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H.HolmanR
The resulting 2.5% SSA plasma supernatant was collected and mixed 1:2.5 with assay buffer to produce a final dilution of 1:5 before assaying
Factor SA, Wolski K, Togasaki DM, et al
Published clinical studies have evaluated investigational retatrutide under controlled research conditions, but those findings should not be interpreted as evidence that this research product is approved for patient care
N Engl J Med 1997;337:5818.PubMed 15
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