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Superose hr6 column

Manufactured by GE Healthcare

The Superose HR6 column is a size exclusion chromatography column designed for the separation and purification of proteins, peptides, and other macromolecules. It features a high-resolution (HR) matrix that provides efficient separation over a wide molecular weight range.

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2 protocols using superose hr6 column

1

Lipoprotein Fractionation by Size-Exclusion Chromatography

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Plasma lipoproteins were fractionated by size-exclusion chromatography (SEC, Superose HR6 column, GE Health) as previously described [27 (link)]. Cholesterol and TG concentrations of each fraction were determined enzymatically using commercial kits (Wako Diagnostics) and expressed as mg/dL in each fraction or percent of TG and cholesterol of each fraction in total fractions [27 (link)].
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2

Fatty Acid Profiling and Lipoprotein Analysis

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For FA profiling by GC-MS, plasma samples from mice were hydrolyzed with 0.5% NaOH for 2 h and then delipidated by organic solvent extraction (CHCl3-CH3OH, 2:1, v/v) to yield total hydrolyzed FAs. In addition, split plasma samples were also analyzed by GC-MS for nonesterified FAs (NEFAs). Both total FAs and NEFAs were derivatized with methanol-acetyl chloride (50:1 (v/v)) to yield methylated FAs. FA methyl esters were analyzed by gas chromatography on a fused silica capillary column (Alltech, Deerfield, IL.; 30 m × 0.25 mm × 0.25 μm film). Analysis was performed on a Hewlett-Packard 6890GC coupled to a 5973 Mass Selective Detector as previous described.18 (link), 19 (link) Dietary FA composition was also examined by the above procedure.
Plasma lipoprotein profiles were determined by size exclusion chromatography (SEC, Superose HR6 column; GE Health) of 200 μL plasma per mouse as previously described.20 (link) Cholesterol and TG concentrations of each fraction were determined enzymatically (Wako Diagnostics).
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