RNAse showing up in gel after plasmid miniprep
"Marianne Leverone ", BIO
leverone at CHUMA.CAS.USF.EDU
Wed Dec 18 10:01:23 EST 1996
Berrnard M: We are using <1 ug/ml. Only one person in our lab is having
this trouble which is wierd. We can't figure out why he is having such
trouble! He is now trying a phenol:chloroform then chloroform extraction
to see if he can get rid of it. this would be a pain because these are
minipreps, and the templates (a lot of them) are being used for DNA
sequencing (for mutation screening). Marianne
On 17 Dec 1996, Bernard Murray wrote:
> In article <Pine.SOL.3.95.961217105000.7159A-100000 at chuma>,
> leverone at CHUMA.CAS.USF.EDU says...
> >Hi Group! When we run plasmid minipreps (alkaline lysis), we add RNAse
> >after the white protein/DNA junk has been pelleted and removed from the
> >neutralization step. After a 30 min incubation, the plasmid is then ppt
> >with isopropanol and 70% etOH washed and dried and resuspended in water.
> >Then a gel is run to check for complete RNA removal. Some of our labgroup
> >people are having trouble getting rid of the RNase becasue it shows up as
> >a band (around the 0.5 kb marker) and we have now run enough controls
> >and other tests and have determined that the band is RNase. ANyone else
> >have this problem and how did you solve it? Thanks. Marianne
> I suspect that you are using *way* too much RNase. If this treatment
> is simply to get rid of the smear to aid visualisation on a gel you
> don't have to use very much at all. If you need RNA free DNA you might
> try LiCl or PEG to differentially precipitate the two of them. If you
> have to get rid of large quantities of RNase then phenol/chloroform
> is probably the best way - isopropanol precipitation will help remove
> the ribonucleotides produced by the digestion but the RNase itself
> will almost certainly co-precipitate with the plasmid.
> I don't see any problems with ethidium staining of gels run with
> aliquots digested with 0.1 mg/ml RNase A (final) and you can probably
> go lower than that. How are you staining your gels? - maybe other
> methods are more sensitive to protein contamination.
> Good luck,
> Bernard Murray, Ph.D.
> bernard at elsie.nci.nih.gov (National Cancer Institute, NIH, Bethesda MD, USA)
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