11 February 2021 1 9K Report

I am using this column with a gradient of acetonitrile vs a phosphate buffer. I clean the column after every run with 2%ACN:98%H20 and store in 30% ACN. I've noticed that my peaks are getting broader as I continue using the column. How do I maintain resolution of my peaks? Am I missing a cleaning step or is there another column I can use?

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