ApoB-depleted serum (2 µL) was separated by native gradient gel electrophoresis (4–16% NativePage; Life Technologies, Carlsbad, CA, USA). The gels were run for 120 min at constant voltage of 150 in NativePage running buffer (Life Technologies, Carlsbad, CA, USA). Subsequently, standard (NativeMark, Life Technologies, Carlsbad, CA, USA) of the gels was fixed with 25% isopropanol/10% acetic acid for 10 min and stained with protein staining solution (PageBlue, Thermo Scientific, Waltham, MA, USA). Separated neutral lipids of the samples were stained with Sudan black (Sigma-Aldrich, Darmstadt, Germany). Size distribution of HDL was analyzed using Image Lab software (version 5.2), as described previously [35 (link)].
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