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Therefore, we measured oxLDL levels in the serum.
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The OxLDL and malondialdehyde-modified low-density lipoprotein (MDA-LDL) levels were measured (oxLDL, Kyowa Medics, Japan; n = 13 and MDA-LDL enzyme-linked immunosorbent assay, SRL, Japan; n = 19).
At first we measured plasma oxLDL levels of FH patients and healthy controls using ELISA, which were significantly increased in homozygous FH patients.
Because apocynin is known to be an NADPH oxidase inhibitor, we examined ROS activity by measuring serum oxLDL levels, and the number of 8‐oxo‐dG adducts per nucleoside in the adipose tissue was quantified by LC‐MS/MS.
Different procedures and kits are available for measuring oxLDL and oxLDL antibodies, and our results represent parameters measured according to the protocols described in the methodology section.
21 Mouse serum oxLDL levels were measured using an ELISA kit (USCN Life Science, Hubei, China) according to the manufacturer's protocol.
OxLDL levels were measured using a competitive enzyme-linked immunosorbent assay (ELISA) kit (Mercodia AB, Uppsala, Sweden).
To investigate the association of the + 3953 IL-1B gene polymorphism in healthy subjects with serum oxidized LDL (oxLDL) levels.
Interestingly, oxidized low-density lipoprotein (oxLDL) levels in obese athletes were reduced and associated with higher adiponectin levels, in contrast to increased levels of oxLDL found in the group of lean-elite athletes [114].
We did not detect any significant differences in oxLDL levels between ApoE−/− and ApoE−/− Nrf2−/− mice (Fig. 4A).
Human anti-oxLDL antibodies play an important role in the regulation of oxLDL levels.
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