Path: utzoo!attcan!uunet!maverick.ksu.ksu.edu!hoss!news From: rdonis@crcvms.unl.edu Newsgroups: bionet.molbio.methds-reagnts Subject: RNA to cDNA then PCR Message-ID: <1990Oct24.205531.26856@hoss.unl.edu> Date: 24 Oct 90 19:36:46 GMT Sender: news@hoss.unl.edu (Network News Administer) Organization: UNL Computing Resource Center Lines: 16 -Message-Text-Follows- We are amplifying a viral RNA by PCR. This requires an initial reverse transcription from RNA to cDNA. We set up a control in which this reverse transcription was carried out without primers. After amplification by PCR we see that the cDNA prepared without primers actually works *better* than with them. I was expecting a negative result in the PCR amplification of cDNA prepared without primers. Since we are using viral RNA extracted from infected cells it may be that there is a cellular RNA/DNA that primes reverse transcription. Has anybody seen something like this? Thank you for your comments, if numerous I will post summary to net. Ruben Donis University of Nebraska rdonis@crcvms.unl.edu rdonis@unlvax1.bitnet 402/472-6063