{"title":"光镜和偏振显微镜下平滑肌细胞显示的嗜银细胞III方法。","authors":"F Gallyas","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>An esterification with n-butyl alcohol containing 0.5% sulphuric acid (at 56 degrees C, for 16 hours) followed by a treatment in a special physical developer renders smooth muscle cells as well as other contractile elements (striated muscle, cilia, flagella, myoepithel cells) visible in light microscope and birefringent in polarization microscope. A few kinds of non-contractile tissue components without oriented fibrillary structure also stain but do not display birefringence.</p>","PeriodicalId":76158,"journal":{"name":"Microscopica acta","volume":"84 2","pages":"139-42"},"PeriodicalIF":0.0000,"publicationDate":"1981-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An argyrophil III method for the demonstration of smooth muscle cells in light and polarization microscopy.\",\"authors\":\"F Gallyas\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>An esterification with n-butyl alcohol containing 0.5% sulphuric acid (at 56 degrees C, for 16 hours) followed by a treatment in a special physical developer renders smooth muscle cells as well as other contractile elements (striated muscle, cilia, flagella, myoepithel cells) visible in light microscope and birefringent in polarization microscope. A few kinds of non-contractile tissue components without oriented fibrillary structure also stain but do not display birefringence.</p>\",\"PeriodicalId\":76158,\"journal\":{\"name\":\"Microscopica acta\",\"volume\":\"84 2\",\"pages\":\"139-42\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1981-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microscopica acta\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microscopica acta","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
An argyrophil III method for the demonstration of smooth muscle cells in light and polarization microscopy.
An esterification with n-butyl alcohol containing 0.5% sulphuric acid (at 56 degrees C, for 16 hours) followed by a treatment in a special physical developer renders smooth muscle cells as well as other contractile elements (striated muscle, cilia, flagella, myoepithel cells) visible in light microscope and birefringent in polarization microscope. A few kinds of non-contractile tissue components without oriented fibrillary structure also stain but do not display birefringence.