The invention in particular relates to a method for the quantification of in vivo RNA from a biological sample comprising the steps of: collecting said biological sample in a tube comprising a compound inhibiting RNA degradation and/or gene induction; forming a precipitate comprising nucleic acids; separating said precipitate from the supernatant; dissolving said precipitate using a buffer, forming a suspension; isolating nucleic acids from said suspension using an automated device; dispersing/distributing a reagent mix for RT-PCR using an automated device; dispersing/distributing the isolated nucleic acids within the dispersed reagent mix using an automated device, and, determining the in vivo levels of transcripts using the nucleic acid/RT-PCR reagent mix in an automated setup.The present invention also relates to the quantification of DNA from a biological sample. The present invention further elucidates a kit for isolating quantifiable nucleic acids from a biological sample. Applications of the method according to present invention are also disclosed.
本发明尤其涉及一种从
生物样本中定量检测体内 RNA 的方法,包括以下步骤在含有抑制 RNA 降解和/或
基因诱导的化合物的试管中收集所述
生物样品;形成包含核酸的沉淀;从上清液中分离所述沉淀;使用缓冲液溶解所述沉淀,形成悬浮液;使用自动装置从所述悬浮液中分离核酸;使用自动装置分散/分配用于 RT-PCR 的混合试剂;使用自动装置在分散的混合试剂中分散/分配分离的核酸,以及,在自动设置中使用核酸/RT-PCR 混合试剂确定转录物的体内
水平。本发明还涉及
生物样本中 DNA 的定量。本发明进一步阐明了一种从
生物样本中分离可定量核酸的试剂盒。还公开了根据本发明的方法的应用。