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Comparing protocols for preparation of DNA-free total yeast RNA suitable for RT-PCR
Authors:Eduardo?M?Del Aguila,Marcio?B?Dutra,Joab?T?Silva,Vania?MF?Paschoalin  author-information"  >  author-information__contact u-icon-before"  >  mailto:paschv@iq.ufrj.br"   title="  paschv@iq.ufrj.br"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:1.Departamento de Bioquímica, Instituto de Química,Universidade Federal do Rio de Janeiro, Centro de Tecnologia,Rio de Janeiro,Brasil;2.Centro de Ciências da Saúde, Universidade Salgado de Oliveira,S?o Gon?alo,Brasil
Abstract:

Background  

Preparation of RNA free from DNA is a critical step before performing RT-PCR assay. Total RNA isolated from several sources, including those obtained from Saccharomyces cerevisiae, using routine methodologies are frequently contaminated with DNA, which can give rise to amplification products that mimic the amplicons expected from the RNA target.
Keywords:
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