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 non-liquid scatter standard for use in nephelometry and turbidimetry systems which comprises a clear silicon rubber gel in which an effective light scattering amount of inorganic particles are suspended. The particles have an index of refraction greater than that of the silicon rubber gel.

Abstract: The invention provides in one aspect a method for generating a schedule for the performance of a process, wherein the process comprises a plurality of steps. Each step of the process comprises one or more operations. The method comprises first obtaining input containing information defining the process and then generating from the input a series of nodes definitions, each node definition corresponding to at least one step of the process. Each node definition includes duration and device usage information relating to at least one step and further includes information identifying at least one previous step and at least one subsequent step. Then, one or more tasks are generated using the series of node definitions, each task comprising at least one step of the process, such that every step in the process is associated with at least one task.

Abstract: A method and device for detecting the presence of hemolysis, icteris and lipemia in a serum sample are provided herein. The method includes the steps of positioning a probe inlet of a probe in a sample container, aspiring at least a portion of the serum sample into a probe lumen of the probe from the sample container, and monitoring the serum sample in a probe lumen to determine whether hemolysis, icteris and lipemia are present in the serum sample. The serum sample is monitored with a detector which performs spectrophotometric analysis of the serum sample in the probe lumen through a substantially transparent section of the probe. From the spectrophotometric analysis, a hemolytic index, an icteric index and a lipemic index of the serum sample can be established. Based upon these serum indices, the serum sample can be transferred to a clinical analyzer for additional tests or can be disposed of because the sample is compromised.

Abstract: A compound of general formula ##STR1## wherein R is methyl R' is selected from the group consisting of trityl and pixyl, and R" is H or OMe. These compounds may advantageously be employed in the synthesis of oligonucleotides by conventional methods, such as automated solid phase synthesis. Use of ethylene diamine in the cleavage and deprotection procedure substantially eliminates the formation of undesirable side products.

Abstract: A centrifuge rotor with a body having a spin axis and a plurality of bores formed therein, each of which is adapted to support a centrifuge container. The rotor includes a load reducing feature to decrease the loading between the rotor body and the centrifuge container, during centrifugation. The load reducing feature includes separating a portion of an annular shoulder of a centrifuge container from the rotor body. The portion of the annular shoulder that is separated is disposed between the spin axis and the bore associated with the centrifuge container.

Abstract: A polarographic sensor device to determine the partial pressure of a gas in a sample medium is disclosed. The device comprises a) a substantially hydroscopic electrolyte composition joining a pair of spaced apart electrodes, one of the pair of electrodes being a sensing electrode; b) a membrane permeable to gas but impermeable to the electrolyte, the membrane having a front section for separating the electrodes and the electrolyte from the sample medium; and c) a fastener comprising a sleeve having a body portion and a lip, the body portion retaining the fastener and a side section of the membrane, and the lip retaining a portion of the front section of the membrane and holding substantially the entire front section in a spaced apart relationship from the sensing electrode.

Abstract: Disclosed herein are N.sup.4 protected deoxycytidines for use in the synthesis of oligonucleotides, the protecting groups being represented by the formula: --CO--(CH.sub.2).sub.0-9 --CH.sub.3. Preferred embodiments are N.sup.4 acetyl deoxycytidines and include N.sup.4 acetyl deoxycytidine phosphoramidites and N.sup.4 acetyl deoxycytidine H-phosphonates. When used to prepare oligonucleotides the protected deoxycytidine compounds provide high quality oligonucleotide products with little side product from cleavage and deprotection reactions carried out with alkyl amine compounds.

Abstract: An assay for determining the presence of an analyte of interest in a test sample containing an interfering substance that interferes with the assay is disclosed. The assay comprises the steps of forming a reaction mixture by combining in an assay medium (i) an assay system containing components for detecting the analyte of interest, (ii) a test sample containing the analyte and an interfering substance, and (iii) an additional amount of the interfering substance in a quantity sufficient to substantially mask the effect of the interfering substance in the test sample. This reaction mixture is incubated under conditions sufficient to allow complex formation. This resultant complex formation is detected and the presence of the analyte in the test sample is determined.

Abstract: An aqueous, liquid-stable thiol activator solution is disclosed. The solution can include a thiol activator, such as N-acetyl-L-cysteine and a stabilizing agent, such as mannitol. The thiol is stabilized in the aqueous solution for at least about one year under storage conditions and for at least about 28 days under open-bottle conditions. The solution can be used as a reactivator of creatine kinase catalytic activity.

Abstract: A swinging bucket centrifuge rotor having free-floating trunnion pins with each pair of trunnion pins having an interlocking mechanism disposed therebetween. The rotor includes a yoke having an axis of rotation, a plurality of spaced arms extending radially outward from the axis of rotation, each of which terminates in a bulwark. The bulwark includes a pair of intersecting bores, each of which extends along an axis lying in a plane spreading transverse to the axis of rotation. Each of the trunnion pins has a lengthwise axis and is disposed in one of the pair of intersecting bores. The trunnion pins include trunnion and coupling portions. The coupling portion has a surface. The interlocking mechanism includes a recess formed into the surface of the coupling portion and a coupling pin. The recess of each of trunnion pin of the pair of trunnion pins is superimposed upon the recess of the remaining trunnion pin, forming a chamber.

Abstract: An improved automated diagnostic analyzer and method of the type which includes a reaction carousel having cuvettes to receive sample and reactant for photometric analysis and to index and park for addition of sample, reactant and washing of cuvettes. Alternative reactant and/or sample addition points are provided so the analyzer controller may index cuvettes to provide greater frequency at which washing of cuvettes may take place simultaneously with addition of sample or reactant.

Abstract: A method for making a homogeneous succinylated polypeptide is disclosed. The method can be carried out by adding a succinyl-containing compound to a polypeptide solution, followed by raising the pH of the polypeptide solution to a pH of between about pH 10 to pH 12.5. The succinylation reaction between the succinyl-containing compound and free amino groups of the polypeptide is essentially complete upon raising the polypeptide solution pH to the alkaline pH.

Abstract: A detection system for sequentially and repetitively scanning a plurality of sample volumes and detecting electromagnetic radiation emitting from each of the sample volumes includes a plurality of coplanar side-by-side capillaries each containing a sample volume, an electromagnetic radiation source, a mirror aligned to receive and reflect electromagnetic radiation, a scanner for moving the mirror, and a detector aligned to receive electromagnetic radiation collected from the sample volumes. In operation, the scanner adjusts the mirror position so that the mirror is positioned to receive the electromagnetic radiation from the electromagnetic radiation source and reflect the electromagnetic radiation sequentially and repetitively to the sample volumes. Emitted electromagnetic radiation from the sample volume is collected and directed to a detector where a signal is generated in response to the interaction of the electromagnetic radiation with the sample.

Abstract: A hybrid fiber-composite centrifuge container having a cylindrical metal sleeve, with a smooth inner surface permanently coupled to the fiber reinforced base. The reinforced base has an open end, a closed end and a cylindrical wall extending between the closed and open ends, with the metal sleeve coupled to the cylindrical wall proximate to the open end forming a sleeve-base interface. The base is formed from a plurality of layers of fiber material wound helically and circumferentially about the axis of the base. Among the plurality of layers of fiber material is a lane-change feature which provides a uniform outer diameter to the cylindrical wall that is coextensive with the interface. The uniform outer diameter helps prevent uncoiling of the plurality of layers of fiber material during centrifugation.

Abstract: A technique and circuit for measuring direct current flowing through a conductor at a high voltage employs a capacitor connected in series with the conductor, and a neon lamp connected in parallel with the capacitor. The series connected capacitor and conductor are connected to a high voltage source such that the current flowing through the series connected capacitor and conductor charges up the capacitor. Since the capacitor and the neon lamp are connected in parallel, the voltage across the electrodes of the neon lamp follows the voltage across the capacitor. When the voltage across the electrodes of the neon lamp reaches the lamp's ignition voltage, the neon lamp fires, and discharges the capacitor until the voltage across the electrodes of the neon lamp falls to the lamp's extinction voltage. The light signal generated by the neon lamp is picked up by a fiber optic cable and transmitted to a remote receiver for processing.

Abstract: Methods for profiling oligosaccharides released from glycoproteins and methods for the electrophoretic separation of high mannose, complex and hybrid oligosaccharides are disclosed. The disclosed methods include first providing an analytical sample which includes at least one released oligosaccharide and introducing the sample into an electrophoretic channel containing an electrophoretic separation medium having a pH less than 8 and greater than 2.5.Then applying a sufficiently high electric field causes the released oligosaccharides to electrophoretically migrate and separate within the electrophoresis channel in accordance with their molecular size or charge to mass ratio. Detecting the separated oligosaccharides provides glycoprotein conjugate profiling information. Preferred embodiments include using an electrophoresis separation medium which includes a lithium acetate buffer having pH of about 4.75 and a gel of about 0.4 wt % polyethylene oxide.

Abstract: A trifunctional conjugate is providing having three chemical moieties attached through a spacer moiety. At least two of the chemical moieties are relatively small molecules, usually less than about 7,000 Daltons in size. The spacer moiety is selected to impart certain steric properties to the conjugate. In one embodiment, the binding of a macromolecular specific binding partner to one of the chemical moieties sterically inhibits the binding of a different macromolecule to another chemical moieties. In another embodiment, the binding of a first chemical moiety to a macromolecule restricts the subsequent binding of a second tridentate member to a proximate location on the same macromolecule. The three chemical moieties are preferably a nitrophenylazido residue, a phenyl boronic acid residue, and a solid support or a label such as biotin. The spacer is preferably cysteine, lysine, glutamic acid, pyroglutamic acid, S-acetylmercaptosuccinic anhydride or .omega.-carbobenzoxylysine.

Abstract: Double stranded nucleic acid duplexes serve as universal harvestable and cleavable link systems in a variety of different types of immunoassays (e.g., sandwich, competitive, etc.). Depending upon the type of assay, at least one specific component involved in the assay system is attached to a first member of a pair of sequences forming a double stranded nucleic acid (i.e., two oligonucleotides comprising substantially complementary sequences). The assay is carried out in the presence of a support to which is attached an oligonucleotide which is the other member of the pair of sequences forming a double-stranded nucleic acid duplex under hybridization conditions. Upon the hybridization of the two complementary oligonucleotides to form a duplex, the component of the assay system to which the first member of the pair of oligonucleotides is attached may thereby be effectively removed from the solution phase and harvested onto the support.

Abstract: A gel pump operated by a stepper motor may be used to deliver fresh gel to one or more capillaries through one or more manifolds and valves. By controlling the valves, fresh gel delivered by the pump will replace the old gel in the capillaries for an automated gel replacement system. In a different setting of the valves, the manifolds may be purged of the old gel prior to delivery of fresh gel to the capillaries. The gel delivery system may also be combined with an electrophoresis system so that sealing connection capable of withstanding high pressure adequate for gel injection need not be frequently broken when the gel is to be replaced. Manifold/reflector assembly is advantageously used in the system that facilitates electrical circuit for electrophoresis and for gel replacement.