Abstract:
PROBLEM TO BE SOLVED: To provide a method and device for quantitatively determining an analyte in a sample. SOLUTION: Based on generated calibration graphs, it is examined whether a signal generated by reaction between an analyte-specific substance and the analyte in the sample enables quantitative determination of the analyte with a desired accuracy. COPYRIGHT: (C)2008,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide an oxidation/reduction-active compound as a detection reagent for measuring fluorescence in analyte, for solving defects in prior art at least partially. SOLUTION: A method for detecting analyte by oxidation/reduction reaction and fluorescence measurement brings a sample, containing analyte into contact with the detection reagent containing a compound expressed by as a fluorescent oxidation reduction indicator. NBD-amine-N-oxide, or its derivative is obtained as a redox indicator. In this manner, NBD-amine formed by reduction features high fluorescence and can be extremely easily excited by blue light irradiation, thus solving nonconformities, where the number of these known as a compound for use, for example, especially strong blue and read LEDs is not sufficient, since an excitation light source to be used is limited mainly to UV and green regions in known fluorescence detection reagents. COPYRIGHT: (C)2004,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide a method and a reagent kit n for fluorometry of an analyte, and a novel oxidation-reduction active compound serving as a fluorescent reagent for the analyte. SOLUTION: In this method for detecting the analyte by an oxidation-reduction reaction and the fluorometry, a sample containing the analyte is brought into contact with a detecting reagent containing a compound expressed by the following general formula (1): Q-F(Q is a quencher group, and F is a fluorophore group) as a fluorescent oxidation-reduction indicator. Examples favorable as the reducible quencher group are quinones, aromatic nitroso compounds such as nitrosoanilines and other nitrosobenzene derivatives, and N-oxides. COPYRIGHT: (C)2004,JPO&NCIPI
Abstract:
The invention relates to a method for increasing the dynamic measuring range of test elements, especially immunological test elements, especially optically readable immunological chromatography strips, that are based on specific bonding reactions. The invention allows to displace the dynamic test range of especially immunological test elements that are based on specific binding reactions towards higher analyte concentrations without forfeiting sensitivity. For this purpose, at least two zones in or on the test element are provided and contain reagents that produce differently strong detectable signals due to different affinities to the analyte (for example in the case of antibodies that have different affinity to the analyte) or due to different principles of interaction with the analyte or with other reagents involved in the detection of the analyte (for example antibodies directed to the analyte in one zone and analyte or analyte analog in a different zone). The signals in the at least two zones are used for evaluation of the analyte concentration/signal strength correlation and used for determining the analyte by way of a suitable method (correlation).
Abstract:
"teste analítico em sanduíche para determinar nt-probnp". a presente invenção refere-se a testes imunológicos rápidos para determinar nt-probnp, que usam combinações especiais de anticorpos. o teste rápido, de acordo com a invenção, pode estar presente com vantagens como uma tira de teste imunocromatográfico.
Abstract:
Detecting an analyte (A) by a redox reaction and fluorimetric measurement, comprises that the (A)-containing sample is treated with a fluorimetric redox indicator (I) that comprises a quencher group (Q) linked to a fluorophore (F). An independent claim is also included for a reagent for the process that comprises (I) where at least one of Q and F is oxidizable or reducible, and the fluorescence can be altered, depending on oxidation or reduction.
Abstract:
An immunological sandwich test determines the presence of NT-proBNP and uses two or more antibodies on the NT-proBNP. An immunological sandwich test determines the presence of NT-proBNP and uses two or more antibodies on the NT-proBNP. At least one antibody is a MAK. One of these antibodies is effective against part of the NT-proBNP epitope incorporating amino-acids 38 to 50. One of these antibodies is directed at parts of the NT-proBNP epitope with amino-acids 1 to 37, or 43 to 76. The epitopes recognised by the anti-bodies have a small overlap range.
Abstract:
The invention relates to a method for increasing the dynamic measuring range of test elements, especially immunological test elements, especially optically readable immunological chromatography strips, that are based on specific bonding reactions. The invention allows to displace the dynamic test range of especially immunological test elements that are based on specific binding reactions towards higher analyte concentrations without forfeiting sensitivity. For this purpose, at least two zones in or on the test element are provided and contain reagents that produce differently strong detectable signals due to different affinities to the analyte (for example in the case of antibodies that have different affinity to the analyte) or due to different principles of interaction with the analyte or with other reagents involved in the detection of the analyte (for example antibodies directed to the analyte in one zone and analyte or analyte analog in a different zone). The signals in the at least two zones are used for evaluation of the analyte concentration/signal strength correlation and used for determining the analyte by way of a suitable method (correlation).