Abstract:
The present invention relates to a technique of measuring a protein based on a degree of coloring in a liquid sample mixed with a protein measurement indicator. In the present invention, information reflecting creatinine concentration in the liquid sample is obtained, and then an influence quantity caused by creatinine to the protein concentration measurement is eliminated based on the information.
Abstract:
PROBLEM TO BE SOLVED: To provide a liquid reagent capable of specifically and simply measuring a very small amount of albumin in a liquid sample such as urine or the like inclusively of modified albumin, which is easily measured by immunoassay, with high sensitivity equal to immunoassay. SOLUTION: The liquid reagent for measuring a very small amount of albumin in the liquid sample contains a buffer solution, an albumin measuring indicator having a chemical structure represented by a chemical formula 1 and a water-soluble polymer such as hydroxypropyl cellulose or the like being a sensitizer. COPYRIGHT: (C)2008,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a liquid reagent reacting with various proteins containing albumin when the total protein in a liquid sample such as a biosample or the like is measured on the basis of the theory of a coloring matter bonding method corresponding to screening inspection to measure the total protein with extremely high sensitivity. SOLUTION: The liquid reagent for measuring the total protein in the liquid sample contains a protein measuring indicator having a chemical structure represented by the chemical formula 1, a formic acid buffer solution the pH of which is adjusted to 1.0-3.5 and a nonionic surfactant. COPYRIGHT: (C)2008,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a liquid reagent capable of specifically and simply measuring a very small amount of albumin in a liquid sample such as urine or the like inclusively of modified albumin (immunological unresponsive albumin), which is not measured by immunoassay, with high sensitivity equal to the immunoassay. SOLUTION: The liquid reagent for measuring a very small amount of albumin in the liquid sample contains an indicator having a chemical structure represented by the chemical formula 1, at least one of a citric acid buffer solution adjusted to 1.0-3.0 in pH and an acetic acid buffer solution and a nonionic interface activator. COPYRIGHT: (C)2008,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a method for assaying saccharogenic albumin, by which the saccharogenic albumin in a specimen can simply be assayed without using a special device. SOLUTION: This method for assaying the saccharogenic albumin, characterized by measuring the concentration of the saccharogenic albumin in a specimen with an enzyme and then determining the ratio to the otherwise measured concentration of all albumins in the specimen.
Abstract:
A technique for performing protein measurement on the basis of the level of coloring upon coexistence of a liquid sample with an indicator for protein measurement. In this technique, information reflecting the concentration of creatinine in a liquid sample is procured, and in accordance with this information, the amount of creatinine influence on the measurement of protein concentration is removed.
Abstract:
A tool for analyzing a specimen having a sufficient volume of information, and being capable of providing the information accurately and reading out that information without requiring any special mechanism. In the tool (1) for analyzing a specimen having a reagent layer (11) and an information recording layer (12) formed on a substrate (13), the information recording layer is divided into one or a plurality of regions and each region is colored with a single color. Information is recorded by at least one of a combination of gray levels of single color in the plurality of regions and the area of each region.
Abstract:
A specimen analyzing tool automatically fed to an analyzing part without inconvenience even if the number of items to be inspected by the tool is small when the tool is set to an analyzer. One or more reagent pads are disposed on a substrate, and a balance pad to keep at least one of a weight balance and a friction balance is disposed on the substrate. The substrate is formed in a strip shape, and one end part of the substrate forms a holding part and the other part than the one end part forms a pad arrangement area. The reagent pads are disposed on the opposite side of the holding part in the pad arrangement area, and the balance pad is disposed on the holding part side in the pad arrangement area.