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If you think you will be purifying the same exact protein again in the future, then you should rinse your elution buffer out with a few column volumes of deionized water (dIH 2 O), and then store the beads in 20% ethanol until youre ready to use them again
Furthermore, the synthesis of such compounds may help in understanding the chemistry at the active site of GPx
Yadlapati R, Dakhoul L, Pandolfino JE, et al
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My Experience: Studying in the first year of a masters degree in Plant Integrative Biology and Breeding in France, I had to do a two-month internship to complete my school year
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