Q:Alternative to RNAse protection
nicholas_theodorakis at urmc.rochester.edu
Fri Oct 29 08:58:09 EST 1999
In article <7vbqon$e8o$1 at nnrp1.deja.com>, ttu00k at sp2.power.uni-essen.de
> We have determined three different transcription start sites for a
> and now want to quantify the relative abundance of transcripts
> from each
> of the starting points. Since we wanted to avoid, if possible,
> establishing quantitative RT-PCR or RNAse protection is anybody
> aware of
> a "simple" technique to answer this question?
> Many thanks in advance.
> Alexander Schramm
> Universitätsklinikum Essen
> Innere Klinik/Tumorforschung
> Sent via Deja.com http://www.deja.com/
> Before you buy.
You could try primer extension. The "Big Red Book" has a reasonable
protocol, and it's pretty "simple."
Also, you could try S1 nuclease protection, but I don't know if you
would have the same objection to it as to whatever you're objection is
to RPA, since they are similar.
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