Here we measure lysozyme nucleation kinetics using an easy-to-use and simply constructed microfluidics setup previously described. We confirm that microfluidics is a direct, accurate, and fast method to measure nucleation frequency using only a few milligrams of molecules. Moreover, our microfluidics setup, by diminishing crystallizer volumes, increases the experimental supersaturation range accessible and can be applied to all water-soluble molecules.
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Ildefonso et al. (2011) studied this question.
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