{"id":5395,"date":"2020-05-27T13:12:34","date_gmt":"2020-05-27T13:12:34","guid":{"rendered":"https:\/\/www.zeulab.com\/producto\/uncategorized\/microcystest\/"},"modified":"2025-05-14T09:37:22","modified_gmt":"2025-05-14T09:37:22","slug":"microcystest","status":"publish","type":"product","link":"https:\/\/www.zeulab.com\/en\/producto\/water-and-marine-toxins\/enzymatic-water-and-marine-toxins\/microcystest\/","title":{"rendered":"Microcystest"},"content":{"rendered":"

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HOW DOES IT HELP YOU?<\/h2>\n

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Microcystest reproduces the biological action of microcystins, detecting all variants independently of their chemical structure. Therefore, the quantitative result obtained with Microcystest will reflect the potential toxicity associated to the water sample.
\nMicrocystest can be used analysis of both raw water and treated water in drinking water stations. The tests can identify free and intracellular toxins. You will be able to know the toxicity associated with microcystins and nodularins in up to 43 samples per assay and just using basic lab equipment and in just 30 minutes.<\/p>\n

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MATRIX<\/h5>\n

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DRINKING WATER<\/h6>

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RAW WATER<\/h6>

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APPLICATIONS AND USERS<\/h5>\n

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DRINKING WATER STATIONS<\/h6>

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LABORATORIES OF WATER AND ENVIRONMENTAL SAMPLES<\/h6>

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ASSAY PROCEDURE<\/h2>\n

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1. Apply Samples\/Standard:<\/h4>\n

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+ Phosphatase<\/p>\n

+ Substrate.<\/p>\n

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2. Incubation:<\/h4>\n

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37\u00baC\/30 min.<\/p>\n

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3. Results:<\/h4>\n

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Photometrical reading at 450 nm<\/p>\n

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Nombre del video<\/h4>\n

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1. Diluci\u00f3n de la muestra:<\/h4>\n

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Aplicar muestra\/patr\u00f3n. Incubaci\u00f3n.<\/p>\n

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2. Conjugado:<\/h4>\n

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Incubaci\u00f3n<\/p>\n

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3. Results:<\/h4>\n

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Lectura fotom\u00e9trica a 450nm<\/p>\n

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TEST PRINCIPLE<\/h2>\n

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Microcystest is based on the inhibition of the enzymatic activity of PP2A by microcystins, reproducing the mechanism of action of these toxins in human beings. Therefore, it detects and quantifies the potential toxicity of a sample derived from microcystins and nodularins. Under normal conditions the phophatase is able to hydrolyse a specific substrate that can be detected at 405 nm. Samples containing microcystins will inhibit the enzyme activity proportionally to the amount of toxin contained in the sample.<\/p>\n

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TECHNICAL DATA<\/h2>\n

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