Hi,
I have some problems with my folmaldehyde gels which I run to assess RNA quality. I can see two distinct bands for 28S and 18S. However I can also see third faded band above the 28S one. Is my RNa degraded? I was wondering if someone else had this issue. Any suggestions, comments will be apreciated.
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#2
Trof
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Posted 06 October 2010 - 08:10 AM
Do you have a picture?
If your band is above the 28S I assume it's bigger. It could be DNA contamination, RNA degradation would produce smaller fragments and visible decrase of 28S in comparison with 18S.
If your band is above the 28S I assume it's bigger. It could be DNA contamination, RNA degradation would produce smaller fragments and visible decrase of 28S in comparison with 18S.
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#3
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Posted 06 October 2010 - 04:18 PM
Not sure how to attach files.can I send it to you by email? What would DNA contamination do to my RT-PCR results.
Thank you.
Thank you.
#4
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Posted 05 November 2010 - 03:24 PM
Trof, on 06 October 2010 - 08:10 AM, said:
Do you have a picture?
If your band is above the 28S I assume it's bigger. It could be DNA contamination, RNA degradation would produce smaller fragments and visible decrase of 28S in comparison with 18S.
If your band is above the 28S I assume it's bigger. It could be DNA contamination, RNA degradation would produce smaller fragments and visible decrase of 28S in comparison with 18S.
