How to check RNA quality - (Sep/30/2010 )
Hi,
I'm extracting RNA from quite old (2 years) and small FFPE slides, for gene expression analysis on qPCR.
So i first want to check my RNA quality before performing qPCR since RNA quality has a profound impact on the results.
Does anyone performed/know some assays to determine RNA quality?
Thanks in advance
greetz
If you have access to a Bioanalyser machine, they are excellent for checking RNA quality. I think you can also run formaldehyde agarose gels but am not certain as I never had to do it myself.
As a general point, see if you can find any papers referring to RNA extraction from your organism of interest; they usually include an image of the RNA run out on a gel (so if yours looks like theirs, it's probably ok) and describe how they assessed the quality of their RNA.
Hope this helps,
hannama
Agilent bioanalyzer if you have it.
If you don't (like me), then try denaturing gel electrophoresis, we prepare it like this:
normal 1% agarose gel with EtBr in it
Load with:
3 ul running buffer (same as for electrophoresis, we use 0.5x TBE)
2 ul 6x loading buffer (contains 30% glycerol and 0.05% bromphenol blue or/and other Elfo dyes)
1.8 ul formamide
1 ul RNA
And look for two bands of 28S and 18S, which should have ratio around 2. More about it (with pictures) in Ambion note.
and the nanodrop? Can that one be used too?
Trof on Thu Sep 30 15:40:40 2010 said:
Agilent bioanalyzer if you have it.
If you don't (like me), then try denaturing gel electrophoresis, we prepare it like this:
normal 1% agarose gel with EtBr in it
Load with:
3 ul running buffer (same as for electrophoresis, we use 0.5x TBE)
2 ul 6x loading buffer (contains 30% glycerol and 0.05% bromphenol blue or/and other Elfo dyes)
1.8 ul formamide
1 ul RNA
And look for two bands of 28S and 18S, which should have ratio around 2. More about it (with pictures) in Ambion note.
Nanodrop only tells you how many nucleotides you have in your samples and how pure it is. It doesn't tell anything about their condition, if they are degraded or not.
why not try to check the OD280 260?
and reextracted RNA from your extracted RNA.
I am a junior student, hope this simple words would work.