Microscopes TRIZ Cases

SCAPE microscopy replaces mechanical sample translation with a single objective and swept light sheet to capture 3D dynamics at over 20 volumes per second.

A light-field microscope uses a microlens array to collect fluorescence while an illumination system radiates excitation light with a predetermined width.

Lowering the laser repetition rate enables time-gated detection that removes background noise and improves signal-to-noise ratio.

Asymmetrical telescope systems with a movable prism group resolve the contradiction between high resolution and compact equipment dimensions.

Automated acquisition planner generates optimized scanning paths using adaptive sampling to record fluorescence signals.

An eccentric second illumination system changes the principal ray angle to resolve inconsistent stereoscopic effects during binocular eye examination.

A microscope system uses chromatic aberration to acquire multiple focal planes simultaneously via wavelength dispersion.

Structured excitation beams create intensity minima to localize individual fluorescent molecules with high spatial accuracy.

A rotatable diaphragm element adjusts the illumination angle in a microscope via a peg-and-hole coupling mechanism.

A microscope autofocus system merges absolute and relative z-position detectors to drive the focus actuator for rapid target acquisition.

Hydrogen gas field ionization generates H3+ beams that reduce sample damage while maintaining narrow energy width for high resolution.

A wavelength selective switch uses a compensating element to stabilize light condensing positions across multiple input ports.

Computational reconstruction synthesizes multi-angle intensity images to resolve high spatial-bandwidth product without mechanical alignment complexity.

Alternating Gaussian and inverted Gaussian pulses enable differential detection that achieves 120 nm resolution while minimizing sample damage.

Segmented detector arrays and acousto-optical beam steering enable rapid volumetric imaging without sacrificing spatial resolution.

Segmenting the optical path into ten groups resolves the trade-off between wide field of view and measurement precision in micro-imaging.

Tilting optical elements by at least 0.5 degrees prevents lens reflection ghosting from coupling into the receiver fiber core.

A movable correction unit in the infinity space adjusts radiation propagation direction to align optical elements.

Information processing apparatus displays analysis results alongside input regions for visual test counts.

A microscope apparatus adjusts activating light irradiation intensity across the observation region to manage fluorescent material activation.

Aspheric lens face compresses outer field regions to expand angular range beyond 45 degrees without mechanical indentation.

Positioning object and intermediate image planes at oblique angles within the detection aperture cone increases the detectable fluorescence angle range.

Replacing torsion springs with an elastic guide member reduces camera module volume while maintaining reliable lens driving engagement.

Lateral reflector turret pivots optical components into the axis, reducing microscope stage height and improving ergonomic access for routine operations.

An auxiliary light beam couples into a microscope at an angle outside the main imaging area to register focus state changes on a detection device.

Structured illumination frequency-mixes high resolution information into the optical passband, resolving lateral and axial details beyond diffraction limits.

Segmenting the microscope into spatially distributed image input and output units reduces mechanical stress and imbalance in confined rotating environments.

Segmenting the ocular and objective lens units allows independent alignment, resolving precision challenges caused by direct connections.

A variable focal length lens device uses electrowetting to adjust magnification and focus position without mechanical drives.

A beam-limiting element in the collimated input path prevents vignetting and stray radiation from corrupting infrared measurements.

An elliptical light shaping diffuser transforms parallel illumination into anisotropically diffuse light for microscopy.

A photo adapter uses a sliding sleeve to adjust focal length for camera attachment.

Two offset focusing cameras measure specimen sharpness to determine the in-focus position, reducing scan time by eliminating sequential adjustments.

Iterative alignment of a microscope objective and pupil relay module reduces residual aberrations below 25 mλ to maintain inspection throughput.

Predictive variable scan speed profiles adjust imaging probe velocity across regions of interest to optimize acquisition throughput.

Segmented lens groups with defined Abbe numbers correct chromatic aberration of magnification and secondary spectrum in high-magnification microscopy.