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PCR reactions were carried out using 0.5 L of gene-specific cDNA samples and that of 16S rRNA as templates with 1 mM final concentration of each of the forward and reverse RT primers (Additional file 12: Table S5) and 4 L of 2 SYBR green PCR mix in a final volume of 10 L
NishimutaH.SatoK.MizukiY.YabukiM.KomuroS.2010Prediction of the intestinal first-pass metabolism of CYP3A substrates in humans using cynomolgus monkeys.381119671975
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SIGEP Study Group for Autoimmune Disorders in Celiac Disease
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