Sharper separation of lipoprotein species by paper electrophoresis in albumin-containing buffer.
RS Lees, FT Hatch - Journal of Laboratory and Clinical Medicine, 1963 - cabdirect.org
RS Lees, FT Hatch
Journal of Laboratory and Clinical Medicine, 1963•cabdirect.orgElectrophoresis was at 110 V for 16 h with barbital buffer, pH 8.6, containing albumin and
0.001 M ethyl-enediamine tetra-acetate and staining was with oil red O. Resolution was best
with 1% albumin (w: v) and the method was particularly suitable for very low density
lipoproteins.-A. Hepburn.
0.001 M ethyl-enediamine tetra-acetate and staining was with oil red O. Resolution was best
with 1% albumin (w: v) and the method was particularly suitable for very low density
lipoproteins.-A. Hepburn.
Abstract
Electrophoresis was at 110 V for 16 h with barbital buffer, pH 8.6, containing albumin and 0.001 M ethyl-enediamine tetra-acetate and staining was with oil red O. Resolution was best with 1% albumin (w: v) and the method was particularly suitable for very low density lipoproteins.-A. Hepburn.
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