Itation at 488 nm and emission at 585 nm. MAGPIX system. Phycoerythrin with excitation at 488 nm and emission at 585 nm.Analytica 2021, 2, FOR PEER Evaluation Analytica 2021,6The two assays enabled us to profile levels of ARG1 and miR-122 in a DILI patient. The two Table enabled us to profile levels of ARG1 high levels inside a DILI patient. As As reported in assays S4, the patient with DILI presentedand miR-122of both ARG1 and reported in Table S4, the patient with DILI presented higher levels of both ARG1 and miR-122, miR-122, when, and as anticipated, the no DILI patient didn’t show important levels of whilst, and as miR-122. the no DILI patient did not show considerable levels of either ARG1 either ARG1 or anticipated,ARG1 and miR-122 levels have been quantified making use of the two calibraor miR-122. ARG1 with the information reported in Tables S2 and S3, respectively. Levels of tion curves generatedand miR-122 levels have been quantified making use of the two calibration curves generated with all the information reported in Tables S2 and S3, respectively. Levels Xanthoangelol Apoptosis Figure 2. ARG1 and miR-122 have been extrapolated and reported in Table S4 and shown inof ARG1 and miR-122 had been extrapolated and reported in Table S4 and shown in Figure 2.Figure 2. ARG1 and miR-122 calibration curves with interpolated ARG1 and miR-122 from DILI Figure 2. ARG1 and miR-122 calibration curves with interpolated ARG1 and miR-122 from DILI samples. Error bars ( s.d.) depending on triplicate measurements. The error bars are smaller than the samples. Error bars ( s.d.) based on triplicate measurements. The error bars are smaller than the size of some information points. n = 3. size of some data points. n = 3.3.two. Tridecanedioic acid Autophagy seqCOMBO Assay–Analysis of ARG1 and miR-122 Simultaneously 3.two. SeqCOMBO Assay–Analysis of ARG1 and miR-122 simultaneously The two individual assays described in Figure 1a,b have been combined delivering the The two to profile assays described the levels of ARG1 combined delivering the seqCOMBOindividual in the identical time in Figure 1a,b had been and miR-122 inside the serum seqCOMBO a DILI patient. As shown in Figure three,of ARG1 and miR-122 within the serum of nine sample of to profile in the similar time the levels the seqCOMBO workflow consists sample of asteps. patient. As shown in Figure three, the seqCOMBO workflow consists of nine major DILI primary steps.seqCOMBO enables profiling levels of ARG1 and miR-122 within the DILI patient. Because the The seqCOMBO and shown in Figure 2, the patient with DILI within the DILI patient. reported in Table S4enables profiling levels of ARG1 and miR-122 presented high levels As reported in Table S4 and shown in Figure 2,expected, the noDILI presented high levels of each ARG1 and miR-122, even though, and as the patient with DILI manage didn’t show ofsignificant levels of ARG1 or miR-122. No signal loss was no DILI controlboth protein and each ARG1 and miR-122, while, and as anticipated, the observed when did not show significantwere analysed via seqCOMBO at the exact same time. observed when both protein miRNA levels of ARG1 or miR-122. No signal loss was and miRNA had been analysed via seqCOMBO at the exact same time. seqCOMBO is employed, an interTo compare how the signal varies when singleplex or CVTo comparegenerated, comparing the MFI signals obtained for person analysis vs. study was how the signal varies when singleplex or seqCOMBO is utilised, an interCV study was generated,in Table 1. TheseMFI signals obtainedthe MILIPLEX xMAP kit can seqCOMBO, as shown comparing the outcomes indicate that for individual analysis vs. seqCOMBO, together with the DCL met.