Abstract: A random access microbiological analyzer for performing AST and ID tests on samples using on-board inventories of different AST test arrays and different ID test rotors within separate AST and ID incubation and analysis chambers.

Abstract: A cup-like broth container comprising four mutually opposed pairs of connected sidewalls with a protruding rib formed on each of four perpendicularly opposed single sidewalls and four Y-shaped clamping ridges attached to and extending outwardly from a single one of the four sidewalls located between the four sidewalls having a protruding rib.

Abstract: A circular shaped rotor to facilitate automated identification testing of microorganisms in a microbiology analyzer having two circular arrays of microwells downwardly projecting from the top of the rotor connected to a recessed central region by a plurality of microchannels formed in the upper surface and connecting the recessed central portion to the second plurality of microwells; the rotor is further adapted to be rotated by a source of rotational energy and moved throughout the analyzer using troughs formed near its outer diameter.

Abstract: An elongate canister having a generally rectangular cross-section sized to house a plurality of antibiotic susceptibility test arrays stacked one atop another and maintained secure within an environmentally controlled inventory chamber in a random access microbiological analyzer.

Abstract: A method for rapidly mixing a liquid solution in a container by causing a small magnetic mixing member to rapidly revolve within the solution in a generally circular pattern in response to a pair of revolving magnetic fields positioned alongside the container.

Abstract: Performing antibiotic testing on samples contained in test arrays by orienting the arrays relative to the direction of gravity so that test solution within the microwells is drawn downwards and air within the microwells is forced to the uppermost portion of the test array. Antibiotic testing is conducted using an interrogating beam of radiation passing horizontally through the microwells at locations devoid of air bubbles.

Abstract: A microbiological test array with a plurality of microwells connected by a microchannel to a solution reservoir. Subsequent to filling the microwells, the microchannels are sealed to protect the integrity of the solution in the test microwells.

Abstract: A method for reducing carryover of and delivering liquid taken from a source container by a dispensing means to a target container by spinning the target container so that any liquid within the target container is removed from the dispensing means prior to dispensing liquid into the target container.

Abstract: Monitoring the intensity pattern of a radiation beam reflected from a sample tube before and after the tube is tilted from an original alignment to determine signal areas that correspond to the location of a liquid interface within the tube.

Abstract: A computer interface module having a first information display screen that is directly linked to a plurality of additional information display screens containing on-line information about the operational status of plurality of interrelated automated devices as well as information describing the location of any specific sample and the status of clinical tests to be performed on the sample. A combination of general function buttons and specific function buttons as well as a scrollable text area where informational messages are displayed.

Abstract: The invention pertains to a novel ionophore having the general structure: wherein R1, R2, R3 and R4 are independently straight or branched chain alkyl having 4 to 12 carbon atoms or the alkyl groups may optionally contain a cycloalkyl group having 3 to 8 carbon atoms or R1 and R2 or R3 and R4 together with N to which they are attached, can form a ring having 5 to 8 carbon atoms. This ionophore has increased selectivity for carbonate ions over other ions, especially salicylate. The invention includes membranes containing effective amounts of the novel ionophores and -sensors containing these membranes.

Abstract: A method for rapidly mixing a liquid solution in a sample container by causing a small magnetic mixing member to rapidly revolve or orbit the container's axis within the solution in a generally circular pattern in response to a revolving magnetic field positioned in close proximity to the sample container.

Abstract: A liquid aspiration method which includes a method for determining the quality of the aspirated sample through mathematical analysis of the pressure profile generated before, during, and after the aspiration process and comparison of the results with predetermined known values.

Abstract: A method is disclosed for modifying an oligonucleotide, which method has application to the detection of a polynucleotide analyte. An oligonucleotide is reversibly hybridized with a polynucleotide, for example, a polynucleotide analyte, in the presence of a 5′-nuclease under isothermal conditions. The polynucleotide analyte serves as a recognition element to enable a 5′-nuclease to cleave the oligonucleotide to provide (i) a first fragment that is substantially non-hybridizable to the polynucleotide analyte and (ii) a second fragment that lies 3′ of the first fragment (in the intact oligonucleotide) and is substantially hybridizable to the polynucleotide analyte. At least a 100-fold molar excess of the first fragment and/or the second fragment are obtained relative to the molar amount of the polynucleotide analyte. The presence of the first fragment and/or the second fragment is detected, the presence thereof indicating the presence of the polynucleotide analyte.

Abstract: The present invention relates to a method for detecting the amount of a target polynucleotide in a sample. A combination is provided in a medium. The combination comprises (i) a sample suspected of containing the target polynucleotide, the target polynucleotide being in single stranded form, (ii) a reference polynucleotide comprising a sequence that is common with a sequence of the target polynucleotide, and (iii) a predetermined amount of an oligonucleotide probe that has a sequence that hybridizes with the sequence that is common. The combination is subjected to conditions for amplifying the target polynucleotide and the reference polynucleotide. The conditions permit formation of substantially non-dissociative complexes of the target polynucleotide and the reference polynucleotide, respectively, with the oligonucleotide probe. Furthermore, the predetermined amount of the oligonucleotide probe is less than the expected amount of the amplified target polynucleotide.

Abstract: The current invention relates to the use of luminescent oxygen channeling immunoassay (“LOCI”) technology to monitor amplification reactions, especially polymerase chain reactions (“PCR”). More specifically, the current invention involves the use of LOCI to measure the kinetics of a PCR reaction in an all-in-one assay format in order to quantitatively and qualitatively detect a target polynucleotide.

Abstract: The invention relates to methods of determining the presence or amount of an analyte in a sample suspected of containing the analyte, said method comprising the steps of: (a) bringing together in an aqueous medium to form a mixture: (i) the sample; (ii) at least one specific binder for the analyte; (iii) a first binding agent coupled to either (1) exogenous analyte or (2) the specific binder for the analyte; (iv) a support comprising a second binding agent; b) adding an activator to the mixture, wherein the activator binds the first binding agent and the second binding agent of the support to immobilize the first binding agent; c)determining the amount of the analyte in the sample by detecting the immobilized first binding agent, the presence or amount thereof being related to the presence or amount of the analyte in the sample.

Abstract: Calibrating an immunoassay by generating two reaction rate measuring curves, from samples having higher and lower relative levels of antigen, extrapolating a combination of the curves to cover sample concentrations known to contain an excess of antigen relative to an amount of capture reagent and combining the low end linear potion of the higher reaction rate measuring curve with the higher end portion of the extrapolated reaction rate measuring curve, thereby eliminating measuring inaccuracies otherwise arising from the hook effect. For antigen concentrations higher than the assay range, a high antigen signal utilizing the two rates avoids reporting false results.

Abstract: A device is provided for both collecting and testing a fluid specimen. The device includes a specimen container having a collection chamber, an isolation chamber and a test chamber. The collection chamber is in fluid communication with the isolation chamber and sealed from the test chamber. The isolation chamber is also sealed from the test chamber. The fluid specimen is collected in the collection chamber and an aliquot is isolated in the isolation chamber. A fluid releasing element is provided to release fluid from the isolation chamber and establish a flow path to the test chamber while sealing the isolation chamber from the collection chamber. In accordance with another aspect of the present invention, the specimen container may include a tamper evident lid which provides an identification of whether or not the container has been opened which may indicate that the contents of the container have been compromised.