When I do the QC for my bead cleaned-up pre-amplified cDNA (Smartseq2) using AATI fragment analyzer and bioanalyzer, the concentration was very low (0.01ng/uL) and almost no peaks. But when I measured the same samples using Qubit, I got about 0.1ng/uL. Why are these methods giving different concentrations? Thanks!
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Originally posted by cmbetts View PostThe FA/BA is probably a more accurate measurement (although I trust qubit more for concentrations >1ng/ul). It's easy to get background readings of 0.1-0.3ng/ul by qubit. Did you run a negative control for comparison?
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