A microscope system (100) configured to record images in at least a first and a second imaging mode (501, 502), comprising: An objective (1) collecting light (201) from a sample (11), An illumination module coupled to the objective, A first reimaging objective (5) generating an intermediate image of the sample and a second reimaging objective (6) that relays the intermediate image onto a detection module, An evaluation module (200) comprising a machine learning method (DL), trained with a first and a second set of images of the same sample, wherein the first and second set has been acquired in the first (501) and second imaging mode (502), respectively, wherein upon acquisition of an image (400) in the second imaging mode (502) the trained machine learning method (DL) outputs a restored image (401) that comprises fewer aberrations than the image (400) acquired in the second imaging mode (52, 53, 57).

An imaging flow cytometer includes at least one flow channel through which an observation target flows, a light source which irradiates the flow channel with sheet-like excitation light, an imaging unit which images a specific cross-section of the observation target by imaging fluorescence from the observation target having passed through a position irradiated with the excitation light, and a three-dimensional image generation unit which generates a three-dimensional image of the observation target as a captured image on the basis of a plurality of captured images obtained by cross-sectional imaging by the imaging unit.

An imaging flow cytometer includes at least one flow channel through which an observation target flows, a light source which irradiates the flow channel with sheet-like excitation light, an imaging unit which images a specific cross-section of the observation target by imaging fluorescence from the observation target having passed through a position irradiated with the excitation light, and a three-dimensional image generation unit which generates a three-dimensional image of the observation target as a captured image on the basis of a plurality of captured images obtained by cross-sectional imaging by the imaging unit.

An objective optical system (43) includes: a reflection surface (RS1) which reflects light traveling toward a sample (SP); a reflection surface (RS2) which reflects light reflected by the reflection surface (RS1) toward the sample (SP); and a transmission portion (TS) which is disposed on an optical path of light reflected by the reflection surface (RS2), which has a liquid contact surface coming into contact with liquid (WT) interposed between the liquid contact surface and the sample (SP), and of which the liquid contact surface is formed to be substantially orthogonal to the optical path of light reflected by the reflection surface (RS2).

An objective optical system (43) includes: a reflection surface (RS1) which reflects light traveling toward a sample (SP); a reflection surface (RS2) which reflects light reflected by the reflection surface (RS1) toward the sample (SP); and a transmission portion (TS) which is disposed on an optical path of light reflected by the reflection surface (RS2), which has a liquid contact surface coming into contact with liquid (WT) interposed between the liquid contact surface and the sample (SP), and of which the liquid contact surface is formed to be substantially orthogonal to the optical path of light reflected by the reflection surface (RS2).

The disclosed flow cytometer includes a wavelength division multiplexer (WDM). The WDM includes an extended light source providing light that forms an object, a collimating optical element that captures light from the extended light source and projects a magnified image of the object as a first light beam, and a first focusing optical element configured to focus the first light beam to a size smaller than the object of the extended light source to a first semiconductor detector. The disclosed flow cytometer further includes a composite microscope objective to direct light emitted by a particle in a flow channel in a viewing zone of the composite microscope to the extended light source, a fluidic system and a peristaltic pump configured to supply liquid sheath and liquid sample to the flow channel, and a laser diode system to illuminate the particle in the flow channel.

The disclosed flow cytometer includes a wavelength division multiplexer (WDM). The WDM includes an extended light source providing light that forms an object, a collimating optical element that captures light from the extended light source and projects a magnified image of the object as a first light beam, and a first focusing optical element configured to focus the first light beam to a size smaller than the object of the extended light source to a first semiconductor detector. The disclosed flow cytometer further includes a composite microscope objective to direct light emitted by a particle in a flow channel in a viewing zone of the composite microscope to the extended light source, a fluidic system and a peristaltic pump configured to supply liquid sheath and liquid sample to the flow channel, and a laser diode system to illuminate the particle in the flow channel.

An image display apparatus according to the present invention includes an image light generator (100) that emits image light, a first reflection element (11) that the image light from the image light generator (100) is to enter, the first reflection element (11) having a transmitting action and a reflecting action on the image light, a second reflection element (12) that reflects, toward the first reflection element (11), the image light that has entered via the first reflection element (11) and causes the image light to re-enter the first reflection element (11), the second reflection element (12) having a reflecting action on the image light, a light-condensing optical system (20) that converges, toward a position of a pupil of an observer, the image light that has re-entered the first reflection element (11), and a controller (40) that controls a placement angle of the first reflection element (11), the second reflection element (12), or both on the basis of the position of the pupil of the observer.

An image display apparatus according to the present invention includes an image light generator (100) that emits image light, a first reflection element (11) that the image light from the image light generator (100) is to enter, the first reflection element (11) having a transmitting action and a reflecting action on the image light, a second reflection element (12) that reflects, toward the first reflection element (11), the image light that has entered via the first reflection element (11) and causes the image light to re-enter the first reflection element (11), the second reflection element (12) having a reflecting action on the image light, a light-condensing optical system (20) that converges, toward a position of a pupil of an observer, the image light that has re-entered the first reflection element (11), and a controller (40) that controls a placement angle of the first reflection element (11), the second reflection element (12), or both on the basis of the position of the pupil of the observer.

The present invention relates to an immersion microscope objective (10) for inspecting a sample (S) in an immersion medium (M), comprising: at least one concave minor (3), at least one optical element (1) comprising an aspherical surface (2) facing the at least one concave minor (3), and an internal space (4) arranged between the at least one concave minor (3) and said aspherical surface (2), said internal space (4) being configured to be filled with an immersion medium (M) such that the immersion medium (M) contacts the at least one concave minor (3) and the aspherical surface (2). According to the present invention, the aspherical interface (2) is shaped such that the working distance (7) of the immersion microscope objective (10) varies by less than 1% when the refractive index n of said immersion medium (M) is increased or decreased by at least 0.025.