文章摘要
Improvement and analysis of cactus totalRNA extraction method
  
DOI:10.16768/j.issn.1004-874X.2017.03.011
Author NameAffiliation
余乃通1,周启林1,罗志文2,胡福初2,张治礼2,刘志昕1 1. 中国热带农业科学院热带生物技术研究所/ 农业部热带作物生物学与遗传资源利用重点实验室海南 海口 571101 2. 海南省农业科学院热带果树研究所/ 海南省热带果树生物学重点实验室海南 海口 571100 
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Abstract:
      High-quality total RNAs of cactus stem were obtained by using Na2SO3 with each of TRIzol reagent, RNA plant plus reagent,BioTeke total RNA extraction reagent,EASY spin Plus plant RNA extraction reagent (Aidlab) or OMEGA plant RNA reagent. The cDNA RT-PCR and specific detection results showed that matK gene fragments were amplified by five total RNA extraction methods. The cDNAs that reverse transcribed from the TRIzol reagent,RNA Plant Plus Reagent,and EASY spin Plus Plant RNA Extraction reagent( Aidlab) were relatively high,as the sensitivity PCR of cDNA highest dilution to 1∶100. While the cDNAs that reverse transcribed from BioTeke total RNA extraction reagent and OMEGA plant RNA reagent were relatively low,as the sensitivity RTPCR indicated the cDNA highest dilution to 1∶10. In this study,Na2SO3 combined with different plant total RNA extraction kits to prepare high quality of RNA is the key of cactus stem cDNA library preparation and molecular biology.
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