I’m trying to separate 20bp circular dsDNA from remaining linear dsDNA post Exonuclease addition.Exonuclease treatment isn’t sufficient as there is relatively large background. I want to ensure the samples are clean from linear dsDNA at a relatively large scale for purity reasons . Gels are not an option as the recovery is low. Any thoughts on MWCO filtration or other size exclusion methods? Apart from conformation the sequences are identical so potential additives would have to distinguish between linear and circular. any suggestions?

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