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Found 3 matching solutions for this experiment
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Cells or tissues were harvested in ProteoJET mammalian cell lysis reagent (Fermentas Life Sciences, Ontario, Canada) or CelLytec MT mammalian tissue lysis-extraction reagent (Sigma) with proteinase inhibitor cocktail (Roche), and protein concentrations were determined with a BCA kit (Pierce, Rockford, IL). |
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Cells or tissues were harvested in ProteoJET mammalian cell lysis reagent (Fermentas Life Sciences, Ontario, Canada) or CelLytec MT mammalian tissue lysis-extraction reagent (Sigma) with proteinase inhibitor cocktail (Roche), and protein concentrations were determined with a BCA kit (Pierce, Rockford, IL). |
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The mesenteric arterioles were homogenized in radioimmunoprecipitation assay (RIPA) buffer (Thermo Fisher Scientific, Inc.) (ratio of 10 mg tissue to 100 µl RIPA buffer) with freshly added protease inhibitor, phenylmethylsulfonyl fluoride (Sigma-Aldrich; Merck Millipore, Darmstadt, Germany). |
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The mesenteric arterioles were homogenized in radioimmunoprecipitation assay (RIPA) buffer (Thermo Fisher Scientific, Inc.) (ratio of 10 mg tissue to 100 µl RIPA buffer) with freshly added protease inhibitor, phenylmethylsulfonyl fluoride (Sigma-Aldrich; Merck Millipore, Darmstadt, Germany). |
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The excised liver tissues or white adipose tissues (including inguinal, periovarian, mesentery, and perirenal fat) were homogenized with tissue protein reagents (T-PER, Pierce Biotechnology, Rockford, IL, USA) and equally quantified before western blotting. |
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The excised liver tissues or white adipose tissues (including inguinal, periovarian, mesentery, and perirenal fat) were homogenized with tissue protein reagents (T-PER, Pierce Biotechnology, Rockford, IL, USA) and equally quantified before western blotting. |
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