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METHOD FOR HEPATIC FIXATION AT NARCOTIZED ANIMAL'S LIFE PERIOD

机译:麻醉动物生命期的肝固定方法

摘要

FIELD: experimental medicine.;SUBSTANCE: the present innovation deals with preparing hepatic preparations for histological testing. In the course of an experiment on inducing hepatic pathology animals should be perfused with glutaraldehyde formaldehyde fixing agent through portal vein under conditions of narcosis. Then comes perfusion with incubation medium containing 0.2%-digitonin in Flickinger's solution at pH being 7.2 at 20-22°C. After incubation hepatic tissue should be reduced to be placed into 0.2%-digitonin for 4-10 h, and then samples should be washed with 0.1 M cacodylate buffer and postfixed with 1%-solution upon cacodylate buffer for 2 h. Then it is necessary to conduct dehydration to be put into araldite followed by contrasting with uranylacetate and lead citrate. The method enables to increase degree of contrast due to fixing hepatic tissues in situ and optimal matching incubation medium.;EFFECT: higher efficiency.;3 ex
机译:领域:实验医学;物质:本发明涉及制备用于组织学测试的肝制剂。在诱导肝病理的实验过程中,应在麻醉状态下通过门静脉向戊二醛甲醛固定剂灌注动物。然后在20-22℃下用pH为7.2的在Flickinger溶液中的含有0.2%洋地黄皂苷的培养培养基进行灌注。孵育后,应减少肝组织,将其放入0.2%洋地黄酮中4-10 h,然后将样品用0.1 M椰油酸缓冲液洗涤,并用1%溶液在椰油酸缓冲液中后固定2 h。然后有必要进行脱水以使其成钠长石,然后与乙酸铀酰酯和柠檬酸铅对比。该方法能够通过原位固定肝组织和最佳匹配的孵育介质来提高对比度,效果:效率更高; 3 ex

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