Biological Procedures Online | |
Optimized RNA Extraction and Northern Hybridization in Streptomycetes | |
Methodology | |
Marcello Tagliavia1  Anna Taravella1  Sandra Marineo1  Mario La Farina1  Anna Maria Puglia1  | |
[1] Dipartimento di Biologia Cellulare e dello Sviluppo, Università di Palermo, Viale delle Scienze (Parco d'Orleans), Edificio 16, 90128, Palermo, Italy; | |
关键词: streptomycetes; total RNA purification; RNA processing; RNA degradation; RNA glyoxylation; alkaline blotting; northern hybridization; | |
DOI : 10.1007/s12575-010-9027-7 | |
received in 2009-12-16, accepted in 2010-02-06, 发布年份 2010 | |
来源: Springer | |
【 摘 要 】
Northern blot hybridization is a useful tool for analyzing transcript patterns. To get a picture of what really occurs in vivo, it is necessary to use a protocol allowing full protection of the RNA integrity and recovery and unbiased transfer of the entire transcripts population. Many protocols suffer from severe limitations including only partial protection of the RNA integrity and/or loss of small sized molecules. Moreover, some of them do not allow an efficient and even transfer in the entire sizes range. These difficulties become more prominent in streptomycetes, where an initial quick lysis step is difficult to obtain. We present here an optimized northern hybridization protocol to purify, fractionate, blot, and hybridize Streptomyces RNA. It is based on grinding by a high-performance laboratory ball mill, followed by prompt lysis with acid phenol-guanidinium, alkaline transfer, and hybridization to riboprobes. Use of this protocol resulted in sharp and intense hybridization signals relative to long mRNAs previously difficult to detect.
【 授权许可】
CC BY
© Tagliavia et al; licensee Springer 2010
【 预 览 】
Files | Size | Format | View |
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RO202311090964481ZK.pdf | 225KB | download |
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