Abstract: An electrophoresis plate includes a substrate and an electrophoresis medium layer on the substrate. The electrophoresis plate may be used for medical testing by placing fluid specimens in wells on the electrophoresis medium layer so that the specimens can be separated into different fractions by applying an electric field across the electrophoresis medium layer. The electrophoresis medium layer includes liquid in a microporous gel such as agarose. The electrophoresis plate is packaged with a protective plastic film across the electrophoresis medium layer, but removal of the protective film prior to use of the electrophoresis plate leaves liquid that has been expressed from the electrophoresis medium layer on the surface of the electrophoresis medium layer.

Abstract: A thromboplastin extract including an aqueous thromboplastin extract of a powdered thromboplastin source including a metal ion chelator. A thromboplastin reagent for use in blood coagulation tests, the thromboplastin reagent includes the extract and calcium ions, and may include one or more of a stabilizer and a preservative.A process for preparing a thromboplastin extract including extracting a powdered thromboplastin source in an aqueous solution having a metal ion chelator, and separating the powder in solution into sedimented powder and supernatant thromboplastin extract. The supernatant thromboplastin extract is mixed with calcium ions, and may be mixed with one or more of a stabilizer and a preservative, to prepare thromboplastin reagent.

Abstract: An electrophoresis apparatus for automatically performing medical assays includes an electrophoresis platform which cooperates with a gantry assembly. The electrophoresis platform and the gantry assembly are movable along paths that are perpendicular to each other. An applicator assembly includes pipettes which transfer fluid samples from a specimen tray to an electrophoresis plate mounted on the electrophoresis platform. The electrophoresis platform then moves to a position into the gantry assembly, where electrophoresis is conducted to separate the samples into different fractions. The electrophoresis platform then moves beneath a reagent pouring station where a reagent is applied to make the separated fractions fluoresce under ultraviolet light. The electrophoresis platform is then moved beneath the gantry assembly again, and an air knife in the gantry assembly spreads the reagent.

Abstract: An analyzer system for automatic column chromatography includes chromatographic columns which are mounted in a rack. A drop removal mechanism system shakes the rack to transfer the last drop of eluate from the tip of a chromatographic column to a receptacle below the tip before the column is repositioned over another receptacle and another fluid or operation is introduced into the column. This prevents one eluate from contaminating another. The chromatographic column may have an upper end which is sealed by a foil member. During use, the foil member is ruptured by lowering a pressure cylinder with a seal-punching head against it. The pressure cylinder, which is part of the pressure tip unit, is then withdrawn so that fluid can be introduced into the column via the ruptured foil member. The pressure tip unit is then lowered into sealing engagement with the column so that pressure can be applied via a bore in the pressure cylinder.

Abstract: A pump for discharging the contents of a sealed container, such as a test tube, is connected to a body member which includes an inlet path and a discharge path with a delivery tube in the discharge path. A predetermined clearance is provided between the exterior of the delivery tube and the interior of the discharge path, the clearance providing venting, or blow-by, such that temperature changes do not cause accidental discharge of the contents of the container, while still maintaining sufficient resistance to venting for permitting pressurizing the interior of the test tube with the pump for accurately controlling the discharge of the test tube contents. A second or supplemental vent is provided in the pump.

Abstract: A platform for conducting electrophoresis includes a support, at least one first electrode which extends upward from the support, and at least one second electrode which also extends upward from the support. An electrophoresis plate is deposited on the support during a medical testing procedure. The electrophoresis plate includes a substrate and an electrophoretic medium layer on the substrate, the electrophoretic medium layer having first and second end regions. The at least one first electrode of the platform extends through a corresponding hole in the substrate to electrically contact the first end region of the electrophoretic medium layer and the at least one second electrode extends through a corresponding hole in the substrate to electrically contact the second end region of the electrophoretic medium layer. This arrangement makes it easy to install the electrophoresis plate on the platform and also provides good electrical contact with the electrodes.

Abstract: An improved method and apparatus for discharging the contents of a test tube which has a resilient self-sealing, reusable stopper at one end. The apparatus includes a flexible member that has a constricted end and a second end. The constricted end defines an outlet area that has an opening. A support having an aperture is disposed proximate to the flexible member. The interior of the flexible member defines a cavity. The apparatus further includes a single fluid transfer tube having a longitudinal bore. The fluid transfer tube has a sharpened end for insertion into and through the seal of the test tube and an outlet end that extends into the aperture. The longitudinal bore establishes a fluid flow path from the sharpened end to the outlet end. When the fluid transfer tube is inserted into the seal of the test tube, the interior of the sealed test tube and the outlet area opening are in fluid communication.

Abstract: A support system for an equipment housing includes a pair of screw-adjustable legs at one end of the housing and a pivoting trestle at the other end. The pivoting trestle is made of two generally U-shaped channel members, one nested inside the other. The channel members have side walls, and a bolt extends through holes in the side walls to pivotally mount one channel with respect to the other. The housing can be levelled by adjusting the effective length of the two legs, and the trestle automatically pivots to accommodate these adjustments as they are made.

Abstract: An analyzer system for automatic column chromatography includes chromatographic columns which are mounted in a rack. A drop removal mechanism system shakes the rack to transfer the last drop of eluate from the tip of a chromatographic column to a receptacle below the tip before the column is repositioned over another receptacle and another fluid or operation is introduced into the column. This prevents one eluate from contaminating another. The chromatographic column may have an upper end which is sealed by a foil member. During use, the foil member is ruptured by lowering a pressure cylinder with a seal-punching head against it. The pressure cylinder, which is part of the pressure tip unit, is then withdrawn so that fluid can be introduced into the column via the ruptured foil member. The pressure tip unit is then lowered into sealing engagement with the column so that pressure can be applied via a bore in the pressure cylinder.

Abstract: A chemical test kit for determining the presence of occult blood in a stool specimen is disclosed which includes an improved monitor system for verifying the effectiveness of the chemicals used in the test. A method of testing for occult blood is also disclosed which method includes verifying the effectiveness of the chemicals utilized in the test.

Abstract: A process for preparing a thromboplastin extract including extracting a powdered thromboplastin source in an aqueous solution having a metal ion chelator, and separating the powder in solution into sedimented powder and supernatant thromboplastin extract is disclosed. The supernatant thromboplastin extract is mixed with calcium ions, and may be mixed with one or more of a stabilizer and a preservative, to prepare thromboplastin reagent.

Abstract: A biological fluid collection and dispensing apparatus for attachment to a test tube includes a pump and a cannula assembly including a fluid transfer cannula and a vent cannula housed partially within the pump. Biological fluid may be both collected and delivered with the apparatus, and the apparatus may remain attached to the test tube during processing of the collected biological fluid sample.

Abstract: An analyzer system for automatic column chromatography includes chromatographic columns which are mounted in a rack. A drop removal mechanism system shakes the rack to transfer the last drop of eluate from the tip of a chromatographic column to a receptacle below the tip before the column is repositioned over another receptacle and another fluid or operation is introduced into the column. This prevents one eluate from contaminating another. The chromatographic column may have an upper end which is sealed by a foil member. During use, the foil member is ruptured by lowering a pressure cylinder with a seal-punching head against it. The pressure cylinder, which is part of the pressure tip unit, is then withdrawn so that fluid can be introduced into the column via the ruptured foil member. The pressure tip unit is then lowered into sealing engagement with the column so that pressure can be applied via a bore in the pressure cylinder.

Abstract: A test sheet for the determination of the presence of a substance having peroxidase-like activity in a throw-in-the-bowl fecal occult blood test, includes a specimen test area and a positive control area. The test area has deposited thereon a test ink having at least one oxygen donor reagent and a chromogen reagent capable of being oxidized by the oxygen donor in the presence of blood or a substance having peroxidase-like activity, to provide a visually observable change of color. The test ink also includes a water soluble polymer for immobilizing the chromogen and oxygen donor. The positive control area has deposited thereon the test ink and a substance having the peroxidase-like activity.

Abstract: An analyzer system for automatic column chromatography, and method for its use, includes an array of chromatograph columns and multi-cell cuvettes associated with each column. Chromatographic separation takes place under a constant, low fluid pressure. A pressure system distributes air to each column during chromatographic separation but prevents leakage of air if the column array is partially empty. The multi-cell cuvette collects and separates the eluates associated with a single column. The system provides for automatic removal of caps from the bottoms of the chromatograph columns and provides for automatic optical density reading.

Abstract: A method and apparatus for removing unreacted protein and unreacted antisera from a gel plate during immunofixation electrophoresis. The apparatus includes a pressure plate movable toward and away from a fixed base for exerting a desired force on the electrophoresis plate. A stop member limits the movement of the pressure plate toward the fixed base thus controlling the amount of pressure on the electrophoresis plate.

Abstract: A biological fluid collection and dispensing apparatus for attachment to a sealed test tube includes a pump and a housing, the housing having a movable portion, and a cannula assembly mounted relative to the housing. Biological fluid is withdrawn from a patient and flows through the pump and housing into the interior of the sealed test tube. The pump is actuated initially to release a delivery conduit and to move the housing such that part of the cannula assembly pierces the test tube seal. The pump is thereafter actuated to pressurize the contents of the test tube such that aliquots may be dispensed through the cannula assembly and delivery tube.

Abstract: A test sheet for the determination of the presence of a substance having peroxidase-like activity in a throw-in-the-bowl fecal occult blood test, includes a specimen test area and a positive control area. The test area has deposited thereon a test ink having at least one oxygen donor reagent and a chromogen reagent capable of being oxidized by the oxygen donor in the presence of blood or a substance having peroxidase-like activity, to provide a visually observable change of color. The test ink also includes a water soluble polymer for immobilizing the chromogen and oxygen donor. The positive control area has deposited thereon the test ink and a substance having the peroxidase-like activity.

Abstract: A method of formulating a test ink for a fecal occult blood test product including the steps of: (a) providing at least one chromogen reagent in a first solution; (b) providing a moisture barrier which is a water-soluble polymer; (c) adding at least one oxygen donor reagent to the moisture barrier; (d) adding at least one color enhancer to the result of step (c) to thereby form a second solution; and (e) adding the second solution to the first solution.

Abstract: An improvement in the immunofixation electrophoresis procedure for detecting proteins in serum, urine or cerebral spinal fluids. Samples are placed on a gel and subjected to electrophoresis for resolving or separating proteins. Thereafter, antisera are applied to the sample areas to cause an antibody-antigen precipitation reaction if the specific proteins are present. The invention includes the provision of a control system for each electrophoretic gel to verify that the antisera have retained their lability, i.e., the ability to react.