Abstract: The problem to be solved by the present invention is to provide a microscope that prevents a dew condensation on an objective lens and allows obtaining a good microscopic image, and a method of preventing a dew condensation on an objective lens. A microscope includes an objective lens having a heater 22 in a cell incubator 3 having a high humidity space. The high humidity space is maintained at 90% to 100% of relative humidity and controlled to be at a predetermined gas temperature. A cultured cell 12 in the cell incubator 3 is observed via the objective lens 1, and the heater 22 is controlled to make the temperature of the objective lens 1 higher than the gas temperature of the high humidity space.

Abstract: A microscope is disclosed which comprises several parts, such as a stand, a stage, a nose piece and several elements used to operate the microscope. At least one of these parts is provided with the ceramic layer on its surface.

Abstract: A displacement prevention sheet that, in order to inhibit a sample from deviating at the time of measurement with a microscope, is disposed between a sample holder in which the sample is set and a sample holder mounting stage on which the sample holder is mounted, wherein at least part of both surfaces of the displacement prevention sheet is provided with displacement prevention means.

Abstract: In the present invention, a micro-pattern embedded optical film for cell-based assays is described. The optical film contains micro-patterns in the form of geometric shapes, such as lines and curves, and numbers and letters. Furthermore, the optical film contains a coordinate system that allows identification of each location on the optical film for cell-based assays, including cell growth, identification, and measurements under an optical microscope. Furthermore, an apparatus with the micro-pattern embedded optical film and a supporting part is described. Methods for making the optical film and apparatus are disclosed. A method for performing cell-based assays using the optical film or apparatus is shown.

Abstract: An assay device (1) comprises a base (2) and glass plate lid (3). The base (2) has an array of shallow microwells (4), each having a flat rim (9), all rims being co-planar. When the lid (3) is placed on the base (2) a thin capillary gap (10) is formed on each rim, acting as a liquid seal for a microwell chamber. The liquid is excess sample liquid and further excess is accommodated in overspill cavities (6) between the microwells (4). Because of the liquid seal and shallow configuration the benefits of microfluidic devices are achieved together with the handling convenience and use of conventional detection equipment of conventional microplate devices.

Abstract: A device for producing rapid temperature changes around microscopic samples comprises two hollow channels (5,6) positioned at the same plane but at an angle to each other, FIG. 1. Streams of solutions (9, 10) flowing from the respective channels are maintained at different temperatures through heating or cooling elements (7, 8) conducting heat to or away from the channels. Initially, the sample (12) is surrounded by stream (9) at initial temperature, FIG. 3. After flow of this stream stops, the sample is surrounded by another stream (10) at a different temperature. This results in the temperature change, which does not depend on the volume of liquid in the system and on the size of heating or cooling elements.

Abstract: Provided is an apparatus for detecting biopolymers (DNA) capable of total analysis including non-reacted samples without complicated operations such as washing. A DNA probe is fixed to one of electrodes and direct current voltage is placed between the electrodes, so that it becomes possible to separate complementary strand sample DNA and non-complementary strand sample DNA. By analyzing from a ratio in the whole reaction system, it is possible to obtain clearer results. Further, by using electrophoresis by gel together, it is possible to separate reacted samples and non-reacted samples to perform measurements therefor in the same reaction field.

Abstract: A multi-aperture high-fill-factor telescope is provided. Specifically a multi-aperture high-fill-factor telescope is provided that includes a plurality of sub-aperture telescopes, each sub-aperture telescope being configured to collect electromagnetic radiation from a scene and including first, second, third, and fourth powered mirrors; a set of combiner optics configured to combine electromagnetic radiation collected by the sub-aperture telescopes to form an image of the scene; and a plurality of sets of relay optics, the sets of relay optics are respectively associated with the sub-aperture telescopes and each set of relay optics includes a first flat fold mirror, a trombone mirror pair, and a last flat fold mirror, wherein the last flat fold mirrors are disposed within about a beam diameter of respective exit pupils of the sub-aperture telescopes.

Abstract: Featured is a long-term cell culture system being configured and arranged so as to be capable of monitoring the dynamic processes that occur during proliferation and differentiation of stem cells such as central nervous system (CNS) stem cells/embryonic stem cells. In particular aspects, the system allows monitoring of such dynamic processes continually and to focally manipulate the cells by focal application of growth factors such as BMP, CNTF and other growth factors. Preferred systems are capable of electrical recording from the cells.

Abstract: An apparatus is provided with a cell culture container having a cell culture region made of a hole formed on a substrate, a semi-permeable membrane covering a top plane of the cell culture region and a culture medium replacement part provided over the semi-permeable membrane, a mechanism for supplying a cell culture medium into the cell culture container, and a microscopic optical mechanism for enabling long-term observation of the cell within the cell culture region. This apparatus makes it possible to culture a cell group originating from a particular single cell, to perform culture and observation while identifying cells to be subjected to interaction during the process of culturing cells, and observe a difference in variation between the particular cell and other cells. There is also provided a mechanism which makes it possible to collect only a cell assuming a particular state and perform analysis or biochemical measurement of a gene of the cell, an expressed mRNA and the like.

Abstract: The slide staining device has a generally rectangular body which includes an upper rectangular frame and a lower rectangular frame. The upper rectangular frame and the lower rectangular frame are aligned and detachably connected together so that multiple microscope slides may be clamped therebetween for staining at the same time. Knobs with threaded bolts projecting therefrom fasten the upper and lower frames together. The lower rectangular frame includes a plurality of ridges to allow for liquid drainage during the washing stage of a staining procedure and a handle to facilitate manipulation of the device. The device of the present invention is designed to complement established and standard laboratory practice.

Abstract: A Microscope Imaging System (CMIS) with intelligent controls is disclosed that provides techniques for scanning, identifying, detecting and tracking microscopic changes in selected characteristics or features of various surfaces including, but not limited to, cells, spheres, and manufactured products subject to difficult-to-see imperfections. The practice of the present invention provides applications that include colloidal hard spheres experiments, biological cell detection for patch clamping, cell movement and tracking, as well as defect identification in products, such as semiconductor devices, where surface damage can be significant, but difficult to detect. The CMIS system is a machine vision system, which combines intelligent image processing with remote control capabilities and provides the ability to auto-focus on a microscope sample, automatically scan an image, and perform machine vision analysis on multiple samples simultaneously.

Abstract: A quantitative cell-counting slide includes a plurality of counting chambers juxtapositionally formed in the slide; each counting chamber including a first counting portion consisting of a plurality of miniature grids of which each miniature grid may be formed to have a volume of 0.01 micro-liter for counting any kind of cells, and a second counting portion formed on a platform and consisting of a plurality of HPF (High Power Field) volumetric grids each formed to have a quantitative volume of 0.0083 micro-liter generally equal to one HPF volume adapted for cell counting used in urinary sediment microscopic examination.

Abstract: A tissue dissecting board assembly for use in tissue restoration and reconstruction surgeries. The assembly is constructed of an optically clear polymeric dissecting board having a plurality of cooperating cavities for holding chemical solutions and compositions required for tissue restoration and reconstruction surgeries. An illumination source is further incorporated in the dissecting board structure to provide an illuminated working area.

Abstract: A tray or holder for tissue specimens, especially of excised tissue, such as biopsied specimens, is used with a confocal imaging system. The tray may be disposable after imaging of the specimen carried therein or may archive the specimen. A window supports the specimen. Clamps mounted inside the tray restrain the tissue. A compliant bag is mounted outside the tray on one side of a window of the tray on which the specimen is disposed. During imaging the specimen is immersed in a liquid contained in the tray having an index of refraction which closely matches the index of refraction of the tissue. The bag also contains an index matching liquid preferably having the same index as the liquid in the tray. Selecting an immersion liquid, which equals the refractive index of the near surface tissue, minimizing wavefront distortion which may result from an effectively corrugated surface of the specimen.

Abstract: This invention describes an integrated microscope with a removable transparent specimen-container that can be directly placed at just beyond the effective focal plane of said microscope, with which schoolchildren can collect live specimens and dispose the specimens in said specimen-container ready for instantaneous microscopic examination of the specimens at a magnification power 20× or higher in the field.

Abstract: An analytic plate such as a microscope slide or a diagnostic plate and kit having the slide or plate, the slide or plate having a containment border for containing a liquid or liquid sample. The containment border is substantially transparent and is substantially flush with the surface of the slide or plate for containing the liquid or liquid sample disposed thereon and thereby preventing spreading or migration of the sample across the slide or plate.

Abstract: A kit (11) is described for the detection of characteristics and parameters of body fluids such as saliva, urine and cervical mucus for the purposes of studying and identifying fertility periods in women, comprising a set of flat plate-shaped supports (3) for samples of said body fluids (F) and a viewer (1) provided with enlargement means, characterized in that each of said flat plate-shape supports (3) for body fluid (F) presents a shallow basin or trap (3p) with a convex bottom entirely surrounded by a raised rim (3r), and is equipped with locking fins (3t) suitable for coupling with structural elements present on said viewer (1) so that it is irreversibly locked onto the latter in a desired relative posititon.

Abstract: An exemplary optical isolator, such as a magnetic-semiconductor composite optical isolator, and method for making the same, is provided that includes a semiconductor waveguide and a magnetic-semiconductor composite layer. The semiconductor waveguide includes a guide layer, a first clad layer and a second clad layer. The guide layer includes one or more layers with a first end, a second end, a top, and a bottom, the guide layer allows a light wave incident the first end of the guide layer to propagate in a positive propagation direction, and allows a light wave incident the second end of the guide layer to propagate in a negative propagation direction. The first clad layer and the second clad layer are provided, respectively, relative to the bottom and the top of the guide layer, and the second clad layer has a thickness to allow an optical field penetration through the second clad layer.

Abstract: A unitary counting device for cells and other microscopic particles is described in this invention. The invention also relates to the method of producing the counting device and to the method of using the device. The counting device is constructed with a top part, a connection layer, a base part, and a grid of microscopic lines that are built inside a counting chamber to define counting areas. Furthermore, the counting chamber has a sample introduction port and an air escape port. A connection layer bonds the top part and the base along perimeter of the chamber and maintains gap uniformity. The connection layer consists of a polymer film sandwiched by two layers of pressure sensitive adhesive. Grid lines are fabricated using polymerizable solutions, for narrow and thin lines, which enable counting small particles under high magnifications.

Abstract: A perfusion incubator having an incubation well assembly is provided. A peristaltic pump may supply medium from a medium supply and pass it through a medium conditioning unit before supplying the medium to the incubation well assembly. Each well assembly may have an upper portion and a lower portion, a medium inlet and a medium outlet. The medium inlet may be positioned at a mid point in the well and the medium outlet is positioned above the medium inlet. An embryo may reside in the lower portion of the well. The well assembly may be formed from a permeable material through which a gas, such as carbon dioxide and/or oxygen, can diffuse.

Abstract: Featured is a long-term cell culture system being configured and arranged so as to be capable of monitoring the dynamic processes that occur during proliferation and differentiation of stem cells such as central nervous system (CNS) stem cells/embryonic stem cells. In particular aspects, the system allows monitoring of such dynamic processes continually and to focally manipulate the cells by focal application of growth factors such as BMP, CNTF and other growth factors. Preferred systems are capable of electrical recording from the cells.

Abstract: A culturing chamber is a closed system to culture cells on a microscope stage for a long time and consists of base (10), a compartment layer (20), and a lid (30) sealingly and detachably combined together. The lid (30) is able to be selectively opened or closed to make the operation such as cell injection convenient. An electronic signal device containing a mult-operational system is applied to the culture chamber to maintain the living circumstance steady for the cells, so that the cultured cells can live long on the microscope stage and be observed and cultured at the same time.

Abstract: The present invention provides an apparatus and methods to evaluate invasive potential of tumor cells. The apparatus permits culturing, staining and analysis of test samples to be performed on the same test plate to facilitate cell invasiveness tests. Methods for testing cell invasiveness in vitro are described.

Abstract: A near field solid immersion lens array, method of using, and making a near field solid immersion lens array. A cover slide is provided having a near field solid optical lens array having least one fiducial mark. The fiducial mark is used by a positioning device for locating the position of each of the lens in the array. A unique identifier may be provided for locating information of the position of each lens in the array that can be used for driving the positioning device.

Abstract: The invention provides devices for packaging a chip shaped carrier having an active surface which is adapted to be read by an electro-optical reading device, e.g. a surface which carries an array of DNA oligonucleotides. The invention further provides processes for assembling the devices. The invention also provides systems for carrying out evaluations and/or monitoring methods involving electro-optical reading of an activce surface of a chip shaped carrier.

Abstract: A sample chamber is formed by a housing sealed against a microscope slide. The housing has fluid ports, including a well formed over at least one port. In a rinse station, rinse solution is drawn from a reservoir through the chamber to a waste reservoir. At a fill station, an aliquot of reagent already placed in the well is driven into the chamber. The reagent may be driven into the chamber by first drawing a vacuum on the chamber through the aliquot of reagent and then releasing the reagent to be drawn into the chamber by the vacuum.

Abstract: A cell and tissue culture modeling device comprising a housing having an interior chamber, an inlet port in fluid communication with the internal chamber, an outlet port in fluid communication with the internal chamber, a plurality of hollow fibers disposed within the interior chamber and traversing the length of the housing between the inlet port and the outlet port. Each of the plurality of hollow fibers has an interior defining an intracapillary space and the interior chamber defines an extracapillary space unoccupied by the plurality of hollow fibers. To access the extracapillary space of the device, a portion of the housing is removable. The device can be used to conduct permeability, drug efficacy, and gene expression studies.

Abstract: The invention involves methods and apparata for manipulating micro-/nanoobjects. A holder exerts a weak attractive force on the micro-/nanoobject (by, for example, suction from negative fluid pressure, electrostatic attraction, magnetic attraction, etc.). A vibrator coupled to the holder generates orbital motion in the holder in at least one plane. As long as the attractive force is not too high, the orbital motion of the holder will cause rotation of the micro-/nanoobject, with the attractive force of the holder maintaining the micro-/nanoobject adjacent the holder during such rotation. Once the micro-/nanoobject has been rotated to a desired orientation, the attractive force of the holder on the micro-/nanoobject can be increased to such a level that the micro-/nanoobject will be firmly fixed to the holder.

Abstract: A panel chip for supporting biological samples for observation with an imaging microscope. The glass panel defines a top flat surface, a bottom bearing surface, and at least a few channels extending generally parallel to each other from top to bottom surfaces. Each of the channels defines a top access mouth for ingress of biological. The channels are arranged in subgroups made of a number of unit cells. Instead of being cylindroid, these channels may form cross sectional rectangular or arcuate channels, or cross sectionally water droplet like channels. Each channel has such an inner diameter as to accommodate flow through viscosity of a biological sample containing fluid. The porous substrate that is created by slot channel can provide the maximum binding surface area per unit cell or pixel, as compared to cylindrical pores, thus achieving higher sensitivity and better imaging. Also, this panel chip is capable of being used as direct in situ synthesizing of molecules and drugs.

Abstract: The invention relates to an in-situ microscope device for reactors, in particular bioreactors, with a dip tube in a reactor connection port which in the inside of the reactor has an inlet for a specimen zone, and with a microscope external tube, arranged coaxially in the dip tube, which at the inner end is directed with a lens towards the specimen zone which lies between a lens cover glass and a slide glass body lying opposite, and is coupled outside with a camera for photographing the image of the specimen zone, the lens cover glass and the slide glass body being movable relative to each other, in order to be able to open and close the specimen zone.

Abstract: In accordance with the invention, a liquid sample for thermal analysis is disposed within a receptacle having a bottom surface and side walls. The top edges of the side walls are bent towards the center of the receptacle. A sheet of flexible, transparent material substantially impermeable to the sample is disposed across the top edges of the side walls, and an open lid compresses an o-ring onto the sheet material, sealing it against the bent top edges of the receptacle. The bottom surface of the receptacle is advantageously coated with a a material not wetted by the sample such as a fluorcarbon.

Abstract: The invention concerns an arrangement for scanning a specimen receiving device (1) for data recording with a laser scanning microscope, preferably with a confocal laser scanning microscope (2), with which imaging of large specimen fields with sufficient speed is possible by scanning of the specimen receiving device (1), which is characterized in that the specimen receiving device (1) is alternatingly rotatable about a first axis (4) by a rotation device (3).

Abstract: A microscope slide having a well formed therein, wherein the well is filled with culture media. The slide is designed for on-site collection, staining, and viewing of cells in biological fluid and tissue samples, preferably with an epi-fluorescence microscope. This novel slide permits point-of-care screening in a matter of minutes of any biological fluid or tissue sample for presence of infectious agents, after which, the slide can be transported to a central lab for culture and/or definitive identification.

Abstract: A biochemical substance is efficiently observed with focusing accurately and rapidly on the substance disposed on an inside of a container. A focusing mark, which is used as a reference when a focal point of an optical system is adjusted, is disposed on the outside of a transparent bottom of each well in a micro plate. A focus-shift-distance corresponding to a distance between the mark and a desired position to be observed is determined. The optical system focuses on the mark, and then, the focal point the optical system is shifted by the focus-shift-distance. This shift allows an object to be focused on accurately and rapidly even when unclear images are obtained.

Abstract: A method for optically coupling a thermoplastic material to an outer surface layer of an organic, dielectric, optical film and the resulting optical filter. Initially, a dielectric film is selected that includes (i) repeating optical layers of at least two polymers having different refractive indexes from each other, (ii) an exterior film surface, (iii) a refractive boundary along the exterior film surface, and (iv) a delamination threshold based on total thermal energy delivered to the film. A thermoplastic material which is miscible with the exterior film surface is fused to the refractive boundary with thermal energy below the delamination threshold to form a polydisperse region having a higher optical transmission than the refractive boundary. Add-on filters in the form of hardcoat layers, anti-reflection layers, holograms, metal dielectric stacks and combinations of these may be combined with the thermoplastic-film construct.

Abstract: A transparent elongated, rectangular glass microscope slide having a specimen observation spot defined by a removable border or frame. The border corresponds to the rectangular perimeter of the glass slide and includes a tab which may be grasped to peel off the border. In use, a cytological GYN PAP smear specimen is placed on the plain glass within the confines of the releasable paper border. The border is then removed after fixing the specimen. The slide also features a frosted end portion for marking identification data. The frosting may include permanent markings such as “NAME” to designate a certain frosted area for marking the desired information such as the patient's name and identification number. A tab is placed on the border end and overlaps a portion of the frosted area, and thus does not protrude outward from the side of the slide.

Abstract: A cassette for retaining a specimen of surgically exposed tissue from a patient in an orientation that facilitates optical sectioning of the tissue by a confocal microscopic or other optical imaging microscope. The cassette includes a base member having a rigid optically transparent window upon which a tissue specimen is situated, a pliable membrane locatable over a substantial portion of the base member including the window, and an upper member, having an aperture therethrough, which can cover the base member to provide an enclosed cavity between the membrane and the window sealing the tissue specimen therein. With the tissue specimen in the enclosed cavity of the cassette, the edges of the tissue specimen may be positioned planar against the window and retained in that position by bonds formed between the membrane and window at multiple points or locations around the tissue specimen.

Abstract: A tray or holder for tissue specimens, especially of excised tissue, such as biopsied specimens, is used with a confocal imaging system, especially a laser scanning confocal microscope system. The tray may be disposable after imaging of the specimen carried therein or may archive the specimen. A window supports the specimen. Clamps mounted inside the tray restrain the tissue. A compliant bag is mounted outside the tray on one side of a window of the tray on which the specimen is disposed. During imaging the specimen is immersed in a liquid contained in the tray having an index of refraction which closely matches the index of refraction of the tissue. The bag also contains an index matching liquid preferably having the same index as the liquid in the tray. A stabilizing plate is attached to a surface of the bag which faces the window.

Abstract: A confocal microscope is provided including a confocal imaging system having an objective lens, and a device which can be an attachment to the confocal imaging system, or a part thereof. The device has a housing with an interior cavity and two opposite ends, where one end of the housing receives the objective lens, and at the other end of the housing which is attached to, or is a part of, the housing which forms that other end. The chamber has first and second plates presenting two opposing sides of the chamber, where the first plate lies adjacent the tissue to be treated, and the second plate is attached to the housing. The interior cavity of the housing has a window defining a first volume between the window and the objective lens, and a second volume between the window and the chamber. The first volume has an immersion liquid optically matched to the objective lens, and the second volume is approximately evacuated.

Abstract: A cassette for retaining a specimen of surgically exposed tissue from a patient in an orientation that facilitates optical sectioning of the tissue by a confocal microscopic or other optical imaging microscope. The cassette includes a base member having a rigid optically transparent window upon which a tissue specimen is situated, a pliable membrane locatable over a substantial portion of the base member including the window, and an upper member, having an aperture therethrough, which can cover the base member to provide an enclosed cavity between the membrane and the window sealing the tissue specimen therein. With the tissue specimen in the enclosed cavity of the cassette, the edges of the tissue specimen may be positioned planar against the window and retained in that position by bonds formed between the membrane and window at multiple points or locations around the tissue specimen.

Abstract: A method for observing the living cell has the steps of erecting a substrate for the living cell; cultivating the living cell on the erected substrate; and observing the living cell with an optical microscope. The system used to incorporate the method has a microscope; and a culture dish having a body with an opening defined in a bottom of the body and a coverslip provided to cover the opening.

Abstract: Provided for heating cultured cells is a controlled heater device comprising a cell culture apparatus, a transparent heater in thermal contact with the cell culture apparatus, and may further comprise one or more of a transparent filter provided to prevent a predetermined spectral range of light from passing through the transparent filter, and a power source for controlling the amount of heat generated by the transparent heater of the controlled heater device.

Abstract: The present invention relates to the field of microscopic sample analysis, and specifically relates to a device for preparing thin microscopic samples of liquids.

Abstract: A microscope slide having a well formed therein, wherein the well is filled with culture media. The slide is designed for on-site collection, staining, and viewing of cells in biological fluid and tissue samples, preferably with an epi-fluorescence microscope. This novel slide permits point-of-care screening in a matter of minutes of any biological fluid or tissue sample for presence of infectious agents, after which, the slide can be transported to a central lab for culture and/or definitive identification.

Abstract: A tray or holder for tissue specimens, especially of excised tissue, such as biopsied specimens, is used with a confocal imaging system, especially a laser scanning confocal microscope system. The tray may be disposable after imaging of the specimen carried therein or may archive the specimen. A window supports the specimen. Clamps mounted inside the tray restrain the tissue. A compliant bag is mounted outside the tray on one side of a window of the tray on which the specimen is disposed. During imaging the specimen is immersed in a liquid contained in the tray having an index of refraction which closely matches the index of refraction of the tissue. The bag also contains an index matching liquid preferably having the same index as the liquid in the tray. A stabilizing plate is attached to a surface of the bag which faces the window.

Abstract: In order to provide an underwater microscope which can obtain a sharp picture of live underwater microorganisms in motion, an underwater microscope 10 comprises at least a camera 12 having an optical axis of an optical system, a channel 22 introducing a water sample, a sample chamber 16 having a thickness ranging from 0.

Abstract: An apparatus and method for efficiently observing a biochemical substance with focusing accurately and rapidly on the substance disposed on an inside of a container is provided. A focusing mark, which is used as a reference when a focal point of an optical system is adjusted, is disposed on the outside of a transparent bottom of each wells in a micro plate. A focus-shift-distance corresponding to a distance between the mark and a desired position to be observed is determined. The optical system focuses on the mark, and then, the focal point the optical system is shifted by the focus-shift-distance. This shift allows an object to be focused on accurately and rapidly even when unclear images are obtained.

Abstract: The present invention provides a culture vessel and microscope that allows a wide area of favorable observation of the sample in the plural wells even when a negative refractive power is generated in the culture medium, wherein a ring-shaped opening, a condenser lens, a lens array, a well plate, an objective lens and a phase contrast plate are disposed in this order viewed from the light source side with a construction to place a phase contrast film of the phase contrast plate in a conjugated relation to the projection pupil position or projection pupil of the objective lens, and the culture vessel is constructed of the lens array and well plate with a relative disposition in which the optical axis of each lens is coaxial with the center line of the confronting each well; the aperture of the ring-shaped opening being smaller than the aperture of the ring-shaped opening that is used when the culture vessel is not disposed in the optical path.

Abstract: The invention is directed to a slide holder for receiving one or more microscope slides. The slide holder includes a generally rectangular frame and at least one slot, each of the slots for receiving one slide. Flexible retaining latches and retaining grooves are provided at each of the slots for facilitating the securing of the slides.