FAQ: I would like to clean up ~1 mg of RNA. Would it be better to use multiple 500 µg columns (NEB #T2050/#T2057) or a single 3 mg column (NEB #T2060/#T2067)?

A few factors should be taken into consideration for ~1 mg RNA input before choosing multiple 500 µg columns vs. a single 3 mg column:

  1. Input Sample Volume. If the starting RNA input volume > 800 µl, it is advisable to use multiple 500 µg columns due to their compatibility with a vacuum manifold. The 3 mg columns are not compatible with a vacuum manifold and require centrifugation for sample loading.

  2. Required Eluate Concentration. 500 µg columns are compatible with elution volumes 50–100 µl (for ~1 mg input, yielding ~5–10 µg/µl eluate concentration). 3 mg columns are compatible with elution volumes 250–500 µl (for ~1 mg input, yielding in ~2–4 µg/µl eluate concentration).

  3. Inaccurate quantification of starting concentration. If the starting sample concentration or input amount is not accurately known, such as RNA synthesized using high yield/scaled-up in vitro transcription (IVT) reactions, the 3 mg columns provide the flexibility to capture input amounts > 500 µg in one column, without the risk of inadvertent RNA loss.