首页> 外国专利> Analysis of contaminants biotoxin mussels, clams and oysters grown, using primary cultures of rat cerebellar neurons.

Analysis of contaminants biotoxin mussels, clams and oysters grown, using primary cultures of rat cerebellar neurons.

机译:使用大鼠小脑神经元的原代培养物分析生长的污染物生物贻贝,蛤和牡蛎。

摘要

ANALYSIS OF CONTAMINANTS BIOTOXINS mussels, clams and OYSTERS GROWN USING PRIMARY CULTURES OF NEURONS rat cerebellar, DEALING WITH THESE DUPLICATE SAMPLES EXTRACT mollusk. The toxicity of each extract was evaluated from neurotoxic effects caused by FOUR dilutions thereof: 0, 10, 50 and 100, FOR A MERGER OF biotoxins, okadaic acid and domoic acid, superiors, peers and below its limit LEGAL IN TISSUE mollusk. The analysis is performed in presence of 2X10BS-6 SC M MK801 SEPARATELY FOR VIEWING okadaic acid neurotoxicity AND domoic. TOXICITY OF EACH EXTRACT IS EVALUATED CROPS TO OBSERVING phase contrast microscopy after 30 '' TREATMENT FOR domoic acid and okadaic 24H for acid. TOXICITY can be checked by staining COMBINATION OF VITAL DYE neurons with a fluorescent ethidium bromide.
机译:使用神经元大鼠小脑的原代培养物分析生物毒素,贻贝,蛤和牡蛎,并用这些双份样品提取物进行处理。从其四种稀释度:0、10、50和100引起的神经毒性作用中评估每种提取物的毒性,以合并生物毒素,冈田酸和多摩酸,上级,对等级以及低于其法律规定的组织软体动物的限度。分析是在2X10BS-6 SC M MK801的存在下进行的,分别用于查看冈田酸的神经毒性和同生反应。评估了30英寸的多摩酸和24小时的冈田酸处理后,每种提取物的毒性都被评估为要观察相差显微镜。毒性可以通过用荧光溴化乙锭染色活体染料神经元的组合来检查。

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