1981
DOI: 10.1016/0003-2697(81)90243-8
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Improved techniques for the separation of serum lipoproteins by density gradient ultracentrifugation: Visualization by prestaining and rapid separation of serum lipoproteins from small volumes of serum

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Cited by 361 publications
(105 citation statements)
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“…To reduce interassay variation of TC, triglycerides and lipoprotein lipid measurements were performed after the completion of the experiment by using aliquots stored at 770 C. Apo determinations were performed in fresh samples. Lipid determinations from very low density lipoprotein (VLDL), LDL or HDL fractions were performed after their isolation from serum by 21 h density gradient ultracentrifugation at 40 000 rpm (272 000 g) and 8 C in a Beckman L8-70M ultracentrifuge, SW-41 rotor (Palo Alto, California), following the method of Terpstra et al (1981). All determinations were carried out in duplicate.…”
Section: Laboratory Analysesmentioning
confidence: 99%
“…To reduce interassay variation of TC, triglycerides and lipoprotein lipid measurements were performed after the completion of the experiment by using aliquots stored at 770 C. Apo determinations were performed in fresh samples. Lipid determinations from very low density lipoprotein (VLDL), LDL or HDL fractions were performed after their isolation from serum by 21 h density gradient ultracentrifugation at 40 000 rpm (272 000 g) and 8 C in a Beckman L8-70M ultracentrifuge, SW-41 rotor (Palo Alto, California), following the method of Terpstra et al (1981). All determinations were carried out in duplicate.…”
Section: Laboratory Analysesmentioning
confidence: 99%
“…The following fractions were sequentially isolated from the top of the tube: very low-density lipoproteins (VLDLs, fraction 1), low-density lipoproteins (LDLs, fraction 2), Cremophor with unbound GePcs (fraction 3), high-density lipoproteins (HDLs, fraction 4), heavy proteins, including mainly albumin and globulins (fraction 5). The identification of the fractions was performed as described elsewhere (Terpstra et al, 1981). The volume of each fraction was measured, then the fractions were dialysed overnight against physiological solution, diluted with a binary solvent mixture (0.4 ml of 4% aqueous SDS plus 1.5 ml of tetrahydrofuran) and the GePc content was determined using the spectrophotofluorimeter.…”
Section: Animals and Tumourmentioning
confidence: 99%
“…The method of Terpstra et al (1981) was used for separating lipoproteins by ultracentrifugation. Plasma samples were stored at 4°C for periods of up to two days.…”
Section: Sampling Of Blood and Analytical Methodsmentioning
confidence: 99%