Abstract:
The use of a multi-spectral imaging system, cell compartment markers, and molecular probes in a method for measuring movement of molecules within a cell by correlation analysis is provided, including measuring molecular movement to a particular compartment in adherent and non-adherent cells, e.g. in response to biological stimuli. A compartment in the cell is defined by the image of a specific compartment marker, e.g., a nuclear fluorescent stain. Molecule location is provided by a probe labeled with a different fluorochrome. A mask is generated based on the compartmental marker, and a correlation measurement is made between the locations of the molecular probe and the compartment marker. The correlation value between the regions defined by the compartment mask and molecular probe gives a quantitative measurement of the translocation of the molecule. The use of only a single masking function simplifies measurement of molecular translocation within a cell.
Abstract:
A system and method for high numeric aperture imaging systems includes a splitter (110), a defocusing system (126), and a combiner (114). The splitter reflects a portion of collected light and transmits another portion of the collected light. The defocusing system is configured to modify optical power of either the transmitted portion or reflected portion of the collected light. The combiner is oriented with respect to a mechanical angle. The combiner recombines portions of the transmitted portion and reflected portion such that the transmitted portion and reflected are subsequently transmitted being separated by an optical separation angle based upon the mechanical angle of orientation of the combiner. Various other implementations are used to maintain focus with regards to the imaging systems involved.
Abstract:
Light (30) from an object (24) such as a cell moving through an imaging syst em (20) is collected and dispersed so that it can be imaged onto a time delay and integration (TDI) detector (44). The light (30) can be emitted from a luminous object (24) or can be light from a light source that has been scattered by the object or can be a fluorescent emission by one or more FISH probes, frequently used to detect substances within cells. Further, light that is absorbed or reflected by the object can also be used to produce images for determining specific characteristics of the object. The movement of the object matches the rate at which a signal is read from the TDI detector. Multiple objects passing through the imaging system (20) can be imaged, producing both scatter images and spectrally dispersed images at different locations on one or more TDI detectors (44).
Abstract:
Light from an object (24), such as a cell, moving through an imaging system (20) is collected and dispersed so that it can be imaged onto a time delay and integration (TDI) detector (44). The light can be emitted from a luminous object or can be light from a light source that has been scattered or not absorbed by the object or can include a light emission by one or more probes within or on the object. Multiple objects passing through the imaging system (20) can be imaged, producing both scatter images and dispersed images at different locations on one or more TDI detectors (44).
Abstract:
Light (30) from an object (24) such as a cell moving through an imaging syst em (20) is collected and dispersed so that it can be imaged onto a time delay a nd integration (TDI) detector (44). The light (30) can be emitted from a lumino us object (24) or can be light from a light source that has been scattered by t he object or can be a fluorescent emission by one or more FISH probes, frequent ly used to detect substances within cells. Further, light that is absorbed or reflected by the object can also be used to produce images for determining specific characteristics of the object. The movement of the object matches t he rate at which a signal is read from the TDI detector. Multiple objects passi ng through the imaging system (20) can be imaged, producing both scatter images and spectrally dispersed images at different locations on one or more TDI detectors (44).
Abstract:
Light from an object (24), such as a cell, moving through an imaging system (20) is collected and dispersed so that it can be imaged onto a time delay and integration (TDI) detector (44). The light can be emitted from a luminous object or can be light from a light source that has been scattered or not absorbed by the object or can include a light emission by one or more probes within or on the object. Multiple objects passing through the imaging system (20) can be imaged, producing both scatter images and dispersed images at different locations on one or more TDI detectors (44).
Abstract:
Provided are methods for determining and analyzing photometric and morphometric features of small objects, such as cells to, for example, identify different cell states. In particularly, methods are provided for identifying apoptotic cells, and for distinguishing between cells undergoing apoptosis versus necrosis.
Abstract:
A system and method for high numeric aperture imaging systems includes a splitter, a defocusing system, and a combiner. The splitter reflects a portion of collected light and transmits another portion of the collected light. The defocusing system is configured to modify optical power of either the transmitted portion or reflected portion of the collected light. The combiner is oriented with respect to a mechanical angle. The combiner recombines portions of the transmitted portion and the reflected portion such that the transmitted portion and reflected portion are subsequently transmitted being separated by an optical separation angle based upon the mechanical angle of orientation of the combiner. Various other implementations are used to maintain focus with regards to the imaging systems involved.