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After deparaffinization, sections were heated in an autoclave at 121 C for 5 min in 10 mM sodium citrate buffer (pH 6.0) or reacted with protease solution (Nichirei Biosciences, Tokyo, Japan) for epitope retrieval, after which endogenous peroxidase was inactivated by 0.3% hydrogen peroxide in methanol

The nature and significance of platelet products in human plasma

Such cases require close follow up for recurrence

Within experimental models, researchers frequently investigate Melanotan II in relation to receptor activation pathways, intracellular signalling mechanisms and peptide-mediated regulatory networks

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