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Figure 4 | BMC Biotechnology

Figure 4

From: Isolation of soybean protein P34 from oil bodies using hydrophobic interaction chromatography

Figure 4

Gel-electrophoretic analysis of a two-step elution in column 1. Column 1 was loaded with soybean feedstock mixture (705 μg total protein, 77% of which are P34) in initial binding buffer (1 M (NH4)2SO4 in 0.05 M phosphate buffer, pH 6.5). Elution was performed at 0.6 M and 0.4 M (NH4)2SO4. In the Coomassie-stained polyacrylamide gel, one fraction is represented by one lane: lanes 1 – 4 show the flow-through in binding buffer, lanes 5 – 12 the fractions eluted with 0.6 M (NH4)2SO4 and lanes 13 – 21 the fractions eluted with 0.4 M (NH4)2SO4 and lanes 22 29 represent the fractions eluted in phosphate buffer during the washing step.

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