Product Details
Catalogue Number
– 500065
Category
– Water
– Metolachlor, ELISA, 96-test, MTO – 5 kit minimum
Brand
– GSD Abraxis
– Water
Features & Benefits
– Immunoassay for the detection of Metolachlor.
Details
– The Metolachlor ELISA is an immunoassay for the detection of Metolachlor. This test is suitable for the quantitative and/or qualitative detection of Metolachlor in contaminated samples. Samples requiring regulatory action should be confirmed by HPLC, GC/MS, or other conventional methods.
The test is a direct competitive ELISA based on the recognition of Metolachlor by specific antibodies. Metolachlor, when present in a sample and a Metolachlor-enzyme conjugate compete for the binding sites of rabbit anti-Metolachlor antibodies in solution. The Metolachlor antibodies are then bound by a second antibody (goat anti-rabbit) immobilized on the microtiter plate. After a washing step and addition of the substrate solution, a color signal is produced. The intensity of the blue color is inversely proportional to the concentration of Metolachlor present in the sample. The color reaction is stopped after a specified time and the color is evaluated using a microplate ELISA photometer. The concentrations of the samples are determined by interpolation using the standard curve constructed with each run.
The test is a direct competitive ELISA based on the recognition of Metolachlor by specific antibodies. Metolachlor, when present in a sample and a Metolachlor-enzyme conjugate compete for the binding sites of rabbit anti-Metolachlor antibodies in solution. The Metolachlor antibodies are then bound by a second antibody (goat anti-rabbit) immobilized on the microtiter plate. After a washing step and addition of the substrate solution, a color signal is produced. The intensity of the blue color is inversely proportional to the concentration of Metolachlor present in the sample. The color reaction is stopped after a specified time and the color is evaluated using a microplate ELISA photometer. The concentrations of the samples are determined by interpolation using the standard curve constructed with each run.
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