Scanning microscope, and method for light microscopy imaging of a specimen
US-9030734-B2 · May 12, 2015 · US
US9829691B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9829691-B2 |
| Application number | US-201314436938-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 4, 2013 |
| Priority date | Oct 23, 2012 |
| Publication date | Nov 28, 2017 |
| Grant date | Nov 28, 2017 |
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A microscope includes at least one illuminating lens configured to guide at least one illuminating beam in the form of a light sheet for illuminating at least one specimen to be examined. The microscope also includes at least one detection lens configured to capture at least one detection beam issuing from the at least one specimen to be examined. The at least one illuminating lens has an optical axis at an angle α, which is not equal to 90°, to an optical axis of the at least one detection lens. The at least one illuminating beam enters the at least one illuminating lens at an entry angle β such that the light sheet lies within a focal plane of the at least one detection lens.
Opening claim text (preview).
The invention claimed is: 1. A microscope comprising: a first illuminating lens configured to guide at least one first illuminating beam in the form of a first light sheet for illuminating at least one specimen to be examined; a second illuminating lens configured to guide at least one second illuminating beam in the form of a second light sheet for illuminating the at least one specimen to be examined; and at least one detection lens configured to capture at least one detection beam issuing from the at least one specimen to be examined, wherein an optical axis of the first illuminating lens is at an angle α, which is not equal to 90°, to an optical axis of the at least one detection lens, wherein an optical axis of the second illuminating lens is at an angle α′, which is not equal to 90°, to an optical axis of the at least one detection lens, wherein the at least one first illuminating beam enters the first illuminating lens at a non-zero entry angle β to the optical axis of the first illuminating lens, as a result of which the first light sheet lies within a focal plane of the at least one detection lens and extends perpendicularly to the optical axis of the detection lens, and wherein the at least one second illuminating beam enters the second illuminating lens at a non-zero entry angle β′ to the optical axis of the second illuminating lens, as a result of which the second light sheet lies within a focal plane of the at least one detection lens and extends perpendicularly to the optical axis of the detection lens. 2. The microscope according to claim 1 , wherein the at least one first illuminating beam enters the first illuminating lens outside the optical axis thereof. 3. The microscope according to claim 2 , wherein the angle α has a value from 120° to 150°. 4. The microscope according to claim 3 , wherein the angle α has a value of approximately 135°. 5. The microscope according to claim 1 , wherein at least two detection lenses are provided and arranged in an objective revolver. 6. The microscope according to claim 1 , wherein structurally identical lenses are used for the at least one detection lens and at least one of the first illuminating lens or the second illuminating lens. 7. The microscope according to claim 1 , further comprising: at least two light sources, which radiate different wavelengths from one another; and at least two detection devices configured to detect the wavelengths that are different from one another. 8. The microscope according to claim 1 , further comprising a first movement arrangement configured to generate a relative movement between a specimen illumination region and the specimen to be examined, wherein the specimen is placed on a stage. 9. The microscope according to claim 8 , further comprising a second movement arrangement configured to move the stage in one plane. 10. The microscope according to claim 8 , wherein the specimen to be examined is placed on the stage by means of a slide. 11. The microscope according to claim 8 , wherein the first illuminating lens and the at least one detection lens are each designed as immersion lenses and are located at least in part in an immersion medium together with the specimen to be examined. 12. The microscope according to claim 1 , wherein the specimen to be examined is placed on a fixed stage, further comprising: at least one device for changing the angle β, and wherein the focal plane of the at least one detection lens can be repositioned. 13. The microscope according to claim 1 , wherein the at least one detection lens configured to capture at least one detection beam issuing from the at least one specimen to be examined comprises a first detection lens configured to capture a first detection beam issuing from the at least one specimen to be examined and a second detection lens configured to capture a second detection beam issuing from the at least one specimen to be examined, wherein the first detection lens has an optical axis and the second detection lens has an optical axis, and wherein the optical axis of the first detection lens is parallel to the optical axis of the second detection lens.
providing an output produced by processing a plurality of individual source images, e.g. image tiling, montage, composite images, depth sectioning, image comparison · CPC title
Condensers · CPC title
Microscope slides, e.g. mounting specimens on microscope slides · CPC title
Optical details, e.g. image relay to the camera or image sensor (G02B21/364 takes precedence; illumination details G02B21/06 and subgroups) · CPC title
Base structure · CPC title
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