This disclosure relates to verifying the operation of cell analyzers, including microscope-based cell imaging and counting analyzers. In one general aspect, a mixture of micro-beads having known characteristics is introduced into the analyzer. One or more images of the mixture are acquired with the analyzer's microscope, the images are analyzed, and a determination is made about whether results meet one or more predetermined quality control thresholds. Also disclosed is a hematology control material that can be used to perform the verification and includes a solvent, a dye dissolved in the solvent, and micro-beads suspended in the solvent. In another general aspect, a quality control method for the analyzers includes capturing images of samples that include patient cells using at least a microscope, extracting sample-specific information about properties of the patient samples from the images, and testing information from the samples against predetermined standards to verify the operation of the analyzer.

Calibration device for a diagnostic device, the diagnostic device comprising a digital imaging device arranged to record an image of at least one sample container containing at least one biological sample. According to the invention, methods include of digitally imaging said at least one sample container, thus obtaining a first image processing the first image, thus obtaining a second image printing a representation of the second image onto a substrate by means of a printing method, thus obtaining the calibration device, wherein said processing of the first image comprises applying at least one transfer function to the first image. The invention further relates to a corresponding calibration device, and a method of calibrating a diagnostic device by means of the calibration device.

Systems and methods for producing a calibration standard for an optical analysis system (e.g., a diagnostic reader) from a live test sample are disclosed. The calibration standard may include an image reproduced on a substrate. The reproduced image may be a replication of a digital image of a live test sample captured using the optical analysis system and then digitally processed to be reproduced on the substrate. The image reproduced on the substrate may include at least one optical feature digitally added to the replication of the digital image of the live test sample. The added optical features may be used to allow for more robust calibration using the calibration standard.

A concentration gradient fluorescence calibration sheet has a glass substrate and an inorganic nano fluorescent liquid lattice disposed on a surface of the glass substrate. The inorganic nano fluorescent liquid lattice has a plurality of inorganic nano fluorescent liquid sub-lattices. Inorganic fluorescent mixed liquid droplets of each inorganic nano fluorescent liquid sub-lattice are arranged in A rows×B columns. The solution concentration of the same row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices is the same, and the solution concentrations of two adjacent rows of inorganic nano fluorescent liquid droplets change in multiples. The concentration gradient fluorescence calibration sheet for the laser microarray chip scanner is utilized to calibrate a scanner under test and a first row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices are taken as index marks.

A calibration suspension unit has a container made of a flexible material that is filled with a calibration suspension for the calibration of a turbidity meter. There exists no air supernatant above the calibration suspension in the container. Further, a method for the manufacture of a calibration suspension unit is provided and its use for the calibration of a turbidity meter is described.

Systems and methods for performing simultaneous nucleic acid amplification and detection. The systems and methods comprise methods for managing a plurality of protocols in conjunction with directing a sensor array across each of a plurality of reaction chambers. In certain embodiments, the protocols comprise thermocycling profiles and the methods may introduce offsets and duration extensions into the thermocycling profiles to achieve more efficient detection behavior.

The present invention provides the use of a composition comprising a block polymer as a support matrix in the manipulation, processing or analysis of particles, such as cells and fluorescent beads. In a preferred embodiment, the composition exhibits gel-sol thermoreversibility, micelle formation under gelling conditions, optically compatible, controllable surfactant properties, molecular sieving properties and biocompatibility. Further aspects of the invention provide (a) a support matrix composition comprising a block polymer, fluorescent beads and/or a dye for use in the manipulation, processing or analysis of particles, (b) a multichamber plate coated in a support matrix composition and (c) kits for producing the same.

The present invention relates generally to a slope spectroscopy standards and methods of making slope spectroscopy standards, specifically standards and methods of developing standards specifically for variable pathlength (slope) measurements.

Refractive index distribution standard in the form of a three-dimensional object which contains in its volume a base medium and regions of variable size and distance with a refractive index other than that of the base medium, characterised in that the difference between the refractive index of said regions and the refractive index of the base medium is not greater than 0.04, at least one of the regions is a set of at least two prisms or cylinders or coaxial rings of variable size and distance, having a dimension in at least one direction similar to the resolving power of the measurement system under assessment and at least one of the regions is sphere-like or ellipsoid-like in shape.

A calibration target for calibrating an optoelectronic device for analyzing biomolecules by detecting fluorescence signals from a sample includes a substrate and a solid fluorescent layer that is disposed on the substrate and capable of being excited by laser light. The fluorescent layer has an optically inactive matrix having embedded therein a carbon-based component that is excitable to light emission.