Hi all
I've run these TruSeq RNA libraries I received on the Bioanalyser HS Kit and they appear to be have strange peaks, almost as if there was a ladder contamination (although the peaks don't correlate with the HS ladder sizes). I've run these samples twice now, preparing fresh gel-dye and using a new tube of marker, but I get the same traces.
Has anyone got any explanations?
I've run these TruSeq RNA libraries I received on the Bioanalyser HS Kit and they appear to be have strange peaks, almost as if there was a ladder contamination (although the peaks don't correlate with the HS ladder sizes). I've run these samples twice now, preparing fresh gel-dye and using a new tube of marker, but I get the same traces.
Has anyone got any explanations?
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