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By gel filtration chromatography, the molecular mass of the enzyme was estimated to be 130 kDa.
(b) Ultracentrifuged cell-free preparations were fractionated by gel filtration chromatography.
The cell-free preparation was incubated with GST-A-CARD or not, and fractionated by using gel filtration chromatography.
(d) Ultracentrifuged cell-free preparations were incubated with recombinant procaspase-3/9-His6, and fractionated by gel filtration chromatography.
After metal affinity, gel filtration chromatography yielded a highly pure 15 kDa gp41-MinTT recombinant protein peak (Fig. 1b).
The 1 1 binding ratio of IL-1α to SL1067 was validated by gel filtration chromatography (Supplementary Fig. 1).
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a, Representative gel-filtration chromatography of NavAb(R3G); highlighted peak fractions were concentrated for crystallization.
Figure 5 Gel-filtration chromatography of ultrafiltrate.
The structure of partially soluble native desmin was studied by gel-filtration chromatography and electron microscopy.
Gel-filtration chromatography of Q-Sepharose FF is shown in Figure 3a.
The ultrafiltrate was subjected to gel-filtration chromatography on Bio-Gel P-2.
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