Abstract:
A thin-wall centrifuge tube (10) having multiple chambers (24, 26) for use in fluid sample investigation with an ultracentrifuge. More particularly, the multiple chamber ultracentrifuge tube (10) can be used, for example, in lipoprotein separation. The ultracentrifuge tube (10) may have two or more separate chambers (24, 26) which, subsequent to centrifugation, can be sealed from each other to retain the separated constituents (50, 54) of the sample under investigation. The chambers (24, 26) in the tube (10) are joined by a constricted area (20) which permits fluid communication between the chambers (24, 26). The tube (10) is designed to be used in conjunction with a support spacer (32) adjacent the constriction (20) in the tube (10) so that the tube (10) is properly supported during high speed centrifugation.
Abstract:
A rotor attachment assembly to provide efficient and secure connection between a rotor (10) and a centrifuge drive mechanism (18). The assembly is designed in such a manner that not only attachment, but also disconnection is accomplished in a convenient one-step operation. The utilization of a single connecting shaft (24) with flexible fingers (30) contributes to the ease of operation as well as the ease of manufacture of the assembly.
Abstract:
A reagent storage and delivery apparatus. The invention includes containers (11, 12, 13) with elastomeric septums (16) in the mouth portions (15) thereof. When attached to a supporting rack (19), a hollow needle (24) on the supporting rack (19) pierces the elastomeric septums (15) and allows the reagent to be dispensed from the containers (11, 12, 13) through the needle (24).
Abstract:
A capillary, interface and holder for a capillary electrophoresis system are provided herein. The capillary is disposed in a substantially planar housing having side surfaces. The capillary includes at least two, substantially coplanar capillary openings which extend through an interface surface located on one of the side surfaces. The interface includes at least two spaced apart receptacles for receiving an ionic fluid. Each receptacle includes a liquid permeable medium having a capillary area and a conductor area. Each capillary area is in fluid communication with one of the capillary openings and each conductor area is in contact with at least one electrical conductor. At least two of the capillary areas are substantially coplanar. The ionic fluid is disposed in each receptacle to create an electrical path between the capillary area and conductor area of each receptacle. The holder selectively retains the housing and the interface so that the capillary areas contact the capillary openings and the conductor areas contact the electrical conductors.
Abstract:
A system for a clinical lab that is capable of automatically processing, including sorting, of multiple specimen containers. The system comprises a central controller, a workstation (100), one or more analyzers (2000), and an automated centrifuge (1000). The workstation (100) has automatic detectors for detecting the presence of a holder (14) holding specimen containers (12). The workstation (100) has a bar code reader for reading bar codes on the containers. The system has a transport subsystem, preferably a workstation robotic arm (700) and an analyzer robotic arm (2002) for transporting the specimen containers (12), moving them to and from the workstation (100), to and from the analyzers (2000), and to and from the centrifuge (1000). The centrifuge is loaded with buckets (1200) containing specimen containers (12). The workstation (100) can be provided with a balance system (800) for balancing the weight of the buckets (1200) used. The workstation (100) can also have a decapper (900) for automatically removing caps from the specimen containers.
Abstract:
A one piece, injection molded single piece, well container (10) suitable for reagents for use in a clinical instrument such as a protein analyzer, normally molded from a high density polyethylene or other recyclable plastic. The container is one or more wells, uses standard caps, and is readily adapted to automatic filling equipment. The molded, single piece reagent cartridge (10) is used in a clinical instrument, the reagent cartridge (10) comprised of a plurality of storage wells (24, 26) located in a line in fixed relationship. The reagent cartridge (10) has a guide (16) at one end which is engageable with a means (40) on the receiving means on an analyzer to restrain the cartridge (10) from radial or lateral movement. Each of the wells (24, 26) has side walls (30) and a closed bottom (28), and the side walls (30) have an upper terminal position including an access opening. An integrally formed hollow shell (14) open at the bottom and otherwise substantially enclosing said wells (24, 26) from a point below the terminal portion is provided to form a hollow space within the shell (14) around the exterior of the wells to permit the flow of conditioned air around the walls. Positive retention is provided by forming a hole (67) through the wall, which engages a detent (68) formed on the retention means.
Abstract:
An assay for detecting in a test sample, an analyte that undergoes auto-oxidation is disclosed. The assay comprises the steps of forming a reaction mixture by combining in an aqueous medium (i) a sample containing the analyte and (ii) a stabilizer that reduces the rate of radical mediated auto-oxidation of the analyte. The reaction mixture is incubated for a period of time and the rate of auto-oxidation is detected. When the detected rate of auto-oxidation is substantially zero, a sufficient quantity of an enzyme is added, that catalyzes the oxidation of the analyte. In the presence of the stabilizer, the analyte can be oxidized to a product species. The product species, the analyte, or both can be detected.
Abstract:
An assay for detecting the presence or amount of a target polynucleotide sequence of interest in a test sample is disclosed. The assay comprises the steps of forming a reaction mixture by combining in an assay medium (i) a first reagent and (ii) an aliquot of the test sample suspected of containing the target polynucleotide sequence. The reaction mixture is subjected to denaturing conditions, and exposed to hybridization conditions allowing the first reagent to hybridize with any target polynucleotide present. A second reagent is then added, the reaction mixture undergoes hybridization conditions and the change in turbidity of the reaction mixture is detected, correlating with the presence of the target polynucleotide in the sample.
Abstract:
A vented probe (10) for adding and removing a sample (30) from a container (28) having an opening (32) which is capped with a stopper (34) and a method for adding and/or removing a sample (30) from the container (28) are provided. The probe (10) comprises a hollow, tubular-shaped body (12) having an outer surface (14), an inner surface (16) which defines a lumen (17), and a first end (18) for inserting through the stopper (34) and a second end (20). A sample aperture (22) extends from the outer surface (14) into the lumen (17) proximate the first end (18) of the body (12) and a regulating aperture (24) extends through the body (12) into the lumen (17) proximate the second end (20) of the body (12). A vent passageway (26) is disposed in the body (12) between the first end (18) and the second end (20). The vent passageway (26) allows for venting of the container (28) when the probe (10) is disposed in the stopper (34). There is no direct communication between the vent passageway (26) and the lumen (17). The vent passageway (26) typically includes three spaced-apart grooves which extend longitudinally in the outer surface (14) of the body (12). These grooves each have a sufficient depth and width so that each groove is not occluded when the probe (10) is positioned in the stopper (34).
Abstract:
A composition, which has utility as a storage buffer and as a sample diluent before analysis by capillary zone electrophoresis (CZE), is comprised of water, a borate compound, a buffer compound and a pH modifier for maintaining a physiological pH. In addition, a conductivity adjusting compound is present so that the conductivity of the composition is about the same as a prospective capillary electrophoresis running buffer. Containers with storage buffer/sample diluent can be assembled in a kit for conducting serum protein electrophoresis (SPE) or immunosubtraction (IFE/s) analysis. Moreover, the storage buffer/sample diluent can be used in methods of preparing samples for CZE analysis, such as quantitative dilutions and enzymatic or immunological reactions.