Provided is a method of inspecting a growth quality of a graphene layer of a graphene-grown copper foil obtained by growing the graphene layer on a copper foil layer by chemical vapor deposition (CVD), the method including reacting oxygen or water molecules with the copper foil layer via a defect portion of the graphene layer, partitioning an entire region of the graphene-grown copper foil into partial regions, sequentially obtaining images of the partial regions, detecting, with respect to each of the images of the partial regions, an oxidized region where the copper foil layer is oxidized, and setting the oxidized region as a graphene defect region, and obtaining a ratio of an area of the graphene defect region to an entire area of each of the images of the partial regions.

Method, kit and composition for analyzing analytes for modifications using modification site specific antibodies to bind an analyte with his specific modification sites of interest to different dyes simultaneously with an antibody which is specific to the non-modificated analyte binding to another dye to determine the concentration of the analyte for quantification of the modified analyte in the identical sample.

Described herein are methods, assays and techniques for detecting and/or measuring anti-drug antibodies that bind to a protein, polypeptide or other compound or molecule that comprises at least one immunoglobulin variable domain with an exposed C-terminal region.

Improved systems and methods for laboratory instrument calibration. A laboratory instrument retrieves a number of sets of past quality control parameters from a data structure. Each set includes a recovered value and a timestamp. The recovered value is equal to an output value adjusted by an initial calibration factor. The laboratory instrument determines that the number of sets is greater than a threshold and that each of the past quality control parameters has a timestamp that is within a time threshold. The laboratory instrument computes an updated calibration factor such that when the updated calibration factor is applied to a representative value of the recovered values, the representative value equals the expected recovered value. The instrument updates the data structure with the calibration factor such that the calibration factor is used in subsequent testing of patient specimens.

Improved systems and methods for laboratory instrument calibration. A laboratory instrument retrieves a number of sets of past quality control parameters from a data structure. Each set includes a recovered value and a timestamp. The recovered value is equal to an output value adjusted by an initial calibration factor. The laboratory instrument determines that the number of sets is greater than a threshold and that each of the past quality control parameters has a timestamp that is within a time threshold. The laboratory instrument computes an updated calibration factor such that when the updated calibration factor is applied to a representative value of the recovered values, the representative value equals the expected recovered value. The instrument updates the data structure with the calibration factor such that the calibration factor is used in subsequent testing of patient specimens.

The oxygen detecting agent composition according to the present invention includes a redox dye, a reducing agent and a basic substance, wherein the redox dye is an iron blue pigment and the reducing agent is lactose.

The oxygen detecting agent composition according to the present invention includes a redox dye, a reducing agent and a basic substance, wherein the redox dye is an iron blue pigment and the reducing agent is lactose.

An exemplary embodiment provides a method of determining formation energy of a multi-element crystal, including: generating information related to a candidate structure of the multi-element crystal and information related to a metal pair included in the multi-element crystal, based on information related to a composition of the multi-element crystal; and determining the formation energy based on the information related to the candidate structure and the information related to the metal pair.

A polymer dye includes at least one repeating unit represented by the following structural formula 1 and at least one selected from the group consisting of repeating units represented by the following structural formulas 2 and 3.

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Hydrogen peroxide present in or generated through enzymatic reaction in a biological sample can be detected by using the polymer dye.

An embodiment provides a method for measuring at least one characteristic of an aqueous sample, including: introducing an aqueous sample into a measurement device comprising one or more electrodes; oxidizing a transition metal to produce a higher valent metal by applying an electrical potential between an anode and a cathode of the measurement device; oxidizing, using the higher valent metal as a catalyst, a material within the aqueous sample; measuring a characteristic of the aqueous sample based upon the oxidized material, using a measurement device selected from the group consisting of: an electrochemical measurement device and an optical measurement device; and optimizing the electrical potential and at least one reagent delivered to the measurement device based on the measurement of the characteristic. Other aspects are described and claimed.