Abstract:
The invention concerns a laboratory product transport element for a laboratory transport system with an energy receiver and/or energy accumulator to provide drive power, at least one signal receiver to receive control signals, a control unit to generate drive signals as a function of at least one control signal obtained from the at least one signal receiver, movement devices for independent movement of the laboratory product transport element on a transfer path as a function of the drive signals of the control unit, in which the drive devices are driven by the drive power and at least one holder to hold a laboratory product being transported. The invention also concerns a laboratory transport system with at least one laboratory product transport element according to an embodiment of the invention and a transfer path arrangement. The invention also concerns methods for operation of laboratory transport systems according to an embodiment of the invention.
Abstract:
A sample tube rack for receiving at least one sample tube comprises an upper part comprising an upper surface, wherein at least one upper opening for receiving the sample tube is provided in the upper surface; an intermediate part comprising an intermediate surface, wherein at least one intermediate opening for receiving the sample tube is provided in the intermediate surface; and a lower part comprising a supporting surface, wherein at least one supporting position for supporting the sample tube is provided in the supporting surface. Therein, the intermediate part is connected to both the upper part and the lower part such that the at least one upper opening is substantially aligned above the at least one intermediate opening and above the at least one supporting position for receiving the at least one sample tube. At least one gripping orifice is provided in a lateral side of the lower part.
Abstract:
The invention concerns a laboratory product transport element for a laboratory transport system with an energy receiver and/or energy accumulator to provide drive power, at least one signal receiver to receive control signals, a control unit to generate drive signals as a function of at least one control signal obtained from the at least one signal receiver, movement devices for independent movement of the laboratory product transport element on a transfer path as a function of the drive signals of the control unit, in which the drive devices are driven by the drive power and at least one holder to hold a laboratory product being transported. The invention also concerns a laboratory transport system with at least one laboratory product transport element according to an embodiment of the invention and a transfer path arrangement. The invention also concerns methods for operation of laboratory transport systems according to an embodiment of the invention.
Abstract:
A system is disclosed. The system includes an aliquotter module. The aliquotter module includes a track including: a travel lane; a first loop; and a second loop configured to transport sample carriers with primary sample containers. The aliquotter module can further include a pipettor that can aspirate a first aliquot volume of a sample in a primary sample container located in an aspiration position and dispense the first aliquot volume of the sample in a secondary sample container located in a dispensing position. The aliquotter module can cause the secondary sample container to leave the aliquotter module before the primary sample container.
Abstract:
Embodiments of the invention are directed to a transfer apparatus and a transport system which may be used in automated medical laboratory in-vitro diagnostic systems for handling patient samples. The transfer apparatus an embodiment of the invention comprises a rotatable disc and a lane gate. The transport system according to an embodiment of the invention comprises a transfer path arrangement including at least a first input lane and two output lanes at the transfer apparatus (i.e., the rotatable disc and the lane gate). The rotatable disc and the lane gate are cooperatively structured to function together to move at least one laboratory product transport element between the at least one input lane and the two output lanes of the transport system. The laboratory product transport element transports laboratory products, such as patient samples.
Abstract:
The present invention relates to methods for labeling intracellular and extracellular targets of leukocytes, as well as to kits for performing said methods.
Abstract:
Assays that can measure the effect of proteasome inhibitors on target cells in a biological sample are provided. The assays include evaluation of the effects of proteasome inhibitors on proteasome activity in cells in a biological sample.
Abstract:
Systems and methods for processing and analyzing samples are disclosed. The system may process samples, such as biological fluids, using assay cartridges which can be processed at different processing locations. In some cases, the system can be used for PCR processing. The different processing locations may include a preparation location where samples can be prepared and an analysis location where samples can be analyzed. To assist with the preparation of samples, the system may also include a number of processing stations which may include processing lanes. During the analysis of samples, in some cases, thermal cycler modules and an appropriate optical detection system can be used to detect the presence or absence of certain nucleic acid sequences in the samples. The system can be used to accurately and rapidly process samples.
Abstract:
A system, method, and apparatus for an integrated console environment for diagnostic instruments are disclosed. An example apparatus includes a laboratory analyzer configured to generate patient sample result data by performing an analysis on a biological sample from a patient and quality control data by performing an analysis on a control biological sample with known properties. The example apparatus also includes a first laboratory instrument memory configured to locally store the patient sample result data among a plurality of other patient sample result data and a first data access component at a first address configured to provide access to the first laboratory instrument memory. The example apparatus further includes a second laboratory instrument memory configured to locally store the quality control data among a plurality of other quality control data and a second data access component at a second address configured to provide access to the second laboratory instrument memory.
Abstract:
In flow cytometry, particles (2) can be distinguished between populations (8) by combining n-dimensional parameter data, which may be derived from signal data from a particle, to mathematically achieve numerical results representative of an alteration (48). An alteration may include a rotational alteration, a scaled alteration, or perhaps even a translational alteration. Alterations may enhance separation of data points which may provide real-time classification (49) of signal data corresponding to individual particles into one of at least two populations.