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Figure Caption
Fig. 2 The aggregation state of recombinant Neu3.2 and Neu3.3. Aliquots of the purified recombinant enzymes (○) were subjected to gel filtration analysis on Superdex 200 HR 10/300. Calibration curve was obtained using the following proteins as molecular weight standards: apoferritin 443 kDa (□), β-amylase 200 kDa (●), alcohol dehydrogenase 150 kDa (■), albumin as monomer 67 kDa (▼) and dimer 134 kDa (▲) and ovalbumin 43 KDa (◆). For details see Material and Methods.
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