Helena Laboratories Corporation

Charles D Kelley

Henry A Garsee

Robert J Sarrine

Philip A Guadagno

Tipton L Golias

Eric H Petersen

Earl W Boone

Michael T Everitt

Gene A Butts

Bruce R Petty

James L Pauley

Gaston Andres Del Pino

Jeffrey Allen Spencer

James Matthew Simmons

An immunofixation electrophoresis applicator system and method deposits antisera in spaced apart locations on a substrate where the antisera is deposited as an elongated bead in a first direction and retained against migration in a direction transverse to said first direction at least by surface tension.

System and method for depositing antisera in immunofixation electrophoresis

Optically scanned data forms an image stored in a computer memory represented as an array having at least two dimensions. The stored image is subjected to virtual scanning. Thus a subset of the array is defined as a portion of the image having first and second dimensions. The value of the subset is derived, the subset is then incremented, and the value of the incremented subset is determined. The steps of incrementing and deriving the value of the incremented subset are repeated. The derived values of the data are compared to a calibrated standard, to create adjusted values of data. The adjusted data values, in the case of electrophoresis, represent the scanned sample which has been subjected to electrophoresis. Thereafter, the adjusted data values can be integrated or otherwise processed.

Scanner densitometer and data evaluation method

An apparatus for electrophoresing a sample and for thereafter either scanning in the visible mode or the fluorescent mode, under control of a central processor, to provide scanning densitometry of the electrophoresed sample, and with the fluorescent mode scanning being performed in situ. The apparatus includes a gantry which moves from left to right in the XY plane. The gantry draws, delivers and deposits the samples and reagents, and includes safety devices to prevent the gantry from movement and damage when there are obstructions in the path of the gantry. A fluorescent scanning unit is moved by X- and Y-direction motors to position a photomultiplier over an electrophoresed sample. In this way, the electrophoretic sample can remain fixed in place during sample delivery, ultraviolet exposure and measurement operations.

Automatic electrophoresis apparatus with fluorescent and visible scanning

An electrophoresis apparatus for automatically performing medical assays includes an electrophoresis platform which cooperates with a gantry assembly. The electrophoresis platform and the gantry assembly are movable along paths that are perpendicular to each other. An applicator assembly includes pipettes which transfer fluid samples from a specimen tray to an electrophoresis plate mounted on the electrophoresis platform. The electrophoresis platform then moves to a position into the gantry assembly, where electrophoresis is conducted to separate the samples into different fractions. The electrophoresis platform then moves beneath a reagent pouring station where a reagent is applied to make the separated fractions fluoresce under ultraviolet light. The electrophoresis platform is then moved beneath the gantry assembly again, and an air knife in the gantry assembly spreads the reagent. After incubation and drying of the electrophoresis plate, the electrophoresis platform and gantry assembly are moved relative to one another while the electrophoresis plate is read with the aid of ultraviolet lamps and a photomultiplier tube mounted in the gantry assembly. The gain of the photomultiplier tube is automatically adjusted and the data gathered is automatically edited to remove background noise. The edited results can be printed or displayed on a video monitor. Techniques for calibrating the electrophoresis apparatus are also disclosed.

Automatic electrophoresis method and apparatus

Method for calibrating a piston and cylinder type applicator

An electrophoresis machine is disclosed in which after a microporous support strip and a sample plate are placed in the machine, all electrophoresis processing, scanning and densitometer functions are automatically performed under computer control. The machine includes apparatus for automatic pipetting of liquid samples from the sample plate to the surface of the support strip, apparatus for applying electrophoresis current to the strip while simultaneously cooling it, apparatus for applying and spreading fluorescent staining reagent to the strip, and apparatus for incubating the strip and subsequently drying it. Mechanical aligning apparatus is provided for precisely aligning pipettes with application wells on the sample strip. Electrode bars and reagent spreader bars are provided to apply electrophoresing current to the strip and to spread reagent dumped onto the strip after electrophoresis. Circular indentations as well as rectangular indentations are provided as application wells on the sample strip. Spring loaded rollers are provided to reduce friction variation of a robotic assembly which translates a pipetting assembly between the sample plate and the sample strip. Multiple reagent bottle assemblies are provided for allowing one or more reagents to be dumped onto the strip after electrophoresing of the sample strip. Alternatively, apparatus is provided for spraying reagent onto the surface of the strip.

Automatic electrophoresis apparatus and method

An automatic electrophoresis machine is provided with a path for refrigerated air to pass over the agarose gel of a support medium during the time that electrophoresis current is applied to the support medium. Such apparatus is also provided with means for applying longitudinal electrophoresis current through the gel of the support medium during one time and applying lateral electrophoresis current through the gel of the support medium during another time.

Automatic electrophoresis apparatus

An electrophoresis machine is disclosed in which after a microporous support strip and a sample plate are placed in the machine, all electrophoresis processing, scanning and densitometer functions are automatically performed under computer control. The machine includes apparatus for automatic pipetting of liquid samples from the sample plate to the surface of the support strip, apparatus for applying electrophoresis current to the strip while simultaneously cooling it, apparatus for applying and spreading flourescent staining reagent to the strip, and apparatus for incubating the strip and subsequently drying it. A T.V. camera, mounted to a flourescent scanning box enclosing the application plate, in cooperation with digital processing equipment, electronically scans electrophoresically longitudinally displaced components of the samples for determining relative component densities. An alternative scanning apparatus including a collimator and photomultiplier is also disclosed.

An electrophoresis machine is disclosed in which after a microporous support strip and a sample plate are placed in the machine, all electrophoresis processing, scanning and densitometer functions are automatically performed under computer control. The machine includes apparatus for automatic pipetting of liquid samples from the sample plate to the surface of the support strip, apparatus for applying electrophoresis current to the strip while simultaneously cooling it, apparatus for applying and spreading flourescent staining reagent to the strip, and apparatus for incubating the strip and subsequently drying it. A T.V. camera, mounted to a flourescent scanning box enlosing the application plate, in cooperation with digital processing equipment, electronically scans electrophoresically longitudinally displaced components of the samples for determining relative component densities. An alternative scanning apparatus including a collimator and photomultiplier is also disclosed.

An electrophoresis machine is disclosed in which after a microporous support strip and a sample plate are placed in the machine, all electrophoresis processing, scanning and densitometer functions are automatically performed under computer control. The machine includes apparatus for automatic pipetting of liquid samples from the sample plate to the surface of the support strip, apparatus for applying electrophoresis current ot the strip while simultaneously cooling it, apparatus for applying and spreading flourescent staining reagent to the strip, and apparatus for incubating the strip and subsequently drying it. A T.V. camera, mounted to a flourescent scanning box enclosing the application plate, in cooperation with digital processing equipment, electronically scans electrophoresically longitudinally displaced components of the samples for determining relative component densities. An alternative scanning apparatus including a collimator and photomultiplier is also disclosed.

A computer controlled diagnostic densitometer for analyzing optical density patterns of blood samples or the like scans a sample and generates an analog waveform signal representative of the scanned optical density pattern. The analog signal is amplified, digitized, stored in a memory and is later read from memory to reconstruct a visual display of the waveform for analysis. Several types of optical density pattens may be scanned which result in analog signals of different amplitudes and signal-to-background noise ratios. An improved amplification system automatically preadjusts the gain and reference value of the analog signal prior to digitization in order to substantially eliminate background noise in the signal and produce substantially full scale analog signal values. The gain and reference value preadjustments are performed by a pair of corresponding multipliers which multiply the analog signal by memory-stored digital data which is unique to the type of optical density pattern being scanned. The gain and reference voltage may also be manually preadjusted in order to assure sample-to-sample analysis consistency for samples from the same patient.

Densitometer with automatic gain and reference value adjustment of

A method of optically scanning a plurality of optical density patterns, such as blood samples or the like is provided wherein the samples are arranged in rows and each include a plurality of optical density segments extending along a first axis, and wherein the segments generally form columns of like segments along a second axis. The optical densities of a row of segments are first scanned along the first axis, following which the centerlines of each segment in the scanned row is determined along the first axis. Then, the segments of each column are scanned along the corresponding, previously determined centerline. The centerline of each segment is determined by displacing a scanning head relative to the sample along the first axis, measuring the optical density of each segment and correlating the magnitude of the measured optical density with the relative displacement between the head and the samples. The scanning of the segments along the centerlines is performed by displacing the scanning head relative to the samples along the second axis, measuring the optical density of each segment in the column being scanned and correlating the magnitude of the measured optical density with the relative displacement of the head and the samples. Voltages are generated which are proportional to the relative displacement between the head and samples along the first and second axes, and these voltages are converted to digital data and stored in memory for later use in the correlation process. A method is also provided for determining the location of each segment in an optical density pattern and for determining the length of the pattern.

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Beaumont, TX, United States of America

Charles D Kelley