{"title":"超灵敏毛细管电泳的痕量组学分析","authors":"T. Kawai","doi":"10.2198/electroph.64.23","DOIUrl":null,"url":null,"abstract":"Firstly, small number of cells (1–100) were manually collected, and they were chemically and/or enzymatically processed in a PCR tube with a micropi-pette. The obtained sample solution was then introduced into a capillary, preconcentrated by LDIS, electrophoretical-ly separated, and detected by highly sensitive detector like laser-induced fluorescence (LIF) or mass spectrometry (MS). The obtained data were processed via a database search and finally metabolome and glycome analyses were achieved for 1–100 cells.","PeriodicalId":369290,"journal":{"name":"Electrophoresis Letters","volume":"77 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Trace omics analysis by ultra-sensitive capillary electrophoresis\",\"authors\":\"T. Kawai\",\"doi\":\"10.2198/electroph.64.23\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Firstly, small number of cells (1–100) were manually collected, and they were chemically and/or enzymatically processed in a PCR tube with a micropi-pette. The obtained sample solution was then introduced into a capillary, preconcentrated by LDIS, electrophoretical-ly separated, and detected by highly sensitive detector like laser-induced fluorescence (LIF) or mass spectrometry (MS). The obtained data were processed via a database search and finally metabolome and glycome analyses were achieved for 1–100 cells.\",\"PeriodicalId\":369290,\"journal\":{\"name\":\"Electrophoresis Letters\",\"volume\":\"77 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Electrophoresis Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2198/electroph.64.23\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrophoresis Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2198/electroph.64.23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Trace omics analysis by ultra-sensitive capillary electrophoresis
Firstly, small number of cells (1–100) were manually collected, and they were chemically and/or enzymatically processed in a PCR tube with a micropi-pette. The obtained sample solution was then introduced into a capillary, preconcentrated by LDIS, electrophoretical-ly separated, and detected by highly sensitive detector like laser-induced fluorescence (LIF) or mass spectrometry (MS). The obtained data were processed via a database search and finally metabolome and glycome analyses were achieved for 1–100 cells.