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Splenocytes from -MYC mice and wild-type littermates were isolated as previously described [53] and stained with APC-conjugated rat anti-mouse CD45R/B220 (ref 561880) and PE-conjugated rat anti-mouse CD43 (ref 561857) antibodies, both from BD Biosciences, before flow cytometry analysis with a FACS Canto II flow cytometer (BD Biosciences) employing Kaluza software (Beckman Coulter)
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Experimental studies describe BPC-157 as interacting with signaling pathways linked to vascular endothelial growth factor receptors and nitric-oxidemediated endothelial signaling [1][6][11]
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