摘要 |
<p>The immunological test element (1) such as a microarray comprises an analyte detection zone (14), and a combined control and calibration zone (15), which comprises fluorophore and binding partner for the specific binding of reagents (6, 7) marked with fluorophore. The analyte detection zone and/or the combined control and calibration zone are present in the form of a bar or circular spots. The fluorophore and/or the binding partner are immobilized in the combined control and calibration zone. The amount of fluorophore in the combined control and calibration zone is 0.001-5 mu g. The immunological test element (1) such as a microarray comprises an analyte detection zone (14), and a combined control and calibration zone (15), which comprises fluorophore and binding partner for the specific binding of reagents (6, 7) marked with fluorophore. The analyte detection zone and/or the combined control and calibration zone are present in the form of a bar or circular spots. The fluorophore and/or the binding partner are immobilized in the combined control and calibration zone. The amount of fluorophore in the combined control and calibration zone is 0.001-5 mu g. The amount of the reagents marked with fluorophore is 1-500 ng. The fluorophore in the combined control and calibration zone and the reagents marked with fluorophore are stimulated with the same wavelength and emit electromagnetic radiation of the same wavelength. An independent claim is included for a method for determining the concentration of an analyte in a sample using a test element and an analysis device suited for the evaluation of the test element.</p> |