本发明提供一种显微镜1,其包括:腔室5,其内部收纳有溶液W2,在该溶液W2中浸渍有与溶液W1一起浸渍有溶液W1的反应杯3,并具有与溶液W1相同的折射率; 浸没物镜11,其设置在腔室5的外侧并且收集从样品S发射的光; 摄像机31,其获取由浸渍物镜11收集的光的图像; 瞄准部12,其使浸渍用物镜11沿着其检测光轴P的方向移动; 以及可移动台7,该可移动台7将腔室5内的反应杯3支承为能够沿着检测光轴P的至少一个方向移动,其中,反应杯3和腔室5具有透明部3b和透明部5b 可以透过来自样品S的光,并且浸渍物镜11被放置为与腔室5的透明部分5b介于其间的反应杯3的透明部分3b相对。
    • 8. 发明公开
    • MEHRFARBEN-SCANNING-MIKROSKOP
    • 更多的色彩扫描显微镜
    • EP3084502A1
    • 2016-10-26
    • EP14827438.4
    • 2014-12-19
    • Carl Zeiss Microscopy GmbH
    • BATHE, Wolfgang
    • G02B21/00
    • G02B21/0076G02B21/0032G02B21/006G02B21/0064G02B21/008G02B21/18
    • The invention relates to a multi-color scanning microscope comprising at least one first light source for emitting a first excitation beam comprising first excitation light having a first wavelength and a second light source for emitting a second excitation beam comprising second excitation light having a second wavelength, which differs from the first wavelength, comprising coupling-in means for coupling the first excitation beam and/or the second excitation beam into an excitation beam path, comprising optical means for guiding the first excitation beam and the second excitation beam to a sample and for guiding detection light emitted by the sample in a detection beam path to a detection unit, wherein the optical means comprise at least the following components: at least one first main color splitter for separating the first excitation light and/or the second excitation light, on the one hand, from the detection light emitted by the sample, on the other hand, a scanner for scanning the sample with at least the first excitation light and the second excitation light, a microscope objective for focusing the first excitation light and the second excitation light onto or into the sample and for guiding the detection light emitted by the sample in the direction of the detection unit, and comprising the detector unit for detecting the detection light emitted by the sample. The microscope is characterized in that the coupling-in means and at least parts of the optical means are designed and arranged in such a way that the first excitation beam having the first wavelength is guided onto a first sample location and the second excitation beam having the second wavelength is guided onto a second sample location, which differs from the first sample location, and in that the detector unit comprises a first detector for detecting the light emitted by the first sample location and a second detector for detecting the light emitted by the second sample location.