http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009536023-A

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filingDate 2007-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2009-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2009536023-A
titleOfInvention Analyte-linked enzyme-immunochemical detection method using an endogenous calibrator
abstract The present invention relates to a large number of analytes, such as metabolites and antigens, in biological fluid samples or other liquid samples, using analytical elements, in particular lateral flow test strips, flow-through-membrane systems (flow-through testing). , For detection using microtiter plate wells / cavities or test tubes, where the method is based on interconnected enzyme and affinity reactions and corrects the dilution of the endogenous calibrator, ie the sample matrix Intrinsically produced substances that can be achieved (eg creatinine, glucose, glucose-6-phosphate, lactate, glutamate, aspartate, cholesterol, pyruvate, urea and triglycerides). The fields of application of the invention are in particular medical diagnosis, the pharmaceutical industry and environmental protection. Advantageously, the present invention relates to the simultaneous or sequential detection of antigens and metabolites. Within the scope of the invention, this is in particular a high molecular antigen, such as a protein or a small hapten, such as an insecticide, neopterin, a toxic substance or a hormone, and a metabolite, such as glucose or creatinine. This result can be measured directly from the assay using a nomogram, a comparator (reference strip), a reader, or by visual comparison with the naked eye.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101118555-B1
priorityDate 2006-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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