Hello,

I've been trying to gel purify my full length tRNA many different ways.
With every attempt, I see degradation on my gel that I run to confirm
purification.

Does anyone have any suggestions for methods that I should try which would
not result in degradation of my purified tRNA?

The samples are heated for 3mins at 70C prior to loading on the gel. This
is our standard protocol for tRNA denaturation. Could this be causing my
degradation?

Any suggestions are welcome.
Thank you,
Rachel Schmidt
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