Abstract: Electrotransfer is performed in an instrument that receives electroblotting cassettes and that contains an integrated power supply, controls, and a display that allows the user to monitor and control each of a plurality of cassettes individually through electrical contacts within the housing that mate with corresponding electrical contacts on the cassettes.

Abstract: In the present vertical slab-gel electrophoresis instrument, all the vertical slab gel cassettes comprise un-notched rectangular sidewalls and flanged spacer strips, but still can form a U-notched upper opening with an even rim for each cassette; one type of cassette can undergo gel casting with an electrophoresis cell, while another two types of cassettes can be used to form a multiple-cassette electrophoresis cell. The present invention can also incorporate a swing-frame chosen for urging a cassette to join an upper buffer chamber, provides an improved cooling device such that there is no need for the use of exogenous coolant, and also provides simple methods to enable cassettes to be tightly enclosed within membrane pouches for gel casting.

Abstract: A first dimension electrophoresis apparatus of vertical type with a gel container 2 having a plurality of rectangular rod-shaped gel chambers is provided. The rod-type gels surrounded with non-conductive material plates are arranged in parallel, an upper open end of the gel container 2 is placed tightly into an upper buffer reservoir 4 and the lower open end thereof is placed tightly into a lower buffer reservoir 1. The gel container 2 and the main parts of the first buffer reservoir 4 and the lower buffer reservoir 1 are sunk in a cooling reservoir 5 filled with cooling liquid. The lower buffer reservoir has a panel portion 1b which is bent upward to penetrate the cooling reservoir. Outlet conductors thereof extend from each of the reservoirs and are insulated physically and electrically from the cooling liquid. As a result, the outer surface of the gel container can directly contact with the cooling liquid.

Abstract: Methods, apparatus and systems are provided for efficient separation of various small and large molecules, especially biomolecules such as proteins, nucleic acids and polysaccharides. In particular, an electrophoresis apparatus is employed in a wide bore electrophoresis of samples in larger amounts than those in conventional capillary electrophoresis. The electrophoresis apparatus comprises: an electrophoresis chamber comprising a cathode, an anode and a housing; and a separation chamber positioned within the housing and comprising an inlet end, an outlet end, and one or more cooling capillaries positioned inside the separation chamber such that the longitudinal axis of at least one of the cooling capillaries is parallel to the direction of electric current flow from the anode to the cathode, wherein the end of the cooling capillary (or capillaries) is adapted to be coupled to a cooling device that allows cooling medium to pass through the cooling capillary.

Abstract: A thermostat array including an array of two or more capillary columns (10) or two or more channels in a microfabricated device is disclosed. A heat conductive material (12) surrounded each individual column or channel in array, each individual column or channel being thermally insulated from every other individual column or channel. One or more independently controlled heating or cooling elements (14) is positioned adjacent to individual columns or channels within the heat conductive material, each heating or cooling element being connected to a source of heating or cooling, and one or more independently controlled temperature sensing elements (16) is positioned adjacent to the individual columns or channels within the heat conductive material. Each temperature sensing element is connected to a temperature controller.

Abstract: The invention relates to a capillary electrophoresis-based method of screening complex materials for any unidentified affinity ligand that binds to a target of interest. The method subjects a plug of a mixture of the target and a complex material sample, and a separate plug of a known, tight-binding competitive ligand, to capillary electrophoresis under conditions optimized to allow mingling of the two plugs during the capillary electrophoresis run. Preferably, migration of the competitive ligand is tracked.

Abstract: In pre-cast slab gel cassettes, the formation of pathways in which proteins can migrate between the gel and the walls of the cassette to form shadow bands is avoided by including a nonionic amphiphilic polymer in the monomer solution from which the gel is formed and casting the gel with the polymer included. The nonionic amphiphilic polymer also prevents the resulting gel from sticking to the walls when the gel is to be removed from the cassette after electrophoresis.

Abstract: High throughput electrophoresis having a plurality of samples migrating through a highly resistive separatory media under an electric field. Multiple electrophoresis runs are conducted using a single separatory media. Automated methods of data analysis yields quantitative and qualitative data using optical densitometer or other detection systems. Controlled operating temperatures and small geometry reduces dispersion inaccuracy in banded data.

Abstract: A machine for sequencing DNA using optical techniques. A sample is loaded in the sample loading area, and place through DNA sequencing gel. The voltage across the reservoir may be increased by improving the cooling and thermal characteristics of the gel device. Preferably materials are used which have at least half and preferably a fifth the thermal transfer characteristics of glass. The materials can also be thin e.g. 50-100 microns. A heat sink can be used to dissipate more of the heat, and a fan can be directed at the heat sink. Moreover, the material can be flexible.

Abstract: The invention relates to capillary electrophoretic methods for detecting ligands or hit compounds that can bind to a selected target at or above a selected binding strength. The method allows one to rank various ligands based on their relative affinity, i.e., the relative stability of the target/ligand complex during capillary electrophoresis under selected conditions. The method also enables selective detection of strong-to-moderate binding hit compounds, even in the presence of high concentrations of weaker, competitive hit compounds.

Abstract: A device is provided for balanced high speed submarine gel electrophoresis. In the device, a conductive balancing liquid is introduced over gel matrix to generate heat, a thicken cooler bottom slows down heat absorption, which results in quick temperature elevation to 33° C. The elevated temperature around 33° C. is utilized to accelerate gel speed and to minimize vertical temperature gradient of the gel matrix.

Abstract: Apparatus for conducting electrophoresis therein includes a chamber with a gel matrix. The chamber has a first sealed region and a second sealed region, and an anode within the first sealed region of the chamber and in contact with the gel matrix, and a cathode within the second sealed region and in contact with the gel matrix. At least one of the electrodes also provides ions for driving the electrophoresis. The apparatus further includes a matrix with at least one sparingly water-soluble salt.

Abstract: The present invention relates to a mold for the manufacture of an electrophoresis cassette, the mold comprising a body having a cassette molding part formed on one face thereof, the cassette molding part being surrounded by a peripheral sheet engaging portion extending in a plane located at a different elevation than the cassette molding part to provide for substantially uniform stretching of the sheet on the cassette molding part.

Abstract: The present invention describes sample loading devices for use in polyacrylamide gel electrophoresis systems. The sample loading devices comprise alternating areas of absorbent membranes and diffusion barriers, where the diffusion barriers are formed by the application of some form of energy, such as heat, pressure, laser energy, RF energy or the like. The present invention also describes devices and methods for making sample loading devices, and methods of loading samples into polyacrylamide gel electrophoresis systems.

Abstract: The present invention provides an integrated, fully automated, high-throughput system for two-dimensional electrophoresis comprised of gel-making machines, gel processing machines, gel compositions and geometries, gel handling systems, sample preparation systems, software and methods. The system is capable of continuous operation at high-throughput to allow construction of large quantitative data sets.

Abstract: The present invention provides an integrated, fully automated, high-throughput system for two-dimensional electrophoresis comprised of gel-making machines, gel processing machines, gel compositions and geometries, gel handling systems, sample preparation systems, software and methods. The system is capable of continuous operation at high-throughput to allow construction of large quantitative data sets.

Abstract: An apparatus for electrophoresing a sample and for thereafter either scanning in the visible mode or the fluorescent mode, under control of a central processor, to provide scanning densitometry of the electrophoresed sample, and with the fluorescent mode scanning being performed in situ. The apparatus includes a gantry which moves from left to right in the XY plane. The gantry draws, delivers and deposits the samples and reagents, and includes safety devices to prevent the gantry from movement and damage when there are obstructions in the path of the gantry. A fluorescent scanning unit is moved by X- and Y-direction motors to position a photomultiplier over an electrophoresed sample. In this way, the electrophoretic sample can remain fixed in place during sample delivery, ultraviolet exposure and measurement operations.

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 present invention involves a power application device including a flat power pad having an electrically insulating support that supports first and second conductive regions. The first conductive region is connected to a positive output terminal of a power supply, and the second conductive region is connected to a negative terminal of the same power supply. The power application device may be used with electrophoresis gel carrier modules of various dimensions having first and second conductive paths leading from the vicinity of each end of the gel to separate external electrical contacts points. The external electrical contact points can each make contact with the conductive regions upon which the electrophoresis gel module sits. When properly positioned on the power pad, the electrophoresis gel module spans the distance between two conductive regions of opposite charge and the external contact points of the electrophoresis module make electrical contact with the conductive regions.

Abstract: Arranging a pair of temperature control units on both sides of gel 1 and arranging light-transmitting slit 134 on one of the elements, irradiation of an excitation beam over the gel 1 and signal detection are practiced through the slit 134. Introducing dry air onto the slit part, mildew occurrence is prevented on the detecting part. Detecting the power level applied to the gel and calculating the temperature of the temperature control units so that the gel temperature might be a predetermined temperature, on the basis of the detected power level, thereafter carrying out the feedback control of the power level, the gel temperature can be controlled appropriately and strictly during electrophoresis in an automatic fluorescent electrophoresis system, so that high-speed analysis can be done highly reproducibly at a higher voltage applied even by SSCP.

Abstract: An improvement in submarine gel electrophoresis apparatus is provided for performing electrophoresis at elevated voltages. A compartmental device is introduced into a conventional submarine gel apparatus to compartmentalize a buffer so that the buffer functions as a potent coolant but without generating massive heat during electrophoresis, which enables the submarine gel electrophoresis to be performed at higher voltages.

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: The heat sink plate of an electrophoresis unit is mounted to a fixed support with studs on the heat sink plate received in sleeves secured to the fixed frame. Compression springs encircle the sleeves and interpose between the heat sink plate and the fixed frame so that when clamping of a gel slab sandwich to the electrophoresis unit is made, a flat face of the heat sink plate orients in substantially full planar face-to-face contact with a flat face of a gel slab sandwich plate and can have following movement with the sandwich plate that is a pivoting thereof about at least two orthogonally disposed axes passing through the heat sink plate so that with said following movement, face-to-face contact is uniform across the plates and hence, heat transfer from the gel slab maintained uniform.

Abstract: A substantially closed cassette for conducting therein electrophoresis separation which includes a closed chamber, the chamber includes therein a body of gel, at least one ion source having a volume smaller than the volume of the gel for providing ions for driving the electrophoresis separation and electrodes for connecting the cassette to an external electrical power source, thereby enabling to drive the electrophoresis separation.

Abstract: An electrophoresis device consists of a housing which has opening(s) for the movement of gases from inside the housing to outside the housing and opening(s) for the movement of gases from outside the housing to inside the housing, whereby the condensation of gases on the inside of the housing is avoided or minimized.

Abstract: A gel electrophoresis separation apparatus comprising, in combination, a gaseous heat-exchange medium, a gaseous heat-exchange medium driving means, and an impingement means, whereby the gaseous heat-exchange medium is driven by the gaseous heat-exchange medium driving means across the impingement means to provide a flow of the gaseous heat-exchange medium on the surface of the gel plates, whereby the flow induced by passage of the gaseous heat-exchange medium through the impingement means thereby minimizes temperature gradients within the gel by forced convection.

Abstract: This invention is a channel plate that facilitates data compaction in DNA sequencing. The channel plate has a length, a width and a thickness, and further has a plurality of channels that are parallel. Each channel has a depth partially through the thickness of the channel plate. Additionally an interface edge permits electrical communication across an interface through a buffer to a deposition membrane surface.

Abstract: A device and method of direct water cooling for horizontal submarine gel electrophoresis is provided. A cooling water is utilized to replace a buffer for immersing a gel matrix during electrophoresis. The replacement offers an excellent heat absorption and a substantial reduction of electric current simultaneously, which enables the horizontal submarine gel electrophoresis to be performed at elevated voltages.

Abstract: This invention relates to an improved real-time scanning fluorescence electrophoresis apparatus for the electrophoretic analysis of fluorescently-labeled polynucleotide fragments. The apparatus is characterized by having an electrophoresis chamber containing an electrophoretic separation medium capable of accommodating multiple electrophoresis lanes arranged in a planar array, a fluorescence detector mounted on a translatable stage, a light source for exciting fluorescent molecules, and a computer for collecting data consisting of time, location, fluorescence wavelength and fluorescent intensity information. The improvements herein disclosed include, (i) using a spectral-array detector for detecting the emission light from the fluorescently-labeled polynucleotide fragments including the simultaneous detection of multiple fluorescent labels, and, (ii) a temperature control means to control the temperature of the electrophoretic separation medium during electrophoresis.