Abstract:
A leakage detection method in an automatic pipetting apparatus for objectively judging leakage by measuring an internal pressure of a pump connected to a nozzle tip. At Step 202, distilled water (90) is sucked, and when an internal pressure P1 of a pump after completion of suction is near the atmospheric pressure, leakage is identified. At Step 203, the tip (36) is kept at halt for 30 seconds, for example, without allowing it to rise after the internal pressure P1 of the pump after completion of suction is measured at Step 202. The internal pressure P2 of the pump is again measured by a pressure sensor. When this internal pressure P2 is different from the internal pressure P1 previously measured, leakage is identified. Further, at Step 204, sucked distilled water (90) is discharged into the same test tube (62), and the internal pressure of the pump is monitored by the pressure sensor. If any sharp fluctuation of the internal pressure is found, leakage is judged. When leakage is detected, leakage detection measurement is terminated.
Abstract:
An apparatus (10) is disclosed which may be employed for determining the relaxation rate of a muscle which has been caused to contract in response to an electrical stimulus. The apparatus comprises a means (13) for supporting the forearm and wrist of a person in a particular palm-up position with the wrist extended; a means (47) for measuring the force exerted upon a load cell (43) by the person's thumb during a test cycle, a means (70) for providing an electrical stimulus to the person's ulnar nerve, and a computer (65) for receiving, storing, plotting and analyzing the force data collected by the transducer (43).
Abstract:
An assay to confirm the presence of antibodies to T. cruzi in a test sample. The assay comprises detecting the presence of antibody to three T. cruzi antigens, Gp90, Gp60/50 and LPPG in a test sample. The presence of antibody in the test sample to at least two of three T. cruzi antibodies is indicative of a confirmed reactive sample. Also provided are diagnostic reagents for detection of T. cruzi, a process for purifying GP60/50, a process for linking a protein and LPPG, and diagnostic test kits for use when assaying for antibodies to T. cruzi.
Abstract:
The present invention relates to the measurement of estradiol using competitive immunoassay methods. The inventors unexpectedly discovered that estrone and its derivatives conjugated to a label is a particularly effective tracer when used in conjunction with estradiol specific antibodies to determine estradiol levels in fluid samples. The present invention also utilizes 5 alpha -dihydrotestosterone to enhance the assay performance.
Abstract:
The present invention involves a method of amplifying RNA by producing complementary DNA (cDNA) by reverse transcription of RNA, and amplification of the cDNA sequences. The analysis of the amplified material facilitates the detection of pathogens and disease states associated with the presence of particular nucleic acid sequences, so the present invention is important in medical diagnostic procedures. A method of producing cDNA of predetermined length is also disclosed.
Abstract:
The present invention relates to the finding that the class of mutant p53 proteins which bind to HSP70 defines a group of mutant p53 proteins which elicit serum autoantibodies. Thus, disclosed is a method of classifying tumor cells for the ability to produce serum p53 autoantibodies in a patient carrying such tumor cells, a method of detecting tumor cells containing a mutant p53 protein capable of forming a complex with a 70 kilodalton heat shock protein (hsp70) in the cells in a patient, a method of distinguishing tumor cells capable of causing more aggressive disease in a patient carrying the tumor cells, and a method of monitoring a patient for the recurrence of disease in a patient previously diagnosed as carrying tumor cells.
Abstract:
A method for administering pyruvate is disclosed which comprises administering a therapeutically effective amount of a pyruvate precursor to a mammal in the form of pyruvamide or a pyruvyl-amino acid. The pyruvyl-amino acid is preferably selected from the group comprising pyruvyl-glycine, pyruvyl-alanine, pyruvyl-leucine, pyruvyl-valine, pyruvyl-isoleucine, pyruvyl-phenylalanine, pyruvyl-proline and pyruvyl-sarcosine, and their amides and esters as well as their salts. Associated with the administration of a pyruvate precursor to a mammal in accordance with this invention are improved insulin resistance, lower fasting insulin levels, and reduced fat gain. Novel methods of synthesizing several pyruvate precursors are also disclosed.
Abstract:
An automated, continuous and random access analytical system (18), having apparatus and methodology capable of simultaneously performing multiple assays of liquid samples using different assay methodologies, and providing continuous and random access while performing a plurality of different assays on the same or different samples during the same time period, is disclosed. A method is also disclosed of operating an automated continuous and random access analytical system (18) capable of simultaneously effecting multiple assays of a plurality of liquid samples wherein scheduling of various assays of the plurality of liquid samples is followed by creating a unit dose disposable and separately transferring a first liquid sample (26) and reagents (30) to a reaction vessel (34) without initiation of an assay reaction sequence, followed by physical transfer of the unit dose disposable to a processing workstation (52), whereby a mixture of the unit dose disposable reagents and sample (34) are achieved during incubation. The system (18) is capable of performing more than one scheduled assay in any order, and assays where more than such scheduled assays are presented. The automated, continuous and random access analytical system (18) is also capable of analyzing the incubated reaction mixtures independently and individually by at least two assay procedures.
Abstract:
Novel haptens and related conjugates based on acridine-9-carboxylic acid, as well as methods for making and using such conjugates. Haptens based on the above core structure may be substituted at positions 3 or 6. Using tethered intermediates, immunogens, tracers, solid supports and labeled oligonucleotides are all described; as are methods for using the intermediates to prepare the conjugates, methods of using the conjugates to make and purify antibodies, as assay tracers, and in nucleic acid hybridization assays. Kits containing haptenated oligonucleotides and anti-hapten conjugates are also described.
Abstract:
Purpose: to judge shortage of a discharge quantity, by identifying the presence of any bubbles at the time of discharge. Constitution: characteristics (101) involving bubbles provides a different internal pressure of a nozzle at nearly the end of discharge of a sample than that provided by characteristics (100) not involving bubbles. The nozzle internal pressure is detected at the time of judgement (105), and this detection value is compared with a threshold value. Accordingly, the occurrence of the bubbles can be judged, and shortage of a discharge quantity is judged on the basis of this judgement to give an alarm.