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Beckman scintillation counter

Manufactured by PerkinElmer

The Beckman scintillation counter is a laboratory instrument used for the detection and quantification of radioactive samples. It measures the emission of light, or scintillations, produced when ionizing radiation interacts with a scintillation material. The instrument is designed to provide accurate and reliable measurements of radioactive samples.

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2 protocols using beckman scintillation counter

1

Quantifying Lactobacillus Fatty Acid Uptake

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Fatty acid consumption of Lactobacillus strains, L. rhamnosus GG (ATCC 53103), L. acidophilus (ATCC 4356), and L. gasseri (ATCC 33323) in bacterial growth medium was evaluated quantitatively using radioactive tracers, [14C]-OA and [14C]-palmitic acid (PA) (PerkinElmer, Waltham, MA). The glucose concentration in each bacterial medium was measured using a GM9 glucose analyzer (Analox Instruments, London, UK). Overnight cultures of Lactobacillus were diluted 100-fold (v/v) and subcultured three times to achieve viability, as described previously27 (link). [14C]-OA (1 µci) was added to 10 ml of MRS growth medium at 20 g/l, and three Lactobacillus strains (1x108 cfu of each strain) were cultured for 6 h with shaking (37 °C at 220 rpm). For L. rhamnosus GG, 1 μci of [14C]-OA and [14C]-PA were further tested. One milliliter of cultured broth was aliquoted every 3 h and centrifuged (10 min, 4000×g), and the supernatant was collected. The pellet was resuspended and washed three times in MRS broth (10 min, 4000×g). 14C radioactivity was measured in both the supernatant and pellet of each aliquoted sample using a β-counter (Beckman scintillation counter, PerkinElmer, Waltham, MA).
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2

Tissue-Specific Fatty Acid Oxidation

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Tissue-specific fatty acid oxidation was measured by the production of 14CO2 from [1-14C]oleic acid (0.3 μCi/mL), with unlabeled oleate present in the medium as previously reported with minor modification (10 (link)). Mice were fed HFD for 6 weeks and fasted overnight. Soleus, extensor digitorum longus, and tibialis anterior muscles and liver tissue were weighed and placed in 50-mL glass flasks. The flasks had an isolated center well containing 1 N NaOH to trap 14CO2. After 30 min of incubation at 37°C, the medium was acidified with 1 mL of 0.5 N sulfuric acid to stop the reaction. Flasks were then held at 50°C for an additional 3 h. The 14C activity of the contents in the center well was counted in scintillation cocktail (Ultima Gold; PerkinElmer) by using a β-counter (Beckman Scintillation Counter; PerkinElmer).
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