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Research from the original patent holders of BPC-157 suggests the arginate form can boost oral bioavailability from less than 3% to greater than 90%

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We may speculate that this study provides an insight into how zinc sufficiency is important for BHMT functionality, since BHMT is a zinc dependent enzyme that catalyses the transmethylation of homocysteine to methionine in the presence of the methyl group donor betaine