Abstract: A multiple capillary florescent detection system employing optical fiber bundles that each fiber bundle has more than one fiber illuminating each sample vessel.

Abstract: A method for determining a concentration of a scale inhibitor in a water system that includes contacting a scale inhibitor with a dye in a capillary channel to form a complex effective to generate fluorescence; measuring a fluorescence signal generated by the complex; and, determining the concentration of the scale inhibitor based on the fluorescence signal.

Abstract: The invention is an improved multiplex capillary electrophoresis instrument or module with at least four and preferably six user-accessible vertically stacked drawers. An x-z stage moves samples from the user accessible drawers to the capillary array for analysis. A computer program allows users to add capillary electrophoresis jobs to a queue corresponding to the analysis of rows or plates of samples without stopping or interrupting runs in progress.

Abstract: The invention includes a high sensitivity and high throughput capillary electrophoresis multiwavelength florescence detection system. The fluorescent detection system is configured to illuminate a relatively large volume of a single capillary or a plurality of capillaries, with a pixelated detection system capable of imaging an area of each capillary that differentiates the capillary walls, the space between the capillaries, and the internal liquid volume within the capillary. Only the desired pixels or image area are used for processing and generating an output signal.

Abstract: The present invention provides a simple method to correct cross-talk, after the data have been generated. Adjacent signals are simply subtracted from the original observed signal with a repeating process. The data processing is stopped when a predefined condition is met. By this technique, cross-talk can be reduced from >5% to less than 0.1%. And as an additional advantage, this method provides a way to correct the cross-talk without the need to know which peaks are caused by the adjacent capillary signal.

Abstract: The invention is a high-throughput multi-capillary system utilizing a 2-dimensional mask onto which the detection windows of the capillaries are lined up in alternating columns and rows. The image of the capillaries is projected onto a 2-dimensional detection system, such as a charge-coupled-detector (CCD) array. Each row and column of the capillary detection windows is imaged in a separate area of the CCD array, which results in reduced cross-talk between capillaries.

Abstract: Using multiple dichroics mirrors to split and redirect different wavelength regions of light in a multi-wavelength fluorescence detection system.

Abstract: The invention includes a method of sample profiling for identification. The method includes the steps of performing less than four nucleotide-specific chemical cleavage reactions to obtain nucleotide sequence fragments, performing size separation on the fragments, detecting the fragments' separation, generating a profile based on the detection, and comparing the profile to a data base to identify the sample.

Abstract: The present invention provides a simple method to correct cross-talk, after the data have been generated. Adjacent signals are simply subtracted from the original observed signal with a repeating process. The data processing is stopped when a predefined condition is met. By this technique, cross-talk can be reduced from >5% to less than 0.1%. And as an additional advantage, this method provides a way to correct the cross-talk without the need to know which peaks are caused by the adjacent capillary signal.

Abstract: The invention includes a high sensitivity and high throughput capillary electrophoresis multiwavelength florescence detection system. The fluorescent detection system is configured to illuminate a relatively large volume of a single capillary or a plurality of capillaries, with a pixelated detection system capable of imaging an area of each capillary that differentiates the capillary walls, the space between the capillaries, and the internal liquid volume within the capillary. Only the desired pixels or image area are used for processing and generating an output signal.

Abstract: A cytometer system includes a fluid input manifold having a sample bore for accommodating a flow of sample fluid surrounded by a frustoconical shaped chamber for accommodating a flow of sheath fluid. A cuvette has a central bore positioned for receiving from the sample bore the flow of the sample fluid surrounded by and in non-mixing contact with the flow of the sheath fluid. The section of the central bore receiving the sample fluid and the sheath fluid has a frustoconical shape that converges and terminates in a section of the central bore that has a square cross section.

Abstract: A bearing assembly includes a housing having a substantially round throughbore, a first side, and a second side. A sleeve bearing is situated within the throughbore. A first spring washer is situated adjacent the first side of the housing and the sleeve bearing, and similarly, a second spring washer is situated adjacent the second side of the housing and the sleeve bearing. A bushing extends into an opening of the first spring washer, an opening of the sleeve bearing, and the throughbore of the housing. A thrust washer is situated adjacent to the second spring washer and a fastener is situated adjacent to the thrust washer. A kit including the aforementioned components is also disclosed.

Abstract: In a biological sample grinding device and method, a bearing having a plurality of rolling elements disposed between a pair of rings is disposed in a container in which a fluid having at least one biological sample particle therein is introduced. With the bearing immersed in the fluid having the biological sample particle therein, one ring of the bearing is rotated relative to the other ring thereof, whereupon the rolling elements roll between the pair of rings and, in response thereto, the biological sample particle is drawn by the fluid between the pair of rings where it is subject to being crushed or ground between at least one of the rolling elements and at least one of the rings. A baffle can be disposed in the container for inhibiting the rotation of the fluid and, hence, the introduction of air into the fluid.

Abstract: A vortexer that includes a base, a plurality of electromagnets mounted in the base, a holder having a body formed, at least in part, of magnetic material pivotably supported on the base and spaced above the electromagnets, a power source and a device in communication with the electromagnets and the power source for selectively activating and deactivating each electromagnet with power from the power source, whereupon the holder pivotably moves toward at least one of the electromagnets when activated.

Abstract: In a biological sample grinding device and method, a bearing having a plurality of rolling elements disposed between a pair of rings is disposed in a container in which a fluid having at least one biological sample particle therein is introduced. With the bearing immersed in the fluid having the biological sample particle therein, one ring of the bearing is rotated relative to the other ring thereof, whereupon the rolling elements roll between the pair of rings and, in response thereto, the biological sample particle is drawn by the fluid between the pair of rings where it is subject to being crushed or ground between at least one of the rolling elements and at least one of the rings. A baffle can be disposed in the container for inhibiting the rotation of the fluid and, hence, the introduction of air into the fluid.

Abstract: This invention relates to methods for reducing background fluorescence in cell detection and measurement systems. In accordance with one aspect of the invention, cell-impermeant chemical agents are used to modify the fluorescent probes that reside outside the cells to be detected. The chemical agents can chemically modify one or more functional groups in the probes, thereby reducing or eliminating the fluorescence of the probes. In accordance with another aspect of the invention, Acid Black 48 is used to reduce background fluorescence produced by fluorescent probes such as SYTO 62.

Abstract: A bearing assembly includes a housing having a substantially round throughbore, a first side, and a second side. A sleeve bearing is situated within the throughbore. A first spring washer is situated adjacent the first side of the housing and the sleeve bearing, and similarly, a second spring washer is situated adjacent the second side of the housing and the sleeve bearing. A bushing extends into an opening of the first spring washer, an opening of the sleeve bearing, and the throughbore of the housing. A thrust washer is situated adjacent to the second spring washer and a fastener is situated adjacent to the thrust washer. A kit including the aforementioned components is also disclosed.

Abstract: A vortexer that includes a base, a plurality of electromagnets mounted in the base, a holder having a body formed, at least in part, of magnetic material pivotably supported on the base and spaced above the electromagnets, a power source and a device in communication with the electromagnets and the power source for selectively activating and deactivating each electromagnet with power from the power source, whereupon the holder pivotably moves toward at least one of the electromagnets when activated.