I know protein structure is very susceptible to degradation as a result of multiple freeze-thaw cycles.  But is it a concern for a sugar like LPS?

Asking because I have 50 uL aliquots of LPS and I only use 1 uL at a time.  Wondering if it's worth it to aliquot it further and/or if I should be recording freeze/thaw cycles for each aliquot.

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