Dear members,

We are planing to purify RNA only or/and RNA-protein complex on FPLC. The
application of the purified materials is for crystallization. However, our
concern is that our FPLC has been frequently used in bacterial expressing
protein purification including purifying proteins from crude lysate, which
is contaminated by RNase. Do you have experience of completely cleaning up
the system before conducting the RNA work? Or it is impossible for 100%
cleaning and we have to use a separate FPLC for this purpose?

Thank you.

Best regards,
Wim

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