Abstract: The present invention relates to the electrophoretic separation of bio-organic molecules using a slab gel electrophoresis apparatus having a pair of spaced, confronting plates defining a multi-lane separation zone adapted to hold a separation medium and an upper loading zone. In one aspect of the invention, at least one of the plates is shaped to provide an expanded loading zone. The plate-to-plate distance within the expanded loading zone is greater than the plate-to-plate width within the separation zone. In another aspect of the invention, a comb is provided with each tooth having a gradual taper beginning at a support member and extending along most of the tooth's longitudinal axis, and a sharp taper beginning immediately beyond the gradual taper and extending to the end of the tooth.

Abstract: The invention relates to improved methods and compositions for loading samples into an analytical instrument having a plurality of sample receiving loading ports. In a principle embodiment of the invention, first and second sample markers are added to sample to be loaded onto an analytical instrument having a plurality of sample receiving loading ports. The first and second samples are compounds are selected so as to produce a distinctive signal upon combination thus a sample containing a first sample marker and a sample containing a second marker are mistakenly loaded into the same sample receiving loading port, a detectable signal indicative of the misloading is produced.

Abstract: Flat plates serving as molds and enclosures for slab gels are held together by a clamping frame in which the side edges of the plates slide into facing channels and are clamped by lever-operated cams that compress the channel walls against the plate surfaces. The joined plates are held on a vertical support rack containing a finger-operated spring-loaded notched clamp that presses down on the plates to seal the opening at the bottom edges of the plates against a gasket. A well-forming comb for insertion between the plates contains flexible outwardly angled fingers to seal against the spacers between the plates.

Abstract: The present invention involves a gel casting and electrophoresis device that simplifies the gel cassette casting and electrophoresis process by providing an integral frame assembly that includes a bottom sealing means movable to a first position where the sealing means seals the bottom of the gel cassette for gel casting purposes and a second position which exposes the bottom of the gel cassette for electrophoresis purposes.

Abstract: A packaging arrangement is disclosed for protecting an electrophoresis gel from damage during shipment and storage. The package arrangement includes first and second sheets that are sealed about their respective edges to form an enclosed cavity. The cavity is at least partially evacuated of air. An electrophoresis gel is located within the cavity. A support sheet may be disposed between the electrophoresis gel and the package to facilitate removal of the gel and to further stiffen the package. In one embodiment of the invention, a plurality of electrophoresis gels are disposed within the cavity. Each gel is preferably separated from adjacent gels by a spacer.

Abstract: A fully automated protein and/or DNA gene fragment analyzing machine and method are disclosed in which, in a simple machine structure, a plurality of electrophoresis calls each containing such fragments, are robotically, under computer programming, inserted into an electrophoresis housing and subjected to voltage for producing electrophoretic migration in one dimension (horizontally), and then preferably after robotic 90.degree. rotating of the cells, are voltage migrated in an orthogonal direction to separate the fragments vertically, and then robotically presented to an optical image scanner for identifying the brightest fragments and classifying the same, with comparison with reference image fragment locations of normal or variant fragments, and for computer storing all relevant data.

Abstract: A gel cassette for electrophoresis includes opposed plastic plates holding a gel therebetween. An upper buffer tank can be adhered to one of the plates by double backed tape that is sandwiched between the tank and plate, thereby avoiding the use of a rubber sealing gasket between the tank and plate. As a result, the distance between the tank and the plate is kept constant. A buffer solution in the tank communicates with the gel. The cassette can then be placed in a lower buffer tank and an electric field applied to the buffer solutions to effect electrophoresis of DNA fragments that have been placed in the gel. In an alternate embodiment, a window is formed in one of the plastic plates to allow laser light to pass into the cassette and excite a fluorescent tag in the DNA. The fluorescence then passes back through the window for detection by a sensor, to automatically determine the DNA sequence of the sample in the gel in accordance with auto DNA sequencing principles.

Abstract: To sequence DNA, DNA samples marked with flourscent infrared dye are applied at a plurality of locations for electrophoresing in a plurality of channels through a gel electrophoresis slab. The channels are scanned with a laser and a sensor, that include a microscope focused on the gel slab. The focal point and slab are adjusted with respect to each other so that the focal point of the microscope remains on the gel slab during a scan. The data from the scan is directly used to amplitude modulate density readings on a display, and the scan is displayed in a horizontal sweep of a cathode ray tube, whereby said cathode ray tube provides intensity displays of bands representing DNA. Different sizes of glass gel sandwiches may be mounted to the same console for different sequencing tasks.

Abstract: The present invention relates to the electrophoretic separation of bio-organic molecules using a slab gel electrophoresis apparatus having a pair of spaced, confronting plates defining a multi-lane separation zone adapted to hold a separation medium and an upper loading zone. In one aspect of the invention, at least one of the plates is shaped to provide an expanded loading zone. The plate-to-plate distance within the expanded loading zone is greater than the plate-to-plate width within the separation zone. In another aspect of the invention, a comb is provided with each tooth having a gradual taper beginning at a support member and extending along most of the tooth's longitudinal axis, and a sharp taper beginning immediately beyond the gradual taper and extending to the end of the tooth.

Abstract: An apparatus and method for loading samples into a gel of an electrophoretic gel system (EGS). The preferred sample loader includes a membrane having a net negative charge, net neutral charge or no charge (preferably nitrocellulose or nylon) which releasably retains the samples such that the samples are actively released when the membrane is inserted into the gel of an EGS. In one preferred embodiment, the sample loader includes a substrate having a plurality of sample loading areas extending therefrom. In an alternative embodiment, the membrane is substantially thick and serves as its own substrate. In another embodiment, sample inhibiting agents such as hydrophobic ink are formed through the membrane to inhibit the diffusion of samples between sample loading areas. Each sample loading area includes an affixed membrane. In use, one or more samples to be subjected to electrophoretic action are applied to the membrane before the membrane is inserted into a previously polymerized gel.

Abstract: A sample holding device for electrophoresis apparatus according to the present invention wherein a plurality of sample holding capillaries are laid out in an array and are immobilized to the supporting jig. This sample holding device is configured to ensure the lower ends of the capillaries can contact the sample injection portion of the electrophoresis separation part of the electrophoresis apparatus, and provides easy sample injection and prevents the gel capillaries of the electrophoresis separation part from being damaged when sample holding capillaries are filled with gels, thereby allowing repeated use of the gel capillaries of the electrophoresis separation part.

Abstract: This invention provides a gel electrophoresis casting cassette for horizontal gel electrophoresis. The tray and lid of the cassette have locking means for securing the two parts to prevent damage to the slab gel and to create slab gels of uniform quality.

Abstract: Changes in polarized light incident on a detection zone within a separation matrix are used to detect optically active molecules within the separation matrix. The separation and detection of optically active molecules within the detection zone is done by loading a sample containing optically active molecules onto a separation matrix; applying a motive force to cause the sample to migrate though the separation matrix and to separate into a plurality of subgroups of optically active molecules; directing an incident beam of polarized radiation to the detection zone; processing the collected exiting beam with an optical component which discriminates between radiation having the same polarization as the incident beam and radiation having a different polarization from the incident beam; and measuring the intensity of the processed exiting beam.

Abstract: An apparatus of conducting electrophoresis experiments including a container for receiving an electrophoresis buffer and a buffer core assembly for holding gel-containing cassettes that are immersed in the buffer for molecular separation of an electrophoresis sample. The buffer core assembly defines a flow path for the electrophoresis buffer which can be circulated by means of a heat exchanger and a pump to effect controlled heat exchange between the buffer and the cassette surfaces thereby maintaining the gel and the electrophoresis process at a desirable temperature uniformly over the surfaces of the gel cassette. The buffer core assembly also has upper well for receiving a second electrically chargeable buffer in contact with the gel so as to impose an electric field on the gel for the electrophoresis in conjunction with the first buffer. The well is isolated from the first buffer to prevent mixing of the buffers and to reduce the risk of an electrical short.

Abstract: A gel electrophoresis apparatus and a cooling system therefor. The apparatus includes a front panel and a back panel. A gel slab is contained in a gel slab platform between the front and back panels. The gel slab platform extends upwardly to the front edge of an upper buffer reservoir and downwardly to a lower buffer reservoir. A conventional gel mold assembly is inserted into the apparatus and supported by the gel slab platform. A cooling unit is disposed below the lower buffer reservoir of the apparatus. A baffle plate is inserted between the front panel and a back panel of the apparatus. When the cooling unit is actuated, the baffle plate directs a cooling medium through the apparatus and between the front panel and the back panel to cool the gel slab. The apparatus also includes dampers which are pivotally mounted on the apparatus at the top of the baffle plate. The dampers are used to control the flow of the cooling medium through each baffle individually.

Abstract: A fully automated protein and/or DNA gene fragment analyzing machine and method are disclosed in which, in a simple machine structure, a plurality of electrophoresis cells each containing such fragments, are robotically, under computer programming, inserted into an electrophoresis housing and subjected to voltage for producing electrophoretic migration in one dimension (horizontally), and then preferably after robotic 90.degree. rotating of the cells, are voltage migrated in an orthogonal direction to separate the fragments vertically, and then robotically presented to an optical image scanner for identifying the brightest fragments and classifying the same, with comparison with reference image fragment locations of normal or variant fragments, and for computer storing all relevant data.

Abstract: An electrophoresis gel cassette that includes a bottom plate with an attached base portion, a cover plate, and a gel chamber formed between the two plates. There is at least one opening, which is in communication with the gel chamber, encompassed in the base portion, thereby making the opening seamless or free of parting lines. Upon assembling the cassette, a contact face of the base portion of the bottom plate and a contact face of the cover plate can be sealed by sonic welding or adhesives to produce a water-tight seal and to facilitate casting.

Abstract: An electrophoresis apparatus which overcomes the safety problems of the conventional apparatus by including a screen for preventing the operator from contacting the exposed surface of the gel chamber to avoid burns or electric shock. Shock due to contact with buffer solutions is also avoided by use of a power engaging mechanism which prevents the operator from accessing either of the buffer reservoirs when one or both of the buffer solutions are connected to the power source. The power engaging mechanism ensures that it is only possible to connect the buffer solutions to the power source when both reservoir covers are in their closed positions.

Abstract: In accordance with the teachings of the present invention, there are provided methods, gels, and transferring devices for loading gels. The methods and devices of the present invention involve the use of ultra-thin, miniature, disposable, slab gels for the quick, inexpensive and high resolution analysis of polynucleotide samples.

Abstract: To sequence DNA, DNA samples marked with flourscent infrared dye are applied at a plurality of locations for electrophoresing in a plurality of channels through a gel electrophoresis slab. The channels are scanned with a laser and a sensor, that include a microscope focused on the gel slab. The focal point and slab are adjusted with respect to each other so that the focal point of the microscope remains on the gel slab during a scan. The data from the scan is directly used to amplitude modulate density readings on a display, and the scan is displayed in a horizontal sweep of a cathode ray tube, whereby said cathode ray tube provides intensity displays of bands representing DNA. Different sizes of glass gel sandwiches may be mounted to the same console for different sequencing tasks.

Abstract: A spacer in the form of an elongated, rectangular parallelepiped for use between the two glass plates of a gel cassette to delimit a space for receiving an electrophoresis gel between the glass plates where the spacer is made of glass.

Abstract: A device and method for vertical slab gel casting and electrophoresis in a single enclosure is provided. Air is utilized as a sealing medium to seal the bottom of a gel space for gel casting by constructing an air-tight connection between a sealable lower buffer chamber and a gel space via a junction. The air is automatically released when a buffer is introduce into the lower buffer chamber so that the bottom of the gel is in direct contact with the buffer without manually removing a solid sealing device from the bottom of the gel, which enables the gel to be directly used for electrophoresis without any movement of the gel space.

Abstract: The loading of samples into wells that are formed in a vertical slab gel is facilitated by a needle guide that provides expanded openings that taper toward the wells, the openings being separated by partitions that help the user distinguish between the wells and the barriers of transparent gel material between the wells.

Abstract: Slab gels in parallel plate gel enclosures are readily placed in an electrophoresis cell where they are in full contact with upper and lower electrode buffers and reliably sealed against leakage with relatively few manual manipulations. The gel enclosures are pressed against an inner frame to form an upper buffer chamber, and the inner frame is inserted in an outer clamping frame in which the pressure between the gel enclosures and the inner frame is maintained by a cam-operated pressure plate. The clamping frame is then placed in a tank serving as the lower buffer chamber.

Abstract: The invention relates to an apparatus for two-dimensional electrophoresis of at least one electrophoresis unit comprising an electrophoresis medium enclosed between two plates, which apparatus comprises a first pair and a second pair of compartments for electrophoresis liquid which are provided with electrodes and which make electrophoretic contact on either side and mutually transversely of each other with the electrophoresis medium of the electrophoresis unit, wherein the compartments are disposed and adapted such that the electrophoresis unit assumes a standing position in the apparatus, and to an electrophoresis unit intended for such an apparatus.

Abstract: The improved DNA base sequencer has a flat plate type gel electrophoretic unit that has multiple tracks for electrophoresing DNA fragments and which is held in a vertical position, a light exciting laser light applying unit that applies laser light to the respective tracks in the electrophoretic unit from one lateral side thereof in such a way that it crosses the tracks at right angles, and a fluorescence detecting unit that detects the fluorescence as generated from the DNA fragments illuminated with the laser light and which converts the detected fluorescence to an electric signal. The sequencer is characterized in that the fluorescence detecting unit comprises a fluorescence condensing lens, a fluorescence filtering unit and a solid-state imaging device, (e.g., a CCD line sensor), the fluorescence filtering unit being composed of at least two filters that selectively transmit fluorescences having different wavelengths and that are staggered with each other along a common longitudinal axis.

Abstract: Changes in polarized light incident on a detection zone within a separation matrix are used to detect optically active molecules within the separation matrix. The separation and detection of optically active molecules within the detection zone is done by loading a sample containing optically active molecules onto a separation matrix; applying a motive force to cause the sample to migrate through the separation matrix and to separate into a plurality of subgroups of optically active molecules; directing an incident beam of polarized radiation to the detection zone; processing the collected exiting beam with an optical component which discriminates between radiation having the same polarization as the incident beam and radiation having a different polarization from the incident beam; and measuring the intensity of the processed exiting beam.

Abstract: This invention relates to a method and system for producing a polyacrylamide gel sample typically for use in electrophoretic analysis. The subject method includes providing a container comprising a bottle and cap assembly for conducting a gel formation sequence. The cap assembly includes a storage compartment. A plurality of premixed chemical materials are employed for producing a polyacrylamide gel used to make the gel samples. The container includes a bottle for storing an acrylamide solution and a cap assembly for storing the premixed chemical materials in dry particulate form therewithin. The cap is located atop the bottle. The premixed chemical materials are stored in the bottle and in the storage compartment for subsequently producing the acrylamide gel solution in situ within the confines of the container so that the step of transferring of the gel stock solutions to an auxiliary container is avoided.