{"title":"补充信息","authors":"Xiaolei Wu, Yuntian Zhu","doi":"10.1201/9781003153078-37","DOIUrl":null,"url":null,"abstract":"In Vitro Callus Production. Induction of in vitro callus production was performed as previously described (Iwase et al., 2011). Etiolated hypocotyls were excised from mutant and wild type seedlings 4 days after germination. Mutant and wild type explants were cultured for 30 days side-by-side on MS medium supplemented with Gamborg’s vitamins, 2% glucose, 0.05% 2-(N-morpholino)ethanesulfonic acid (MES), pH 5.8 with KOH, 0.8% phytoagar, and the indicated concentrations of NAA and kinetin.","PeriodicalId":106290,"journal":{"name":"Heterostructured Materials","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Supplementary Information Text\",\"authors\":\"Xiaolei Wu, Yuntian Zhu\",\"doi\":\"10.1201/9781003153078-37\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In Vitro Callus Production. Induction of in vitro callus production was performed as previously described (Iwase et al., 2011). Etiolated hypocotyls were excised from mutant and wild type seedlings 4 days after germination. Mutant and wild type explants were cultured for 30 days side-by-side on MS medium supplemented with Gamborg’s vitamins, 2% glucose, 0.05% 2-(N-morpholino)ethanesulfonic acid (MES), pH 5.8 with KOH, 0.8% phytoagar, and the indicated concentrations of NAA and kinetin.\",\"PeriodicalId\":106290,\"journal\":{\"name\":\"Heterostructured Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-09-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Heterostructured Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1201/9781003153078-37\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Heterostructured Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1201/9781003153078-37","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
In Vitro Callus Production. Induction of in vitro callus production was performed as previously described (Iwase et al., 2011). Etiolated hypocotyls were excised from mutant and wild type seedlings 4 days after germination. Mutant and wild type explants were cultured for 30 days side-by-side on MS medium supplemented with Gamborg’s vitamins, 2% glucose, 0.05% 2-(N-morpholino)ethanesulfonic acid (MES), pH 5.8 with KOH, 0.8% phytoagar, and the indicated concentrations of NAA and kinetin.