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1 14c linoleic acid

Manufactured by PerkinElmer

1-14C-linoleic acid is a radioactive tracer used for research purposes. It is a labeled form of the essential fatty acid linoleic acid, with the carbon-14 isotope incorporated at the first carbon position. This product is intended for use in scientific investigations, but a detailed description of its specific applications is not available within the scope of this request.

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3 protocols using 1 14c linoleic acid

1

Rat Cardiomyocyte Lipid Metabolism

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Cardiac myocytes were prepared from the hearts of control and PVR pups as described [16 (link)]. The protocol allows for rat cardiomyocytes to be cultured for up to 72 h at 37°C in 5% CO2 without significant change in phenotype [17 (link)]. Enough hearts were collected to yield approximately 15-20million cardiac myocytes sufficient to plate 15–20 x 35mm dishes (1 million/dish, Corning PrimeriaTM). Isolated cardiac myocytes were incubated with 0.1 mM [1,3-3H]glycerol (2 μCi/dish, Perkin Elmer) or 0.1 μM [1-14C]linoleic acid (2 μCi/dish, Perkin Elmer) bound to albumin (1:1 molar ratio) or 0.1 μM [1-14C]oleic acid (2 μCi/dish Perkin Elmer) bound to albumin (1:1 molar ratio) for up to 360 min (6 h) and radioactivity incorporated into phospholipids determined as previously described [18 (link)].
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2

Fatty Acid Oxidation Measurement

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Fatty acid oxidation was measured according to previous publication 37 . 1-14C-linoleic acid and 1-14C-palmitic acid were purchased from PerkinElmer. Briefly, isolated CD4+ or CD8+ T lymphocytes were pretreated with linoleic acid or kept in regular media. After 24 hrs. cell media was changed to media containing 50 μM cold linoleic acid plus 1μCi 1-14C-linoleic acid/ml or 50 μM cold palmitic acid plus 1μCi 1-14C-palmitic acid /ml. After 2 hours medium was removed and mixed with concentrated perchloric acid (final concentration 0.3M) plus BSA (final concentration 2%) to precipitate the radiolabeled fatty acids. Samples were vortexed and centrifuged (10,000x g for 10 min). Radioactivity was determined in the supernatant to measure water-soluble β-oxidation products.
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3

Fatty Acid Oxidation Measurement

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Fatty acid oxidation was measured according to previous publication 37 . 1-14C-linoleic acid and 1-14C-palmitic acid were purchased from PerkinElmer. Briefly, isolated CD4+ or CD8+ T lymphocytes were pretreated with linoleic acid or kept in regular media. After 24 hrs. cell media was changed to media containing 50 μM cold linoleic acid plus 1μCi 1-14C-linoleic acid/ml or 50 μM cold palmitic acid plus 1μCi 1-14C-palmitic acid /ml. After 2 hours medium was removed and mixed with concentrated perchloric acid (final concentration 0.3M) plus BSA (final concentration 2%) to precipitate the radiolabeled fatty acids. Samples were vortexed and centrifuged (10,000x g for 10 min). Radioactivity was determined in the supernatant to measure water-soluble β-oxidation products.
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