I have a set of frozen mammalian brain and lung samples which I need to screen for RNA viruses. I have seen some protocols e.g. mag max core kit (MagMAX™ CORE Nucleic Acid Purification Kit Catalog number: A32702) which seems to suggest disruption of tissue before adding lysis buffer. But this seems wrong to me - won't the viral RNA be degraded? My samples were directly frozen and not in any preservative like RNAlater and such.

I have to send half of each of my samples to a collaborator and I don't have duplicates. So I need to stop at the tissue homogenate step, split samples and and freeze at -80 to ship them.

Wondering if anyone has experience with tissue homogenisation without lysis buffer when testing for RNA virus? And storing samples before actual extraction?

Thanks very much!

More Divya Venkatesh's questions See All
Similar questions and discussions