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Regulatory T cells license macrophage pro-resolving functions during atherosclerosis regression

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Then, serial dilutions of unlabeled binding partner samples (inhibitor or substrate) were mixed with 0.377 M of dye-labeled TyrBm in 50 mM PBS buffer pH 7.4 and incubated for 5 minutes

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Contaminants in BPC-157 samples directly skew mucosal repair data, which is why researchers rely on high purity peptides for research with independently verified third-party COAs