In this complex, single copies of Sec61 and TRAP associate with a nontranslating ribosome and this stoichiometry was verified by quantitative mass spectrometry.
Regulation of subsets of these genes was verified by quantitative PCR in an independent experiment.
Reduction of α-gustducin message was verified by quantitative real time PCR.
The inocula used were verified by quantitative culture on YPD agar.
This enhancement of Aβ1 42 phagocytosis peptides was verified by quantitative immunofluorescence assay (Fig. 1B).
The inocula used for immunizations and challenge were verified by quantitative culture on YPD agar.
The expression pattern of eight miRNAs was verified by quantitative (q) RT-PCR (Fig. 2).
This was verified by quantitative RT-PCR, which showed 5.7-fold upregulation (Fig. 4A).
The differential regulation of the flagellum by temperature and pressure was verified by quantitative RT-PCR (Fig. 7C, D).
Up-regulation of COX-2 and other inflammatory mediators was verified by quantitative real-time PCR (Figure 3).
