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Soybean oil

Manufactured by Oriental Yeast
Sourced in Japan

Soybean oil is a laboratory equipment product used for various applications. It is a vegetable oil derived from the seeds of the soybean plant. The core function of soybean oil is to serve as a lubricant, solvent, or sample preparation agent in laboratory settings.

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3 protocols using soybean oil

1

Dietary Composition Analysis Protocol

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Milk casein, corn starch, α-corn starch, mineral AIN-93G mixture and vitamin AIN-93VX mixture were purchased from Clea Japan (Osaka, Japan). Soybean oil and lard were purchased from Oriental Yeast (Tokyo, Japan) and Yamakei (Osaka, Japan), respectively. OPZ was purchased from LKT Laboratories, Inc. (St. Paul, MN) and all other chemicals were purchased from Wako Pure Chemical Industries (Osaka, Japan), unless noted.
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2

Dietary Modulation of Cholesterol Metabolism

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Milk casein, corn starch, α-corn starch, mineral AIN-93 mixture and vitamin AIN-93 VX mixture were purchased from CLEA Japan (Osaka, Japan). Soybean oil and lard were purchased from Oriental Yeast (Tokyo, Japan) and Yamakei (Osaka, Japan), respectively. Ezetimibe was kindly provided by Schering-Plough Co., Ltd. (Osaka, Japan). All other chemicals were purchased from Wako Pure Chem. Ind., Ltd. (Osaka, Japan), unless noted.
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3

Dietary Fatty Acid Effects on Mice

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Four-week-old male ICR mice were placed in one of 4 experimental groups and were fed one of the following diets for 28 days: (1) Soybean oil diet. Soybean oil (Nisshin OilliO, Tokyo, Japan) was added to AIN-93G (a standard purified diet without fat, Oriental Yeast Co. Ltd., Tokyo, Japan) at a final concentration of 7% (w/w). (2) Cottonseed oil diet. Cottonseed oil (Nisshin OilliO) was added to AIN-93G at a final concentration of 7% (w/w). (3) Cottonseed oil diet supplemented with DHA. DHA was added to a cottonseed oil diet at a final concentration of 4% (w/w) of total fat. (4) Cottonseed oil diet supplemented with DHA with the administration of letrozole. The mice were fed a cottonseed oil diet supplemented with DHA. Letrozole was suspended in a 0.5% (w/v) methylcellulose 400 and intraperitoneally injected (10 mg/kg) every other day during the intake of the diet. The chow was maintained at −30 °C until use. Experiments shown in Figs 13 were performed using (1–3) treatment groups, while those shown in Figs 4 and 5 were done with (1–4) treatment groups.
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