To use an object information acquiring apparatus that has: a plurality of detection elements that detect acoustic waves generated from an object irradiated with light from a light source and output electric signals; a supporting member that supports the plurality of detection elements so that the axes of directivity of at least part of the detection elements gather; an inputting unit that receives an input of a measurement condition from a user; a selecting unit that selects at least part of the plurality of detection elements in response to the measurement condition input by the user; and a processing unit that acquires property information on the inside of the object, using electric signals output from the selected detection elements.

A super resolution microscope system is disclosed and described. The system can include a sample stage (180) adapted to receive a sample (185) including probe molecules. At least one light source (105) is provided to produce a coherent excitation light to excite the probe molecules and cause luminescence of the probe molecules. An image detector (100) can detect the luminescence from the probe molecules. A microlens array (125) can be positioned in a beam path (110) of the coherent light from the at least one light source (105). The beam path (110) of the coherent light extends between the light source (105) and the sample stage (180). The microlens array (125) can also be positioned in a beam path (112) of the luminescence from the probe molecules. The beam path (112) of the luminescence extends between the sample stage (180) and the image detector (100).

Disclosed is an apparatus and method for processing a bio optical signal based on a spread spectrum scheme including a demodulator configured to collect a bio optical signal generated in response to an incident beam modulated based on a spreading code being scattered from a target analyte, and remove a noise from the bio optical signal by demodulating the bio optical signal based on the spreading code, wherein the bio optical signal has a correlation with the modulated incident beam.

A single cell apparatus and method for single ion addressing are described herein. One apparatus includes a single cell configured to set a frequency, intensity, and a polarization of a laser, shutter the laser, align the shuttered laser to an ion in an ion trap such that the ion fluoresces light and/or performs a quantum operation, and detect the light fluoresced from the ion.

An objective cell is irradiated with laser beam of a predetermined wavelength. Only Stokes light is selected out of detected light including reflected light and scattered light of the laser beam, and a Raman scattering spectrum is obtained by dispersion of the selected Stokes light. A transcriptome of the objective cells is estimated, based on the Raman scattering spectrum. It is preferable to estimate the transcriptome of the objective cells, based on N-dimensional Raman data obtained by dimensional reduction of the Raman scattering spectrum. This configuration only needs to irradiate the objective cell with the laser beam and does not require to destroy the objective cell. As a result, this enables the transcriptome of the cell to be estimated in a short time period without destroying the cell.

An optical sensor and a method of operating the optical sensor are provided. The optical sensor includes a light source configured to emit a light, and a path adjuster configured to adjust a traveling path of the light to reflect the light at a first time, and allow the light to pass through the path adjuster at a second time. The optical sensor further includes a light receiver configured to receive a reference light among the reflected light, and receive, among the light passing through the path adjuster, a measurement light related to a target material.

A multiband IR adjunct (MIRA) sensor to spectroscopically determine the content and the concentration of chemical composition of a targeted object, includes a sensor housing, a first front optics in a first optical channel, a second front optics in the first optical channel, an acousto-optic tunable filter (AOTF), a photo detector (PD), a set of back optics in the first optical channel that focuses polarized narrow-band light beams received from the AOTF device onto the PD, the PD converting the polarized narrow-band light beams into an electrical signal, and a data acquisition unit signal-connected to the PD, the data acquisition unit collecting the electrical signals. Multiple optical channels can be provided within the housing to analyze UV/VIS/near infrared (NIR), short-wavelength infrared (SWIR), mid-wavelength infrared (MWIR), and LWIR wavelength ranges respectively.

For determining a molecule position of a singularized fluorophore molecule, a light beam including fluorescence excitation light and fluorescence influencing light is shaped and focused such as to form a light intensity distribution having a central intensity minimum of the fluorescence influencing light. The central intensity minimum is continuously moved along a track repeatedly extending around an estimated position. Individual photons of fluorescence light emitted by the fluorophore molecule due to excitation by the fluorescence excitation light are registered; and an intensity minimum position of the intensity minimum is recorded for the excitation of each individual photon registered. In response, the estimated position around which the track extends is updated on basis of the recorded intensity minimum position, and extensions of the track around the estimated position are reduced and an effectiveness of the fluorescence influencing light is increased.

Embodiments of the present disclosure are directed to a compact, mobile, digital spatial profiling (DSP) system, and associated apparatuses, devices and methods, which are configured to image one or more regions-of-interest (ROIs), and then using UV light to cleave, for example, oligos off antibodies in one or more ROIs (photocleaving), and collect the photocleaved oligos for later hybridization and counting.

Preparation cell systems and methods are described herein. One example of a system for a preparation cell includes a laser coupled to a fiber bundle comprising a plurality of fibers, a preparation cell to prepare a state of laser light received by the fiber bundle, and an exiting fiber bundle coupled to the preparation cell.