Accepted answer
Nobody has published a cycle count, and at 1 mg/mL the concentration tells you what a wrong guess costs: a 0.1 mL aliquot holds 0.1 mg and every microlitre is 1 µg. Damage from freezing is not gradual attrition — it is concentrated at the phase transitions, where ice excludes solute and the unfrozen fraction climbs well above 1 mg/mL for as long as the transition lasts. Two slow cycles can therefore do more than four fast ones, which is why a cycle count is the wrong unit in the first place. The way to make the number one is to make it one: split at reconstitution into single-draw aliquots, label each with 1 mg/mL and the date, and never thaw a container you will refreeze.
The short version: aliquot before freezing, thaw slowly, never refreeze a thawed aliquot, and count your cycles.
Let a frozen vial reach room temperature before opening it. Opening a cold vial in humid air condenses water into the cake, which raises residual moisture and undoes what lyophilisation achieved.
Buffer salts crystallise at different points during freezing. Sodium phosphate is the classic example: the dibasic form crystallises first and the pH of the residual liquid falls by several units. That pH excursion is the real damage in many cases.
Cryoconcentration of solutes at the ice front is a well-documented mechanism in freeze-thaw damage to proteins and peptides.
The caveat is that aggregation is invisible in a clear solution below the threshold where it becomes visible.
Aliquot before the first freeze. That is the whole answer.
edited 28 Mar 2025 by marta_okonkwo — fixed an arithmetic slip in the third paragraph