| 摘要 |
<p num="1">The present invention in general provides a method for amplification of a target RNA, comprising the steps of (i) transfering a liquid with a first volume comprising at least one or more living cells into a vessel (ii) adding to said vessel an RT-PCR reaction buffer with a second volume, whereas said second volume is at least 2x as large as said first volume (iii) lysing said at least one or more living cells within said vessel by means of incubation for at least 20 seconds at at least 90°C, and (iv) amplifying said target by means of a one-step RT-PCR without performance of an intermediate purification step.
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