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Here, we also present a modified version of the triolein-based substrate assay to answer specific research questions pertaining to the relative abundance of circulating factors that may inhibit LPL
As a complementary approach to probing the Arr pathway, we quantified agonist-induced GLP-1R internalization using human embryonic kidney (HEK) 293 cells stably expressing a fluorogen-activated protein (FAP)-tagged version of the human GLP-1R (Fig
TMG for glutathione synthesis
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